Summary of medicine characteristics - VALNI 20 RETARD
1 NAME OF THE MEDICINAL PRODUCT
Valni 20 Retard (Nifedipine).
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains 20 mg Nifedipine.
Excipient with known effect: Each tablet contains 11.980mg lactose (as lactose monohydrate)
For full list of excipients, see section 6.1
3 PHARMACEUTICAL FORM
Modified Release Tablet.
Pale red, round, biconvex tablets, marked NTF 20 on one side
4 CLINICAL PARTICULARS
4 CLINICAL PARTICULARS4.1 Therapeutic indications
Valni 20 Retard tablets are indicated for the following:
(i) Hypertension
(ii) The prophylaxis of chronic stable angina pectoris
4.2 Posology and method of administration
Posology
It is recommended that these tablets are swallowed with a glass of water. These tablets must be swallowed whole and not broken or chewed.
Adults: The recommended dose is one tablet (20 mg) every 12 hours. The dosage may be increased up to 40 mg every 12 hours to achieve the desired effect.
Paediatric population
The safety and efficacy of nifedipine in children under the age 18 years have not been established. Currently available data for the use of nifedipine in hypertension are described in section 5.1.
Elderly
There are no special dosage requirements for the elderly, however, the pharmacokinetics of nifedipine are altered in the elderly so that lower maintenance doses of nifedipine may be required compared to younger patients.
Patients with hepatic dysfunction must be carefully monitored when treatment is commenced as Nifedipine is primarily metabolised in the liver. If hepatic function is impaired, the dosage requirements of nifedipine should be established before use of Valni 20 Retard.
Dosage adjustments should not be required for patients with renal impairment.
Treatment with Valni 20 Retard may be continued long term.
Method of Administration
Oral Administration.
4.3 Contraindications
Hypersensitivity to nifedipine, any of the excipients listed in section 6.1. or other dihydropyridines because of the theoretical risk of cross reactivity.
Nifedipine should not be used in cardiogenic shock, clinically significant aortic stenosis, unstable angina, or during or within one month of a myocardial infarction.
Nifedipine should not be used for the treatment of acute attacks of angina.
The safety of nifedipine in malignant hypertension has not been established.
Nifedipine should not be used for secondary prevention of myocardial infarction.
Owing to the duration of action of the formulation, Nifedipine should not be administered to patients with hepatic impairment.
Nifedipine should not be administered to patients with a history of gastrointestinal obstruction, oesophageal obstruction, or any degree of decreased lumen diameter of the gastro-intestinal tract.
Nifedipine must not be used in patients with a Kock pouch (ileostomy after Proctocolectomy).
Nifedipine is contra-indicated in patients with inflammatory bowel disease or Crohn's disease
Nifedipine should not be administered concomitantly with rifampicin since effective plasma levels of nifedipine may not be achieved owing to enzyme induction (see section 4.5).
4.4 Special warnings and precautions for use
Nifedipine should be used with caution in patients with severe hypotension and in patients whose cardiac reserve is poor. Deterioration of heart failure has occasionally been observed with nifedipine.
Nifedipine may enhance the effects of other antihypertensive agents such as betablockers (although this combination is well tolerated) resulting in postural hypotension. Nifedipine will not prevent the occurrence of rebound effects following the discontinuation of other antihypertensive agents.
Caution should be exercised in patients with hypotension as there is a risk of further reduction in blood pressure and care must be exercised in patients with very low blood pressure (severe hypotension with systolic pressure less than 90 mm Hg).
C ardiac ischaemic pain has been reported to have occurred in some patients within 1–4 hours of receiving nifedipine. In such cases treatment should be discontinued.
Careful monitoring of blood pressure must be exercised when administering nifedipine with I.V. magnesium sulphate, owing to the possibility of an excessive fall in blood pressure, which could harm both mother and foetus.
Caution should be exercised when nifedipine is given to diabetic patients as nifedipine may impair glucose tolerance, and may require adjustment of diabetic therapy.
In patients with malignant hypertension and hypovolaemia who are on dialysis, a significant decrease in blood pressure can occur.
