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

STOMATITIS ( 16 FDA reports)
DERMATITIS ACNEIFORM ( 13 FDA reports)
DUODENAL ULCER ( 12 FDA reports)
ASTHMA ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
HYPERTENSION ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
GRANULOCYTE COUNT DECREASED ( 5 FDA reports)
PANCREATIC ENZYMES INCREASED ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
TOXIC SKIN ERUPTION ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
ENTEROCOLITIS ( 4 FDA reports)
FALL ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
PARKINSONISM ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
COLORECTAL CANCER ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
HEPATIC VEIN OCCLUSION ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
INTRACARDIAC MASS ( 3 FDA reports)
NEURODEGENERATIVE DISORDER ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RASH ( 2 FDA reports)
SPINAL CORD INJURY ( 2 FDA reports)
SPINAL SHOCK ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
URTICARIA CHRONIC ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACNE ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMOGRAPHISM ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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