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

DEATH ( 351 FDA reports)
DYSPNOEA ( 330 FDA reports)
PNEUMONIA ( 215 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 100 FDA reports)
HEADACHE ( 90 FDA reports)
SYNCOPE ( 90 FDA reports)
CHEST PAIN ( 88 FDA reports)
HYPOTENSION ( 85 FDA reports)
FLUID RETENTION ( 84 FDA reports)
DIZZINESS ( 75 FDA reports)
FALL ( 73 FDA reports)
OEDEMA PERIPHERAL ( 73 FDA reports)
RENAL FAILURE ( 71 FDA reports)
NAUSEA ( 70 FDA reports)
FATIGUE ( 63 FDA reports)
PULMONARY HYPERTENSION ( 63 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 61 FDA reports)
PYREXIA ( 58 FDA reports)
DIARRHOEA ( 56 FDA reports)
OEDEMA ( 54 FDA reports)
ANAEMIA ( 51 FDA reports)
BACK PAIN ( 51 FDA reports)
RIGHT VENTRICULAR FAILURE ( 51 FDA reports)
COUGH ( 49 FDA reports)
PAIN ( 49 FDA reports)
CARDIAC FAILURE ( 48 FDA reports)
VOMITING ( 47 FDA reports)
ATRIAL FIBRILLATION ( 44 FDA reports)
CONDITION AGGRAVATED ( 44 FDA reports)
INFECTION ( 43 FDA reports)
FLUID OVERLOAD ( 42 FDA reports)
ASTHENIA ( 41 FDA reports)
OXYGEN SATURATION DECREASED ( 41 FDA reports)
PULMONARY OEDEMA ( 40 FDA reports)
RESPIRATORY FAILURE ( 39 FDA reports)
DEVICE RELATED INFECTION ( 38 FDA reports)
HAEMORRHAGE ( 38 FDA reports)
UNEVALUABLE EVENT ( 38 FDA reports)
HOSPITALISATION ( 37 FDA reports)
DEHYDRATION ( 35 FDA reports)
EPISTAXIS ( 34 FDA reports)
MALAISE ( 34 FDA reports)
DISEASE PROGRESSION ( 33 FDA reports)
BRONCHITIS ( 31 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 29 FDA reports)
HEART RATE INCREASED ( 29 FDA reports)
URINARY TRACT INFECTION ( 29 FDA reports)
VISION BLURRED ( 29 FDA reports)
CHEST DISCOMFORT ( 28 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 28 FDA reports)
LOSS OF CONSCIOUSNESS ( 28 FDA reports)
PAIN IN EXTREMITY ( 28 FDA reports)
FLUSHING ( 27 FDA reports)
MYOCARDIAL INFARCTION ( 27 FDA reports)
RASH ( 27 FDA reports)
VISUAL IMPAIRMENT ( 27 FDA reports)
LUNG TRANSPLANT ( 26 FDA reports)
PLEURAL EFFUSION ( 25 FDA reports)
ASCITES ( 24 FDA reports)
CEREBROVASCULAR ACCIDENT ( 24 FDA reports)
DRUG DOSE OMISSION ( 24 FDA reports)
SEPSIS ( 23 FDA reports)
ARTHRALGIA ( 22 FDA reports)
HAEMOGLOBIN DECREASED ( 22 FDA reports)
LUNG DISORDER ( 22 FDA reports)
SWELLING ( 22 FDA reports)
PALPITATIONS ( 21 FDA reports)
CARDIAC PACEMAKER INSERTION ( 19 FDA reports)
INSOMNIA ( 19 FDA reports)
TRANSFUSION ( 19 FDA reports)
ABDOMINAL PAIN ( 18 FDA reports)
HAEMOPTYSIS ( 18 FDA reports)
PRESYNCOPE ( 18 FDA reports)
SCLERODERMA ( 18 FDA reports)
WEIGHT INCREASED ( 18 FDA reports)
OFF LABEL USE ( 17 FDA reports)
CARDIAC ARREST ( 16 FDA reports)
CONVULSION ( 16 FDA reports)
DECREASED APPETITE ( 16 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 16 FDA reports)
ABDOMINAL DISTENSION ( 15 FDA reports)
CARDIAC DISORDER ( 15 FDA reports)
HEAD INJURY ( 15 FDA reports)
NASOPHARYNGITIS ( 15 FDA reports)
PULMONARY EMBOLISM ( 15 FDA reports)
RENAL FAILURE ACUTE ( 15 FDA reports)
INTESTINAL OBSTRUCTION ( 14 FDA reports)
MYALGIA ( 14 FDA reports)
RENAL DISORDER ( 14 FDA reports)
CATHETERISATION CARDIAC ( 13 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 13 FDA reports)
NASAL CONGESTION ( 13 FDA reports)
PAIN IN JAW ( 13 FDA reports)
BLOOD POTASSIUM DECREASED ( 12 FDA reports)
CIRCULATORY FAILURE NEONATAL ( 12 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
FEELING ABNORMAL ( 12 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 12 FDA reports)
HYPERTENSION ( 12 FDA reports)
LOW BIRTH WEIGHT BABY ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
THROMBOCYTOPENIA ( 12 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 12 FDA reports)
TREATMENT NONCOMPLIANCE ( 12 FDA reports)
ABDOMINAL DISCOMFORT ( 11 FDA reports)
BLOOD COUNT ABNORMAL ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
CARDIO-RESPIRATORY ARREST ( 11 FDA reports)
CHILLS ( 11 FDA reports)
DIALYSIS ( 11 FDA reports)
DIVERTICULITIS ( 11 FDA reports)
MUSCLE SPASMS ( 11 FDA reports)
SKIN ULCER ( 11 FDA reports)
WEIGHT DECREASED ( 11 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
CONTUSION ( 10 FDA reports)
HIP FRACTURE ( 10 FDA reports)
HYPOAESTHESIA ( 10 FDA reports)
HYPOXIA ( 10 FDA reports)
INFUSION SITE INFECTION ( 10 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 10 FDA reports)
LOCALISED INFECTION ( 10 FDA reports)
MACULAR DEGENERATION ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
PREGNANCY ( 10 FDA reports)
STAPHYLOCOCCAL INFECTION ( 10 FDA reports)
TACHYCARDIA ( 10 FDA reports)
THROMBOSIS ( 10 FDA reports)
ATRIAL FLUTTER ( 9 FDA reports)
BRADYCARDIA ( 9 FDA reports)
CATHETER SITE PAIN ( 9 FDA reports)
CELLULITIS ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
ERYTHEMA ( 9 FDA reports)
GASTRIC DISORDER ( 9 FDA reports)
GOUT ( 9 FDA reports)
HAEMATOCHEZIA ( 9 FDA reports)
HAEMATOCRIT DECREASED ( 9 FDA reports)
HEPATIC FAILURE ( 9 FDA reports)
