Summary of Product Characteristics (SmPC) - Cytisinicline Adamed 1.5 mg film-coated tablets
1 NAME OF THE MEDICINAL PRODUCT
Cytisinicline Adamed 1.5 mg film-coated tablets
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains 1.5 mg of cytisinicline, also known as cytisine.
Excipient with known effect:
Each tablet contains 0.12 mg aspartame.
For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Film-coated tablet (tablet)
Round, biconvex, light green or greenish film-coated tablets of 5 mm diameter.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
Smoking cessation and reduction of nicotine cravings in smokers who are willing to stop smoking.
The treatment goal of Cytisinicline Adamed is the permanent cessation of the nicotine-containing products use.
4.2 Posology and method of administration
Posology
One package of Cytisinicline Adamed (100 tablets) is sufficient for a complete treatment course.
The duration of therapy is 25 days.
Cytisinicline Adamed should be taken according to the following schedule: From the 1st to the 3rd day 1 tablet should be taken every 2 hours (6 tablets daily). From the 4th to the 12th day 1 tablet should be taken every 2.5 hours (5 tablets daily). From the13th to the 16th day 1 tablet should be taken every 3 hours (4 tablets daily). From the 17th to the 20th day 1 tablet should be taken every 5 hours (3 tablets daily).
From the 21st to the 25th day 1 to 2 tablets daily should be taken.
Special population (renal impairment, hepatic impairment)
There is no clinical experience of Cytisinicline Adamed in patients with renal or hepatic impairment, therefore the drug product is not recommended for use in this patient population.
Elderly population
Due to limited clinical experience, Cytisinicline Adamed is not recommended for use in elderly patients over 65 years of age.
Paediatric population
The safety and efficacy of Cytisinicline Adamed in persons under 18 years of age have not been established. Cytisinicline Adamed is not recommended for use in persons under 18 years of age.
Method of administration
Cytisinicline Adamed should be taken orally with a suitable amount of water.
4.3 Contraindications
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1,
Unstable angina,
A history of recent myocardial infarction,
Clinically significant arrhythmias,
A history of recent stroke,
Pregnancy and breastfeeding.
4.4 Special warnings and precautions for use
Cytisinicline Adamed should be taken only by those with a serious intention of weaning off nicotine. Patient should be aware, that the simultaneous administration of the drug and smoking or use of products containing nicotine could lead to aggravated adverse reactions of nicotine.
Cytisinicline Adamed should be taken with caution in case of ischemic heart disease, heart failure, hypertension, pheochromocytoma, atherosclerosis and other peripheral vascular diseases, gastric and duodenal ulcer, gastroesophageal reflux disease, hyperthyroidism, diabetes and schizophrenia.
Women of childbearing potential
Women of childbearing potential must use highly effective contraception while taking Cytisinicline Adamed (see section 4.5 and 4.6).
4.5 Interaction with other medicinal products and other forms of interaction
Cytisinicline Adamed should not be used with anti-tuberculosis drugs. No other clinical data on significant interaction with other drugs.
Hormonal contraceptives
It is currently unknown whether Cytisinicline Adamed may reduce the effectiveness of systemically acting hormonal contraceptives, and therefore women using systemically acting hormonal contraceptives should add a second barrier method.
4.6 Fertility, pregnancy and lactation
Pregnancy
There are no or limited amount of data from the use of cytisine in pregnant women. Animal studies are insufficient with respect to reproductive toxicity (see section 5.3). Cytisinicline Adamed is contraindicated during pregnancy (see section 4.3).
Breastfeeding
Cytisinicline Adamed is contraindicated during breast-feeding (see section 4.3).
Fertility
No data on the effects of Cytisinicline Adamed on fertility.
Women of childbearing potential
Women of childbearing potential must use highly effective contraception while taking Cytisinicline Adamed (see section 4.5 and 4.4). Women using systemically acting hormonal contraceptives should add a second barrier method.
