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

NAUSEA ( 765 FDA reports)
DIZZINESS ( 641 FDA reports)
DRUG INEFFECTIVE ( 544 FDA reports)
DYSPNOEA ( 526 FDA reports)
PAIN ( 526 FDA reports)
FATIGUE ( 512 FDA reports)
DIARRHOEA ( 473 FDA reports)
HEADACHE ( 468 FDA reports)
HYPERTENSION ( 465 FDA reports)
ANXIETY ( 425 FDA reports)
ASTHENIA ( 425 FDA reports)
WEIGHT DECREASED ( 394 FDA reports)
BLOOD PRESSURE INCREASED ( 368 FDA reports)
FALL ( 358 FDA reports)
MYOCARDIAL INFARCTION ( 358 FDA reports)
OEDEMA PERIPHERAL ( 357 FDA reports)
PAIN IN EXTREMITY ( 355 FDA reports)
VOMITING ( 353 FDA reports)
BLOOD GLUCOSE INCREASED ( 347 FDA reports)
DEPRESSION ( 345 FDA reports)
CHEST PAIN ( 337 FDA reports)
ANAEMIA ( 330 FDA reports)
ARTHRALGIA ( 291 FDA reports)
RENAL FAILURE ( 286 FDA reports)
BACK PAIN ( 285 FDA reports)
CEREBROVASCULAR ACCIDENT ( 272 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 263 FDA reports)
INSOMNIA ( 262 FDA reports)
HYPOTENSION ( 260 FDA reports)
COUGH ( 257 FDA reports)
INJURY ( 244 FDA reports)
MALAISE ( 238 FDA reports)
CONSTIPATION ( 226 FDA reports)
ABDOMINAL PAIN ( 223 FDA reports)
PRURITUS ( 223 FDA reports)
DEHYDRATION ( 218 FDA reports)
WEIGHT INCREASED ( 212 FDA reports)
MYALGIA ( 210 FDA reports)
DECREASED APPETITE ( 208 FDA reports)
DEATH ( 207 FDA reports)
RASH ( 206 FDA reports)
PALPITATIONS ( 203 FDA reports)
DYSGEUSIA ( 201 FDA reports)
CORONARY ARTERY DISEASE ( 199 FDA reports)
FEELING ABNORMAL ( 196 FDA reports)
PYREXIA ( 193 FDA reports)
TREMOR ( 191 FDA reports)
ABDOMINAL PAIN UPPER ( 189 FDA reports)
MUSCLE SPASMS ( 189 FDA reports)
LOSS OF CONSCIOUSNESS ( 183 FDA reports)
ATRIAL FIBRILLATION ( 182 FDA reports)
HYPOAESTHESIA ( 177 FDA reports)
URINARY TRACT INFECTION ( 176 FDA reports)
CONFUSIONAL STATE ( 174 FDA reports)
PNEUMONIA ( 171 FDA reports)
VISION BLURRED ( 171 FDA reports)
EMOTIONAL DISTRESS ( 169 FDA reports)
RENAL FAILURE ACUTE ( 166 FDA reports)
GAIT DISTURBANCE ( 165 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 161 FDA reports)
SYNCOPE ( 160 FDA reports)
FLUSHING ( 157 FDA reports)
DYSPEPSIA ( 151 FDA reports)
PARAESTHESIA ( 150 FDA reports)
CHEST DISCOMFORT ( 146 FDA reports)
MUSCULAR WEAKNESS ( 145 FDA reports)
HYPERHIDROSIS ( 132 FDA reports)
SOMNOLENCE ( 129 FDA reports)
PLEURAL EFFUSION ( 123 FDA reports)
CHILLS ( 120 FDA reports)
BURNING SENSATION ( 118 FDA reports)
PANCREATITIS ( 118 FDA reports)
RENAL IMPAIRMENT ( 118 FDA reports)
UNEVALUABLE EVENT ( 118 FDA reports)
CONDITION AGGRAVATED ( 116 FDA reports)
RENAL FAILURE CHRONIC ( 115 FDA reports)
ABDOMINAL DISTENSION ( 114 FDA reports)
ALOPECIA ( 114 FDA reports)
NEUROPATHY PERIPHERAL ( 114 FDA reports)
ERYTHEMA ( 112 FDA reports)
URTICARIA ( 111 FDA reports)
BLOOD GLUCOSE DECREASED ( 110 FDA reports)
ANHEDONIA ( 109 FDA reports)
HAEMOGLOBIN DECREASED ( 109 FDA reports)
OSTEOARTHRITIS ( 109 FDA reports)
DRY MOUTH ( 108 FDA reports)
DYSPHAGIA ( 108 FDA reports)
FEAR ( 108 FDA reports)
HYPOGLYCAEMIA ( 108 FDA reports)
ABDOMINAL DISCOMFORT ( 103 FDA reports)
NEPHROLITHIASIS ( 103 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 102 FDA reports)
BLOOD PRESSURE DECREASED ( 102 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 102 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 101 FDA reports)
CONVULSION ( 100 FDA reports)
ARRHYTHMIA ( 98 FDA reports)
BLOOD CREATININE INCREASED ( 98 FDA reports)
CELLULITIS ( 98 FDA reports)
HEART RATE INCREASED ( 97 FDA reports)
HYPONATRAEMIA ( 97 FDA reports)
DIABETES MELLITUS ( 95 FDA reports)
STRESS ( 95 FDA reports)
NERVOUSNESS ( 93 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 93 FDA reports)
CARDIAC DISORDER ( 91 FDA reports)
GASTRITIS ( 91 FDA reports)
RESPIRATORY FAILURE ( 91 FDA reports)
SINUSITIS ( 91 FDA reports)
SLEEP APNOEA SYNDROME ( 90 FDA reports)
ANOREXIA ( 88 FDA reports)
ARTHRITIS ( 88 FDA reports)
POLLAKIURIA ( 87 FDA reports)
DEEP VEIN THROMBOSIS ( 86 FDA reports)
FEELING HOT ( 86 FDA reports)
NECK PAIN ( 86 FDA reports)
ASTHMA ( 84 FDA reports)
JOINT SWELLING ( 84 FDA reports)
SWELLING ( 84 FDA reports)
CATARACT ( 83 FDA reports)
HYPERSENSITIVITY ( 83 FDA reports)
OVERDOSE ( 83 FDA reports)
DIVERTICULUM ( 82 FDA reports)
TYPE 2 DIABETES MELLITUS ( 82 FDA reports)
MUSCULOSKELETAL PAIN ( 81 FDA reports)
RENAL DISORDER ( 81 FDA reports)
OEDEMA ( 80 FDA reports)
BRADYCARDIA ( 79 FDA reports)
DYSPNOEA EXERTIONAL ( 79 FDA reports)
HYPERKALAEMIA ( 78 FDA reports)
OSTEONECROSIS OF JAW ( 78 FDA reports)
BRONCHITIS ( 77 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 77 FDA reports)
CONTUSION ( 77 FDA reports)
DRUG INTERACTION ( 77 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 76 FDA reports)
HYPERLIPIDAEMIA ( 75 FDA reports)
INFECTION ( 75 FDA reports)
NASOPHARYNGITIS ( 75 FDA reports)
EPISTAXIS ( 73 FDA reports)
LETHARGY ( 73 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 73 FDA reports)
RENAL INJURY ( 73 FDA reports)
CARDIOMEGALY ( 72 FDA reports)
ERECTILE DYSFUNCTION ( 72 FDA reports)
BALANCE DISORDER ( 71 FDA reports)
MITRAL VALVE INCOMPETENCE ( 71 FDA reports)
DRUG HYPERSENSITIVITY ( 70 FDA reports)
OSTEOPOROSIS ( 70 FDA reports)
INJECTION SITE PAIN ( 69 FDA reports)
MENTAL STATUS CHANGES ( 69 FDA reports)
SEPSIS ( 69 FDA reports)
AMNESIA ( 67 FDA reports)
THROMBOCYTOPENIA ( 67 FDA reports)
BONE PAIN ( 66 FDA reports)
CARDIAC ARREST ( 66 FDA reports)
ECONOMIC PROBLEM ( 66 FDA reports)
FLATULENCE ( 66 FDA reports)
HEART RATE DECREASED ( 66 FDA reports)
THROMBOSIS ( 66 FDA reports)
CHOLELITHIASIS ( 65 FDA reports)
HEART RATE IRREGULAR ( 65 FDA reports)
MEMORY IMPAIRMENT ( 65 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 65 FDA reports)
HOT FLUSH ( 64 FDA reports)
SWELLING FACE ( 64 FDA reports)
ARTERIOSCLEROSIS ( 63 FDA reports)
BLOOD SODIUM DECREASED ( 63 FDA reports)
DYSPHONIA ( 63 FDA reports)
HAEMORRHAGE ( 62 FDA reports)
HYPERGLYCAEMIA ( 62 FDA reports)
PULMONARY EMBOLISM ( 62 FDA reports)
CYSTITIS ( 61 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 61 FDA reports)
HALLUCINATION ( 61 FDA reports)
RHABDOMYOLYSIS ( 61 FDA reports)
TOOTH LOSS ( 60 FDA reports)
URINARY RETENTION ( 60 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 59 FDA reports)
PLATELET COUNT DECREASED ( 59 FDA reports)
MEDICATION ERROR ( 58 FDA reports)
OSTEOMYELITIS ( 58 FDA reports)
ATELECTASIS ( 57 FDA reports)
HYPOTHYROIDISM ( 57 FDA reports)
ROAD TRAFFIC ACCIDENT ( 57 FDA reports)
WHEEZING ( 57 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 56 FDA reports)
ANGINA PECTORIS ( 56 FDA reports)
BONE DISORDER ( 56 FDA reports)
INFLUENZA ( 56 FDA reports)
INGROWING NAIL ( 56 FDA reports)
MIGRAINE ( 56 FDA reports)
MULTI-ORGAN FAILURE ( 56 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 55 FDA reports)
DYSURIA ( 55 FDA reports)
HAEMATURIA ( 55 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 55 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 55 FDA reports)
FEMUR FRACTURE ( 54 FDA reports)
HYPOKALAEMIA ( 54 FDA reports)
MOBILITY DECREASED ( 54 FDA reports)
RENAL CYST ( 54 FDA reports)
SLEEP DISORDER ( 54 FDA reports)
TINNITUS ( 54 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 53 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 53 FDA reports)
OROPHARYNGEAL PAIN ( 53 FDA reports)
SUICIDAL IDEATION ( 53 FDA reports)
ADVERSE EVENT ( 52 FDA reports)
ARTHROPATHY ( 52 FDA reports)
BREAST CANCER ( 52 FDA reports)
DISORIENTATION ( 52 FDA reports)
OSTEOPENIA ( 52 FDA reports)
ABASIA ( 51 FDA reports)
AGITATION ( 51 FDA reports)
HAEMORRHOIDS ( 51 FDA reports)
HERPES ZOSTER ( 51 FDA reports)
MYOCARDIAL ISCHAEMIA ( 51 FDA reports)
PULMONARY OEDEMA ( 51 FDA reports)
VERTIGO ( 51 FDA reports)
CHOLECYSTECTOMY ( 50 FDA reports)
INCORRECT DOSE ADMINISTERED ( 50 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 50 FDA reports)
LUNG NEOPLASM ( 49 FDA reports)
MENISCUS LESION ( 49 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 48 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 48 FDA reports)
CORONARY ARTERY OCCLUSION ( 48 FDA reports)
HAEMATOCHEZIA ( 48 FDA reports)
HEPATIC ENZYME INCREASED ( 48 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 48 FDA reports)
RASH PRURITIC ( 48 FDA reports)
URINARY INCONTINENCE ( 48 FDA reports)
COLONIC POLYP ( 47 FDA reports)
GASTRIC DISORDER ( 47 FDA reports)
OFF LABEL USE ( 47 FDA reports)
RIB FRACTURE ( 47 FDA reports)
SWOLLEN TONGUE ( 47 FDA reports)
GALLBLADDER DISORDER ( 46 FDA reports)
HIATUS HERNIA ( 46 FDA reports)
STOMATITIS ( 46 FDA reports)
CARDIOVASCULAR DISORDER ( 45 FDA reports)
DRUG DOSE OMISSION ( 45 FDA reports)
OSTEONECROSIS ( 45 FDA reports)
SPEECH DISORDER ( 45 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 45 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 44 FDA reports)
BONE DENSITY DECREASED ( 44 FDA reports)
DIVERTICULITIS ( 44 FDA reports)
INFLUENZA LIKE ILLNESS ( 44 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 44 FDA reports)
TACHYCARDIA ( 44 FDA reports)
VISUAL ACUITY REDUCED ( 44 FDA reports)
ANGIOEDEMA ( 43 FDA reports)
BLOOD POTASSIUM INCREASED ( 43 FDA reports)
CARDIAC FAILURE ( 43 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 43 FDA reports)
DENTAL CARIES ( 42 FDA reports)
HEPATITIS ( 42 FDA reports)
RHINORRHOEA ( 42 FDA reports)
TOOTH DISORDER ( 42 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 42 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 42 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 41 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 41 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 41 FDA reports)
FLUID RETENTION ( 41 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 41 FDA reports)
PANCYTOPENIA ( 41 FDA reports)
RECTAL HAEMORRHAGE ( 41 FDA reports)
ROTATOR CUFF SYNDROME ( 41 FDA reports)
SCAR ( 41 FDA reports)
STAPHYLOCOCCAL INFECTION ( 41 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 40 FDA reports)
INJECTION SITE HAEMORRHAGE ( 40 FDA reports)
IRRITABILITY ( 40 FDA reports)
LEUKOPENIA ( 40 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 40 FDA reports)