HYPERHIDROSIS ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 9 FDA reports)
LACERATION ( 9 FDA reports)
PERICARDIAL EFFUSION ( 9 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 9 FDA reports)
RESPIRATORY ARREST ( 9 FDA reports)
UNRESPONSIVE TO STIMULI ( 9 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
VIRAL INFECTION ( 9 FDA reports)
ACUTE RESPIRATORY FAILURE ( 8 FDA reports)
ARRHYTHMIA ( 8 FDA reports)
ASTHMA ( 8 FDA reports)
BLINDNESS ( 8 FDA reports)
CATHETER SITE INFECTION ( 8 FDA reports)
CYANOSIS ( 8 FDA reports)
DEAFNESS ( 8 FDA reports)
DYSPNOEA EXERTIONAL ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
HERPES ZOSTER ( 8 FDA reports)
LUNG NEOPLASM MALIGNANT ( 8 FDA reports)
MULTI-ORGAN FAILURE ( 8 FDA reports)
NECK PAIN ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
PULMONARY MASS ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
RIB FRACTURE ( 8 FDA reports)
ROAD TRAFFIC ACCIDENT ( 8 FDA reports)
THROAT IRRITATION ( 8 FDA reports)
VENTRICULAR TACHYCARDIA ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
ABSCESS ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
CATHETER SITE DISCHARGE ( 7 FDA reports)
CATHETER SITE ERYTHEMA ( 7 FDA reports)
CHOKING ( 7 FDA reports)
CLOSTRIDIAL INFECTION ( 7 FDA reports)
COLD SWEAT ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
DIPLOPIA ( 7 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 7 FDA reports)
GASTROINTESTINAL DISORDER ( 7 FDA reports)
HYPERTHYROIDISM ( 7 FDA reports)
HYPOTHYROIDISM ( 7 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
LEFT VENTRICULAR FAILURE ( 7 FDA reports)
MECHANICAL VENTILATION ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
PELVIC FRACTURE ( 7 FDA reports)
POLLAKIURIA ( 7 FDA reports)
PULMONARY HAEMORRHAGE ( 7 FDA reports)
PULMONARY THROMBOSIS ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
ANAEMIA NEONATAL ( 6 FDA reports)
ARTHRITIS ( 6 FDA reports)
CARDIAC OPERATION ( 6 FDA reports)
CATHETER PLACEMENT ( 6 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 6 FDA reports)
COLON OPERATION ( 6 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
FLATULENCE ( 6 FDA reports)
GALLBLADDER OPERATION ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
KNEE ARTHROPLASTY ( 6 FDA reports)
LIVER INJURY ( 6 FDA reports)
MENTAL DISORDER ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
NO THERAPEUTIC RESPONSE ( 6 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 6 FDA reports)
PREMATURE BABY ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
RESPIRATORY DISORDER ( 6 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 6 FDA reports)
SURGERY ( 6 FDA reports)
TREMOR ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
WHEEZING ( 6 FDA reports)
ABASIA ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 5 FDA reports)
ARTHROPATHY ( 5 FDA reports)
ATRIAL TACHYCARDIA ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
CARDIAC ABLATION ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
CORONARY ARTERY OCCLUSION ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
HEART AND LUNG TRANSPLANT ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
LABILE BLOOD PRESSURE ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
NEOPLASM MALIGNANT ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
OSTEOARTHRITIS ( 5 FDA reports)
OSTEOMYELITIS ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 5 FDA reports)
PERICARDITIS ( 5 FDA reports)
PULMONARY CONGESTION ( 5 FDA reports)
PULMONARY FIBROSIS ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
RHEUMATOID ARTHRITIS ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
SKIN DISCOLOURATION ( 5 FDA reports)
SLEEP APNOEA SYNDROME ( 5 FDA reports)
STENT PLACEMENT ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 5 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
ARTERIAL INJURY ( 4 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CARDIAC FIBRILLATION ( 4 FDA reports)
CATHETER SITE HAEMORRHAGE ( 4 FDA reports)
CATHETER SITE SWELLING ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
COLOSTOMY ( 4 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 4 FDA reports)
DEAFNESS UNILATERAL ( 4 FDA reports)
DEVICE RELATED SEPSIS ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
FEEDING TUBE COMPLICATION ( 4 FDA reports)
FIBROMYALGIA ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEART VALVE REPLACEMENT ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HERNIA ( 4 FDA reports)
HIGH FREQUENCY ABLATION ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 4 FDA reports)
KIDNEY INFECTION ( 4 FDA reports)
LEG AMPUTATION ( 4 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MENINGITIS ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
NECK INJURY ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
SUDDEN HEARING LOSS ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
WHEELCHAIR USER ( 4 FDA reports)
ABORTION ( 3 FDA reports)
