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

PYREXIA ( 446 FDA reports)
DIARRHOEA ( 327 FDA reports)
HYPERTENSION ( 294 FDA reports)
ANAEMIA ( 271 FDA reports)
DIZZINESS ( 268 FDA reports)
DYSPNOEA ( 266 FDA reports)
MALAISE ( 263 FDA reports)
NAUSEA ( 249 FDA reports)
VOMITING ( 248 FDA reports)
FALL ( 232 FDA reports)
OEDEMA PERIPHERAL ( 223 FDA reports)
BLOOD CREATININE INCREASED ( 222 FDA reports)
BLOOD PRESSURE INCREASED ( 221 FDA reports)
CHEST PAIN ( 218 FDA reports)
FATIGUE ( 218 FDA reports)
PNEUMONIA ( 203 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 200 FDA reports)
RENAL FAILURE ( 198 FDA reports)
HEADACHE ( 196 FDA reports)
PLEURAL EFFUSION ( 192 FDA reports)
HAEMOGLOBIN DECREASED ( 191 FDA reports)
RENAL FAILURE ACUTE ( 190 FDA reports)
RENAL IMPAIRMENT ( 189 FDA reports)
ASTHENIA ( 186 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 170 FDA reports)
PAIN ( 170 FDA reports)
HYPOTENSION ( 158 FDA reports)
MYOCARDIAL INFARCTION ( 156 FDA reports)
INTERSTITIAL LUNG DISEASE ( 153 FDA reports)
DECREASED APPETITE ( 150 FDA reports)
CONDITION AGGRAVATED ( 147 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 146 FDA reports)
PLATELET COUNT DECREASED ( 146 FDA reports)
DEPRESSION ( 145 FDA reports)
DEHYDRATION ( 143 FDA reports)
CARDIAC FAILURE ( 142 FDA reports)
ANXIETY ( 137 FDA reports)
ABDOMINAL PAIN ( 136 FDA reports)
CONFUSIONAL STATE ( 136 FDA reports)
CONSTIPATION ( 136 FDA reports)
CEREBROVASCULAR ACCIDENT ( 135 FDA reports)
HYPOGLYCAEMIA ( 135 FDA reports)
BLOOD UREA INCREASED ( 134 FDA reports)
CEREBRAL INFARCTION ( 131 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 129 FDA reports)
DRUG INEFFECTIVE ( 129 FDA reports)
ARTHRALGIA ( 128 FDA reports)
LOSS OF CONSCIOUSNESS ( 128 FDA reports)
RASH ( 124 FDA reports)
BACK PAIN ( 122 FDA reports)
DRUG INTERACTION ( 120 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 118 FDA reports)
DEATH ( 117 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 116 FDA reports)
GAIT DISTURBANCE ( 116 FDA reports)
BLOOD PRESSURE DECREASED ( 115 FDA reports)
PAIN IN EXTREMITY ( 114 FDA reports)
RHABDOMYOLYSIS ( 114 FDA reports)
CARDIAC ARREST ( 113 FDA reports)
ANOREXIA ( 111 FDA reports)
PALPITATIONS ( 111 FDA reports)
WEIGHT DECREASED ( 111 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 110 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 108 FDA reports)
DIABETES MELLITUS ( 107 FDA reports)
INSOMNIA ( 105 FDA reports)
URINARY TRACT INFECTION ( 104 FDA reports)
LIVER DISORDER ( 103 FDA reports)
ANGINA PECTORIS ( 99 FDA reports)
ATRIAL FIBRILLATION ( 99 FDA reports)
ERYTHEMA ( 97 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 96 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 96 FDA reports)
SPEECH DISORDER ( 95 FDA reports)
PRURITUS ( 94 FDA reports)
OEDEMA ( 90 FDA reports)
CONVULSION ( 88 FDA reports)
SOMNOLENCE ( 88 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 87 FDA reports)
RESPIRATORY FAILURE ( 87 FDA reports)
JAUNDICE ( 86 FDA reports)
OSTEONECROSIS ( 85 FDA reports)
HYPERGLYCAEMIA ( 84 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 83 FDA reports)
HYPOAESTHESIA ( 83 FDA reports)
THROMBOCYTOPENIA ( 83 FDA reports)
ABDOMINAL PAIN UPPER ( 80 FDA reports)
BRADYCARDIA ( 80 FDA reports)
PANCYTOPENIA ( 80 FDA reports)
DYSARTHRIA ( 79 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 79 FDA reports)
HYPERKALAEMIA ( 79 FDA reports)
BLOOD GLUCOSE INCREASED ( 78 FDA reports)
BRONCHITIS ( 78 FDA reports)
HYPOKALAEMIA ( 78 FDA reports)
DISORIENTATION ( 76 FDA reports)
RENAL FAILURE CHRONIC ( 76 FDA reports)
SEPSIS ( 75 FDA reports)
CATARACT ( 74 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 74 FDA reports)
INFECTION ( 73 FDA reports)
CHEST DISCOMFORT ( 72 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 72 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 72 FDA reports)
ASTHMA ( 71 FDA reports)
CHILLS ( 71 FDA reports)
COUGH ( 71 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 71 FDA reports)
HYPONATRAEMIA ( 71 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 70 FDA reports)
LEUKOPENIA ( 70 FDA reports)
SWELLING ( 69 FDA reports)
CARDIOMEGALY ( 68 FDA reports)
CEREBRAL HAEMORRHAGE ( 68 FDA reports)
BONE DISORDER ( 67 FDA reports)
POLLAKIURIA ( 67 FDA reports)
ASCITES ( 66 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 65 FDA reports)
FEELING ABNORMAL ( 65 FDA reports)
CORONARY ARTERY DISEASE ( 63 FDA reports)
EMOTIONAL DISTRESS ( 63 FDA reports)
MYALGIA ( 63 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 63 FDA reports)
RENAL DISORDER ( 63 FDA reports)
SHOCK ( 63 FDA reports)
MELAENA ( 62 FDA reports)
MULTI-ORGAN FAILURE ( 62 FDA reports)
PULMONARY OEDEMA ( 62 FDA reports)
TREMOR ( 62 FDA reports)
URINARY INCONTINENCE ( 62 FDA reports)
DELIRIUM ( 61 FDA reports)
IMPAIRED HEALING ( 61 FDA reports)
MUSCULAR WEAKNESS ( 61 FDA reports)
HEPATITIS ( 59 FDA reports)
MEMORY IMPAIRMENT ( 59 FDA reports)
TACHYCARDIA ( 59 FDA reports)
AMNESIA ( 58 FDA reports)
DIVERTICULUM INTESTINAL ( 58 FDA reports)
NEUTROPENIA ( 58 FDA reports)
OSTEOMYELITIS ( 58 FDA reports)
DYSPHAGIA ( 57 FDA reports)
PULMONARY EMBOLISM ( 57 FDA reports)
OVERDOSE ( 56 FDA reports)
URTICARIA ( 56 FDA reports)
ARRHYTHMIA ( 55 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 55 FDA reports)
STEVENS-JOHNSON SYNDROME ( 55 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 54 FDA reports)
BURSITIS ( 54 FDA reports)
GASTROENTERITIS ( 54 FDA reports)
SYNCOPE ( 54 FDA reports)
HAEMODIALYSIS ( 53 FDA reports)
PARAESTHESIA ( 53 FDA reports)
RESPIRATORY DISTRESS ( 53 FDA reports)
VISION BLURRED ( 53 FDA reports)
AGRANULOCYTOSIS ( 52 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 52 FDA reports)
HAEMATOCRIT DECREASED ( 52 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 51 FDA reports)
INJURY ( 51 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 50 FDA reports)
EOSINOPHIL COUNT INCREASED ( 50 FDA reports)
OSTEOARTHRITIS ( 50 FDA reports)
RECTAL HAEMORRHAGE ( 50 FDA reports)
HYPOPHAGIA ( 49 FDA reports)
NEOPLASM MALIGNANT ( 49 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 49 FDA reports)
DISEASE PROGRESSION ( 48 FDA reports)
HEART RATE INCREASED ( 48 FDA reports)
HEPATIC ENZYME INCREASED ( 48 FDA reports)
DRUG ERUPTION ( 47 FDA reports)
GLAUCOMA ( 47 FDA reports)
HAEMATOCHEZIA ( 47 FDA reports)
HYPERLIPIDAEMIA ( 47 FDA reports)
PERICARDIAL EFFUSION ( 47 FDA reports)
SEPTIC SHOCK ( 47 FDA reports)
WEIGHT INCREASED ( 47 FDA reports)
HEPATIC FAILURE ( 46 FDA reports)
DEFORMITY ( 45 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 45 FDA reports)
COGNITIVE DISORDER ( 44 FDA reports)
OSTEONECROSIS OF JAW ( 44 FDA reports)
DIALYSIS ( 43 FDA reports)
DYSPNOEA EXERTIONAL ( 43 FDA reports)
HYPERHIDROSIS ( 43 FDA reports)
LUNG DISORDER ( 43 FDA reports)
NASOPHARYNGITIS ( 43 FDA reports)
BLOOD POTASSIUM INCREASED ( 42 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 42 FDA reports)
COMA ( 42 FDA reports)
GASTRIC ULCER ( 42 FDA reports)
GINGIVAL BLEEDING ( 42 FDA reports)
HERPES ZOSTER ( 42 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 42 FDA reports)
ABDOMINAL DISTENSION ( 41 FDA reports)
DRUG TOXICITY ( 41 FDA reports)
HALLUCINATION ( 41 FDA reports)
FEMUR FRACTURE ( 40 FDA reports)
CARDIO-RESPIRATORY ARREST ( 39 FDA reports)
CAROTID ARTERY STENOSIS ( 39 FDA reports)
GASTRITIS ( 39 FDA reports)
GENERALISED OEDEMA ( 39 FDA reports)
HEPATIC STEATOSIS ( 39 FDA reports)
MUSCULOSKELETAL PAIN ( 39 FDA reports)
PULMONARY HYPERTENSION ( 39 FDA reports)
ROTATOR CUFF SYNDROME ( 39 FDA reports)
CARDIAC DISORDER ( 38 FDA reports)
CELLULITIS ( 38 FDA reports)
HIP FRACTURE ( 38 FDA reports)
PURULENT DISCHARGE ( 38 FDA reports)
SPINAL COLUMN STENOSIS ( 38 FDA reports)
STOMATITIS ( 38 FDA reports)
ABSCESS JAW ( 37 FDA reports)
EPISTAXIS ( 37 FDA reports)
HYPERSENSITIVITY ( 37 FDA reports)
NEUTROPHIL COUNT DECREASED ( 37 FDA reports)
RESTLESSNESS ( 37 FDA reports)
EYELID PTOSIS ( 36 FDA reports)
HYPERCALCAEMIA ( 36 FDA reports)
HYPERTENSIVE CRISIS ( 36 FDA reports)
MENTAL STATUS CHANGES ( 36 FDA reports)
MUSCLE SPASMS ( 36 FDA reports)
STAPHYLOCOCCAL INFECTION ( 36 FDA reports)
SUICIDE ATTEMPT ( 36 FDA reports)
TOOTH EXTRACTION ( 36 FDA reports)
CARPAL TUNNEL SYNDROME ( 35 FDA reports)
CHROMATURIA ( 35 FDA reports)
DYSPEPSIA ( 35 FDA reports)
NEUROPATHY PERIPHERAL ( 35 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 35 FDA reports)
VISUAL ACUITY REDUCED ( 35 FDA reports)
ABDOMINAL DISCOMFORT ( 34 FDA reports)
ALOPECIA ( 34 FDA reports)
BLOOD POTASSIUM DECREASED ( 34 FDA reports)
BLOOD SODIUM DECREASED ( 34 FDA reports)
DRY MOUTH ( 34 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 34 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 34 FDA reports)
LUNG NEOPLASM MALIGNANT ( 34 FDA reports)
MITRAL VALVE INCOMPETENCE ( 34 FDA reports)
PANCREATITIS ( 34 FDA reports)
SKIN EXFOLIATION ( 34 FDA reports)
SPINAL OSTEOARTHRITIS ( 34 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 34 FDA reports)
URINE ODOUR ABNORMAL ( 34 FDA reports)
URINE OUTPUT DECREASED ( 34 FDA reports)
ABNORMAL BEHAVIOUR ( 33 FDA reports)
