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

DIARRHOEA ( 294 FDA reports)
PYREXIA ( 287 FDA reports)
PAIN ( 254 FDA reports)
PRURITUS ( 228 FDA reports)
DYSPNOEA ( 227 FDA reports)
VOMITING ( 227 FDA reports)
NAUSEA ( 222 FDA reports)
ANXIETY ( 205 FDA reports)
ANAEMIA ( 185 FDA reports)
RASH ( 177 FDA reports)
FATIGUE ( 162 FDA reports)
ASTHENIA ( 161 FDA reports)
PNEUMONIA ( 149 FDA reports)
HYPOTENSION ( 144 FDA reports)
ABDOMINAL PAIN ( 143 FDA reports)
RENAL FAILURE ( 140 FDA reports)
ERYTHEMA ( 132 FDA reports)
OEDEMA PERIPHERAL ( 131 FDA reports)
RENAL FAILURE ACUTE ( 131 FDA reports)
HEADACHE ( 120 FDA reports)
CONFUSIONAL STATE ( 119 FDA reports)
THROMBOCYTOPENIA ( 119 FDA reports)
INJURY ( 115 FDA reports)
JAUNDICE ( 115 FDA reports)
MALAISE ( 115 FDA reports)
HYPERTENSION ( 112 FDA reports)
DIZZINESS ( 111 FDA reports)
CHEST PAIN ( 110 FDA reports)
DEHYDRATION ( 110 FDA reports)
ARTHRALGIA ( 105 FDA reports)
DEPRESSION ( 103 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 102 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 102 FDA reports)
PAIN IN EXTREMITY ( 101 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 96 FDA reports)
ATRIAL FIBRILLATION ( 94 FDA reports)
FALL ( 94 FDA reports)
WEIGHT DECREASED ( 94 FDA reports)
PLEURAL EFFUSION ( 92 FDA reports)
URTICARIA ( 91 FDA reports)
BACK PAIN ( 90 FDA reports)
CELLULITIS ( 88 FDA reports)
DRUG INTERACTION ( 88 FDA reports)
SEPSIS ( 88 FDA reports)
DEEP VEIN THROMBOSIS ( 85 FDA reports)
DRUG INEFFECTIVE ( 83 FDA reports)
MYOCARDIAL INFARCTION ( 82 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 81 FDA reports)
EMOTIONAL DISTRESS ( 81 FDA reports)
RESPIRATORY FAILURE ( 78 FDA reports)
URINARY TRACT INFECTION ( 78 FDA reports)
HYPOAESTHESIA ( 77 FDA reports)
PANCYTOPENIA ( 77 FDA reports)
ABDOMINAL PAIN UPPER ( 74 FDA reports)
CONSTIPATION ( 74 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 73 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 73 FDA reports)
LEUKOPENIA ( 73 FDA reports)
NEUTROPENIA ( 73 FDA reports)
SINUSITIS ( 73 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 72 FDA reports)
HYPOKALAEMIA ( 72 FDA reports)
DEATH ( 71 FDA reports)
CONDITION AGGRAVATED ( 68 FDA reports)
DECREASED APPETITE ( 68 FDA reports)
HYPERSENSITIVITY ( 68 FDA reports)
INSOMNIA ( 68 FDA reports)
OSTEONECROSIS OF JAW ( 68 FDA reports)
PULMONARY EMBOLISM ( 68 FDA reports)
RASH MACULO-PAPULAR ( 68 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 67 FDA reports)
CHOLESTASIS ( 66 FDA reports)
CORONARY ARTERY DISEASE ( 65 FDA reports)
INFECTION ( 65 FDA reports)
OEDEMA ( 65 FDA reports)
SOMNOLENCE ( 65 FDA reports)
CHILLS ( 64 FDA reports)
BRONCHITIS ( 63 FDA reports)
TACHYCARDIA ( 63 FDA reports)
DYSPEPSIA ( 62 FDA reports)
ANHEDONIA ( 61 FDA reports)
LOSS OF CONSCIOUSNESS ( 61 FDA reports)
COUGH ( 60 FDA reports)
SEPTIC SHOCK ( 60 FDA reports)
TOXIC SKIN ERUPTION ( 60 FDA reports)
ECONOMIC PROBLEM ( 59 FDA reports)
HEPATITIS CHOLESTATIC ( 59 FDA reports)
HEPATITIS ( 58 FDA reports)
BLOOD BILIRUBIN INCREASED ( 57 FDA reports)
OSTEOMYELITIS ( 57 FDA reports)
CYTOLYTIC HEPATITIS ( 56 FDA reports)
DYSPHAGIA ( 56 FDA reports)
NEUROPATHY PERIPHERAL ( 56 FDA reports)
OSTEOARTHRITIS ( 56 FDA reports)
CONVULSION ( 55 FDA reports)
EOSINOPHILIA ( 55 FDA reports)
HAEMOGLOBIN DECREASED ( 55 FDA reports)
ANAPHYLACTIC SHOCK ( 54 FDA reports)
FACE OEDEMA ( 54 FDA reports)
OVERDOSE ( 53 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 52 FDA reports)
PURPURA ( 52 FDA reports)
HYPONATRAEMIA ( 51 FDA reports)
MYALGIA ( 51 FDA reports)
CARDIAC ARREST ( 50 FDA reports)
CHOLELITHIASIS ( 50 FDA reports)
INFLAMMATION ( 50 FDA reports)
FEBRILE NEUTROPENIA ( 49 FDA reports)
GAIT DISTURBANCE ( 49 FDA reports)
SPINAL OSTEOARTHRITIS ( 49 FDA reports)
GASTRITIS ( 47 FDA reports)
LEUKOCYTOSIS ( 47 FDA reports)
AGRANULOCYTOSIS ( 46 FDA reports)
IMPAIRED HEALING ( 46 FDA reports)
LYMPHADENOPATHY ( 46 FDA reports)
PAIN IN JAW ( 46 FDA reports)
ATELECTASIS ( 45 FDA reports)
BLOOD CREATININE INCREASED ( 45 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 45 FDA reports)
HAEMATURIA ( 45 FDA reports)
HEPATIC ENZYME INCREASED ( 45 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 44 FDA reports)
ENCEPHALOPATHY ( 44 FDA reports)
MULTIPLE INJURIES ( 44 FDA reports)
SKIN EXFOLIATION ( 44 FDA reports)
TREMOR ( 44 FDA reports)
ANAPHYLACTIC REACTION ( 43 FDA reports)
CARDIAC FAILURE ( 43 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 43 FDA reports)
PARAESTHESIA ( 43 FDA reports)
RESPIRATORY DISTRESS ( 43 FDA reports)
CEREBROVASCULAR ACCIDENT ( 42 FDA reports)
HAEMORRHOIDS ( 42 FDA reports)
HEPATIC FAILURE ( 42 FDA reports)
DRUG HYPERSENSITIVITY ( 41 FDA reports)
PALPITATIONS ( 41 FDA reports)
VISION BLURRED ( 41 FDA reports)
DISORIENTATION ( 40 FDA reports)
MITRAL VALVE INCOMPETENCE ( 40 FDA reports)
RASH ERYTHEMATOUS ( 40 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 40 FDA reports)
BRADYCARDIA ( 39 FDA reports)
CARDIAC DISORDER ( 39 FDA reports)
CARDIOMEGALY ( 39 FDA reports)
DIABETES MELLITUS ( 39 FDA reports)
LUNG DISORDER ( 39 FDA reports)
PULMONARY OEDEMA ( 39 FDA reports)
RENAL FAILURE CHRONIC ( 39 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 39 FDA reports)
WEIGHT INCREASED ( 39 FDA reports)
ABDOMINAL DISTENSION ( 38 FDA reports)
ANGINA PECTORIS ( 38 FDA reports)
EPISTAXIS ( 38 FDA reports)
HIATUS HERNIA ( 38 FDA reports)
SLEEP APNOEA SYNDROME ( 38 FDA reports)
STEVENS-JOHNSON SYNDROME ( 38 FDA reports)
SWELLING FACE ( 38 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 38 FDA reports)
ASTHMA ( 37 FDA reports)
BLOOD GLUCOSE INCREASED ( 37 FDA reports)
CHROMATURIA ( 37 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 37 FDA reports)
HYPERHIDROSIS ( 37 FDA reports)
BLISTER ( 36 FDA reports)
BRONCHOSPASM ( 36 FDA reports)
CANDIDIASIS ( 36 FDA reports)
CHEST DISCOMFORT ( 36 FDA reports)
EXPOSED BONE IN JAW ( 36 FDA reports)
RENAL IMPAIRMENT ( 36 FDA reports)
ASCITES ( 35 FDA reports)
BONE DISORDER ( 35 FDA reports)
SKIN LESION ( 35 FDA reports)
HYPERKALAEMIA ( 34 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 34 FDA reports)
MULTI-ORGAN FAILURE ( 34 FDA reports)
MUSCULAR WEAKNESS ( 34 FDA reports)
OSTEOPENIA ( 34 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 33 FDA reports)
HAEMATOCHEZIA ( 33 FDA reports)
HAEMATOMA ( 33 FDA reports)
LIVER INJURY ( 33 FDA reports)
OESOPHAGITIS ( 33 FDA reports)
CROHN'S DISEASE ( 32 FDA reports)
DENTAL CARIES ( 32 FDA reports)
HERPES ZOSTER ( 32 FDA reports)
HYPERGLYCAEMIA ( 32 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 32 FDA reports)
NEOPLASM MALIGNANT ( 32 FDA reports)
OSTEONECROSIS ( 32 FDA reports)
RECTAL HAEMORRHAGE ( 32 FDA reports)
STAPHYLOCOCCAL INFECTION ( 32 FDA reports)
BONE PAIN ( 31 FDA reports)
CARDIOMYOPATHY ( 31 FDA reports)
HEPATIC STEATOSIS ( 31 FDA reports)
HYPERLIPIDAEMIA ( 31 FDA reports)
HYPOXIA ( 31 FDA reports)
OSTEOPOROSIS ( 31 FDA reports)
PNEUMONIA ASPIRATION ( 31 FDA reports)
ARRHYTHMIA ( 30 FDA reports)
DERMATITIS BULLOUS ( 30 FDA reports)
DERMATITIS EXFOLIATIVE ( 30 FDA reports)
GENERALISED ERYTHEMA ( 30 FDA reports)
MASTICATION DISORDER ( 30 FDA reports)
MUSCLE SPASMS ( 30 FDA reports)
OSTEOLYSIS ( 30 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 30 FDA reports)
SKIN ULCER ( 30 FDA reports)
ABDOMINAL DISCOMFORT ( 29 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 29 FDA reports)
ARTERIOSCLEROSIS ( 29 FDA reports)
COMA ( 29 FDA reports)
PULMONARY CONGESTION ( 29 FDA reports)
PULMONARY HYPERTENSION ( 29 FDA reports)
UNEVALUABLE EVENT ( 29 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 28 FDA reports)
FEAR ( 28 FDA reports)
RASH MACULAR ( 28 FDA reports)
RASH PUSTULAR ( 28 FDA reports)
SYNCOPE ( 28 FDA reports)
CARDIAC MURMUR ( 27 FDA reports)
CONTUSION ( 27 FDA reports)
DYSPNOEA EXERTIONAL ( 27 FDA reports)
GINGIVITIS ( 27 FDA reports)
LIP OEDEMA ( 27 FDA reports)
NEPHROLITHIASIS ( 27 FDA reports)
PLATELET COUNT DECREASED ( 27 FDA reports)
TRANSAMINASES INCREASED ( 27 FDA reports)
VENTRICULAR TACHYCARDIA ( 27 FDA reports)
VERTIGO ( 27 FDA reports)
ANGIOEDEMA ( 26 FDA reports)
