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

PYREXIA ( 46 FDA reports)
ASTHENIA ( 38 FDA reports)
THROMBOCYTOPENIA ( 37 FDA reports)
RENAL FAILURE ACUTE ( 32 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 29 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 29 FDA reports)
PRURITUS ( 28 FDA reports)
MALAISE ( 27 FDA reports)
NEUTROPENIA ( 27 FDA reports)
FALL ( 26 FDA reports)
AGRANULOCYTOSIS ( 24 FDA reports)
LEUKOPENIA ( 24 FDA reports)
ANAEMIA ( 23 FDA reports)
CHOLESTASIS ( 23 FDA reports)
DYSPNOEA ( 23 FDA reports)
ERYTHEMA ( 22 FDA reports)
MYOCARDIAL INFARCTION ( 22 FDA reports)
RECTAL HAEMORRHAGE ( 21 FDA reports)
CYTOLYTIC HEPATITIS ( 20 FDA reports)
DRUG INTERACTION ( 20 FDA reports)
INFLAMMATION ( 20 FDA reports)
MYALGIA ( 20 FDA reports)
LOSS OF CONSCIOUSNESS ( 19 FDA reports)
VARICELLA ( 19 FDA reports)
VOMITING ( 19 FDA reports)
CARDIAC FAILURE ( 18 FDA reports)
HYPONATRAEMIA ( 18 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 17 FDA reports)
CONFUSIONAL STATE ( 17 FDA reports)
NAUSEA ( 17 FDA reports)
PAIN IN EXTREMITY ( 17 FDA reports)
COMA ( 16 FDA reports)
DIARRHOEA ( 16 FDA reports)
LUNG DISORDER ( 16 FDA reports)
OEDEMA PERIPHERAL ( 16 FDA reports)
RENAL FAILURE ( 16 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
BLOOD CREATININE INCREASED ( 15 FDA reports)
DERMATITIS BULLOUS ( 15 FDA reports)
FATIGUE ( 15 FDA reports)
CONDITION AGGRAVATED ( 14 FDA reports)
HAEMOGLOBIN DECREASED ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
HYPOTENSION ( 14 FDA reports)
EOSINOPHILIA ( 13 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 13 FDA reports)
HAEMATEMESIS ( 13 FDA reports)
ABDOMINAL PAIN ( 12 FDA reports)
CARDIAC ARREST ( 12 FDA reports)
HEADACHE ( 12 FDA reports)
HYPERTENSION ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 12 FDA reports)
PULMONARY OEDEMA ( 12 FDA reports)
PURPURA ( 12 FDA reports)
SEPTIC SHOCK ( 12 FDA reports)
TOXIC SKIN ERUPTION ( 12 FDA reports)
ARRHYTHMIA ( 11 FDA reports)
BONE MARROW DEPRESSION ( 11 FDA reports)
CHEST PAIN ( 11 FDA reports)
DEEP VEIN THROMBOSIS ( 11 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 11 FDA reports)
FACE OEDEMA ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 11 FDA reports)
JAUNDICE ( 11 FDA reports)
NEPHROTIC SYNDROME ( 11 FDA reports)
PAIN ( 11 FDA reports)
PANCYTOPENIA ( 11 FDA reports)
RHABDOMYOLYSIS ( 11 FDA reports)
SKIN EXFOLIATION ( 11 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 11 FDA reports)
ACUTE CORONARY SYNDROME ( 10 FDA reports)
ARTHRALGIA ( 10 FDA reports)
BONE MARROW FAILURE ( 10 FDA reports)
DERMATITIS EXFOLIATIVE ( 10 FDA reports)
DISORIENTATION ( 10 FDA reports)
HAEMATOMA ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
ATRIAL FIBRILLATION ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 9 FDA reports)
COUGH ( 9 FDA reports)
DYSPHAGIA ( 9 FDA reports)
HEPATITIS ( 9 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 9 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
VERTIGO ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
ABDOMINAL PAIN UPPER ( 8 FDA reports)
ALOPECIA ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 8 FDA reports)
CEREBRAL HAEMORRHAGE ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
MUSCLE SPASMS ( 8 FDA reports)
OVERDOSE ( 8 FDA reports)
PHLEBITIS ( 8 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
SKIN DISORDER ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
TRANSAMINASES INCREASED ( 8 FDA reports)
VASCULAR PURPURA ( 8 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
CEREBRAL HAEMATOMA ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
CYANOSIS ( 7 FDA reports)
DEHYDRATION ( 7 FDA reports)
DRY MOUTH ( 7 FDA reports)
HEPATOCELLULAR DAMAGE ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
LEUKOCYTOSIS ( 7 FDA reports)
MIOSIS ( 7 FDA reports)
MUCOUS MEMBRANE DISORDER ( 7 FDA reports)
PERICARDIAL EFFUSION ( 7 FDA reports)
PREMATURE BABY ( 7 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 7 FDA reports)
PULMONARY FIBROSIS ( 7 FDA reports)
RASH ERYTHEMATOUS ( 7 FDA reports)
SCAB ( 7 FDA reports)
SYMBLEPHARON ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
ACUTE PULMONARY OEDEMA ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 6 FDA reports)
ANOREXIA ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
ARTERIOSPASM CORONARY ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 6 FDA reports)
CARDIOGENIC SHOCK ( 6 FDA reports)
CHOLANGITIS ( 6 FDA reports)
CONJUNCTIVITIS ( 6 FDA reports)
CORNEAL NEOVASCULARISATION ( 6 FDA reports)
DECEREBRATION ( 6 FDA reports)
DIALYSIS ( 6 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
ENDOCARDITIS ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
HYPOKINESIA ( 6 FDA reports)
INCORRECT DOSE ADMINISTERED ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 6 FDA reports)
INTUBATION ( 6 FDA reports)
IRIS ADHESIONS ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
PANCREATITIS ACUTE ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
CAESAREAN SECTION ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIOMYOPATHY ( 5 FDA reports)
CELL DEATH ( 5 FDA reports)
CORNEAL TRANSPLANT ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DEPILATION ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HEPATOSPLENOMEGALY ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PERIORBITAL HAEMATOMA ( 5 FDA reports)
RASH ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RASH PAPULAR ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
SUDDEN DEATH ( 5 FDA reports)
TREMOR ( 5 FDA reports)
TUMOUR LYSIS SYNDROME ( 5 FDA reports)
ULCERATIVE KERATITIS ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
AGITATION ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 4 FDA reports)
