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

ANAEMIA ( 16 FDA reports)
DIARRHOEA ( 16 FDA reports)
PYREXIA ( 15 FDA reports)
RASH ( 15 FDA reports)
BRADYCARDIA ( 14 FDA reports)
ABDOMINAL PAIN ( 13 FDA reports)
BRONCHOSPASM ( 13 FDA reports)
HYPOTENSION ( 13 FDA reports)
CARDIAC FAILURE ( 12 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
SHOCK ( 12 FDA reports)
DRUG INTERACTION ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
MUSCLE RIGIDITY ( 11 FDA reports)
VOMITING ( 11 FDA reports)
OSTEONECROSIS ( 10 FDA reports)
STEVENS-JOHNSON SYNDROME ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
ASCITES ( 9 FDA reports)
DISEASE PROGRESSION ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
MEGACOLON ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
BACTERIAL INFECTION ( 8 FDA reports)
CIRCULATORY COLLAPSE ( 8 FDA reports)
CYANOSIS ( 8 FDA reports)
ERYTHEMA ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
CHOLESTASIS ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 7 FDA reports)
ACUTE CORONARY SYNDROME ( 6 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
HYPERTHERMIA ( 6 FDA reports)
ILEUS PARALYTIC ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
MELAENA ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
ABSCESS ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
PURPURA ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
ACUTE ABDOMEN ( 4 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CHILLS ( 4 FDA reports)
FALL ( 4 FDA reports)
GASTROINTESTINAL PERFORATION ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPERPYREXIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SEQUESTRECTOMY ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
COUGH ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FRACTURED SACRUM ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
PAIN ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BILIARY ISCHAEMIA ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
BRUGADA SYNDROME ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EMBOLISM ARTERIAL ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEPATIC CANCER METASTATIC ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
LAPAROTOMY ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
MENINGITIS TUBERCULOUS ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
METASTASES TO THE MEDIASTINUM ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TONGUE HAEMATOMA ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
VENTRICULAR FLUTTER ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ADRENAL GLAND TUBERCULOSIS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
CONGENITAL FOOT MALFORMATION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
EXTRASKELETAL OSSIFICATION ( 1 FDA reports)
FEMORAL NERVE INJURY ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL MUCOSITIS ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC EMBOLISATION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OBESITY ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRACHEAL OBSTRUCTION ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSIENT PSYCHOSIS ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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