BLOOD PRESSURE INCREASED ( 26 FDA reports)
CARDIO-RESPIRATORY ARREST ( 26 FDA reports)
GASTROINTESTINAL DISORDER ( 26 FDA reports)
HALLUCINATION ( 26 FDA reports)
HYPOGLYCAEMIA ( 26 FDA reports)
OXYGEN SATURATION DECREASED ( 26 FDA reports)
SINUS TACHYCARDIA ( 26 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 26 FDA reports)
ANOREXIA ( 25 FDA reports)
BLOOD SODIUM DECREASED ( 25 FDA reports)
DYSURIA ( 25 FDA reports)
HYPOTHYROIDISM ( 25 FDA reports)
MALNUTRITION ( 25 FDA reports)
MUSCULOSKELETAL PAIN ( 25 FDA reports)
RASH GENERALISED ( 25 FDA reports)
STRESS ( 25 FDA reports)
BLOOD PRESSURE DECREASED ( 24 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 24 FDA reports)
DYSARTHRIA ( 24 FDA reports)
EJECTION FRACTION DECREASED ( 24 FDA reports)
GINGIVAL INFECTION ( 24 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 24 FDA reports)
MENTAL STATUS CHANGES ( 24 FDA reports)
NECK PAIN ( 24 FDA reports)
PROTEINURIA ( 24 FDA reports)
SINUS DISORDER ( 24 FDA reports)
SKIN DISORDER ( 24 FDA reports)
TREATMENT NONCOMPLIANCE ( 24 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 24 FDA reports)
AMNESIA ( 23 FDA reports)
CATARACT ( 23 FDA reports)
CLOSTRIDIUM COLITIS ( 23 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 23 FDA reports)
DIPLOPIA ( 23 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 23 FDA reports)
DIVERTICULUM ( 23 FDA reports)
FEELING ABNORMAL ( 23 FDA reports)
HAEMOPTYSIS ( 23 FDA reports)
HEPATOCELLULAR INJURY ( 23 FDA reports)
HYPERTHERMIA ( 23 FDA reports)
JAUNDICE CHOLESTATIC ( 23 FDA reports)
OSTEITIS ( 23 FDA reports)
PALLOR ( 23 FDA reports)
PANCREATITIS ( 23 FDA reports)
PRURITUS GENERALISED ( 23 FDA reports)
SPEECH DISORDER ( 23 FDA reports)
TOOTH EXTRACTION ( 23 FDA reports)
ABNORMAL BEHAVIOUR ( 22 FDA reports)
DEFORMITY ( 22 FDA reports)
DIVERTICULITIS ( 22 FDA reports)
EAR PAIN ( 22 FDA reports)
LUNG NEOPLASM ( 22 FDA reports)
PHARYNGITIS ( 22 FDA reports)
PRODUCTIVE COUGH ( 22 FDA reports)
SCOLIOSIS ( 22 FDA reports)
SWELLING ( 22 FDA reports)
WHEEZING ( 22 FDA reports)
AGITATION ( 21 FDA reports)
DISEASE PROGRESSION ( 21 FDA reports)
HEPATOMEGALY ( 21 FDA reports)
JAW FRACTURE ( 21 FDA reports)
METABOLIC ACIDOSIS ( 21 FDA reports)
MYOCARDIAL ISCHAEMIA ( 21 FDA reports)
PURULENT DISCHARGE ( 21 FDA reports)
ARTHRITIS ( 20 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 20 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 20 FDA reports)
BRONCHOPNEUMONIA ( 20 FDA reports)
CHOLECYSTITIS ( 20 FDA reports)
CHOLECYSTITIS CHRONIC ( 20 FDA reports)
CHRONIC SINUSITIS ( 20 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 20 FDA reports)
DYSLIPIDAEMIA ( 20 FDA reports)
HEPATIC CIRRHOSIS ( 20 FDA reports)
HEPATITIS ACUTE ( 20 FDA reports)
ILEUS ( 20 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 20 FDA reports)
PANIC ATTACK ( 20 FDA reports)
PRIMARY SEQUESTRUM ( 20 FDA reports)
SUICIDAL IDEATION ( 20 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 20 FDA reports)
VISUAL IMPAIRMENT ( 20 FDA reports)
ANGIONEUROTIC OEDEMA ( 19 FDA reports)
BONE LESION ( 19 FDA reports)
CAROTID ARTERY STENOSIS ( 19 FDA reports)
COAGULOPATHY ( 19 FDA reports)
COLONIC POLYP ( 19 FDA reports)
DISCOMFORT ( 19 FDA reports)
DISTURBANCE IN ATTENTION ( 19 FDA reports)
ECZEMA ( 19 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 19 FDA reports)
PERIODONTITIS ( 19 FDA reports)
SHOCK ( 19 FDA reports)
SLEEP DISORDER ( 19 FDA reports)
TENDONITIS ( 19 FDA reports)
ACTINIC KERATOSIS ( 18 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 18 FDA reports)
BURSITIS ( 18 FDA reports)
ERYTHEMA MULTIFORME ( 18 FDA reports)
EYE PAIN ( 18 FDA reports)
FACIAL PAIN ( 18 FDA reports)
HAEMATEMESIS ( 18 FDA reports)
HAEMOLYTIC ANAEMIA ( 18 FDA reports)
IRRITABILITY ( 18 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 18 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 18 FDA reports)
MASS ( 18 FDA reports)
MULTIPLE MYELOMA ( 18 FDA reports)
NEOPLASM PROGRESSION ( 18 FDA reports)
NEUTROPHIL COUNT DECREASED ( 18 FDA reports)
PERICARDIAL EFFUSION ( 18 FDA reports)
RETINAL HAEMORRHAGE ( 18 FDA reports)
SURGERY ( 18 FDA reports)
TINNITUS ( 18 FDA reports)
ALOPECIA ( 17 FDA reports)
ARTHROPATHY ( 17 FDA reports)
BODY TEMPERATURE INCREASED ( 17 FDA reports)
CYANOSIS ( 17 FDA reports)
DEAFNESS ( 17 FDA reports)
DEAFNESS NEUROSENSORY ( 17 FDA reports)
DERMATITIS ( 17 FDA reports)
GALLBLADDER DISORDER ( 17 FDA reports)
HYPOPHAGIA ( 17 FDA reports)
ILL-DEFINED DISORDER ( 17 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 17 FDA reports)
JOINT SWELLING ( 17 FDA reports)
LETHARGY ( 17 FDA reports)
MEDICATION ERROR ( 17 FDA reports)
MEMORY IMPAIRMENT ( 17 FDA reports)
METASTASES TO BONE ( 17 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 17 FDA reports)
MYOCLONUS ( 17 FDA reports)
OBESITY ( 17 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 17 FDA reports)
PNEUMOTHORAX ( 17 FDA reports)
PROTHROMBIN TIME PROLONGED ( 17 FDA reports)
RENAL CYST ( 17 FDA reports)
RESPIRATORY DISORDER ( 17 FDA reports)
SINUS BRADYCARDIA ( 17 FDA reports)
TOOTH ABSCESS ( 17 FDA reports)
TOOTH LOSS ( 17 FDA reports)
URINARY RETENTION ( 17 FDA reports)
VENTRICULAR HYPOKINESIA ( 17 FDA reports)
AORTIC VALVE INCOMPETENCE ( 16 FDA reports)
BACK DISORDER ( 16 FDA reports)
BACTERIAL INFECTION ( 16 FDA reports)
BLOOD UREA INCREASED ( 16 FDA reports)
BONE LOSS ( 16 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 16 FDA reports)
DECREASED INTEREST ( 16 FDA reports)
DILATATION VENTRICULAR ( 16 FDA reports)
EYELID OEDEMA ( 16 FDA reports)
FAECES DISCOLOURED ( 16 FDA reports)
HEART RATE INCREASED ( 16 FDA reports)
HYPERBILIRUBINAEMIA ( 16 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 16 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 16 FDA reports)
MIGRAINE ( 16 FDA reports)
OROPHARYNGEAL PAIN ( 16 FDA reports)
PANCREATITIS ACUTE ( 16 FDA reports)
RENAL INJURY ( 16 FDA reports)
RHABDOMYOLYSIS ( 16 FDA reports)
RHEUMATOID ARTHRITIS ( 16 FDA reports)
ROAD TRAFFIC ACCIDENT ( 16 FDA reports)
ROTATOR CUFF SYNDROME ( 16 FDA reports)
SCAR ( 16 FDA reports)
STATUS EPILEPTICUS ( 16 FDA reports)
SUDDEN DEATH ( 16 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 16 FDA reports)
THROMBOSIS ( 16 FDA reports)
ANURIA ( 15 FDA reports)
COLITIS ( 15 FDA reports)
DEPRESSED MOOD ( 15 FDA reports)
FEELING HOT ( 15 FDA reports)
FIBROMYALGIA ( 15 FDA reports)
FLUSHING ( 15 FDA reports)
HEPATOCELLULAR DAMAGE ( 15 FDA reports)
LYMPHOEDEMA ( 15 FDA reports)
MELAENA ( 15 FDA reports)
MOUTH ULCERATION ( 15 FDA reports)
NASAL CONGESTION ( 15 FDA reports)
ORTHOSTATIC HYPOTENSION ( 15 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 15 FDA reports)
PLEURAL FIBROSIS ( 15 FDA reports)
POLLAKIURIA ( 15 FDA reports)
PSEUDOMONAS INFECTION ( 15 FDA reports)
RALES ( 15 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 15 FDA reports)
WOUND INFECTION ( 15 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 14 FDA reports)
CAESAREAN SECTION ( 14 FDA reports)
CIRCULATORY COLLAPSE ( 14 FDA reports)
DENTAL FISTULA ( 14 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 14 FDA reports)
DIALYSIS ( 14 FDA reports)
DRUG ERUPTION ( 14 FDA reports)
GENERALISED OEDEMA ( 14 FDA reports)
GINGIVAL PAIN ( 14 FDA reports)
INFLUENZA LIKE ILLNESS ( 14 FDA reports)
LUNG INFILTRATION ( 14 FDA reports)
PERIODONTAL DISEASE ( 14 FDA reports)
PHARYNGEAL OEDEMA ( 14 FDA reports)
PHYSICAL DISABILITY ( 14 FDA reports)
PRESYNCOPE ( 14 FDA reports)
PULMONARY FIBROSIS ( 14 FDA reports)
PYELONEPHRITIS ( 14 FDA reports)
RASH PAPULAR ( 14 FDA reports)
RASH PRURITIC ( 14 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 14 FDA reports)
ULCER ( 14 FDA reports)
VIRAL INFECTION ( 14 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 13 FDA reports)
BURNING SENSATION ( 13 FDA reports)
CARDIAC VALVE DISEASE ( 13 FDA reports)
CARDIOVASCULAR DISORDER ( 13 FDA reports)
CHEILITIS ( 13 FDA reports)
CLOSTRIDIAL INFECTION ( 13 FDA reports)
COLITIS ULCERATIVE ( 13 FDA reports)
DIABETIC NEUROPATHY ( 13 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 13 FDA reports)
DRUG TOXICITY ( 13 FDA reports)
DYSPHONIA ( 13 FDA reports)