THROAT IRRITATION ( 40 FDA reports)
MULTIPLE INJURIES ( 39 FDA reports)
NEOPLASM MALIGNANT ( 39 FDA reports)
CEREBRAL INFARCTION ( 38 FDA reports)
DEMENTIA ( 38 FDA reports)
EMOTIONAL DISORDER ( 38 FDA reports)
EXPOSED BONE IN JAW ( 38 FDA reports)
GOUT ( 38 FDA reports)
LIMB DISCOMFORT ( 38 FDA reports)
OBESITY ( 38 FDA reports)
SPINAL COLUMN STENOSIS ( 38 FDA reports)
BLOOD COUNT ABNORMAL ( 37 FDA reports)
DRUG EFFECT DECREASED ( 37 FDA reports)
FOOT FRACTURE ( 37 FDA reports)
HYPOXIA ( 37 FDA reports)
NASAL CONGESTION ( 37 FDA reports)
ORAL PAIN ( 37 FDA reports)
TREATMENT NONCOMPLIANCE ( 37 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 37 FDA reports)
FEELING JITTERY ( 36 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 36 FDA reports)
ABNORMAL DREAMS ( 35 FDA reports)
DYSSTASIA ( 35 FDA reports)
ERUCTATION ( 35 FDA reports)
HAEMATOCRIT DECREASED ( 35 FDA reports)
RESPIRATORY DISTRESS ( 35 FDA reports)
SINUS TACHYCARDIA ( 35 FDA reports)
CARDIAC MURMUR ( 34 FDA reports)
CARDIOMYOPATHY ( 34 FDA reports)
CAROTID ARTERY STENOSIS ( 34 FDA reports)
CEREBRAL ATROPHY ( 34 FDA reports)
DRY SKIN ( 34 FDA reports)
FEELING COLD ( 34 FDA reports)
HAEMATOMA ( 34 FDA reports)
ORTHOPNOEA ( 34 FDA reports)
ORTHOSTATIC HYPOTENSION ( 34 FDA reports)
ANGIONEUROTIC OEDEMA ( 33 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 33 FDA reports)
BLOOD UREA INCREASED ( 33 FDA reports)
BURSITIS ( 33 FDA reports)
CARPAL TUNNEL SYNDROME ( 33 FDA reports)
CRYING ( 33 FDA reports)
DELIRIUM ( 33 FDA reports)
GASTROENTERITIS ( 33 FDA reports)
GASTROINTESTINAL DISORDER ( 33 FDA reports)
HEPATIC STEATOSIS ( 33 FDA reports)
IMPAIRED HEALING ( 33 FDA reports)
MASTICATION DISORDER ( 33 FDA reports)
OXYGEN SATURATION DECREASED ( 33 FDA reports)
PANCREATITIS ACUTE ( 33 FDA reports)
RASH MACULAR ( 33 FDA reports)
SKIN BURNING SENSATION ( 33 FDA reports)
SPINAL OSTEOARTHRITIS ( 33 FDA reports)
TOE OPERATION ( 33 FDA reports)
VENTRICULAR TACHYCARDIA ( 33 FDA reports)
BLINDNESS UNILATERAL ( 32 FDA reports)
DEFORMITY ( 32 FDA reports)
DYSKINESIA ( 32 FDA reports)
EYE DISORDER ( 32 FDA reports)
FLANK PAIN ( 32 FDA reports)
LYMPHADENOPATHY ( 32 FDA reports)
SKIN EXFOLIATION ( 32 FDA reports)
BLOOD POTASSIUM DECREASED ( 31 FDA reports)
DEAFNESS ( 31 FDA reports)
DYSARTHRIA ( 31 FDA reports)
PERICARDIAL EFFUSION ( 31 FDA reports)
PHARYNGEAL OEDEMA ( 31 FDA reports)
PRODUCT QUALITY ISSUE ( 31 FDA reports)
PULMONARY HYPERTENSION ( 31 FDA reports)
RETCHING ( 31 FDA reports)
SKIN DISCOLOURATION ( 31 FDA reports)
VISUAL DISTURBANCE ( 31 FDA reports)
ASCITES ( 30 FDA reports)
CANDIDIASIS ( 30 FDA reports)
DISCOMFORT ( 30 FDA reports)
DISEASE PROGRESSION ( 30 FDA reports)
DISTURBANCE IN ATTENTION ( 30 FDA reports)
EYE PAIN ( 30 FDA reports)
LIMB INJURY ( 30 FDA reports)
MACULAR DEGENERATION ( 30 FDA reports)
NOCTURIA ( 30 FDA reports)
PAIN IN JAW ( 30 FDA reports)
PANIC ATTACK ( 30 FDA reports)
PRODUCTIVE COUGH ( 30 FDA reports)
PRURITUS GENERALISED ( 30 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 30 FDA reports)
TOOTHACHE ( 30 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 30 FDA reports)
AORTIC VALVE INCOMPETENCE ( 29 FDA reports)
DIFFICULTY IN WALKING ( 29 FDA reports)
DYSLIPIDAEMIA ( 29 FDA reports)
GASTRIC ULCER ( 29 FDA reports)
HAEMATEMESIS ( 29 FDA reports)
JOINT STIFFNESS ( 29 FDA reports)
LACUNAR INFARCTION ( 29 FDA reports)
NEUTROPENIA ( 29 FDA reports)
RESTLESS LEGS SYNDROME ( 29 FDA reports)
TENDONITIS ( 29 FDA reports)
ABDOMINAL PAIN LOWER ( 28 FDA reports)
APHASIA ( 28 FDA reports)
BLOOD URINE PRESENT ( 28 FDA reports)
CIRCULATORY COLLAPSE ( 28 FDA reports)
FEBRILE NEUTROPENIA ( 28 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 28 FDA reports)
HEPATIC FAILURE ( 28 FDA reports)
HIP FRACTURE ( 28 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 28 FDA reports)
PATHOLOGICAL FRACTURE ( 28 FDA reports)
PSORIASIS ( 28 FDA reports)
SINUS BRADYCARDIA ( 28 FDA reports)
THROAT TIGHTNESS ( 28 FDA reports)
THYROID DISORDER ( 28 FDA reports)
UPPER LIMB FRACTURE ( 28 FDA reports)
ATRIAL FLUTTER ( 27 FDA reports)
CARDIO-RESPIRATORY ARREST ( 27 FDA reports)
DIABETIC RETINOPATHY ( 27 FDA reports)
FAECES DISCOLOURED ( 27 FDA reports)
GROIN PAIN ( 27 FDA reports)
ILL-DEFINED DISORDER ( 27 FDA reports)
INJECTION SITE ERYTHEMA ( 27 FDA reports)
LEUKOCYTOSIS ( 27 FDA reports)
LUNG INFILTRATION ( 27 FDA reports)
PRESYNCOPE ( 27 FDA reports)
SINUS DISORDER ( 27 FDA reports)
SKIN INDURATION ( 27 FDA reports)
TOOTH ABSCESS ( 27 FDA reports)
ANAPHYLACTIC REACTION ( 26 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 26 FDA reports)
BLINDNESS ( 26 FDA reports)
BLISTER ( 26 FDA reports)
COAGULOPATHY ( 26 FDA reports)
DECREASED INTEREST ( 26 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 26 FDA reports)
DIABETIC NEUROPATHY ( 26 FDA reports)
EYE SWELLING ( 26 FDA reports)
HYPERTHYROIDISM ( 26 FDA reports)
KIDNEY INFECTION ( 26 FDA reports)
LIVER DISORDER ( 26 FDA reports)
LUNG DISORDER ( 26 FDA reports)
PHOTOSENSITIVITY REACTION ( 26 FDA reports)
SHOCK ( 26 FDA reports)
SURGERY ( 26 FDA reports)
TONGUE ULCERATION ( 26 FDA reports)
VENTRICULAR FIBRILLATION ( 26 FDA reports)
ANGINA UNSTABLE ( 25 FDA reports)
BIPOLAR I DISORDER ( 25 FDA reports)
COMA ( 25 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 25 FDA reports)
DIABETIC KETOACIDOSIS ( 25 FDA reports)
DIALYSIS ( 25 FDA reports)
DRY EYE ( 25 FDA reports)
FULL BLOOD COUNT DECREASED ( 25 FDA reports)
KNEE ARTHROPLASTY ( 25 FDA reports)
LOBAR PNEUMONIA ( 25 FDA reports)
METABOLIC ACIDOSIS ( 25 FDA reports)
MOUTH ULCERATION ( 25 FDA reports)
MOVEMENT DISORDER ( 25 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 25 FDA reports)
AORTIC ANEURYSM ( 24 FDA reports)
BLOOD URIC ACID INCREASED ( 24 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 24 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 24 FDA reports)
DIZZINESS POSTURAL ( 24 FDA reports)
EJECTION FRACTION DECREASED ( 24 FDA reports)
HAEMOPTYSIS ( 24 FDA reports)
INTESTINAL OBSTRUCTION ( 24 FDA reports)
MIDDLE INSOMNIA ( 24 FDA reports)
NIGHT SWEATS ( 24 FDA reports)
NIGHTMARE ( 24 FDA reports)
ORAL HERPES ( 24 FDA reports)
PHYSICAL DISABILITY ( 24 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 24 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 24 FDA reports)
SPINAL COMPRESSION FRACTURE ( 24 FDA reports)
UNRESPONSIVE TO STIMULI ( 24 FDA reports)
BODY TEMPERATURE INCREASED ( 23 FDA reports)
CAROTID ARTERY OCCLUSION ( 23 FDA reports)
HAND FRACTURE ( 23 FDA reports)
HYDRONEPHROSIS ( 23 FDA reports)
HYPERCHOLESTEROLAEMIA ( 23 FDA reports)
HYPOPHAGIA ( 23 FDA reports)
IRON DEFICIENCY ANAEMIA ( 23 FDA reports)
JOINT INJURY ( 23 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 23 FDA reports)
LYMPHOEDEMA ( 23 FDA reports)
MELAENA ( 23 FDA reports)
MENTAL DISORDER ( 23 FDA reports)
MICTURITION URGENCY ( 23 FDA reports)
OESOPHAGITIS ( 23 FDA reports)
PERICARDITIS ( 23 FDA reports)
SCIATICA ( 23 FDA reports)
SUBDURAL HAEMATOMA ( 23 FDA reports)
TOOTH EXTRACTION ( 23 FDA reports)
ULCER ( 23 FDA reports)
UROSEPSIS ( 23 FDA reports)
VISUAL IMPAIRMENT ( 23 FDA reports)
BACK INJURY ( 22 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 22 FDA reports)
CHOLECYSTITIS CHRONIC ( 22 FDA reports)
DERMATITIS EXFOLIATIVE ( 22 FDA reports)
FIBROSIS ( 22 FDA reports)
HEAD INJURY ( 22 FDA reports)
LACERATION ( 22 FDA reports)
MASS ( 22 FDA reports)
ORAL DISORDER ( 22 FDA reports)
RESPIRATORY DISORDER ( 22 FDA reports)
SENSORY LOSS ( 22 FDA reports)
SEXUAL DYSFUNCTION ( 22 FDA reports)
SPINAL CORD COMPRESSION ( 22 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 22 FDA reports)
ABSCESS ( 21 FDA reports)
AGEUSIA ( 21 FDA reports)
CEREBRAL HAEMORRHAGE ( 21 FDA reports)
CHOLECYSTITIS ( 21 FDA reports)
CORONARY ARTERY STENOSIS ( 21 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 21 FDA reports)
DRUG DEPENDENCE ( 21 FDA reports)
FIBULA FRACTURE ( 21 FDA reports)
FLUID OVERLOAD ( 21 FDA reports)
FRACTURE ( 21 FDA reports)
HEPATIC CIRRHOSIS ( 21 FDA reports)
HERNIA ( 21 FDA reports)
INTERSTITIAL LUNG DISEASE ( 21 FDA reports)
NEURALGIA ( 21 FDA reports)
RETINAL VEIN OCCLUSION ( 21 FDA reports)
SEPTIC SHOCK ( 21 FDA reports)
SICK SINUS SYNDROME ( 21 FDA reports)
SKIN FIBROSIS ( 21 FDA reports)
STOMACH DISCOMFORT ( 21 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 21 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 21 FDA reports)
ABDOMINAL HERNIA ( 20 FDA reports)
ANGER ( 20 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 20 FDA reports)
COLITIS ( 20 FDA reports)
CONJUNCTIVITIS ( 20 FDA reports)
DECUBITUS ULCER ( 20 FDA reports)
DIPLOPIA ( 20 FDA reports)
GLOSSODYNIA ( 20 FDA reports)
ISCHAEMIA ( 20 FDA reports)
JAUNDICE ( 20 FDA reports)
METASTASES TO LIVER ( 20 FDA reports)
MULTIPLE MYELOMA ( 20 FDA reports)
NEOPLASM PROGRESSION ( 20 FDA reports)
PNEUMONIA ASPIRATION ( 20 FDA reports)
RASH ERYTHEMATOUS ( 20 FDA reports)
SENSATION OF HEAVINESS ( 20 FDA reports)
SKIN TIGHTNESS ( 20 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 20 FDA reports)
ACCIDENTAL OVERDOSE ( 19 FDA reports)
BONE LESION ( 19 FDA reports)
DIASTOLIC DYSFUNCTION ( 19 FDA reports)
EMPHYSEMA ( 19 FDA reports)
EYE PRURITUS ( 19 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 19 FDA reports)
HYPERSOMNIA ( 19 FDA reports)
INFUSION RELATED REACTION ( 19 FDA reports)
ISCHAEMIC STROKE ( 19 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 19 FDA reports)
PALLOR ( 19 FDA reports)
PELVIC PAIN ( 19 FDA reports)
PROSTATE CANCER ( 19 FDA reports)
PULMONARY FIBROSIS ( 19 FDA reports)
RENAL ARTERY STENOSIS ( 19 FDA reports)
SKIN LESION ( 19 FDA reports)
SUICIDE ATTEMPT ( 19 FDA reports)
AORTIC STENOSIS ( 18 FDA reports)
ATRIOVENTRICULAR BLOCK ( 18 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 18 FDA reports)
BACK DISORDER ( 18 FDA reports)
CEREBRAL ISCHAEMIA ( 18 FDA reports)
COLD SWEAT ( 18 FDA reports)
EATING DISORDER ( 18 FDA reports)
EYE HAEMORRHAGE ( 18 FDA reports)
GENERALISED OEDEMA ( 18 FDA reports)
HYPERURICAEMIA ( 18 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 18 FDA reports)