BASAL CELL CARCINOMA ( 33 FDA reports)
BLISTER ( 33 FDA reports)
HEART RATE DECREASED ( 33 FDA reports)
MYOCARDIAL ISCHAEMIA ( 33 FDA reports)
NEPHROLITHIASIS ( 33 FDA reports)
UROSEPSIS ( 33 FDA reports)
AGITATION ( 32 FDA reports)
BREAST CANCER ( 32 FDA reports)
DRUG HYPERSENSITIVITY ( 32 FDA reports)
ENCEPHALOPATHY ( 32 FDA reports)
HAEMATURIA ( 32 FDA reports)
PANCREATITIS ACUTE ( 32 FDA reports)
POOR QUALITY SLEEP ( 32 FDA reports)
PROTEINURIA ( 32 FDA reports)
ABSCESS ( 31 FDA reports)
COLONIC POLYP ( 31 FDA reports)
DUODENAL ULCER ( 31 FDA reports)
DYSURIA ( 31 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 31 FDA reports)
INFLAMMATION ( 31 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 31 FDA reports)
MEDICATION ERROR ( 31 FDA reports)
PARALYSIS ( 31 FDA reports)
PROSTATE CANCER ( 31 FDA reports)
RADICULOPATHY ( 31 FDA reports)
ROSACEA ( 31 FDA reports)
VERTIGO ( 31 FDA reports)
DEEP VEIN THROMBOSIS ( 30 FDA reports)
DYSGEUSIA ( 30 FDA reports)
HAEMATEMESIS ( 30 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 30 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 30 FDA reports)
NECK PAIN ( 30 FDA reports)
SINUSITIS ( 30 FDA reports)
BLADDER CANCER RECURRENT ( 29 FDA reports)
BURNING SENSATION ( 29 FDA reports)
COLITIS ( 29 FDA reports)
FACE OEDEMA ( 29 FDA reports)
HYPERPARATHYROIDISM ( 29 FDA reports)
METABOLIC ACIDOSIS ( 29 FDA reports)
RESPIRATORY DISORDER ( 29 FDA reports)
ACUTE PULMONARY OEDEMA ( 28 FDA reports)
ADVERSE EVENT ( 28 FDA reports)
BENIGN COLONIC NEOPLASM ( 28 FDA reports)
BONE MARROW FAILURE ( 28 FDA reports)
DERMATITIS EXFOLIATIVE ( 28 FDA reports)
LUNG INFILTRATION ( 28 FDA reports)
PURPURA ( 28 FDA reports)
SPINAL HAEMANGIOMA ( 28 FDA reports)
BLOOD BILIRUBIN INCREASED ( 27 FDA reports)
BONE PAIN ( 27 FDA reports)
DIPLOPIA ( 27 FDA reports)
FLUSHING ( 27 FDA reports)
HAEMORRHOIDS ( 27 FDA reports)
HYPOGLYCAEMIC COMA ( 27 FDA reports)
OESOPHAGEAL ULCER ( 27 FDA reports)
OFF LABEL USE ( 27 FDA reports)
PRURITUS GENERALISED ( 27 FDA reports)
TINNITUS ( 27 FDA reports)
URINARY RETENTION ( 27 FDA reports)
ATELECTASIS ( 26 FDA reports)
BLOOD URIC ACID INCREASED ( 26 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 26 FDA reports)
DYSSTASIA ( 26 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 26 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 26 FDA reports)
OXYGEN SATURATION DECREASED ( 26 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 26 FDA reports)
POST PROCEDURAL COMPLICATION ( 26 FDA reports)
STRESS ( 26 FDA reports)
ARTERIOSCLEROSIS ( 25 FDA reports)
ARTHRITIS ( 25 FDA reports)
HAEMATOMA ( 25 FDA reports)
HEART RATE IRREGULAR ( 25 FDA reports)
HYPOTHYROIDISM ( 25 FDA reports)
HYPOXIA ( 25 FDA reports)
INTESTINAL OBSTRUCTION ( 25 FDA reports)
IRRITABLE BOWEL SYNDROME ( 25 FDA reports)
OSTEOPENIA ( 25 FDA reports)
PNEUMONIA ASPIRATION ( 25 FDA reports)
PREMATURE BABY ( 25 FDA reports)
SINUS BRADYCARDIA ( 25 FDA reports)
TREATMENT NONCOMPLIANCE ( 25 FDA reports)
WHEEZING ( 25 FDA reports)
APLASIA PURE RED CELL ( 24 FDA reports)
BALANCE DISORDER ( 24 FDA reports)
CARDIAC FAILURE ACUTE ( 24 FDA reports)
CARDIOVASCULAR DISORDER ( 24 FDA reports)
CEREBRAL ISCHAEMIA ( 24 FDA reports)
DIFFICULTY IN WALKING ( 24 FDA reports)
DRY SKIN ( 24 FDA reports)
HEPATIC ENCEPHALOPATHY ( 24 FDA reports)
OLIGURIA ( 24 FDA reports)
RHEUMATOID ARTHRITIS ( 24 FDA reports)
SWELLING FACE ( 24 FDA reports)
UTERINE CANCER ( 24 FDA reports)
VENTRICULAR TACHYCARDIA ( 24 FDA reports)
ANGINA UNSTABLE ( 23 FDA reports)
ANURIA ( 23 FDA reports)
BLOOD ALBUMIN DECREASED ( 23 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 23 FDA reports)
BONE DEBRIDEMENT ( 23 FDA reports)
FLUID RETENTION ( 23 FDA reports)
HAEMORRHAGE ( 23 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 23 FDA reports)
NOCTURIA ( 23 FDA reports)
PYELONEPHRITIS ( 23 FDA reports)
RENAL ARTERY STENOSIS ( 23 FDA reports)
TOXIC SKIN ERUPTION ( 23 FDA reports)
ABASIA ( 22 FDA reports)
ACUTE RESPIRATORY FAILURE ( 22 FDA reports)
ANAPHYLACTIC SHOCK ( 22 FDA reports)
DEMENTIA ( 22 FDA reports)
EAR PAIN ( 22 FDA reports)
ECZEMA ( 22 FDA reports)
HEPATOMEGALY ( 22 FDA reports)
ILEUS ( 22 FDA reports)
SUBDURAL HAEMATOMA ( 22 FDA reports)
CHRONIC SINUSITIS ( 21 FDA reports)
DIVERTICULITIS ( 21 FDA reports)
EATING DISORDER ( 21 FDA reports)
FEELING HOT ( 21 FDA reports)
GOUT ( 21 FDA reports)
HALLUCINATION, VISUAL ( 21 FDA reports)
HYPERCHOLESTEROLAEMIA ( 21 FDA reports)
INCONTINENCE ( 21 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 21 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 21 FDA reports)
NERVOUS SYSTEM DISORDER ( 21 FDA reports)
PERITONITIS ( 21 FDA reports)
PULMONARY CONGESTION ( 21 FDA reports)
RESPIRATORY TRACT INFECTION ( 21 FDA reports)
SINUS CONGESTION ( 21 FDA reports)
SUDDEN DEATH ( 21 FDA reports)
ANAPHYLACTIC REACTION ( 20 FDA reports)
CAESAREAN SECTION ( 20 FDA reports)
CIRCULATORY COLLAPSE ( 20 FDA reports)
DELUSION ( 20 FDA reports)
EROSIVE OESOPHAGITIS ( 20 FDA reports)
ERYTHEMA MULTIFORME ( 20 FDA reports)
FEBRILE NEUTROPENIA ( 20 FDA reports)
ILEUS PARALYTIC ( 20 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 20 FDA reports)
LEUKOCYTOSIS ( 20 FDA reports)
LIVER CARCINOMA RUPTURED ( 20 FDA reports)
MYELODYSPLASTIC SYNDROME ( 20 FDA reports)
ONYCHOMYCOSIS ( 20 FDA reports)
ORTHOSTATIC HYPOTENSION ( 20 FDA reports)
ROAD TRAFFIC ACCIDENT ( 20 FDA reports)
SKIN DISORDER ( 20 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 20 FDA reports)
THROMBOSIS ( 20 FDA reports)
TONGUE DISORDER ( 20 FDA reports)
TOOTH FRACTURE ( 20 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 19 FDA reports)
AORTIC ANEURYSM ( 19 FDA reports)
BLOOD CHLORIDE DECREASED ( 19 FDA reports)
CYANOSIS ( 19 FDA reports)
GASTROINTESTINAL PAIN ( 19 FDA reports)
HEPATITIS FULMINANT ( 19 FDA reports)
HYPERKERATOSIS ( 19 FDA reports)
HYPERURICAEMIA ( 19 FDA reports)
IRON DEFICIENCY ANAEMIA ( 19 FDA reports)
MOBILITY DECREASED ( 19 FDA reports)
PERIODONTITIS ( 19 FDA reports)
PROTEIN URINE PRESENT ( 19 FDA reports)
RESPIRATORY ARREST ( 19 FDA reports)
SKIN LESION ( 19 FDA reports)
SLEEP APNOEA SYNDROME ( 19 FDA reports)
TENDON RUPTURE ( 19 FDA reports)
TENDONITIS ( 19 FDA reports)
VENTRICULAR FIBRILLATION ( 19 FDA reports)
VIRAL INFECTION ( 19 FDA reports)
CARDIAC MURMUR ( 18 FDA reports)
CHOLELITHIASIS ( 18 FDA reports)
CHOLESTASIS ( 18 FDA reports)
COLD SWEAT ( 18 FDA reports)
EPILEPSY ( 18 FDA reports)
HEMIPLEGIA ( 18 FDA reports)
HOT FLUSH ( 18 FDA reports)
HYPERBILIRUBINAEMIA ( 18 FDA reports)
HYPOACUSIS ( 18 FDA reports)
HYPOALBUMINAEMIA ( 18 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 18 FDA reports)
JOINT SWELLING ( 18 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 18 FDA reports)
NEPHROTIC SYNDROME ( 18 FDA reports)
OCULAR HYPERAEMIA ( 18 FDA reports)
PHLEBITIS ( 18 FDA reports)
POLYURIA ( 18 FDA reports)
PSORIASIS ( 18 FDA reports)
SEQUESTRECTOMY ( 18 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 18 FDA reports)
CATARACT OPERATION ( 17 FDA reports)
CYSTITIS ( 17 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 17 FDA reports)
GINGIVITIS ( 17 FDA reports)
INFLUENZA ( 17 FDA reports)
JOINT SPRAIN ( 17 FDA reports)
MENTAL DISORDER ( 17 FDA reports)
MYOPATHY ( 17 FDA reports)
NEOPLASM PROGRESSION ( 17 FDA reports)
NIGHT SWEATS ( 17 FDA reports)
ORAL INTAKE REDUCED ( 17 FDA reports)
PALLOR ( 17 FDA reports)
PLEURISY ( 17 FDA reports)
PRODUCTIVE COUGH ( 17 FDA reports)
RETINAL DETACHMENT ( 17 FDA reports)
SURGERY ( 17 FDA reports)
THIRST ( 17 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 17 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 17 FDA reports)
ACNE ( 16 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 16 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 16 FDA reports)
BONE MARROW DEPRESSION ( 16 FDA reports)
BRONCHOPNEUMONIA ( 16 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 16 FDA reports)
CEREBRAL ATROPHY ( 16 FDA reports)
CORONARY ARTERY STENOSIS ( 16 FDA reports)
DEPRESSED MOOD ( 16 FDA reports)
DERMAL CYST ( 16 FDA reports)
DRUG LEVEL INCREASED ( 16 FDA reports)
FEMORAL NECK FRACTURE ( 16 FDA reports)
FLATULENCE ( 16 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 16 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 16 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 16 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 16 FDA reports)
MASTICATION DISORDER ( 16 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 16 FDA reports)
PNEUMONITIS ( 16 FDA reports)
PSYCHOTIC DISORDER ( 16 FDA reports)
PURULENCE ( 16 FDA reports)
RIB FRACTURE ( 16 FDA reports)
SKIN PAPILLOMA ( 16 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 16 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 16 FDA reports)
TYPE 1 DIABETES MELLITUS ( 16 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 16 FDA reports)
VERTIGO POSITIONAL ( 16 FDA reports)
VISUAL IMPAIRMENT ( 16 FDA reports)
ANGIONEUROTIC OEDEMA ( 15 FDA reports)
APHASIA ( 15 FDA reports)
ATRIOVENTRICULAR BLOCK ( 15 FDA reports)
CHOLECYSTITIS ( 15 FDA reports)
COORDINATION ABNORMAL ( 15 FDA reports)
DRUG EFFECT DECREASED ( 15 FDA reports)
