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

RENAL FAILURE ACUTE ( 68 FDA reports)
RENAL FAILURE ( 60 FDA reports)
PYREXIA ( 58 FDA reports)
THROMBOCYTOPENIA ( 56 FDA reports)
DRUG INTERACTION ( 50 FDA reports)
ANAEMIA ( 49 FDA reports)
MALAISE ( 47 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 42 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 41 FDA reports)
DYSPNOEA ( 41 FDA reports)
VOMITING ( 39 FDA reports)
FALL ( 38 FDA reports)
AGRANULOCYTOSIS ( 37 FDA reports)
CYTOLYTIC HEPATITIS ( 37 FDA reports)
MULTI-ORGAN FAILURE ( 34 FDA reports)
MYOCARDIAL INFARCTION ( 34 FDA reports)
HYPOTENSION ( 33 FDA reports)
ASTHENIA ( 32 FDA reports)
BRADYCARDIA ( 32 FDA reports)
CARDIAC FAILURE ( 32 FDA reports)
DIARRHOEA ( 31 FDA reports)
EOSINOPHILIA ( 31 FDA reports)
HYPERKALAEMIA ( 31 FDA reports)
SEPTIC SHOCK ( 30 FDA reports)
LOSS OF CONSCIOUSNESS ( 28 FDA reports)
ATRIAL FIBRILLATION ( 27 FDA reports)
COMA ( 27 FDA reports)
PRURITUS ( 26 FDA reports)
NEUTROPENIA ( 25 FDA reports)
CONDITION AGGRAVATED ( 24 FDA reports)
DEHYDRATION ( 24 FDA reports)
HYPONATRAEMIA ( 24 FDA reports)
PANCYTOPENIA ( 23 FDA reports)
RECTAL HAEMORRHAGE ( 22 FDA reports)
WEIGHT DECREASED ( 22 FDA reports)
OEDEMA PERIPHERAL ( 21 FDA reports)
RHABDOMYOLYSIS ( 20 FDA reports)
VENTRICULAR FIBRILLATION ( 20 FDA reports)
CARDIO-RESPIRATORY ARREST ( 19 FDA reports)
LUNG DISORDER ( 19 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
HAEMOGLOBIN DECREASED ( 18 FDA reports)
NAUSEA ( 18 FDA reports)
OEDEMA ( 18 FDA reports)
CHEST PAIN ( 17 FDA reports)
EPISTAXIS ( 17 FDA reports)
FATIGUE ( 17 FDA reports)
INTESTINAL ISCHAEMIA ( 17 FDA reports)
PREMATURE BABY ( 17 FDA reports)
ANURIA ( 16 FDA reports)
CARDIOGENIC SHOCK ( 16 FDA reports)
CONFUSIONAL STATE ( 16 FDA reports)
DERMATITIS EXFOLIATIVE ( 16 FDA reports)
DRUG INEFFECTIVE ( 16 FDA reports)
ERYTHEMA ( 16 FDA reports)
PAIN IN EXTREMITY ( 16 FDA reports)
PULMONARY EMBOLISM ( 16 FDA reports)
CAESAREAN SECTION ( 15 FDA reports)
HAEMATOMA ( 15 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 14 FDA reports)
CARDIAC ARREST ( 14 FDA reports)
CONVULSION ( 14 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 14 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 14 FDA reports)
HEADACHE ( 14 FDA reports)
HEPATITIS ( 14 FDA reports)
INFLAMMATION ( 14 FDA reports)
LACTIC ACIDOSIS ( 14 FDA reports)
OVERDOSE ( 14 FDA reports)
SEPSIS ( 14 FDA reports)
ABORTION INDUCED ( 13 FDA reports)
HEPATIC FAILURE ( 13 FDA reports)
HYPERTENSION ( 13 FDA reports)
INFECTION ( 13 FDA reports)
ISCHAEMIC STROKE ( 13 FDA reports)
LEUKOPENIA ( 13 FDA reports)
PLEURAL EFFUSION ( 13 FDA reports)
RASH MACULO-PAPULAR ( 13 FDA reports)
TOXIC SKIN ERUPTION ( 13 FDA reports)
COUGH ( 12 FDA reports)
CYANOSIS ( 12 FDA reports)
DEATH ( 12 FDA reports)
DECREASED APPETITE ( 12 FDA reports)
HAEMATURIA ( 12 FDA reports)
HYPOGLYCAEMIA ( 12 FDA reports)
INTERSTITIAL LUNG DISEASE ( 12 FDA reports)
METABOLIC ACIDOSIS ( 12 FDA reports)
MUSCLE HAEMORRHAGE ( 12 FDA reports)
PULMONARY OEDEMA ( 12 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 12 FDA reports)
TRANSAMINASES INCREASED ( 12 FDA reports)
ULCER HAEMORRHAGE ( 12 FDA reports)
VERTIGO ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
AGITATION ( 11 FDA reports)
ANGINA PECTORIS ( 11 FDA reports)
ARTHRALGIA ( 11 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 11 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 11 FDA reports)
BONE MARROW FAILURE ( 11 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 11 FDA reports)
CHOLESTASIS ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
GASTROENTERITIS ( 11 FDA reports)
HYPERHIDROSIS ( 11 FDA reports)
HYPOKALAEMIA ( 11 FDA reports)
ILIAC ARTERY OCCLUSION ( 11 FDA reports)
INCORRECT DOSE ADMINISTERED ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 11 FDA reports)
LYMPHADENOPATHY ( 11 FDA reports)
MYALGIA ( 11 FDA reports)
PALLOR ( 11 FDA reports)
RESPIRATORY DISORDER ( 11 FDA reports)
SOMNOLENCE ( 11 FDA reports)
THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
TINNITUS ( 11 FDA reports)
URINARY TRACT INFECTION ( 11 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 10 FDA reports)
BLOOD BILIRUBIN INCREASED ( 10 FDA reports)
CEREBROVASCULAR ACCIDENT ( 10 FDA reports)
DYSPHAGIA ( 10 FDA reports)
ENCEPHALOPATHY ( 10 FDA reports)
GASTRIC ULCER ( 10 FDA reports)
HAEMATEMESIS ( 10 FDA reports)
LYMPHOPENIA ( 10 FDA reports)
PANCREATITIS ACUTE ( 10 FDA reports)
PERICARDIAL EFFUSION ( 10 FDA reports)
PNEUMONIA ASPIRATION ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
ACUTE CORONARY SYNDROME ( 9 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 9 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
CHILLS ( 9 FDA reports)
