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

PNEUMONIA ( 11 FDA reports)
PYREXIA ( 11 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
SEPSIS ( 8 FDA reports)
RENAL FAILURE ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
INFECTION ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
RETINAL ARTERY OCCLUSION ( 4 FDA reports)
SHOCK ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
WOUND DEHISCENCE ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BONE MARROW TOXICITY ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
LEIOMYOMA ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
NIKOLSKY'S SIGN ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
TOOTH DEPOSIT ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLADDER CANDIDIASIS ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
COMA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 1 FDA reports)
BILE DUCT NECROSIS ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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