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However, cases of prolonged visual disturbance have been reported, including after Clomid 50 mg Tablets have been discontinued. The visual disturbances may be irreversible, especially with increased dosage or duration of therapy. There are reports of new cases of endometriosis and exacerbation of pre-existing endometriosis during Clomid 50 mg Tablets therapy. Multiple pregnancies, including simultaneous intrauterine and extrauterine pregnancies, have been reported. There is an increased chance of ectopic pregnancy in women who conceive following Clomid 50 mg Tablets therapy. Reduced endometrial thickness (frequency not known) Isolated reports have been received on the occurrence of endocrine-related or dependent neoplasms or their aggravation (see section 4. Central nervous system : Convulsions have been reported; patients with a history of seizures may be predisposed, transient paraesthesia (frequency not known), dizziness (frequency not known). In investigational patients, CNS symptoms/signs, conditions of dizziness, light-headedness/vertigo (0. After prescription availability, there were isolated additional reports of these conditions and also reports of other conditions such as syncope/fainting, cerebrovascular accident, cerebral thrombosis, psychotic reactions including paranoid psychosis, neurologic impairment, disorientation and speech disturbance. Anxiety (frequency not known), depression (frequency not known), mood disturbances (including mood altered, mood swings and irritability) (frequency not known), nervousness (frequency not known), insomnia (frequency not known). Dermatitis and rash were reported by investigational patients. Conditions such as rash and urticaria were the most common ones reported after prescription availability but also reported were conditions such as allergic reaction, erythema multiforme, ecchymosis and angioneurotic oedema. Hair thinning (alopecia) has been reported very rarely. Bromsulphalein (BSP) retention of greater than 5% was reported in 32 of 141 patients in whom it was measured, including 5 of 43 patients who took approximately the dose of Clomid 50 mg Tablets now recommended. Retention was usually minimal unless associated with prolonged continuous Clomid 50 mg Tablets administration or with apparently unrelated liver disease. Other liver function tests were usually normal. In a later study in which patients were given 6 consecutive monthly courses of Clomid 50 mg Tablets (50 mg or 100 mg daily for 3 days) or matching placebo, BSP tests were done on 94 patients. Values in excess of 5% retention were recorded in 11 patients, 6 of whom had taken drug and 5 placebos. In a separate report, one patient taking 50 mg of Clomid 50 mg Tablets daily developed jaundice on the 19 th day of treatment; liver biopsy revealed bile stasis without evidence of hepatitis, virigen testocaps 40 mg oral steroids nebido. Hypertriglyceridemia (frequency not known), in some cases with pancreatitis, has been observed in patients with pre-existing or a family history of hypertriglyceridemia and/or with dose and duration of treatment exceeding the label recommendations. Tachycardia, (frequency not known) palpitations (frequency not known) Pancreatitis (frequency not known) 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 Yellow Card Scheme at: www. Toxic effects of acute overdosage of Clomid 50 mg Tablets have not been reported but the number of overdose cases recorded is small. undefined

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