Summary of medicine characteristics - Emtricitabine/Tenofovir disoproxil Krka
1. NAME OF THE MEDICINAL PRODUCT
Emtricitabine/Tenofovir disoproxil Krka 200 mg/245 mg film-coated tablets
2. QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains 200 mg of emtricitabine and 245 mg of tenofovir disoproxil (equivalent to 300.7 mg of tenofovir disoproxil succinate or 136 mg of tenofovir).
Excipient(s) with known effect
Each film-coated tablet contains 80 mg lactose monohydrate.
For the full list of excipients, see section 6.1.
3. PHARMACEUTICAL FORM
Film-coated tablet (tablet).
Emtricitabine/Tenofovir disoproxil Krka film coated tablets are blue, oval, biconvex tablets, of dimensions 20 mm x 10 mm.
4. CLINICAL PARTICULARS4.1 Therapeutic indications
Treatment of HIV-1 infection
Emtricitabine/Tenofovir disoproxil Krka is indicated in antiretroviral combination therapy for the treatment of HIV-1 infected adults (see section 5.1).
Emtricitabine/Tenofovir disoproxil Krka is also indicated for the treatment of HIV-1 infected adolescents, with NRTI resistance or toxicities precluding the use of first line agents (see sections 4.2, 4.4 and 5.1).
Pre-exposure prophylaxis (PrEP)
Emtricitabine/Tenofovir disoproxil Krka is indicated in combination with safer sex practices for preexposure prophylaxis to reduce the risk of sexually acquired HIV-1 infection in adults and adolescents at high risk (see sections 4.2, 4.4 and 5.1).
4.2 Posology and method of administration
Emtricitabine/Tenofovir disoproxil Krka should be initiated by a physician experienced in the management of HIV infection.
Posology
Treatment of HIV in adults and adolescents aged 12 years and older, weighing at least 35 kg: One tablet, once daily.
Prevention of HIV in adults and adolescents aged 12 years and older, weighing at least 35 kg: One tablet, once daily.
Separate preparations of emtricitabine and tenofovir disoproxil are available for treatment of HIV-1 infection if it becomes necessary to discontinue or modify the dose of one of the components of Emtricitabine/Tenofovir disoproxil Krka. Please refer to the Summary of Product Characteristics for these medicinal products.
If a dose of Emtricitabine/Tenofovir disoproxil Krka is missed within 12 hours of the time it is usually taken, Emtricitabine/Tenofovir disoproxil Krka should be taken as soon as possible and the normal dosing schedule should be resumed. If a dose of Emtricitabine/Tenofovir disoproxil Krka is missed by more than 12 hours and it is almost time for the next dose, the missed dose should not be taken and the usual dosing schedule should be resumed.
If vomiting occurs within 1 hour of taking Emtricitabine/Tenofovir disoproxil Krka, another tablet should be taken. If vomiting occurs more than 1 hour after taking Emtricitabine/Tenofovir disoproxil Krka a second dose should not be taken.
Special populations
Elderly
No dose adjustment is required (see section 5.2).
Renal impairment
Emtricitabine and tenofovir are eliminated by renal excretion and the exposure to emtricitabine and tenofovir increases in individuals with renal dysfunction (see sections 4.4 and 5.2).
Adults with renal impairment
Emtricitabine/Tenofovir disoproxil Krka should only be used in individuals with creatinine clearance (CrCl) <80 mL/min if the potential benefits are considered to outweigh the potential risks. See Table 1.
Table 1: Dosing recommendations in adults with renal impairment
| Treatment of HIV-1 infection | Pre-exposure prophylaxis | |
| Mild renal impairment (CrCl 50–80 mL/min) | Limited data from clinical studies support once daily dosing (see section 4.4). | Limited data from clinical studies support once daily dosing in HIV-1 uninfected individuals with CrCl 60–80 mL/min. Use is not recommended in HIV-1 uninfected individuals with CrCl < 60 mL/min as it has not been studied in this population (see sections 4.4 and 5.2). |
| Moderate renal impairment (CrCl 3049 mL/min) | Administration every 48 hours is recommended based on modelling of single-dose pharmacokinetic data for emtricitabine and tenofovir disoproxil in non-HIV infected subjects with varying degrees of renal impairment (see section 4.4). | Not recommended for use in this population. |
| Severe renal impairment (CrCl < 30 mL/min) and haemodialysis patients | Not recommended because appropriate dose reductions cannot be achieved with the combination tablet. | Not recommended for use in this population |
Paediatrics with renal impairment
Not recommended for use in individuals under the age of 18 years with renal impairment (see section 4.4).
Hepatic impairment
No dose adjustment is required in patients with hepatic impairment (see sections 4.4 and 5.2).
Paediatric population
The safety and efficacy of emtricitabine/tenofovir disoproxil in children under the age of 12 years have not been established (see section 5.2).
Method of administration
Oral administration. It is preferable that Emtricitabine/Tenofovir disoproxil Krka is taken with food.
The film-coated tablet can be disintegrated in approximately 100 mL of water, orange juice or grape juice and taken immediately.
4.3 Contraindications
Hypersensitivity to the active substances or to any of the excipients listed in section 6.1.
Use for pre exposure prophylaxis in individuals with unknown or positive HIV 1 status.
4.4 Special warnings and precautions for use
Transmission of HIV
While effective viral suppression with antiretroviral therapy has been proven to substantially reduce the risk of sexual transmission, a residual risk cannot be excluded. Precautions to prevent transmission of HIV by infected individuals should be taken in accordance with national guidelines.
Patients with HIV-1 harbouring mutations
Emtricitabine/Tenofovir disoproxil Krka should be avoided in antiretroviral-experienced patients with HIV-1 harbouring the K65R mutation (see section 5.1).
Overall HIV-1 infection prevention strategy
Emtricitabine/tenofovir disoproxil is not always effective in preventing the acquisition of HIV-1. The time to onset of protection after commencing Emtricitabine/Tenofovir disoproxil Krka is unknown. Emtricitabine/Tenofovir disoproxil Krka should only be used for pre-exposure prophylaxis as part of an overall HIV-1 infection prevention strategy including the use of other HIV-1 prevention measures (e.g. consistent and correct condom use, knowledge of HIV-1 status, regular testing for other sexually transmitted infections).
Risk of resistance with undetected HIV-1 infection
Emtricitabine/Tenofovir disoproxil Krka should only be used to reduce the risk of acquiring HIV-1 in individuals confirmed to be HIV negative (see section 4.3). Individuals should be re-confirmed to be HIV-negative at frequent intervals (e.g. at least every 3 months) using a combined antigen/antibody test while taking Emtricitabine/Tenofovir disoproxil Krka for pre-exposure prophylaxis.
Emtricitabine/Tenofovir disoproxil Krka alone does not constitute a complete regimen for the treatment of HIV-1 and HIV-1 resistance mutations have emerged in individuals with undetected HIV-1 infection who are only taking Emtricitabine/Tenofovir disoproxil Krka.
If clinical symptoms consistent with acute viral infection are present and recent (< 1 month) exposures to HIV-1 are suspected, use of Emtricitabine/Tenofovir disoproxil Krka should be delayed for at least one month and HIV-1 status reconfirmed before starting Emtricitabine/Tenofovir disoproxil Krka for pre-exposure prophylaxis.
Importance of adherence
The effectiveness of Emtricitabine/Tenofovir disoproxil Krka in reducing the risk of acquiring HIV-1 is strongly correlated with adherence as demonstrated by measurable drug levels in blood (see section 5.1). HIV-1 uninfected individuals should be counselled at frequent intervals to strictly adhere to the recommended Emtricitabine/Tenofovir disoproxil Krka dosing schedule.
Patients with hepatitis B or C virus infection
HIV-1 infected patients with chronic hepatitis B or C treated with antiretroviral therapy are at an increased risk for severe and potentially fatal hepatic adverse reactions. Physicians should refer to current HIV treatment guidelines for the management of HIV infection in patients co-infected with hepatitis B virus (HBV) or hepatitis C virus (HCV).
The safety and efficacy of emtricitabine/tenofovir disoproxil for pre-exposure prophylaxis in patients with HBV or HCV infection has not been established.
In case of concomitant antiviral therapy for hepatitis B or C, please refer also to the relevant Summary of Product Characteristics for these medicinal products. See also under Use with ledipasvir and sofosbuvir or sofosbuvir and velpatasvir below.
Tenofovir disoproxil is indicated for the treatment of HBV and emtricitabine has shown activity against HBV in pharmacodynamic studies but the safety and efficacy of emtricitabine/tenofovir disoproxil have not been specifically established in patients with chronic HBV infection.
Discontinuation of Emtricitabine/Tenofovir disoproxil Krka therapy in patients infected with HBV may be associated with severe acute exacerbations of hepatitis. Patients infected with HBV who discontinue Emtricitabine/Tenofovir disoproxil Krka should be closely monitored with both clinical and laboratory follow-up for at least several months after stopping treatment. If appropriate, resumption of hepatitis B therapy may be warranted. In patients with advanced liver disease or cirrhosis, treatment discontinuation is not recommended since post-treatment exacerbation of hepatitis may lead to hepatic decompensation.
Liver disease
The safety and efficacy of emtricitabine/tenofovir disoproxil have not been established in patients with significant underlying liver disorders. The pharmacokinetics of tenofovir has been studied in patients with hepatic impairment and no dose adjustment is required. The pharmacokinetics of emtricitabine has not been studied in patients with hepatic impairment. Based on minimal hepatic metabolism and the renal route of elimination for emtricitabine, it is unlikely that a dose adjustment would be required for Emtricitabine/Tenofovir disoproxil Krka in patients with hepatic impairment (see sections 4.2 and 5.2).
