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

BACK PAIN ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
ANURIA ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DIZZINESS ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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