ADMINISTRATION SITE INFECTION ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ASPIRATION PLEURAL CAVITY ( 3 FDA reports)
BACK DISORDER ( 3 FDA reports)
BACK INJURY ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
CARDIAC FAILURE CHRONIC ( 3 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
COR PULMONALE ( 3 FDA reports)
DENTAL DISCOMFORT ( 3 FDA reports)
DEVICE DAMAGE ( 3 FDA reports)
DEVICE OCCLUSION ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
FACE INJURY ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HERNIA REPAIR ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INFUSION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
INTESTINAL OPERATION ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LACRIMATION INCREASED ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LIVER TRANSPLANT ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
OESOPHAGEAL DISORDER ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
OVARIAN CYST RUPTURED ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PULMONARY VEIN OCCLUSION ( 3 FDA reports)
RECTAL PROLAPSE ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN OPERATION ( 3 FDA reports)
SKIN TIGHTNESS ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VARICOSE VEIN RUPTURED ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
WOUND TREATMENT ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ABSCESS DRAINAGE ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BIOPSY LIVER ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST OPERATION ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CATHETER SITE INFLAMMATION ( 2 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CONDUCTIVE DEAFNESS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DEVICE INFUSION ISSUE ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEMALE STERILISATION ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GOITRE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMODIALYSIS COMPLICATION ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HOSPICE CARE ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INGUINAL HERNIA REPAIR ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NASAL INFLAMMATION ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OXYGEN SATURATION INCREASED ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PLATELET TRANSFUSION ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POLIOMYELITIS ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SHOULDER OPERATION ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SPINAL CORD INJURY ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROXINE FREE INCREASED ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
VASCULAR CAUTERISATION ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VIRAL TEST POSITIVE ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL EXPLORATION ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADMINISTRATION SITE ABSCESS ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALTERNARIA INFECTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AUTOMATIC BLADDER ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC SARCOIDOSIS ( 1 FDA reports)
CARDIAC SEPTAL DEFECT REPAIR ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CASTLEMAN'S DISEASE ( 1 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYST ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIURETIC THERAPY ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR INFECTION BACTERIAL ( 1 FDA reports)
ELECTROCAUTERISATION ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
IMPLANT SITE ABSCESS ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION SITE ABSCESS ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE PUSTULE ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT INJECTION ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LACRIMAL DUCT PROCEDURE ( 1 FDA reports)
LAPAROSCOPY ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEDICAL INDUCTION OF COMA ( 1 FDA reports)
MEDICAL OBSERVATION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCARDIAL STRAIN ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARADOXICAL EMBOLISM ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POEMS SYNDROME ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY HYPERTENSIVE CRISIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULMONARY VALVE REPLACEMENT ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RENAL AND LIVER TRANSPLANT ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL CYST RUPTURED ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STATUS MIGRAINOSUS ( 1 FDA reports)
STENT MALFUNCTION ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOEMBOLECTOMY ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL OBSTRUCTION ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRANSPLANT EVALUATION ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
ULCER ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use