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

HYPOGLYCAEMIA ( 110 FDA reports)
DYSPNOEA ( 71 FDA reports)
CARDIAC ARREST ( 61 FDA reports)
DRUG INTERACTION ( 59 FDA reports)
ANAEMIA ( 55 FDA reports)
RENAL FAILURE ACUTE ( 55 FDA reports)
CARDIAC FAILURE ( 48 FDA reports)
SEPSIS ( 48 FDA reports)
PYREXIA ( 45 FDA reports)
THROMBOCYTOPENIA ( 43 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 42 FDA reports)
RENAL FAILURE ( 42 FDA reports)
PULMONARY EMBOLISM ( 40 FDA reports)
HYPOTENSION ( 39 FDA reports)
LEUKOPENIA ( 39 FDA reports)
DEHYDRATION ( 35 FDA reports)
DIABETES MELLITUS ( 35 FDA reports)
FALL ( 35 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 35 FDA reports)
HYPERGLYCAEMIA ( 35 FDA reports)
VOMITING ( 33 FDA reports)
DEATH ( 32 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 32 FDA reports)
MULTI-ORGAN FAILURE ( 32 FDA reports)
BLOOD GLUCOSE INCREASED ( 31 FDA reports)
DRUG INEFFECTIVE ( 30 FDA reports)
MYOCARDIAL INFARCTION ( 29 FDA reports)
HAEMATOMA ( 28 FDA reports)
HYPERTENSION ( 28 FDA reports)
PLEURAL EFFUSION ( 28 FDA reports)
BLOOD CREATININE INCREASED ( 27 FDA reports)
DIARRHOEA ( 27 FDA reports)
OEDEMA PERIPHERAL ( 27 FDA reports)
CELLULITIS ( 25 FDA reports)
CHOLESTASIS ( 25 FDA reports)
MALAISE ( 25 FDA reports)
PNEUMONIA ( 25 FDA reports)
PREGNANCY ( 25 FDA reports)
STEVENS-JOHNSON SYNDROME ( 25 FDA reports)
URINARY TRACT INFECTION ( 24 FDA reports)
HYPERKALAEMIA ( 23 FDA reports)
NAUSEA ( 23 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 23 FDA reports)
ATRIAL FIBRILLATION ( 22 FDA reports)
FATIGUE ( 21 FDA reports)
HYPOKALAEMIA ( 21 FDA reports)
SEPTIC SHOCK ( 21 FDA reports)
WOUND INFECTION ( 21 FDA reports)
ASTHENIA ( 20 FDA reports)
CHEST PAIN ( 20 FDA reports)
CONVULSION ( 20 FDA reports)
DEEP VEIN THROMBOSIS ( 20 FDA reports)
HYPOGLYCAEMIC COMA ( 20 FDA reports)
PREMATURE BABY ( 20 FDA reports)
RESPIRATORY FAILURE ( 20 FDA reports)
SOMNOLENCE ( 20 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 19 FDA reports)
ABDOMINAL PAIN ( 18 FDA reports)
CONFUSIONAL STATE ( 18 FDA reports)
RECTAL HAEMORRHAGE ( 18 FDA reports)
ANURIA ( 17 FDA reports)
ASCITES ( 17 FDA reports)
CONDITION AGGRAVATED ( 17 FDA reports)
DECREASED APPETITE ( 17 FDA reports)
HAEMOGLOBIN DECREASED ( 17 FDA reports)
HAEMORRHAGIC ANAEMIA ( 17 FDA reports)
NEUTROPENIA ( 17 FDA reports)
PRURITUS ( 17 FDA reports)
SYNCOPE ( 17 FDA reports)
ABORTION INDUCED ( 16 FDA reports)
BLOOD GLUCOSE DECREASED ( 16 FDA reports)
CARDIAC DISORDER ( 16 FDA reports)
DIZZINESS ( 16 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 16 FDA reports)
HEADACHE ( 16 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 16 FDA reports)
BRADYCARDIA ( 15 FDA reports)
CAESAREAN SECTION ( 15 FDA reports)
CATHETER RELATED COMPLICATION ( 15 FDA reports)
CIRCULATORY COLLAPSE ( 15 FDA reports)
HYPERHIDROSIS ( 15 FDA reports)
OEDEMA ( 15 FDA reports)
RENAL IMPAIRMENT ( 15 FDA reports)
COMA ( 14 FDA reports)
DISTURBANCE IN ATTENTION ( 14 FDA reports)
GOITRE ( 14 FDA reports)
KETOSIS ( 14 FDA reports)
LYMPHOCELE ( 14 FDA reports)
PERITONITIS ( 14 FDA reports)
POST PROCEDURAL COMPLICATION ( 14 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
BACTERIAL INFECTION ( 13 FDA reports)
CALCULUS URETERIC ( 13 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 13 FDA reports)
HAEMATEMESIS ( 13 FDA reports)
HEPATITIS ( 13 FDA reports)
LEUKOCYTOSIS ( 13 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 13 FDA reports)
OFF LABEL USE ( 13 FDA reports)
PAIN ( 13 FDA reports)
PREMATURE LABOUR ( 13 FDA reports)
RHABDOMYOLYSIS ( 13 FDA reports)
SHOCK ( 13 FDA reports)
VENTRICULAR FIBRILLATION ( 13 FDA reports)
ABORTION SPONTANEOUS ( 12 FDA reports)
ANGIOEDEMA ( 12 FDA reports)
BICYTOPENIA ( 12 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 12 FDA reports)
ENTEROCOCCAL INFECTION ( 12 FDA reports)
GASTRITIS EROSIVE ( 12 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 12 FDA reports)
HAEMORRHAGE ( 12 FDA reports)