LACRIMATION INCREASED ( 18 FDA reports)
LIP SWELLING ( 18 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 18 FDA reports)
MUSCLE STRAIN ( 18 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 18 FDA reports)
POST PROCEDURAL COMPLICATION ( 18 FDA reports)
PROCEDURAL PAIN ( 18 FDA reports)
PROTEINURIA ( 18 FDA reports)
RASH GENERALISED ( 18 FDA reports)
RASH MACULO-PAPULAR ( 18 FDA reports)
RESTLESSNESS ( 18 FDA reports)
TARDIVE DYSKINESIA ( 18 FDA reports)
TOOTH REPAIR ( 18 FDA reports)
URETHRAL STENOSIS ( 18 FDA reports)
URINE OUTPUT DECREASED ( 18 FDA reports)
VASCULITIS ( 18 FDA reports)
VITAMIN D DEFICIENCY ( 18 FDA reports)
ANKLE FRACTURE ( 17 FDA reports)
CARDIAC VALVE DISEASE ( 17 FDA reports)
CARDIOGENIC SHOCK ( 17 FDA reports)
CHROMATURIA ( 17 FDA reports)
COMPLETED SUICIDE ( 17 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 17 FDA reports)
DERMATITIS ( 17 FDA reports)
DIVERTICULUM INTESTINAL ( 17 FDA reports)
EXCORIATION ( 17 FDA reports)
GLAUCOMA ( 17 FDA reports)
INGUINAL HERNIA ( 17 FDA reports)
INJECTION SITE BRUISING ( 17 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 17 FDA reports)
MENTAL IMPAIRMENT ( 17 FDA reports)
MULTIPLE SCLEROSIS ( 17 FDA reports)
MUSCLE TIGHTNESS ( 17 FDA reports)
ONYCHOMYCOSIS ( 17 FDA reports)
SCOLIOSIS ( 17 FDA reports)
SKIN HYPERPIGMENTATION ( 17 FDA reports)
SKIN HYPERTROPHY ( 17 FDA reports)
STENT PLACEMENT ( 17 FDA reports)
VENTRICULAR DYSFUNCTION ( 17 FDA reports)
VENTRICULAR HYPERTROPHY ( 17 FDA reports)
ABNORMAL BEHAVIOUR ( 16 FDA reports)
AGGRESSION ( 16 FDA reports)
ANGIOPATHY ( 16 FDA reports)
APATHY ( 16 FDA reports)
APPLICATION SITE PRURITUS ( 16 FDA reports)
BLADDER CANCER ( 16 FDA reports)
BLOOD CALCIUM DECREASED ( 16 FDA reports)
CAROTID BRUIT ( 16 FDA reports)
DEVICE FAILURE ( 16 FDA reports)
DRUG DISPENSING ERROR ( 16 FDA reports)
FIBROMYALGIA ( 16 FDA reports)
HYPOVOLAEMIA ( 16 FDA reports)
ILEUS ( 16 FDA reports)
IMPAIRED DRIVING ABILITY ( 16 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 16 FDA reports)
INCISIONAL HERNIA ( 16 FDA reports)
INFLAMMATION ( 16 FDA reports)
JAW DISORDER ( 16 FDA reports)
KYPHOSIS ( 16 FDA reports)
MALNUTRITION ( 16 FDA reports)
METASTASES TO SPINE ( 16 FDA reports)
MOOD SWINGS ( 16 FDA reports)
NEUTROPHIL COUNT DECREASED ( 16 FDA reports)
OCCULT BLOOD POSITIVE ( 16 FDA reports)
PANCREATIC CYST ( 16 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 16 FDA reports)
SKIN ULCER ( 16 FDA reports)
STENT OCCLUSION ( 16 FDA reports)
STEVENS-JOHNSON SYNDROME ( 16 FDA reports)
URETHRAL OBSTRUCTION ( 16 FDA reports)
ACUTE RESPIRATORY FAILURE ( 15 FDA reports)
APPLICATION SITE ERYTHEMA ( 15 FDA reports)
CEREBELLAR HAEMORRHAGE ( 15 FDA reports)
COORDINATION ABNORMAL ( 15 FDA reports)
DRUG ADMINISTRATION ERROR ( 15 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 15 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 15 FDA reports)
EYE IRRITATION ( 15 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 15 FDA reports)
HEPATIC LESION ( 15 FDA reports)
IMPAIRED WORK ABILITY ( 15 FDA reports)
INTENTIONAL DRUG MISUSE ( 15 FDA reports)
IRRITABLE BOWEL SYNDROME ( 15 FDA reports)
LACTIC ACIDOSIS ( 15 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 15 FDA reports)
MUSCLE CRAMP ( 15 FDA reports)
NECK INJURY ( 15 FDA reports)
NEPHROSCLEROSIS ( 15 FDA reports)
PERIPHERAL COLDNESS ( 15 FDA reports)
PNEUMOTHORAX ( 15 FDA reports)
PROTHROMBIN TIME PROLONGED ( 15 FDA reports)
PULMONARY CONGESTION ( 15 FDA reports)
RADICULOPATHY ( 15 FDA reports)
RHEUMATOID ARTHRITIS ( 15 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 15 FDA reports)
SENSORY DISTURBANCE ( 15 FDA reports)
SINUS CONGESTION ( 15 FDA reports)
SKIN DISORDER ( 15 FDA reports)
SPLENOMEGALY ( 15 FDA reports)
TEMPERATURE INTOLERANCE ( 15 FDA reports)
TOOTH FRACTURE ( 15 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 15 FDA reports)
VENTRICULAR HYPOKINESIA ( 15 FDA reports)
WEIGHT LOSS POOR ( 15 FDA reports)
ACUTE CORONARY SYNDROME ( 14 FDA reports)
ATAXIA ( 14 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 14 FDA reports)
BODY HEIGHT DECREASED ( 14 FDA reports)
CORONARY ARTERY BYPASS ( 14 FDA reports)
CROHN'S DISEASE ( 14 FDA reports)
DRUG TOXICITY ( 14 FDA reports)
EAR INFECTION ( 14 FDA reports)
EAR PAIN ( 14 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 14 FDA reports)
ELECTROLYTE IMBALANCE ( 14 FDA reports)
EYELID OEDEMA ( 14 FDA reports)
HAEMOGLOBIN INCREASED ( 14 FDA reports)
HAEMOLYTIC ANAEMIA ( 14 FDA reports)
HEARING IMPAIRED ( 14 FDA reports)
HYPERCALCAEMIA ( 14 FDA reports)
INJECTION SITE IRRITATION ( 14 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 14 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 14 FDA reports)
LIBIDO DECREASED ( 14 FDA reports)
LOCALISED INFECTION ( 14 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 14 FDA reports)
MUSCLE ATROPHY ( 14 FDA reports)
NO ADVERSE EVENT ( 14 FDA reports)
ORAL DISCOMFORT ( 14 FDA reports)
ORGAN FAILURE ( 14 FDA reports)
PARALYSIS ( 14 FDA reports)
QUALITY OF LIFE DECREASED ( 14 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 14 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 14 FDA reports)
THINKING ABNORMAL ( 14 FDA reports)
UTERINE LEIOMYOMA ( 14 FDA reports)
VIRAL INFECTION ( 14 FDA reports)
ACCIDENT AT WORK ( 13 FDA reports)
APNOEA ( 13 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 13 FDA reports)
BLOOD BILIRUBIN INCREASED ( 13 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 13 FDA reports)
BREAST CANCER FEMALE ( 13 FDA reports)
CERVICAL SPINAL STENOSIS ( 13 FDA reports)
COR PULMONALE ( 13 FDA reports)
DEPRESSED MOOD ( 13 FDA reports)
DILATATION ATRIAL ( 13 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 13 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 13 FDA reports)
ENCEPHALOPATHY ( 13 FDA reports)
EXOSTOSIS ( 13 FDA reports)
EXPIRED DRUG ADMINISTERED ( 13 FDA reports)
GASTROINTESTINAL PAIN ( 13 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 13 FDA reports)
GYNAECOMASTIA ( 13 FDA reports)
HAEMODIALYSIS ( 13 FDA reports)
HAIR TEXTURE ABNORMAL ( 13 FDA reports)
HEMIPARESIS ( 13 FDA reports)
HIP ARTHROPLASTY ( 13 FDA reports)
HYPERKERATOSIS ( 13 FDA reports)
HYPOMAGNESAEMIA ( 13 FDA reports)
INCREASED APPETITE ( 13 FDA reports)
INJECTION SITE HAEMATOMA ( 13 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 13 FDA reports)
LUNG NEOPLASM MALIGNANT ( 13 FDA reports)
MAJOR DEPRESSION ( 13 FDA reports)
METASTASES TO BONE ( 13 FDA reports)
OEDEMA MOUTH ( 13 FDA reports)
OTITIS MEDIA ( 13 FDA reports)
PLATELET COUNT INCREASED ( 13 FDA reports)
POOR PERSONAL HYGIENE ( 13 FDA reports)
RADIUS FRACTURE ( 13 FDA reports)
RENAL TUBULAR NECROSIS ( 13 FDA reports)
RESPIRATORY ARREST ( 13 FDA reports)
RIGHT ATRIAL DILATATION ( 13 FDA reports)
SYNOVIAL CYST ( 13 FDA reports)
TEARFULNESS ( 13 FDA reports)
THIRST ( 13 FDA reports)
VAGINAL HAEMORRHAGE ( 13 FDA reports)
WEIGHT FLUCTUATION ( 13 FDA reports)
ADENOCARCINOMA ( 12 FDA reports)
ADRENAL MASS ( 12 FDA reports)
BACTERAEMIA ( 12 FDA reports)
BACTERIAL INFECTION ( 12 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 12 FDA reports)
BIPOLAR DISORDER ( 12 FDA reports)
BLADDER DISORDER ( 12 FDA reports)
BLOOD ALBUMIN DECREASED ( 12 FDA reports)
BLOOD CALCIUM INCREASED ( 12 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 12 FDA reports)
BONE DEBRIDEMENT ( 12 FDA reports)
CHOKING ( 12 FDA reports)
COLON CANCER ( 12 FDA reports)
CONDUCTION DISORDER ( 12 FDA reports)
CYST ( 12 FDA reports)
DIABETIC NEPHROPATHY ( 12 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 12 FDA reports)
FUNGAL INFECTION ( 12 FDA reports)
GASTRIC HAEMORRHAGE ( 12 FDA reports)
GINGIVAL DISORDER ( 12 FDA reports)
HAEMANGIOMA OF LIVER ( 12 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 12 FDA reports)
HAEMORRHAGIC STROKE ( 12 FDA reports)
HAIR GROWTH ABNORMAL ( 12 FDA reports)
HOMICIDAL IDEATION ( 12 FDA reports)
HYDROURETER ( 12 FDA reports)
HYPOKINESIA ( 12 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 12 FDA reports)
INTERMITTENT CLAUDICATION ( 12 FDA reports)
LABORATORY TEST ABNORMAL ( 12 FDA reports)
LOCAL SWELLING ( 12 FDA reports)
LOWER LIMB FRACTURE ( 12 FDA reports)
MEDICATION RESIDUE ( 12 FDA reports)
METASTASIS ( 12 FDA reports)
OCULAR HYPERAEMIA ( 12 FDA reports)
OSTEOLYSIS ( 12 FDA reports)
PANCREATIC MASS ( 12 FDA reports)
PANIC REACTION ( 12 FDA reports)
PARANOIA ( 12 FDA reports)
PELVIC FRACTURE ( 12 FDA reports)
PIRIFORMIS SYNDROME ( 12 FDA reports)
PLANTAR FASCIITIS ( 12 FDA reports)
PLATELET AGGREGATION INCREASED ( 12 FDA reports)
POOR QUALITY SLEEP ( 12 FDA reports)
PROSTATOMEGALY ( 12 FDA reports)
PULSE ABSENT ( 12 FDA reports)
RASH PAPULAR ( 12 FDA reports)
READING DISORDER ( 12 FDA reports)
RHEUMATIC FEVER ( 12 FDA reports)
SYNCOPE VASOVAGAL ( 12 FDA reports)
THROMBOPHLEBITIS ( 12 FDA reports)
TYPE 1 DIABETES MELLITUS ( 12 FDA reports)
ULCER HAEMORRHAGE ( 12 FDA reports)
VITAMIN B12 DEFICIENCY ( 12 FDA reports)
ACIDOSIS ( 11 FDA reports)
AGORAPHOBIA ( 11 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 11 FDA reports)
APPLICATION SITE RASH ( 11 FDA reports)
BEDRIDDEN ( 11 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 11 FDA reports)
BONE EROSION ( 11 FDA reports)
CALCULUS BLADDER ( 11 FDA reports)
DEAFNESS NEUROSENSORY ( 11 FDA reports)
DEVICE RELATED INFECTION ( 11 FDA reports)
DRUG INTOLERANCE ( 11 FDA reports)
DRY THROAT ( 11 FDA reports)
ECCHYMOSIS ( 11 FDA reports)
ESCHERICHIA BACTERAEMIA ( 11 FDA reports)
ESSENTIAL HYPERTENSION ( 11 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 11 FDA reports)
EXTRASYSTOLES ( 11 FDA reports)
FACIAL PALSY ( 11 FDA reports)
FURUNCLE ( 11 FDA reports)
GASTROENTERITIS VIRAL ( 11 FDA reports)
GOITRE ( 11 FDA reports)
HALLUCINATION, VISUAL ( 11 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 11 FDA reports)
HOSPITALISATION ( 11 FDA reports)
HUMERUS FRACTURE ( 11 FDA reports)
HUNGER ( 11 FDA reports)
HYPERCHLORHYDRIA ( 11 FDA reports)
HYSTERECTOMY ( 11 FDA reports)
