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לוסטרל טבליות 100 מ"ג LUSTRAL TABLETS 100 MG (SERTRALINE AS HYDROCHLORIDE)
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תרופה בסל
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צורת מתן:
פומי : PER OS
צורת מינון:
טבליות מצופות פילם : FILM COATED 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 Nausea is the most common undesirable effect. In the treatment of social anxiety disorder, sexual dysfunction (ejaculation failure) in men occurred in 14% for sertraline vs 0% in placebo. These undesirable effects are dose dependent and are often transient in nature with continued treatment. Table 1 displays adverse reactions observed from post-marketing experience (frequency not known) and placebo-controlled clinical trials (comprising a total of 2542 patients on sertraline and 2145 on placebo) in depression, OCD, panic disorder, PTSD and social anxiety disorder. Some adverse drug reactions listed in Table 1 may decrease in intensity and frequency with continued treatment and do not generally lead to cessation of therapy. Table 1: Adverse Reactions Frequency of adverse reactions observed from placebo-controlled clinical trials in depression, OCD, panic disorder, PTSD and social anxiety disorder. Pooled analysis and post-marketing experience. System Organ Very Common Uncommon Rare Frequency Class Common (≥1/100 to (≥1/1,000 to (≥1/10,000 to Not Known (≥1/10) <1/10) <1/100) <1/1,000) (Cannot be Estimated From the Available Data) Infections and upper respiratory gastroenteritis, otitis diverticulitis§ infestations tract infection, media pharyngitis, rhinitis Neoplasms neoplasm benign, malignant and unspecified (including cysts and polyps) Blood and lymphadenopathy, lymphatic thrombocytopenia*§, system disorders leukopenia*§ Immune system hypersensitivity, anaphylactoid reaction disorders seasonal allergy Endocrine hypothyroidism hyperprolactinaemia§, disorders inappropriate antidiuretic hormone secretion§ Metabolism and decreased appetite, hypercholesterolaemia, diabetes nutrition increased appetite* mellitus, hypoglycaemia, disorders hyperglycaemia§, hyponatraemia§ Psychiatric insomnia anxiety*, depression*, suicidal conversion disorder§, disorders agitation*, ideation/behaviour, paroniria§, drug dependence, libido decreased*, psychotic disorder, sleep walking, premature nervousness, thinking abnormal, ejaculation depersonalisation, apathy,hallucination*, nightmare, bruxism* aggression*, euphoric mood*, paranoia Nervous system dizziness, tremor, movement amnesia, coma*, akathisia (see section disorders headache*, disorders (including hypoaesthesia*, muscle 4.4), dyskinesia, hyperaesthesia, somnolence extrapyramidal contractions cerebrovascular spasm symptoms such as involuntary*, syncope*, (including reversible cerebral hyperkinesia, hyperkinesia*, vasoconstriction syndrome and hypertonia, dystonia, migraine*, convulsion*, Call-Fleming syndrome)§, teeth grinding or gait dizziness postural, psychomotor restlessness§ (see abnormalities), coordination abnormal, section 4.4), sensory paraesthesia*, speech disorder disturbance, choreoathetosis§, hypertonia*, also reported were signs and disturbance in symptoms associated with attention, dysgeusia serotonin syndrome or neuroleptic malignant syndrome: In some cases associated with concomitant use of serotonergic drugs that included agitation, confusion, diaphoresis, diarrhoea, fever, hypertension, rigidity and tachycardia§ Table 1: Adverse Reactions Frequency of adverse reactions observed from placebo-controlled clinical trials in depression, OCD, panic disorder, PTSD and social anxiety disorder. Pooled analysis and post-marketing experience. System Organ Very Common Uncommon Rare Frequency Class Common (≥1/100 to <1/10) (≥1/1,000 to <1/100) (≥1/10,000 to <1/1,000) Not Known (≥1/10) (Cannot be Estimated From the Available Data) Eye disorders visual disturbance mydriasis scotoma, glaucoma, diplopia, maculopathy photophobia, hyphaema§, pupils unequal§, vision abnormal§, lacrimal disorder Ear and labyrinth tinnitus ear pain disorders Cardiac palpitations tachycardia, cardiac myocardial infarction§, Torsade disorders disorder de Pointes§ (see sections 4.4, 4.5 and 5.1), bradycardia, QTc prolongation (see sections 4.4, 4.5 and 5.1) Vascular hot flush abnormal bleeding peripheral ischaemia disorders (such as gastrointestinal