JOINT DISLOCATION ( 12 FDA reports)
STAPHYLOCOCCAL INFECTION ( 12 FDA reports)
VENTRICULAR TACHYCARDIA ( 12 FDA reports)
ANAPHYLACTIC SHOCK ( 11 FDA reports)
ANGINA PECTORIS ( 11 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 11 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 11 FDA reports)
EPILEPSY ( 11 FDA reports)
HYPOAESTHESIA ( 11 FDA reports)
HYPONATRAEMIA ( 11 FDA reports)
INFECTION ( 11 FDA reports)
LOSS OF CONSCIOUSNESS ( 11 FDA reports)
MELAENA ( 11 FDA reports)
PLATELET COUNT DECREASED ( 11 FDA reports)
PRE-ECLAMPSIA ( 11 FDA reports)
URTICARIA ( 11 FDA reports)
ANGINA UNSTABLE ( 10 FDA reports)
ANOREXIA ( 10 FDA reports)
BRONCHOPNEUMONIA ( 10 FDA reports)
CEREBROVASCULAR ACCIDENT ( 10 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 10 FDA reports)
CORONARY ARTERY DISEASE ( 10 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 10 FDA reports)
EPISTAXIS ( 10 FDA reports)
ERYTHEMA ( 10 FDA reports)
INFLAMMATION ( 10 FDA reports)
INJECTION SITE INFLAMMATION ( 10 FDA reports)
LUNG DISORDER ( 10 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
SUDDEN DEATH ( 10 FDA reports)
TOXIC SKIN ERUPTION ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
ARRHYTHMIA ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
BRAIN OEDEMA ( 9 FDA reports)
CARDIOGENIC SHOCK ( 9 FDA reports)
CYANOSIS ( 9 FDA reports)
DISEASE PROGRESSION ( 9 FDA reports)
DRUG ERUPTION ( 9 FDA reports)
DYSPHAGIA ( 9 FDA reports)
GAIT DISTURBANCE ( 9 FDA reports)
INTENTIONAL OVERDOSE ( 9 FDA reports)
METABOLIC ACIDOSIS ( 9 FDA reports)
PANCYTOPENIA ( 9 FDA reports)
PROTEINURIA ( 9 FDA reports)
RASH ( 9 FDA reports)
RASH ERYTHEMATOUS ( 9 FDA reports)
RESPIRATORY DISTRESS ( 9 FDA reports)
TREMOR ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
WEIGHT INCREASED ( 9 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 8 FDA reports)
AGRANULOCYTOSIS ( 8 FDA reports)
ARTHRALGIA ( 8 FDA reports)
ATRIAL SEPTAL DEFECT ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 8 FDA reports)
CACHEXIA ( 8 FDA reports)
DIABETIC KETOACIDOSIS ( 8 FDA reports)
DYSPNOEA EXERTIONAL ( 8 FDA reports)
ENDOCARDITIS ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
HEART DISEASE CONGENITAL ( 8 FDA reports)
HEPATIC STEATOSIS ( 8 FDA reports)
HYPERTENSIVE CRISIS ( 8 FDA reports)
HYPERTHERMIA ( 8 FDA reports)
HYPOTHERMIA ( 8 FDA reports)
INTESTINAL INFARCTION ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
LACTIC ACIDOSIS ( 8 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 8 FDA reports)
MUCOSAL INFLAMMATION ( 8 FDA reports)
NERVOUS SYSTEM DISORDER ( 8 FDA reports)
ORAL CANDIDIASIS ( 8 FDA reports)
OSTEOMYELITIS ( 8 FDA reports)
OVERDOSE ( 8 FDA reports)
OXYGEN SATURATION DECREASED ( 8 FDA reports)
PANCREATITIS ( 8 FDA reports)
POLYHYDRAMNIOS ( 8 FDA reports)
PSEUDOMONAS INFECTION ( 8 FDA reports)
RESPIRATORY ARREST ( 8 FDA reports)
SHOCK HAEMORRHAGIC ( 8 FDA reports)
TRANSAMINASES INCREASED ( 8 FDA reports)
ABDOMINAL DISTENSION ( 7 FDA reports)
ACUTE CORONARY SYNDROME ( 7 FDA reports)
BACTERIAL SEPSIS ( 7 FDA reports)
BLISTER ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
CYTOLYTIC HEPATITIS ( 7 FDA reports)
DIALYSIS ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 7 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 7 FDA reports)
ENCEPHALOPATHY ( 7 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 7 FDA reports)
GASTROENTERITIS ( 7 FDA reports)
HELLP SYNDROME ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
HEPATOCELLULAR INJURY ( 7 FDA reports)
HERPES ZOSTER ( 7 FDA reports)
HYDRONEPHROSIS ( 7 FDA reports)
ILL-DEFINED DISORDER ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
INTESTINAL OBSTRUCTION ( 7 FDA reports)
KLEBSIELLA INFECTION ( 7 FDA reports)
LEG AMPUTATION ( 7 FDA reports)
LUNG INFILTRATION ( 7 FDA reports)
MOOD ALTERED ( 7 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 7 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 7 FDA reports)
RESPIRATORY DISORDER ( 7 FDA reports)
RESPIRATORY TRACT INFECTION ( 7 FDA reports)
