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

DYSPNOEA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
RENAL FAILURE ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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