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

HYPOTENSION ( 4 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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