EMOTIONAL DISORDER ( 15 FDA reports)
FAECES DISCOLOURED ( 15 FDA reports)
GASTROINTESTINAL PERFORATION ( 15 FDA reports)
HYPOAESTHESIA ORAL ( 15 FDA reports)
HYPOTHERMIA ( 15 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 15 FDA reports)
INTESTINAL ISCHAEMIA ( 15 FDA reports)
LEFT VENTRICULAR FAILURE ( 15 FDA reports)
LUNG NEOPLASM ( 15 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 15 FDA reports)
ORTHOPNOEA ( 15 FDA reports)
RECTAL POLYP ( 15 FDA reports)
RETINAL HAEMORRHAGE ( 15 FDA reports)
SQUAMOUS CELL CARCINOMA ( 15 FDA reports)
TYPE 2 DIABETES MELLITUS ( 15 FDA reports)
ABSCESS DRAINAGE ( 14 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 14 FDA reports)
ARTHROPATHY ( 14 FDA reports)
AZOTAEMIA ( 14 FDA reports)
BLADDER CATHETERISATION ( 14 FDA reports)
CANDIDIASIS ( 14 FDA reports)
CHEST X-RAY ABNORMAL ( 14 FDA reports)
COAGULOPATHY ( 14 FDA reports)
COMMUNICATION DISORDER ( 14 FDA reports)
CONTUSION ( 14 FDA reports)
DIABETIC NEPHROPATHY ( 14 FDA reports)
DYSLALIA ( 14 FDA reports)
ERECTILE DYSFUNCTION ( 14 FDA reports)
FEAR ( 14 FDA reports)
GENERALISED ERYTHEMA ( 14 FDA reports)
GINGIVAL INFECTION ( 14 FDA reports)
HAEMOPTYSIS ( 14 FDA reports)
HEPATITIS ACUTE ( 14 FDA reports)
HYPERTHYROIDISM ( 14 FDA reports)
ILL-DEFINED DISORDER ( 14 FDA reports)
INGROWING NAIL ( 14 FDA reports)
INTENTIONAL OVERDOSE ( 14 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 14 FDA reports)
LUNG ADENOCARCINOMA ( 14 FDA reports)
METASTASES TO LUNG ( 14 FDA reports)
NEUROPATHY ( 14 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 14 FDA reports)
PNEUMOTHORAX ( 14 FDA reports)
PO2 DECREASED ( 14 FDA reports)
SHOCK HAEMORRHAGIC ( 14 FDA reports)
TACHYPNOEA ( 14 FDA reports)
TOOTH LOSS ( 14 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 14 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 13 FDA reports)
ATAXIA ( 13 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 13 FDA reports)
BLOOD SODIUM INCREASED ( 13 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 13 FDA reports)
CARDIOMYOPATHY ( 13 FDA reports)
DISEASE RECURRENCE ( 13 FDA reports)
DRUG DOSE OMISSION ( 13 FDA reports)
DYSKINESIA ( 13 FDA reports)
ELECTROLYTE IMBALANCE ( 13 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 13 FDA reports)
EYE PAIN ( 13 FDA reports)
GASTRIC CANCER ( 13 FDA reports)
GASTROINTESTINAL DISORDER ( 13 FDA reports)
GINGIVAL PAIN ( 13 FDA reports)
GINGIVAL SWELLING ( 13 FDA reports)
GINGIVAL ULCERATION ( 13 FDA reports)
GRANULOCYTOPENIA ( 13 FDA reports)
HIATUS HERNIA ( 13 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 13 FDA reports)
INFLUENZA LIKE ILLNESS ( 13 FDA reports)
LETHARGY ( 13 FDA reports)
LUNG INFECTION ( 13 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 13 FDA reports)
PATHOLOGICAL FRACTURE ( 13 FDA reports)
PREMATURE LABOUR ( 13 FDA reports)
PRIMARY SEQUESTRUM ( 13 FDA reports)
RASH GENERALISED ( 13 FDA reports)
REFLUX OESOPHAGITIS ( 13 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 13 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 13 FDA reports)
TENDERNESS ( 13 FDA reports)
VENTRICULAR HYPERTROPHY ( 13 FDA reports)
AORTIC VALVE INCOMPETENCE ( 12 FDA reports)
BLADDER CANCER ( 12 FDA reports)
BLOOD CHLORIDE INCREASED ( 12 FDA reports)
BONE OPERATION ( 12 FDA reports)
BRAIN STEM INFARCTION ( 12 FDA reports)
BREAST CANCER IN SITU ( 12 FDA reports)
BREAST LUMP REMOVAL ( 12 FDA reports)
CORONARY ARTERY OCCLUSION ( 12 FDA reports)
CRYING ( 12 FDA reports)
DIASTOLIC DYSFUNCTION ( 12 FDA reports)
DIVERTICULUM ( 12 FDA reports)
DRY EYE ( 12 FDA reports)
HYDRONEPHROSIS ( 12 FDA reports)
HYPOCALCAEMIA ( 12 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 12 FDA reports)
LIMB DISCOMFORT ( 12 FDA reports)
METABOLIC ENCEPHALOPATHY ( 12 FDA reports)
MIGRAINE ( 12 FDA reports)
MOOD SWINGS ( 12 FDA reports)
MUCOSAL INFLAMMATION ( 12 FDA reports)
MULTIPLE MYELOMA ( 12 FDA reports)
MYOCLONUS ( 12 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 12 FDA reports)
NEPHROGENIC ANAEMIA ( 12 FDA reports)
NERVE INJURY ( 12 FDA reports)
ORAL CANDIDIASIS ( 12 FDA reports)
ORAL INFECTION ( 12 FDA reports)
ORAL PAIN ( 12 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 12 FDA reports)
PRESYNCOPE ( 12 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 12 FDA reports)
PULMONARY FIBROSIS ( 12 FDA reports)
RALES ( 12 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 12 FDA reports)
RESTLESS LEGS SYNDROME ( 12 FDA reports)
RHINITIS ALLERGIC ( 12 FDA reports)
SENSORY DISTURBANCE ( 12 FDA reports)
SKIN INDURATION ( 12 FDA reports)
SKIN TIGHTNESS ( 12 FDA reports)
SPONDYLOLISTHESIS ( 12 FDA reports)
SYNOVIAL CYST ( 12 FDA reports)
TOOTH INFECTION ( 12 FDA reports)
ULCER ( 12 FDA reports)
WOUND SECRETION ( 12 FDA reports)
ACUTE SINUSITIS ( 11 FDA reports)
AGGRESSION ( 11 FDA reports)
ANGIOPATHY ( 11 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 11 FDA reports)
ATRIAL SEPTAL DEFECT ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 11 FDA reports)
BASEDOW'S DISEASE ( 11 FDA reports)
BLOOD CALCIUM DECREASED ( 11 FDA reports)
BLOOD GLUCOSE DECREASED ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 11 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 11 FDA reports)
CARDIOGENIC SHOCK ( 11 FDA reports)
DENTAL CARIES ( 11 FDA reports)
EOSINOPHILIA ( 11 FDA reports)
FISTULA ( 11 FDA reports)
HEPATIC CIRRHOSIS ( 11 FDA reports)
HUMERUS FRACTURE ( 11 FDA reports)
INCORRECT DOSE ADMINISTERED ( 11 FDA reports)
IRRITABILITY ( 11 FDA reports)
LYMPHOMA ( 11 FDA reports)
MACULAR DEGENERATION ( 11 FDA reports)
MOVEMENT DISORDER ( 11 FDA reports)
OBESITY ( 11 FDA reports)
ORGANISING PNEUMONIA ( 11 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 11 FDA reports)
PEPTIC ULCER ( 11 FDA reports)
PNEUMONIA BACTERIAL ( 11 FDA reports)
PSYCHIATRIC SYMPTOM ( 11 FDA reports)
RENAL HAEMORRHAGE ( 11 FDA reports)
RETCHING ( 11 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 11 FDA reports)
SCAR ( 11 FDA reports)
SENSORY LOSS ( 11 FDA reports)
SEROTONIN SYNDROME ( 11 FDA reports)
SINUS TACHYCARDIA ( 11 FDA reports)
SKIN HYPERTROPHY ( 11 FDA reports)
SKIN ULCER ( 11 FDA reports)
SOFT TISSUE INFECTION ( 11 FDA reports)
STRIDOR ( 11 FDA reports)
TOOTH ABSCESS ( 11 FDA reports)
TORSADE DE POINTES ( 11 FDA reports)
URINE OUTPUT INCREASED ( 11 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 11 FDA reports)
ABORTION ( 10 FDA reports)
AORTIC DISSECTION ( 10 FDA reports)
APLASTIC ANAEMIA ( 10 FDA reports)
ASPIRATION ( 10 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 10 FDA reports)
BODY TEMPERATURE INCREASED ( 10 FDA reports)
BRONCHOSPASM ( 10 FDA reports)
CAROTID ARTERY OCCLUSION ( 10 FDA reports)
CEREBRAL ARTERY STENOSIS ( 10 FDA reports)
CEREBROSCLEROSIS ( 10 FDA reports)
CERUMEN IMPACTION ( 10 FDA reports)
CLOSTRIDIAL INFECTION ( 10 FDA reports)
COLONOSCOPY ABNORMAL ( 10 FDA reports)
DECUBITUS ULCER ( 10 FDA reports)
DIABETIC KETOACIDOSIS ( 10 FDA reports)
DIABETIC RETINOPATHY ( 10 FDA reports)
DISCOMFORT ( 10 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 10 FDA reports)
EXPOSED BONE IN JAW ( 10 FDA reports)
FLUID OVERLOAD ( 10 FDA reports)
GLOSSITIS ( 10 FDA reports)
GRAND MAL CONVULSION ( 10 FDA reports)
HERPES SIMPLEX ( 10 FDA reports)
HIP ARTHROPLASTY ( 10 FDA reports)
INCISIONAL DRAINAGE ( 10 FDA reports)
INCOHERENT ( 10 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 10 FDA reports)
ISCHAEMIA ( 10 FDA reports)
JAW OPERATION ( 10 FDA reports)
JOINT CONTRACTURE ( 10 FDA reports)
LARYNGEAL OEDEMA ( 10 FDA reports)
LIVER INJURY ( 10 FDA reports)
LOCALISED INFECTION ( 10 FDA reports)
METRORRHAGIA ( 10 FDA reports)
MOUTH ULCERATION ( 10 FDA reports)
MUSCLE CONTRACTURE ( 10 FDA reports)
PAIN IN JAW ( 10 FDA reports)
POST PROCEDURAL HAEMATOMA ( 10 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 10 FDA reports)
RENAL CYST ( 10 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 10 FDA reports)
SPINAL DISORDER ( 10 FDA reports)
SUICIDAL IDEATION ( 10 FDA reports)
SWOLLEN TONGUE ( 10 FDA reports)
THERAPY NON-RESPONDER ( 10 FDA reports)
THROMBOCYTOPENIC PURPURA ( 10 FDA reports)
TOOTH DISCOLOURATION ( 10 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 10 FDA reports)
UNEVALUABLE EVENT ( 10 FDA reports)
VITREOUS HAEMORRHAGE ( 10 FDA reports)
ALCOHOL USE ( 9 FDA reports)
AMMONIA INCREASED ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 9 FDA reports)
BILE DUCT CANCER ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 9 FDA reports)
CAPILLARY LEAK SYNDROME ( 9 FDA reports)
CARDIAC VALVE DISEASE ( 9 FDA reports)
CONGENITAL AORTIC ANOMALY ( 9 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 9 FDA reports)
DEAFNESS ( 9 FDA reports)
DERMATITIS ACNEIFORM ( 9 FDA reports)
ENTEROCOLITIS ( 9 FDA reports)
EXOSTOSIS ( 9 FDA reports)
FEELING COLD ( 9 FDA reports)
FIBRIN INCREASED ( 9 FDA reports)
GYNAECOMASTIA ( 9 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 9 FDA reports)
HYPERTENSIVE HEART DISEASE ( 9 FDA reports)
INGUINAL HERNIA ( 9 FDA reports)
LACTIC ACIDOSIS ( 9 FDA reports)
LACUNAR INFARCTION ( 9 FDA reports)
LIP SWELLING ( 9 FDA reports)
MOTOR DYSFUNCTION ( 9 FDA reports)
