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

NAUSEA ( 427 FDA reports)
RHABDOMYOLYSIS ( 392 FDA reports)
DYSPNOEA ( 381 FDA reports)
RENAL FAILURE ACUTE ( 370 FDA reports)
DIZZINESS ( 367 FDA reports)
PAIN ( 355 FDA reports)
ASTHENIA ( 347 FDA reports)
DIARRHOEA ( 319 FDA reports)
FATIGUE ( 311 FDA reports)
ANXIETY ( 301 FDA reports)
CHEST PAIN ( 282 FDA reports)
DEPRESSION ( 270 FDA reports)
VOMITING ( 261 FDA reports)
MYOCARDIAL INFARCTION ( 260 FDA reports)
MYALGIA ( 255 FDA reports)
ANAEMIA ( 247 FDA reports)
DIABETES MELLITUS ( 243 FDA reports)
DRUG INTERACTION ( 236 FDA reports)
PAIN IN EXTREMITY ( 233 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 230 FDA reports)
HEADACHE ( 228 FDA reports)
DRUG INEFFECTIVE ( 225 FDA reports)
WEIGHT DECREASED ( 224 FDA reports)
OEDEMA PERIPHERAL ( 223 FDA reports)
FALL ( 220 FDA reports)
BACK PAIN ( 217 FDA reports)
ARTHRALGIA ( 216 FDA reports)
BLOOD GLUCOSE INCREASED ( 213 FDA reports)
PNEUMONIA ( 197 FDA reports)
ABDOMINAL PAIN ( 190 FDA reports)
RENAL FAILURE ( 181 FDA reports)
HYPOTENSION ( 179 FDA reports)
WEIGHT INCREASED ( 176 FDA reports)
HYPERTENSION ( 170 FDA reports)
DEHYDRATION ( 168 FDA reports)
PANCREATITIS ( 164 FDA reports)
MALAISE ( 161 FDA reports)
PYREXIA ( 161 FDA reports)
INSOMNIA ( 157 FDA reports)
CONSTIPATION ( 156 FDA reports)
RASH ( 156 FDA reports)
MUSCLE SPASMS ( 154 FDA reports)
HYPOAESTHESIA ( 151 FDA reports)
COUGH ( 148 FDA reports)
INJURY ( 148 FDA reports)
PARAESTHESIA ( 148 FDA reports)
CEREBROVASCULAR ACCIDENT ( 145 FDA reports)
DEATH ( 145 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 144 FDA reports)
CONFUSIONAL STATE ( 139 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 138 FDA reports)
CORONARY ARTERY DISEASE ( 137 FDA reports)
FLUSHING ( 137 FDA reports)
ATRIAL FIBRILLATION ( 131 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 129 FDA reports)
SYNCOPE ( 125 FDA reports)
TYPE 2 DIABETES MELLITUS ( 122 FDA reports)
FEELING ABNORMAL ( 120 FDA reports)
GAIT DISTURBANCE ( 118 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 117 FDA reports)
URINARY TRACT INFECTION ( 117 FDA reports)
ABDOMINAL PAIN UPPER ( 115 FDA reports)
PRURITUS ( 114 FDA reports)
LOSS OF CONSCIOUSNESS ( 111 FDA reports)
THROMBOCYTOPENIA ( 107 FDA reports)
HYPOGLYCAEMIA ( 106 FDA reports)
BLOOD CREATININE INCREASED ( 102 FDA reports)
HAEMOGLOBIN DECREASED ( 102 FDA reports)
VISION BLURRED ( 101 FDA reports)
HYPERLIPIDAEMIA ( 100 FDA reports)
PALPITATIONS ( 100 FDA reports)
HYPERKALAEMIA ( 98 FDA reports)
DECREASED APPETITE ( 95 FDA reports)
MENTAL STATUS CHANGES ( 95 FDA reports)
MUSCULAR WEAKNESS ( 94 FDA reports)
TREMOR ( 94 FDA reports)
HYPERHIDROSIS ( 93 FDA reports)
NEUROPATHY PERIPHERAL ( 92 FDA reports)
OSTEOARTHRITIS ( 92 FDA reports)
CONDITION AGGRAVATED ( 90 FDA reports)
HYPERCHOLESTEROLAEMIA ( 90 FDA reports)
RENAL IMPAIRMENT ( 89 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 88 FDA reports)
RENAL FAILURE CHRONIC ( 88 FDA reports)
CONVULSION ( 87 FDA reports)
OSTEONECROSIS OF JAW ( 84 FDA reports)
CARDIAC ARREST ( 83 FDA reports)
HYPERGLYCAEMIA ( 83 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 82 FDA reports)
BRADYCARDIA ( 82 FDA reports)
ECONOMIC PROBLEM ( 82 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 80 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 79 FDA reports)
COMPLETED SUICIDE ( 79 FDA reports)
PLEURAL EFFUSION ( 79 FDA reports)
SOMNOLENCE ( 79 FDA reports)
CELLULITIS ( 78 FDA reports)
BLOOD PRESSURE INCREASED ( 77 FDA reports)
CARDIAC DISORDER ( 77 FDA reports)
SEPSIS ( 77 FDA reports)
CONTUSION ( 75 FDA reports)
RESPIRATORY FAILURE ( 74 FDA reports)
MUSCULOSKELETAL PAIN ( 73 FDA reports)
DYSURIA ( 72 FDA reports)
HYPERSENSITIVITY ( 71 FDA reports)
ERYTHEMA ( 70 FDA reports)
MEMORY IMPAIRMENT ( 70 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 70 FDA reports)
ANHEDONIA ( 68 FDA reports)
CHILLS ( 68 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 68 FDA reports)
ABDOMINAL DISTENSION ( 66 FDA reports)
AGITATION ( 66 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 66 FDA reports)
BRONCHITIS ( 65 FDA reports)
STRESS ( 65 FDA reports)
ANGINA PECTORIS ( 64 FDA reports)
DYSPEPSIA ( 64 FDA reports)
DYSPHAGIA ( 64 FDA reports)
SINUSITIS ( 64 FDA reports)
BLOOD GLUCOSE DECREASED ( 63 FDA reports)
PLATELET COUNT DECREASED ( 63 FDA reports)
MIGRAINE ( 62 FDA reports)
TACHYCARDIA ( 62 FDA reports)
TOOTHACHE ( 62 FDA reports)
BALANCE DISORDER ( 61 FDA reports)
BONE DISORDER ( 61 FDA reports)
TINNITUS ( 61 FDA reports)
UNEVALUABLE EVENT ( 61 FDA reports)
CHEST DISCOMFORT ( 60 FDA reports)
EMOTIONAL DISTRESS ( 60 FDA reports)
FLATULENCE ( 60 FDA reports)
HAEMORRHOIDS ( 60 FDA reports)
HYPOTHYROIDISM ( 60 FDA reports)
SLEEP DISORDER ( 60 FDA reports)
DYSGEUSIA ( 59 FDA reports)
OVERDOSE ( 59 FDA reports)
CARDIOMEGALY ( 58 FDA reports)
DRY MOUTH ( 58 FDA reports)
OBESITY ( 58 FDA reports)
ATELECTASIS ( 57 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 57 FDA reports)
OSTEONECROSIS ( 57 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 57 FDA reports)
CHOLELITHIASIS ( 56 FDA reports)
EXOSTOSIS ( 56 FDA reports)
HAEMATURIA ( 56 FDA reports)
IRRITABILITY ( 56 FDA reports)
DRUG DOSE OMISSION ( 55 FDA reports)
AMNESIA ( 54 FDA reports)
EPISTAXIS ( 54 FDA reports)
GASTRITIS ( 54 FDA reports)
HEPATIC ENZYME INCREASED ( 54 FDA reports)
SLEEP APNOEA SYNDROME ( 54 FDA reports)
ABNORMAL DREAMS ( 53 FDA reports)
ARRHYTHMIA ( 53 FDA reports)
HEART RATE IRREGULAR ( 53 FDA reports)
HEPATIC STEATOSIS ( 53 FDA reports)
OSTEOPOROSIS ( 52 FDA reports)
RECTAL HAEMORRHAGE ( 52 FDA reports)
SWELLING ( 52 FDA reports)
UNRESPONSIVE TO STIMULI ( 52 FDA reports)
ABASIA ( 51 FDA reports)
VISUAL ACUITY REDUCED ( 51 FDA reports)
DEEP VEIN THROMBOSIS ( 49 FDA reports)
DIABETIC NEUROPATHY ( 49 FDA reports)
DIVERTICULITIS ( 49 FDA reports)
INFECTION ( 49 FDA reports)
ABDOMINAL DISCOMFORT ( 48 FDA reports)
DRY SKIN ( 48 FDA reports)
HALLUCINATION ( 48 FDA reports)
OSTEOMYELITIS ( 48 FDA reports)
ARTHRITIS ( 47 FDA reports)
DRUG EFFECT DECREASED ( 47 FDA reports)
HYPONATRAEMIA ( 47 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 47 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 47 FDA reports)
CARDIAC MURMUR ( 46 FDA reports)
DYSPNOEA EXERTIONAL ( 46 FDA reports)
HEART RATE INCREASED ( 46 FDA reports)
HYPOACUSIS ( 46 FDA reports)
LETHARGY ( 46 FDA reports)
MITRAL VALVE INCOMPETENCE ( 46 FDA reports)
RASH PRURITIC ( 46 FDA reports)
DISABILITY ( 45 FDA reports)
MULTI-ORGAN FAILURE ( 45 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 45 FDA reports)
TREATMENT NONCOMPLIANCE ( 45 FDA reports)
DISTURBANCE IN ATTENTION ( 44 FDA reports)
HAEMORRHAGE ( 44 FDA reports)
HIATUS HERNIA ( 44 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 44 FDA reports)
NECK PAIN ( 44 FDA reports)
PULMONARY EMBOLISM ( 44 FDA reports)
OEDEMA ( 43 FDA reports)
SURGERY ( 43 FDA reports)
CORONARY ARTERY OCCLUSION ( 42 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 42 FDA reports)
MULTIPLE INJURIES ( 42 FDA reports)
TOOTH EXTRACTION ( 42 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 42 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 42 FDA reports)
BLOOD PRESSURE DECREASED ( 41 FDA reports)
DRUG HYPERSENSITIVITY ( 41 FDA reports)
EMOTIONAL DISORDER ( 41 FDA reports)
HYPERSOMNIA ( 41 FDA reports)
INFLUENZA ( 41 FDA reports)
MEDICATION ERROR ( 41 FDA reports)
MYOPATHY ( 41 FDA reports)
MYOSITIS ( 41 FDA reports)
NEPHROLITHIASIS ( 41 FDA reports)
ORAL PAIN ( 41 FDA reports)
SPINAL OSTEOARTHRITIS ( 41 FDA reports)
VENTRICULAR HYPERTROPHY ( 41 FDA reports)
BLOOD UREA INCREASED ( 40 FDA reports)
FEAR ( 40 FDA reports)
HEPATITIS ( 40 FDA reports)
MULTIPLE MYELOMA ( 40 FDA reports)
PANCYTOPENIA ( 40 FDA reports)
SINUS CONGESTION ( 40 FDA reports)
SUICIDAL IDEATION ( 40 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 39 FDA reports)
ANOREXIA ( 39 FDA reports)
BARRETT'S OESOPHAGUS ( 39 FDA reports)
DYSLIPIDAEMIA ( 39 FDA reports)
OFF LABEL USE ( 39 FDA reports)
ROTATOR CUFF SYNDROME ( 39 FDA reports)
AORTIC VALVE INCOMPETENCE ( 38 FDA reports)
ASTHMA ( 38 FDA reports)
INJECTION SITE PAIN ( 38 FDA reports)
NEUTROPENIA ( 38 FDA reports)
ORTHOSTATIC HYPOTENSION ( 38 FDA reports)
PULMONARY OEDEMA ( 38 FDA reports)
RESPIRATORY ARREST ( 38 FDA reports)
DIABETIC KETOACIDOSIS ( 37 FDA reports)
DYSKINESIA ( 37 FDA reports)
EAR PAIN ( 37 FDA reports)
HAEMATOCRIT DECREASED ( 37 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 37 FDA reports)