HIV-1 infected patients with pre-existing liver dysfunction, including chronic active hepatitis, have an increased frequency of liver function abnormalities during combination antiretroviral therapy (CART) and should be monitored according to standard practice. If there is evidence of worsening liver disease in such patients, interruption or discontinuation of treatment must be considered.
Renal and bone effects in adults
Renal effects
Emtricitabine and tenofovir are primarily excreted by the kidneys by a combination of glomerular filtration and active tubular secretion. Renal failure, renal impairment, elevated creatinine, hypophosphataemia and proximal tubulopathy (including Fanconi syndrome) have been reported with the use of tenofovir disoproxil (see section 4.8).
Renal monitoring
Prior to initiating Emtricitabine/Tenofovir disoproxil Krka for the treatment of HIV-1 infection or for use in pre-exposure prophylaxis, it is recommended that creatinine clearance is calculated in all individuals.
In individuals without risk factors for renal disease, it is recommended that renal function (creatinine clearance and serum phosphate) is monitored after two to four weeks of use, after three months of use and every three to six months thereafter.
In individuals at risk for renal disease more frequent monitoring of renal function is required.
See also under Co-administration o f other medicinal products below.
Renal management in HIV-1 infected patients
If serum phosphate is < 1.5 mg/dL (0.48 mmol/L) or creatinine clearance is decreased to < 50 mL/min in any patient receiving Emtricitabine/Tenofovir disoproxil Krka, renal function should be reevaluated within one week, including measurements of blood glucose, blood potassium and urine glucose concentrations (see section 4.8, proximal tubulopathy). Consideration should be given to interrupting treatment with Emtricitabine/Tenofovir disoproxil Krka in patients with creatinine clearance decreased to < 50 mL/min or decreases in serum phosphate to < 1.0 mg/dL (0.32 mmol/L). Interrupting treatment with Emtricitabine/Tenofovir disoproxil Krka should also be considered in case of progressive decline of renal function when no other cause has been identified.
Renal safety with emtricitabine/tenofovir disoproxil has only been studied to a very limited degree in HIV-1 infected patients with impaired renal function (creatinine clearance < 80 mL/min). Dose interval adjustments are recommended for HIV-1 infected patients with creatinine clearance 30–49 mL/min (see section 4.2). Limited clinical study data suggest that the prolonged dose interval is not optimal and could result in increased toxicity and possibly inadequate response. Furthermore, in a small clinical study, a subgroup of patients with creatinine clearance between 50 and 60 mL/min who received tenofovir disoproxil in combination with emtricitabine every 24 hours had a 2–4-fold higher exposure to tenofovir and worsening of renal function (see section 5.2). Therefore, a careful benefitrisk assessment is needed when Emtricitabine/Tenofovir disoproxil Krka is used in patients with creatinine clearance < 60 mL/min, and renal function should be closely monitored. In addition, the clinical response to treatment should be closely monitored in patients receiving Emtricitabine/Tenofovir disoproxil Krka at a prolonged dosing interval. The use of Emtricitabine/Tenofovir disoproxil Krka is not recommended in patients with severe renal impairment (creatinine clearance < 30 mL/min) and in patients who require haemodialysis since appropriate dose reductions cannot be achieved with the combination tablet (see sections 4.2 and 5.2).
Renal management in pre-exposure prophylaxis
Emtricitabine/tenofovir disoproxil has not been studied in HIV-1 uninfected individuals with creatinine clearance < 60 mL/min and is therefore not recommended for use in this population. If serum phosphate is < 1.5 mg/dL (0.48 mmol/L) or creatinine clearance is decreased to < 60 mL/min in any individual receiving Emtricitabine/Tenofovir disoproxil Krka for pre-exposure prophylaxis, renal function should be re-evaluated within one week, including measurements of blood glucose, blood potassium and urine glucose concentrations (see section 4.8, proximal tubulopathy). Consideration should be given to interrupting use of Emtricitabine/Tenofovir disoproxil Krka in individuals with creatinine clearance decreased to < 60 mL/min or decreases in serum phosphate to < 1.0 mg/dL (0.32 mmol/L). Interrupting use of Emtricitabine/Tenofovir disoproxil Krka should also be considered in case of progressive decline of renal function when no other cause has been identified.
Bone effects
Bone abnormalities such as osteomalacia which can manifest as persistent or worsening bone pain, and which can infrequently contribute to fractures, may be associated with tenofovir disoproxil-induced proximal renal tubulopathy (see section 4.8).
Tenofovir disoproxil may also cause a reduction in bone mineral density (BMD).
If bone abnormalities are suspected or detected then appropriate consultation should be obtained.
Treatment ofHIV-1 infection
In a 144-week controlled clinical study (GS-99–903) that compared tenofovir disoproxil with stavudine in combination with lamivudine and efavirenz in antiretroviral-naïve patients, small decreases in BMD of the hip and spine were observed in both treatment groups. Decreases in BMD of spine and changes in bone biomarkers from baseline were significantly greater in the tenofovir disoproxil treatment group at 144 weeks. Decreases in BMD of hip were significantly greater in this group until 96 weeks. However, there was no increased risk of fractures or evidence for clinically relevant bone abnormalities over 144 weeks in this study.
In other studies (prospective and cross-sectional), the most pronounced decreases in BMD were seen in patients treated with tenofovir disoproxil as part of a regimen containing a boosted protease inhibitor. Overall in view of the bone abnormalities associated with tenofovir disoproxil and the limitations of long term data on the impact of tenofovir disoproxil on bone health and fracture risk, alternative treatment regimens should be considered for patients with osteoporosis that are at a high risk for fractures.
Pre-exposure prophylaxis
In clinical studies of HIV-1 uninfected individuals, small decreases in BMD were observed. In a study of 498 men, the mean changes from baseline to week 24 in BMD ranged from – 0.4% to – 1.0% across hip, spine, femoral neck and trochanter in men who received daily emtricitabine/tenofovir disoproxil prophylaxis (n = 247) vs. placebo (n = 251).
Renal and bone effects in the paediatric population
There are uncertainties associated with the long-term renal and bone effects of tenofovir disoproxil during the treatment of HIV-1 infection in the paediatric population and the long term renal and bone effects of emtricitabine/tenofovir when used for pre-exposure prophylaxis in uninfected adolescents (see section 5.1). Moreover, the reversibility of renal toxicity after cessation of tenofovir disoproxil for treatment of HIV-1 or after cessation of emtricitabine/tenofovir for pre-exposure prophylaxis cannot be fully ascertained.
A multidisciplinary approach is recommended to weigh the benefit/risk balance of the use of emtricitabine/tenofovir for the treatment of HIV-1 infection or for pre-exposure prophylaxis, decide the appropriate monitoring during treatment (including decision for treatment withdrawal) and consider the need for supplementation on a case by case basis.
When using emtricitabine/tenofovir for pre-exposure prophylaxis individuals should be reassessed at each visit to ascertain whether they remain at high risk of HIV-1 infection. The risk of HIV-1 infection should be balanced against the potential for renal and bone effects with long-term use of emtricitabine/tenofovir.
Renal effects:
Renal adverse reactions consistent with proximal renal tubulopathy have been reported in HIV 1 infected paediatric patients aged 2 to < 12 years in clinical study GS-US-104–0352 (see sections 4.8 and 5.1).
Renal monitoring
Renal function (creatinine clearance and serum phosphate) should be evaluated prior to initiating emtricitabine/tenofovir for treatment of HIV-1 or for pre-exposure prophylaxis, and should be monitored during use as in adults (see above).
Renal management
If serum phosphate is confirmed to be < 3.0 mg/dl (0.96 mmol/l) in any paediatric patient receiving Emtricitabine/Tenofovir disoproxil Krka, renal function should be re-evaluated within one week, including measurements of blood glucose, blood potassium and urine glucose concentrations (see section 4.8, proximal tubulopathy). If renal abnormalities are suspected or detected then consultation with a nephrologist should be obtained to consider interruption of emtricitabine/tenofovir use. Interrupting use of Emtricitabine/Tenofovir disoproxil Krka should also be considered in case of progressive decline of renal function when no other cause has been identified.
Co-administration and risk of renal toxicity
The same recommendations apply as in adults (see Co-administration of other medicinal products below).
Renal impairment
The use of Emtricitabine/Tenofovir disoproxil Krka is not recommended in individuals under the age of 18 years with renal impairment (see section 4.2). Emtricitabine/Tenofovir disoproxil Krka should not be initiated in paediatric patients with renal impairment and should be discontinued in paediatric patients who develop renal impairment during Emtricitabine/Tenofovir disoproxil Krka use.
Bone effects
Use of tenofovir disoproxil may cause a reduction in BMD. The effects of tenofovir disoproxil -associated changes in BMD on long-term bone health and future fracture risk are uncertain (see section 5.1).
If bone abnormalities are detected or suspected during use of emtricitabine/tenofovir in any paediatric patients, consultation with an endocrinologist and/or nephrologist should be obtained.
Weight and metabolic parameters
An increase in weight and in levels of blood lipids and glucose may occur during antiretroviral therapy. Such changes may in part be linked to disease control and life style. For lipids, there is in some cases evidence for a treatment effect, while for weight gain there is no strong evidence relating this to any particular treatment. For monitoring of blood lipids and glucose reference is made to established HIV treatment guidelines. Lipid disorders should be managed as clinically appropriate.