INJECTION SITE PRURITUS ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 11 FDA reports)
INTRAOCULAR LENS IMPLANT ( 11 FDA reports)
JOINT EFFUSION ( 11 FDA reports)
LEFT ATRIAL DILATATION ( 11 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
LUMBAR SPINAL STENOSIS ( 11 FDA reports)
MANIA ( 11 FDA reports)
MEDICAL DEVICE COMPLICATION ( 11 FDA reports)
MELANOCYTIC NAEVUS ( 11 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 11 FDA reports)
MUCOSAL INFLAMMATION ( 11 FDA reports)
MUSCLE TWITCHING ( 11 FDA reports)
MYOPATHY ( 11 FDA reports)
NASAL SEPTUM DEVIATION ( 11 FDA reports)
NERVOUS SYSTEM DISORDER ( 11 FDA reports)
ORAL CANDIDIASIS ( 11 FDA reports)
ORAL INTAKE REDUCED ( 11 FDA reports)
PARONYCHIA ( 11 FDA reports)
PEPTIC ULCER ( 11 FDA reports)
PROSTATE CANCER METASTATIC ( 11 FDA reports)
PROTEIN URINE ( 11 FDA reports)
PULMONARY MASS ( 11 FDA reports)
RESPIRATORY RATE INCREASED ( 11 FDA reports)
RHINITIS ALLERGIC ( 11 FDA reports)
SKIN CANCER ( 11 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 11 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 11 FDA reports)
SYNOVITIS ( 11 FDA reports)
TESTICULAR PAIN ( 11 FDA reports)
TINEL'S SIGN ( 11 FDA reports)
TONGUE DISORDER ( 11 FDA reports)
TRANSAMINASES INCREASED ( 11 FDA reports)
TRIGGER FINGER ( 11 FDA reports)
ULNA FRACTURE ( 11 FDA reports)
VASCULAR CALCIFICATION ( 11 FDA reports)
VEIN DISORDER ( 11 FDA reports)
WHIPLASH INJURY ( 11 FDA reports)
ANEURYSM ( 10 FDA reports)
ANGIOPLASTY ( 10 FDA reports)
ARTHROPOD BITE ( 10 FDA reports)
BLOOD IRON INCREASED ( 10 FDA reports)
BRADYPHRENIA ( 10 FDA reports)
BREAST TENDERNESS ( 10 FDA reports)
BRONCHOSPASM ( 10 FDA reports)
CAROTID ARTERY DISEASE ( 10 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 10 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 10 FDA reports)
CHROMATOPSIA ( 10 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 10 FDA reports)
DIABETIC FOOT ( 10 FDA reports)
DILATATION VENTRICULAR ( 10 FDA reports)
FACE OEDEMA ( 10 FDA reports)
FAILURE TO THRIVE ( 10 FDA reports)
FEELING DRUNK ( 10 FDA reports)
FLUID INTAKE REDUCED ( 10 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 10 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 10 FDA reports)
HERPES SIMPLEX ( 10 FDA reports)
HICCUPS ( 10 FDA reports)
HYDROCELE ( 10 FDA reports)
IMMOBILE ( 10 FDA reports)
IMMUNOSUPPRESSION ( 10 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 10 FDA reports)
JAW FRACTURE ( 10 FDA reports)
MONOCLONAL GAMMOPATHY ( 10 FDA reports)
NERVE INJURY ( 10 FDA reports)
NEUROPATHY ( 10 FDA reports)
NON-CARDIAC CHEST PAIN ( 10 FDA reports)
OESOPHAGEAL DISORDER ( 10 FDA reports)
PETECHIAE ( 10 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 10 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 10 FDA reports)
PURULENT DISCHARGE ( 10 FDA reports)
PYELONEPHRITIS ( 10 FDA reports)
RENAL CANCER METASTATIC ( 10 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 10 FDA reports)
RETINAL HAEMORRHAGE ( 10 FDA reports)
SCAB ( 10 FDA reports)
SKIN PLAQUE ( 10 FDA reports)
SPLEEN DISORDER ( 10 FDA reports)
SPONDYLOLISTHESIS ( 10 FDA reports)
STATUS ASTHMATICUS ( 10 FDA reports)
STRESS SYMPTOMS ( 10 FDA reports)
SUDDEN DEATH ( 10 FDA reports)
URETERAL NEOPLASM ( 10 FDA reports)
UTERINE MASS ( 10 FDA reports)
WALKING AID USER ( 10 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 9 FDA reports)
ACUTE PULMONARY OEDEMA ( 9 FDA reports)
ADVERSE DRUG REACTION ( 9 FDA reports)
ANAEMIA POSTOPERATIVE ( 9 FDA reports)
ANURIA ( 9 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 9 FDA reports)
BLOOD IRON DECREASED ( 9 FDA reports)
BLOOD LACTIC ACID INCREASED ( 9 FDA reports)
BLOOD PRESSURE ABNORMAL ( 9 FDA reports)
BULLOUS LUNG DISEASE ( 9 FDA reports)
CARBUNCLE ( 9 FDA reports)
CARDIAC TAMPONADE ( 9 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 9 FDA reports)
COGNITIVE DISORDER ( 9 FDA reports)
DIABETIC COMA ( 9 FDA reports)
DIVERTICULAR PERFORATION ( 9 FDA reports)
DRUG PRESCRIBING ERROR ( 9 FDA reports)
EAR DISCOMFORT ( 9 FDA reports)
EARLY SATIETY ( 9 FDA reports)
FASCIITIS ( 9 FDA reports)
FOOT DEFORMITY ( 9 FDA reports)
GASTROENTERITIS RADIATION ( 9 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 9 FDA reports)
IMPAIRED SELF-CARE ( 9 FDA reports)
INCONTINENCE ( 9 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 9 FDA reports)
INJECTION SITE SWELLING ( 9 FDA reports)
INTRACRANIAL ANEURYSM ( 9 FDA reports)
LARYNGEAL OEDEMA ( 9 FDA reports)
LIGAMENT SPRAIN ( 9 FDA reports)
MACULOPATHY ( 9 FDA reports)
MICTURITION FREQUENCY DECREASED ( 9 FDA reports)
MUSCLE CONTRACTURE ( 9 FDA reports)
NAIL DISORDER ( 9 FDA reports)
NASAL DISCOMFORT ( 9 FDA reports)
NEUTROPENIC COLITIS ( 9 FDA reports)
OBSTRUCTION GASTRIC ( 9 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 9 FDA reports)
OROPHARYNGEAL BLISTERING ( 9 FDA reports)
OTITIS EXTERNA ( 9 FDA reports)
PENILE INFECTION ( 9 FDA reports)
PERIORBITAL OEDEMA ( 9 FDA reports)
PERIPHERAL EMBOLISM ( 9 FDA reports)
PHOTOPSIA ( 9 FDA reports)
PROSTATITIS ( 9 FDA reports)
PSYCHOTIC DISORDER ( 9 FDA reports)
RESPIRATORY TRACT CONGESTION ( 9 FDA reports)
RHEUMATIC HEART DISEASE ( 9 FDA reports)
SERUM FERRITIN INCREASED ( 9 FDA reports)
SQUAMOUS CELL CARCINOMA ( 9 FDA reports)
STRESS FRACTURE ( 9 FDA reports)
TOE AMPUTATION ( 9 FDA reports)
TONGUE BITING ( 9 FDA reports)
UMBILICAL HERNIA ( 9 FDA reports)
URETERIC STENOSIS ( 9 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 9 FDA reports)
ABSCESS JAW ( 8 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 8 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 8 FDA reports)
APHAGIA ( 8 FDA reports)
APPLICATION SITE REACTION ( 8 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 8 FDA reports)
BARRETT'S OESOPHAGUS ( 8 FDA reports)
BONE MARROW GRANULOMA ( 8 FDA reports)
BONE OPERATION ( 8 FDA reports)
BRAIN SCAN ABNORMAL ( 8 FDA reports)
BUTTOCK PAIN ( 8 FDA reports)
CARDIAC PACEMAKER INSERTION ( 8 FDA reports)
CEREBROVASCULAR DISORDER ( 8 FDA reports)
CERVICOBRACHIAL SYNDROME ( 8 FDA reports)
CHOLECYSTITIS ACUTE ( 8 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 8 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 8 FDA reports)
CLOSTRIDIUM COLITIS ( 8 FDA reports)
COMMINUTED FRACTURE ( 8 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 8 FDA reports)
CSF TEST ABNORMAL ( 8 FDA reports)
CYANOPSIA ( 8 FDA reports)
DEPERSONALISATION ( 8 FDA reports)
DEVICE MALFUNCTION ( 8 FDA reports)
DIABETIC COMPLICATION ( 8 FDA reports)
DISABILITY ( 8 FDA reports)
EATING DISORDER SYMPTOM ( 8 FDA reports)
EPIGASTRIC DISCOMFORT ( 8 FDA reports)
EXTREMITY CONTRACTURE ( 8 FDA reports)
EYE LASER SURGERY ( 8 FDA reports)
EYELID DISORDER ( 8 FDA reports)
FOOT OPERATION ( 8 FDA reports)
GINGIVAL EROSION ( 8 FDA reports)
HAEMATOCRIT INCREASED ( 8 FDA reports)
HEPATIC ENCEPHALOPATHY ( 8 FDA reports)
HEPATOMEGALY ( 8 FDA reports)
HEPATOTOXICITY ( 8 FDA reports)
HYPERTENSIVE CRISIS ( 8 FDA reports)
HYPERTONIC BLADDER ( 8 FDA reports)
HYPERVENTILATION ( 8 FDA reports)
HYPOACUSIS ( 8 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 8 FDA reports)
INITIAL INSOMNIA ( 8 FDA reports)
INJECTION SITE REACTION ( 8 FDA reports)
INTESTINAL PERFORATION ( 8 FDA reports)
MACULAR OEDEMA ( 8 FDA reports)
MALIGNANT MELANOMA ( 8 FDA reports)
MENOPAUSAL SYMPTOMS ( 8 FDA reports)
METAPLASIA ( 8 FDA reports)
MUSCLE INJURY ( 8 FDA reports)
NARCOLEPSY ( 8 FDA reports)
NEPHRITIS INTERSTITIAL ( 8 FDA reports)
NEPHROPATHY ( 8 FDA reports)
NEPHROTIC SYNDROME ( 8 FDA reports)
NERVE COMPRESSION ( 8 FDA reports)
NO THERAPEUTIC RESPONSE ( 8 FDA reports)
NODULE ( 8 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 8 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 8 FDA reports)
ORAL CAVITY FISTULA ( 8 FDA reports)
ORAL INFECTION ( 8 FDA reports)
ORAL SURGERY ( 8 FDA reports)
PAIN OF SKIN ( 8 FDA reports)
PAPILLOMA VIRAL INFECTION ( 8 FDA reports)
PARAESTHESIA ORAL ( 8 FDA reports)
PAROTID GLAND ENLARGEMENT ( 8 FDA reports)
PARTIAL SEIZURES ( 8 FDA reports)
PERIODONTITIS ( 8 FDA reports)
PERITONITIS ( 8 FDA reports)
PHOTOPHOBIA ( 8 FDA reports)
PIGMENTARY GLAUCOMA ( 8 FDA reports)
POLYMYALGIA RHEUMATICA ( 8 FDA reports)
POSITIVE ROMBERGISM ( 8 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 8 FDA reports)
PRESCRIBED OVERDOSE ( 8 FDA reports)
PROCEDURAL COMPLICATION ( 8 FDA reports)
PROCTITIS ( 8 FDA reports)
PROTEIN TOTAL DECREASED ( 8 FDA reports)
PSEUDOMONAS INFECTION ( 8 FDA reports)
RECTAL CRAMPS ( 8 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 8 FDA reports)
RENAL COLIC ( 8 FDA reports)
RETINAL DETACHMENT ( 8 FDA reports)
SHOULDER PAIN ( 8 FDA reports)
SKIN IRRITATION ( 8 FDA reports)
SKIN LACERATION ( 8 FDA reports)
SLUGGISHNESS ( 8 FDA reports)
SPINAL FUSION SURGERY ( 8 FDA reports)
SUBCUTANEOUS ABSCESS ( 8 FDA reports)
SUDDEN CARDIAC DEATH ( 8 FDA reports)
TACHYPHRENIA ( 8 FDA reports)
TENDERNESS ( 8 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 8 FDA reports)
TOE DEFORMITY ( 8 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 8 FDA reports)
VISUAL FIELD DEFECT ( 8 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 8 FDA reports)
WOUND ( 8 FDA reports)
WRONG DRUG ADMINISTERED ( 8 FDA reports)
YELLOW SKIN ( 8 FDA reports)
ABDOMINAL HAEMATOMA ( 7 FDA reports)
AORTIC VALVE REPLACEMENT ( 7 FDA reports)
ASPIRATION ( 7 FDA reports)
ATRIAL TACHYCARDIA ( 7 FDA reports)
AUTOIMMUNE THYROIDITIS ( 7 FDA reports)
BILE DUCT STONE ( 7 FDA reports)
BLEPHARITIS ( 7 FDA reports)
BLOOD CHLORIDE DECREASED ( 7 FDA reports)
BLOOD DISORDER ( 7 FDA reports)
BODY TEMPERATURE DECREASED ( 7 FDA reports)
BREAST PAIN ( 7 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 7 FDA reports)
CATARACT OPERATION ( 7 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 7 FDA reports)
CORONARY ARTERY THROMBOSIS ( 7 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 7 FDA reports)
CYANOSIS ( 7 FDA reports)
DEMYELINATION ( 7 FDA reports)
DENTURE WEARER ( 7 FDA reports)
DISEASE RECURRENCE ( 7 FDA reports)
DRUG ERUPTION ( 7 FDA reports)
DUODENAL ULCER ( 7 FDA reports)
DUODENITIS ( 7 FDA reports)
