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

VASCULITIS ( 6 FDA reports)
FATIGUE ( 5 FDA reports)
PLATELET DISORDER ( 5 FDA reports)
NAUSEA ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE EXFOLIATION ( 2 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PRODUCT ADHESION ISSUE ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABSCESS ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENITIS BACTERIAL ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NAIL PITTING ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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