Mitochondrial dysfunction following exposure in utero
Nucleos(t)ide analogues may impact mitochondrial function to a variable degree, which is most pronounced with stavudine, didanosine and zidovudine. There have been reports of mitochondrial dysfunction in HIV negative infants exposed in utero and/or postnatally to nucleoside analogues; these have predominantly concerned treatment with regimens containing zidovudine. The main adverse reactions reported are haematological disorders (anaemia, neutropenia) and metabolic disorders (hyperlactatemia, hyperlipasemia). These events have often been transitory. Late onset neurological disorders have been reported rarely (hypertonia, convulsion, abnormal behaviour). Whether such neurological disorders are transient or permanent is currently unknown. These findings should be considered for any child exposed in utero to nucleos(t)ide analogues, who present with severe clinical findings of unknown etiology, particularly neurologic findings. These findings do not affect current national recommendations to use antiretroviral therapy in pregnant women to prevent vertical transmission of HIV.
Immune Reactivation Syndrome
In HIV infected patients with severe immune deficiency at the time of institution of CART, an inflammatory reaction to asymptomatic or residual opportunistic pathogens may arise and cause serious clinical conditions, or aggravation of symptoms. Typically, such reactions have been observed within the first few weeks or months of initiation of CART. Relevant examples are cytomegalovirus retinitis, generalised and/or focal mycobacterial infections, and Pneumocystis jirovecii pneumonia. Any inflammatory symptoms should be evaluated and treatment instituted when necessary. Autoimmune disorders (such as Graves' disease and autoimmune hepatitis) have also been reported to occur in the setting of immune reactivation; however, the reported time to onset is more variable and these events can occur many months after initiation of treatment.
Opportunistic infections
HIV-1 infected patients receiving Emtricitabine/Tenofovir disoproxil Krka or any other antiretroviral therapy may continue to develop opportunistic infections and other complications of HIV infection, and therefore should remain under close clinical observation by physicians experienced in the treatment of patients with HIV associated diseases.
Osteonecrosis
Although the aetiology is considered to be multifactorial (including corticosteroid use, alcohol consumption, severe immunosuppression, higher body mass index), cases of osteonecrosis have been reported particularly in patients with advanced HIV-disease and/or long-term exposure to CART. Patients should be advised to seek medical advice if they experience joint aches and pain, joint stiffness or difficulty in movement.
Co-administration of other medicinal products
Use of Emtricitabine/Tenofovir disoproxil Krka should be avoided with concurrent or recent use of a nephrotoxic medicinal product (see section 4.5). If concomitant use with nephrotoxic agents is unavoidable, renal function should be monitored weekly.
Cases of acute renal failure after initiation of high dose or multiple non-steroidal anti-inflammatory drugs (NSAIDs) have been reported in HIV-1 infected patients treated with tenofovir disoproxil and with risk factors for renal dysfunction. If Emtricitabine/Tenofovir disoproxil Krka is co-administered with an NSAID, renal function should be monitored adequately.
A higher risk of renal impairment has been reported in HIV-1 infected patients receiving tenofovir disoproxil in combination with a ritonavir or cobicistat boosted protease inhibitor. Close monitoring of renal function is required in these patients (see section 4.5). In HIV-1 infected patients with renal risk factors, the co-administration of tenofovir disoproxil with a boosted protease inhibitor should be carefully evaluated.
Emtricitabine/Tenofovir disoproxil Krka should not be administered concomitantly with other medicinal products containing emtricitabine, tenofovir disoproxil, tenofovir alafenamide, or other cytidine analogues, such as lamivudine (see section 4.5). Emtricitabine/Tenofovir disoproxil Krka should not be administered concomitantly with adefovir dipivoxil.
Use with ledipasvir and sofosbuvir, sofosbuvir and velpatasvir or sofosbuvir, velpatasvir and voxilaprevir
Co-administration of tenofovir disoproxil with ledipasvir/sofosbuvir, sofosbuvir/velpatasvir or sofosbuvir/velpatasvir/voxilaprevir has been shown to increase plasma concentrations of tenofovir, especially when used together with an HIV regimen containing tenofovir disoproxil and a pharmacokinetic enhancer (ritonavir or cobicistat).
The safety of tenofovir disoproxil when co-administered with ledipasvir/sofosbuvir, sofosbuvir/velpatasvir or sofosbuvir/velpatasvir/voxilaprevir and a pharmacokinetic enhancer has not been established. The potential risks and benefits associated with co-administration should be considered, particularly in patients at increased risk of renal dysfunction. Patients receiving ledipasvir/sofosbuvir, sofosbuvir/velpatasvir or sofosbuvir/velpatasvir/voxilaprevir concomitantly with tenofovir disoproxil and a boosted HIV protease inhibitor should be monitored for adverse reactions related to tenofovir disoproxil.
Co-administration of tenofovir disoproxil and didanosine
Co-administration of tenofovir disoproxil and didanosine is not recommended (see section 4.5).
Triple nucleoside therapy
There have been reports of a high rate of virological failure and of emergence of resistance at an early stage in HIV-1 infected patients when tenofovir disoproxil was combined with lamivudine and abacavir as well as with lamivudine and didanosine as a once daily regimen. There is close structural similarity between lamivudine and emtricitabine and similarities in the pharmacokinetics and pharmacodynamics of these two agents. Therefore, the same problems may be seen if Emtricitabine/Tenofovir disoproxil Krka is administered with a third nucleoside analogue.
Elderly
Emtricitabine/tenofovir disoproxil has not been studied in individuals over the age of 65 years. Individuals over the age of 65 years are more likely to have decreased renal function, therefore caution should be exercised when administering Emtricitabine/Tenofovir disoproxil Krka to older people.
Lactose
Emtricitabine/Tenofovir disoproxil Krka contains lactosemonohydrate. Patients with rare hereditary problems of galactose intolerance, total lactase deficiency or glucose-galactose malabsorption should not take this medicine.
Sodium
Emtricitabine/Tenofovir disoproxil Krka contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially ‘sodium-free’.
4.5 Interaction with other medicinal products and other forms of interaction
Interaction studies have only been performed in adults.
As Emtricitabine/Tenofovir disoproxil Krka contains emtricitabine and tenofovir disoproxil, any interactions that have been identified with these agents individually may occur with Emtricitabine/Tenofovir disoproxil Krka. Interaction studies have only been performed in adults.
The steady-state pharmacokinetics of emtricitabine and tenofovir were unaffected when emtricitabine and tenofovir disoproxil were administered together versus each medicinal product dosed alone.
In vitro and clinical pharmacokinetic interaction studies have shown the potential for CYP450 mediated interactions involving emtricitabine and tenofovir disoproxil with other medicinal products is low.
Concomitant use not recommended
Emtricitabine/Tenofovir disoproxil Krka should not be administered concomitantly with other medicinal products containing emtricitabine, tenofovir disoproxil, tenofovir alafenamide or other cytidine analogues, such as lamivudine (see section 4.4). Emtricitabine/Tenofovir disoproxil Krka should not be administered concomitantly with adefovir dipivoxil.
Didanosine
The co-administration of Emtricitabine/Tenofovir disoproxil Krka and didanosine is not recommended (see section 4.4 and Table 2).
Renally eliminated medicinal products
Since emtricitabine and tenofovir are primarily eliminated by the kidneys, co-administration of Emtricitabine/Tenofovir disoproxil Krka with medicinal products that reduce renal function or compete for active tubular secretion (e.g. cidofovir) may increase serum concentrations of emtricitabine, tenofovir and/or the co-administered medicinal products.
Use of Emtricitabine/Tenofovir disoproxil Krka should be avoided with concurrent or recent use of a nephrotoxic medicinal product. Some examples include, but are not limited to, aminoglycosides, amphotericin B, foscarnet, ganciclovir, pentamidine, vancomycin, cidofovir or interleukin-2 (see
section 4.4).
Other interactions
Interactions between emtricitabine/tenofovir disoproxil or its individual component(s) and other medicinal products are listed in Table 2 below (increase is indicated as “t”, decrease as “j”, no change as “^”, twice daily as “b.i.d.” and once daily as “q.d.”). If available, 90% confidence intervals are shown in parentheses.
