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

HYPONATRAEMIA ( 6 FDA reports)
MALAISE ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLISTER ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
FALL ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
NAIL DISORDER ( 3 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 3 FDA reports)
ONYCHOMYCOSIS ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PELVIC FRACTURE ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
CHILLS ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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