DYSAESTHESIA ( 7 FDA reports)
DYSPNOEA EXACERBATED ( 7 FDA reports)
EAR DISORDER ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 7 FDA reports)
ENDODONTIC PROCEDURE ( 7 FDA reports)
ENERGY INCREASED ( 7 FDA reports)
EYELID PTOSIS ( 7 FDA reports)
FAECAL INCONTINENCE ( 7 FDA reports)
FAMILY STRESS ( 7 FDA reports)
FORMICATION ( 7 FDA reports)
GINGIVAL BLEEDING ( 7 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 7 FDA reports)
GRIP STRENGTH DECREASED ( 7 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 7 FDA reports)
HAEMORRHAGIC ANAEMIA ( 7 FDA reports)
HAIR DISORDER ( 7 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 7 FDA reports)
HYPOALBUMINAEMIA ( 7 FDA reports)
HYPOTRICHOSIS ( 7 FDA reports)
ILEUS PARALYTIC ( 7 FDA reports)
INADEQUATE ANALGESIA ( 7 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 7 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 7 FDA reports)
JOINT DISLOCATION ( 7 FDA reports)
LICHEN PLANUS ( 7 FDA reports)
LIP BLISTER ( 7 FDA reports)
LIP INJURY ( 7 FDA reports)
LUNG INFECTION ( 7 FDA reports)
MENORRHAGIA ( 7 FDA reports)
MITRAL VALVE DISEASE ( 7 FDA reports)
MOOD ALTERED ( 7 FDA reports)
MUSCLE DISORDER ( 7 FDA reports)
MUSCLE FATIGUE ( 7 FDA reports)
MYELODYSPLASTIC SYNDROME ( 7 FDA reports)
MYOCLONUS ( 7 FDA reports)
MYOFASCIAL SPASM ( 7 FDA reports)
MYOSITIS ( 7 FDA reports)
OESOPHAGEAL PAIN ( 7 FDA reports)
PANCREATIC DISORDER ( 7 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 7 FDA reports)
PERITONEAL DIALYSIS ( 7 FDA reports)
POST PROCEDURAL OEDEMA ( 7 FDA reports)
PULMONARY THROMBOSIS ( 7 FDA reports)
PULMONARY VASCULAR DISORDER ( 7 FDA reports)
RALES ( 7 FDA reports)
RELAPSING FEVER ( 7 FDA reports)
RHINITIS ( 7 FDA reports)
SALIVARY HYPERSECRETION ( 7 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 7 FDA reports)
SCLERODERMA ( 7 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 7 FDA reports)
SKIN FISSURES ( 7 FDA reports)
SKIN PAPILLOMA ( 7 FDA reports)
SNEEZING ( 7 FDA reports)
SPINAL DISORDER ( 7 FDA reports)
SPINAL FRACTURE ( 7 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 7 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 7 FDA reports)
THYROID MASS ( 7 FDA reports)
TONGUE OEDEMA ( 7 FDA reports)
TOXOPLASMOSIS ( 7 FDA reports)
URETHRAL STRICTURE ( 7 FDA reports)
URINARY TRACT DISORDER ( 7 FDA reports)
VASCULAR GRAFT ( 7 FDA reports)
VENOUS INSUFFICIENCY ( 7 FDA reports)
WITHDRAWAL SYNDROME ( 7 FDA reports)
WOUND INFECTION ( 7 FDA reports)
WRIST FRACTURE ( 7 FDA reports)
ACCIDENTAL EXPOSURE ( 6 FDA reports)
ACUTE PRERENAL FAILURE ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
ALLERGIC SINUSITIS ( 6 FDA reports)
ANOSMIA ( 6 FDA reports)
ANOXIC ENCEPHALOPATHY ( 6 FDA reports)
AORTIC VALVE CALCIFICATION ( 6 FDA reports)
AORTIC VALVE SCLEROSIS ( 6 FDA reports)
APHONIA ( 6 FDA reports)
APPENDICITIS ( 6 FDA reports)
APPENDICITIS PERFORATED ( 6 FDA reports)
ARTHROSCOPY ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
AZOTAEMIA ( 6 FDA reports)
BASEDOW'S DISEASE ( 6 FDA reports)
BEREAVEMENT REACTION ( 6 FDA reports)
BLADDER PAIN ( 6 FDA reports)
BLOOD CREATINE INCREASED ( 6 FDA reports)
BLOOD MAGNESIUM DECREASED ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 6 FDA reports)
BODY TINEA ( 6 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 6 FDA reports)
BREAST CANCER METASTATIC ( 6 FDA reports)
BREAST LUMP REMOVAL ( 6 FDA reports)
BREAST NEOPLASM ( 6 FDA reports)
BREATH SOUNDS ABNORMAL ( 6 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 6 FDA reports)
CACHEXIA ( 6 FDA reports)
CALCULUS URETHRAL ( 6 FDA reports)
CARDIAC FLUTTER ( 6 FDA reports)
CARTILAGE INJURY ( 6 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 6 FDA reports)
CEREBELLAR INFARCTION ( 6 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 6 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 6 FDA reports)
DEAFNESS UNILATERAL ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DYSTONIA ( 6 FDA reports)
EAR CONGESTION ( 6 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
EJACULATION DISORDER ( 6 FDA reports)
ENDOTRACHEAL INTUBATION ( 6 FDA reports)
ENTEROBACTER INFECTION ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
EPICONDYLITIS ( 6 FDA reports)
FACE INJURY ( 6 FDA reports)
FIBROUS HISTIOCYTOMA ( 6 FDA reports)
GASTRIC CANCER ( 6 FDA reports)
GINGIVAL PAIN ( 6 FDA reports)
GUN SHOT WOUND ( 6 FDA reports)
HAEMORRHAGE URINARY TRACT ( 6 FDA reports)
HEAD DISCOMFORT ( 6 FDA reports)
HEPATITIS C ( 6 FDA reports)
HYPERCOAGULATION ( 6 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 6 FDA reports)
INJECTION SITE EXTRAVASATION ( 6 FDA reports)
INTESTINAL POLYP ( 6 FDA reports)
INTRACARDIAC THROMBUS ( 6 FDA reports)
INTRACRANIAL HYPOTENSION ( 6 FDA reports)
JOINT CONTRACTURE ( 6 FDA reports)
KERATITIS ( 6 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 6 FDA reports)
LARYNGITIS ( 6 FDA reports)
LARYNGOSPASM ( 6 FDA reports)
LIGAMENT RUPTURE ( 6 FDA reports)
LIP DRY ( 6 FDA reports)
LIPOMA ( 6 FDA reports)
LISTLESS ( 6 FDA reports)
LIVER INJURY ( 6 FDA reports)
LOSS OF EMPLOYMENT ( 6 FDA reports)
LYMPHOMA ( 6 FDA reports)
MICTURITION DISORDER ( 6 FDA reports)
MONOPLEGIA ( 6 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 6 FDA reports)
MUSCULOSKELETAL DISORDER ( 6 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 6 FDA reports)
NEOPLASM ( 6 FDA reports)
NODAL RHYTHM ( 6 FDA reports)
NONSPECIFIC REACTION ( 6 FDA reports)
PAROSMIA ( 6 FDA reports)
PERNICIOUS ANAEMIA ( 6 FDA reports)
PERONEAL NERVE PALSY ( 6 FDA reports)
PERSONALITY CHANGE ( 6 FDA reports)
PHARYNGITIS ( 6 FDA reports)
PLEURITIC PAIN ( 6 FDA reports)
POLYNEUROPATHY ( 6 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 6 FDA reports)
PORTAL HYPERTENSION ( 6 FDA reports)
PROSTATIC DISORDER ( 6 FDA reports)
PROTEIN URINE PRESENT ( 6 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 6 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 6 FDA reports)
PURPURA ( 6 FDA reports)
RENAL ATROPHY ( 6 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 6 FDA reports)
RENAL PAIN ( 6 FDA reports)
RESPIRATORY TRACT INFECTION ( 6 FDA reports)
RETINOPATHY ( 6 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 6 FDA reports)
SELF-MEDICATION ( 6 FDA reports)
SINOBRONCHITIS ( 6 FDA reports)
SKIN INFECTION ( 6 FDA reports)
SOCIAL PROBLEM ( 6 FDA reports)
STRESS URINARY INCONTINENCE ( 6 FDA reports)
STRIDOR ( 6 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 6 FDA reports)
THERAPY NON-RESPONDER ( 6 FDA reports)
THROMBOEMBOLIC STROKE ( 6 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 6 FDA reports)
TOOTH INFECTION ( 6 FDA reports)
UMBILICAL HERNIA REPAIR ( 6 FDA reports)
VARICOSE VEIN ( 6 FDA reports)
VENOUS THROMBOSIS LIMB ( 6 FDA reports)
ABDOMINAL ADHESIONS ( 5 FDA reports)
ABDOMINAL INFECTION ( 5 FDA reports)
ABDOMINAL MASS ( 5 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
ALCOHOL ABUSE ( 5 FDA reports)
ANXIETY DISORDER ( 5 FDA reports)
AORTIC VALVE STENOSIS ( 5 FDA reports)
APPLICATION SITE IRRITATION ( 5 FDA reports)
ARTERIAL DISORDER ( 5 FDA reports)
ARTERIAL STENOSIS ( 5 FDA reports)
ATHEROSCLEROSIS ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 5 FDA reports)
ATROPHY ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BLINDNESS TRANSIENT ( 5 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 5 FDA reports)
BLOOD CREATININE ABNORMAL ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 5 FDA reports)
BLOOD SODIUM INCREASED ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 5 FDA reports)
BONE LOSS ( 5 FDA reports)
BREAST ENLARGEMENT ( 5 FDA reports)
BRONCHIECTASIS ( 5 FDA reports)
BRUXISM ( 5 FDA reports)
CALCINOSIS ( 5 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 5 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 5 FDA reports)
CATARACT NUCLEAR ( 5 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 5 FDA reports)
CHEST X-RAY ABNORMAL ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 5 FDA reports)
CHRONIC SINUSITIS ( 5 FDA reports)
CITROBACTER INFECTION ( 5 FDA reports)
CLOSTRIDIAL INFECTION ( 5 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 5 FDA reports)
COMPRESSION FRACTURE ( 5 FDA reports)
CONTRALATERAL BREAST CANCER ( 5 FDA reports)
CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
CSF SHUNT REMOVAL ( 5 FDA reports)
DERMATITIS ALLERGIC ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DEVICE OCCLUSION ( 5 FDA reports)
DIAPHRAGMATIC DISORDER ( 5 FDA reports)
DRUG LEVEL INCREASED ( 5 FDA reports)
DRUG TOLERANCE INCREASED ( 5 FDA reports)
DYSGRAPHIA ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 5 FDA reports)
ERYTHEMA MULTIFORME ( 5 FDA reports)
ESCHERICHIA INFECTION ( 5 FDA reports)
EYE INJURY ( 5 FDA reports)
EYE OEDEMA ( 5 FDA reports)
EYELID IRRITATION ( 5 FDA reports)
FACET JOINT SYNDROME ( 5 FDA reports)
FOAMING AT MOUTH ( 5 FDA reports)
FRACTURE DELAYED UNION ( 5 FDA reports)
FRACTURE DISPLACEMENT ( 5 FDA reports)
GENERAL SYMPTOM ( 5 FDA reports)
HAEMOLYSIS ( 5 FDA reports)
HAIR COLOUR CHANGES ( 5 FDA reports)
HAND DEFORMITY ( 5 FDA reports)
HEART TRANSPLANT ( 5 FDA reports)
HEPATIC CYST ( 5 FDA reports)
HERNIA REPAIR ( 5 FDA reports)
HYPERPARATHYROIDISM ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
INFARCTION ( 5 FDA reports)
INJECTION SITE RASH ( 5 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 5 FDA reports)
JOINT SPRAIN ( 5 FDA reports)
LEUKOPLAKIA ( 5 FDA reports)
LIMB OPERATION ( 5 FDA reports)
LIP PAIN ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
LIVEDO RETICULARIS ( 5 FDA reports)
LOW TURNOVER OSTEOPATHY ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 5 FDA reports)
METRORRHAGIA ( 5 FDA reports)
MOUTH HAEMORRHAGE ( 5 FDA reports)
MUSCLE SPASTICITY ( 5 FDA reports)
NASAL POLYPS ( 5 FDA reports)
NEOPLASM PROSTATE ( 5 FDA reports)
NEPHROGENIC ANAEMIA ( 5 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 5 FDA reports)
NYSTAGMUS ( 5 FDA reports)
OESOPHAGEAL ULCER ( 5 FDA reports)
OPEN WOUND ( 5 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 5 FDA reports)
