Quest for the right Drug
אביליפיי מיינטנה 400 מ"ג ABILIFY MAINTENA 400 MG (ARIPIPRAZOLE AS MONOHYDRATE)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
תוך-שרירי : I.M
צורת מינון:
אבקה וממס להכנת תרחיף בשחרור ממושך להזרקה : POWDER AND SOLVENT FOR PROLONGED-RELEASE SUSPENSION FOR INJECTION
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 Summary of the safety profile The most frequently observed adverse drug reactions (ADRs) reported in ≥ 5 % of patients in two double-blind , long-term trials of Abilify Maintena were weight increased (9.0 %), akathisia (7.9 %), insomnia (5.8 %), and injection site pain (5.1 %). Tabulated list of adverse reactions The incidences of the ADRs associated with aripiprazole therapy are tabulated below. The table is based on adverse reactions reported during clinical trials and/or post-marketing use. All ADRs are listed by system organ class and frequency; 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) and not known (cannot be estimated from the available data). Within each frequency grouping, adverse reactions are presented in order of decreasing seriousness. The frequency of adverse reactions reported during post-marketing use cannot be determined as they are derived from spontaneous reports. Consequently, the frequency of these adverse events is qualified as "not known". Common Uncommon Not known Blood and Neutropenia Leukopenia lymphatic Anaemia system Thrombocytopenia disorders Neutrophil count decreased White blood cell count decreased Immune Hypersensitivity Allergic reaction (e.g. system anaphylactic reaction, disorders angioedema including swollen tongue, tongue oedema, face oedema, pruritus, or urticaria) Endocrine Blood prolactin decreased Diabetic hyperosmolar coma disorders Hyperprolactinaemia Diabetic ketoacidosis Metabolism Weight Hyperglycaemia Anorexia and increased Hypercholesterolaemia Hyponatraemia nutrition Diabetes Hyperinsulinaemia disorders mellitus Hyperlipidaemia Weight Hypertriglyceridaemia decreased Appetite disorder Psychiatric Agitation Suicidal ideation Completed suicide disorders Anxiety Psychotic disorder Suicide attempt Restlessness Hallucination Pathological gambling Insomnia Delusion Impulse-control disorders Hypersexuality Binge eating Panic reaction Compulsive shopping Depression Poriomania Affect lability Nervousness Apathy Aggression Dysphoria Sleep disorder Bruxism Libido decreased Mood altered Nervous Extrapyramidal Dystonia Neuroleptic malignant system disorder Tardive dyskinesia syndrome disorders Akathisia Parkinsonism Grand mal convulsion Tremor Movement disorder Serotonin syndrome Dyskinesia Psychomotor hyperactivity Speech disorder Sedation Restless legs syndrome Common Uncommon Not known Somnolence Cogwheel rigidity Dizziness Hypertonia Headache Bradykinesia Drooling Dysgeusia Parosmia Eye Oculogyric crisis disorders Vision blurred Eye pain Diplopia Photophobia Cardiac Ventricular extrasystoles Sudden unexplained death disorders Bradycardia Cardiac arrest Tachycardia Torsades de pointes Electrocardiogram T wave Ventricular arrhythmias amplitude decreased QT prolongation Electrocardiogram abnormal Electrocardiogram T wave inversion Vascular Hypertension Syncope disorders Orthostatic hypotension Venous thromboembolism Blood pressure increased (including pulmonary embolism and deep vein thrombosis) Respiratory, Cough Oropharyngeal spasm thoracic and Hiccups Laryngospasm mediastinal Aspiration pneumonia disorders Gastrointesti Dry mouth Gastrooesophageal reflux Pancreatitis nal disorders disease Dysphagia Dyspepsia Vomiting Diarrhoea Nausea Abdominal pain upper Abdominal discomfort Constipation Frequent bowel movement Salivary hypersecretion Hepatobiliary Liver function test Hepatic failure disorders abnormal Jaundice Hepatic enzyme increased Hepatitis Alanine aminotransferase Alkaline phosphatase increased increased Gamma-glutamyl transferase increased Blood bilirubin increased Aspartate aminotransferase Common Uncommon Not known increased Skin and Alopecia Rash subcutaneous Acne Photosensitivity reaction tissue Rosacea Hyperhidrosis disorders Eczema Drug Reaction with Skin induration Eosinophilia and Systemic Symptoms (DRESS) Musculoskel Musculoskeletal Muscle rigidity Rhabdomyolysis etal and stiffness Muscle spasms connective Muscle twitching tissue Muscle tightness disorders Myalgia Pain in extremity Arthralgia Back pain Joint range of motion decreased Nuchal rigidity Trismus Renal and Nephrolithiasis Urinary retention, Urinary urinary Glycosuria incontinence disorders Pregnancy, Drug withdrawal syndrome puerperium neonatal (see section 4.6) and perinatal conditions Reproductive Erectile Galactorrhoea Priapism system and dysfunction Gynaecomastia breast Breast tenderness disorders Vulvovaginal dryness General Injection site Pyrexia Temperature regulation disorders pain Asthenia disorder (e.g. hypothermia, and Injection site Gait disturbance pyrexia) administrati induration Chest discomfort Chest pain on site Fatigue Injection site reaction Peripheral oedema conditions Injection site erythema Injection site swelling Injection site discomfort Injection site pruritus Thirst Sluggishness Common Uncommon Not known Investigations Blood creatine Blood glucose increased Blood glucose fluctuation phosphokinase Blood glucose decreased increased Glycosylated haemoglobin increased Waist