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סיפרול 0.25 מ"ג SIFROL TABLETS 0.25 MG (PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE)
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צורת מתן:
פומי : PER OS
צורת מינון:
טבליה : TABLETS
עלון לרופא
מינוניםPosology התוויות
Indications תופעות לוואי
Adverse reactions התוויות נגד
Contraindications אינטראקציות
Interactions מינון יתר
Overdose הריון/הנקה
Pregnancy & Lactation אוכלוסיות מיוחדות
Special populations תכונות פרמקולוגיות
Pharmacological properties מידע רוקחי
Pharmaceutical particulars אזהרת שימוש
Special Warning עלון לרופא
Physicians Leaflet
Adverse reactions : תופעות לוואי
4.8 Undesirable effects Based on the analysis of pooled placebo-controlled trials, comprising a total of 1,923 patients on pramipexole and 1,354 patients on placebo, adverse drug reactions were frequently reported for both groups. 63% of patients on pramipexole and 52% of patients on placebo reported at least one adverse drug reaction. The majority of adverse drug reactions usually start early in therapy and most tend to disappear even as therapy is continued. Sifrol IR Updated Prescribing Information 0.25 mg, 1 mg April 2020 Within the system organ classes, adverse reactions are listed under headings of frequency (number of patients expected to experience the reaction), using the following categories: 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). Parkinson's disease, most common adverse reactions The most commonly ( 5%) reported adverse drug reactions in patients with Parkinson's disease more frequent with pramipexole treatment than with Placebo were nausea, dyskinesia, hypotension, dizziness, somnolence, insomnia, constipation, hallucination, headache and fatigue. The incidence of somnolence is increased at doses higher than 1.5 mg pramipexole salt per day (see section 4.2.). A more frequent adverse drug reaction in combination with levodopa was dyskinesia. Hypotension may occur at the beginning of treatment, especially if pramipexole is titrated too fast. Table 1: Parkinson’s disease Body System Very common Common Uncommon Rare Not known (≥1/10) (≥1/100 to (≥1/1,000 to (≥1/10,000 <1/10) < 1/100) To <1/1,000) Infections and pneumonia infestations Endocrine inappropriate disorders antidiuretic hormone secretion1 Psychiatric Insomnia, compulsive mania disorders Hallucinations, shopping, abnormal pathological dreams, gambling, confusion, restlessness, behavioural hypersexuality, symptoms of delusion, impulse control libido disorder, disorders and paranoia, compulsions delirium, binge eating1 hyperphagia1 Nervous system Somnolence, headache sudden onset of disorders Dizziness, sleep, Dyskinesia amnesia, hyperkinesia, syncope Eye disorders visual impairment including diplopia, vision blurred, visual acuity reduced Cardiac cardiac failure1 disorders Vascular hypotension disorders Respiratory, Dyspnoea, thoracic, and hiccups mediastinal disorders Gastrointestinal nausea Constipation, disorders vomiting Skin and Hypersensitivity, Sifrol IR Updated Prescribing Information 0.25 mg, 1 mg April 2020 subcutaneous Pruritus, tissue disorders rash General Fatigue, Dopamine disorders and peripheral agonist administration oedema withdrawal site conditions syndrome including apathy, anxiety, depression, fatigue, sweating and pain. Investigations weight decrease weight increase including decreased appetite 1 This side effect has been observed in post-marketing experience. With 95 % certainty, the frequency category is not greater than uncommon, but might be lower. A precise frequency estimation is not possible as the side effect did not occur in a clinical trial database of 2,762 patients with Parkinson’s Disease treated with pramipexole. Restless Legs Syndrome, most common adverse reactions The most commonly ( 5%) reported adverse drug reactions in patients with Restless Legs Syndrome treated with Pramipexole were nausea, headache, dizziness and fatigue. Nausea and fatigue were more often reported in female patients treated with SIFROL (20.8% and 10.5%, respectively) compared to males (6.7% and 7.3%, respectively). Table 2: Restless Legs Syndrome Body Very common Common Uncommon (≥1/1,000 to < Not known System (≥1/10) (≥1/100 to 1/100) <1/10) Infections