4.7 Effects on ability to drive and use machines
Cytisinicline Adamed has no influence on the ability to drive and use machines.
4.8 Undesirable effects
The clinical studies and previous experience with use of cytisine-containing product indicate a good tolerability of cytisine. The proportion of patients who discontinued treatment because adverse reactions was 6-15,5% and in controlled studies it was comparable to the proportion of patients who discontinued treatment in the placebo group. Mild to moderate adverse reactions have usually been observed, most frequently concerning the gastrointestinal tract. The majority of adverse reactions occurred at the beginning of the therapy and resolved during treatment. These symptoms could also be the result of smoking cessation, rather than the use of drug product.
All adverse reactions by system organ class and frequency of occurrence in clinical trials are listed below. The frequency of occurrence is defined as follows: very common (≥ 1/10), common (≥ 1/100 to < 1/10), uncommon (≥ 1/1,000 to < 1/100), rare (≥ 1/10,000 to < 1/1,000), very rare (<1/10,000), not known (cannot be estimated from the available data).
Metabolism and nutrition disorders:
very common: change in appetite (mainly increase), weight gain
Nervous system disorders:
very common: dizziness, irritability, mood changes, anxiety, sleep disorders (insomnia, drowsiness, lethargy, abnormal dreams, nightmares), headaches
common: difficulty in concentration
uncommon: feeling of heaviness in the head, decreased libido
Eye disorders:
uncommon: lacrimation
Cardiac disorders:
very common: tachycardia
common: slow heart rate
Vascular disorders:
very common: hypertension
Respiratory, thoracic and mediastinal disorders:
uncommon: dyspnea, increased sputum
Gastrointestinal disorders:
very common: dry mouth, diarrhea, nausea, changes flavour, heartburn, constipation, vomiting, abdominal pain (especially in the upper abdomen)
common: abdominal distension, burning tongue uncommon: excessive salivation
Skin and subcutaneous tissue disorders:
very common: rash
uncommon: sweating, decreased elasticity of the skin
Musculoskeletal and connective tissue disorders:
very common: myalgia
General disorders and administration site conditions:
very common: fatigue
common: malaise
uncommon: tiredness
Investigations:
uncommon: increase in serum transaminase levels
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:
Yellow Card Scheme
Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
4.9 Overdose
Symptoms of nicotine intoxication are observed in Cytisinicline Adamed overdose. Symptoms of overdose include malaise, nausea, vomiting, increased heart rate, blood pressure fluctuations, breathing disorders, visual disturbances, clonic convulsions. In all cases of overdose, standard procedure should be taken as in acute poisoning; gastric lavage should be performed and the diuresis should be controlled with infusion fluids and diuretics. The anti-epileptic drugs, acting on the cardiovascular system and stimulating the respiration may be used, if necessary. Breathing, blood pressure and heart rate should be monitored.
5. PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: drugs used in nicotine dependence, ATC code: N07BA04
The use of Cytisinicline Adamed allows for a gradual reduction of nicotine dependence by relieving withdrawal symptoms.
The active ingredient of Cytisinicline Adamed is a plant alkaloid cytisine (found, among others, in seeds of golden chain, genus Laburnum), with a chemical structure similar to nicotine. It has an effect on acetylcholine nicotinic receptors. The action of cytisine is similar to that of nicotine, but in general weaker. Cytisine competes with nicotine for the same receptors and gradually displaces nicotine due to its stronger binding. It has lower ability to stimulate nicotinic receptors, mainly α4β2 subtype (it is their partial agonist) and less than nicotine passes into the central nervous system. It is hypothesized that in the central nervous system cytisine acts on the mechanism involved in nicotine dependence and on the release of neurotransmitters. It prevents nicotine-dependent full activation of the mesolimbic dopamine system and moderately increases level of dopamine in the brain, what alleviates the central symptoms of nicotine withdrawal. In the peripheral nervous system, cytisine stimulates and then infects the autonomic ganglia of the nervous system, causes a reflex stimulation of breathing and secretion of catecholamines from the core part of the adrenal gland, raises blood pressure and prevents peripheral symptoms of nicotine withdrawal.