SPEECH DISORDER ( 7 FDA reports)
VERTIGO ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
BRONCHOSPASM ( 6 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 6 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 6 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 6 FDA reports)
CATHETER RELATED INFECTION ( 6 FDA reports)
CEREBRAL ISCHAEMIA ( 6 FDA reports)
CHILLS ( 6 FDA reports)
DEVICE LEAKAGE ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 6 FDA reports)
EXTREMITY NECROSIS ( 6 FDA reports)
EYE HAEMORRHAGE ( 6 FDA reports)
FUNGAL INFECTION ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
HEART RATE IRREGULAR ( 6 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 6 FDA reports)
INFLUENZA LIKE ILLNESS ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
JEJUNAL PERFORATION ( 6 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 6 FDA reports)
LUNG INFECTION ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
PARALYSIS ( 6 FDA reports)
PERICARDIAL HAEMORRHAGE ( 6 FDA reports)
PROTHROMBIN TIME PROLONGED ( 6 FDA reports)
PSYCHOMOTOR RETARDATION ( 6 FDA reports)
RASH MACULAR ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 6 FDA reports)
RETINOPATHY ( 6 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 6 FDA reports)
STILLBIRTH ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
TORSADE DE POINTES ( 6 FDA reports)
VENA CAVA THROMBOSIS ( 6 FDA reports)
ABASIA ( 5 FDA reports)
ABSCESS BACTERIAL ( 5 FDA reports)
ACUTE PULMONARY OEDEMA ( 5 FDA reports)
APHASIA ( 5 FDA reports)
BACTERAEMIA ( 5 FDA reports)
BLEEDING TIME PROLONGED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 5 FDA reports)
BONE MARROW FAILURE ( 5 FDA reports)
BRAIN INJURY ( 5 FDA reports)
CARDIAC FAILURE CHRONIC ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CHOLECYSTITIS ( 5 FDA reports)
COLON CANCER ( 5 FDA reports)
COORDINATION ABNORMAL ( 5 FDA reports)
DERMATITIS ALLERGIC ( 5 FDA reports)
DRUG LEVEL INCREASED ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 5 FDA reports)
ERYSIPELAS ( 5 FDA reports)
ERYSIPELOID ( 5 FDA reports)
FLUID RETENTION ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 5 FDA reports)
HEPATIC ENCEPHALOPATHY ( 5 FDA reports)
HYPERTENSIVE HEART DISEASE ( 5 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 5 FDA reports)
INTRA-UTERINE DEATH ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 5 FDA reports)
MENINGITIS ENTEROCOCCAL ( 5 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
OCULAR HYPERAEMIA ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
POST PROCEDURAL BILE LEAK ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
PURULENT DISCHARGE ( 5 FDA reports)
PUSTULAR PSORIASIS ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
RALES ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 5 FDA reports)
SKIN NECROSIS ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
SLEEP DISORDER ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
SUDDEN CARDIAC DEATH ( 5 FDA reports)
SUICIDE ATTEMPT ( 5 FDA reports)
SWELLING ( 5 FDA reports)
THIRST ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
TYPE 1 DIABETES MELLITUS ( 5 FDA reports)
URETERIC OBSTRUCTION ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ACIDOSIS ( 4 FDA reports)
AGITATION ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
AZOTAEMIA ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLOOD KETONE BODY ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CANDIDA SEPSIS ( 4 FDA reports)
CARDIAC TAMPONADE ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
DECREASED INSULIN REQUIREMENT ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DERMATITIS ACNEIFORM ( 4 FDA reports)
DERMATITIS BULLOUS ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DIABETIC COMA ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DIVERTICULUM ( 4 FDA reports)
DRUG EFFECT INCREASED ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