EMPHYSEMA ( 13 FDA reports)
ERECTILE DYSFUNCTION ( 13 FDA reports)
ESSENTIAL HYPERTENSION ( 13 FDA reports)
FLANK PAIN ( 13 FDA reports)
FLUID RETENTION ( 13 FDA reports)
FUNGAL INFECTION ( 13 FDA reports)
GINGIVAL SWELLING ( 13 FDA reports)
HAEMATOCRIT DECREASED ( 13 FDA reports)
HEPATIC CYST ( 13 FDA reports)
HYPERCHOLESTEROLAEMIA ( 13 FDA reports)
HYPOTHERMIA ( 13 FDA reports)
IMPETIGO ( 13 FDA reports)
INTERSTITIAL LUNG DISEASE ( 13 FDA reports)
LIVER DISORDER ( 13 FDA reports)
LOCALISED INFECTION ( 13 FDA reports)
LUNG INFECTION ( 13 FDA reports)
PETECHIAE ( 13 FDA reports)
RASH MORBILLIFORM ( 13 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 13 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 13 FDA reports)
RESTLESS LEGS SYNDROME ( 13 FDA reports)
RIB FRACTURE ( 13 FDA reports)
SEQUESTRECTOMY ( 13 FDA reports)
SPINAL COLUMN STENOSIS ( 13 FDA reports)
SQUAMOUS CELL CARCINOMA ( 13 FDA reports)
SUICIDE ATTEMPT ( 13 FDA reports)
SYNOVIAL CYST ( 13 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 13 FDA reports)
TORSADE DE POINTES ( 13 FDA reports)
VASCULAR PURPURA ( 13 FDA reports)
ADRENAL INSUFFICIENCY ( 12 FDA reports)
BACTERAEMIA ( 12 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 12 FDA reports)
CARPAL TUNNEL SYNDROME ( 12 FDA reports)
COLON CANCER ( 12 FDA reports)
DRUG DEPENDENCE ( 12 FDA reports)
DRY MOUTH ( 12 FDA reports)
DUODENAL ULCER ( 12 FDA reports)
DYSGEUSIA ( 12 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 12 FDA reports)
ELECTROLYTE IMBALANCE ( 12 FDA reports)
EMOTIONAL DISORDER ( 12 FDA reports)
ESCHERICHIA INFECTION ( 12 FDA reports)
FLATULENCE ( 12 FDA reports)
HAEMORRHAGE ( 12 FDA reports)
HEPATIC NECROSIS ( 12 FDA reports)
HYDRONEPHROSIS ( 12 FDA reports)
INGUINAL HERNIA ( 12 FDA reports)
INTESTINAL OBSTRUCTION ( 12 FDA reports)
LARYNGEAL OEDEMA ( 12 FDA reports)
LOCAL SWELLING ( 12 FDA reports)
METASTASES TO SPINE ( 12 FDA reports)
MOOD SWINGS ( 12 FDA reports)
MUSCLE HAEMORRHAGE ( 12 FDA reports)
MUSCLE STRAIN ( 12 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 12 FDA reports)
NEPHRITIS INTERSTITIAL ( 12 FDA reports)
NEURALGIA ( 12 FDA reports)
NEURODERMATITIS ( 12 FDA reports)
ORAL PAIN ( 12 FDA reports)
OSTEOSCLEROSIS ( 12 FDA reports)
PARONYCHIA ( 12 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 12 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 12 FDA reports)
PROTEIN URINE PRESENT ( 12 FDA reports)
RHINITIS ALLERGIC ( 12 FDA reports)
SPINAL COMPRESSION FRACTURE ( 12 FDA reports)
SPONDYLOLISTHESIS ( 12 FDA reports)
TYPE 2 DIABETES MELLITUS ( 12 FDA reports)
UPPER LIMB FRACTURE ( 12 FDA reports)
VENOUS INSUFFICIENCY ( 12 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 12 FDA reports)
ANGER ( 11 FDA reports)
BACK INJURY ( 11 FDA reports)
BASAL CELL CARCINOMA ( 11 FDA reports)
BONE DEBRIDEMENT ( 11 FDA reports)
BRUXISM ( 11 FDA reports)
CARDIAC PACEMAKER INSERTION ( 11 FDA reports)
CEREBRAL ISCHAEMIA ( 11 FDA reports)
CONJUNCTIVITIS ( 11 FDA reports)
CRYING ( 11 FDA reports)
DISEASE RECURRENCE ( 11 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 11 FDA reports)
EXOSTOSIS ( 11 FDA reports)
FEMUR FRACTURE ( 11 FDA reports)
HALLUCINATION, VISUAL ( 11 FDA reports)
HEART RATE IRREGULAR ( 11 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
HEPATIC PAIN ( 11 FDA reports)
HYPOMAGNESAEMIA ( 11 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 11 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 11 FDA reports)
JOINT DISLOCATION ( 11 FDA reports)
MENORRHAGIA ( 11 FDA reports)
MITRAL VALVE CALCIFICATION ( 11 FDA reports)
MUSCLE TWITCHING ( 11 FDA reports)
ORAL CAVITY FISTULA ( 11 FDA reports)
OVARIAN CYST ( 11 FDA reports)
PNEUMONIA BACTERIAL ( 11 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 11 FDA reports)
PRURIGO ( 11 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 11 FDA reports)
RECTAL ULCER ( 11 FDA reports)
RENAL DISORDER ( 11 FDA reports)
RESPIRATORY TRACT INFECTION ( 11 FDA reports)
SENSORY DISTURBANCE ( 11 FDA reports)
SPLENIC LESION ( 11 FDA reports)
SUPERINFECTION ( 11 FDA reports)
TOOTHACHE ( 11 FDA reports)
VENTRICULAR FIBRILLATION ( 11 FDA reports)
VISUAL ACUITY REDUCED ( 11 FDA reports)
WOUND DRAINAGE ( 11 FDA reports)
ABNORMAL FAECES ( 10 FDA reports)
ABSCESS JAW ( 10 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 10 FDA reports)
ACUTE PULMONARY OEDEMA ( 10 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 10 FDA reports)
BALANCE DISORDER ( 10 FDA reports)
BLOOD CALCIUM DECREASED ( 10 FDA reports)
BLOOD POTASSIUM DECREASED ( 10 FDA reports)
BLOOD URINE PRESENT ( 10 FDA reports)
CERVICAL SPINAL STENOSIS ( 10 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 10 FDA reports)
COR PULMONALE ( 10 FDA reports)
DUODENITIS ( 10 FDA reports)
GASTROENTERITIS ( 10 FDA reports)
GRAND MAL CONVULSION ( 10 FDA reports)
HEMIPARESIS ( 10 FDA reports)
HIP FRACTURE ( 10 FDA reports)
LACERATION ( 10 FDA reports)
MOBILITY DECREASED ( 10 FDA reports)
MUCOSAL INFLAMMATION ( 10 FDA reports)
MYELODYSPLASTIC SYNDROME ( 10 FDA reports)
NIKOLSKY'S SIGN ( 10 FDA reports)
ORTHOPNOEA ( 10 FDA reports)
OVERWEIGHT ( 10 FDA reports)
PARAESTHESIA ORAL ( 10 FDA reports)
PATHOLOGICAL FRACTURE ( 10 FDA reports)
PHLEBITIS ( 10 FDA reports)
PLATELET COUNT INCREASED ( 10 FDA reports)
PREMATURE BABY ( 10 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 10 FDA reports)
RESPIRATORY ARREST ( 10 FDA reports)
RHINORRHOEA ( 10 FDA reports)
SICK SINUS SYNDROME ( 10 FDA reports)
SKIN BURNING SENSATION ( 10 FDA reports)
SKIN PLAQUE ( 10 FDA reports)
SPLENOMEGALY ( 10 FDA reports)
STREPTOCOCCAL INFECTION ( 10 FDA reports)
TYPE I HYPERSENSITIVITY ( 10 FDA reports)
ABASIA ( 9 FDA reports)
ACNE ( 9 FDA reports)
ACUTE HEPATIC FAILURE ( 9 FDA reports)
ACUTE RESPIRATORY FAILURE ( 9 FDA reports)
ADNEXA UTERI MASS ( 9 FDA reports)
ALCOHOL USE ( 9 FDA reports)
ANGINA UNSTABLE ( 9 FDA reports)
ANIMAL BITE ( 9 FDA reports)
APLASTIC ANAEMIA ( 9 FDA reports)
ASPIRATION ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 9 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 9 FDA reports)
BLOOD ALBUMIN DECREASED ( 9 FDA reports)
CARDIOGENIC SHOCK ( 9 FDA reports)
CEREBRAL HAEMORRHAGE ( 9 FDA reports)
CHARLES BONNET SYNDROME ( 9 FDA reports)
CHEST X-RAY ABNORMAL ( 9 FDA reports)
CHOLECYSTECTOMY ( 9 FDA reports)
COGNITIVE DISORDER ( 9 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 9 FDA reports)
DYSAESTHESIA ( 9 FDA reports)
DYSTONIA ( 9 FDA reports)
EAR INFECTION ( 9 FDA reports)
EAR NEOPLASM ( 9 FDA reports)
ECCHYMOSIS ( 9 FDA reports)
ENDODONTIC PROCEDURE ( 9 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 9 FDA reports)
EYE SWELLING ( 9 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 9 FDA reports)
GANGRENE ( 9 FDA reports)
GINGIVAL ULCERATION ( 9 FDA reports)
GROIN PAIN ( 9 FDA reports)
HAEMODIALYSIS ( 9 FDA reports)
HAEMODYNAMIC INSTABILITY ( 9 FDA reports)
HEPATIC LESION ( 9 FDA reports)
HOT FLUSH ( 9 FDA reports)
HYPERSOMNIA ( 9 FDA reports)
INFLUENZA ( 9 FDA reports)
INTRACRANIAL ANEURYSM ( 9 FDA reports)
JAW OPERATION ( 9 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 9 FDA reports)
LACTOSE INTOLERANCE ( 9 FDA reports)
LACUNAR INFARCTION ( 9 FDA reports)
LIP SWELLING ( 9 FDA reports)
LUNG CONSOLIDATION ( 9 FDA reports)
LUNG NEOPLASM MALIGNANT ( 9 FDA reports)
LYMPHOPENIA ( 9 FDA reports)
MACROGLOSSIA ( 9 FDA reports)
METASTASES TO LIVER ( 9 FDA reports)
MIXED LIVER INJURY ( 9 FDA reports)
NASOPHARYNGITIS ( 9 FDA reports)
NIGHTMARE ( 9 FDA reports)
OEDEMA MOUTH ( 9 FDA reports)
OFF LABEL USE ( 9 FDA reports)
ORAL CANDIDIASIS ( 9 FDA reports)
ORAL INFECTION ( 9 FDA reports)
PANCREATIC HAEMORRHAGE ( 9 FDA reports)
POST PROCEDURAL COMPLICATION ( 9 FDA reports)
PULMONARY GRANULOMA ( 9 FDA reports)
RECTAL POLYP ( 9 FDA reports)
RHINITIS ( 9 FDA reports)
SCIATICA ( 9 FDA reports)
SKIN CANCER ( 9 FDA reports)
SKIN DISCOLOURATION ( 9 FDA reports)
SPINAL DISORDER ( 9 FDA reports)
STENT OCCLUSION ( 9 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 9 FDA reports)
TACHYPNOEA ( 9 FDA reports)
TARDIVE DYSKINESIA ( 9 FDA reports)
TONGUE DISCOLOURATION ( 9 FDA reports)