Nifedipine is metabolised via the cytochrome P450 3A4 system. Drugs that are known to either inhibit or to induce this enzyme system may therefore alter the first pass or the clearance of nifedipine (see section 4.5).
Drugs that are known inhibitors of the cytochrome P450 3A4 system, and which may therefore lead to increased plasma concentrations of nifedipine include, for example:
– macrolide antibiotics (e.g., erythromycin)
– anti-HIV protease inhibitors (e.g., ritonavir)
– azole antimycotics (e.g., ketoconazole)
– the antidepressants, nefazodone and fluoxetine
– quinupristin/dalfopristin
– valproic acid
– cimetidine
Upon co-administration with these drugs, the blood pressure should be monitored and, if necessary, a reduction of the nifedipine dose should be considered.
Nifedipine should not be used during pregnancy unless the clinical condition of the woman requires treatment with nifedipine. Nifedipine should be reserved for women with severe hypertension who are unresponsive to standard therapy (see section 4.6).
Nifedipine is not recommended for use during breastfeeding because nifedipine has been reported to be excreted in human milk and the effects of oral absorption of small amounts of nifedipine are not known (see section 4.6).
For use in special population see section 4.2.
Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicine because it contains lactose
4.5 Interaction with other medicinal products and other forms of interaction
Nifedipine is metabolised via the cytochrome P450 3A4 system, located both in the intestinal mucosa and in the liver. Drugs that are known to either inhibit or to induce this enzyme system may therefore alter the first pass (after oral administration) or the clearance of nifedipine (see section 4.4).
The extent as well as the duration of interactions should be taken into account when administering nifedipine together with the following drugs:
Rifampicin strongly induces the cytochrome P450 3A4 system. Upon coadministration with rifampicin, the bioavailability of nifedipine is distinctly reduced and thus its efficacy weakened. The use of nifedipine in combination with rifampicin is therefore contraindicated (see section 4.3).
Upon co-administration of the following weak to moderate inhibitors of the cytochrome P450 3A4 system, the blood pressure should be monitored and, if necessary, a reduction in the nifedipine dose considered.
In the majority of these cases, no formal studies to assess the potential for a drug interaction between nifedipine and the drug(s) listed have been undertaken, thus far.
No interaction studies have been carried out between nifedipine and macrolide antibiotics. Certain macrolide antibiotics are known to inhibit the cytochrome P450 3A4 mediated metabolism of other drugs. Therefore the potential for an increase of nifedipine plasma concentrations upon co-administration of both drugs cannot be excluded (see section 4.4).
Azithromycin, although structurally related to the class of macrolide antibiotics is void of CYP3A4 inhibition.
A clinical study investigating the potential of a drug interaction between nifedipine and certain anti-HIV protease inhibitors has not yet been performed. Drugs of this class are known to inhibit the cytochrome P450 3A4 system. In addition, drugs of this class have been shown to inhibit in vitro the cytochrome P450 3A4 mediated metabolism of nifedipine. When administered together with nifedipine, a substantial increase in plasma concentrations of nifedipine due to a decreased first pass metabolism and a decreased elimination cannot be excluded (see section 4.4).
A formal interaction study investigating the potential of a drug interaction between nifedipine and certain azole anti-mycotics has not yet been performed. Drugs of this class are known to inhibit the cytochrome P450 3A4 system. When administered orally together with nifedipine, a substantial increase in systemic bioavailability of nifedipine due to a decreased first pass metabolism cannot be excluded (see section 4.4).
A clinical study investigating the potential of a drug interaction between nifedipine and fluoxetine has not yet been performed. Fluoxetine has been shown to inhibit in vitro the cytochrome P450 3A4 mediated metabolism of nifedipine. Therefore an increase of nifedipine plasma concentrations upon co-administration of both drugs cannot be excluded (see section 4.4).
A clinical study investigating the potential of a drug interaction between nifedipine and nefazodone has not yet been performed. Nefazodone is known to inhibit the cytochrome P450 3A4 mediated metabolism of other drugs. Therefore an increase of nifedipine plasma concentrations upon co-administration of both drugs cannot be excluded (see section 4.4).