Table 2: Interactions between emtricitabine/tenofovir disoproxil or its individual component(s) and other medicinal products
| Medicinal product by therapeutic areas | Effects on drug levels Mean percent change in AUC, C max , C min with 90% confidence intervals if available (mechanism) | Recommendation concerning coadministration with Emtricitabine/Tenofovir disoproxil Krka (emtricitabine 200 mg, tenofovir disoproxil 245 mg) |
| ANTI-INFECTIVES | ||
| Antiretrovirals | ||
| Protease inhibitors | ||
| Atazanavir/Ritonavir/Tenofovir disoproxil (300 mg q.d./100 mg q.d./245 mg q.d.) | Atazanavir: AUC: j 25% (4 42 to 4 3) Cmax: j 28% (j 50 to t 5) Cmin: j 26% (j 46 to t 10) Tenofovir: AUC: t 37% Cmax: t 34% Cmin: t 29% | No dose adjustment is recommended. The increased exposure of tenofovir could potentiate tenofovir associated adverse events, including renal disorders. Renal function should be closely monitored (see section 4.4). |
| Atazanavir/Ritonavir/Emtricitabine | Interaction not studied. | |
| Darunavir/Ritonavir/Tenofovir disoproxil (300 mg q.d./100 mg q.d./245 mg q.d.) | Darunavir: AUC: ~ Cmin: Tenofovir: AUC: t 22% Cmin: t 37% | No dose adjustment is recommended. The increased exposure of tenofovir could potentiate tenofovir associated adverse events, including renal disorders. Renal function should be closely monitored (see section 4.4). |
| Darunavir/Ritonavir/Emtricitabine | Interaction not studied. | |
| Lopinavir/Ritonavir/Tenofovir disoproxil (400 mg b.i.d./100 mg b.i.d/245 mg q.d.) | Lopinavir/Ritonavir: AUC: ~ Cmax: < > Cmin: Tenofovir: AUC: t 32% (t 25 to t 38) Cmax: Cmin: t 51% (t 37 to t 66) | No dose adjustment is recommended. The increased exposure of tenofovir could potentiate tenofovir associated adverse events, including renal disorders. Renal function should be closely monitored (see section 4.4). |
| Lopinavir/Ritonavir/Emtricitabine | Interaction not studied. | |
| NRTIs | ||
| Didanosine/Tenofovir disoproxil | Co-administration of tenofovir disoproxil and didanosine results in a 40–60% increase in systemic exposure to didanosine. | Co-administration of Emtricitabine/Tenofovir disoproxil Krka and didanosine is not recommended (see section 4.4). Increased systemic exposure to didanosine may increase didanosine related adverse reactions. Rarely, pancreatitis and lactic acidosis, sometimes fatal, have been reported. Co-administration of tenofovir disoproxil and didanosine at a dose of |
| Didanosine/Emtricitabine | Interaction not studied. | |
| 400 mg daily has been associated with a significant decrease in CD4 cell count, possibly due to an intracellular interaction increasing phosphorylated (i.e. active) didanosine. A decreased dosage of 250 mg didanosine coadministered with tenofovir disoproxil therapy has been associated with reports of high rates of virological failure within several tested combinations for the treatment of HIV-1 infection. | ||
| Lamivudine/Tenofovir disoproxil | Lamivudine: AUC: 1 3% (1 8% to Î 15) Cmax: 1 24% (1 44 to | 12) Cmin: NC Tenofovir: AUC: | 4% (| 15 to Î 8) Cmax: Î 102% (| 96 to Î 108) Cmin: NC | Lamivudine and Emtricitabine/Tenofovir disoproxil Krka should not be administered concomitantly (see section 4.4). |
| Efavirenz/Tenofovir disoproxil | Efavirenz: AUC: | 4% (| 7 to | 1) Cmax: | 4% (| 9 to Î 2) Cmin: NC Tenofovir: AUC: | 1% (| 8 to Î 6) Cmax: Î 7% (| 6 to Î 22) Cmin: NC | No dose adjustment of efavirenz is required. |
| ANTI-INFECTIVES | ||
| Hepatitis B virus (HBV) antiviral agents | ||
| Adefovir dipivoxil /Tenofovir disoproxil | Adefovir dipivoxil: AUC: | 11% (| 14 to | 7) Cmax: | 7% (| 13 to | 0) Cmin: NC Tenofovir: AUC: | 2% (| 5 to Î 0) Cmax: | 1% (| 7 to Î 6) Cmin: NC | Adefovir dipivoxil and Emtricitabine/Tenofovir disoproxil Krka should not be administered concomitantly (see section 4.4). |
| Hepatitis C virus (HCV) antiviral agents | ||
| Ledipasvir/Sofosbuvir (90 mg/400 mg q.d.) + Atazanavir/Ritonavir (300 mg q.d./100 mg q.d.) + Emtricitabine/Tenofovir disoproxil (200 mg/245 mg q.d.)1 | Ledipasvir: AUC: t 96% (t 74 to t 121) Cmax: t 68% (t 54 to t 84) Cmin: t 118% (t 91 to t 150) Sofosbuvir: AUC: ~ Cmax: GS-3310072: AUC: ~ Cmax: < > Cmin: t 42% (t 34 to t 49) Atazanavir: AUC: ~ Cmax: Cmin: t 63% (t 45 to t 84) Ritonavir: AUC: ~ Cmax: < > Cmin: t 45% (t 27 to t 64) Emtricitabine: AUC: ~ Cmax: < > | Increased plasma concentrations of tenofovir resulting from coadministration of tenofovir disoproxil, ledipasvir/sofosbuvir and atazanavir/ritonavir may increase adverse reactions related to tenofovir disoproxil, including renal disorders. The safety of tenofovir disoproxil when used with ledipasvir/sofosbuvir and a pharmacokinetic enhancer (e.g. ritonavir or cobicistat) has not been established. The combination should be used with caution with frequent renal monitoring, if other alternatives are not available (see section 4.4). |
| Cmin: Tenofovir: AUC: ~ Cmax: í 47% (í 37 to Î 58) Cmin: Î 47% (Î 38 to Î 57) | ||
| Ledipasvir/Sofosbuvir (90 mg/400 mg q.d.) + Darunavir/Ritonavir (800 mg q.d./100 mg q.d.) + Emtricitabine/Tenofovir disoproxil (200 mg/245 mg q.d.)1 | Ledipasvir: AUC: ~ Cmax: Cmin: Sofosbuvir: AUC: 1 27% (1 35 to | 18) Cmax: | 37% (| 48 to | 25) GS-3310072: AUC: ~ Cmax: Cmin: Darunavir: AUC: ~ Cmax: < > Cmin: Ritonavir: AUC: ~ Cmax: < > Cmin: Î 48% (Î 34 to Î 63) Emtricitabine: AUC: ~ Cmax: Cmin: Tenofovir: AUC: Î 50% (Î 42 to Î 59) Cmax: Î 64% (Î 54 to Î 74) Cmin: Î 59% (Î 49 to Î 70) | Increased plasma concentrations of tenofovir resulting from coadministration of tenofovir disoproxil, ledipasvir/sofosbuvir and darunavir/ritonavir may increase adverse reactions related to tenofovir disoproxil, including renal disorders. The safety of tenofovir disoproxil when used with ledipasvir/sofosbuvir and a pharmacokinetic enhancer (e.g. ritonavir or cobicistat) has not been established. The combination should be used with caution with frequent renal monitoring, if other alternatives are not available (see section 4.4). |
| Ledipasvir/Sofosbuvir (90 mg/400 mg q.d.) + Efavirenz/Emtricitabine/Tenofovir disoproxil (600 mg/200 mg/245 mg q.d.) | Ledipasvir: AUC: | 34% (| 41 to | 25) Cmax: | 34% (| 41 to Î 25) Cmin: | 34% (| 43 to Î 24) Sofosbuvir: AUC: ~ Cmax: < > GS-3310072: AUC: ~ Cmax: < > Cmin: Efavirenz: AUC: ~ Cmax: < > Cmin: Emtricitabine: AUC: ~ Cmax: Cmin: Tenofovir: AUC: Î 98% (Î 77 to Î 123) Cmax: Î 79% (Î 56 to Î 104) Cmin: Î 163% (Î 137 to Î 197) | No dose adjustment is recommended. The increased exposure of tenofovir could potentiate adverse reactions associated with tenofovir disoproxil, including renal disorders. Renal function should be closely monitored (see section 4.4). |
| Ledipasvir/Sofosbuvir (90 mg/400 mg q.d.) + Emtricitabine/Rilpivirine/ Tenofovir disoproxil (200 mg/25 mg/245 mg q.d.) | Ledipasvir: AUC: ~ Cmax: < > Cmin: Sofosbuvir: AUC: ~ | No dose adjustment is recommended. The increased exposure of tenofovir could potentiate adverse reactions associated with tenofovir disoproxil, including renal disorders. Renal function should be closely monitored |
| Cmax: < > GS-3310072: AUC: ~ Cmax: Cmin: Emtricitabine: AUC: ~ Cmax: < > Cmin: Rilpivirine: AUC: ~ Cmax: < > Cmin: Tenofovir: AUC: t 40% (t 31 to t 50) Cmax: Cmin: t 91% (t 74 to t 110) | (see section 4.4). | |
| Ledipasvir/Sofosbuvir (90 mg/400 mg q.d.) + Dolutegravir (50 mg q.d.) + Emtricitabine/Tenofovir disoproxil (200 mg/245 mg q.d.) | Sofosbuvir: AUC: ~ Cmax: ^ GS-3310072 AUC: ~ Cmax: ^ Cmin: ^ Ledipasvir: AUC: ~ Cmax: ^ Cmin: ^ Dolutegravir AUC: ~ Cmax: ^ Cmin: ^ Emtricitabine: AUC: ~ Cmax: ^ Cmin: ^ Tenofovir: AUC: t 65% (t 59 to t 71) Cmax: t 61% (t 51 to t 72) Cmin: t 115% (t 105 to t 126) | No dose adjustment is required. The increased exposure of tenofovir could potentiate adverse reactions associated with tenofovir disoproxil, including renal disorders. Renal function should be closely monitored (see section 4.4). |