VENTRICULAR HYPERTROPHY ( 9 FDA reports)
VOMITING PROJECTILE ( 9 FDA reports)
ACIDOSIS ( 8 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 8 FDA reports)
ADRENAL DISORDER ( 8 FDA reports)
ANAPHYLACTOID REACTION ( 8 FDA reports)
APHASIA ( 8 FDA reports)
APHTHOUS STOMATITIS ( 8 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 8 FDA reports)
BONE MARROW FAILURE ( 8 FDA reports)
BONE MARROW TRANSPLANT ( 8 FDA reports)
BRAIN INJURY ( 8 FDA reports)
BULLOUS LUNG DISEASE ( 8 FDA reports)
CARDIAC TAMPONADE ( 8 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 8 FDA reports)
COLECTOMY ( 8 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 8 FDA reports)
CONDUCTION DISORDER ( 8 FDA reports)
CYSTITIS ( 8 FDA reports)
DRUG LEVEL INCREASED ( 8 FDA reports)
DRY EYE ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 8 FDA reports)
EXOPHTHALMOS ( 8 FDA reports)
FAECES PALE ( 8 FDA reports)
FISTULA REPAIR ( 8 FDA reports)
HEPATIC ENCEPHALOPATHY ( 8 FDA reports)
HEPATIC MASS ( 8 FDA reports)
HEPATITIS FULMINANT ( 8 FDA reports)
HEPATOTOXICITY ( 8 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 8 FDA reports)
HYPERURICAEMIA ( 8 FDA reports)
HYPOALBUMINAEMIA ( 8 FDA reports)
INTESTINAL DILATATION ( 8 FDA reports)
JOINT CONTRACTURE ( 8 FDA reports)
JOINT EFFUSION ( 8 FDA reports)
KERATITIS ( 8 FDA reports)
LABORATORY TEST ABNORMAL ( 8 FDA reports)
LUMBAR SPINAL STENOSIS ( 8 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 8 FDA reports)
METASTASES TO LUNG ( 8 FDA reports)
MUCOSAL EROSION ( 8 FDA reports)
MUSCLE CRAMP ( 8 FDA reports)
NECROSIS ( 8 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 8 FDA reports)
ODYNOPHAGIA ( 8 FDA reports)
ORAL DISORDER ( 8 FDA reports)
PAINFUL RESPIRATION ( 8 FDA reports)
PELVIC PAIN ( 8 FDA reports)
PEPTIC ULCER ( 8 FDA reports)
PERIPHERAL ISCHAEMIA ( 8 FDA reports)
PNEUMONITIS ( 8 FDA reports)
PRODUCT QUALITY ISSUE ( 8 FDA reports)
QUALITY OF LIFE DECREASED ( 8 FDA reports)
RENAL TUBULAR NECROSIS ( 8 FDA reports)
SENSITIVITY OF TEETH ( 8 FDA reports)
SINUS OPERATION ( 8 FDA reports)
SKIN HYPERPIGMENTATION ( 8 FDA reports)
SKIN TIGHTNESS ( 8 FDA reports)
SNORING ( 8 FDA reports)
SPUTUM CULTURE POSITIVE ( 8 FDA reports)
STOMATITIS ( 8 FDA reports)
STREPTOCOCCAL SEPSIS ( 8 FDA reports)
TENDERNESS ( 8 FDA reports)
TENOSYNOVITIS ( 8 FDA reports)
THINKING ABNORMAL ( 8 FDA reports)
UNRESPONSIVE TO STIMULI ( 8 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
VARICES OESOPHAGEAL ( 8 FDA reports)
VENA CAVA FILTER INSERTION ( 8 FDA reports)
VENTRICULAR DYSFUNCTION ( 8 FDA reports)
ABSCESS ( 7 FDA reports)
ACCIDENT ( 7 FDA reports)
ACCIDENTAL OVERDOSE ( 7 FDA reports)
AGEUSIA ( 7 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 7 FDA reports)
ALVEOLITIS ( 7 FDA reports)
BILE DUCT OBSTRUCTION ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 7 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 7 FDA reports)
BREATH ODOUR ( 7 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 7 FDA reports)
CARDIOPULMONARY FAILURE ( 7 FDA reports)
CATHETERISATION CARDIAC ( 7 FDA reports)
CHOLANGITIS ( 7 FDA reports)
CLAUSTROPHOBIA ( 7 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 7 FDA reports)
CYST ( 7 FDA reports)
DELIRIUM ( 7 FDA reports)
DIZZINESS POSTURAL ( 7 FDA reports)
DRUG ADMINISTRATION ERROR ( 7 FDA reports)
DYSKINESIA ( 7 FDA reports)
EAR DISORDER ( 7 FDA reports)
EATING DISORDER ( 7 FDA reports)
ENDOTRACHEAL INTUBATION ( 7 FDA reports)
ENTEROBACTER INFECTION ( 7 FDA reports)
EPILEPSY ( 7 FDA reports)
FAT NECROSIS ( 7 FDA reports)
FLUID OVERLOAD ( 7 FDA reports)
FOOT AMPUTATION ( 7 FDA reports)
GINGIVAL BLEEDING ( 7 FDA reports)
GOUT ( 7 FDA reports)
HEART DISEASE CONGENITAL ( 7 FDA reports)
HEART RATE DECREASED ( 7 FDA reports)
HYDROCELE ( 7 FDA reports)
HYPERKERATOSIS ( 7 FDA reports)
HYPERPARATHYROIDISM ( 7 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 7 FDA reports)
IRON DEFICIENCY ( 7 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 7 FDA reports)
JOINT INJURY ( 7 FDA reports)
KLEBSIELLA INFECTION ( 7 FDA reports)
LACTIC ACIDOSIS ( 7 FDA reports)
LEG AMPUTATION ( 7 FDA reports)
LIMB DISCOMFORT ( 7 FDA reports)
LUMBAR RADICULOPATHY ( 7 FDA reports)
LYMPHADENITIS ( 7 FDA reports)
MENINGITIS ( 7 FDA reports)
MENTAL DISORDER ( 7 FDA reports)
METRORRHAGIA ( 7 FDA reports)
MITRAL VALVE PROLAPSE ( 7 FDA reports)
MULTI-ORGAN DISORDER ( 7 FDA reports)
NASAL SEPTUM DEVIATION ( 7 FDA reports)
NEPHROTIC SYNDROME ( 7 FDA reports)
NERVOUS SYSTEM DISORDER ( 7 FDA reports)
NEURITIS ( 7 FDA reports)
NEUTROPHIL COUNT INCREASED ( 7 FDA reports)
NOCTURIA ( 7 FDA reports)
ONYCHOMADESIS ( 7 FDA reports)
OTITIS EXTERNA ( 7 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 7 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 7 FDA reports)
PORTAL HYPERTENSION ( 7 FDA reports)
PROSTATE CANCER ( 7 FDA reports)
PULMONARY MASS ( 7 FDA reports)
RADICULOPATHY ( 7 FDA reports)
RESPIRATORY RATE INCREASED ( 7 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 7 FDA reports)
SEBORRHOEIC DERMATITIS ( 7 FDA reports)
SKIN DESQUAMATION ( 7 FDA reports)
SKIN FISSURES ( 7 FDA reports)
SKIN INDURATION ( 7 FDA reports)
SKIN NECROSIS ( 7 FDA reports)
SKIN REACTION ( 7 FDA reports)
SKIN TEST POSITIVE ( 7 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 7 FDA reports)
SOFT TISSUE DISORDER ( 7 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 7 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
TONGUE OEDEMA ( 7 FDA reports)
TONSILLITIS ( 7 FDA reports)
TOOTH DISCOLOURATION ( 7 FDA reports)
TOOTH DISORDER ( 7 FDA reports)
TUBERCULOSIS ( 7 FDA reports)
TUMOUR HAEMORRHAGE ( 7 FDA reports)
URINARY INCONTINENCE ( 7 FDA reports)
VASCULAR COMPRESSION ( 7 FDA reports)
VASCULITIS ( 7 FDA reports)
VISUAL FIELD DEFECT ( 7 FDA reports)
VITREOUS FLOATERS ( 7 FDA reports)
X-RAY ABNORMAL ( 7 FDA reports)
ABSCESS LIMB ( 6 FDA reports)
ACTINOMYCOSIS ( 6 FDA reports)
ADDISON'S DISEASE ( 6 FDA reports)
ADENOCARCINOMA ( 6 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 6 FDA reports)
ANOSMIA ( 6 FDA reports)
AORTIC STENOSIS ( 6 FDA reports)
APNOEA ( 6 FDA reports)
APPENDICITIS ( 6 FDA reports)
ARTHRITIS INFECTIVE ( 6 FDA reports)
AUTISM ( 6 FDA reports)
BENIGN OVARIAN TUMOUR ( 6 FDA reports)
BILE DUCT STONE ( 6 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 6 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 6 FDA reports)
BLOOD GLUCOSE DECREASED ( 6 FDA reports)
BLOOD POTASSIUM INCREASED ( 6 FDA reports)
BONE EROSION ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 6 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 6 FDA reports)
CELLULITIS ORBITAL ( 6 FDA reports)
CEREBRAL INFARCTION ( 6 FDA reports)
CEREBROVASCULAR DISORDER ( 6 FDA reports)
CHOLESTEATOMA ( 6 FDA reports)
COLITIS ISCHAEMIC ( 6 FDA reports)
CONGENITAL ANOMALY ( 6 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 6 FDA reports)
CORONARY ARTERY STENOSIS ( 6 FDA reports)
CULTURE URINE POSITIVE ( 6 FDA reports)
DERMAL CYST ( 6 FDA reports)
DERMATITIS CONTACT ( 6 FDA reports)
DIVERTICULUM INTESTINAL ( 6 FDA reports)
DRUG DISPENSING ERROR ( 6 FDA reports)
DRUG EFFECT DECREASED ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 6 FDA reports)
EDENTULOUS ( 6 FDA reports)
ENTEROCOCCAL INFECTION ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
EXOMPHALOS ( 6 FDA reports)
EYE DISORDER ( 6 FDA reports)
EYE HAEMORRHAGE ( 6 FDA reports)
FEELING GUILTY ( 6 FDA reports)
FIBROMA ( 6 FDA reports)
FLUID INTAKE REDUCED ( 6 FDA reports)
FOREIGN BODY TRAUMA ( 6 FDA reports)
FRACTURED SACRUM ( 6 FDA reports)
FUNGAL SKIN INFECTION ( 6 FDA reports)
GASTRIC DISORDER ( 6 FDA reports)
GASTRIC POLYPS ( 6 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 6 FDA reports)
GENERALISED ANXIETY DISORDER ( 6 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 6 FDA reports)
GOITRE ( 6 FDA reports)
GROWTH RETARDATION ( 6 FDA reports)
HAEMOLYSIS ( 6 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 6 FDA reports)
HEPATIC FIBROSIS ( 6 FDA reports)
HEPATIC TRAUMA ( 6 FDA reports)
HEPATIC VEIN THROMBOSIS ( 6 FDA reports)
HEPATITIS C ( 6 FDA reports)