Simultaneous administration of quinupristin / dalfopristin and nifedipine may lead to increased plasma concentrations of nifedipine (see section 4.4).
No formal studies have been performed to investigate the potential interaction between nifedipine and valproic acid. As valproic acid has been shown to increase the plasma concentrations of the structurally similar calcium channel blocker nimodipine due to enzyme inhibition, an increase in nifedipine plasma concentrations and hence an increase in efficacy cannot be excluded (see section 4.4).
Due to its inhibition of cytochrome P450 3A4, cimetidine elevates the plasma concentrations of nifedipine and may potentiate the antihypertensive effect (see section 4.4).
Upon co-administration of inducers of the cytochrome P450 3A4 system, the clinical response to nifedipine should be monitored and, if necessary, an increase in the nifedipine dose considered. If the dose of nifedipine is increased during coadministration of both drugs, a reduction of the nifedipine dose should be considered when the treatment is discontinued.
Simultaneous administration of cisapride and nifedipine may lead to increased plasma concentrations of nifedipine.
Phenytoin induces the cytochrome P450 3A4 system. Upon co-administration with phenytoin, the bioavailability of nifedipine is reduced and thus its efficacy weakened. When both drugs are concomitantly administered, the clinical response to nifedipine should be monitored and, if necessary, an increase of the nifedipine dose considered. If the dose of nifedipine is increased during co-administration of both drugs, a reduction of the nifedipine dose should be considered when the treatment with phenytoin is discontinued.
No formal studies have been performed to investigate the potential interaction between nifedipine and carbamazepine or phenobarbitone. As both drugs have been shown to reduce the plasma concentrations of the structurally similar calcium channel blocker nimodipine due to enzyme induction, a decrease in nifedipine plasma concentrations and hence a decrease in efficacy cannot be excluded.
Nifedipine may increase the blood pressure lowering effect of concomitant applied antihypertensives. such as:
– diuretics,
– P-blockers,
– ACE-inhibitors,
– Angiotensin 1(AT1) receptor- antagonists,
– other calcium antagonists,
– a-adrenergic blocking agents,
– PDE5 inhibitors,
– a-methyldopa
When nifedipine is administered simultaneously with beta-receptor blockers, the patient should be carefully monitored, since deterioration of heart failure is also known to develop in isolated cases. Withdrawal of any previous antihypertensive agents should be gradual as nifedipine will not compensate for any possible rebound effects.
Quinidine
It is reported that serum quinidine levels have been shown to be reduced when it is used in combination with nifedipine and after discontinuation of nifedipine, a distinct increase in plasma quinidine levels may be observed in individual cases. Consequently, when nifedipine is either additionally administered or discontinued, monitoring of the quinidine plasma concentration, and if necessary, adjustment of the quinidine dose are recommended. Some authors reported increased plasma concentrations of nifedipine upon co-administration of both drugs, while others did not observe an alteration in the pharmacokinetics of nifedipine.
Therefore, the blood pressure should be carefully monitored, if quinidine is added to an existing therapy with nifedipine. If necessary, the dose of nifedipine should be decreased.
Tacrolimus is metabolised via the cytochrome P450 3A4 system. Published data indicate that the dose of tacrolimus administered simultaneously with nifedipine may be reduced in individual cases. Upon co-administration of both drugs, the tacrolimus plasma concentrations should be monitored and, if necessary, a reduction in the tacrolimus dose considered.
Concurrent administration of nifedipine along with theophylline and phenytoin will lead to increased plasma levels of theophylline and phenytoin. and the enhanced effect of non-polarising muscle relaxants such as tubocurarine.
The simultaneous administration of nifedipine and digoxin may lead to reduced digoxin clearance and therefore bring about an increase in the plasma concentrations of digoxin level.. The patient should therefore be checked for symptoms of digoxin overdosage as a precaution and if necessary, the glycoside dose should be reduced taking account of the plasma concentration of digoxin.
As with other dihydropyridines, nifedipine should not be taken with grapefruit juice because bioavailability is increased.