| Sofosbuvir/Velpatasvir (400 mg/100 mg q.d.) + Atazanavir/Ritonavir (300 mg q.d./100 mg q.d.) + Emtricitabine/Tenofovir disoproxil (200 mg/245 mg q.d.) | Sofosbuvir: AUC: ~ Cmax: ^ GS-3310072: AUC: ~ Cmax: ^ Cmin: t 42% (t 37 to t 49) Velpatasvir: AUC: t 142% (t 123 to t 164) Cmax: t 55% (t 41 to t 71) Cmin: t 301% (t 257 to t 350) Atazanavir: AUC: ~ Cmax: ^ | Increased plasma concentrations of tenofovir resulting from co administration of tenofovir disoproxil, sofosbuvir/velpatasvir and atazanavir/ritonavir may increase adverse reactions related to tenofovir disoproxil, including renal disorders. The safety of tenofovir disoproxil when used with sofosbuvir/velpatasvir and a pharmacokinetic enhancer (e.g. ritonavir or cobicistat) has not been established. The combination should be used with caution with frequent renal monitoring (see section 4.4). |
| Cmin: Î 39% (Î 20 to Î 61) Ritonavir: AUC: ~ Cmax: ^ Cmin: Î 29% (Î 15 to Î 44) Emtricitabine: AUC: ~ Cmax: ^ Cmin: ^ Tenofovir: AUC: ~ Cmax: Î 55% (Î 43 to Î 68) Cmin: Î 39% (Î 31 to Î 48) | ||
| Sofosbuvir/Velpatasvir (400 mg/100 mg q.d.) + Darunavir/Ritonavir (800 mg q.d./100 mg q.d.) + Emtricitabine/Tenofovir disoproxil (200 mg/245 mg q.d.) | Sofosbuvir: AUC: 1 28% (1 34 to | 20) Cmax: | 38% (| 46 to | 29) GS-3310072: AUC: ~ Cmax: ^ Cmin: ^ Velpatasvir: AUC: ~ Cmax: | 24% (| 35 to | 11) Cmin: ^ Darunavir: AUC: ~ Cmax: ^ Cmin: ^ Ritonavir: AUC: ~ Cmax: ^ Cmin: ^ Emtricitabine: AUC: ~ Cmax: ^ Cmin: ^ Tenofovir: AUC: Î 39% (Î 33 to Î 44) Cmax: Î 55% (Î 45 to Î 66) Cmin: Î 52% (Î 45 to Î 59) | Increased plasma concentrations of tenofovir resulting from co administration of tenofovir disoproxil, sofosbuvir/velpatasvir and darunavir/ritonavir may increase adverse reactions related to tenofovir disoproxil, including renal disorders. The safety of tenofovir disoproxil when used with sofosbuvir/velpatasvir and a pharmacokinetic enhancer (e.g. ritonavir or cobicistat) has not been established. The combination should be used with caution with frequent renal monitoring (see section 4.4). |
| Sofosbuvir/Velpatasvir (400 mg/100 mg q.d.) + Lopinavir/Ritonavir (800 mg/200 mg q.d.) + Emtricitabine/Tenofovir disoproxil (200 mg/245 mg q.d.) | Sofosbuvir: AUC: | 29% (| 36 to | 22) Cmax: | 41% (| 51 to | 29) GS-3310072: AUC: ~ Cmax: ^ Cmin: ^ Velpatasvir: AUC: ~ Cmax: | 30% (| 41 to | 17) Cmin: Î 63% (Î 43 to Î 85) | Increased plasma concentrations of tenofovir resulting from co administration of tenofovir disoproxil, sofosbuvir/velpatasvir and lopinavir/ritonavir may increase adverse reactions related to tenofovir disoproxil, including renal disorders. The safety of tenofovir disoproxil when used with sofosbuvir/velpatasvir and a pharmacokinetic enhancer (e.g. ritonavir or cobicistat) has not been established. The combination should be used with |
| Lopinavir: AUC: ~ Cmax: ^ Cmin: ^ Ritonavir: AUC: ~ Cmax: ^ Cmin: ^ Emtricitabine: AUC: ~ Cmax: ^ Cmin: ^ Tenofovir: AUC: ~ Cmax: Î 42% (Î 27 to Î 57) Cmin: ^ | caution with frequent renal monitoring (see section 4.4). | |
| Sofosbuvir/Velpatasvir (400 mg/100 mg q.d.) + Raltegravir (400 mg b.i.d) + Emtricitabine/Tenofovir disoproxil (200 mg/245 mg q.d.) | Sofosbuvir: AUC: ~ Cmax: ^ GS-3310072: AUC: ~ Cmax: ^ Cmin: ^ Velpatasvir: AUC: ~ Cmax: ^ Cmin: ^ Raltegravir: AUC: ~ Cmax: ^ Cmin: | 21% (| 58 to Î 48) Emtricitabine: AUC: ~ Cmax: ^ Cmin: ^ Tenofovir: AUC: î 40% (Î 34 to Î 45) Cmax: Î 46% (Î 39 to Î 54) Cmin: Î 70% (Î 61 to Î 79) | No dose adjustment is recommended. The increased exposure of tenofovir could potentiate adverse reactions associated with tenofovir disoproxil, including renal disorders. Renal function should be closely monitored (see section 4.4). |
| Sofosbuvir/Velpatasvir (400 mg/100 mg q.d.) + Efavirenz/Emtricitabine/Tenofovir disoproxil (600 mg/200 mg/245 mg q.d.) | Sofosbuvir: AUC: ~ Cmax: Î 38% (Î 14 to Î 67) GS-3310072: AUC: ~ Cmax: ^ Cmin: ^ Velpatasvir: AUC: 1 53% (1 61 to | 43) Cmax: | 47% (| 57 to | 36) Cmin: | 57% (| 64 to | 48) | Concomitant administration of sofosbuvir/velpatasvir and efavirenz is expected to decrease plasma concentrations of velpatasvir. Co administration of sofosbuvir/velpatasvir with efavirenz-containing regimens is not recommended. |
| Efavirenz: AUC: ~ Cmax: ^ Cmin: ^ Emtricitabine: AUC: ~ Cmax: ^ Cmin: ^ Tenofovir: AUC: Î 81% (Î 68 to Î 94) Cmax: Î 77% (Î 53 to Î 104) Cmin: Î 121% (Î 100 to Î 143) | ||
| Sofosbuvir/Velpatasvir (400 mg/100 mg q.d.) + Emtricitabine/Rilpivirine/Tenofovir disoproxil (200 mg/25 mg/245 mg q.d.) | Sofosbuvir: AUC: ~ Cmax: ^ GS-3310072: AUC: ~ Cmax: ^ Cmin: ^ Velpatasvir: AUC: ~ Cmax: ^ Cmin: ^ Emtricitabine: AUC: ~ Cmax: ^ Cmin: ^ Rilpivirine: AUC: ~ Cmax: ^ Cmin: ^ Tenofovir: AUC: Î 40% (Î 34 to Î 46) Cmax: Î 44% (Î 33 to Î 55) Cmin: Î 84% (Î 76 to Î 92) | No dose adjustment is recommended. The increased exposure of tenofovir could potentiate adverse reactions associated with tenofovir disoproxil, including renal disorders. Renal function should be closely monitored (see section 4.4). |
| Sofosbuvir/Velpatasvir/ Voxilaprevir (400 mg/100 mg/ 100 mg+100 mg q.d.)3 + Darunavir (800 mg q.d.) + Ritonavir (100 mg q.d.) + Emtricitabine/Tenofovir disoproxil (200 mg/245 mg q.d.) | Sofosbuvir: AUC: ~ Cmax: i 30% Cmin: N/A GS-3310072: AUC: ~ Cmax: Cmin: N/A Velpatasvir: AUC: ~ Cmax: Cmin: Voxilaprevir: AUC: Î 143% Cmax:Î72% Cmin: Î 300% | Increased plasma concentrations of tenofovir resulting from co administration of tenofovir disoproxil, sofosbuvir/velpatasvir/voxilaprevir and darunavir/ritonavir may increase adverse reactions related to tenofovir disoproxil, including renal disorders. The safety of tenofovir disoproxil when used with sofosbuvir/velpatasvir/voxilaprevir and a pharmacokinetic enhancer (e.g. ritonavir or cobicistat) has not been established. The combination should be used with caution with frequent renal monitoring (see section 4.4). |
| Darunavir: AUC: ~ Cmax: < > Cmin: i 34% Ritonavir: AUC: Î 45% Cmax: Î 60% Cmin: ^^ Emtricitabine: AUC: ~ Cmax: < > Cmin: Tenofovir: AUC: Î 39% Cmax: Î 48% Cmin: Î 47% | ||
| Sofosbuvir (400 mg q.d.) + Efavirenz/Emtricitabine/Tenofovir disoproxil (600 mg/200 mg/245 mg q.d.) | Sofosbuvir: AUC: ~ Cmax: i 19% (i 40 to Î 10) GS-3310072: AUC: ~ Cmax: i 23% (i 30 to Î 16) Efavirenz: AUC: ~ Cmax: < > Cmin: Emtricitabine: AUC: ~ Cmax: ^^ Cmin: Tenofovir: AUC: ~ Cmax: Î 25% (Î 8 to Î 45) Cmin: | No dose adjustment is required. |
| Ribavirin/Tenofovir disoproxil | Ribavirin: AUC: Î 26% (Î 20 to Î 32) Cmax: i 5% (i 11 to Î 1) Cmin: NC | No dose adjustment of ribavirin is required. |
| Herpes virus antiviral agents | ||
| Famciclovir/Emtricitabine | Famciclovir: AUC: i 9% (i 16 to i 1) Cmax: i 7% (i 22 to Î 11) Cmin: NC Emtricitabine: AUC: i 7% (i 13 to i 1) Cmax: i 11% (i 20 to Î 1) Cmin: NC | No dose adjustment of famciclovir is required. |
| Antimycobacterials | ||
| Rifampicin/Tenofovir disoproxil | Tenofovir: AUC: i 12% (i 16 to i 8) Cmax: i 16% (i 22 to i 10) Cmin: i 15% (i 12 to i 9) | No dose adjustment is required. |
| ORAL CONTRACEPTIVES | ||
| Norgestimate/Ethinyl oestradiol/Tenofovir disoproxil | Norgestimate: AUC: j 4% (¡ 32 to $ 34) Cmax: j 5% (j 27 to $ 24) Cmin: NC | No dose adjustment of norgestimate/ethinyl oestradiol is required. |
| Ethinyl oestradiol: AUC: 1 4% (1 9 to Î 0) Cmax: 1 6% (1 13 to Î 0) Cmin: 1 2% (1 9 to Î 6) | ||
| IMMUNOSUPPRESSANTS | ||
| Tacrolimus/Tenofovir disoproxil /Emtricitabine | Tacrolimus: AUC: Î 4% (1 3 to Î 11) Cmax: Î 3% (1 3 to Î 9) Cmin: NC Emtricitabine: AUC: 1 5% (1 9 to | 1) Cmax: | 11% (| 17 to | 5) Cmin: NC Tenofovir: AUC: Î 6% (| 1 to Î 13) Cmax: Î13% (Î 1 to Î 27) Cmin: NC | No dose adjustment of tacrolimus is required. |
| NARCOTIC ANALGESICS | ||
| Methadone/Tenofovir disoproxil | Methadone: AUC: Î 5% (| 2 to Î 13) Cmax: Î 5% (| 3 to Î 14) Cmin: NC | No dose adjustment of methadone is required. |
NC = not calculated.