PRODUCTIVE COUGH ( 37 FDA reports)
SEPTIC SHOCK ( 37 FDA reports)
UMBILICAL HERNIA ( 37 FDA reports)
DISORIENTATION ( 36 FDA reports)
GINGIVAL ULCERATION ( 36 FDA reports)
METABOLIC ACIDOSIS ( 36 FDA reports)
TARDIVE DYSKINESIA ( 36 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 35 FDA reports)
CARDIO-RESPIRATORY ARREST ( 35 FDA reports)
FEELING HOT ( 35 FDA reports)
HYPOXIA ( 35 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 35 FDA reports)
CHROMATURIA ( 34 FDA reports)
DENTAL CARIES ( 34 FDA reports)
HAEMATOCHEZIA ( 34 FDA reports)
NERVOUSNESS ( 34 FDA reports)
PANCREATITIS ACUTE ( 34 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 34 FDA reports)
WOUND DEHISCENCE ( 34 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 33 FDA reports)
BURNING SENSATION ( 33 FDA reports)
CARDIAC FAILURE ( 33 FDA reports)
DYSARTHRIA ( 33 FDA reports)
HYPOKALAEMIA ( 33 FDA reports)
RENAL INJURY ( 33 FDA reports)
SEBORRHOEIC DERMATITIS ( 33 FDA reports)
SUICIDE ATTEMPT ( 33 FDA reports)
VERTIGO ( 33 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 33 FDA reports)
AORTIC STENOSIS ( 32 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 32 FDA reports)
DIABETIC RETINOPATHY ( 32 FDA reports)
IMPAIRED HEALING ( 32 FDA reports)
LACTIC ACIDOSIS ( 32 FDA reports)
THROMBOSIS ( 32 FDA reports)
URTICARIA ( 32 FDA reports)
ACUTE RESPIRATORY FAILURE ( 31 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 31 FDA reports)
ERECTILE DYSFUNCTION ( 31 FDA reports)
HOT FLUSH ( 31 FDA reports)
INCORRECT DOSE ADMINISTERED ( 31 FDA reports)
PRODUCT QUALITY ISSUE ( 31 FDA reports)
REFLUX OESOPHAGITIS ( 31 FDA reports)
RENAL DISORDER ( 31 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 31 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 31 FDA reports)
X-RAY ABNORMAL ( 31 FDA reports)
ARTERIOSCLEROSIS ( 30 FDA reports)
BASAL CELL CARCINOMA ( 30 FDA reports)
FEBRILE NEUTROPENIA ( 30 FDA reports)
HYPOVOLAEMIA ( 30 FDA reports)
LOOSE TOOTH ( 30 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 30 FDA reports)
MOOD SWINGS ( 30 FDA reports)
MYOCARDIAL ISCHAEMIA ( 30 FDA reports)
POLLAKIURIA ( 30 FDA reports)
SOFT TISSUE INFLAMMATION ( 30 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 30 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 29 FDA reports)
BLOOD POTASSIUM INCREASED ( 29 FDA reports)
CARDIOMYOPATHY ( 29 FDA reports)
EMPHYSEMA ( 29 FDA reports)
EYE SWELLING ( 29 FDA reports)
GALLBLADDER DISORDER ( 29 FDA reports)
GRANULOCYTOPENIA ( 29 FDA reports)
HAEMODIALYSIS ( 29 FDA reports)
ILEUS ( 29 FDA reports)
INCREASED APPETITE ( 29 FDA reports)
LEUKOCYTOSIS ( 29 FDA reports)
MENTAL DISORDER ( 29 FDA reports)
NIGHT SWEATS ( 29 FDA reports)
OSTEOPENIA ( 29 FDA reports)
SWELLING FACE ( 29 FDA reports)
SWOLLEN TONGUE ( 29 FDA reports)
ANGER ( 28 FDA reports)
ANGIOEDEMA ( 28 FDA reports)
ATRIAL TACHYCARDIA ( 28 FDA reports)
DEPRESSED MOOD ( 28 FDA reports)
DRUG TOXICITY ( 28 FDA reports)
FIBROMYALGIA ( 28 FDA reports)
FLUID RETENTION ( 28 FDA reports)
IRON DEFICIENCY ANAEMIA ( 28 FDA reports)
JOINT SWELLING ( 28 FDA reports)
MOBILITY DECREASED ( 28 FDA reports)
NEOPLASM MALIGNANT ( 28 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 28 FDA reports)
PULMONARY HYPERTENSION ( 28 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 28 FDA reports)
URINARY RETENTION ( 28 FDA reports)
BIPOLAR DISORDER ( 27 FDA reports)
COMA ( 27 FDA reports)
DELIRIUM ( 27 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 27 FDA reports)
GASTROENTERITIS ( 27 FDA reports)
LUNG NEOPLASM ( 27 FDA reports)
MOVEMENT DISORDER ( 27 FDA reports)
PERIPHERAL COLDNESS ( 27 FDA reports)
SPEECH DISORDER ( 27 FDA reports)
BONE DENSITY DECREASED ( 26 FDA reports)
CARDIOVASCULAR DISORDER ( 26 FDA reports)
DEFORMITY ( 26 FDA reports)
DIVERTICULUM INTESTINAL ( 26 FDA reports)
EYE PAIN ( 26 FDA reports)
GINGIVAL PAIN ( 26 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 26 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 26 FDA reports)
PAIN IN JAW ( 26 FDA reports)
PRESYNCOPE ( 26 FDA reports)
RIB FRACTURE ( 26 FDA reports)
ANGINA UNSTABLE ( 25 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 25 FDA reports)
BLOOD BILIRUBIN INCREASED ( 25 FDA reports)
DIVERTICULUM ( 25 FDA reports)
DYSSTASIA ( 25 FDA reports)
ENDODONTIC PROCEDURE ( 25 FDA reports)
GINGIVAL RECESSION ( 25 FDA reports)
LEUKOPENIA ( 25 FDA reports)
LYMPHADENOPATHY ( 25 FDA reports)
OROPHARYNGEAL PAIN ( 25 FDA reports)
PANIC ATTACK ( 25 FDA reports)
RESPIRATORY DISTRESS ( 25 FDA reports)
STAPHYLOCOCCAL INFECTION ( 25 FDA reports)
STOMACH DISCOMFORT ( 25 FDA reports)
ADVERSE EVENT ( 24 FDA reports)
ANKLE FRACTURE ( 24 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 24 FDA reports)
BLOOD POTASSIUM DECREASED ( 24 FDA reports)
COLONIC POLYP ( 24 FDA reports)
DECREASED INTEREST ( 24 FDA reports)
GASTRIC ULCER ( 24 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 24 FDA reports)
METASTASES TO BONE ( 24 FDA reports)
SINUS TACHYCARDIA ( 24 FDA reports)
ARTHROPATHY ( 23 FDA reports)
BREAST CANCER ( 23 FDA reports)
HERPES ZOSTER ( 23 FDA reports)
INFLUENZA LIKE ILLNESS ( 23 FDA reports)
NASOPHARYNGITIS ( 23 FDA reports)
PEPTIC ULCER ( 23 FDA reports)
PULMONARY CONGESTION ( 23 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 23 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 23 FDA reports)
TROPONIN INCREASED ( 23 FDA reports)
VISUAL IMPAIRMENT ( 23 FDA reports)
ACUTE SINUSITIS ( 22 FDA reports)
ANXIETY DISORDER ( 22 FDA reports)
BLOOD SODIUM DECREASED ( 22 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 22 FDA reports)
CANDIDIASIS ( 22 FDA reports)
CAROTID ARTERY STENOSIS ( 22 FDA reports)
CATARACT ( 22 FDA reports)
CORONARY ARTERY STENOSIS ( 22 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 22 FDA reports)
DIALYSIS ( 22 FDA reports)
DIFFICULTY IN WALKING ( 22 FDA reports)
DRUG DEPENDENCE ( 22 FDA reports)
DYSPHONIA ( 22 FDA reports)
ERUCTATION ( 22 FDA reports)
GLAUCOMA ( 22 FDA reports)
HAEMATOCRIT ABNORMAL ( 22 FDA reports)
JAUNDICE ( 22 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 22 FDA reports)
NIGHTMARE ( 22 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 22 FDA reports)
RHINITIS ALLERGIC ( 22 FDA reports)
ROAD TRAFFIC ACCIDENT ( 22 FDA reports)
STEM CELL TRANSPLANT ( 22 FDA reports)
VENTRICULAR TACHYCARDIA ( 22 FDA reports)
ALOPECIA ( 21 FDA reports)
ATRIAL FLUTTER ( 21 FDA reports)
BLISTER ( 21 FDA reports)
CARDIAC PACEMAKER INSERTION ( 21 FDA reports)
ECZEMA ( 21 FDA reports)
GASTROINTESTINAL DISORDER ( 21 FDA reports)
HAEMATEMESIS ( 21 FDA reports)
IMPAIRED WORK ABILITY ( 21 FDA reports)
OESOPHAGITIS ( 21 FDA reports)
PERIODONTITIS ( 21 FDA reports)
SKIN BURNING SENSATION ( 21 FDA reports)
SKIN INFECTION ( 21 FDA reports)
SPINAL COLUMN STENOSIS ( 21 FDA reports)
VISUAL DISTURBANCE ( 21 FDA reports)
WHEEZING ( 21 FDA reports)
BLOOD URINE PRESENT ( 20 FDA reports)
FEELING GUILTY ( 20 FDA reports)
GRAND MAL CONVULSION ( 20 FDA reports)
ILL-DEFINED DISORDER ( 20 FDA reports)
LUNG INFILTRATION ( 20 FDA reports)
MELANOCYTIC NAEVUS ( 20 FDA reports)
MIDDLE INSOMNIA ( 20 FDA reports)
NERVOUS SYSTEM DISORDER ( 20 FDA reports)
POLYDIPSIA ( 20 FDA reports)
RADICULOPATHY ( 20 FDA reports)
RENAL TUBULAR NECROSIS ( 20 FDA reports)
RESTLESSNESS ( 20 FDA reports)
RHINORRHOEA ( 20 FDA reports)
SEBORRHOEIC KERATOSIS ( 20 FDA reports)
SINUS HEADACHE ( 20 FDA reports)
ADVERSE DRUG REACTION ( 19 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 19 FDA reports)
BONE LESION ( 19 FDA reports)
CHOLECYSTECTOMY ( 19 FDA reports)
COAGULOPATHY ( 19 FDA reports)
DRUG DISPENSING ERROR ( 19 FDA reports)
EJECTION FRACTION DECREASED ( 19 FDA reports)
FEELING COLD ( 19 FDA reports)
FLUID OVERLOAD ( 19 FDA reports)
KIDNEY INFECTION ( 19 FDA reports)
MAJOR DEPRESSION ( 19 FDA reports)
MELAENA ( 19 FDA reports)
NASAL CONGESTION ( 19 FDA reports)
RENAL CYST ( 19 FDA reports)
TOOTH ABSCESS ( 19 FDA reports)
TOOTH DISORDER ( 19 FDA reports)
ABNORMAL BEHAVIOUR ( 18 FDA reports)
ACUTE CORONARY SYNDROME ( 18 FDA reports)
APHASIA ( 18 FDA reports)
BLOOD CHLORIDE DECREASED ( 18 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 18 FDA reports)
CAROTID ARTERY DISEASE ( 18 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 18 FDA reports)
EXTRASYSTOLES ( 18 FDA reports)
FACIAL PALSY ( 18 FDA reports)
FAECES DISCOLOURED ( 18 FDA reports)
FRUSTRATION ( 18 FDA reports)
GASTRIC DISORDER ( 18 FDA reports)
HEPATOMEGALY ( 18 FDA reports)