APHASIA ( 4 FDA reports)
ASPHYXIA ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GINGIVAL BLEEDING ( 4 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HAIR COLOUR CHANGES ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
INFECTION ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
LARYNGEAL OEDEMA ( 4 FDA reports)
LIFE SUPPORT ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
PETECHIAE ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
SUPERINFECTION ( 4 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BRONCHIAL INFECTION ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CORNEAL OPACITY ( 3 FDA reports)
DEATH ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DILATATION VENTRICULAR ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSMORPHISM ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FLUID REPLACEMENT ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
HAEMANGIOMA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
IRON METABOLISM DISORDER ( 3 FDA reports)
LIPIDS ABNORMAL ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
MELAENA ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
MYASTHENIA GRAVIS ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PORTAL VEIN THROMBOSIS ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
VASCULAR MALFORMATION PERIPHERAL ( 3 FDA reports)
VENOUS THROMBOSIS ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CARDIAC PERFORATION ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBELLAR HYPOPLASIA ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHOLANGITIS SCLEROSING ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONGENITAL VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CROSS SENSITIVITY REACTION ( 2 FDA reports)
CRYOGLOBULINAEMIA ( 2 FDA reports)
CRYSTAL URINE ( 2 FDA reports)
CYSTIC LYMPHANGIOMA ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DUODENAL FISTULA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ECTOPIC PREGNANCY ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAEMATOSPERMIA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC INFECTION ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LABIA ENLARGED ( 2 FDA reports)
LACRIMATION DECREASED ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MICROLITHIASIS ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MYASTHENIC SYNDROME ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POLYP ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RENAL CANCER METASTATIC ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN DEPIGMENTATION ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN TEST NEGATIVE ( 2 FDA reports)
SODIUM RETENTION ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
TENDON CALCIFICATION ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TENDON INJURY ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VESICOURETERIC REFLUX ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUPUNCTURE ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AGITATION NEONATAL ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 1 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ASCITES INFECTION ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALINT'S SYNDROME ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN LARYNGEAL NEOPLASM ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLADDER STENOSIS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE LESION EXCISION ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARTILAGE DEVELOPMENT DISORDER ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOROIDAL DETACHMENT ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLUTTERING ( 1 FDA reports)
COAGULATION FACTOR V LEVEL INCREASED ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL MEGAURETER ( 1 FDA reports)
CONGENITAL VESICOURETERIC REFLUX ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRAIN OF CEREBRAL SUBDURAL SPACE ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EAR, NOSE AND THROAT EXAMINATION ABNORMAL ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBRIN INCREASED ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
FOETAL ARRHYTHMIA ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENITAL LABIAL ADHESIONS ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOGLOBINAEMIA ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFANTILE GENETIC AGRANULOCYTOSIS ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOSS OF VISUAL CONTRAST SENSITIVITY ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGOCOCCAL SEPSIS ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
ODDI'S SPHINCTER CONSTRICTION ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
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OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC FISTULA ( 1 FDA reports)
PAO2/FIO2 RATIO DECREASED ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROSTATIC ADENOMA ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDO LYMPHOMA ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY PARALYSIS ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOMNOLENCE NEONATAL ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROID CANCER METASTATIC ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULTRAFILTRATION FAILURE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
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URETERAL CATHETERISATION ( 1 FDA reports)
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VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VULVAR EROSION ( 1 FDA reports)
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WHEEZING ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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