HERPES SIMPLEX ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HODGKIN'S DISEASE ( 6 FDA reports)
HYDROURETER ( 6 FDA reports)
HYPERMETABOLISM ( 6 FDA reports)
HYPOTONIA ( 6 FDA reports)
HYPOVOLAEMIC SHOCK ( 6 FDA reports)
IMPAIRED WORK ABILITY ( 6 FDA reports)
INJECTION SITE THROMBOSIS ( 6 FDA reports)
INTENTIONAL OVERDOSE ( 6 FDA reports)
INTESTINAL HAEMORRHAGE ( 6 FDA reports)
IRON DEFICIENCY ANAEMIA ( 6 FDA reports)
JOINT CREPITATION ( 6 FDA reports)
JUGULAR VEIN THROMBOSIS ( 6 FDA reports)
KYPHOSCOLIOSIS ( 6 FDA reports)
LEFT ATRIAL DILATATION ( 6 FDA reports)
LIMB INJURY ( 6 FDA reports)
LIP DRY ( 6 FDA reports)
LOBAR PNEUMONIA ( 6 FDA reports)
MAJOR DEPRESSION ( 6 FDA reports)
MECHANICAL VENTILATION ( 6 FDA reports)
MOOD ALTERED ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MUCOUS MEMBRANE DISORDER ( 6 FDA reports)
MYELOMA RECURRENCE ( 6 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
NODULE ( 6 FDA reports)
OCULAR ICTERUS ( 6 FDA reports)
OLIGURIA ( 6 FDA reports)
OSTEOCHONDROSIS ( 6 FDA reports)
PAPILLOMA ( 6 FDA reports)
PHARYNGEAL ERYTHEMA ( 6 FDA reports)
PLEURISY ( 6 FDA reports)
POLYARTHRITIS ( 6 FDA reports)
POLYURIA ( 6 FDA reports)
PRESCRIBED OVERDOSE ( 6 FDA reports)
PROSTATITIS ( 6 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 6 FDA reports)
RENAL ARTERY STENOSIS ( 6 FDA reports)
RESPIRATION ABNORMAL ( 6 FDA reports)
RESPIRATORY ACIDOSIS ( 6 FDA reports)
SCAB ( 6 FDA reports)
SELF ESTEEM DECREASED ( 6 FDA reports)
SENSORY LOSS ( 6 FDA reports)
SHOCK HAEMORRHAGIC ( 6 FDA reports)
SKELETAL INJURY ( 6 FDA reports)
SKIN ATROPHY ( 6 FDA reports)
SKIN HYPERTROPHY ( 6 FDA reports)
SKIN INFECTION ( 6 FDA reports)
SPLEEN DISORDER ( 6 FDA reports)
SPONDYLOLYSIS ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
STOMACH DISCOMFORT ( 6 FDA reports)
SUBCUTANEOUS ABSCESS ( 6 FDA reports)
TENDON RUPTURE ( 6 FDA reports)
THROMBOSIS IN DEVICE ( 6 FDA reports)
TONGUE ULCERATION ( 6 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 6 FDA reports)
TROPONIN INCREASED ( 6 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 6 FDA reports)
VAGINAL DISCHARGE ( 6 FDA reports)
VARICOSE VEIN ( 6 FDA reports)
VIBRATION TEST ABNORMAL ( 6 FDA reports)
VULVOVAGINITIS ( 6 FDA reports)
WHIPLASH INJURY ( 6 FDA reports)
YELLOW SKIN ( 6 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
ABSCESS NECK ( 5 FDA reports)
ABSCESS ORAL ( 5 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
AMMONIA INCREASED ( 5 FDA reports)
ANAEMIA MACROCYTIC ( 5 FDA reports)
ANAL ABSCESS ( 5 FDA reports)
ANGIOPATHY ( 5 FDA reports)
AORTIC ANEURYSM ( 5 FDA reports)
AORTIC VALVE DISEASE ( 5 FDA reports)
AORTIC VALVE SCLEROSIS ( 5 FDA reports)
AREFLEXIA ( 5 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
ARTHROSCOPY ( 5 FDA reports)
ATAXIA ( 5 FDA reports)
ATRIAL FLUTTER ( 5 FDA reports)
ATRIAL SEPTAL DEFECT ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 5 FDA reports)
BIOPSY BONE ABNORMAL ( 5 FDA reports)
BIPOLAR I DISORDER ( 5 FDA reports)
BLINDNESS ( 5 FDA reports)
BLOOD IRON DECREASED ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
BREATH SOUNDS ABNORMAL ( 5 FDA reports)
BRONCHIAL HYPERACTIVITY ( 5 FDA reports)
BRONCHIECTASIS ( 5 FDA reports)
BRONCHITIS ACUTE ( 5 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 5 FDA reports)
CACHEXIA ( 5 FDA reports)
CARDIAC FLUTTER ( 5 FDA reports)
CHOLESTATIC LIVER INJURY ( 5 FDA reports)
CLUMSINESS ( 5 FDA reports)
CONJUNCTIVITIS VIRAL ( 5 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 5 FDA reports)
CORONARY ARTERY OCCLUSION ( 5 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 5 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 5 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
DIABETIC FOOT ( 5 FDA reports)
DIABETIC KETOACIDOSIS ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 5 FDA reports)
DUODENOGASTRIC REFLUX ( 5 FDA reports)
DYSHIDROSIS ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 5 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 5 FDA reports)
EPIDERMAL NECROSIS ( 5 FDA reports)
ERYTHEMA OF EYELID ( 5 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 5 FDA reports)
EXANTHEM ( 5 FDA reports)
EXCORIATION ( 5 FDA reports)
EXTREMITY NECROSIS ( 5 FDA reports)
EYE ALLERGY ( 5 FDA reports)
EYE ROLLING ( 5 FDA reports)
FANCONI SYNDROME ( 5 FDA reports)
FIBULA FRACTURE ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
GASTROENTERITIS RADIATION ( 5 FDA reports)
GLAUCOMA ( 5 FDA reports)
GLOBULINS INCREASED ( 5 FDA reports)
GLOSSITIS ( 5 FDA reports)
HAEMATOMA INFECTION ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 5 FDA reports)
HEPATIC ENZYME ABNORMAL ( 5 FDA reports)
HEPATIC NEOPLASM ( 5 FDA reports)
HIP ARTHROPLASTY ( 5 FDA reports)
HOMICIDAL IDEATION ( 5 FDA reports)
HYPERVIGILANCE ( 5 FDA reports)
HYPOACUSIS ( 5 FDA reports)
HYPOAESTHESIA ORAL ( 5 FDA reports)
HYPOGONADISM MALE ( 5 FDA reports)
HYPOVOLAEMIA ( 5 FDA reports)
ILEITIS ( 5 FDA reports)
INGROWING NAIL ( 5 FDA reports)
INTENTIONAL SELF-INJURY ( 5 FDA reports)
INTRACARDIAC THROMBUS ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
LOOSE TOOTH ( 5 FDA reports)
MALIGNANT MELANOMA ( 5 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 5 FDA reports)
METASTASES TO PANCREAS ( 5 FDA reports)
METASTASES TO PELVIS ( 5 FDA reports)
MICROCYTIC ANAEMIA ( 5 FDA reports)
NASAL ULCER ( 5 FDA reports)
NECK MASS ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
OCULAR HYPERAEMIA ( 5 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 5 FDA reports)
ORAL HERPES ( 5 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 5 FDA reports)
PELVIC ABSCESS ( 5 FDA reports)
PENILE INFECTION ( 5 FDA reports)
PERIORBITAL CELLULITIS ( 5 FDA reports)
POLYNEUROPATHY ( 5 FDA reports)
POSTOPERATIVE INFECTION ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
PROSTATE CANCER METASTATIC ( 5 FDA reports)
PROSTATOMEGALY ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
RASH SCARLATINIFORM ( 5 FDA reports)
RASH VESICULAR ( 5 FDA reports)
RENAL COLIC ( 5 FDA reports)
RENAL PAIN ( 5 FDA reports)
RHONCHI ( 5 FDA reports)
RIGHT ATRIAL DILATATION ( 5 FDA reports)
SCREAMING ( 5 FDA reports)
SEASONAL ALLERGY ( 5 FDA reports)
SKIN OEDEMA ( 5 FDA reports)
STRESS FRACTURE ( 5 FDA reports)
SUBDURAL HAEMATOMA ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
TESTICULAR PAIN ( 5 FDA reports)
THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TONGUE DISORDER ( 5 FDA reports)
URETERAL NEOPLASM ( 5 FDA reports)
URETHRAL OBSTRUCTION ( 5 FDA reports)
URINE OUTPUT DECREASED ( 5 FDA reports)
URTICARIA GENERALISED ( 5 FDA reports)
UTERINE HAEMORRHAGE ( 5 FDA reports)
UTERINE MASS ( 5 FDA reports)
UVEITIS ( 5 FDA reports)
WOUND SECRETION ( 5 FDA reports)
ABDOMINAL MASS ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 4 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 4 FDA reports)
ADENOIDECTOMY ( 4 FDA reports)
ADRENOCORTICAL CARCINOMA ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
AKATHISIA ( 4 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 4 FDA reports)
ALCOHOL ABUSE ( 4 FDA reports)
ALVEOLAR OSTEITIS ( 4 FDA reports)
ALVEOLAR PROTEINOSIS ( 4 FDA reports)
ANAEMIA NEONATAL ( 4 FDA reports)
ANAEMIA POSTOPERATIVE ( 4 FDA reports)
ANOXIC ENCEPHALOPATHY ( 4 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 4 FDA reports)
APLASIA PURE RED CELL ( 4 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 4 FDA reports)
ATROPHIC GLOSSITIS ( 4 FDA reports)
AUTOIMMUNE HEPATITIS ( 4 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 4 FDA reports)
BLOOD CALCIUM INCREASED ( 4 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
BLOOD DISORDER ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 4 FDA reports)
BLOOD LACTIC ACID INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 4 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 4 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
BREAST CANCER RECURRENT ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
BRONCHOPLEURAL FISTULA ( 4 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 4 FDA reports)
CALCIFICATION METASTATIC ( 4 FDA reports)
