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

DYSPNOEA ( 4 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
SEDATION ( 2 FDA reports)
RASH ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
HYPOTONIA ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
COUGH ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)

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