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

HYPONATRAEMIA ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
VOMITING ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COMA ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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