OTORRHOEA ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
OVARIAN CYST ( 5 FDA reports)
PANCREATIC INSUFFICIENCY ( 5 FDA reports)
PANCREATITIS CHRONIC ( 5 FDA reports)
PENIS DISORDER ( 5 FDA reports)
PERINEAL PAIN ( 5 FDA reports)
PITTING OEDEMA ( 5 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
PROCTALGIA ( 5 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 5 FDA reports)
PRODUCT TASTE ABNORMAL ( 5 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 5 FDA reports)
PSORIATIC ARTHROPATHY ( 5 FDA reports)
QRS AXIS ABNORMAL ( 5 FDA reports)
RECTAL CANCER ( 5 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 5 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 5 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 5 FDA reports)
RENAL MASS ( 5 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 5 FDA reports)
ROSACEA ( 5 FDA reports)
SEDATION ( 5 FDA reports)
SLEEP TERROR ( 5 FDA reports)
SOMNAMBULISM ( 5 FDA reports)
SPUTUM DISCOLOURED ( 5 FDA reports)
SUPERINFECTION BACTERIAL ( 5 FDA reports)
TENDON RUPTURE ( 5 FDA reports)
TENSION ( 5 FDA reports)
TENSION HEADACHE ( 5 FDA reports)
THYROID NEOPLASM ( 5 FDA reports)
TIBIA FRACTURE ( 5 FDA reports)
TONGUE HAEMORRHAGE ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
TRANSPLANT REJECTION ( 5 FDA reports)
UNDERDOSE ( 5 FDA reports)
URETERIC OBSTRUCTION ( 5 FDA reports)
URINARY TRACT OBSTRUCTION ( 5 FDA reports)
VAGINAL DISCHARGE ( 5 FDA reports)
VAGINAL MYCOSIS ( 5 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
VITAMIN D DECREASED ( 5 FDA reports)
VITREOUS FLOATERS ( 5 FDA reports)
ABDOMINAL RIGIDITY ( 4 FDA reports)
ACUTE SINUSITIS ( 4 FDA reports)
ADHESION ( 4 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 4 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 4 FDA reports)
ANIMAL BITE ( 4 FDA reports)
APPLICATION SITE ULCER ( 4 FDA reports)
ARTERIAL RESTENOSIS ( 4 FDA reports)
ARTHRITIS INFECTIVE ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
BIFASCICULAR BLOCK ( 4 FDA reports)
BLADDER OBSTRUCTION ( 4 FDA reports)
BLEPHAROSPASM ( 4 FDA reports)
BLISTER INFECTED ( 4 FDA reports)
BLOOD CHLORIDE INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BREAST CANCER STAGE I ( 4 FDA reports)
BREAST MASS ( 4 FDA reports)
BRONCHITIS ACUTE ( 4 FDA reports)
BRONCHITIS VIRAL ( 4 FDA reports)
BURSA CALCIFICATION ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 4 FDA reports)
CARDIAC OUTPUT DECREASED ( 4 FDA reports)
CATHETER RELATED COMPLICATION ( 4 FDA reports)
CEREBRAL ARTERY STENOSIS ( 4 FDA reports)
CEREBRAL DISORDER ( 4 FDA reports)
CERVIX CARCINOMA ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CHONDROPATHY ( 4 FDA reports)
CLAVICLE FRACTURE ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
CONTRAST MEDIA REACTION ( 4 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 4 FDA reports)
CYSTOCELE ( 4 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 4 FDA reports)
DEPRESSION SUICIDAL ( 4 FDA reports)
DERMAL CYST ( 4 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
DYSLEXIA ( 4 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EXERCISE LACK OF ( 4 FDA reports)
FINGER DEFORMITY ( 4 FDA reports)
FOREIGN BODY ASPIRATION ( 4 FDA reports)
FRACTURE MALUNION ( 4 FDA reports)
GALLBLADDER OPERATION ( 4 FDA reports)
GASTRIC NEOPLASM ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GINGIVAL INFECTION ( 4 FDA reports)
GINGIVITIS ( 4 FDA reports)
GROWTH OF EYELASHES ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HEART RATE ABNORMAL ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 4 FDA reports)
HEPATIC MASS ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 4 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HILAR LYMPHADENOPATHY ( 4 FDA reports)
HOSTILITY ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
INAPPROPRIATE AFFECT ( 4 FDA reports)
INCISION SITE INFECTION ( 4 FDA reports)
INJECTION SITE DISCOMFORT ( 4 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 4 FDA reports)
INTERNAL INJURY ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
MALIGNANT HYPERTENSION ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MEDIASTINAL HAEMATOMA ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
METABOLIC ENCEPHALOPATHY ( 4 FDA reports)
MICROALBUMINURIA ( 4 FDA reports)
MITRAL VALVE PROLAPSE ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 4 FDA reports)
MYOPIA ( 4 FDA reports)
NASAL ULCER ( 4 FDA reports)
NEPHRECTOMY ( 4 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
NODAL ARRHYTHMIA ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 4 FDA reports)
OCULAR DISCOMFORT ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
ORAL MUCOSAL BLISTERING ( 4 FDA reports)
OSTEOSCLEROSIS ( 4 FDA reports)
OVARIAN CANCER METASTATIC ( 4 FDA reports)
PANCREATIC CARCINOMA ( 4 FDA reports)
PARKINSONISM ( 4 FDA reports)
PCO2 DECREASED ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
POLYARTHRITIS ( 4 FDA reports)
POLYPECTOMY ( 4 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 4 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 4 FDA reports)
POSTOPERATIVE INFECTION ( 4 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 4 FDA reports)
PRECANCEROUS CELLS PRESENT ( 4 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 4 FDA reports)
PULMONARY GRANULOMA ( 4 FDA reports)
PUPIL FIXED ( 4 FDA reports)
RECTAL CANCER STAGE III ( 4 FDA reports)
RENAL CANCER ( 4 FDA reports)
RETINAL OEDEMA ( 4 FDA reports)
SALIVA ALTERED ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SENSATION OF PRESSURE ( 4 FDA reports)
SHOCK HAEMORRHAGIC ( 4 FDA reports)
SKIN WRINKLING ( 4 FDA reports)
SPONDYLOSIS ( 4 FDA reports)
SPONTANEOUS PENILE ERECTION ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
SUBSTANCE ABUSE ( 4 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 4 FDA reports)
TRANSFUSION REACTION ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 4 FDA reports)
URINE ANALYSIS ABNORMAL ( 4 FDA reports)
URINE COLOUR ABNORMAL ( 4 FDA reports)
URINE FLOW DECREASED ( 4 FDA reports)
UTERINE DISORDER ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VASCULAR PSEUDOANEURYSM ( 4 FDA reports)
VEIN PAIN ( 4 FDA reports)
VENOUS THROMBOSIS ( 4 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 4 FDA reports)
WOUND DEBRIDEMENT ( 4 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACANTHOSIS NIGRICANS ( 3 FDA reports)
ACNE ( 3 FDA reports)
ACTINIC KERATOSIS ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ADRENAL ADENOMA ( 3 FDA reports)
ADRENAL NEOPLASM ( 3 FDA reports)
ALCOHOL INTERACTION ( 3 FDA reports)
ALCOHOL POISONING ( 3 FDA reports)
ALCOHOLISM ( 3 FDA reports)
AMENORRHOEA ( 3 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 3 FDA reports)
APPETITE DISORDER ( 3 FDA reports)
APPLICATION SITE BLEEDING ( 3 FDA reports)
APPLICATION SITE DISCOMFORT ( 3 FDA reports)
APPLICATION SITE PAIN ( 3 FDA reports)
APPLICATION SITE URTICARIA ( 3 FDA reports)
ARTERIAL THROMBOSIS ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
AXILLARY PAIN ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BELLIGERENCE ( 3 FDA reports)
BENIGN OVARIAN TUMOUR ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BILIARY TRACT DISORDER ( 3 FDA reports)
BIOPSY COLON ( 3 FDA reports)
BK VIRUS INFECTION ( 3 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 3 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 3 FDA reports)
BLOOD TEST ABNORMAL ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
BREAST DISCOLOURATION ( 3 FDA reports)
BREATH ODOUR ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CARDIAC FIBRILLATION ( 3 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CAROTID ARTERY ANEURYSM ( 3 FDA reports)
CATARACT SUBCAPSULAR ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 3 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 3 FDA reports)
CENTRAL LINE INFECTION ( 3 FDA reports)
CEREBELLAR ATROPHY ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CHOLECYSTITIS INFECTIVE ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CHONDROMALACIA ( 3 FDA reports)
COLONIC STENOSIS ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CORONARY ANGIOPLASTY ( 3 FDA reports)
COSTOCHONDRITIS ( 3 FDA reports)
CREATININE RENAL CLEARANCE ( 3 FDA reports)
CYSTITIS INTERSTITIAL ( 3 FDA reports)
CYSTOID MACULAR OEDEMA ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DEVICE CONNECTION ISSUE ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DEVICE ISSUE ( 3 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 3 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
ENCEPHALOMALACIA ( 3 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 3 FDA reports)
ENTEROCUTANEOUS FISTULA ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
EXERCISE TOLERANCE DECREASED ( 3 FDA reports)
EYE DISCHARGE ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
EYELIDS PRURITUS ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
FAECES PALE ( 3 FDA reports)
FAT INTOLERANCE ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FOLLICULITIS ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
FRACTURE NONUNION ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 3 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 3 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 3 FDA reports)
GASTROINTESTINAL ULCER ( 3 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
GENITAL ERYTHEMA ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
GUTTATE PSORIASIS ( 3 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HEART INJURY ( 3 FDA reports)
HEART VALVE INCOMPETENCE ( 3 FDA reports)
HEPATITIS B ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HYPERPHAGIA ( 3 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
INCISION SITE PAIN ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INFUSION SITE HAEMATOMA ( 3 FDA reports)
INFUSION SITE REACTION ( 3 FDA reports)
INJECTION SITE BURNING ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE STINGING ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
INTESTINAL MASS ( 3 FDA reports)
INTESTINAL OPERATION ( 3 FDA reports)