bleeding), hypertension, flushing, haematuria Respiratory, yawning dyspnoea, epistaxis, hyperventilation, interstitial lung thoracic and bronchospasm* disease§, eosinophilic mediastinal pneumonia*§, laryngospasm, disorders dysphonia, stridor§, hypoventilation, hiccups Gastrointestinal nausea, dyspepsia, melaena, tooth disorder, mouth ulceration, pancreatitis§, colitis disorders diarrhoea, dry constipation*, oesophagitis, glossitis, haematochezia, tongue microscopic* mouth abdominal pain*, haemorrhoids, salivary ulceration, stomatitis vomiting*, flatulence hypersecretion, dysphagia, eructation, tongue disorder Hepatobiliary hepatic function abnormal, disorders serious liver events (including hepatitis, jaundice and hepatic failure) Skin and hyperhidrosis, rash* periorbital oedema*, rare reports of severe cutaneous subcutaneous urticaria*, alopecia*, adverse reactions (SCAR): e.g. tissue disorders pruritus*, purpura*, Stevens-Johnson syndrome and dermatitis, dry skin, epidermal necrolysis§, skin face oedema, cold reaction§, photosensitivity§, sweat angioedema, hair texture abnormal, skin odour abnormal, dermatitis bullous, rash follicular Musculoskeletal back pain, arthralgia, osteoarthritis, muscle rhabdomyolysis§, bone disorder trismus* and connective myalgia twitching, muscle tissue disorders cramps, muscular weakness Renal and pollakiuria, micturition urinary hesitation*, oliguria urinary disorders disorder, urinary retention, urinary incontinence*, polyuria, nocturia Table 1: Adverse Reactions Frequency of adverse reactions observed from placebo-controlled clinical trials in depression, OCD, panic disorder, PTSD and social anxiety disorder. Pooled analysis and post-marketing experience. System Organ Very Common Uncommon Rare Frequency Class Common (≥1/100 to <1/10) (≥1/1,000 to <1/100) (≥1/10,000 to <1/1,000) Not Known (≥1/10) (Cannot be Estimated From the Available Data) Reproductive ejaculation menstruation sexual dysfunction (see galactorrhoea*, atrophic postpartum system and failure irregular, erectile section 4.4), vulvovaginitis, genital discharge, haemorrhage*† breast disorders dysfunction menorrhagia, vaginal balanoposthitis§, haemorrhage, female gynaecomastia, priapism* sexual dysfunction (see section 4.4) General fatigue* malaise*, oedema peripheral*, hernia, drug tolerance decreased disorders and chest pain*, chills, gait disturbance*, administration asthenia, pyrexia thirst site conditions Investigations weight increased* alanine blood cholesterol increased, aminotransferase abnormal clinical laboratory increased*, aspartate results, semen abnormal, altered aminotransferase platelet function§ increased*, weight decreased* Injury, poisoning injury and procedural complications Surgical and vasodilation procedure medical procedures ADR identified post-marketing § ADR frequency represented by the estimated upper limit of the 95% confidence interval using “The Rule of 3”. † This event has been reported for the therapeutic class of SSRIs/SNRIs (see sections 4.4, 4.6). Withdrawal symptoms seen on discontinuation of sertraline treatment Discontinuation of sertraline (particularly when abrupt) commonly leads to withdrawal symptoms. Dizziness, sensory disturbances (including paraesthesia), sleep disturbances (including insomnia and intense dreams), agitation or anxiety, nausea and/or vomiting, tremor and headache are the most commonly reported. Generally these events are mild to moderate and are self-limiting; however, in some patients they may be severe and/or prolonged. It is therefore advised that when sertraline treatment is no longer required, gradual discontinuation by dose tapering should be carried out (see sections 4.2 and 4.4). Elderly population SSRIs or SNRIs including sertraline have been associated with cases of clinically significant hyponatraemia in elderly patients, who may be at greater risk for this adverse event (see section 4.4). Class effects Epidemiological studies, mainly conducted in patients 50 years of age and older, show an increased risk of bone fractures in patients receiving SSRIs and TCAs. The mechanism leading to this risk is unknown. 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.
שימוש לפי פנקס קופ''ח כללית 1994
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תאריך הכללה מקורי בסל
01/03/2008
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לוסטרל טבליות 100 מ"ג