Grapefruit juice inhibits the cytochrome P450 3A4 system, thus results in elevated plasma concentrations and prolonged action of nifedipine due to a decreased first pass metabolism or reduced clearance. As a consequence, the blood pressure lowering effect of nifedipine may be increased. After regular intake of grapefruit juice, this effect may last for at least three days after the last ingestion of grapefruit juice.
Ingestion of grapefruit/grapefruit juice is therefore to be avoided while taking nifedipine.
Nifedipine may increase the spectrophotometric values of urinary vanillylmandelic acid falsely. However, HPLC measurements are unaffected.
4.6 Fertility, pregnancy and lactation
Nifedipine should not be used during pregnancy unless the clinical condition of the woman requires treatment with nifedipine. Nifedipine should be reserved for women with severe hypertension who are unresponsive to standard therapy (see section 4.4).
There are no adequate and well-controlled studies in pregnant women.
In animal studies, nifedipine has been shown to produce embryotoxicity, foetotoxicity and teratogenicity.
From the clinical evidence available, a specific prenatal risk has not been identified, although an increase in perinatal asphyxia, caesarean delivery, as well as prematurity and intrauterine growth retardation have been reported. It is unclear whether these reports are due to the underlying hypertension, its treatment, or to a specific drug effect.
The available information is inadequate to rule out adverse drug effects on the unborn and newborn child.
Acute pulmonary oedema has been observed when calcium channel blockers, among others nifedipine, have been used as a tocolytic agent during pregnancy (see section 4.8), especially in cases of multiple pregnancy (twins or more), with the intravenous route and/or concomitant use of beta-2 agonists.
Nifedipine passes into the breast milk. The nifedipine concentration in the milk is almost comparable with mother serum concentration. For immediate release formulations, it is proposed to delay breastfeeding or milk expression for 3 to 4 hours after drug administration to decrease the nifedipine exposure to the infant (see section 4.4).
In single cases of in vitro fertilisation, calcium antagonists like nifedipine have been associated with reversible biochemical changes in the spermatozoa's head section that may result in impaired sperm function. In those men who are repeatedly unsuccessful in fathering a child by in vitro fertilisation, and where no other explanation can be found, calcium antagonists like nifedipine should be considered as possible causes.
4.7
4.8
Effects on ability to drive and use machines
Reactions to the drug, which vary in intensity from individual to individual, may impair the ability to drive or to operate machinery. This applies particularly at the start of treatment, on changing the medication and in combination with alcohol.
Nausea, headaches, lethargy and dizziness have been reported to occur and therefore the patient should be warned of these possible effects.
Undesirable effects
Adverse drug reactions (ADRs) based on placebo-controlled studies with nifedipine sorted by CIOMS III categories of frequency (clinical trial data base: nifedipine n = 2,661; placebo n = 1,486; status: 22 Feb 2006 and the ACTION study: nifedipine n = 3,825; placebo n = 3,840) are listed below: ADRs listed under „common“ were observed with a frequency below 3% with the exception of oedema (9.9%) and headache (3.9%). ADRs derived from post marketing reports, and for which a frequency could not be estimated are printed in bold italic.