HYPOAESTHESIA FACIAL ( 18 FDA reports)
INCISIONAL HERNIA ( 18 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 18 FDA reports)
METABOLIC SYNDROME ( 18 FDA reports)
MUCOSAL INFLAMMATION ( 18 FDA reports)
MUSCLE ATROPHY ( 18 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 18 FDA reports)
MYELODYSPLASTIC SYNDROME ( 18 FDA reports)
OCULAR HYPERAEMIA ( 18 FDA reports)
PERICARDIAL EFFUSION ( 18 FDA reports)
POLYP ( 18 FDA reports)
PSORIASIS ( 18 FDA reports)
RETINAL DETACHMENT ( 18 FDA reports)
VENOUS INSUFFICIENCY ( 18 FDA reports)
VIRAL INFECTION ( 18 FDA reports)
VITAMIN B12 DEFICIENCY ( 18 FDA reports)
ACTINIC KERATOSIS ( 17 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 17 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 17 FDA reports)
BONE PAIN ( 17 FDA reports)
BURSITIS ( 17 FDA reports)
CARPAL TUNNEL SYNDROME ( 17 FDA reports)
CATARACT OPERATION ( 17 FDA reports)
CEREBRAL ISCHAEMIA ( 17 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 17 FDA reports)
ELECTROLYTE IMBALANCE ( 17 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 17 FDA reports)
FEMUR FRACTURE ( 17 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 17 FDA reports)
HEAD INJURY ( 17 FDA reports)
HEMIPARESIS ( 17 FDA reports)
HYPOMAGNESAEMIA ( 17 FDA reports)
MACULAR HOLE ( 17 FDA reports)
MITRAL VALVE DISEASE ( 17 FDA reports)
ORTHOPNOEA ( 17 FDA reports)
RASH ERYTHEMATOUS ( 17 FDA reports)
SKIN EXFOLIATION ( 17 FDA reports)
AGGRESSION ( 16 FDA reports)
ANGIONEUROTIC OEDEMA ( 16 FDA reports)
BENIGN LUNG NEOPLASM ( 16 FDA reports)
BLADDER DISORDER ( 16 FDA reports)
BLINDNESS ( 16 FDA reports)
BREAST MASS ( 16 FDA reports)
CHOROIDAL DETACHMENT ( 16 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 16 FDA reports)
DIPLOPIA ( 16 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 16 FDA reports)
EATING DISORDER ( 16 FDA reports)
ENCEPHALOPATHY ( 16 FDA reports)
EXPOSED BONE IN JAW ( 16 FDA reports)
FEELING JITTERY ( 16 FDA reports)
FOOT FRACTURE ( 16 FDA reports)
HAEMOPTYSIS ( 16 FDA reports)
HOSPITALISATION ( 16 FDA reports)
INTENTIONAL DRUG MISUSE ( 16 FDA reports)
INTENTIONAL OVERDOSE ( 16 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 16 FDA reports)
LIMB OPERATION ( 16 FDA reports)
LIVER DISORDER ( 16 FDA reports)
LUNG INFECTION ( 16 FDA reports)
METASTASES TO LIVER ( 16 FDA reports)
MUSCLE DISORDER ( 16 FDA reports)
MYELOPATHY ( 16 FDA reports)
OSTEOLYSIS ( 16 FDA reports)
PARANOIA ( 16 FDA reports)
PROSTATE CANCER ( 16 FDA reports)
PSYCHOTIC DISORDER ( 16 FDA reports)
RASH GENERALISED ( 16 FDA reports)
RETCHING ( 16 FDA reports)
RHINITIS ( 16 FDA reports)
SCAR ( 16 FDA reports)
SCIATICA ( 16 FDA reports)
SINUS BRADYCARDIA ( 16 FDA reports)
SKIN DISCOLOURATION ( 16 FDA reports)
SKIN FIBROSIS ( 16 FDA reports)
SKIN PAPILLOMA ( 16 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 16 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 16 FDA reports)
VITREOUS FLOATERS ( 16 FDA reports)
WALKING AID USER ( 16 FDA reports)
WRIST FRACTURE ( 16 FDA reports)
ACTINIC ELASTOSIS ( 15 FDA reports)
ACTINOMYCOSIS ( 15 FDA reports)
BREAST CANCER METASTATIC ( 15 FDA reports)
BREAST PAIN ( 15 FDA reports)
CATHETER RELATED COMPLICATION ( 15 FDA reports)
CENTRAL LINE INFECTION ( 15 FDA reports)
DERMAL CYST ( 15 FDA reports)
DUODENITIS ( 15 FDA reports)
FACIAL PAIN ( 15 FDA reports)
FLANK PAIN ( 15 FDA reports)
GINGIVAL INFECTION ( 15 FDA reports)
GOUT ( 15 FDA reports)
HEART INJURY ( 15 FDA reports)
LOBAR PNEUMONIA ( 15 FDA reports)
LUNG DISORDER ( 15 FDA reports)
MANIA ( 15 FDA reports)
METASTASES TO LUNG ( 15 FDA reports)
NO THERAPEUTIC RESPONSE ( 15 FDA reports)
NON-CARDIAC CHEST PAIN ( 15 FDA reports)
OTITIS EXTERNA ( 15 FDA reports)
OXYGEN SATURATION DECREASED ( 15 FDA reports)
PALLOR ( 15 FDA reports)
PANCREATITIS CHRONIC ( 15 FDA reports)
PRESBYOPIA ( 15 FDA reports)
THYROID DISORDER ( 15 FDA reports)
TYPE 1 DIABETES MELLITUS ( 15 FDA reports)
UMBILICAL HERNIA REPAIR ( 15 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 15 FDA reports)
ABDOMINAL HERNIA ( 14 FDA reports)
ATRIOVENTRICULAR BLOCK ( 14 FDA reports)
BLOOD ALBUMIN DECREASED ( 14 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 14 FDA reports)
BONE NEOPLASM MALIGNANT ( 14 FDA reports)
CATHETERISATION CARDIAC ( 14 FDA reports)
CHOLESTASIS ( 14 FDA reports)
DIABETIC NEPHROPATHY ( 14 FDA reports)
DRUG LEVEL INCREASED ( 14 FDA reports)
EPICONDYLITIS ( 14 FDA reports)
EYE DISORDER ( 14 FDA reports)
HAEMATOMA ( 14 FDA reports)
HEPATOCELLULAR DAMAGE ( 14 FDA reports)
HERNIA ( 14 FDA reports)
HYPERKERATOSIS ( 14 FDA reports)
HYPOPHAGIA ( 14 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 14 FDA reports)
LIPOMA ( 14 FDA reports)
LOCALISED INFECTION ( 14 FDA reports)
NOCTURIA ( 14 FDA reports)
OVERWEIGHT ( 14 FDA reports)
PRESCRIBED OVERDOSE ( 14 FDA reports)
PROTHROMBIN TIME PROLONGED ( 14 FDA reports)
PRURITUS GENERALISED ( 14 FDA reports)
QUALITY OF LIFE DECREASED ( 14 FDA reports)
SPLENOMEGALY ( 14 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 14 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
ACIDOSIS ( 13 FDA reports)
ACROCHORDON ( 13 FDA reports)
AGEUSIA ( 13 FDA reports)
ASCITES ( 13 FDA reports)
BONE LESION EXCISION ( 13 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 13 FDA reports)
CHOLECYSTITIS ( 13 FDA reports)
CHOLECYSTITIS CHRONIC ( 13 FDA reports)
CORONARY ARTERY BYPASS ( 13 FDA reports)
DEAFNESS ( 13 FDA reports)
DIABETIC COMA ( 13 FDA reports)
DIABETIC COMPLICATION ( 13 FDA reports)
DRUG ERUPTION ( 13 FDA reports)
EROSIVE DUODENITIS ( 13 FDA reports)
EYE LASER SURGERY ( 13 FDA reports)
GOITRE ( 13 FDA reports)
HEPATIC FAILURE ( 13 FDA reports)
INTERSTITIAL LUNG DISEASE ( 13 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 13 FDA reports)
INTESTINAL OBSTRUCTION ( 13 FDA reports)
JAW FRACTURE ( 13 FDA reports)
JOINT INJURY ( 13 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 13 FDA reports)
LIGAMENT SPRAIN ( 13 FDA reports)
LUMBAR RADICULOPATHY ( 13 FDA reports)
LUNG NEOPLASM MALIGNANT ( 13 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 13 FDA reports)
OCCULT BLOOD POSITIVE ( 13 FDA reports)
ORAL INTAKE REDUCED ( 13 FDA reports)
PERSONALITY CHANGE ( 13 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 13 FDA reports)
POST PROCEDURAL COMPLICATION ( 13 FDA reports)
PROSTATOMEGALY ( 13 FDA reports)
RASH PAPULAR ( 13 FDA reports)
RENAL PAIN ( 13 FDA reports)
RESPIRATORY RATE INCREASED ( 13 FDA reports)
RESTLESS LEGS SYNDROME ( 13 FDA reports)
SCOLIOSIS ( 13 FDA reports)
SYNOVIAL CYST ( 13 FDA reports)
TACHYPNOEA ( 13 FDA reports)
THROAT IRRITATION ( 13 FDA reports)
ULCER ( 13 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 13 FDA reports)
UTERINE HAEMORRHAGE ( 13 FDA reports)
VENTRICULAR FIBRILLATION ( 13 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 13 FDA reports)
ABSCESS ORAL ( 12 FDA reports)
AFFECTIVE DISORDER ( 12 FDA reports)
ANAPHYLACTIC REACTION ( 12 FDA reports)
AORTIC VALVE SCLEROSIS ( 12 FDA reports)
AZOTAEMIA ( 12 FDA reports)
BACK INJURY ( 12 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 12 FDA reports)
CEREBRAL ATROPHY ( 12 FDA reports)
CHRONIC SINUSITIS ( 12 FDA reports)
DEAFNESS NEUROSENSORY ( 12 FDA reports)
ECCHYMOSIS ( 12 FDA reports)
EYE HAEMORRHAGE ( 12 FDA reports)
GASTRIC POLYPS ( 12 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 12 FDA reports)
HEPATOTOXICITY ( 12 FDA reports)
HYPERNATRAEMIA ( 12 FDA reports)
HYPOCALCAEMIA ( 12 FDA reports)
HYPOKINESIA ( 12 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 12 FDA reports)
LABORATORY TEST ABNORMAL ( 12 FDA reports)
LEFT ATRIAL DILATATION ( 12 FDA reports)
MUSCLE CRAMP ( 12 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 12 FDA reports)
PANCREATIC DISORDER ( 12 FDA reports)
PELVIC PAIN ( 12 FDA reports)
PULMONARY GRANULOMA ( 12 FDA reports)
PYELONEPHRITIS ( 12 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 12 FDA reports)
RENAL MASS ( 12 FDA reports)
SCHIZOPHRENIA ( 12 FDA reports)
SCLERAL OPERATION ( 12 FDA reports)
SKIN LESION ( 12 FDA reports)
SPINAL COMPRESSION FRACTURE ( 12 FDA reports)
STENT PLACEMENT ( 12 FDA reports)
TOOTH FRACTURE ( 12 FDA reports)
TRANSAMINASES INCREASED ( 12 FDA reports)
TRIGEMINAL NEURALGIA ( 12 FDA reports)
URINARY INCONTINENCE ( 12 FDA reports)
ACCIDENTAL OVERDOSE ( 11 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 11 FDA reports)
CEREBRAL HAEMORRHAGE ( 11 FDA reports)
COLITIS ( 11 FDA reports)
CRYING ( 11 FDA reports)