5.2 Pharmacokinetic properties
Pharmacokinetics in animals:
After oral administration of labeled cytisine in mice at a dose of 2 mg/kg, 42% of the administered dose was absorbed. The maximum concentration of cytisine in the blood was reported after 120 minutes, and within 24 hours 18% of the dose was excreted in the urine. The half-life of cytisine, determined after intravenous administration, was 200 minutes. Nearly 1/3 of the dose administered intravenously was excreted in the urine in 24 hours and 3% of the dose within 6 hours with faeces. The highest concentrations of drug were obtained in liver, adrenal glands and kidneys. After intravenous administration, the concentration of cytisine in the bile was 200 times higher than in blood. Constant level of cytisine concentration in the blood was accomplished in two phases after its percutaneous administration to the rabbits. The first phase lasted 24 hours and the second phase for the next three days. In the first phase, the rate of absorption and the blood level of the drug were two times higher than in the second phase. The volume of distribution (Vd) in rabbits after oral and intravenous administration was 6.21 l/kg and 1.02 l/kg, respectively. After subcutaneous administration of 1 mg/kg cytisine to male rats, the blood concentration was 516 ng/ml, and the concentration in the brain was 145 ng/ml. The concentration in the brain was less than 30% of the concentration in the blood. In similar experiments with subcutaneously administered nicotine, the concentration of nicotine in the brain was 65% of the concentration in the blood.
Pharmacokinetics in humans:
Absorption
The pharmacokinetic properties of cytisine were tested after a single oral dose of the formulation containing 1.5 mg of cytisine in 36 healthy volunteers. After oral administration, cytisine was quickly absorbed from the gastrointestinal tract. The mean maximum plasma concentration of 15.55 ng/ml was achieved after a mean of 0.92 hours.
Biotransformation
Cytisine was slightly metabolised.
Elimination
64% of the dose was excreted unchanged in the urine within 24 hours. The mean halflife in plasma was approx. 4 hours. The mean residence time (MRT) was approx. 6 hours.
There is no data in renally and hepatically impaired patients and the influence of food on the exposure of cytosine is unknown.
5.3 Preclinical safety data
Non-clinical data reveal no special hazard for humans based on non-GLP studies of repeat dose toxicity, genotoxicity and toxicity to reproduction and development.
Repeat dose toxicity studies in mice, rats and dogs did not show significant toxicity in relation to haematopoiesis, gastric mucosa, kidneys, liver and other internal organs.
Cytisine was not genotoxic in an in vivo study in mice. There was no evidence of embryotoxicity of cytisine in rats.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Tablet core: hypromellose, mannitol, maize starch, magnesium aluminometasilicate type A, silica colloidal anhydrous, magnesium stearate.
Film-coat: Aqua Polish P green [hypromellose (E464), cellulose microcrystalline (E460), talcum (E553b), glycerol (E422), titanium dioxide (E171), quinoline yellow Al-lake (E104), indigo carmine (blue 2) Al-lake ( E132)], menthol flavour powder (SC552873), aspartame (E951).
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
3 years
6.4 Special precautions for storage
Store in the original package in order to protect from light.
This medicinal product does not require any special temperature storage conditions.
6.5 Nature and contents of container
Carton includes 100 film-coated tablets in PVC / PVDC / Aluminum blisters.
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
Adamed Pharma S.A.
Pieńków, ul. M. Adamkiewicza 6A
05-152 Czosnów
Poland
8 MARKETING AUTHORISATION NUMBER(S)
PL 32556/0025
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE
AUTHORISATION
06/02/2024
10 DATE OF REVISION OF THE TEXT
16/05/2024