| Common > 1% to <10% | Uncommon > 0.1% to <1% | Rare > 0.01% to <0.1% | Frequency Not Known |
| Blood and Lymphatic System Disorders | |||
| Agranulocytosis Leucopenia | |||
| Immune System Disorder | |||
| Allergic reaction Allergic oedema / angioedema (incl. larynx oedema*) | Pruritus Urticaria Rash | Anaphylactic/ anaphylactoid reaction | |
| Metabolism and Nutrition Disorders | |||
| Hyperglycaemia | |||
| Psychiatric Disorders | |||
| Anxiety reactions Sleep disorders | |||
| Nervous System Disorders | |||
| Headache | Migraine Vertigo Dizziness Tremor | Dysaesthesia, paraesthesia, lethargy | Hypoaesthesia, Somnolence |
| Eye disorders | |||
| Visual disturbances | Eye pain | ||
| Cardiac Disorders | |||
| Tachycardia Palpitations | Chest pain (Angina pectoris) | ||
| Vascular Disorders | |||
| Oedema (incl. peripheral oedema) Vasodilatation | Hypotension Syncope | ||
| Respiratory, Thoracic and Mediastinal Disorders | |||
| Nasal congestion Nosebleed | Dyspnoea Pulmonary oedema | ||
| Gastrointestinal Disorders | |||
| Constipation | Gastrointestinal and abdominal pain Dyspepsia | Gingival hyperplasia | Vomiting, Bezoar Dysphagia, Intestinal obstruction, |
| Flatulence Dry mouth, nausea | Intestinal ulcer, Gastroesophageal sphincter insufficiency | ||
| Hepatobiliary Disorders | |||
| Transient increase in liver enzymes | Jaundice | ||
| Skin and Subcutaneous Tissue Disorders | |||
| Erythema | Toxic Epidermal Necrolysis Photosensitivity allergic reaction Palpable purpura | ||
| Musculoskeletal and Connective Tissue Disorders | |||
| Muscle cramps Joint swelling | Myalgia, Arthralgia | ||
| Renal and Urinary Disorders | |||
| Dysuria, Polyuria | Increased frequency of micturition | ||
| Reproductive System and Breast Disorders | |||
| Erectile dysfunction | |||
| General Disorders and Administration Site Conditions | |||
| Feeling unwell | Unspecific pain Chills | ||
* = may result in life-threatening outcome
cases have been reported when used as tocolytic during pregnancy (see section 4.6)
Exacerbation of angina pectoris may occur frequently at the start of treatment with short acting formulations of nifedipine. The occurrence of myocardial infarction has been described although it is not possible to distinguish such an event from the natural course of ischaemic heart disease.
Gingival hyperplasia and, in older men, gynaecomastia have been reported but these are usually reversible on drug withdrawal. Hypersensitivity reactions such as skin rashes and abnormalities of liver function have occurred. These symptoms disappear upon discontinuation of nifedipine.
In dialysis patients with malignant hypertension and hypovolaemia, a distinct fall in blood pressure can occur as a result of vasodilation.
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 Yellow Card Scheme at www.mhra.gov.uk/yellowcard
4.9 Overdose
This may be associated with severe hypotension, tachycardia or bradycardia and unconsciousness although there are few reports and the symptoms are not necessarily dose-related.
The metabolic disturbances which can occur include hyperglycaemia and metabolic acidosis. The cardiac effects which may occur include heart block, AV dissociation and asystole and cardiogenic shock with pulmonary oedema.
Other effects include drowsiness, dizziness, confusion, nausea, vomiting, lethargy, flushing, hypoxia, disturbances of consciousness to the point of coma.
Treatment-
As far as treatment is concerned, elimination of nifedipine and the restoration of stable cardiovascular conditions have priority. After oral ingestion thorough gastric lavage is indicated, if necessary in combination with irrigation of the small intestine. Particularly in the cases of intoxication with slow release nifedipine formulations such as Nifedipine Retard, elimination must be complete as possible including the small intestine, to prevent the otherwise inevitable subsequent absorption of the active substance.
The benefit of gastric decontamination is uncertain.
1. Consider activated charcoal (50 g for adults, 1 g/kg for children) if the patient presents within 1 hour of ingestion of a potentially toxic amount.
2. Alternatively consider gastric lavage in adults within 1 hour of a potentially lifethreatening overdose.
3. Consider further doses of activated charcoal (alternatively ipecacuanha) every 4 hours, if a clinically significant amount of a sustained release preparation has been ingested with a single dose of an osmotic laxative (e.g. sorbitol, lactulose or magnesium sulphate).
4. Asymptomatic patients should be observed for at least 4 hours after ingestion.
Haemodialysis serves no purpose as nifedipine is not dialysable but plasmapheresis is advisable (high plasma protein binding, relatively low volume of distribution).