DEVICE MALFUNCTION ( 11 FDA reports)
DIZZINESS POSTURAL ( 11 FDA reports)
DYSPLASTIC NAEVUS ( 11 FDA reports)
EYE IRRITATION ( 11 FDA reports)
FAT TISSUE INCREASED ( 11 FDA reports)
FORMICATION ( 11 FDA reports)
GINGIVAL BLEEDING ( 11 FDA reports)
GROIN PAIN ( 11 FDA reports)
GUN SHOT WOUND ( 11 FDA reports)
INADEQUATE ANALGESIA ( 11 FDA reports)
INJECTION SITE ERYTHEMA ( 11 FDA reports)
INJECTION SITE HAEMORRHAGE ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 11 FDA reports)
JOINT SPRAIN ( 11 FDA reports)
JOINT STIFFNESS ( 11 FDA reports)
LYMPHOMA ( 11 FDA reports)
MONOCLONAL GAMMOPATHY ( 11 FDA reports)
MOUTH ULCERATION ( 11 FDA reports)
NEPHROPATHY ( 11 FDA reports)
OPEN REDUCTION OF FRACTURE ( 11 FDA reports)
OPEN WOUND ( 11 FDA reports)
ORAL CANDIDIASIS ( 11 FDA reports)
ORAL DISORDER ( 11 FDA reports)
PERITONITIS ( 11 FDA reports)
PNEUMOTHORAX ( 11 FDA reports)
PROSTATITIS ( 11 FDA reports)
PROTEINURIA ( 11 FDA reports)
PULSE ABSENT ( 11 FDA reports)
RADICAL MASTECTOMY ( 11 FDA reports)
RECTAL FISSURE ( 11 FDA reports)
SINUS DISORDER ( 11 FDA reports)
SPINAL FRACTURE ( 11 FDA reports)
SUDDEN DEATH ( 11 FDA reports)
ABDOMINAL PAIN LOWER ( 10 FDA reports)
ACNE ( 10 FDA reports)
ANAL FISSURE ( 10 FDA reports)
BACTERIAL INFECTION ( 10 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 10 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 10 FDA reports)
BLOOD URIC ACID INCREASED ( 10 FDA reports)
BODY TEMPERATURE INCREASED ( 10 FDA reports)
BONE FRAGMENTATION ( 10 FDA reports)
CATARACT CORTICAL ( 10 FDA reports)
CEREBRAL INFARCTION ( 10 FDA reports)
CHOKING ( 10 FDA reports)
COLD SWEAT ( 10 FDA reports)
CROHN'S DISEASE ( 10 FDA reports)
CYSTITIS ( 10 FDA reports)
DISCOMFORT ( 10 FDA reports)
DISEASE PROGRESSION ( 10 FDA reports)
EXCORIATION ( 10 FDA reports)
EYE PRURITUS ( 10 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 10 FDA reports)
HAEMOTHORAX ( 10 FDA reports)
HEART RATE DECREASED ( 10 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 10 FDA reports)
HEPATIC CIRRHOSIS ( 10 FDA reports)
INFUSION RELATED REACTION ( 10 FDA reports)
INJECTION SITE HAEMATOMA ( 10 FDA reports)
INJECTION SITE PRURITUS ( 10 FDA reports)
INTESTINAL PERFORATION ( 10 FDA reports)
LACRIMATION INCREASED ( 10 FDA reports)
LIPIDS INCREASED ( 10 FDA reports)
MEDICATION RESIDUE ( 10 FDA reports)
MOOD ALTERED ( 10 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 10 FDA reports)
MUSCLE STRAIN ( 10 FDA reports)
MYOGLOBINURIA ( 10 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 10 FDA reports)
ODYNOPHAGIA ( 10 FDA reports)
ONYCHOMYCOSIS ( 10 FDA reports)
PANIC DISORDER ( 10 FDA reports)
PARTNER STRESS ( 10 FDA reports)
PHARYNGITIS ( 10 FDA reports)
RHEUMATOID ARTHRITIS ( 10 FDA reports)
SENSORY DISTURBANCE ( 10 FDA reports)
SEQUESTRECTOMY ( 10 FDA reports)
STRESS URINARY INCONTINENCE ( 10 FDA reports)
TENDERNESS ( 10 FDA reports)
TENOSYNOVITIS ( 10 FDA reports)
THYROID NEOPLASM ( 10 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 10 FDA reports)
ABSCESS ( 9 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 9 FDA reports)
ACUTE PRERENAL FAILURE ( 9 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 9 FDA reports)
APPLICATION SITE ERYTHEMA ( 9 FDA reports)
CALCULUS URINARY ( 9 FDA reports)
CEREBROVASCULAR DISORDER ( 9 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 9 FDA reports)
DECREASED ACTIVITY ( 9 FDA reports)
DIABETIC FOOT ( 9 FDA reports)
DILATATION ATRIAL ( 9 FDA reports)
DILATATION VENTRICULAR ( 9 FDA reports)
DRUG LEVEL DECREASED ( 9 FDA reports)
DYSTONIA ( 9 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 9 FDA reports)
ENTERITIS ( 9 FDA reports)
FIBULA FRACTURE ( 9 FDA reports)
FRACTURE ( 9 FDA reports)
GASTROENTERITIS VIRAL ( 9 FDA reports)
GINGIVAL SWELLING ( 9 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 9 FDA reports)
HAEMORRHAGE URINARY TRACT ( 9 FDA reports)
HEPATITIS CHOLESTATIC ( 9 FDA reports)
HIP FRACTURE ( 9 FDA reports)
HYPERTHYROIDISM ( 9 FDA reports)
HYPOAESTHESIA ORAL ( 9 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 9 FDA reports)
IRRITABLE BOWEL SYNDROME ( 9 FDA reports)
LIBIDO DECREASED ( 9 FDA reports)
LIPASE INCREASED ( 9 FDA reports)
LUMBAR SPINAL STENOSIS ( 9 FDA reports)
LYMPHOEDEMA ( 9 FDA reports)
MAMMOGRAM ABNORMAL ( 9 FDA reports)
MENTAL IMPAIRMENT ( 9 FDA reports)
MYOPIA ( 9 FDA reports)
NECROSIS ( 9 FDA reports)
OSTEITIS ( 9 FDA reports)
PERIODONTAL INFECTION ( 9 FDA reports)
PNEUMONIA ASPIRATION ( 9 FDA reports)
RETINOPATHY ( 9 FDA reports)
SEDATION ( 9 FDA reports)
SKIN IRRITATION ( 9 FDA reports)
SKIN ULCER ( 9 FDA reports)
STOMATITIS ( 9 FDA reports)
SUBDURAL HAEMATOMA ( 9 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 9 FDA reports)
TENDON RUPTURE ( 9 FDA reports)
THROAT TIGHTNESS ( 9 FDA reports)
TOBACCO USER ( 9 FDA reports)
VAGINAL HAEMORRHAGE ( 9 FDA reports)
VASCULAR PSEUDOANEURYSM ( 9 FDA reports)
ACCIDENTAL EXPOSURE ( 8 FDA reports)
ADNEXA UTERI CYST ( 8 FDA reports)
ADRENAL INSUFFICIENCY ( 8 FDA reports)
ALCOHOL USE ( 8 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 8 FDA reports)
ANOXIC ENCEPHALOPATHY ( 8 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 8 FDA reports)
ATAXIA ( 8 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 8 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 8 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 8 FDA reports)
CARDIAC VALVE DISEASE ( 8 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 8 FDA reports)
CIRCULATORY COLLAPSE ( 8 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 8 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 8 FDA reports)
CYST ( 8 FDA reports)
DERMATITIS ( 8 FDA reports)
DRUG ABUSE ( 8 FDA reports)
DRUG INTOLERANCE ( 8 FDA reports)
DRUG SCREEN POSITIVE ( 8 FDA reports)
DRY EYE ( 8 FDA reports)
EAR DISORDER ( 8 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 8 FDA reports)
EXCESSIVE EYE BLINKING ( 8 FDA reports)
EXERCISE TOLERANCE DECREASED ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
GINGIVITIS ( 8 FDA reports)
GRIMACING ( 8 FDA reports)
HEPATIC VEIN THROMBOSIS ( 8 FDA reports)
HEPATITIS TOXIC ( 8 FDA reports)
HYDRONEPHROSIS ( 8 FDA reports)
HYPERCALCAEMIA ( 8 FDA reports)
INFLAMMATION ( 8 FDA reports)
INTRAOCULAR LENS IMPLANT ( 8 FDA reports)
ISCHAEMIA ( 8 FDA reports)
ISCHAEMIC STROKE ( 8 FDA reports)
LOCAL SWELLING ( 8 FDA reports)
MACULAR DEGENERATION ( 8 FDA reports)
MUSCULOSKELETAL DISORDER ( 8 FDA reports)
NEURALGIA ( 8 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 8 FDA reports)
NEUROPATHY ( 8 FDA reports)
NEUTROPHIL COUNT DECREASED ( 8 FDA reports)
PANCREATITIS RELAPSING ( 8 FDA reports)
PARALYSIS ( 8 FDA reports)
PARKINSON'S DISEASE ( 8 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 8 FDA reports)
PHOTOSENSITIVITY REACTION ( 8 FDA reports)
PNEUMONITIS ( 8 FDA reports)
POISONING ( 8 FDA reports)
POLYURIA ( 8 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 8 FDA reports)
PROTEIN TOTAL INCREASED ( 8 FDA reports)
PSEUDOMONAS INFECTION ( 8 FDA reports)
PULMONARY MASS ( 8 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 8 FDA reports)
SENSATION OF HEAVINESS ( 8 FDA reports)
SHOCK ( 8 FDA reports)
SKIN CANCER ( 8 FDA reports)
SNEEZING ( 8 FDA reports)
TONGUE DISORDER ( 8 FDA reports)
VENTRICULAR DYSFUNCTION ( 8 FDA reports)
VITREOUS HAEMORRHAGE ( 8 FDA reports)
ADENOMA BENIGN ( 7 FDA reports)
AMMONIA INCREASED ( 7 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 7 FDA reports)
APHAGIA ( 7 FDA reports)
ASTIGMATISM ( 7 FDA reports)
BILIARY DILATATION ( 7 FDA reports)
BLADDER CANCER ( 7 FDA reports)
BLINDNESS UNILATERAL ( 7 FDA reports)
BLOOD CALCIUM DECREASED ( 7 FDA reports)
BRUXISM ( 7 FDA reports)
CALCULUS URETERIC ( 7 FDA reports)
CHOLECYSTITIS ACUTE ( 7 FDA reports)
COGNITIVE DISORDER ( 7 FDA reports)
COLON CANCER ( 7 FDA reports)
CONCUSSION ( 7 FDA reports)
CYANOSIS ( 7 FDA reports)
DELUSION ( 7 FDA reports)
DEVICE BREAKAGE ( 7 FDA reports)
DUODENAL ULCER ( 7 FDA reports)
EOSINOPHIL COUNT INCREASED ( 7 FDA reports)
ESCHERICHIA INFECTION ( 7 FDA reports)
EXPIRED DRUG ADMINISTERED ( 7 FDA reports)
FACIAL BONES FRACTURE ( 7 FDA reports)
FAMILY STRESS ( 7 FDA reports)
FOREIGN BODY TRAUMA ( 7 FDA reports)
FUNGAL INFECTION ( 7 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 7 FDA reports)
GRAVITATIONAL OEDEMA ( 7 FDA reports)
HALLUCINATION, AUDITORY ( 7 FDA reports)
HEPATIC ENZYME ABNORMAL ( 7 FDA reports)
HEPATIC LESION ( 7 FDA reports)
HEPATITIS ACUTE ( 7 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 7 FDA reports)