MUSCLE RIGIDITY ( 9 FDA reports)
MUSCLE TIGHTNESS ( 9 FDA reports)
NEPHRITIS INTERSTITIAL ( 9 FDA reports)
NEPHROPATHY ( 9 FDA reports)
OESOPHAGITIS ( 9 FDA reports)
ORAL DISCOMFORT ( 9 FDA reports)
ORAL FUNGAL INFECTION ( 9 FDA reports)
OROPHARYNGEAL PAIN ( 9 FDA reports)
OSTEOLYSIS ( 9 FDA reports)
PERICARDITIS ( 9 FDA reports)
PETECHIAE ( 9 FDA reports)
PHARYNGEAL OEDEMA ( 9 FDA reports)
PNEUMATOSIS INTESTINALIS ( 9 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 9 FDA reports)
POLYNEUROPATHY ( 9 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 9 FDA reports)
PROTEIN TOTAL DECREASED ( 9 FDA reports)
RASH PAPULAR ( 9 FDA reports)
RASH PRURITIC ( 9 FDA reports)
RENAL ATROPHY ( 9 FDA reports)
RESPIRATORY DEPRESSION ( 9 FDA reports)
RETINAL ARTERY OCCLUSION ( 9 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 9 FDA reports)
SCIATICA ( 9 FDA reports)
SICK SINUS SYNDROME ( 9 FDA reports)
SINUS ARREST ( 9 FDA reports)
SKIN DISCOLOURATION ( 9 FDA reports)
SNORING ( 9 FDA reports)
STENT PLACEMENT ( 9 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 9 FDA reports)
TRANSAMINASES INCREASED ( 9 FDA reports)
TUMOUR HAEMORRHAGE ( 9 FDA reports)
VITAMIN B12 DEFICIENCY ( 9 FDA reports)
WOUND DEHISCENCE ( 9 FDA reports)
WOUND HAEMORRHAGE ( 9 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 9 FDA reports)
ABDOMINAL PAIN LOWER ( 8 FDA reports)
ADRENAL INSUFFICIENCY ( 8 FDA reports)
AMINOACIDURIA ( 8 FDA reports)
ANGER ( 8 FDA reports)
ANKLE FRACTURE ( 8 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 8 FDA reports)
BACK INJURY ( 8 FDA reports)
BACTERIAL INFECTION ( 8 FDA reports)
BLADDER DISORDER ( 8 FDA reports)
BLADDER PERFORATION ( 8 FDA reports)
BLINDNESS ( 8 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 8 FDA reports)
BLOOD PRESSURE ABNORMAL ( 8 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 8 FDA reports)
BRAIN STEM HAEMORRHAGE ( 8 FDA reports)
CATHETER RELATED INFECTION ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 8 FDA reports)
COMA HEPATIC ( 8 FDA reports)
COMPLETED SUICIDE ( 8 FDA reports)
COMPRESSION FRACTURE ( 8 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 8 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 8 FDA reports)
CONJUNCTIVITIS ( 8 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 8 FDA reports)
CYST ( 8 FDA reports)
CYSTIC LYMPHANGIOMA ( 8 FDA reports)
DISTURBANCE IN ATTENTION ( 8 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 8 FDA reports)
DYSPHONIA ( 8 FDA reports)
ECONOMIC PROBLEM ( 8 FDA reports)
EXCITABILITY ( 8 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 8 FDA reports)
EXTRASYSTOLES ( 8 FDA reports)
EYE DISORDER ( 8 FDA reports)
EYE IRRITATION ( 8 FDA reports)
FACIAL PALSY ( 8 FDA reports)
FALLOT'S TETRALOGY ( 8 FDA reports)
FIBRINOUS BRONCHITIS ( 8 FDA reports)
FIBROMYALGIA ( 8 FDA reports)
GANGRENE ( 8 FDA reports)
GASTROINTESTINAL INFECTION ( 8 FDA reports)
GLUCOSE URINE PRESENT ( 8 FDA reports)
GOITRE ( 8 FDA reports)
HAEMORRHAGE URINARY TRACT ( 8 FDA reports)
HYPERAMMONAEMIA ( 8 FDA reports)
HYPOKINESIA ( 8 FDA reports)
HYPOPHOSPHATAEMIA ( 8 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 8 FDA reports)
INFARCTION ( 8 FDA reports)
INFECTIOUS PERITONITIS ( 8 FDA reports)
LABORATORY TEST ABNORMAL ( 8 FDA reports)
LIP EROSION ( 8 FDA reports)
LOOSE TOOTH ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 8 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 8 FDA reports)
MUSCLE DISORDER ( 8 FDA reports)
MUSCLE TWITCHING ( 8 FDA reports)
NEPHRITIS ( 8 FDA reports)
NEPHROPATHY TOXIC ( 8 FDA reports)
NEUROMYOPATHY ( 8 FDA reports)
NOONAN SYNDROME ( 8 FDA reports)
OVARIAN CANCER ( 8 FDA reports)
PANCREATIC CYST ( 8 FDA reports)
PANIC ATTACK ( 8 FDA reports)
PARAESTHESIA ORAL ( 8 FDA reports)
PAROSMIA ( 8 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 8 FDA reports)
PULMONARY VALVE STENOSIS ( 8 FDA reports)
RASH ERYTHEMATOUS ( 8 FDA reports)
RENAL CELL CARCINOMA ( 8 FDA reports)
RENAL TUBULAR DISORDER ( 8 FDA reports)
STUPOR ( 8 FDA reports)
SUDDEN HEARING LOSS ( 8 FDA reports)
THERMAL BURN ( 8 FDA reports)
TONGUE OEDEMA ( 8 FDA reports)
TOXIC ENCEPHALOPATHY ( 8 FDA reports)
VARICOSE VEIN ( 8 FDA reports)
VENA CAVA THROMBOSIS ( 8 FDA reports)
VITAMIN B12 DECREASED ( 8 FDA reports)
WHITE BLOOD CELL DISORDER ( 8 FDA reports)
ACCIDENTAL OVERDOSE ( 7 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 7 FDA reports)
AGEUSIA ( 7 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 7 FDA reports)
ANION GAP NORMAL ( 7 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 7 FDA reports)
AORTIC VALVE STENOSIS ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 7 FDA reports)
ASPIRATION PLEURAL CAVITY ( 7 FDA reports)
ATROPHY ( 7 FDA reports)
BACTERAEMIA ( 7 FDA reports)
BACTERIAL TEST POSITIVE ( 7 FDA reports)
BARRETT'S OESOPHAGUS ( 7 FDA reports)
BREAST MASS ( 7 FDA reports)
BREAST PAIN ( 7 FDA reports)
CHOKING SENSATION ( 7 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 7 FDA reports)
CLOSTRIDIUM COLITIS ( 7 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 7 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 7 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 7 FDA reports)
DECREASED ACTIVITY ( 7 FDA reports)
DIABETIC NEUROPATHY ( 7 FDA reports)
DISSOCIATION ( 7 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 7 FDA reports)
DUODENITIS ( 7 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 7 FDA reports)
EMBOLISM ( 7 FDA reports)
EXANTHEM ( 7 FDA reports)
EYE HAEMORRHAGE ( 7 FDA reports)
FAECAL INCONTINENCE ( 7 FDA reports)
FOETAL DISTRESS SYNDROME ( 7 FDA reports)
GASTRITIS EROSIVE ( 7 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 7 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 7 FDA reports)
HAEMOLYTIC ANAEMIA ( 7 FDA reports)
HEAD INJURY ( 7 FDA reports)
HEMIANOPIA ( 7 FDA reports)
HEMIPARESIS ( 7 FDA reports)
HEPATITIS B ( 7 FDA reports)
HOSPITALISATION ( 7 FDA reports)
HYPERACUSIS ( 7 FDA reports)
HYPOMAGNESAEMIA ( 7 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 7 FDA reports)
INJECTION SITE HAEMATOMA ( 7 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 7 FDA reports)
LOBAR PNEUMONIA ( 7 FDA reports)
LOCALISED OEDEMA ( 7 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
LOWER LIMB FRACTURE ( 7 FDA reports)
LUNG CONSOLIDATION ( 7 FDA reports)
MENINGITIS ( 7 FDA reports)
METASTASES TO BONE ( 7 FDA reports)
MONOCYTE COUNT INCREASED ( 7 FDA reports)
MOUTH HAEMORRHAGE ( 7 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 7 FDA reports)
NON-CARDIAC CHEST PAIN ( 7 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 7 FDA reports)
PARKINSON'S DISEASE ( 7 FDA reports)
PERIPHERAL COLDNESS ( 7 FDA reports)
PHOTOPHOBIA ( 7 FDA reports)
PULMONARY HAEMORRHAGE ( 7 FDA reports)
RAYNAUD'S PHENOMENON ( 7 FDA reports)
RENAL GLYCOSURIA ( 7 FDA reports)
RENAL PAIN ( 7 FDA reports)
RETINAL DEGENERATION ( 7 FDA reports)
RIGHT VENTRICULAR FAILURE ( 7 FDA reports)
SPLENOMEGALY ( 7 FDA reports)
STOMACH DISCOMFORT ( 7 FDA reports)
THYROIDITIS FIBROUS CHRONIC ( 7 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 7 FDA reports)
URETERIC STENOSIS ( 7 FDA reports)
URINE URIC ACID INCREASED ( 7 FDA reports)
VASCULITIS ( 7 FDA reports)
VENOUS OCCLUSION ( 7 FDA reports)
VISUAL DISTURBANCE ( 7 FDA reports)
ABDOMINAL ADHESIONS ( 6 FDA reports)
ACIDOSIS ( 6 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 6 FDA reports)
ACUTE CORONARY SYNDROME ( 6 FDA reports)
ACUTE PRERENAL FAILURE ( 6 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 6 FDA reports)
APNOEA ( 6 FDA reports)
ARTERIOVENOUS MALFORMATION ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 6 FDA reports)
BLOOD MAGNESIUM DECREASED ( 6 FDA reports)
BLOOD URIC ACID DECREASED ( 6 FDA reports)
BLOOD URINE PRESENT ( 6 FDA reports)
BONE SCAN ABNORMAL ( 6 FDA reports)
BRADYCARDIA FOETAL ( 6 FDA reports)
BRAIN NEOPLASM ( 6 FDA reports)
BRAIN OEDEMA ( 6 FDA reports)
BREAST CANCER FEMALE ( 6 FDA reports)
BRONCHIECTASIS ( 6 FDA reports)
BRUXISM ( 6 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 6 FDA reports)
CATARACT CORTICAL ( 6 FDA reports)
CATHETER RELATED COMPLICATION ( 6 FDA reports)
CATHETER SITE PAIN ( 6 FDA reports)
CELL MARKER INCREASED ( 6 FDA reports)
CEREBELLAR HAEMORRHAGE ( 6 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 6 FDA reports)
CHONDROCALCINOSIS ( 6 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 6 FDA reports)
COLITIS ISCHAEMIC ( 6 FDA reports)
CYSTOCELE ( 6 FDA reports)
CYTOLYTIC HEPATITIS ( 6 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 6 FDA reports)
DIPLEGIA ( 6 FDA reports)
DRUG INTOLERANCE ( 6 FDA reports)
DYSTHYMIC DISORDER ( 6 FDA reports)
EMBOLIC STROKE ( 6 FDA reports)
ESCHERICHIA INFECTION ( 6 FDA reports)
ESSENTIAL HYPERTENSION ( 6 FDA reports)
EYE SWELLING ( 6 FDA reports)
FOOT AMPUTATION ( 6 FDA reports)
FUNGAL INFECTION ( 6 FDA reports)
GASTROENTERITIS VIRAL ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE ( 6 FDA reports)
HALLUCINATION, AUDITORY ( 6 FDA reports)
HIP SURGERY ( 6 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 6 FDA reports)
HYPOVOLAEMIA ( 6 FDA reports)
