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

BLOOD UREA INCREASED ( 12 FDA reports)
INTERSTITIAL LUNG DISEASE ( 12 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 11 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
CARDIAC FAILURE ( 10 FDA reports)
DECREASED APPETITE ( 10 FDA reports)
HYPONATRAEMIA ( 9 FDA reports)
SHOCK ( 9 FDA reports)
VENTRICULAR TACHYCARDIA ( 9 FDA reports)
CHOLESTASIS ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ANAEMIA ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
GRANULOCYTOPENIA ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
DIVERTICULUM INTESTINAL ( 5 FDA reports)
GASTROINTESTINAL PERFORATION ( 5 FDA reports)
HEMIPLEGIA ( 5 FDA reports)
INTESTINAL HAEMATOMA ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
MELAENA ( 5 FDA reports)
PERITONITIS ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 5 FDA reports)
ANOREXIA ( 4 FDA reports)
ASTERIXIS ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
ENTEROCOLITIS ( 4 FDA reports)
GASTRIC CANCER ( 4 FDA reports)
HYPOCHLORAEMIA ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BRONCHITIS BACTERIAL ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
ENTERITIS INFECTIOUS ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HEPATITIS CHOLESTATIC ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PSEUDOALDOSTERONISM ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FUSOBACTERIUM INFECTION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIPHERAL ARTERY DISSECTION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SPLEEN SCAN ABNORMAL ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VITAMIN B1 DEFICIENCY ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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