HOMICIDAL IDEATION ( 7 FDA reports)
HYPERBILIRUBINAEMIA ( 7 FDA reports)
HYPERTENSIVE EMERGENCY ( 7 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 7 FDA reports)
ILEUS PARALYTIC ( 7 FDA reports)
INFARCTION ( 7 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 7 FDA reports)
LIP SWELLING ( 7 FDA reports)
LIPID METABOLISM DISORDER ( 7 FDA reports)
LIVER INJURY ( 7 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 7 FDA reports)
MENISCUS LESION ( 7 FDA reports)
METASTASES TO ADRENALS ( 7 FDA reports)
METASTASES TO SPINE ( 7 FDA reports)
MUSCLE FATIGUE ( 7 FDA reports)
MUSCLE INJURY ( 7 FDA reports)
MUSCLE TWITCHING ( 7 FDA reports)
NASAL ULCER ( 7 FDA reports)
NEOPLASM PROGRESSION ( 7 FDA reports)
NO ADVERSE EVENT ( 7 FDA reports)
ORAL DISCOMFORT ( 7 FDA reports)
OTITIS MEDIA ( 7 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 7 FDA reports)
PANCREATIC PSEUDOCYST ( 7 FDA reports)
PETECHIAE ( 7 FDA reports)
PHARYNGEAL OEDEMA ( 7 FDA reports)
PIGMENTED NAEVUS ( 7 FDA reports)
PLEURITIC PAIN ( 7 FDA reports)
POLYNEUROPATHY ( 7 FDA reports)
POOR QUALITY SLEEP ( 7 FDA reports)
PROCEDURAL PAIN ( 7 FDA reports)
RALES ( 7 FDA reports)
RENAL ARTERY STENOSIS ( 7 FDA reports)
RESPIRATORY DISORDER ( 7 FDA reports)
RESPIRATORY TRACT CONGESTION ( 7 FDA reports)
SCAB ( 7 FDA reports)
SENSATION OF FOREIGN BODY ( 7 FDA reports)
SKIN DISORDER ( 7 FDA reports)
SKIN HAEMORRHAGE ( 7 FDA reports)
SKIN WARM ( 7 FDA reports)
SOFT TISSUE INJURY ( 7 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 7 FDA reports)
SWEAT DISCOLOURATION ( 7 FDA reports)
TENDONITIS ( 7 FDA reports)
TESTICULAR MASS ( 7 FDA reports)
TOE AMPUTATION ( 7 FDA reports)
UPPER LIMB FRACTURE ( 7 FDA reports)
URETERIC OBSTRUCTION ( 7 FDA reports)
URETHRAL STENOSIS ( 7 FDA reports)
VARICOSE VEIN ( 7 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 7 FDA reports)
WRONG DRUG ADMINISTERED ( 7 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 6 FDA reports)
ALLODYNIA ( 6 FDA reports)
ANAL HAEMORRHAGE ( 6 FDA reports)
ANGIOMYOLIPOMA ( 6 FDA reports)
ANION GAP INCREASED ( 6 FDA reports)
ANOSMIA ( 6 FDA reports)
APLASIA PURE RED CELL ( 6 FDA reports)
ARTERIOSPASM CORONARY ( 6 FDA reports)
BENCE JONES PROTEINURIA ( 6 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 6 FDA reports)
BLOOD CALCIUM INCREASED ( 6 FDA reports)
BLOOD COUNT ABNORMAL ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 6 FDA reports)
BREAST CALCIFICATIONS ( 6 FDA reports)
BREAST CANCER IN SITU ( 6 FDA reports)
BREATH SOUNDS ABNORMAL ( 6 FDA reports)
BRONCHOSPASM ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 6 FDA reports)
CARDIOGENIC SHOCK ( 6 FDA reports)
CAROTID ARTERY OCCLUSION ( 6 FDA reports)
CAROTID BRUIT ( 6 FDA reports)
CERVICAL NEURITIS ( 6 FDA reports)
CHEST WALL PAIN ( 6 FDA reports)
COLITIS ISCHAEMIC ( 6 FDA reports)
COMMUNICATION DISORDER ( 6 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 6 FDA reports)
COORDINATION ABNORMAL ( 6 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 6 FDA reports)
ENTEROCOLITIS ( 6 FDA reports)
ESCHERICHIA SEPSIS ( 6 FDA reports)
FACE OEDEMA ( 6 FDA reports)
FISTULA ( 6 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 6 FDA reports)
GASTROINTESTINAL INFECTION ( 6 FDA reports)
GLOSSITIS ( 6 FDA reports)
GLOSSODYNIA ( 6 FDA reports)
HEPATIC FIBROSIS ( 6 FDA reports)
HEPATIC NECROSIS ( 6 FDA reports)
HUMERUS FRACTURE ( 6 FDA reports)
HYPERPARATHYROIDISM ( 6 FDA reports)
HYPERTENSIVE CRISIS ( 6 FDA reports)
HYSTERECTOMY ( 6 FDA reports)
INFECTED SKIN ULCER ( 6 FDA reports)
INJECTION SITE IRRITATION ( 6 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 6 FDA reports)
ISCHAEMIC HEPATITIS ( 6 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 6 FDA reports)
LACUNAR INFARCTION ( 6 FDA reports)
LARYNGITIS ( 6 FDA reports)
LIMB DISCOMFORT ( 6 FDA reports)
LIMB INJURY ( 6 FDA reports)
MENINGITIS ( 6 FDA reports)
METABOLIC DISORDER ( 6 FDA reports)
METABOLIC ENCEPHALOPATHY ( 6 FDA reports)
METASTATIC PAIN ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 6 FDA reports)
MULTIPLE SCLEROSIS ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
NEOPLASM ( 6 FDA reports)
NEPHRITIS INTERSTITIAL ( 6 FDA reports)
NEPHROSCLEROSIS ( 6 FDA reports)
NERVE COMPRESSION ( 6 FDA reports)
NEUROGENIC BLADDER ( 6 FDA reports)
OEDEMA MOUTH ( 6 FDA reports)
OLIGURIA ( 6 FDA reports)
OSTEOCHONDROSIS ( 6 FDA reports)
OSTEOSCLEROSIS ( 6 FDA reports)
PATHOLOGICAL GAMBLING ( 6 FDA reports)
PCO2 DECREASED ( 6 FDA reports)
PERIODONTAL DISEASE ( 6 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 6 FDA reports)
POLYMYOSITIS ( 6 FDA reports)
POLYP COLORECTAL ( 6 FDA reports)
POLYPECTOMY ( 6 FDA reports)
POOR DENTAL CONDITION ( 6 FDA reports)
PORTAL VEIN THROMBOSIS ( 6 FDA reports)
PROCTALGIA ( 6 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 6 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 6 FDA reports)
PULMONARY FIBROSIS ( 6 FDA reports)
RETINAL DISORDER ( 6 FDA reports)
SACRALISATION ( 6 FDA reports)
SPINAL CORD COMPRESSION ( 6 FDA reports)
SPLENIC INJURY ( 6 FDA reports)
SPONDYLOLISTHESIS ( 6 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 6 FDA reports)
SUBSTANCE ABUSE ( 6 FDA reports)
SYNCOPE VASOVAGAL ( 6 FDA reports)
TENDON DISORDER ( 6 FDA reports)
THIRST ( 6 FDA reports)
TROPONIN I INCREASED ( 6 FDA reports)
URETHRITIS ( 6 FDA reports)
UTERINE LEIOMYOMA ( 6 FDA reports)
VARICES OESOPHAGEAL ( 6 FDA reports)
VASCULAR INSUFFICIENCY ( 6 FDA reports)
VENTRICULAR HYPOKINESIA ( 6 FDA reports)
VISUAL FIELD DEFECT ( 6 FDA reports)
VITAMIN D DEFICIENCY ( 6 FDA reports)
WEIGHT LOSS POOR ( 6 FDA reports)
ABDOMINAL MASS ( 5 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
ANAL FISTULA ( 5 FDA reports)
ANGIOPLASTY ( 5 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 5 FDA reports)
ANURIA ( 5 FDA reports)
AORTIC ANEURYSM ( 5 FDA reports)
APHTHOUS STOMATITIS ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
APPLICATION SITE PRURITUS ( 5 FDA reports)
ARTHROPOD BITE ( 5 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 5 FDA reports)
BACK DISORDER ( 5 FDA reports)
BACTERAEMIA ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BED REST ( 5 FDA reports)
BILE DUCT STONE ( 5 FDA reports)
BLOOD CREATINE INCREASED ( 5 FDA reports)
BLOOD MAGNESIUM DECREASED ( 5 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 5 FDA reports)
BODY HEIGHT DECREASED ( 5 FDA reports)
BREAST CANCER FEMALE ( 5 FDA reports)
BREAST CANCER RECURRENT ( 5 FDA reports)
BREAST LUMP REMOVAL ( 5 FDA reports)
BREAST OPERATION ( 5 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
CARDIAC ENZYMES INCREASED ( 5 FDA reports)
CATHETER BACTERAEMIA ( 5 FDA reports)
CAUDA EQUINA SYNDROME ( 5 FDA reports)
CHEILITIS ( 5 FDA reports)
CHOKING SENSATION ( 5 FDA reports)
CLOSTRIDIAL INFECTION ( 5 FDA reports)
CONNECTIVE TISSUE DISORDER ( 5 FDA reports)
CONVERSION DISORDER ( 5 FDA reports)
CORONARY ARTERY THROMBOSIS ( 5 FDA reports)
CYST REMOVAL ( 5 FDA reports)
DEBRIDEMENT ( 5 FDA reports)
DENTAL FISTULA ( 5 FDA reports)
DERMATITIS CONTACT ( 5 FDA reports)
DIABETIC GASTROPARESIS ( 5 FDA reports)
DIASTOLIC DYSFUNCTION ( 5 FDA reports)
DISEASE RECURRENCE ( 5 FDA reports)
DROOLING ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 5 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 5 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 5 FDA reports)
EOSINOPHILIA ( 5 FDA reports)
EPIGASTRIC DISCOMFORT ( 5 FDA reports)
EYE INJURY ( 5 FDA reports)
EYE OPERATION ( 5 FDA reports)
EYELID PTOSIS ( 5 FDA reports)
FAECES HARD ( 5 FDA reports)
FAILURE TO THRIVE ( 5 FDA reports)
FIBROSIS ( 5 FDA reports)
FLUID INTAKE REDUCED ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
FURUNCLE ( 5 FDA reports)
GALLBLADDER POLYP ( 5 FDA reports)
GANGRENE ( 5 FDA reports)
GASTRODUODENITIS ( 5 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 5 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 5 FDA reports)
GASTROINTESTINAL PAIN ( 5 FDA reports)
GASTROINTESTINAL ULCER ( 5 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 5 FDA reports)
HAEMORRHOID OPERATION ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HEPATIC ENCEPHALOPATHY ( 5 FDA reports)
HEPATITIS C ( 5 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
HIP ARTHROPLASTY ( 5 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 5 FDA reports)
HYPERPHAGIA ( 5 FDA reports)
HYPERPHOSPHATAEMIA ( 5 FDA reports)
HYPOPHOSPHATAEMIA ( 5 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 5 FDA reports)