IMMUNODEFICIENCY ( 6 FDA reports)
IMPAIRED INSULIN SECRETION ( 6 FDA reports)
INJECTION SITE REACTION ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 6 FDA reports)
INTESTINAL PERFORATION ( 6 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 6 FDA reports)
LEFT VENTRICULAR HEAVE ( 6 FDA reports)
LIMB INJURY ( 6 FDA reports)
LISTLESS ( 6 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 6 FDA reports)
LYMPHOPENIA ( 6 FDA reports)
MANIA ( 6 FDA reports)
MANTLE CELL LYMPHOMA ( 6 FDA reports)
MENISCUS LESION ( 6 FDA reports)
MENOPAUSAL SYMPTOMS ( 6 FDA reports)
METABOLIC DISORDER ( 6 FDA reports)
METASTASES TO LIVER ( 6 FDA reports)
METASTASIS ( 6 FDA reports)
MIDDLE INSOMNIA ( 6 FDA reports)
MIOSIS ( 6 FDA reports)
MUCOUS STOOLS ( 6 FDA reports)
MUSCLE CRAMP ( 6 FDA reports)
MYOSITIS ( 6 FDA reports)
NAIL DYSTROPHY ( 6 FDA reports)
NEONATAL DISORDER ( 6 FDA reports)
ORAL MUCOSA EROSION ( 6 FDA reports)
PANCREATITIS CHRONIC ( 6 FDA reports)
PIGMENTATION DISORDER ( 6 FDA reports)
PLATELET COUNT INCREASED ( 6 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 6 FDA reports)
POST HERPETIC NEURALGIA ( 6 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 6 FDA reports)
PRE-ECLAMPSIA ( 6 FDA reports)
PROCEDURAL PAIN ( 6 FDA reports)
PSEUDOMONAS INFECTION ( 6 FDA reports)
PULMONARY INFARCTION ( 6 FDA reports)
QUADRIPLEGIA ( 6 FDA reports)
RASH MACULO-PAPULAR ( 6 FDA reports)
RESPIRATORY RATE INCREASED ( 6 FDA reports)
RETINAL DISORDER ( 6 FDA reports)
SENSATION OF HEAVINESS ( 6 FDA reports)
SENSORY LEVEL ABNORMAL ( 6 FDA reports)
SEROMA ( 6 FDA reports)
SHOULDER PAIN ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
SPINAL FRACTURE ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
STROKE VOLUME DECREASED ( 6 FDA reports)
SUBDURAL HAEMORRHAGE ( 6 FDA reports)
SYNCOPE VASOVAGAL ( 6 FDA reports)
TUBERCULOSIS ( 6 FDA reports)
UNRESPONSIVE TO STIMULI ( 6 FDA reports)
UTERINE LEIOMYOMA ( 6 FDA reports)
VAGINAL HAEMORRHAGE ( 6 FDA reports)
WOUND DECOMPOSITION ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
ABORTION INDUCED ( 5 FDA reports)
ACCIDENTAL EXPOSURE ( 5 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 5 FDA reports)
AMAUROSIS FUGAX ( 5 FDA reports)
AMYLOIDOSIS ( 5 FDA reports)
ANAPHYLACTOID SHOCK ( 5 FDA reports)
ANHEDONIA ( 5 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 5 FDA reports)
ANXIETY DISORDER ( 5 FDA reports)
APATHY ( 5 FDA reports)
APPENDICECTOMY ( 5 FDA reports)
ASPIRATION BONE MARROW ( 5 FDA reports)
AUTOIMMUNE HEPATITIS ( 5 FDA reports)
BACK DISORDER ( 5 FDA reports)
BEDRIDDEN ( 5 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 5 FDA reports)
BLOOD CREATINE INCREASED ( 5 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 5 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 5 FDA reports)
BONE FISTULA ( 5 FDA reports)
BONE MARROW TRANSPLANT ( 5 FDA reports)
BRAIN STEM SYNDROME ( 5 FDA reports)
BREAST DISORDER ( 5 FDA reports)
BREECH PRESENTATION ( 5 FDA reports)
BRONCHITIS ACUTE ( 5 FDA reports)
BUNION ( 5 FDA reports)
CARDIAC PACEMAKER INSERTION ( 5 FDA reports)
CAROTID ARTERY ATHEROMA ( 5 FDA reports)
CATHETER PLACEMENT ( 5 FDA reports)
CATHETER REMOVAL ( 5 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 5 FDA reports)
COLLAGEN DISORDER ( 5 FDA reports)
COLON CANCER ( 5 FDA reports)
CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
CREPITATIONS ( 5 FDA reports)
CROHN'S DISEASE ( 5 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 5 FDA reports)
DECREASED INTEREST ( 5 FDA reports)
DEMYELINATION ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
DIABETIC FOOT INFECTION ( 5 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
DUODENAL OBSTRUCTION ( 5 FDA reports)
DYSGRAPHIA ( 5 FDA reports)
DYSLIPIDAEMIA ( 5 FDA reports)
EFFUSION ( 5 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 5 FDA reports)
ENDOPHTHALMITIS ( 5 FDA reports)
ENTERITIS INFECTIOUS ( 5 FDA reports)
EOSINOPHILIC PNEUMONIA ( 5 FDA reports)
ERYTHRODERMIC PSORIASIS ( 5 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 5 FDA reports)
EYE DISCHARGE ( 5 FDA reports)
EYE INFECTION ( 5 FDA reports)
EYELID OEDEMA ( 5 FDA reports)
FAECES PALE ( 5 FDA reports)
FANCONI SYNDROME ACQUIRED ( 5 FDA reports)
FRACTURE ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 5 FDA reports)
GASTRIC POLYPS ( 5 FDA reports)
GRANULOCYTE COUNT DECREASED ( 5 FDA reports)
HAEMARTHROSIS ( 5 FDA reports)
HAEMOLYSIS ( 5 FDA reports)
HEAD DISCOMFORT ( 5 FDA reports)
HEPATITIS CHOLESTATIC ( 5 FDA reports)
HEPATORENAL SYNDROME ( 5 FDA reports)
HICCUPS ( 5 FDA reports)
HYPERMAGNESAEMIA ( 5 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 5 FDA reports)
HYPERVENTILATION ( 5 FDA reports)
HYPERVIGILANCE ( 5 FDA reports)
HYPOAESTHESIA FACIAL ( 5 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 5 FDA reports)
HYPOTONIA ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
INTESTINAL ULCER ( 5 FDA reports)
INTRA-UTERINE DEATH ( 5 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 5 FDA reports)
JAUNDICE CHOLESTATIC ( 5 FDA reports)
JAW DISORDER ( 5 FDA reports)
JOINT ARTHROPLASTY ( 5 FDA reports)
LEFT ATRIAL DILATATION ( 5 FDA reports)
LIP OEDEMA ( 5 FDA reports)
LIPIDS ABNORMAL ( 5 FDA reports)
MAJOR DEPRESSION ( 5 FDA reports)
MALNUTRITION ( 5 FDA reports)
MENORRHAGIA ( 5 FDA reports)
MENSTRUATION IRREGULAR ( 5 FDA reports)
MICROANGIOPATHY ( 5 FDA reports)
MICTURITION DISORDER ( 5 FDA reports)
MONOPARESIS ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE ( 5 FDA reports)
MUSCLE ATROPHY ( 5 FDA reports)
MYOGLOBINURIA ( 5 FDA reports)
NASAL DISORDER ( 5 FDA reports)
NASAL SEPTUM DEVIATION ( 5 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 5 FDA reports)
NIKOLSKY'S SIGN ( 5 FDA reports)
NO THERAPEUTIC RESPONSE ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER ( 5 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 5 FDA reports)
NYSTAGMUS ( 5 FDA reports)
OCCULT BLOOD POSITIVE ( 5 FDA reports)
OCULAR ICTERUS ( 5 FDA reports)
ONYCHOMADESIS ( 5 FDA reports)
OPPORTUNISTIC INFECTION ( 5 FDA reports)
ORAL DISORDER ( 5 FDA reports)
ORAL HERPES ( 5 FDA reports)
OROPHARYNGEAL SPASM ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
PANCREATIC CARCINOMA ( 5 FDA reports)
PARKINSONISM ( 5 FDA reports)
PARONYCHIA ( 5 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 5 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 5 FDA reports)
PERSONALITY CHANGE ( 5 FDA reports)
PERSONALITY DISORDER ( 5 FDA reports)
PO2 ABNORMAL ( 5 FDA reports)
POLYMYOSITIS ( 5 FDA reports)
POSTPARTUM HAEMORRHAGE ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 5 FDA reports)
PYELONEPHRITIS ACUTE ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
RECTAL CANCER ( 5 FDA reports)
RECTOCELE ( 5 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 5 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 5 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
SCAB ( 5 FDA reports)
SCOLIOSIS ( 5 FDA reports)
SEASONAL ALLERGY ( 5 FDA reports)
SEBORRHOEIC KERATOSIS ( 5 FDA reports)
SERUM FERRITIN INCREASED ( 5 FDA reports)
SKIN EROSION ( 5 FDA reports)
SKIN HYPERPIGMENTATION ( 5 FDA reports)
SKIN SWELLING ( 5 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 5 FDA reports)
STENT OCCLUSION ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
TACHYARRHYTHMIA ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
THROMBOPHLEBITIS ( 5 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TONGUE COATED ( 5 FDA reports)
TONGUE DISCOLOURATION ( 5 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 5 FDA reports)
TRISMUS ( 5 FDA reports)
TUBERCULOUS PLEURISY ( 5 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 5 FDA reports)
VENOUS INSUFFICIENCY ( 5 FDA reports)
VITREOUS DETACHMENT ( 5 FDA reports)
WOUND DEBRIDEMENT ( 5 FDA reports)
WOUND DRAINAGE ( 5 FDA reports)
YAWNING ( 5 FDA reports)
ABDOMINAL HERNIA ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ANGIOPLASTY ( 4 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 4 FDA reports)
AORTIC ANEURYSM RUPTURE ( 4 FDA reports)
AORTIC STENOSIS ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
ASPERGILLOSIS ( 4 FDA reports)
BASOPHIL COUNT INCREASED ( 4 FDA reports)
BENIGN NEOPLASM OF SKIN ( 4 FDA reports)
BLADDER NEOPLASM ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD BICARBONATE INCREASED ( 4 FDA reports)
BLOOD CALCIUM INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 4 FDA reports)
BLOOD DISORDER ( 4 FDA reports)
BLOOD OSMOLARITY DECREASED ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 4 FDA reports)
BODY HEIGHT DECREASED ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
BONE CYST ( 4 FDA reports)
BONE LESION ( 4 FDA reports)
BONE MARROW DISORDER ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BRADYCARDIA NEONATAL ( 4 FDA reports)
CARDIAC FAILURE CHRONIC ( 4 FDA reports)
CARDIAC FLUTTER ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 4 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
CHOKING ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 4 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 4 FDA reports)
CUTANEOUS VASCULITIS ( 4 FDA reports)
