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

SHOCK HAEMORRHAGIC ( 4 FDA reports)
OESOPHAGITIS ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
VOMITING ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
RADIAL PULSE ABNORMAL ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
ANURIA ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
FEMORAL PULSE ABNORMAL ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
ASCITES ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)

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