IMPAIRED DRIVING ABILITY ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 5 FDA reports)
INTERMITTENT CLAUDICATION ( 5 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 5 FDA reports)
IRITIS ( 5 FDA reports)
IRREGULAR SLEEP PHASE ( 5 FDA reports)
JOINT DISLOCATION ( 5 FDA reports)
LACERATION ( 5 FDA reports)
LICHEN PLANUS ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 5 FDA reports)
LOW TURNOVER OSTEOPATHY ( 5 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
LUNG LOBECTOMY ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
MALIGNANT MELANOMA ( 5 FDA reports)
MASTICATION DISORDER ( 5 FDA reports)
MEDIASTINOSCOPY ( 5 FDA reports)
MELANOSIS COLI ( 5 FDA reports)
MIXED HYPERLIPIDAEMIA ( 5 FDA reports)
MOTOR DYSFUNCTION ( 5 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 5 FDA reports)
MYOPATHY TOXIC ( 5 FDA reports)
NAIL DISORDER ( 5 FDA reports)
NASAL SEPTUM DEVIATION ( 5 FDA reports)
NEPHRITIS ( 5 FDA reports)
NEUROLOGICAL SYMPTOM ( 5 FDA reports)
NEUROPATHIC ARTHROPATHY ( 5 FDA reports)
NODULE ( 5 FDA reports)
ORAL TORUS ( 5 FDA reports)
ORGANISING PNEUMONIA ( 5 FDA reports)
PAIN OF SKIN ( 5 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 5 FDA reports)
PELVIC FRACTURE ( 5 FDA reports)
PLATELET COUNT INCREASED ( 5 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 5 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
PROCEDURAL COMPLICATION ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 5 FDA reports)
PURULENT DISCHARGE ( 5 FDA reports)
RECTAL POLYP ( 5 FDA reports)
RESPIRATORY ACIDOSIS ( 5 FDA reports)
RETINAL HAEMORRHAGE ( 5 FDA reports)
ROSACEA ( 5 FDA reports)
SCRATCH ( 5 FDA reports)
SCROTAL OEDEMA ( 5 FDA reports)
SELF-INJURIOUS IDEATION ( 5 FDA reports)
SJOGREN'S SYNDROME ( 5 FDA reports)
SKELETAL INJURY ( 5 FDA reports)
SKIN FISSURES ( 5 FDA reports)
SKIN LACERATION ( 5 FDA reports)
SMOKER ( 5 FDA reports)
SNORING ( 5 FDA reports)
SPUTUM DISCOLOURED ( 5 FDA reports)
STRABISMUS ( 5 FDA reports)
SUICIDAL BEHAVIOUR ( 5 FDA reports)
SUNBURN ( 5 FDA reports)
TEARFULNESS ( 5 FDA reports)
TEMPERATURE INTOLERANCE ( 5 FDA reports)
THERAPY REGIMEN CHANGED ( 5 FDA reports)
THINKING ABNORMAL ( 5 FDA reports)
TOOTH IMPACTED ( 5 FDA reports)
TOOTH LOSS ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
TRACHEOBRONCHITIS ( 5 FDA reports)
ULCER HAEMORRHAGE ( 5 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 5 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 5 FDA reports)
URINARY TRACT OBSTRUCTION ( 5 FDA reports)
VERTIGO POSITIONAL ( 5 FDA reports)
VULVOVAGINAL DRYNESS ( 5 FDA reports)
WOUND DRAINAGE ( 5 FDA reports)
WOUND HAEMORRHAGE ( 5 FDA reports)
ABDOMINAL INJURY ( 4 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ACHLORHYDRIA ( 4 FDA reports)
AMYLOIDOSIS ( 4 FDA reports)
AORTIC BRUIT ( 4 FDA reports)
AORTIC VALVE DISEASE ( 4 FDA reports)
APHONIA ( 4 FDA reports)
ASEPTIC NECROSIS BONE ( 4 FDA reports)
AUTOIMMUNE HEPATITIS ( 4 FDA reports)
BEDRIDDEN ( 4 FDA reports)
BENIGN COLONIC POLYP ( 4 FDA reports)
BIPOLAR I DISORDER ( 4 FDA reports)
BLADDER OBSTRUCTION ( 4 FDA reports)
BLOOD BICARBONATE INCREASED ( 4 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 4 FDA reports)
BONE OPERATION ( 4 FDA reports)
BRADYKINESIA ( 4 FDA reports)
BRAIN INJURY ( 4 FDA reports)
BRAIN MASS ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
BREAST HAEMORRHAGE ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIAC OPERATION ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 4 FDA reports)
CATARACT NUCLEAR ( 4 FDA reports)
CERUMEN IMPACTION ( 4 FDA reports)
CHEST X-RAY ABNORMAL ( 4 FDA reports)
CHORIORETINAL ATROPHY ( 4 FDA reports)
CLOSTRIDIUM COLITIS ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
COMPRESSION FRACTURE ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 4 FDA reports)
CORNEAL REFLEX DECREASED ( 4 FDA reports)
COSTOCHONDRITIS ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DIABETES INSIPIDUS ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 4 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 4 FDA reports)
DRY GANGRENE ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 4 FDA reports)
FACE INJURY ( 4 FDA reports)
FOOD CRAVING ( 4 FDA reports)
FULL BLOOD COUNT DECREASED ( 4 FDA reports)
GALLBLADDER ENLARGEMENT ( 4 FDA reports)
GASTRIC DILATATION ( 4 FDA reports)
GASTRIC OPERATION ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GYNAECOMASTIA ( 4 FDA reports)
HALLUCINATION, TACTILE ( 4 FDA reports)
HANGOVER ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEART RATE ABNORMAL ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
HERPES VIRUS INFECTION ( 4 FDA reports)
HOSTILITY ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPERTROPHY ( 4 FDA reports)
HYPOCHLORAEMIA ( 4 FDA reports)
HYPOCHROMASIA ( 4 FDA reports)
INCISION SITE HAEMORRHAGE ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
INITIAL INSOMNIA ( 4 FDA reports)
INJECTION SITE BRUISING ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 4 FDA reports)
INTESTINAL ISCHAEMIA ( 4 FDA reports)
INTRACRANIAL ANEURYSM ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
JOINT EFFUSION ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
LARGE INTESTINAL ULCER ( 4 FDA reports)
LIGAMENT INJURY ( 4 FDA reports)
LOWER LIMB FRACTURE ( 4 FDA reports)
LUNG TRANSPLANT ( 4 FDA reports)
MALABSORPTION ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
MARITAL PROBLEM ( 4 FDA reports)
MASS ( 4 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 4 FDA reports)
METASTATIC CARCINOID TUMOUR ( 4 FDA reports)
MICROCYTOSIS ( 4 FDA reports)
MICROVASCULAR ANGINA ( 4 FDA reports)
MONOCYTE COUNT INCREASED ( 4 FDA reports)
MULTIPLE FRACTURES ( 4 FDA reports)
NECROTISING FASCIITIS ( 4 FDA reports)
NEPHROGENIC ANAEMIA ( 4 FDA reports)
NERVE INJURY ( 4 FDA reports)
NERVE ROOT COMPRESSION ( 4 FDA reports)
NICOTINE DEPENDENCE ( 4 FDA reports)
OESOPHAGEAL PAIN ( 4 FDA reports)
PAINFUL ERECTION ( 4 FDA reports)
PANCREATIC INSUFFICIENCY ( 4 FDA reports)
PANIC REACTION ( 4 FDA reports)
PARANEOPLASTIC SYNDROME ( 4 FDA reports)
PARKINSONISM ( 4 FDA reports)
PATHOLOGICAL FRACTURE ( 4 FDA reports)
PHIMOSIS ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
PLANTAR FASCIITIS ( 4 FDA reports)
PORTAL TRIADITIS ( 4 FDA reports)
PRIMARY SEQUESTRUM ( 4 FDA reports)
PROSTATIC DISORDER ( 4 FDA reports)
PROTEIN URINE PRESENT ( 4 FDA reports)
PSORIATIC ARTHROPATHY ( 4 FDA reports)
RENAL TRANSPLANT ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
SHORT-BOWEL SYNDROME ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
SKIN CANDIDA ( 4 FDA reports)
SKIN ODOUR ABNORMAL ( 4 FDA reports)
SKIN REACTION ( 4 FDA reports)
SLUGGISHNESS ( 4 FDA reports)
SPINAL DISORDER ( 4 FDA reports)
SPLENECTOMY ( 4 FDA reports)
STARING ( 4 FDA reports)
STATUS EPILEPTICUS ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 4 FDA reports)
SYNOVITIS ( 4 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 4 FDA reports)
TESTICULAR CYST ( 4 FDA reports)
TESTICULAR PAIN ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
THORACOTOMY ( 4 FDA reports)
TIBIA FRACTURE ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 4 FDA reports)
URETHRAL INJURY ( 4 FDA reports)
URETHRAL STRICTURE ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
VIITH NERVE PARALYSIS ( 4 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 4 FDA reports)
VITAMIN D DECREASED ( 4 FDA reports)
VULVOVAGINAL PRURITUS ( 4 FDA reports)
WEIGHT FLUCTUATION ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
ABSCESS JAW ( 3 FDA reports)
ADENOVIRUS INFECTION ( 3 FDA reports)
ADJUSTMENT DISORDER ( 3 FDA reports)
ALCOHOLIC PANCREATITIS ( 3 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 3 FDA reports)
AMNESTIC DISORDER ( 3 FDA reports)
ANAEMIA POSTOPERATIVE ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANEURYSM ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC CALCIFICATION ( 3 FDA reports)
AORTIC VALVE REPLACEMENT ( 3 FDA reports)
APOPTOSIS ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
APPETITE DISORDER ( 3 FDA reports)
APPLICATION SITE BURNING ( 3 FDA reports)
APPLICATION SITE IRRITATION ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ARTHRITIS BACTERIAL ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
ATHEROSCLEROSIS ( 3 FDA reports)
AUTOMATIC BLADDER ( 3 FDA reports)
BACTERIAL TEST POSITIVE ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BONE GRAFT ( 3 FDA reports)