CARDIAC FAILURE CHRONIC ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CHOLECYSTITIS ACUTE ( 4 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
COMPRESSION FRACTURE ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
DEBRIDEMENT ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
DIAPHRAGMATIC HERNIA ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
DRUG ABUSE ( 4 FDA reports)
EAR HAEMORRHAGE ( 4 FDA reports)
ECZEMA INFECTED ( 4 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 4 FDA reports)
EMBOLISM ( 4 FDA reports)
ENANTHEMA ( 4 FDA reports)
ENCEPHALITIS HERPES ( 4 FDA reports)
ENDOCARDITIS ( 4 FDA reports)
ENTEROCOLONIC FISTULA ( 4 FDA reports)
EOSINOPHIL COUNT DECREASED ( 4 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 4 FDA reports)
ERUCTATION ( 4 FDA reports)
ERYSIPELAS ( 4 FDA reports)
EXTRASYSTOLES ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
FACIAL BONES FRACTURE ( 4 FDA reports)
FEBRILE BONE MARROW APLASIA ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FEELING JITTERY ( 4 FDA reports)
FISTULA ( 4 FDA reports)
FOLATE DEFICIENCY ( 4 FDA reports)
FURUNCLE ( 4 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 4 FDA reports)
GASTROENTERITIS VIRAL ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 4 FDA reports)
GINGIVAL DISORDER ( 4 FDA reports)
GLOSSODYNIA ( 4 FDA reports)
GOUTY ARTHRITIS ( 4 FDA reports)
GRANULOCYTOPENIA ( 4 FDA reports)
HAEMOTHORAX ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HEPATITIS A ( 4 FDA reports)
HEPATITIS TOXIC ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
HISTOPLASMOSIS ( 4 FDA reports)
HIV INFECTION ( 4 FDA reports)
HUMERUS FRACTURE ( 4 FDA reports)
HYPERAEMIA ( 4 FDA reports)
HYPERTHYROIDISM ( 4 FDA reports)
HYPERTRANSAMINASAEMIA ( 4 FDA reports)
IMMUNE SYSTEM DISORDER ( 4 FDA reports)
IMPAIRED DRIVING ABILITY ( 4 FDA reports)
IMPAIRED SELF-CARE ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 4 FDA reports)
INTRA-UTERINE DEATH ( 4 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
JAW DISORDER ( 4 FDA reports)
JOINT STIFFNESS ( 4 FDA reports)
KAPOSI'S SARCOMA ( 4 FDA reports)
KNEE OPERATION ( 4 FDA reports)
LARYNGITIS ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LEUKODYSTROPHY ( 4 FDA reports)
LUNG ABSCESS ( 4 FDA reports)
LUNG INJURY ( 4 FDA reports)
LYMPH NODE PALPABLE ( 4 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 4 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
MENISCUS LESION ( 4 FDA reports)
MENOPAUSAL SYMPTOMS ( 4 FDA reports)
MIXED HYPERLIPIDAEMIA ( 4 FDA reports)
MONOCYTE COUNT DECREASED ( 4 FDA reports)
MOTOR DYSFUNCTION ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
NASAL VESTIBULITIS ( 4 FDA reports)
NECK INJURY ( 4 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 4 FDA reports)
NEUROPATHY ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
OESOPHAGEAL DISORDER ( 4 FDA reports)
OLIGOMENORRHOEA ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
ORAL SURGERY ( 4 FDA reports)
ORGAN FAILURE ( 4 FDA reports)
OTITIS MEDIA ACUTE ( 4 FDA reports)
OTITIS MEDIA CHRONIC ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 4 FDA reports)
PANCREATIC CYST ( 4 FDA reports)
PARKINSON'S DISEASE ( 4 FDA reports)
PAROTITIS ( 4 FDA reports)
PERIPHERAL COLDNESS ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PERIVASCULAR DERMATITIS ( 4 FDA reports)
PIGMENTATION DISORDER ( 4 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 4 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 4 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 4 FDA reports)
PROSTATE INFECTION ( 4 FDA reports)
PROTEUS INFECTION ( 4 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
PYELOCALIECTASIS ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
RECTAL ABSCESS ( 4 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
RETINOPATHY ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 4 FDA reports)
SENSATION OF HEAVINESS ( 4 FDA reports)
SERUM FERRITIN INCREASED ( 4 FDA reports)
SINUS ARRHYTHMIA ( 4 FDA reports)
SINUS HEADACHE ( 4 FDA reports)
SKIN TEST NEGATIVE ( 4 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 4 FDA reports)
SOCIAL PROBLEM ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 4 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
THROMBOPHLEBITIS ( 4 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 4 FDA reports)
THYROID NEOPLASM ( 4 FDA reports)
TOOTH FRACTURE ( 4 FDA reports)
TRISMUS ( 4 FDA reports)
TROPONIN T INCREASED ( 4 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
URETERIC STENOSIS ( 4 FDA reports)
URINARY TRACT OBSTRUCTION ( 4 FDA reports)
UROSEPSIS ( 4 FDA reports)
VASCULAR OCCLUSION ( 4 FDA reports)
VIITH NERVE PARALYSIS ( 4 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
WOUND ( 4 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
WRIST FRACTURE ( 4 FDA reports)
ABDOMINAL HAEMATOMA ( 3 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
ABORTION MISSED ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ALLERGY TEST POSITIVE ( 3 FDA reports)
AMENORRHOEA ( 3 FDA reports)
ANAL FISTULA ( 3 FDA reports)
ANEURYSM ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
APGAR SCORE LOW ( 3 FDA reports)
APLASIA ( 3 FDA reports)
ARTERIAL INSUFFICIENCY ( 3 FDA reports)
ARTHROPOD BITE ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BACTERIAL TEST POSITIVE ( 3 FDA reports)
BARRETT'S OESOPHAGUS ( 3 FDA reports)
BILIARY DYSKINESIA ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLINDNESS CORTICAL ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BODY TINEA ( 3 FDA reports)
BONE CYST ( 3 FDA reports)
BONE FISTULA ( 3 FDA reports)
BONE SCAN ABNORMAL ( 3 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 3 FDA reports)
BRONCHIAL INFECTION ( 3 FDA reports)
BUNION OPERATION ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
CALCULUS BLADDER ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CARDIAC DEATH ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CATHETER RELATED COMPLICATION ( 3 FDA reports)
CAUDA EQUINA SYNDROME ( 3 FDA reports)
CEREBELLAR HAEMORRHAGE ( 3 FDA reports)
CEREBRAL DISORDER ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHAPPED LIPS ( 3 FDA reports)
CHOLURIA ( 3 FDA reports)
CHONDROMALACIA ( 3 FDA reports)
COAGULATION FACTOR DECREASED ( 3 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 3 FDA reports)
COARCTATION OF THE AORTA ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COLON ADENOMA ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DISBACTERIOSIS ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DYSPNOEA EXACERBATED ( 3 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
EJACULATION DISORDER ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
EMPYEMA ( 3 FDA reports)
ENTEROCOCCAL SEPSIS ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
EXFOLIATIVE RASH ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
FEBRILE INFECTION ( 3 FDA reports)
FOETAL DISTRESS SYNDROME ( 3 FDA reports)
FOETAL HEART RATE DECELERATION ( 3 FDA reports)
FOLLICULITIS ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
GASTRODUODENITIS ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HAEMORRHAGIC DISORDER ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEAD DISCOMFORT ( 3 FDA reports)
HEPATITIS ALCOHOLIC ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HOSTILITY ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
HYPOAESTHESIA FACIAL ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
INCISION SITE COMPLICATION ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INFERTILITY ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
LIPOMA ( 3 FDA reports)
LIVER TRANSPLANT ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
LUNG CREPITATION ( 3 FDA reports)
LYMPHOCELE ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MEDIASTINITIS ( 3 FDA reports)
MENINGIOMA ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
METATARSUS PRIMUS VARUS ( 3 FDA reports)
MONOCYTOPENIA ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
MYCOSIS FUNGOIDES ( 3 FDA reports)
MYOFASCIAL SPASM ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NEONATAL DISORDER ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 3 FDA reports)