DELIVERY ( 4 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
DEVICE DISLOCATION ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
DYSPNOEA EXACERBATED ( 4 FDA reports)
EAR HAEMORRHAGE ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
ELECTROLYTE DEPLETION ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 4 FDA reports)
ERUCTATION ( 4 FDA reports)
ERYTHROID MATURATION ARREST ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
EYE LASER SURGERY ( 4 FDA reports)
FACIAL PAIN ( 4 FDA reports)
FACIAL PARESIS ( 4 FDA reports)
FANCONI SYNDROME ( 4 FDA reports)
FLANK PAIN ( 4 FDA reports)
FLOPPY INFANT ( 4 FDA reports)
FOLLICULITIS ( 4 FDA reports)
FOREARM FRACTURE ( 4 FDA reports)
GALLBLADDER DISORDER ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
GASTROINTESTINAL INJURY ( 4 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 4 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 4 FDA reports)
GENITAL PRURITUS FEMALE ( 4 FDA reports)
GINGIVAL ABSCESS ( 4 FDA reports)
GINGIVAL HYPERTROPHY ( 4 FDA reports)
GLIOSARCOMA ( 4 FDA reports)
GLOSSODYNIA ( 4 FDA reports)
GLOSSOPTOSIS ( 4 FDA reports)
HAEMOGLOBIN INCREASED ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HAEMORRHAGIC STROKE ( 4 FDA reports)
HALLUCINATIONS, MIXED ( 4 FDA reports)
HEART RATE ABNORMAL ( 4 FDA reports)
HEPATIC HAEMATOMA ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HEPATIC VEIN OCCLUSION ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
HERNIA ( 4 FDA reports)
HILAR LYMPHADENOPATHY ( 4 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
HYPOREFLEXIA ( 4 FDA reports)
HYPOVENTILATION ( 4 FDA reports)
ILEAL ULCER ( 4 FDA reports)
INITIAL INSOMNIA ( 4 FDA reports)
INJECTION SITE EXTRAVASATION ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTESTINAL POLYP ( 4 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 4 FDA reports)
INTRAOCULAR LENS IMPLANT ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
KIDNEY RUPTURE ( 4 FDA reports)
KNEE OPERATION ( 4 FDA reports)
LARYNGEAL CANCER ( 4 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 4 FDA reports)
LIFE EXPECTANCY SHORTENED ( 4 FDA reports)
LIGAMENT SPRAIN ( 4 FDA reports)
LIP ULCERATION ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
MALIGNANT HYPERTENSION ( 4 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 4 FDA reports)
MASS ( 4 FDA reports)
MENINGIOMA BENIGN ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
METABOLIC SYNDROME ( 4 FDA reports)
MICROCEPHALY ( 4 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 4 FDA reports)
MULTI-ORGAN DISORDER ( 4 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 4 FDA reports)
MYOGLOBIN URINE PRESENT ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 4 FDA reports)
NERVE BLOCK ( 4 FDA reports)
NERVE COMPRESSION ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NEUTROPENIC SEPSIS ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 4 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 4 FDA reports)
OCCULT BLOOD ( 4 FDA reports)
OLIGOHYDRAMNIOS ( 4 FDA reports)
OPISTHOTONUS ( 4 FDA reports)
ORAL MUCOSAL ERUPTION ( 4 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 4 FDA reports)
ORGAN FAILURE ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
PERFORMANCE STATUS DECREASED ( 4 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
PERITONITIS BACTERIAL ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PITTING OEDEMA ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
POLYARTHRITIS ( 4 FDA reports)
POLYDIPSIA ( 4 FDA reports)
POOR SUCKING REFLEX ( 4 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 4 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 4 FDA reports)
PROTEIN URINE ( 4 FDA reports)
PROTHROMBIN TIME SHORTENED ( 4 FDA reports)
PULMONARY TUBERCULOSIS ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
RECTAL ULCER ( 4 FDA reports)
RENAL HYPERTENSION ( 4 FDA reports)
RENAL INJURY ( 4 FDA reports)
RESPIRATION ABNORMAL ( 4 FDA reports)
RESPIRATORY TRACT OEDEMA ( 4 FDA reports)
RESUSCITATION ( 4 FDA reports)
RETINAL TEAR ( 4 FDA reports)
SCHIZOPHRENIA ( 4 FDA reports)
SCOTOMA ( 4 FDA reports)
SKIN LACERATION ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 4 FDA reports)
SNEEZING ( 4 FDA reports)
SPINAL CORD OEDEMA ( 4 FDA reports)
SPLENIC INFARCTION ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
STRESS INCONTINENCE ( 4 FDA reports)
STRESS SYMPTOMS ( 4 FDA reports)
SUBILEUS ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
TETANY ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 4 FDA reports)
THYROID GLAND CANCER ( 4 FDA reports)
TOOTH DISORDER ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 4 FDA reports)
TRANSPLANT REJECTION ( 4 FDA reports)
UPPER LIMB FRACTURE ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
UTERINE HYPOTONUS ( 4 FDA reports)
VAGINAL BURNING SENSATION ( 4 FDA reports)
VASCULAR PSEUDOANEURYSM ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
VOLVULUS ( 4 FDA reports)
WOUND ( 4 FDA reports)
YELLOW SKIN ( 4 FDA reports)
ABDOMINAL ABSCESS ( 3 FDA reports)
ACCIDENT ( 3 FDA reports)
ACTIVATION SYNDROME ( 3 FDA reports)
ACUTE ABDOMEN ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 3 FDA reports)
ADAMS-STOKES SYNDROME ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
AGORAPHOBIA ( 3 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANEURYSM ( 3 FDA reports)
ANISOCYTOSIS ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ARTERIOSPASM CORONARY ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 3 FDA reports)
ASBESTOSIS ( 3 FDA reports)
ASEPTIC NECROSIS BONE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ASTERIXIS ( 3 FDA reports)
ATRIAL TACHYCARDIA ( 3 FDA reports)
AUTOANTIBODY POSITIVE ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
BACTERIAL CULTURE POSITIVE ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
BILE DUCT STONE ( 3 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 3 FDA reports)
BIPOLAR I DISORDER ( 3 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
BLEEDING TIME PROLONGED ( 3 FDA reports)
BLEPHARAL PIGMENTATION ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD CREATININE DECREASED ( 3 FDA reports)
BLOOD FOLATE DECREASED ( 3 FDA reports)
BLOOD PH INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 3 FDA reports)
BLOOD UREA ABNORMAL ( 3 FDA reports)
BONE INFECTION ( 3 FDA reports)
BONE NEOPLASM MALIGNANT ( 3 FDA reports)
BONE SARCOMA ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
BREAST CANCER STAGE I ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
BULBAR PALSY ( 3 FDA reports)
BURNING SENSATION MUCOSAL ( 3 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 3 FDA reports)
CARCINOID TUMOUR OF THE DUODENUM ( 3 FDA reports)
CARDIAC FIBRILLATION ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CARDIORENAL SYNDROME ( 3 FDA reports)
CATHETERISATION CARDIAC ( 3 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CEREBROVASCULAR DISORDER ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHEMOTHERAPY ( 3 FDA reports)
CHEST WALL PAIN ( 3 FDA reports)
CHOLANGITIS ACUTE ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHOLESTATIC LIVER INJURY ( 3 FDA reports)
CHRONIC HEPATITIS ( 3 FDA reports)
COARCTATION OF THE AORTA ( 3 FDA reports)
COLITIS EROSIVE ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
COLONIC HAEMATOMA ( 3 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 3 FDA reports)
CONVULSIONS LOCAL ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
CORONARY ANGIOPLASTY ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
DECEREBRATION ( 3 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DERMATITIS PSORIASIFORM ( 3 FDA reports)
DERMATOMYOSITIS ( 3 FDA reports)
DESQUAMATION MOUTH ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 3 FDA reports)
DIVERTICULAR PERFORATION ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
DRUG-INDUCED LIVER INJURY ( 3 FDA reports)
DUODENAL PERFORATION ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DUPUYTREN'S CONTRACTURE ( 3 FDA reports)
DYSPHASIA ( 3 FDA reports)
DYSPLASIA ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
ENDOCARDITIS BACTERIAL ( 3 FDA reports)
ENTEROBACTER SEPSIS ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
EPIDERMAL NECROSIS ( 3 FDA reports)
EPIDIDYMITIS ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 3 FDA reports)
EYELASH THICKENING ( 3 FDA reports)
FAECAL VOMITING ( 3 FDA reports)
FEELING GUILTY ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FIBROSIS ( 3 FDA reports)
FLOPPY IRIS SYNDROME ( 3 FDA reports)
FOETAL DISORDER ( 3 FDA reports)
FOOD INTERACTION ( 3 FDA reports)
FRACTURE NONUNION ( 3 FDA reports)
FUNGAEMIA ( 3 FDA reports)
GASTRITIS ATROPHIC ( 3 FDA reports)
GASTROENTERITIS BACILLUS ( 3 FDA reports)
GASTROINTESTINAL ULCER ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GENITAL ULCERATION ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
HAEMOGLOBINAEMIA ( 3 FDA reports)
HAND FRACTURE ( 3 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
HEPATIC CONGESTION ( 3 FDA reports)