N/A = not applicable.
1 Data generated from simultaneous dosing with ledipasvir/sofosbuvir. Staggered administration (12 hours apart) provided similar results.
2 The predominant circulating metabolite of sofosbuvir.
3 Study conducted with additional voxilaprevir 100 mg to achieve voxilaprevir exposures expected in HCV-infected patients.
4.6 Fertility, pregnancy and lactation
Pregnancy
A large amount of data on pregnant women (more than 1,000 pregnancy outcomes) indicate no malformations or foetal/neonatal toxicity associated with emtricitabine and tenofovir disoproxil. Animal studies on emtricitabine and tenofovir disoproxil do not indicate reproductive toxicity (see section 5.3). Therefore the use of Emtricitabine/Tenofovir disoproxil Krka may be considered during pregnancy, if necessary.
Breast-feeding
Emtricitabine and tenofovir have been shown to be excreted in human milk. There is insufficient information on the effects of emtricitabine and tenofovir in newborns/infants. Therefore Emtricitabine/Tenofovir disoproxil Krka should not be used during breast-feeding.
As a general rule, it is recommended that HIV infected women do not breast-feed their infants under any circumstances in order to avoid transmission of HIV to the infant.
Fertility
No human data on the effect of emtricitabine/tenofovir disoproxil are available. Animal studies do not indicate harmful effects of emtricitabine or tenofovir disoproxil on fertility.
4.7 Effects on ability to drive and use machines
No studies on the effects on the ability to drive and use machines have been performed. However, individuals should be informed that dizziness has been reported during treatment with both emtricitabine and tenofovir disoproxil.
4.8 Undesirable effects
Summary of the safety profile
HIV-1 infection
The most frequently reported adverse reactions considered possibly or probably related to emtricitabine and/or tenofovir disoproxil were nausea (12%) and diarrhoea (7%) in an open-label randomised clinical study in adults (GS-01–934, see section 5.1). The safety profile of emtricitabine and tenofovir disoproxil in this study was consistent with the previous experience with these agents when each was administered with other antiretroviral agents.
Pre-exposure prophylaxis
No new adverse reactions to emtricitabine/tenofovir disoproxil were identified from two randomised placebo-controlled studies (iPrEx, Partners PrEP) in which 2,830 HIV-1 uninfected adults received emtricitabine/tenofovir disoproxil once daily for pre-exposure prophylaxis. Patients were followed for a median of 71 weeks and 87 weeks, respectively. The most frequent adverse reaction reported in the emtricitabine/tenofovir disoproxil group in the iPrEx study was headache (1%).
Tabulated summary of adverse reactions
The adverse reactions considered at least possibly related to treatment with the tenofovir disoproxil and emtricitabine from clinical study and post-marketing experience in HIV-1 infected patients are listed in Table 3, below, by body system organ class and frequency. Within each frequency grouping, undesirable effects are presented in order of decreasing seriousness. Frequencies are defined as very common (> 1/10), common (> 1/100 to < 1/10), uncommon (> 1/1,000 to < 1/100) or rare (> 1/10,000 to < 1/1,000).
Table 3: Tabulated summary of adverse reactions associated with tenofovir disoproxil and emtricitabine based on clinical study and post-marketing experience
| Frequency | Emtricitabine | Tenofovir disoproxil |
| Blood and lymphatic system disorders: | ||
| Common: | neutropenia | |
| Uncommon: | 2 anaemia2 | |
| Immune system disorders: | ||
| Common: | allergic reaction | |
| Metabolism and nutrition disorders: | ||
| Very common: | hypophosphataemia1 | |
| Common: | hyperglycaemia, hypertriglyceridaemia | |
| Uncommon: | hypokalaemia1 | |
| Rare: | lactic acidosis | |
| Psychiatric disorders: | ||
| Common: | insomnia, abnormal dreams | |
| Nervous system disorders: | ||
| Very common: | headache | dizziness |
| Common: | dizziness | headache |
| Gastrointestinal disorders: | ||
| Very common: | diarrhoea, nausea | diarrhoea, vomiting, nausea |
| Common: | elevated amylase including elevated pancreatic amylase, elevated serum lipase, vomiting, abdominal pain, dyspepsia | abdominal pain, abdominal distension, flatulence |
| Uncommon: | pancreatitis | |
| Hepatobiliary disorders: | ||
| Common: | elevated serum aspartate aminotransferase (AST) and/or elevated serum alanine aminotransferase (ALT), hyperbilirubinaemia | increased transaminases |
| Rare: | hepatic steatosis, hepatitis | |
| Skin and subcutaneous tissue disorders: | ||
| Very common: | rash | |
| Common: | vesiculobullous rash, pustular rash, maculopapular rash, rash, pruritus, urticaria, skin discolouration (increased pigmentation)2 | |
| Uncommon: | angioedema3 | |
| Rare: | angioedema | |
| Musculoskeletal and connective tissue disorders: | ||
| Very common: | elevated creatine kinase | |
| Uncommon: | rhabdomyolysis1, muscular weakness1 | |
| Rare: | osteomalacia (manifested as bone pain and infrequently contributing to fractures)1,3, myopathy1 | |
| Renal and urinary disorders: | ||
| Uncommon: | increased creatinine, proteinuria, proximal renal tubulopathy including Fanconi syndrome | |
| Rare: | renal failure (acute and chronic), acute tubular necrosis, nephritis (including acute interstitial nephritis)3, nephrogenic diabetes insipidus | |
| General disorders and administration site conditions: | ||
| Very common: | asthenia | |
| Common: | pain, asthenia | |
1 This adverse reaction may occur as a consequence of proximal renal tubulopathy. It is not considered to be causally associated with tenofovir disoproxil in the absence of this condition.
2 Anaemia was common and skin discolouration (increased pigmentation) was very common when emtricitabine was administered to paediatric patients.
3 This adverse reaction was identified through post-marketing surveillance but not observed in randomised controlled clinical studies in adults or paediatric HIV clinical studies for emtricitabine or in randomised controlled clinical studies or the tenofovir disoproxil expanded access program for tenofovir disoproxil. The frequency category was estimated from a statistical calculation based on the total number of patients exposed to emtricitabine in randomised controlled clinical studies (n = 1,563) or tenofovir disoproxil in randomised controlled clinical studies and the expanded access program (n = 7,319).
Description of selected adverse reactions
Renal impairment
As Emtricitabine/Tenofovir disoproxil Krka may cause renal damage monitoring of renal function is recommended (see section 4.4). Proximal renal tubulopathy generally resolved or improved after tenofovir disoproxil discontinuation. However, in some HIV-1 infected patients, declines in creatinine clearance did not completely resolve despite tenofovir disoproxil discontinuation. Patients at risk of renal impairment (such as patients with baseline renal risk factors, advanced HIV disease, or patients receiving concomitant nephrotoxic medications) are at increased risk of experiencing incomplete recovery of renal function despite tenofovir disoproxil discontinuation (see section 4.4).
Lactic acidosis
Cases of lactic acidosis have been reported with tenofovir disoproxil alone or in combination with other antiretrovirals. Patients with predisposing factors such as patients with decompensated liver 21
disease, or patients receiving concomitant medications known to induce lactic acidosis are at increased risk of experiencing severe lactic acidosis during tenofovir disoproxil treatment, including fatal outcomes.
Metabolic parameters
Weight and levels of blood lipids and glucose may increase during antiretroviral therapy (see section 4.4).
Immune Reactivation Syndrome
In HIV infected patients with severe immune deficiency at the time of initiation of CART, an inflammatory reaction to asymptomatic or residual opportunistic infections may arise. Autoimmune disorders (such as Graves' disease and autoimmune hepatitis) have also been reported; however, the reported time to onset is more variable and these events can occur many months after initiation of treatment (see section 4.4).