NUCHAL RIGIDITY ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
OEDEMA GENITAL ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
OVARIAN ABSCESS ( 3 FDA reports)
PALATAL DISORDER ( 3 FDA reports)
PARAPROTEINAEMIA ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PIGMENTARY GLAUCOMA ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
POLYP ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
PORTAL VEIN THROMBOSIS ( 3 FDA reports)
POSTNASAL DRIP ( 3 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 3 FDA reports)
POVERTY OF THOUGHT CONTENT ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
PRINZMETAL ANGINA ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PROCEDURAL SITE REACTION ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULMONARY ARTERY DILATATION ( 3 FDA reports)
PULMONARY VASCULAR DISORDER ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RETCHING ( 3 FDA reports)
RETROPERITONEAL HAEMATOMA ( 3 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SCROTAL SWELLING ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SHOULDER ARTHROPLASTY ( 3 FDA reports)
SINUS CONGESTION ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
SLEEP TERROR ( 3 FDA reports)
SMEAR CERVIX ABNORMAL ( 3 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 3 FDA reports)
SPUTUM ABNORMAL ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SUPERINFECTION LUNG ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
TENDON CALCIFICATION ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THERAPY REGIMEN CHANGED ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
TIBIA FRACTURE ( 3 FDA reports)
TINEA PEDIS ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TOOTH INFECTION ( 3 FDA reports)
TOOTH INJURY ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 3 FDA reports)
ULNAR NERVE INJURY ( 3 FDA reports)
UMBILICAL HERNIA ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
UTERINE CANCER ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
VITAMIN B12 DEFICIENCY ( 3 FDA reports)
WOUND DEBRIDEMENT ( 3 FDA reports)
WOUND DEHISCENCE ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
XEROSIS ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABSCESS MANAGEMENT ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ACROCHORDON ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANOGENITAL WARTS ( 2 FDA reports)
ANTI FACTOR V ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APALLIC SYNDROME ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ASTHMA EXERCISE INDUCED ( 2 FDA reports)
ASTIGMATISM ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BENIGN BONE NEOPLASM ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BONE MARROW OEDEMA ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRAIN COMPRESSION ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BREAST OEDEMA ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BREATH SOUNDS DECREASED ( 2 FDA reports)
BRONCHITIS BACTERIAL ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
BUNION ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CAROTID ARTERY DISEASE ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CHEILOSIS ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CHOLESTEROSIS ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CLEFT LIP ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 2 FDA reports)
COAGULATION TIME SHORTENED ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 2 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 2 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
CYSTITIS RADIATION ( 2 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 2 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DENTAL IMPLANTATION ( 2 FDA reports)
DENTAL PLAQUE ( 2 FDA reports)
DERMATITIS INFECTED ( 2 FDA reports)
DERMO-HYPODERMITIS ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DUODENAL POLYP ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
EOSINOPHILIC CELLULITIS ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 2 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FACTOR V DEFICIENCY ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROENTERITIS HELICOBACTER ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GENITAL EROSION ( 2 FDA reports)
GENITAL ERYTHEMA ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
GINGIVAL ERYTHEMA ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GLOMERULONEPHROPATHY ( 2 FDA reports)
HAEMATOMA EVACUATION ( 2 FDA reports)
HAEMATOMETRA ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEART TRANSPLANT ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEPATITIS VIRAL ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HISTAMINE LEVEL INCREASED ( 2 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERSPLENISM ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPERTONIC BLADDER ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOGONADISM ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
IMPLANT SITE EROSION ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTERCOSTAL NEURALGIA ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTESTINAL MASS ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LICE INFESTATION ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LOCALISED SKIN REACTION ( 2 FDA reports)
LUNG HYPERINFLATION ( 2 FDA reports)
LYMPH GLAND INFECTION ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MANIA ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 2 FDA reports)
MAXILLOFACIAL OPERATION ( 2 FDA reports)
MEDICATION CRYSTALS IN URINE ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENINGOCELE ( 2 FDA reports)
MENINGORRHAGIA ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTATIC GASTRIC CANCER ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
MICROCYTOSIS ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MONOCLONAL GAMMOPATHY ( 2 FDA reports)
MONOCYTOSIS ( 2 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
MYELOCYTOSIS ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYOFASCITIS ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NARCOTIC INTOXICATION ( 2 FDA reports)
NASAL ODOUR ( 2 FDA reports)
NEPHRITIC SYNDROME ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESTROGENIC EFFECT ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
ORAL DISCHARGE ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OVARIAN NEOPLASM ( 2 FDA reports)
OVERGROWTH BACTERIAL ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PELVIC MASS ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIDIVERTICULAR ABSCESS ( 2 FDA reports)
PERIRENAL HAEMATOMA ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PH URINE INCREASED ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 2 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PREMATURE DELIVERY ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
PSEUDOPHAKIA ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY ARTERY STENOSIS ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 2 FDA reports)
PYOTHORAX ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RECTOSIGMOID CANCER ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 2 FDA reports)
REHABILITATION THERAPY ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL LIPOMATOSIS ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETICULOCYTOSIS ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLEEP INERTIA ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPECIFIC GRAVITY URINE DECREASED ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STARING ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 2 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 2 FDA reports)
STRESS AT WORK ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBRETINAL FIBROSIS ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TACHYCARDIA FOETAL ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TONGUE BLACK HAIRY ( 2 FDA reports)
TONGUE COATED ( 2 FDA reports)
TONGUE ERUPTION ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TOOTH IMPACTED ( 2 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 2 FDA reports)
TRANSAMINASES ABNORMAL ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
