Please choose an event type to view the corresponding MedsFacts report:

TRANSIENT ISCHAEMIC ATTACK ( 10 FDA reports)
HYDROCEPHALUS ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 6 FDA reports)
PREGNANCY ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
CONGENITAL HYDROCEPHALUS ( 4 FDA reports)
ULCER HAEMORRHAGE ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
THIRST ( 2 FDA reports)
CATARACT ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FALL ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EPILEPSY ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PIGMENTED NAEVUS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOMITING ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)

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