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

PNEUMONIA ( 84 FDA reports)
PYREXIA ( 79 FDA reports)
INTERSTITIAL LUNG DISEASE ( 31 FDA reports)
CARDIAC FAILURE ( 25 FDA reports)
RESPIRATORY FAILURE ( 25 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 24 FDA reports)
MALAISE ( 24 FDA reports)
RASH ( 23 FDA reports)
VOMITING ( 23 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 22 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 20 FDA reports)
DYSPNOEA ( 20 FDA reports)
RHABDOMYOLYSIS ( 20 FDA reports)
COUGH ( 19 FDA reports)
HEADACHE ( 19 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 18 FDA reports)
DRUG INTERACTION ( 18 FDA reports)
BRADYCARDIA ( 17 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 17 FDA reports)
CARDIAC ARREST ( 15 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 15 FDA reports)
HYPOGLYCAEMIA ( 15 FDA reports)
CHROMATURIA ( 14 FDA reports)
CONVULSION ( 14 FDA reports)
LIVER DISORDER ( 14 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 14 FDA reports)
ARTHRALGIA ( 13 FDA reports)
DEATH ( 13 FDA reports)
MYALGIA ( 13 FDA reports)
RESPIRATORY ARREST ( 13 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 12 FDA reports)
BLOOD CREATININE INCREASED ( 12 FDA reports)
BRONCHOPNEUMONIA ( 12 FDA reports)
CARDIO-RESPIRATORY ARREST ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 12 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
PLEURAL EFFUSION ( 12 FDA reports)
ABNORMAL BEHAVIOUR ( 11 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 11 FDA reports)
CONDITION AGGRAVATED ( 11 FDA reports)
DIZZINESS ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
PNEUMONIA ASPIRATION ( 11 FDA reports)
ASTHMA ( 10 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 10 FDA reports)
BLOOD UREA INCREASED ( 10 FDA reports)
MELAENA ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 10 FDA reports)
ANURIA ( 9 FDA reports)
ASTHENIA ( 9 FDA reports)
BLOOD BILIRUBIN INCREASED ( 9 FDA reports)
BLOOD PRESSURE DECREASED ( 9 FDA reports)
CARNITINE DECREASED ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
FACE OEDEMA ( 9 FDA reports)
RESPIRATORY DISORDER ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 8 FDA reports)
ANAEMIA ( 8 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
DRUG ERUPTION ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
HYPONATRAEMIA ( 8 FDA reports)
INFECTION ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 8 FDA reports)
PNEUMONIA BACTERIAL ( 8 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
BLOOD POTASSIUM INCREASED ( 7 FDA reports)
BRONCHITIS CHRONIC ( 7 FDA reports)
DEHYDRATION ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
GENERALISED OEDEMA ( 7 FDA reports)
HAEMOPTYSIS ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HYPOXIA ( 7 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
NEUTROPENIA ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
OEDEMA ( 7 FDA reports)
PALLOR ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
URINARY RETENTION ( 7 FDA reports)
ABASIA ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 6 FDA reports)
ASPIRATION ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
CHILLS ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
DYSLALIA ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
FALL ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
HALLUCINATION ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HERPES ZOSTER ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
MALNUTRITION ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
PERICARDIAL EFFUSION ( 6 FDA reports)
PRODUCTIVE COUGH ( 6 FDA reports)
RESPIRATORY DEPRESSION ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
SINUS ARRHYTHMIA ( 6 FDA reports)
STEVENS-JOHNSON SYNDROME ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
URINE OUTPUT DECREASED ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
AGRANULOCYTOSIS ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
APNOEIC ATTACK ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 5 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 5 FDA reports)
BRAIN STEM HAEMORRHAGE ( 5 FDA reports)
BRONCHITIS ACUTE ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CRYING ( 5 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 5 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 5 FDA reports)
DISEASE RECURRENCE ( 5 FDA reports)
FLUID INTAKE REDUCED ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
GENERALISED ERYTHEMA ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 5 FDA reports)
PAIN ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
STRABISMUS ( 5 FDA reports)
THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TREMOR ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
AGGRESSION ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
CANDIDA SEPSIS ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CARDIAC FAILURE CHRONIC ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
EMPYEMA ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 4 FDA reports)
HYDRONEPHROSIS ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
HYPOPROTEINAEMIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 4 FDA reports)
MIDDLE LOBE SYNDROME ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PSEUDOMONAL SEPSIS ( 4 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 4 FDA reports)
PYOTHORAX ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 4 FDA reports)
SPUTUM INCREASED ( 4 FDA reports)
STATUS EPILEPTICUS ( 4 FDA reports)
SUBCUTANEOUS ABSCESS ( 4 FDA reports)
SUFFOCATION FEELING ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VOCAL CORD PARALYSIS ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ALVEOLITIS ALLERGIC ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 3 FDA reports)
CONGENITAL CYSTIC LUNG ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
EYE DISCHARGE ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
FANCONI SYNDROME ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 3 FDA reports)
GLOSSOPTOSIS ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
INFUSION SITE ERYTHEMA ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
OPISTHOTONUS ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PNEUMOMEDIASTINUM ( 3 FDA reports)
PNEUMONIA MYCOPLASMAL ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
STRABISMUS CONGENITAL ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TIC ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 2 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLORECTAL CANCER METASTATIC ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DERMOID CYST ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPERTROPHY BREAST ( 2 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INFUSION SITE PHLEBITIS ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 2 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOGLOBIN URINE PRESENT ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PERIANAL ABSCESS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
PORTAL VEIN PHLEBITIS ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RADIAL NERVE PALSY ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SHOCK ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
TENSION ( 2 FDA reports)
TESTICULAR EMBRYONAL CARCINOMA ( 2 FDA reports)
TESTICULAR SEMINOMA (PURE) ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TRACHEAL OEDEMA ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VITAMIN K DEFICIENCY ( 2 FDA reports)
VITH NERVE DISORDER ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABORTION THREATENED ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALVEOLAR PROTEINOSIS ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BASOSQUAMOUS CARCINOMA ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILEVEL POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOKINE STORM ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
FRONTAL LOBE EPILEPSY ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFECTIVE SPONDYLITIS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
KAWASAKI'S DISEASE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNX IRRITATION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST NEGATIVE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO URINARY TRACT ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEISSERIA TEST POSITIVE ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POOR SUCKING REFLEX ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPONDYLITIC MYELOPATHY ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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