TWIN PREGNANCY ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
VAGINAL LESION ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VENOUS STENOSIS ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENOUS VALVE RUPTURED ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VITAMIN K DEFICIENCY ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
VULVOVAGINAL PRURITUS ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABDOMINAL X-RAY ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACHOLIA ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 1 FDA reports)
AIRWAY PEAK PRESSURE INCREASED ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANAL POLYP ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANAL STENOSIS ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC ANTIBODY NEGATIVE ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTA HYPOPLASIA ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE REPAIR ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APICAL GRANULOMA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTHROPOD-BORNE DISEASE ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ASPLENIA ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTISM SPECTRUM DISORDER ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AZOOSPERMIA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLAST CELLS ABSENT ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLEPHAROSYNECHIA ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PYRUVIC ACID DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BONE SARCOMA ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOMALACIA ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE RASH ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 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 ACCIDENT PROPHYLAXIS ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEMICAL EYE INJURY ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHLAMYDIA TEST POSITIVE ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLANGIOLITIS ( 1 FDA reports)
CHOLESTASIS OF PREGNANCY ( 1 FDA reports)
CHONDROMA ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR IX LEVEL DECREASED ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 1 FDA reports)
CONGENITAL TRACHEOMALACIA ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIOSYNOSTOSIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CRYOFIBRINOGENAEMIA ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CRYSTALLURIA ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DACRYOSTENOSIS CONGENITAL ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE BATTERY ISSUE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DEXTROCARDIA ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC CARDIOMYOPATHY ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPLASTIC NAEVUS ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ELECTROPHORESIS ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ERYTHEMA MARGINATUM ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 1 FDA reports)
EUTHANASIA ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR IX INHIBITION ( 1 FDA reports)
FACTOR VII DEFICIENCY ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FEMORAL NERVE PALSY ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA DIFFUSE SMALL CELL LYMPHOMA ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL LABIAL ADHESIONS ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GENITAL TRACT INFLAMMATION ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE PARALYSIS ( 1 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOLYTIC ICTEROANAEMIA ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAIR PLUCKING ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC EMBOLISATION ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 1 FDA reports)
HETEROTAXIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERGLOBULINAEMIA ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HYPERSPLENISM ACQUIRED ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPACTED FRACTURE ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE MASS ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAUNDICE HEPATOCELLULAR ( 1 FDA reports)
JEJUNITIS ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LABOUR COMPLICATION ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGOMALACIA ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP SLOUGHING ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHANGIECTASIA ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOCYTE TRANSFORMATION TEST POSITIVE ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
LYMPHORRHOEA ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACROPHAGE ACTIVATION ( 1 FDA reports)
MACROPHAGES INCREASED ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MAMMOPLASTY ( 1 FDA reports)
MANTLE CELL LYMPHOMA RECURRENT ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 1 FDA reports)
MEDIASTINAL SHIFT ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYOGLOBIN BLOOD DECREASED ( 1 FDA reports)
MYOKYMIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEPHROSTOMY ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPENIA NEONATAL ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL MASS ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PENILE EXFOLIATION ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL CYST ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL NERVE TRANSPOSITION ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PH BODY FLUID INCREASED ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBOSCLEROSIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PITYRIASIS ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET FACTOR 4 INCREASED ( 1 FDA reports)
PLEURAL CALCIFICATION ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POISONING ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 1 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTPARTUM DEPRESSION ( 1 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROLONGED LABOUR ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PROSTATIC CALCIFICATION ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURITUS ALLERGIC ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
RADIATION OESOPHAGITIS ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
REACTION TO DRUG EXCIPIENT ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RED BLOOD CELL COUNT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL AMYLOIDOSIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL CYST INFECTION ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
RETROPHARYNGEAL ABSCESS ( 1 FDA reports)
RETROSTERNAL INFECTION ( 1 FDA reports)
RHESUS ANTIBODIES POSITIVE ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
SCAN BONE MARROW ABNORMAL ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCAR EXCISION ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SEIZURE ANOXIC ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SHONE COMPLEX ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUS POLYP ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPINOCEREBELLAR ATAXIA ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
THALASSAEMIA ( 1 FDA reports)
THALASSAEMIA BETA ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYMECTOMY ( 1 FDA reports)
THYMUS ENLARGEMENT ( 1 FDA reports)
THYROID CYST ( 1 FDA reports)
THYROID FIBROSIS ( 1 FDA reports)
THYROID HAEMORRHAGE ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE DESQUAMATION ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONGUE PRURITUS ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 1 FDA reports)
TRYPTASE ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE FIBROSIS ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL CYST ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENOUS HAEMORRHAGE ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS RECANALISATION ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIRAL TONSILLITIS ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WHITE CLOT IN BLOOD PRESENT ( 1 FDA reports)
WOUND EVISCERATION ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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