BORDERLINE GLAUCOMA ( 3 FDA reports)
BRAIN NEOPLASM ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
CARCINOMA IN SITU ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
CHORDOMA ( 3 FDA reports)
CHOREA ( 3 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CLAUSTROPHOBIA ( 3 FDA reports)
CLUMSINESS ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
COLON INJURY ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
COLORECTAL CANCER ( 3 FDA reports)
CONSTRICTED AFFECT ( 3 FDA reports)
CRANIAL NERVE DISORDER ( 3 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DIARRHOEA INFECTIOUS ( 3 FDA reports)
DIPLEGIA ( 3 FDA reports)
DRUG INTERACTION POTENTIATION ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
EJACULATION DISORDER ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
ESSENTIAL HYPERTENSION ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
EXOPHTHALMOS ( 3 FDA reports)
EXTRADURAL HAEMATOMA ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FLAT AFFECT ( 3 FDA reports)
FOOD INTOLERANCE ( 3 FDA reports)
FOOD POISONING ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FRACTURE NONUNION ( 3 FDA reports)
GALLBLADDER OPERATION ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTRIC INFECTION ( 3 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
GENERALISED ANXIETY DISORDER ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GILBERT'S SYNDROME ( 3 FDA reports)
GLYCOSURIA ( 3 FDA reports)
GROWTH HORMONE DEFICIENCY ( 3 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 3 FDA reports)
HAIR TEXTURE ABNORMAL ( 3 FDA reports)
HEART VALVE CALCIFICATION ( 3 FDA reports)
HEART VALVE INCOMPETENCE ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HYPERMETROPIA ( 3 FDA reports)
HYPERTENSIVE HEART DISEASE ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
INCISION SITE PAIN ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INGROWING NAIL ( 3 FDA reports)
INGUINAL HERNIA ( 3 FDA reports)
INJECTION SITE INFLAMMATION ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INSULIN RESISTANCE ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 3 FDA reports)
IRON DEFICIENCY ( 3 FDA reports)
JOINT CREPITATION ( 3 FDA reports)
JUDGEMENT IMPAIRED ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
KIDNEY ENLARGEMENT ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LICHENOID KERATOSIS ( 3 FDA reports)
LIPIDS ABNORMAL ( 3 FDA reports)
LIPODYSTROPHY ACQUIRED ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LOSS OF CONTROL OF LEGS ( 3 FDA reports)
LUNG OPERATION ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MASKED FACIES ( 3 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
METASTASIS ( 3 FDA reports)
METASTATIC NEOPLASM ( 3 FDA reports)
MITRAL VALVE CALCIFICATION ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MUSCLE SWELLING ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MYELITIS ( 3 FDA reports)
NASAL DISCOMFORT ( 3 FDA reports)
NEGATIVE THOUGHTS ( 3 FDA reports)
NEOPLASM PROSTATE ( 3 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 3 FDA reports)
NODAL ARRHYTHMIA ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OBSESSIVE THOUGHTS ( 3 FDA reports)
OBSTRUCTION ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
OESOPHAGEAL DISCOMFORT ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
OTORRHOEA ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
PANCREAS INFECTION ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 3 FDA reports)
PARATHYROIDECTOMY ( 3 FDA reports)
PENILE OEDEMA ( 3 FDA reports)
PENIS DISORDER ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PERIPHERAL NERVE LESION ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PITTING OEDEMA ( 3 FDA reports)
POLYCYTHAEMIA ( 3 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 3 FDA reports)
PORTAL HYPERTENSION ( 3 FDA reports)
POST PROCEDURAL PAIN ( 3 FDA reports)
POSTNASAL DRIP ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 3 FDA reports)
PREVENTIVE SURGERY ( 3 FDA reports)
PRODUCT ADHESION ISSUE ( 3 FDA reports)
PROTRUSION TONGUE ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
PUPIL FIXED ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RENAL CANCER ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
RETINAL DEGENERATION ( 3 FDA reports)
RETINAL VASCULAR DISORDER ( 3 FDA reports)
RETROPERITONEAL HAEMATOMA ( 3 FDA reports)
RHONCHI ( 3 FDA reports)
SALIVARY GLAND CALCULUS ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 3 FDA reports)
SEBORRHOEA ( 3 FDA reports)
SECONDARY HYPOTHYROIDISM ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SINUS POLYP ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SOMATISATION DISORDER ( 3 FDA reports)
SPLENIC CYST ( 3 FDA reports)
SPONDYLOSIS ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
STASIS DERMATITIS ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SUPRAPUBIC PAIN ( 3 FDA reports)
TENSION ( 3 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TONGUE ULCERATION ( 3 FDA reports)
TORTICOLLIS ( 3 FDA reports)
TOXIC DILATATION OF COLON ( 3 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
URETHRAL HAEMORRHAGE ( 3 FDA reports)
URETHRAL MEATUS STENOSIS ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
UTERINE ATROPHY ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VASCULAR PUNCTURE SITE SEALING ( 3 FDA reports)
VENA CAVA THROMBOSIS ( 3 FDA reports)
VENOUS STASIS ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VOMITING PROJECTILE ( 3 FDA reports)
WOUND ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
XANTHOPSIA ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABDOMINAL WALL DISORDER ( 2 FDA reports)
ABNORMAL CLOTTING FACTOR ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ABSCESS DRAINAGE ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ADENOMYOSIS ( 2 FDA reports)
ADENOTONSILLECTOMY ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALVEOLAR OSTEITIS ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
APATHY ( 2 FDA reports)
APNOEA ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPLICATION SITE BURN ( 2 FDA reports)
APPLICATION SITE DRYNESS ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
APPLICATION SITE WARMTH ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ARTHRODESIS ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BASILAR ARTERY STENOSIS ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BILE OUTPUT INCREASED ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BILIARY TRACT OPERATION ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLADDER NEOPLASM SURGERY ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CREATINE ( 2 FDA reports)
BLOOD INSULIN INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 2 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BOREDOM ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREAST CANCER STAGE I ( 2 FDA reports)
BREAST MALFORMATION ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARCINOID SYNDROME ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
COLON ADENOMA ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
CRANIOPHARYNGIOMA ( 2 FDA reports)
CREATINE URINE ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CUBITAL TUNNEL SYNDROME ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
CYANOSIS CENTRAL ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC EYE DISEASE ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
DYSTROPHIC CALCIFICATION ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ENDOCRINE PANCREATIC DISORDER ( 2 FDA reports)
ENDOSCOPY ABNORMAL ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
ESSENTIAL TREMOR ( 2 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 2 FDA reports)
EXERCISE LACK OF ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FOOD INTERACTION ( 2 FDA reports)
FRACTURE DELAYED UNION ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GENERAL SYMPTOM ( 2 FDA reports)
GLIOSIS ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HIDRADENITIS ( 2 FDA reports)
HILAR LYMPHADENOPATHY ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERLACTACIDAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTRANSAMINASAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
HYSTEROSCOPY ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
IMPLANT SITE HAEMATOMA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INFECTED INSECT BITE ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INGROWN HAIR ( 2 FDA reports)
INJECTION SITE COLDNESS ( 2 FDA reports)