HEPATITIS C VIRUS ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPERCREATININAEMIA ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPERPYREXIA ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 3 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 3 FDA reports)
ICHTHYOSIS ACQUIRED ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
INCISION SITE INFECTION ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INDUCED LABOUR ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
INTESTINAL INFARCTION ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
INTRACRANIAL ANEURYSM ( 3 FDA reports)
INTUSSUSCEPTION ( 3 FDA reports)
IRIS HYPERPIGMENTATION ( 3 FDA reports)
ISCHAEMIC ULCER ( 3 FDA reports)
JEJUNAL PERFORATION ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
JUGULAR VEIN DISTENSION ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
KNEE ARTHROPLASTY ( 3 FDA reports)
KYPHOSIS ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
LIVER TRANSPLANT ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LOCALISED OSTEOARTHRITIS ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
LUNG TRANSPLANT ( 3 FDA reports)
LYMPHOEDEMA ( 3 FDA reports)
MACROCYTOSIS ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MALIGNANT MELANOMA ( 3 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 3 FDA reports)
MENOPAUSE ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
METASTASES TO SPINE ( 3 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 3 FDA reports)
MICROCYTIC ANAEMIA ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
MITRAL VALVE PROLAPSE ( 3 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NEGATIVE THOUGHTS ( 3 FDA reports)
NEOPLASM RECURRENCE ( 3 FDA reports)
NEPHRECTOMY ( 3 FDA reports)
NO ADVERSE DRUG EFFECT ( 3 FDA reports)
NOCTURNAL DYSPNOEA ( 3 FDA reports)
NODULE ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 3 FDA reports)
ORAL NEOPLASM ( 3 FDA reports)
OTOTOXICITY ( 3 FDA reports)
PANCREATIC ENZYMES INCREASED ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PATELLA FRACTURE ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PELVIC VENOUS THROMBOSIS ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERIOSTITIS ( 3 FDA reports)
PERITONITIS SCLEROSING ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 3 FDA reports)
PLATELET COUNT ABNORMAL ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
POLYCYTHAEMIA ( 3 FDA reports)
POLYTRAUMATISM ( 3 FDA reports)
PORIOMANIA ( 3 FDA reports)
PORPHYRIA ACUTE ( 3 FDA reports)
PORTAL VENOUS GAS ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 3 FDA reports)
POTTER'S SYNDROME ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 3 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PULMONARY CAVITATION ( 3 FDA reports)
PULMONARY GRANULOMA ( 3 FDA reports)
PULMONARY MASS ( 3 FDA reports)
PULSE ABNORMAL ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
RADIUS FRACTURE ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RENAL INFARCT ( 3 FDA reports)
SALIVARY HYPERSECRETION ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SENILE DEMENTIA ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SENSE OF OPPRESSION ( 3 FDA reports)
SHUNT MALFUNCTION ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SINUS HEADACHE ( 3 FDA reports)
SKIN CANCER ( 3 FDA reports)
SKIN FIBROSIS ( 3 FDA reports)
SKIN FISSURES ( 3 FDA reports)
SKIN PLAQUE ( 3 FDA reports)
SKIN WRINKLING ( 3 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
THYROID DISORDER ( 3 FDA reports)
THYROIDITIS CHRONIC ( 3 FDA reports)
TINEA CAPITIS ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
VASCULAR BYPASS GRAFT ( 3 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 3 FDA reports)
VENOUS THROMBOSIS ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
VESTIBULAR NEURONITIS ( 3 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VISUAL PATHWAY DISORDER ( 3 FDA reports)
VITRECTOMY ( 3 FDA reports)
VULVAR EROSION ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 3 FDA reports)
ABDOMINAL OPERATION ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ABSCESS MANAGEMENT ( 2 FDA reports)
ABSCESS ORAL ( 2 FDA reports)
ABULIA ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ADENOIDITIS ( 2 FDA reports)
ADRENAL NEOPLASM ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
AGNOSIA ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 2 FDA reports)
ALPHA HYDROXYBUTYRATE DEHYDROGENASE INCREASED ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANAL ULCER ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
ANTI-INSULIN ANTIBODY ( 2 FDA reports)
AORTIC DISSECTION RUPTURE ( 2 FDA reports)
APALLIC SYNDROME ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BACTERIA WOUND IDENTIFIED ( 2 FDA reports)
BENIGN OVARIAN TUMOUR ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BEZOAR ( 2 FDA reports)
BICUSPID AORTIC VALVE ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 2 FDA reports)
BIOPSY LIVER ( 2 FDA reports)
BLADDER DYSFUNCTION ( 2 FDA reports)
BLADDER HYPERTROPHY ( 2 FDA reports)
BLINDNESS CORTICAL ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLUE TOE SYNDROME ( 2 FDA reports)
BODY MASS INDEX INCREASED ( 2 FDA reports)
BONE DENSITY DECREASED ( 2 FDA reports)
BONE FORMATION INCREASED ( 2 FDA reports)
BONE FRAGMENTATION ( 2 FDA reports)
BOWEN'S DISEASE ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN TUMOUR OPERATION ( 2 FDA reports)
BREAST DISCOMFORT ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CALCIUM DEFICIENCY ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CARBON DIOXIDE ABNORMAL ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 2 FDA reports)
CARDIOMYOPATHY NEONATAL ( 2 FDA reports)
CAROTID ARTERY DISEASE ( 2 FDA reports)
CAROTID PULSE ABNORMAL ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CELLULITIS PHARYNGEAL ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBROVASCULAR STENOSIS ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHEILITIS GRANULOMATOSA ( 2 FDA reports)
CHEST EXPANSION DECREASED ( 2 FDA reports)
CHEST TUBE INSERTION ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
COLON ADENOMA ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
CONFUSION POSTOPERATIVE ( 2 FDA reports)
CONGENITAL MITOCHONDRIAL CYTOPATHY ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORNEAL LESION ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CRYOGLOBULINAEMIA ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CYSTITIS ESCHERICHIA ( 2 FDA reports)
CYSTITIS NONINFECTIVE ( 2 FDA reports)
CYSTITIS RADIATION ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DEBRIDEMENT ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DENTAL OPERATION ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DEVICE DAMAGE ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DIZZINESS EXERTIONAL ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DROWNING ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DYSCHEZIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
EPIPHYSEAL DISORDER ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
ERYTHROBLAST COUNT DECREASED ( 2 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EXTRASKELETAL OSSIFICATION ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FOETAL ACIDOSIS ( 2 FDA reports)
FOETAL HEART RATE DECELERATION ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FOREIGN BODY IN EYE ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL LESION ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 2 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GROWTH OF EYELASHES ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEAT EXHAUSTION ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERTONIC BLADDER ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPOCAPNIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOSPADIAS ( 2 FDA reports)
ILEAL PERFORATION ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INDIFFERENCE ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INJECTION SITE DESQUAMATION ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LARYNGOPHARYNGITIS ( 2 FDA reports)
LENS IMPLANT ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE I ( 2 FDA reports)
LUPUS NEPHRITIS ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
LYMPHORRHOEA ( 2 FDA reports)
MACULOPATHY ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MALIGNANT NEOPLASM OF RENAL PELVIS ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONONEURITIS ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MUCOSAL ULCERATION ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE ENZYME INCREASED ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NECROTISING OESOPHAGITIS ( 2 FDA reports)
NEONATAL HYPOXIA ( 2 FDA reports)
NEONATAL PNEUMONIA ( 2 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
NEUROSIS ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OSTEOCHONDROSIS ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC INJURY ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PERICARDIAL DRAINAGE ( 2 FDA reports)
PERICARDITIS TUBERCULOUS ( 2 FDA reports)
PERIHEPATIC ABSCESS ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PEYRONIE'S DISEASE ( 2 FDA reports)
