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PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUCOCUTANEOUS RASH ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
CONSTIPATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FALL ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AMIMIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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