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

SEPSIS ( 14 FDA reports)
BLOOD PRESSURE DECREASED ( 13 FDA reports)
HYPOTENSION ( 13 FDA reports)
TACHYCARDIA ( 10 FDA reports)
RESPIRATORY DISTRESS ( 9 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
POST PROCEDURAL COMPLICATION ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
SHOCK ( 7 FDA reports)
CIRCULATORY COLLAPSE ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
HYPOVOLAEMIA ( 6 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 6 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 6 FDA reports)
VOMITING ( 6 FDA reports)
CARDIAC OUTPUT DECREASED ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HEPATITIS C POSITIVE ( 5 FDA reports)
HEPATITIS C VIRUS ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
PROCEDURAL COMPLICATION ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RASH ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
GRAFT THROMBOSIS ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SERRATIA INFECTION ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANAPHYLACTOID SHOCK ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMORRHAGE ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
NEGATIVE CARDIAC INOTROPIC EFFECT ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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