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

ASTHENIA ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
VOMITING ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
ANOREXIA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
FALL ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EXANTHEM ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INFECTION ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MULTIPLE ENDOCRINE ADENOMATOSIS TYPE I ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WHITE BLOOD CELLS URINE ( 2 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
APHONIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL RUPTURE ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
NECROTISING OESOPHAGITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
PYRUVATE KINASE INCREASED ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VIRAL DNA TEST POSITIVE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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