Osteonecrosis
Cases of osteonecrosis have been reported, particularly in patients with generally acknowledged risk factors, advanced HIV disease or long-term exposure to CART. The frequency of this is unknown (see section 4.4).
Paediatric population
Assessment of adverse reactions related to emtricitabine is based on experience in three paediatric studies (n = 169) where treatment-naïve (n = 123) and treatment-experienced (n = 46) paediatric HIV infected patients aged 4 months to 18 years were treated with emtricitabine in combination with other antiretroviral agents. In addition to the adverse reactions reported in adults, anaemia (9.5%) and skin discolouration (31.8%) occurred more frequently in clinical trials in paediatric patients than in adults (see section 4.8, Tabulated summary of adverse reactions).
Assessment of adverse reactions related to tenofovir disoproxil is based on two randomised trials (studies GS-US-104–0321 and GS-US-104–0352) in 184 HIV 1 infected paediatric patients (aged 2 to < 18 years) who received treatment with tenofovir disoproxil (n = 93) or placebo/active comparator (n = 91) in combination with other antiretroviral agents for 48 weeks (see section 5.1). The adverse reactions observed in paediatric patients who received treatment with tenofovir disoproxil were consistent with those observed in clinical studies of tenofovir disoproxil in adults (see section 4.8 Tabulated summary of adverse reactions and 5.1).
Reductions in BMD have been reported in paediatric patients. In HIV 1 infected adolescents (aged 12 to < 18 years), the BMD Z scores observed in subjects who received tenofovir disoproxil were lower than those observed in subjects who received placebo. In HIV 1 infected children (aged 2 to 15 years), the BMD Z scores observed in subjects who switched to tenofovir disoproxil were lower than those observed in subjects who remained on their stavudine- or zidovudine-containing regimen (see sections 4.4 and 5.1).
In study GS-US-104–0352, 89 HIV-1 infected paediatric patients with a median age of 7 years (range 2 to 15 years) were exposed to tenofovir disoproxil for a median of 331 weeks. Eight of the 89 patients (9.0%) discontinued study drug due to renal adverse events. Five subjects (5.6%) had laboratory findings clinically consistent with proximal renal tubulopathy, 4 of whom discontinued tenofovir disoproxil therapy. Seven patients had estimated glomerular filtration rate (GFR) values between 70 and 90 mL/min/1.73 m2. Among them, 3 patients experienced a clinically meaningful decline in estimated GFR during therapy which improved after discontinuation of tenofovir disoproxil.
Other special populations
Individuals with renal impairment
Since tenofovir disoproxil can cause renal toxicity, close monitoring of renal function is recommended in any adults with renal impairment receiving Emtricitabine/Tenofovir disoproxil Krka (see sections
4.2, 4.4 and 5.2). The use of Emtricitabine/Tenofovir disoproxil Krka is not recommended in individuals under the age of 18 years with renal impairment (see sections 4.2 and 4.4).
HIV/HBV or HCV co-infected patients
The adverse reaction profile of emtricitabine and tenofovir disoproxil in a limited number of HIV-infected patients in study GS-01–934 who were co-infected with HBV (n = 13) or HCV (n = 26) was similar to that observed in patients infected with HIV without co-infection. However, as would be expected in this patient population, elevations in AST and ALT occurred more frequently than in the general HIV infected population.
Exacerbations of hepatitis after discontinuation of treatment
In HBV infected patients, clinical and laboratory evidence of hepatitis have occurred after discontinuation of treatment (see section 4.4).
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the national reporting system listed in Appendix V.
4.9 Overdose
If overdose occurs the individual must be monitored for evidence of toxicity (see section 4.8), and standard supportive treatment applied as necessary.
Up to 30% of the emtricitabine dose and approximately 10% of the tenofovir dose can be removed by haemodialysis. It is not known whether emtricitabine or tenofovir can be removed by peritoneal dialysis.
5. PHARMACOLOGICAL PROPERTIES5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Antiviral for systemic use; antivirals for treatment of HIV infections, combinations. ATC code: J05AR03
Mechanism of action
Emtricitabine is a nucleoside analogue of cytidine. Tenofovir disoproxil is converted in vivo to tenofovir, a nucleoside monophosphate (nucleotide) analogue of adenosine monophosphate. Both emtricitabine and tenofovir have activity that is specific to human immunodeficiency virus (HIV-1 and HIV-2) and hepatitis B virus.
Emtricitabine and tenofovir are phosphorylated by cellular enzymes to form emtricitabine triphosphate and tenofovir diphosphate, respectively. In vitro studies have shown that both emtricitabine and tenofovir can be fully phosphorylated when combined together in cells. Emtricitabine triphosphate and tenofovir diphosphate competitively inhibit HIV-1 reverse transcriptase, resulting in DNA chain termination.
Both emtricitabine triphosphate and tenofovir diphosphate are weak inhibitors of mammalian DNA polymerases and there was no evidence of toxicity to mitochondria in vitro and in vivo.
Antiviral activity in vitro
Synergistic antiviral activity was observed with the combination of emtricitabine and tenofovir in 23
vitro. Additive to synergistic effects were observed in combination studies with protease inhibitors, and with nucleoside and non-nucleoside analogue inhibitors of HIV reverse transcriptase.
Resistance
In vitro
Resistance has been seen in vitro and in some HIV-1 infected patients due to the development of the M184V/I mutation with emtricitabine or the K65R mutation with tenofovir.
Emtricitabine-resistant viruses with the M184V/I mutation were cross-resistant to lamivudine, but retained sensitivity to didanosine, stavudine, tenofovir and zidovudine. The K65R mutation can also be selected by abacavir or didanosine and results in reduced susceptibility to these agents plus lamivudine, emtricitabine and tenofovir. Tenofovir disoproxil should be avoided in patients with HIV-1 harbouring the K65R mutation. In addition, a K70E substitution in HIV-1 reverse transcriptase has been selected by tenofovir and results in low-level reduced susceptibility to abacavir, emtricitabine, lamivudine and tenofovir. HIV-1 expressing three or more thymidine analogue associated mutations (TAMs) that included either the M41L or L210W reverse transcriptase mutation showed reduced susceptibility to tenofovir disoproxil.
In vivo – treatment of HIV-1
In an open-label randomised clinical study (GS-01–934) in antiretroviral-naïve patients, genotyping was performed on plasma HIV-1 isolates from all patients with confirmed HIV RNA > 400 copies/mL at weeks 48, 96 or 144 or at the time of early study drug discontinuation. As of week 144:
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– The M184V/I mutation developed in 2/19 (10.5%) isolates analysed from patients in the
emtricitabine/tenofovir disoproxil /efavirenz group and in 10/29 (34.5%) isolates analysed from the lamivudine/zidovudine/efavirenz group (p-value < 0.05, Fisher's Exact test comparing the emtricitabine+tenofovir disoproxil group to the lamivudine/zidovudine group among all patients).
-
– No virus analysed contained the K65R or K70E mutation.
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– Genotypic resistance to efavirenz, predominantly the K103N mutation, developed in virus from
5.2 Pharmacokinetic properties
Absorption
The bioequivalence of one emtricitabine/tenofovir disoproxil film-coated tablet with one emtricitabine 200 mg hard capsule and one tenofovir disoproxil 245 mg film-coated tablet was established following single dose administration to fasting healthy subjects. Following oral administration of emtricitabine/tenofovir disoproxil to healthy subjects, emtricitabine and tenofovir disoproxil are rapidly absorbed and tenofovir disoproxil is converted to tenofovir. Maximum emtricitabine and tenofovir concentrations are observed in serum within 0.5 to 3.0 h of dosing in the fasted state. Administration of emtricitabine/tenofovir disoproxil with food resulted in a delay of approximately three quarters of an hour in reaching maximum tenofovir concentrations and increases in tenofovir AUC and Cmax of approximately 35% and 15%, respectively, when administered with a high fat or light meal, compared to administration in the fasted state. In order to optimise the absorption of tenofovir, it is recommended that Emtricitabine/Tenofovir disoproxil Krka should preferably be taken with food.
Distribution
Following intravenous administration the volume of distribution of emtricitabine and tenofovir was approximately 1.4 L/kg and 800 mL/kg, respectively. After oral administration of emtricitabine or tenofovir disoproxil, emtricitabine and tenofovir are widely distributed throughout the body. In vitro binding of emtricitabine to human plasma proteins was < 4% and independent of concentration over the range of 0.02 to 200 pg/mL. In vitro protein binding of tenofovir to plasma or serum protein was less than 0.7 and 7.2%, respectively, over the tenofovir concentration range 0.01 to 25 pg/mL.
Biotransformation
There is limited metabolism of emtricitabine. The biotransformation of emtricitabine includes oxidation of the thiol moiety to form the 3'-sulphoxide diastereomers (approximately 9% of dose) and conjugation with glucuronic acid to form 2'-O-glucuronide (approximately 4% of dose). In vitro studies have determined that neither tenofovir disoproxil nor tenofovir are substrates for the CYP450 enzymes. Neither emtricitabine nor tenofovir inhibited in vitro drug metabolism mediated by any of the major human CYP450 isoforms involved in drug biotransformation. Also, emtricitabine did not inhibit uridine-5'-diphosphoglucuronyl transferase, the enzyme responsible for glucuronidation.
Elimination
Emtricitabine is primarily excreted by the kidneys with complete recovery of the dose achieved in urine (approximately 86%) and faeces (approximately 14%). Thirteen percent of the emtricitabine dose was recovered in urine as three metabolites. The systemic clearance of emtricitabine averaged 307 mL/min. Following oral administration, the elimination half-life of emtricitabine is approximately
10 hours.