Hypotension as a result of cardiogenic shock and arterial vasodilatation can be treated with calcium (10–20ml of a 10% calcium gluconate solution administered slowly i.v. and repeated if necessary).. As a result, the serum calcium can reach the upper normal range to slightly elevated levels. If an insufficient increase in blood pressure is achieved with calcium, vasoconstricting sympathomimetics such as dopamine or noradrenaline are additionally administered. The dosage of these drugs is determined solely by the effect obtained.Bradycardiac heart rhythm disturbances may be treated symptomatically with beta-sympathomimetics, and in life-threatening bradycardiac disturbances of heart rhythm, temporaray pacemaker therapy can be advisable. It has also been reported that the use of metaraminol combined with calcium salts has been beneficial. Care should be exercised to avoid cardiac overload when administering additional fluids or volume
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
ATC Code: C08
Nifedipine is a dihydropyridine and is a potent antagonist of calcium influx through the slow channel of the cell membrane of cardiac and smooth muscle cells. Nifedipine also binds to intracellular calcium binding proteins.
Calcium is normally released from the sarcoplasmic reticulum intracellularly and this combined with the influx of extracellular calcium results in enhanced binding calcium to calmodulin. Calcium channel blockers such as Nifedipine act as arteriolar dilators by inhibiting this calcium entry into the channel. The effects are more pronounced on vascular smooth muscle because depolarisation of cardiac muscle cells is dependent on both sodium ion influx and calcium ion influx and also nifedipine has little effect on the rate of recovery of the slow calcium channel.
Nifedipine is known to be an effective and relatively well tolerated treatment for angina and mild to severe hypertension.
The antihypertensive effects of nifedipine are achieved by causing peripheral vasodilatation resulting in a reduction in peripheral resistance. Nifedipine reduces blood pressure in hypertension but has little or no effect in normotensive individuals.
Nifedipine produces its effects in the treatment of angina by reducing peripheral and coronary vascular resistance, leading to an increase in coronary blood flow, cardiac output and stroke volume and causing a decrease in after-load.
Paediatric population:
Limited information on comparison of nifedipine with other antihypertensives is available for both acute hypertension and long-term hypertension with different formulations in different dosages. Antihypertensive effects of nifedipine have been demonstrated but dose recommendations, long term safety and effect on cardiovascular outcome remain unestablished. Paediatric dosing forms are lacking.
5.2 Pharmacokinetic properties
Nifedipine is rapidly and almost completely absorbed from the gastro-intestinal tract after oral administration, however due to extensive hepatic first pass metabolism, the resultant bioavailability lies between 45% and 75%. Administration in the presence of food slightly alters the early rate of absorption but does not influence the extent of drug availability.
The terminal elimination half-life is 1.7 to 3.4 h in conventional formulations (nifedipine capsules). The terminal half-life following Nifedipine retard administration does not represent a meaningful parameter as a plateau-like plasma concentration is maintained during release from the tablets and absorption. After release and absorption of the last dose, the plasma concentration finally declines with an elimination half-life as seen in conventional formulations
Nifedipine is about 92%-98% bound to plasma proteins (albumin). The distribution halflife after intravenous administration has been determined to be 5 to 6 minutes.
After oral administration, nifedipine is metabolised in the gut wall and in the liver, primarily by oxidative processes. These metabolites show no pharmacodynamic activity. Nifedipine is eliminated in the form of its metabolites, predominantly via the kidneys, with approximately 5–15% being excreted via the bile in the faeces. Non-metabolised nifedipine can be detected only in traces (below 0.1%) in the urine.
There are no significant differences in the pharmacokinetics of nifedipine between healthy subjects and subjects with renal impairment. Therefore, dosage adjustment is not needed in these patients.
In patients with hepatic impairment, the elimination half-life is distinctly prolonged and the total clearance is reduced. Owing to the duration of action of the formulation, nifedipine retard should not be administered in these patients.
The dosage schedule for a standard capsule formulation of nifedipine is 10 mg three times daily leading to a maximum of 20 mg three times daily. The nifedipine tablet is designed as a modified release product to provide a twice daily dosing of 20 mg which can be increased to 40 mg twice daily if necessary.
Adalat Retard is a modified release formulation currently available on the UK market. A comparative bioavailability study has been carried out comparing this preparation with Valni 20 Retard. The results of the study are provided below and demonstrate that these two preparations are bioequivalent.