INTESTINAL STENOSIS ( 3 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
LABILE BLOOD PRESSURE ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LAZINESS ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LIP DISCOLOURATION ( 3 FDA reports)
LIVER CARCINOMA RUPTURED ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LOWER EXTREMITY MASS ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
MALIGNANT MELANOMA IN SITU ( 3 FDA reports)
MARITAL PROBLEM ( 3 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 3 FDA reports)
MEAN CELL VOLUME DECREASED ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
METASTASES TO LUNG ( 3 FDA reports)
METASTATIC NEOPLASM ( 3 FDA reports)
METATARSALGIA ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MUSCLE NECROSIS ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 3 FDA reports)
MYOCARDIAL CALCIFICATION ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
NASAL SEPTUM PERFORATION ( 3 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 3 FDA reports)
NECK MASS ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NEOPLASM SKIN ( 3 FDA reports)
NEPHROCALCINOSIS ( 3 FDA reports)
NEUROFIBROMATOSIS ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NIPPLE SWELLING ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
ODYNOPHAGIA ( 3 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
ORAL TORUS ( 3 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
PATHOLOGICAL GAMBLING ( 3 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 3 FDA reports)
PERIRECTAL ABSCESS ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PITUITARY TUMOUR RECURRENT ( 3 FDA reports)
PLASTIC SURGERY ( 3 FDA reports)
PNEUMATOSIS INTESTINALIS ( 3 FDA reports)
PNEUMONIA LEGIONELLA ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
POLYP ( 3 FDA reports)
POLYP COLORECTAL ( 3 FDA reports)
POLYTRAUMATISM ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
POST HERPETIC NEURALGIA ( 3 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 3 FDA reports)
POSTPARTUM DISORDER ( 3 FDA reports)
PROCEDURAL SITE REACTION ( 3 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 3 FDA reports)
PRODUCT ODOUR ABNORMAL ( 3 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 3 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PSYCHOLOGICAL TRAUMA ( 3 FDA reports)
PULMONARY CALCIFICATION ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
PYURIA ( 3 FDA reports)
RECTAL POLYP ( 3 FDA reports)
RED BLOOD CELL ABNORMALITY ( 3 FDA reports)
REFRACTORY ANAEMIA ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
REPETITIVE SPEECH ( 3 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 3 FDA reports)
RETINAL DISORDER ( 3 FDA reports)
RETROPERITONEAL HAEMATOMA ( 3 FDA reports)
RHEUMATOID LUNG ( 3 FDA reports)
ROTATOR CUFF REPAIR ( 3 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SEASONAL ALLERGY ( 3 FDA reports)
SEROMA ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SHOCK HYPOGLYCAEMIC ( 3 FDA reports)
SIALOADENITIS ( 3 FDA reports)
SNORING ( 3 FDA reports)
SOFT TISSUE DISORDER ( 3 FDA reports)
SOFT TISSUE MASS ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 3 FDA reports)
SPLENECTOMY ( 3 FDA reports)
SPLENIC HAEMORRHAGE ( 3 FDA reports)
SPLENIC INFARCTION ( 3 FDA reports)
SPONDYLITIS ( 3 FDA reports)
STARVATION ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SUBDURAL HAEMORRHAGE ( 3 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 3 FDA reports)
SUDDEN ONSET OF SLEEP ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
TACHYARRHYTHMIA ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
TENDON CALCIFICATION ( 3 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
TINEA PEDIS ( 3 FDA reports)
TOBACCO USER ( 3 FDA reports)
TONGUE COATED ( 3 FDA reports)
TONGUE DISCOLOURATION ( 3 FDA reports)
TONSIL CANCER ( 3 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 3 FDA reports)
TUMOUR FLARE ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINARY SEDIMENT PRESENT ( 3 FDA reports)
URINARY TRACT PAIN ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
URTICARIA CHRONIC ( 3 FDA reports)
VASCULAR DEMENTIA ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VENTRICULAR DRAINAGE ( 3 FDA reports)
VERTEBROPLASTY ( 3 FDA reports)
VERTIGO LABYRINTHINE ( 3 FDA reports)
VESTIBULAR NEURONITIS ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VIRAL TEST POSITIVE ( 3 FDA reports)
VITAMIN B12 DECREASED ( 3 FDA reports)
VOMITING PROJECTILE ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
ABDOMINAL INJURY ( 2 FDA reports)
ABDOMINAL NEOPLASM ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACCESSORY NAVICULAR SYNDROME ( 2 FDA reports)
ACETABULUM FRACTURE ( 2 FDA reports)
ACROCHORDON ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADENOMA BENIGN ( 2 FDA reports)
ADJUSTMENT DISORDER ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
AMPUTATION ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANALGESIC THERAPY ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPLICATION SITE DERMATITIS ( 2 FDA reports)
APPLICATION SITE DISCHARGE ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 2 FDA reports)
ARTHROSCOPIC SURGERY ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ATHETOSIS ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BED REST ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BIOPSY STOMACH ABNORMAL ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLADDER SPASM ( 2 FDA reports)
BLAST CELLS PRESENT ( 2 FDA reports)
BLEPHAROCHALASIS ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL ( 2 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BONE METABOLISM DISORDER ( 2 FDA reports)
BONE NEOPLASM ( 2 FDA reports)
BORDERLINE GLAUCOMA ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BREAKTHROUGH PAIN ( 2 FDA reports)
BREAST CANCER STAGE III ( 2 FDA reports)
BREAST DISORDER ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BRONCHIAL DISORDER ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
BURN OESOPHAGEAL ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
BUTTERFLY RASH ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CHORIORETINOPATHY ( 2 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CLOSED HEAD INJURY ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COMPLICATED FRACTURE ( 2 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 2 FDA reports)
CONFUSION POSTOPERATIVE ( 2 FDA reports)
CORONARY ARTERY DISSECTION ( 2 FDA reports)
CRANIAL NERVE DISORDER ( 2 FDA reports)
CRYSTAL ARTHROPATHY ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DEVICE MISUSE ( 2 FDA reports)
DIAPHRAGMATIC HERNIA ( 2 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 2 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
ECTROPION OF CERVIX ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
ENTROPION ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
EPINEPHRINE INCREASED ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 2 FDA reports)
ESSENTIAL TREMOR ( 2 FDA reports)
EXERCISE CAPACITY DECREASED ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EYE INFECTION FUNGAL ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
EYELID MARGIN CRUSTING ( 2 FDA reports)
EYELID OPERATION ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FEMORAL BRUIT ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FRACTURED SACRUM ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GASTRIC BANDING ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTRITIS ATROPHIC ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GINGIVAL ERYTHEMA ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GINGIVAL ULCERATION ( 2 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMOGLOBINURIA ( 2 FDA reports)
HAEMORRHAGIC CYST ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HALLUCINATION, TACTILE ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC CALCIFICATION ( 2 FDA reports)
HEPATITIS B VIRUS TEST ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS VIRAL ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HERNIA HIATUS REPAIR ( 2 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTROPHY ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
HYPERVOLAEMIA ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOCHONDRIASIS ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 2 FDA reports)
HYPOGONADISM ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
INCISION SITE CELLULITIS ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INCREASED INSULIN REQUIREMENT ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INFUSION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INSULIN RESISTANCE ( 2 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 2 FDA reports)
INTRAOCULAR MELANOMA ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KETOSIS ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
LABOUR COMPLICATION ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LENS IMPLANT ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LIMB ASYMMETRY ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOOSE TOOTH ( 2 FDA reports)
LOSS OF ANATOMICAL ALIGNMENT AFTER FRACTURE REDUCTION ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
MALE SEXUAL DYSFUNCTION ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MENISCUS OPERATION ( 2 FDA reports)
MERALGIA PARAESTHETICA ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MOLE EXCISION ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MORBID THOUGHTS ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCLE FIBROSIS ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 2 FDA reports)
MYOTONIC DYSTROPHY ( 2 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NEAR DROWNING ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEOVASCULARISATION ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 2 FDA reports)
NEUROSURGERY ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NIGHT BLINDNESS ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NODAL OSTEOARTHRITIS ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NOREPINEPHRINE INCREASED ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