and pneumonia1 infestations Endocrine inappropriate antidiuretic disorders hormone secretion1 Psychiatric Insomnia, Restlessness, confusion, disorders abnormal hallucinations, libido disorder, dreams delusion1, hyperphagia1, paranoia1 , mania1 , delirium1, behavioural symptoms of impulse control disorders and compulsions1 (such as: compulsive shopping, pathological gambling, hypersexuality, binge eating) Nervous Headache, sudden onset of sleep, syncope, system dizziness, dyskinesia, amnesia1, disorders somnolence hyperkinesia1 Eye disorders visual impairment including visual acuity, reduced diplopia, vision blurred Sifrol IR Updated Prescribing Information 0.25 mg, 1 mg April 2020 Cardiac cardiac failure1 disorders Vascular Hypotension disorders Respiratory, Dyspnoea, hiccups thoracic, and mediastinal disorders Gastrointestina nausea constipation, l disorders vomiting Skin and Hypersensitivity, pruritus, rash subcutaneous tissue disorders General fatigue peripheral oedema Dopamine disorders and agonist administration withdrawal site conditions syndrome including apathy, anxiety, depression, fatigue, sweating and pain Investigations weight decrease including decreased appetite weight increase 1 This side effect has been observed in post-marketing experience. With 95 % certainty, the frequency category is not greater than uncommon, but might be lower. A precise frequency estimation is not possible as the side effect did not occur in a clinical trial database of 1,395 patients with Restless Legs Syndrome treated with pramipexole Description of selected adverse reactions Somnolence Pramipexole is commonly associated with somnolence and has been associated uncommonly with excessive daytime somnolence and sudden sleep onset episodes (see also section 4.4). Libido disorders Pramipexole may uncommonly be associated with libido disorders (increased or decreased). Impulse control disorders Pathological gambling, increased libido, hypersexuality, compulsive spending or buying, binge eating and compulsive eating can occur in patients treated with dopamine agonists including SIFROL (see section 4.4). In a cross-sectional, retrospective screening and case-control study including 3,090 Parkinson’s disease patients, 13.6% of all patients receiving dopaminergic or non-dopaminergic treatment had symptoms of an impulse control disorder during the past six months. Manifestations observed include pathological gambling, compulsive shopping, binge eating, and compulsive sexual behaviour (hypersexuality). Possible independent risk factors for impulse control disorders included dopaminergic treatments and higher doses of dopaminergic treatment, younger age ( ≤ 65 years), not being married and self-reported family history of gambling behaviours. Dopamine agonist withdrawal syndrome Non-motor adverse effects may occur when tapering or discontinuing dopamine agonists including pramipexole. Symptoms include apathy, anxiety, depression, fatigue, sweating and pain (see section Sifrol IR Updated Prescribing Information 0.25 mg, 1 mg April 2020 4.4). Cardiac failure In clinical studies and post-marketing experience cardiac failure has been reported in patients with pramipexole. In a pharmacoepidemiological study pramipexole use was associated with an increased risk of cardiac failure compared with non-use of pramipexole (observed risk ratio 1.86; 95% CI, 1.21-2.85). You can report side effects to the Ministry of Health by following the link ‘Reporting Side Effects of Drug Treatment' on the Ministry of Health home page (www.health.gov.il) which links to an online form for reporting side effects. You can also use this link: https://sideeffects.health.gov.il
פרטי מסגרת הכללה בסל
התרופה תינתן בהתקיים כל אלה: א. התרופה תינתן לטיפול בפרקינסון באחת הדרכים האלה: 1. כטיפול יחיד 2. כטיפול משולב עם levodopa ב. לא יינתנו התרופות Pergolide Ropinirole או Pramipexole בו בזמן ג. מתן התרופה ייעשה לפי מרשם של רופא מומחה בנוירולוגיה.
מסגרת הכללה בסל
התוויות הכלולות במסגרת הסל
התוויה | תאריך הכללה | תחום קליני | Class Effect | מצב מחלה |
---|---|---|---|---|
פרקינסון | 01/03/2008 |
שימוש לפי פנקס קופ''ח כללית 1994
לא צוין
תאריך הכללה מקורי בסל
01/03/2008
הגבלות
תרופה מוגבלת לרישום ע'י רופא מומחה או הגבלה אחרת
מידע נוסף