DIZZINESS ( 9 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
HEPATITIS CHOLESTATIC ( 9 FDA reports)
JAUNDICE ( 9 FDA reports)
NEONATAL DISORDER ( 9 FDA reports)
RESPIRATORY DISTRESS ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
SHOCK ( 9 FDA reports)
STATUS EPILEPTICUS ( 9 FDA reports)
ACUTE PULMONARY OEDEMA ( 8 FDA reports)
CEREBELLAR HYPOPLASIA ( 8 FDA reports)
COLITIS ISCHAEMIC ( 8 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
DISTURBANCE IN ATTENTION ( 8 FDA reports)
EPILEPSY ( 8 FDA reports)
ERYTHEMA MULTIFORME ( 8 FDA reports)
FOETAL GROWTH RETARDATION ( 8 FDA reports)
HEART DISEASE CONGENITAL ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
NERVOUS SYSTEM DISORDER ( 8 FDA reports)
NEUROPATHY PERIPHERAL ( 8 FDA reports)
ORTHOSTATIC HYPOTENSION ( 8 FDA reports)
PAIN ( 8 FDA reports)
PERICARDITIS ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
RASH ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
SHOCK HAEMORRHAGIC ( 8 FDA reports)
SKIN EXFOLIATION ( 8 FDA reports)
STAPHYLOCOCCAL INFECTION ( 8 FDA reports)
TREMOR ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
ALOPECIA ( 7 FDA reports)
ANAPHYLACTIC SHOCK ( 7 FDA reports)
ANGIOEDEMA ( 7 FDA reports)
BACTERIAL INFECTION ( 7 FDA reports)
BLOOD CULTURE POSITIVE ( 7 FDA reports)
BRADYCARDIA NEONATAL ( 7 FDA reports)
BRONCHITIS ( 7 FDA reports)
CARDIOMYOPATHY ( 7 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 7 FDA reports)
GASTROINTESTINAL NECROSIS ( 7 FDA reports)
HAEMODYNAMIC INSTABILITY ( 7 FDA reports)
HAEMOPTYSIS ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 7 FDA reports)
HYDROCEPHALUS ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
KAPOSI'S SARCOMA ( 7 FDA reports)
LARYNGEAL OEDEMA ( 7 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 7 FDA reports)
MELAENA ( 7 FDA reports)
MITRAL VALVE INCOMPETENCE ( 7 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
PURPURA ( 7 FDA reports)
TROPONIN INCREASED ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
APLASIA ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
ARTERIAL DISORDER ( 6 FDA reports)
ATRIAL FLUTTER ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
CIRCULATORY COLLAPSE ( 6 FDA reports)
COGNITIVE DISORDER ( 6 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 6 FDA reports)
DIALYSIS ( 6 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 6 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 6 FDA reports)
HAEMOLYTIC ANAEMIA ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 6 FDA reports)
PERITONEAL HAEMORRHAGE ( 6 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
TACHYPNOEA ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
AMYOTROPHY ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
CONGENITAL BLADDER ANOMALY ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
FLATULENCE ( 5 FDA reports)
GASTRITIS HYPERTROPHIC ( 5 FDA reports)
GINGIVITIS ( 5 FDA reports)
GRAND MAL CONVULSION ( 5 FDA reports)
HEMIPLEGIA ( 5 FDA reports)
HEPATITIS FULMINANT ( 5 FDA reports)
HYPERCALCAEMIA ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
HYPOALBUMINAEMIA ( 5 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
NEONATAL HYPOTENSION ( 5 FDA reports)
NEPHRITIS ( 5 FDA reports)
OEDEMA NEONATAL ( 5 FDA reports)
OROANTRAL FISTULA ( 5 FDA reports)
PANCREATITIS NECROTISING ( 5 FDA reports)
PNEUMONIA BACTERIAL ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
RENAL HYPOPLASIA ( 5 FDA reports)
SKIN LESION ( 5 FDA reports)
STRESS CARDIOMYOPATHY ( 5 FDA reports)
SUBDURAL HAEMATOMA ( 5 FDA reports)
SUDDEN DEATH ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 5 FDA reports)
URETHRAL VALVES ( 5 FDA reports)
URTICARIA GENERALISED ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABASIA ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
AORTIC INTRAMURAL HAEMATOMA ( 4 FDA reports)
APGAR SCORE LOW ( 4 FDA reports)
APHASIA ( 4 FDA reports)
ARTERIOSPASM CORONARY ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 4 FDA reports)
BACTERIAL SEPSIS ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BRAIN HYPOXIA ( 4 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 4 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CARDIOVERSION ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CEREBRAL DISORDER ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
CYANOSIS NEONATAL ( 4 FDA reports)
CYTOTOXIC OEDEMA ( 4 FDA reports)
DERMATITIS BULLOUS ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
ERYSIPELAS ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HAPTOGLOBIN DECREASED ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HERPES VIRUS INFECTION ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HUMERUS FRACTURE ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