ONYCHALGIA ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PENILE ARTERY OCCLUSION ( 2 FDA reports)
PERICARDITIS CONSTRICTIVE ( 2 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERISTALSIS VISIBLE ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 2 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PINGUECULA ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
POST POLIO SYNDROME ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
POSTRENAL FAILURE ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
PROTEUS INFECTION ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PRURITUS ALLERGIC ( 2 FDA reports)
PUBIC RAMI FRACTURE ( 2 FDA reports)
PUBIS FRACTURE ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RECTOCELE ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
REMOVAL OF FOREIGN BODY ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 2 FDA reports)
RESORPTION BONE INCREASED ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 2 FDA reports)
RETINAL VASCULAR OCCLUSION ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SACROILIITIS ( 2 FDA reports)
SALIVARY GLAND MASS ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCHAMBERG'S DISEASE ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SHOULDER OPERATION ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SPINAL LAMINECTOMY ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 2 FDA reports)
STEAL SYNDROME ( 2 FDA reports)
STRESS AT WORK ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THORACIC OUTLET SYNDROME ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
TRACHEOBRONCHITIS ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 2 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 2 FDA reports)
TRAUMATIC FRACTURE ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TRICHORRHEXIS ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
UPPER EXTREMITY MASS ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URETHRAL PAIN ( 2 FDA reports)
URGE INCONTINENCE ( 2 FDA reports)
UTERINE CERVIX ATROPHY ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
VARICOSE VEIN OPERATION ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VIRAL PHARYNGITIS ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 2 FDA reports)
VITREOUS DETACHMENT ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 2 FDA reports)
WEIGHT BEARING DIFFICULTY ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WHITE BLOOD CELLS URINE ( 2 FDA reports)
WHITE CLOT SYNDROME ( 2 FDA reports)
WHOLE BLOOD TRANSFUSION ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
XERODERMA ( 2 FDA reports)
ZYGOMYCOSIS ( 2 FDA reports)
ABDOMINAL AORTIC BRUIT ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACTINOMYCOSIS ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAL INJURY ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC DISSECTION RUPTURE ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASBESTOSIS ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 1 FDA reports)
ATONIC SEIZURES ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILATERAL HYDRONEPHROSIS ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE NORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCIFICATION OF MUSCLE ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC MALPOSITION ( 1 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVICAL SPASM ( 1 FDA reports)
CERVICAL SPINE FLATTENING ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHONDRITIS ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 0 ( 1 FDA reports)
CLITORAL ENGORGEMENT ( 1 FDA reports)
CLUMSY CHILD SYNDROME ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON CANCER STAGE I ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CUTIS LAXA ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DEVICE INTERACTION ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG CHEMICAL INCOMPATIBILITY ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSTROPHIC CALCIFICATION ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENLARGED CLITORIS ( 1 FDA reports)
ENOPHTHALMOS ( 1 FDA reports)
ENTEROCHROMAFFIN CELL HYPERPLASIA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ERYTHROPSIA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE OPERATION COMPLICATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELASH DISCOLOURATION ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FORCED EXPIRATORY VOLUME ABNORMAL ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GAIT SPASTIC ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER CANCER METASTATIC ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL ULCER PERFORATION ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GREENSTICK FRACTURE ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA OF SPLEEN ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEADACHE POSTOPERATIVE ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HIP DEFORMITY ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HISTIOCYTOSIS ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HYALOSIS ASTEROID ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERVISCOSITY SYNDROME ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPONATRAEMIC SYNDROME ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPINGEMENT SYNDROME ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REMOVAL ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INJECTION SITE CALCIFICATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE PUSTULE ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 1 FDA reports)
INSULIN TOLERANCE TEST ABNORMAL ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT STABILISATION ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LAPAROSCOPIC SURGERY ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL MASS ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LATERAL MEDULLARY SYNDROME ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGAMENT PAIN ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MALIGNANT OMENTUM NEOPLASM ( 1 FDA reports)
MALOCCLUSION ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEIBOMIANITIS ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MIXED INCONTINENCE ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
MYOSCLEROSIS ( 1 FDA reports)
MYXOEDEMA ( 1 FDA reports)
NAIL AVULSION ( 1 FDA reports)
NAIL BED INFECTION ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NASAL TURBINATE ABNORMALITY ( 1 FDA reports)
NASOPHARYNGEAL CANCER ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OCULAR MYASTHENIA ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OLIVOPONTOCEREBELLAR ATROPHY ( 1 FDA reports)
OMENTECTOMY ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OOPHORECTOMY BILATERAL ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL NEOPLASM ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOPETROSIS ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
OVULATION DISORDER ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARATHYROID GLAND OPERATION ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDITIS LUPUS ( 1 FDA reports)
PERIDIVERTICULITIS ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLASTIC SURGERY TO THE FACE ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURAL DECORTICATION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POST-TRAUMATIC PAIN ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY FUNCTION CHALLENGE TEST ABNORMAL ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RENIN ABNORMAL ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
RESIDUAL URINE VOLUME INCREASED ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY SIGHS ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL ANEURYSM ( 1 FDA reports)
RETINAL NEOVASCULARISATION ( 1 FDA reports)
RETINAL SCAR ( 1 FDA reports)
RETROPERITONEAL EFFUSION ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEBACEOUS CARCINOMA ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSATION OF BLOCK IN EAR ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SHOULDER DEFORMITY ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUS POLYP ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPHEROCYTIC ANAEMIA ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPINAL CORD HAEMORRHAGE ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPINOCEREBELLAR DISORDER ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STARING ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
SUBMANDIBULAR MASS ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
TEETH BRITTLE ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERAPY NAIVE ( 1 FDA reports)
THERMOHYPOAESTHESIA ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THORACOTOMY ( 1 FDA reports)
THREAT OF REDUNDANCY ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THROMBOSIS PROPHYLAXIS ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLAR ATROPHY ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
UMBILICAL MALFORMATION ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URETHRAL SPASM ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
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URTICARIA GENERALISED ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
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UTERINE ISCHAEMIA ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
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VAGINAL REMOVAL OF INTRAUTERINE FOREIGN BODY ( 1 FDA reports)
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VAGINITIS ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
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VASODILATATION ( 1 FDA reports)
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VENOUS OCCLUSION ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
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VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
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X-RAY ABNORMAL ( 1 FDA reports)
YAWNING ( 1 FDA reports)
YELLOW NAIL SYNDROME ( 1 FDA reports)

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