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

X-RAY ABNORMAL ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
PAIN ( 2 FDA reports)
MENISCUS OPERATION ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTHENIA ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
ANAL FISTULA EXCISION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL MEMBRANE FAILURE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
RASH ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)

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