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

NEUROPATHY PERIPHERAL ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
DEPRESSIVE SYMPTOM ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
LIVER DISORDER ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ARTHROSCOPY ( 3 FDA reports)
DEATH ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
PERICARDITIS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DYSKINESIA ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
ABASIA ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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