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

DYSGEUSIA ( 9 FDA reports)
PAIN ( 9 FDA reports)
PIGMENTATION DISORDER ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
FALL ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
ORTHOSTATIC HYPOTENSION ( 7 FDA reports)
VOMITING ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
CHILLS ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
PLATELET COUNT INCREASED ( 6 FDA reports)
RASH ( 6 FDA reports)
ACCIDENT ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
LIP EXFOLIATION ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
CHANGE OF BOWEL HABIT ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
APHASIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAL POLYP ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MELANOMA RECURRENT ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STRESS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)

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