Tenofovir is primarily excreted by the kidney by both filtration and an active tubular transport system with approximately 70–80% of the dose excreted unchanged in urine following intravenous administration. The apparent clearance of tenofovir averaged approximately 307 mL/min. Renal clearance has been estimated to be approximately 210 mL/min, which is in excess of the glomerular filtration rate. This indicates that active tubular secretion is an important part of the elimination of tenofovir. Following oral administration, the elimination half-life of tenofovir is approximately 12 to 18 hours.
Elderly
Pharmacokinetic studies have not been performed with emtricitabine or tenofovir (administered as tenofovir disoproxil) in the elderly (over 65 years of age).
Gender
Emtricitabine and tenofovir pharmacokinetics are similar in male and female patients.
Ethnicity
No clinically important pharmacokinetic difference due to ethnicity has been identified for emtricitabine. The pharmacokinetics of tenofovir (administered as tenofovir disoproxil) have not been specifically studied in different ethnic groups.
Paediatric population
Pharmacokinetic studies have not been performed with emtricitabine/tenofovir disoproxil in children and adolescents (under 18 years of age). Steady-state pharmacokinetics of tenofovir were evaluated in 8 HIV-1 infected adolescent patients (aged 12 to < 18 years) with body weight > 35 kg and in 23 HIV-1 infected children aged 2 to < 12 years. Tenofovir exposure achieved in these paediatric patients receiving oral daily doses of tenofovir disoproxil 245 mg or 6.5 mg/kg body weight tenofovir disoproxil up to a maximum dose of 245 mg was similar to exposures achieved in adults receiving once-daily doses of tenofovir disoproxil 245 mg. Pharmacokinetic studies have not been performed with tenofovir disoproxil in children under 2 years. In general, the pharmacokinetics of emtricitabine in infants, children and adolescents (aged 4 months up to 18 years) are similar to those seen in adults.
The pharmacokinetics of emtricitabine and tenofovir (administered as tenofovir disoproxil) are expected to be similar in HIV-1 infected and uninfected adolescents based on the similar exposures of emtricitabine and tenofovir in HIV-1 infected adolescents and adults, and the similar exposures of emtricitabine and tenofovir in HIV-1 infected and uninfected adults.
Renal impairment
Limited pharmacokinetic data are available for emtricitabine and tenofovir after co-administration of separate preparations or as emtricitabine/tenofovir disoproxil in patients with renal impairment. Pharmacokinetic parameters were mainly determined following administration of single doses of emtricitabine 200 mg or tenofovir disoproxil 245 mg to non-HIV infected subjects with varying degrees of renal impairment. The degree of renal impairment was defined according to baseline creatinine clearance (CrCl) (normal renal function when CrCl > 80 mL/min; mild impairment with CrCl = 50–79 mL/min; moderate impairment with CrCl = 30–49 mL/min and severe impairment with CrCl = 10–29 mL/min).
The mean (%CV) emtricitabine drug exposure increased from 12 (25%) gg^h/mL in subjects with normal renal function, to 20 (6%) gg^h/mL, 25 (23%) gg^h/mL and 34 (6%) gg^h/mL, in subjects with mild, moderate and severe renal impairment, respectively. The mean (%CV) tenofovir drug exposure increased from 2,185 (12%) ng^h/mL in subjects with normal renal function, to 3,064 (30%) ng^h/mL, 6,009 (42%) ng^h/mL and 15,985 (45%) ng^h/mL, in subjects with mild, moderate and severe renal impairment, respectively.
The increased dose interval for emtricitabine/tenofovir disoproxil in HIV-1 infected patients with moderate renal impairment is expected to result in higher peak plasma concentrations and lower Cmm levels as compared to patients with normal renal function. In subjects with end-stage renal disease (ESRD) requiring haemodialysis, between dialysis drug exposures substantially increased over 72 hours to 53 (19%) gg^h/mL of emtricitabine, and over 48 hours to 42,857 (29%) ng^h/mL of tenofovir.
A small clinical study was conducted to evaluate the safety, antiviral activity and pharmacokinetics of tenofovir disoproxil in combination with emtricitabine in HIV infected patients with renal impairment. A subgroup of patients with baseline creatinine clearance between 50 and 60 mL/min, receiving once daily dosing, had a 2–4-fold increase in tenofovir exposure and worsening renal function.
The pharmacokinetics of emtricitabine and tenofovir (administered as tenofovir disoproxil) in paediatric patients with renal impairment have not been studied. No data are available to make dose recommendations (see sections 4.2 and 4.4).
Hepatic impairment
The pharmacokinetics of emtricitabine/tenofovir disoproxil have not been studied in subjects with hepatic impairment.
The pharmacokinetics of emtricitabine have not been studied in non-HBV infected subjects with varying degrees of hepatic insufficiency. In general, emtricitabine pharmacokinetics in HBV infected subjects were similar to those in healthy subjects and in HIV infected patients.
A single 245 mg dose of tenofovir disoproxil was administered to non-HIV infected subjects with varying degrees of hepatic impairment defined according to Child-Pugh-Turcotte (CPT) classification. Tenofovir pharmacokinetics were not substantially altered in subjects with hepatic impairment suggesting that no dose adjustment is required in these subjects. The mean (%CV) tenofovir Cmax and AUG-, values were 223 (34.8%) ng/mL and 2,050 (50.8%) ng^h/mL, respectively, in normal subjects compared with 289 (46.0%) ng/mL and 2,310 (43.5%) ng^h/mL in subjects with moderate hepatic impairment, and 305 (24.8%) ng/mL and 2,740 (44.0%) ng^h/mL in subjects with severe hepatic impairment.
5.3 Preclinical safety data
Emtricitabine
Non-clinical data on emtricitabine reveal no special hazard for humans based on conventional studies of safety pharmacology, repeated dose toxicity, genotoxicity, carcinogenic potential and toxicity to reproduction and development.
Tenofovir disoproxil
Non-clinical safety pharmacology studies on tenofovir disoproxil reveal no special hazard for humans. Repeated dose toxicity studies in rats, dogs and monkeys at exposure levels greater than or equal to clinical exposure levels and with possible relevance to clinical use include renal and bone toxicity and a decrease in serum phosphate concentration. Bone toxicity was diagnosed as osteomalacia (monkeys) and reduced BMD (rats and dogs). The bone toxicity in young adult rats and dogs occurred at exposures > 5-fold the exposure in paediatric or adult patients; bone toxicity occurred in juvenile infected monkeys at very high exposures following subcutaneous dosing (> 40-fold the exposure in patients). Findings in the rat and monkey studies indicated that there was a substance-related decrease in intestinal absorption of phosphate with potential secondary reduction in BMD.
Genotoxicity studies revealed positive results in the in vitro mouse lymphoma assay, equivocal results in one of the strains used in the Ames test, and weakly positive results in an UDS test in primary rat hepatocytes. However, it was negative in an in vivo mouse bone marrow micronucleus assay.
Oral carcinogenicity studies in rats and mice only revealed a low incidence of duodenal tumours at an extremely high dose in mice. These tumours are unlikely to be of relevance to humans.
Reproductive toxicity studies in rats and rabbits showed no effects on mating, fertility, pregnancy or foetal parameters. However, tenofovir disoproxil reduced the viability index and weight of pups in a periand postnatal toxicity study at maternally toxic doses.
Combination of emtricitabine and tenofovir disoproxil
Genotoxicity and repeated dose toxicity studies of one month or less with the combination of these two components found no exacerbation of toxicological effects compared to studies with the separate components.
6. PHARMACEUTICAL PARTICULARS6.1 List of excipients
Tablet core
Pregelatinized starch
Croscarmellose sodium
Lactose monohydrate
Microcrystalline cellulose
Sodium stearyl fumarate
Stearic acid
Film coating
Hypromellose 5 cP
Titanum dioxide (E171)
Macrogol
Indigo carmine aluminium lake (E132)
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
3 years
Shelf life after first opening of the bottle: 2 months.
6.4 Special precautions for storage
Blisters
Do not store above 30°C.
Store in the original blister in order to protect from moisture and light.
HDPE bottle
Do not store above 30°C.
Keep the bottle tightly closed in order to protect from moisture and light.
6.5 Nature and contents of container
Blisters
OPA/Alu/PE+DES/ – Aluminium blisters.
Pack sizes: 28, 84 film-coated tablets and 28 × 1 film-coated tablet.
HDPE bottle
High density polyethylene (HDPE) bottle with a child-resistant tamper evident polypropylene closure with integrated a silica gel desiccant.
Pack sizes: 30 film coated tablets (1×30) and 90 film-coated tablets (3×30).
Not all pack sizes may be marketed.
6.6 Special precautions for disposal
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
7. MARKETING AUTHORISATION HOLDER
KRKA, d.d., Novo mesto, Šmarješka cesta 6, 8501 Novo mesto, Slovenia
8. MARKETING AUTHORISATION NUMBER(S)
Blisters
EU/1/16/1151/001 –28 film-coated tablets
EU/1/16/1151/003 – 84 film-coated tablets
EU/1/16/1151/005 – 28 × 1 film-coated tablet
Bottle
EU/1/16/1151/002 –30 film-coated tablets
EU/1/16/1151/004 –90 (3 × 30) film-coated tablets
9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
Date of first authorisation: 8 December 2016
Date of latest renewal: 15 September 2021