circumference increased Blood cholesterol decreased Blood triglycerides decreased Description of selected adverse reactions Injection site reactions During the double-blind, controlled phases of the two long-term trials, injection site reactions were observed; those seen were generally mild to moderate in severity, and resolved over time. Injection site pain (incidence 5.1 %), had a median onset on day 2 after the injection and a median duration of 4 days. In an open label study comparing bioavailability of Abilify Maintena administered in the deltoid or gluteal muscle, injection site related reactions were slightly more frequent in the deltoid muscle. The majority were mild and improved on subsequent injections. When compared to studies where Abilify Maintena was injected in the gluteal muscle, repeated occurrence of injection site pain was more frequent in the deltoid muscle. Leukopenia Neutropenia has been reported in the clinical program with Abilify Maintena and typically started around day 16 after first injection, and lasted a median of 18 days. Extrapyramidal Symptoms (EPS) In trials in stable patients with schizophrenia, Abilify Maintena was associated with a higher frequency of EPS symptoms (18.4 %) than oral aripiprazole treatment (11.7 %). Akathisia was the most frequently observed symptom (8.2 %) and typically started around day 10 after first injection, and lasted a median of 56 days. Subjects with akathisia typically received anti-cholinergic medicines as treatment, primarily benzatropine mesilate and trihexyphenidyl. Less often substances such as propranolol and benzodiazepines (clonazepam and diazepam) were administered to control akathisia. Parkinsonism events followed in frequency of 6.9 % for Abilify Maintena, 4.15 % for oral aripiprazole 10-30 mg tablets and 3.0 % for placebo, respectively. Dystonia Class effect: Symptoms of dystonia, prolonged abnormal contractions of muscle groups, may occur in susceptible individuals during the first few days of treatment. Dystonic symptoms include spasm of the neck muscles, sometimes progressing to tightness of the throat, swallowing difficulty, difficulty breathing, and/or protrusion of the tongue. While these symptoms can occur at low doses, they occur more frequently and with greater severity with high potency and at higher doses of first generation antipsychotic medicinal products. An elevated risk of acute dystonia is observed in males and younger age groups. Weight During the Double-blind, Active-controlled Phase of the 38-week long-term trial, the incidence of weight gain of ≥ 7 % from baseline to last visit was 9.5 % for Abilify Maintena and 11.7 % for the oral aripiprazole tablets 10-30 mg. The incidence of weight loss of ≥ 7 % from baseline to last visit was 10.2 % for Abilify Maintena and 4.5 % for oral aripiprazole tablets 10-30 mg. During the Double-blind, Placebo-controlled Phase of the 52-week long-term trial, the incidence of weight gain of ≥ 7 % from baseline to last visit was 6.4 % for Abilify Maintena and 5.2 % for placebo. The incidence of weight loss of ≥ 7 % from baseline to last visit was 6.4 % for Abilify Maintena and 6.7 % for placebo. During double-blind treatment, mean change in body weight from baseline to last visit was -0.2 kg for Abilify Maintena and -0.4 kg for placebo (p = 0.812). Prolactin In clinical trials for the approved indications and post-marketing, both increase and decrease in serum prolactin as compared to baseline was observed with aripiprazole (section 5.1). Pathological gambling and other impulse control disorders Pathological gambling, hypersexuality, compulsive shopping and binge or compulsive eating can occur in patients treated with aripiprazole (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. Any suspected adverse events should be reported to the Ministry of Health according to the National Regulation by using an online form https://sideeffects.health.gov.il/
פרטי מסגרת הכללה בסל
1. הטיפול בתרופה האמורה יינתן לאחד מאלה: א. למבוטח בגיר שהוא חולה סכיזופרניה;ב. למבוטח קטין הסובל מסכיזופרניה או מפסיכוזה אחרת;ג. טיפול בהפרעה ביפולרית כקו טיפולי שני. ד. טיפול אוגמנטציה בדיכאון מסוג (major depressive disorder (MDD2. התחלת הטיפול בתרופה תהיה על פי הוראתו של רופא מומחה בפסיכיאטריה או בפסיכיאטריה של הילד והמתבגר או בנוירולוגיה, לפי העניין; 3. לא יינתנו לחולה בו בזמן שתי תרופות או יותר ממשפחת התרופות האנטיפסיכוטיות האטיפיות, למעט לעניין סעיף 1(ד).
מסגרת הכללה בסל
התוויות הכלולות במסגרת הסל
התוויה | תאריך הכללה | תחום קליני | Class Effect | מצב מחלה |
---|---|---|---|---|
טיפול אוגמנטציה בדיכאון מסוג (major depressive disorder (MDD | 21/01/2016 | פסיכיאטריה | ||
מבוטח בגיר שהוא חולה סכיזופרניה | 12/01/2014 | פסיכיאטריה | ZIPRASIDONE, ARIPIPRAZOLE, SERTINDOLE, PALIPERIDONE, QUETIAPINE, ILOPERIDONE, AMISULPRIDE, OLANZAPINE, RISPERIDONE, ASENAPINE | סכיזופרניה |
הפרעה ביפולרית כקו טיפולי שני. | 10/01/2012 | פסיכיאטריה | ARIPIPRAZOLE, OLANZAPINE, QUETIAPINE | |
למבוטח קטין הסובל מסכיזופרניה או מפסיכוזה אחרת; | 03/01/2010 | פסיכיאטריה | ARIPIPRAZOLE, ILOPERIDONE, OLANZAPINE, QUETIAPINE, RISPERIDONE, AMISULPRIDE, ASENAPINE, PALIPERIDONE, SERTINDOLE, ZIPRASIDONE | |
מבוטח בגיר שהוא חולה סכיזופרניה - קו שני | 03/01/2010 | פסיכיאטריה |
שימוש לפי פנקס קופ''ח כללית 1994
לא צוין
תאריך הכללה מקורי בסל
03/01/2010
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אביליפיי מיינטנה 400 מ"ג