Mean data from the comparative bioavailability study is presented below:
| Pharmacokinetic parameters | Adalat Retard | Valni 20 Retard |
| measured after 6 days at Tablet steady state (mean N=24) | Tablet | |
| CMAX | 58.7ng/ml | 58.5ng/ml |
| T/ B | 13.31 hours | 17.30 hours |
| AUC 0–48 hours | 407 ng/ml/hour 413 ng/ml/hour | |
| AUC0-INF | 480 ng/ml/hour 517 ng/ml/hour | |
| TMAX | 2.00 hours | 2.21 hours |
5.3 Preclinical safety data
Preclinical data reveal no special hazards for humans based on conventional studies of single and repeated dose toxicity, genotoxicity and carcinogenic potential.
Following acute oral and intravenous administration of nifedipine in various animal species, the following LD50 (mg/kg) values were obtained:
| Mouse: | Oral: 494 (421–572); | i.v.: 4.2 (3.8–4.6). |
| Rat: | Oral: 1022 (950–1087); | i.v.: 15.5 (13.7–17.5). |
| Rabbit | Oral: 250–500; | i.v.: 2–3. |
| Cat: | Oral: ~ 100; | i.v.: 0.5–8. |
| Dog: | Oral: > 250; | i.v.: 2–3. |
* 95% confidence interval.
In subacute and subchronic toxicity studies in rats and dogs, nifedipine was tolerated without damage at doses of up to 50 mg/kg (rats) and 100 mg/kg (dogs) p.o. over periods of thirteen and four weeks, respectively. Following intravenous administration, dogs tolerated up to 0.1 mg/kg nifedipine for six days without damage. Rats tolerated daily intravenous administration of 2.5 mg/kg nifedipine over a period of three weeks without damage.
In chronic toxicity studies in dogs with treatment lasting up to one year, nifedipine was tolerated without damage at doses up to and including 100 mg/kg p.o. In rats, toxic effects occurred at concentrations above 100 ppm in the feed (approximately 5–7 mg/kg bodyweight).
In a carcinogenicity study in rats (two years), there was no evidence of a carcinogenic effect of nifedipine.
Nifedipine has been shown to produce teratogenic findings in rats, mice and rabbits, including digital anomalies, malformation of the extremities, cleft palates, cleft sternum and malformation of the ribs.
Digital anomalies and malformation of the extremities are possibly a result of compromised uterine blood flow, but have also been observed in animals treated with nifedipine solely after the end of the organogenesis period.
Nifedipine administration was associated with a variety of embryotoxic, placentotoxic and foetotoxic effects, including stunted foetuses (rats, mice, rabbits), small placentas and underdeveloped chorionic villi (monkeys), embryonic and foetal deaths (rats, mice, rabbits) and prolonged pregnancy/decreased neonatal survival (rats; not evaluated in other species). The risk to humans cannot be ruled out if a sufficiently high systemic exposure is achieved, however, all of the doses associated with the teratogenic, embryotoxic or foetotoxic effects in animals were maternally toxic and were several times the recommended maximum dose for humans.
In in vitro and in vivo tests, nifedipine has not been associated with mutagenic properties
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Microcrystalline cellulose, lactose, corn starch, talc, hydroxypropylmethyl cellulose, magnesium stearate, polysorbate 80, polyethylene glycol 4000, iron oxide (E172) and titanium dioxide (E171).
6.2 Incompatibilities
None reported.
6.3 Shelf life
3 years.
6.4 Special precautions for storage
Store in a dry place below 25°C. Store in the original package in order to protect from light.
6.5 Nature and contents of container
Blister strips composed of: PVC foil 250^m ± 5%, PVdC 25^m ± 5%, aluminium foil 25iim ± 8%, PVdC 20GSM ± 10%.
Pack size: 28, 30, 56, 60, 84, 100, 250, 500, 1,000.
Not all pack sizes may be marketed.
6.6 Special precautions for disposal and other handling
No special requirements for disposal
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
Tillomed Laboratories Ltd
220 Butterfield, Great Marlings
Luton
LU2 8DL
UK
8 MARKETING AUTHORISATION NUMBER(S)
PL 11311/0458
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
Date of first authorisation: 10/10/1995
Date of renewal: 20/08/2001