INJECTION SITE DISCOLOURATION ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE JOINT SWELLING ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INSULIN RESISTANCE SYNDROME ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 2 FDA reports)
INTERCEPTED MEDICATION ERROR ( 2 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
IRIDOTOMY ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LDL/HDL RATIO INCREASED ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 2 FDA reports)
LIMB ASYMMETRY ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIPOATROPHY ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LYMPH GLAND INFECTION ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
MALFORMATION VENOUS ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MIDDLE EAR DISORDER ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOTONIA ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NASAL OPERATION ( 2 FDA reports)
NASAL SEPTUM PERFORATION ( 2 FDA reports)
NECK MASS ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NERVE DEGENERATION ( 2 FDA reports)
NIGHT BLINDNESS ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OSTEOMYELITIS ACUTE ( 2 FDA reports)
OSTEOMYELITIS CHRONIC ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATIC NECROSIS ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PLICA SYNDROME ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POST PROCEDURAL SWELLING ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PROSTATIC ABSCESS ( 2 FDA reports)
PSYCHOSOMATIC DISEASE ( 2 FDA reports)
PUBIC RAMI FRACTURE ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RADIUS FRACTURE ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH SCALY ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RECTAL ABSCESS ( 2 FDA reports)
RECTAL SPASM ( 2 FDA reports)
RED BLOOD CELL ABNORMALITY ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETICULOCYTE COUNT DECREASED ( 2 FDA reports)
RETROPERITONEAL OEDEMA ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SEMEN VOLUME DECREASED ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SHOULDER OPERATION ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN MACERATION ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 2 FDA reports)
SPINAL LAMINECTOMY ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
STEREOTYPY ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SYSTOLIC DYSFUNCTION ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
TENDON INJURY ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URINARY HESITATION ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 2 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 2 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABSCESS NECK ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACOUSTIC STIMULATION TESTS ABNORMAL ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOID CYSTIC CARCINOMA ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL SPASM ( 1 FDA reports)
ANAL SPHINCTER HYPERTONIA ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANORECTAL STENOSIS ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BASAL GANGLIA STROKE ( 1 FDA reports)
BASOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 1 FDA reports)
BETA GLOBULIN DECREASED ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE NORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN ABNORMAL ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD HIV RNA INCREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL NEOPLASM ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHITIS ACUTE VIRAL ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOGENIC CYST ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BURN INFECTION ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARDIAC CIRRHOSIS ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CIRCUMCISION ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLON CANCER STAGE III ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLORECTAL CANCER STAGE II ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 1 FDA reports)
CORNEAL STRIAE ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DELIRIUM FEBRILE ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DUODENAL OBSTRUCTION ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
ECZEMA VESICULAR ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXERCISE CAPACITY DECREASED ( 1 FDA reports)
EXTERNAL EAR LESION EXCISION ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE PROSTHESIS USER ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYELID RETRACTION ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FAECAL OCCULT BLOOD ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FISTULA REPAIR ( 1 FDA reports)
FLAIL CHEST ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FULGURATION ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GALLBLADDER EMPYEMA ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS RADIATION ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT HAEMORRHAGE ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMODIALYSIS COMPLICATION ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERALBUMINAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPHAEMA ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPINGEMENT SYNDROME ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTION PROPHYLAXIS ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFUSION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE STINGING ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRANASAL FUNGAL INFECTION ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIFE EXPECTANCY SHORTENED ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGHT CHAIN DISEASE ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVER SARCOIDOSIS ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MOANING ( 1 FDA reports)
MODERATE MENTAL RETARDATION ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYELOMA RECURRENCE ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NAIL AVULSION ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL INJURY ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPIATES NEGATIVE ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PAPILLARY MUSCLE INFARCTION ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PENILE ERYTHEMA ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET COUNT NORMAL ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA ADENOVIRAL ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PRODUCT COMMINGLING ( 1 FDA reports)
PRODUCT CONTAINER SEAL ISSUE ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT IDENTIFICATION NUMBER ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROTEIN S ABNORMAL ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYURIA ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL EXAMINATION ABNORMAL ( 1 FDA reports)
RECTAL FISTULA REPAIR ( 1 FDA reports)
RECTAL STENOSIS ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL ONCOCYTOMA ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHABDOMYOMA ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCLEROTHERAPY ( 1 FDA reports)
SCROTAL HAEMATOMA ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SENSATION OF PRESSURE IN EAR ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEPTOPLASTY ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SEX HORMONE BINDING GLOBULIN DECREASED ( 1 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN NEOPLASM BLEEDING ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SMOKING CESSATION THERAPY ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPERM CONCENTRATION DECREASED ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STENT-GRAFT ENDOLEAK ( 1 FDA reports)
STITCH ABSCESS ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THYMIC CANCER METASTATIC ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE IV HYPERLIPIDAEMIA ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
ULTRASONIC ANGIOGRAM ABNORMAL ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UROGENITAL FISTULA ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
VAGINAL CANCER RECURRENT ( 1 FDA reports)
VAGINAL CYST ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS PRESSURE INCREASED ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENOUS VALVE RUPTURED ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORD NEOPLASM ( 1 FDA reports)
VULVAL CANCER ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND SEPSIS ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)
YAWNING ( 1 FDA reports)