FISTULA ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GESTATIONAL HYPERTENSION ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HEPATOTOXICITY ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LOCALISED INFECTION ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
NEUTROPENIC COLITIS ( 4 FDA reports)
NIKOLSKY'S SIGN ( 4 FDA reports)
OEDEMATOUS PANCREATITIS ( 4 FDA reports)
OSTEITIS ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
OSTEOMYELITIS CHRONIC ( 4 FDA reports)
OTORRHOEA ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
PORTAL VEIN THROMBOSIS ( 4 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PULMONARY HAEMORRHAGE ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
THIRST DECREASED ( 4 FDA reports)
TONGUE ULCERATION ( 4 FDA reports)
TRAUMATIC LUNG INJURY ( 4 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 4 FDA reports)
VASOSPASM ( 4 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
WOUND DECOMPOSITION ( 4 FDA reports)
WRONG DRUG ADMINISTERED ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ACUTE ABDOMEN ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD INSULIN ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD PROLACTIN DECREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CATHETERISATION CARDIAC ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
COMPLICATION OF PREGNANCY ( 3 FDA reports)
CONGENITAL HYDROCEPHALUS ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
COUGH ( 3 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 3 FDA reports)
CUTANEOUS VASCULITIS ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
EMERGENCY CARE ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
ERECTION INCREASED ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FISTULA REPAIR ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
FOETAL MACROSOMIA ( 3 FDA reports)
FOETAL MOVEMENTS DECREASED ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTROINTESTINAL CARCINOMA ( 3 FDA reports)
GASTROINTESTINAL NECROSIS ( 3 FDA reports)
GASTROINTESTINAL PAIN ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INFLAMMATORY MARKER INCREASED ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INTENSIVE CARE ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
JUGULAR VEIN THROMBOSIS ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LARYNGOSPASM ( 3 FDA reports)
LEARNING DISORDER ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MEGACOLON ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 3 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
NEONATAL DISORDER ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
PAIN OF SKIN ( 3 FDA reports)
PANCREATIC ENZYMES INCREASED ( 3 FDA reports)
PANCREATIC NECROSIS ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PITUITARY INFARCTION ( 3 FDA reports)
PNEUMONIA KLEBSIELLA ( 3 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 3 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
VANISHING BILE DUCT SYNDROME ( 3 FDA reports)
VASCULAR PURPURA ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VENTRICULAR FLUTTER ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
WOUND DEHISCENCE ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
AMAUROSIS ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANGIOSARCOMA ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
ARTERIOPATHIC DISEASE ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CARDIAC INDEX DECREASED ( 2 FDA reports)
CARDIAC PERFORATION ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBRAL CALCIFICATION ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBRAL MALARIA ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CLONUS ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DERMATOMYOSITIS ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DRUG PHYSIOLOGIC INCOMPATIBILITY ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DUODENAL ATRESIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EXOMPHALOS ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRIC STENOSIS ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROSCHISIS ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC VEIN OCCLUSION ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HERPES OESOPHAGITIS ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYDROPNEUMOTHORAX ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTONIA NEONATAL ( 2 FDA reports)
HYPERVOLAEMIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOPITUITARISM ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INCREASED INSULIN REQUIREMENT ( 2 FDA reports)
INFUSION SITE PHLEBITIS ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE ATROPHY ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJURY ( 2 FDA reports)
INSULIN RESISTANCE ( 2 FDA reports)
INSULIN RESISTANCE SYNDROME ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LEIOMYOSARCOMA ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MACROSOMIA ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MESOTHELIOMA ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
MYOGLOBINAEMIA ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEISSERIA INFECTION ( 2 FDA reports)
NEONATAL HYPOTENSION ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NODULE ( 2 FDA reports)
NOROVIRUS TEST POSITIVE ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PANCREATIC ABSCESS ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERITONITIS SCLEROSING ( 2 FDA reports)
PIERRE ROBIN SYNDROME ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POST PROCEDURAL PNEUMONIA ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULMONARY FISTULA ( 2 FDA reports)
PULMONARY MALFORMATION ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RENAL VEIN OCCLUSION ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
SHOULDER DYSTOCIA ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THREATENED LABOUR ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TRISOMY 21 ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ADENOVIRAL HEPATITIS ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
APATHY ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARRESTED LABOUR ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CALCIFICATION OF MUSCLE ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLINODACTYLY ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYANOSIS NEONATAL ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEVICE ISSUE ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERTENSION NEONATAL ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFUSION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LDL/HDL RATIO DECREASED ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYMPHOCELE MARSUPIALISATION ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NEONATAL DIABETES MELLITUS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUROGLYCOPENIA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OEDEMA NEONATAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PAROPHTHALMIA ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERICARDITIS INFECTIVE ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PLACENTAL INSUFFICIENCY ( 1 FDA reports)
PLAGIOCEPHALY ( 1 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
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PULMONARY HYPERTENSION ( 1 FDA reports)
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PULMONARY TOXICITY ( 1 FDA reports)
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PUPILLARY DISORDER ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RENAL AGENESIS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINOPATHY PROLIFERATIVE ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SHUNT STENOSIS ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYCARDIA FOETAL ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSIENT PSYCHOSIS ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WALKING DISTANCE TEST ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND EVISCERATION ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)

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