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

NAUSEA ( 11 FDA reports)
FATIGUE ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BLINDNESS TRANSIENT ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
PARAESTHESIA ( 5 FDA reports)
POLYARTHRITIS ( 5 FDA reports)
RASH ( 5 FDA reports)
HAEMATOMA ( 4 FDA reports)
MONOPLEGIA ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
CONVERSION DISORDER ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
FALL ( 3 FDA reports)
GENITAL PRURITUS FEMALE ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE URTICARIA ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
BLISTER ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
JOINT TUBERCULOSIS ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
POLYMORPHIC LIGHT ERUPTION ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABSCESS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATOPY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
COMA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPRAXIA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
JC VIRUS TEST POSITIVE ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NODULE ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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