JUGULAR VEIN THROMBOSIS ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
MIOSIS ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
MUSCLE ABSCESS ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
PARTIAL SEIZURES ( 4 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 4 FDA reports)
PEMPHIGOID ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PSOAS ABSCESS ( 4 FDA reports)
PSYCHOMOTOR RETARDATION ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
PULMONARY VASCULAR DISORDER ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
RESPIRATORY ACIDOSIS ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
SERUM FERRITIN INCREASED ( 4 FDA reports)
SINOATRIAL BLOCK ( 4 FDA reports)
SMALL FOR DATES BABY ( 4 FDA reports)
TACHYARRHYTHMIA ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 4 FDA reports)
THROMBOSIS IN DEVICE ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
VASCULAR COMPLICATION ASSOCIATED WITH DEVICE ( 4 FDA reports)
VASCULAR PURPURA ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ALLERGIC OEDEMA ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD COPPER INCREASED ( 3 FDA reports)
BLOOD GASES ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
CANDIDA SEPSIS ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CEREBROVASCULAR DISORDER ( 3 FDA reports)
CLONUS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
CONGENITAL HYDROCEPHALUS ( 3 FDA reports)
CONGENITAL NOSE MALFORMATION ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
CORYNEBACTERIUM INFECTION ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EAR MALFORMATION ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
EPIDERMOLYSIS BULLOSA ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FEBRILE BONE MARROW APLASIA ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
FOETAL GROWTH RESTRICTION ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GLOMERULOSCLEROSIS ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
GROWTH RETARDATION ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEPATIC ENZYME ABNORMAL ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPOPROTHROMBINAEMIA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
HYPOSPADIAS ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
INTESTINAL INFARCTION ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
KIDNEY FIBROSIS ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
MACROGLOSSIA ( 3 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 3 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
MICROLITHIASIS ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 3 FDA reports)
NONSPECIFIC REACTION ( 3 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 3 FDA reports)
OLIGOHYDRAMNIOS ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PROSTHESIS IMPLANTATION ( 3 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
Q FEVER ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SKIN TEST POSITIVE ( 3 FDA reports)
STOMATITIS NECROTISING ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACQUIRED HAEMOPHILIA ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUPUNCTURE ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAL ATRESIA ( 2 FDA reports)
ANAL CANDIDIASIS ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CAUDAL REGRESSION SYNDROME ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLESTATIC LIVER INJURY ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL HAND MALFORMATION ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CRYING ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYSTIC LYMPHANGIOMA ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DECREASED INSULIN REQUIREMENT ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EATON-LAMBERT SYNDROME ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EVANS SYNDROME ( 2 FDA reports)
FAECALITH ( 2 FDA reports)
FANCONI SYNDROME ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FOETAL DEATH ( 2 FDA reports)
FOETAL HEART RATE DISORDER ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
GASTRITIS ATROPHIC ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GOUT ( 2 FDA reports)
HAEMATOSPERMIA ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERCORTICOIDISM ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOGONADISM ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE THROMBOSIS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIMB MALFORMATION ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MASS ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENINGOCOCCAL SEPSIS ( 2 FDA reports)
MENINGORRHAGIA ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MICROGNATHIA ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEPHRITIC SYNDROME ( 2 FDA reports)