PHARYNGEAL ABSCESS ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PHRENIC NERVE PARALYSIS ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PLACENTA PRAEVIA ( 2 FDA reports)
PLATELET AGGREGATION ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
PLEURODESIS ( 2 FDA reports)
PNEUMONIA CHLAMYDIAL ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POST PROCEDURAL BILE LEAK ( 2 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
POSTOPERATIVE THROMBOSIS ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROSTATE CANCER STAGE IV ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 2 FDA reports)
PSYCHOGENIC ERECTILE DYSFUNCTION ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY HYPOPLASIA ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 2 FDA reports)
PUTAMEN HAEMORRHAGE ( 2 FDA reports)
PYURIA ( 2 FDA reports)
RECTAL NEOPLASM ( 2 FDA reports)
RED BLOOD CELL ABNORMALITY ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 2 FDA reports)
REGURGITATION OF FOOD ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RESORPTION BONE INCREASED ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 2 FDA reports)
RETINAL NEOVASCULARISATION ( 2 FDA reports)
RETINAL PIGMENTATION ( 2 FDA reports)
RETROPERITONEAL ABSCESS ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SCAN WITH CONTRAST ABNORMAL ( 2 FDA reports)
SCLERAL DISCOLOURATION ( 2 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 2 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SEPSIS NEONATAL ( 2 FDA reports)
SHUNT THROMBOSIS ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SKIN NEOPLASM EXCISION ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SPEECH REHABILITATION ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
SPLENITIS ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
TENSION ( 2 FDA reports)
THALAMUS HAEMORRHAGE ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
THYMECTOMY ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
THYROIDITIS SUBACUTE ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TONGUE ATROPHY ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TONSILLAR DISORDER ( 2 FDA reports)
TRACHEOBRONCHITIS ( 2 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
TUMOUR ASSOCIATED FEVER ( 2 FDA reports)
TUMOUR EXCISION ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
UTERINE HYPERTONUS ( 2 FDA reports)
VASCULAR INSUFFICIENCY ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VOCAL CORD CYST ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
VOCAL CORD THICKENING ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
VULVOVAGINAL RASH ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACTINOMYCOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALLERGIC BRONCHITIS ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANGIOSCLEROSIS ( 1 FDA reports)
ANOREXIA NERVOSA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY ( 1 FDA reports)
ANTIBIOTIC PROPHYLAXIS ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
AORTA HYPOPLASIA ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE DISEASE MIXED ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL ANEURYSM REPAIR ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOGRAM RENAL ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATYPICAL FEMUR FRACTURE ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BENIGN RENAL NEOPLASM ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILE DUCT NECROSIS ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER CANCER STAGE III ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER TAMPONADE ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GASTRIN INCREASED ( 1 FDA reports)
BLOOD HYPOSMOSIS ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOLITHIASIS ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR ISCHAEMIA ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLELITHOTOMY ( 1 FDA reports)
CHOLESTASIS OF PREGNANCY ( 1 FDA reports)
CHOLINERGIC SYNDROME ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLORECTAL CANCER RECURRENT ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 1 FDA reports)
DENTAL FISTULA ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DURAL FISTULA ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR CANAL ERYTHEMA ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENCEPHALITIS FUNGAL ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPIDIDYMAL CYST ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ERYTHROMELALGIA ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EWING'S SARCOMA ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACTOR V INHIBITION ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEMORAL ARTERY ANEURYSM ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE NORMAL ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL GANGRENE ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GENERAL ANAESTHESIA ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GINGIVAL OEDEMA ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLAUCOMA SURGERY ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEPATIC ARTERY ANEURYSM ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RESECTABLE ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HISTOLOGY ABNORMAL ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HYPERALBUMINAEMIA ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERSTHENURIA ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGLOBULINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOPHARYNGEAL CANCER ( 1 FDA reports)
HYPOPLASTIC ANAEMIA ( 1 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTHERMIA NEONATAL ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILEAL ULCER PERFORATION ( 1 FDA reports)
ILEECTOMY ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPLANT SITE HAEMATOMA ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JEJUNAL ULCER PERFORATION ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL PAIN ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
LEUKAEMIC INFILTRATION EXTRAMEDULLARY ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LUMBAR HERNIA ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT LYMPHOMA UNCLASSIFIABLE LOW GRADE ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MEAN PLATELET VOLUME ABNORMAL ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS FUNGAL ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MUCOSAL EXCORIATION ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELOCYTE COUNT DECREASED ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYOCARDIAL OEDEMA ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL OPERATION ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECROSIS OF ARTERY ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEOPLASM GROWTH ACCELERATED ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROSTOMY ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUTROPHIL FUNCTION DISORDER ( 1 FDA reports)
NEUTROPHIL HYPERSEGMENTED MORPHOLOGY PRESENT ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
ODONTOGENIC CYST ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OSTEOTOMY ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PACHYMENINGITIS ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PELVIC HAEMATOMA OBSTETRIC ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENIS DEVIATION ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PEPTIC ULCER REACTIVATED ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDIAL NEOPLASM ( 1 FDA reports)
PERICARDITIS MALIGNANT ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL REVASCULARISATION ( 1 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGOLARYNGEAL ABSCESS ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLACENTAL INSUFFICIENCY ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYP ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POPLITEAL STENOSIS ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE CONSTIPATION ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTPARTUM DISORDER ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RADIOTHERAPY TO BRAIN ( 1 FDA reports)
REACTIVE PSYCHOSIS ( 1 FDA reports)
RECTAL CANCER STAGE II ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
RELAPSING FEVER ( 1 FDA reports)
RENAL AMYLOIDOSIS ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL OSTEODYSTROPHY ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHESUS ANTIBODIES POSITIVE ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SKELETON DYSPLASIA ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPINAL VASCULAR DISORDER ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STARING ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STRANGURY ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THYMOMA ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSURETHRAL BLADDER RESECTION ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
UTERINE ATONY ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VERTEBRAL ABSCESS ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VIOLENT IDEATION ( 1 FDA reports)
VISUAL MIDLINE SHIFT SYNDROME ( 1 FDA reports)
VITAMIN B1 DEFICIENCY ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

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