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

NAUSEA ( 5 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
RETCHING ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DEATH ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
BLISTER ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
AGITATION ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)

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