NEPHRITIS ALLERGIC ( 2 FDA reports)
NEPHROANGIOSCLEROSIS ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NERVE ROOT LESION ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
OROPHARYNGITIS FUNGAL ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PARANEOPLASTIC SYNDROME ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PARVOVIRUS INFECTION ( 2 FDA reports)
PELVIC HAEMATOMA ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERIRENAL HAEMATOMA ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLEUROPERICARDITIS ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RENAL ISCHAEMIA ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETROGNATHIA ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
RHABDOMYOSARCOMA ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SCAB ( 2 FDA reports)
SCAR ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SMOKER ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUBSTANCE ABUSE ( 2 FDA reports)
SUPERINFECTION LUNG ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
TENDON CALCIFICATION ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
URETERAL NECROSIS ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
VAGINAL CANDIDIASIS ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
APATHY ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BRONCHIAL DYSPLASIA ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BULBAR PALSY ( 1 FDA reports)
BULLOUS IMPETIGO ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILAIDITI'S SYNDROME ( 1 FDA reports)
CHOLINERGIC SYNDROME ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLEFT LIP ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL URETERIC ANOMALY ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORNEAL NEOVASCULARISATION ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 1 FDA reports)
DACRYOSTENOSIS CONGENITAL ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPILATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DIABETES COMPLICATING PREGNANCY ( 1 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOMETRITIS DECIDUAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
ERYTHROBLASTOSIS ( 1 FDA reports)
ERYTHROMELALGIA ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FOETAL ARRHYTHMIA ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FONTANELLE BULGING ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GINGIVITIS ULCERATIVE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLOMERULONEPHROPATHY ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART AND LUNG TRANSPLANT ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HYGROMA COLLI ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERKALIURIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSION NEONATAL ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOSIDERAEMIA ( 1 FDA reports)
HYPOTHERMIA NEONATAL ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOVENTILATION NEONATAL ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGEAL DISCOMFORT ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LUMBAR VERTEBRA INJURY ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEASLES ANTIBODY POSITIVE ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEGAKARYOCYTES ( 1 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 1 FDA reports)
MENINGITIS ENTEROVIRAL ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM CHELONAE INFECTION ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAEVUS FLAMMEUS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
NEONATAL CHOLESTASIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NON-OBSTRUCTIVE CARDIOMYOPATHY ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARVOVIRUS B19 TEST POSITIVE ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLACENTAL INSUFFICIENCY ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL DYSPLASIA ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY PARALYSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL ANEURYSM ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL MIGRAINE ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETRO-ORBITAL NEOPLASM ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SECONDARY HYPOGONADISM ( 1 FDA reports)
SECONDARY HYPOTHYROIDISM ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE UNSPECIFIED ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SYMBLEPHARON ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TOBACCO POISONING ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TYPE II HYPERSENSITIVITY ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URETERAL CATHETERISATION ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT MALFORMATION ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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