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

JOINT SWELLING ( 20 FDA reports)
RENAL IMPAIRMENT ( 17 FDA reports)
ABDOMINAL DISTENSION ( 16 FDA reports)
ABDOMINAL DISCOMFORT ( 15 FDA reports)
ANAEMIA ( 15 FDA reports)
ANKLE FRACTURE ( 15 FDA reports)
BONE ATROPHY ( 15 FDA reports)
DECREASED APPETITE ( 15 FDA reports)
DEHYDRATION ( 15 FDA reports)
HYPOPHAGIA ( 15 FDA reports)
HYPOTENSION ( 15 FDA reports)
MALAISE ( 15 FDA reports)
OCULAR ICTERUS ( 15 FDA reports)
PALLOR ( 15 FDA reports)
ROTATOR CUFF SYNDROME ( 15 FDA reports)
SWELLING ( 15 FDA reports)
BURNING SENSATION ( 14 FDA reports)
CHOLELITHIASIS ( 14 FDA reports)
CONSTIPATION ( 14 FDA reports)
EYELID OEDEMA ( 14 FDA reports)
FACE OEDEMA ( 14 FDA reports)
MUSCULOSKELETAL PAIN ( 14 FDA reports)
OEDEMA PERIPHERAL ( 14 FDA reports)
ABDOMINAL PAIN UPPER ( 13 FDA reports)
HERPES ZOSTER ( 13 FDA reports)
METASTASIS ( 13 FDA reports)
ABDOMINAL PAIN ( 12 FDA reports)
CHEST PAIN ( 12 FDA reports)
FALL ( 12 FDA reports)
PROSTATE CANCER ( 12 FDA reports)
ABDOMINAL PAIN LOWER ( 11 FDA reports)
PANCYTOPENIA ( 11 FDA reports)
FAECES DISCOLOURED ( 10 FDA reports)
CARDIAC FAILURE ACUTE ( 9 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
ADENOCARCINOMA ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
ANOREXIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
GASTRIC ULCER PERFORATION ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHOLINERGIC SYNDROME ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL ULCER PERFORATION ( 2 FDA reports)
HEPATIC CALCIFICATION ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTRIC LAVAGE ABNORMAL ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC PH INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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