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

NAUSEA ( 1046 FDA reports)
FATIGUE ( 834 FDA reports)
PAIN ( 797 FDA reports)
DYSPNOEA ( 788 FDA reports)
DIZZINESS ( 761 FDA reports)
ASTHENIA ( 689 FDA reports)
MYOCARDIAL INFARCTION ( 672 FDA reports)
CHEST PAIN ( 624 FDA reports)
DIARRHOEA ( 624 FDA reports)
BLOOD GLUCOSE INCREASED ( 615 FDA reports)
DRUG INEFFECTIVE ( 615 FDA reports)
WEIGHT DECREASED ( 608 FDA reports)
ANXIETY ( 604 FDA reports)
HEADACHE ( 579 FDA reports)
VOMITING ( 549 FDA reports)
ARTHRALGIA ( 548 FDA reports)
DEPRESSION ( 536 FDA reports)
FLUSHING ( 525 FDA reports)
MYALGIA ( 523 FDA reports)
PAIN IN EXTREMITY ( 510 FDA reports)
OEDEMA PERIPHERAL ( 487 FDA reports)
BACK PAIN ( 455 FDA reports)
PANCREATITIS ( 451 FDA reports)
INSOMNIA ( 450 FDA reports)
ABDOMINAL PAIN ( 416 FDA reports)
WEIGHT INCREASED ( 413 FDA reports)
DIABETES MELLITUS ( 412 FDA reports)
MUSCLE SPASMS ( 409 FDA reports)
FALL ( 405 FDA reports)
HYPERTENSION ( 400 FDA reports)
CORONARY ARTERY DISEASE ( 396 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 395 FDA reports)
ANAEMIA ( 393 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 389 FDA reports)
RENAL FAILURE ( 383 FDA reports)
PRURITUS ( 378 FDA reports)
ABDOMINAL PAIN UPPER ( 348 FDA reports)
PNEUMONIA ( 326 FDA reports)
DEHYDRATION ( 313 FDA reports)
RASH ( 311 FDA reports)
MALAISE ( 295 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 294 FDA reports)
RENAL FAILURE ACUTE ( 291 FDA reports)
FEELING ABNORMAL ( 288 FDA reports)
CONSTIPATION ( 284 FDA reports)
ATRIAL FIBRILLATION ( 283 FDA reports)
HYPOTENSION ( 282 FDA reports)
PARAESTHESIA ( 282 FDA reports)
CEREBROVASCULAR ACCIDENT ( 277 FDA reports)
PYREXIA ( 274 FDA reports)
INJURY ( 270 FDA reports)
COUGH ( 261 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 261 FDA reports)
TYPE 2 DIABETES MELLITUS ( 260 FDA reports)
PALPITATIONS ( 250 FDA reports)
URINARY TRACT INFECTION ( 250 FDA reports)
HYPOAESTHESIA ( 246 FDA reports)
DECREASED APPETITE ( 242 FDA reports)
MUSCULAR WEAKNESS ( 242 FDA reports)
SOMNOLENCE ( 240 FDA reports)
HYPERHIDROSIS ( 232 FDA reports)
CARDIAC DISORDER ( 231 FDA reports)
GAIT DISTURBANCE ( 223 FDA reports)
ERYTHEMA ( 221 FDA reports)
EMOTIONAL DISTRESS ( 217 FDA reports)
BLOOD CREATININE INCREASED ( 216 FDA reports)
HYPERLIPIDAEMIA ( 215 FDA reports)
CONFUSIONAL STATE ( 214 FDA reports)
CHOLELITHIASIS ( 209 FDA reports)
LOSS OF CONSCIOUSNESS ( 202 FDA reports)
BLOOD GLUCOSE DECREASED ( 201 FDA reports)
VISION BLURRED ( 201 FDA reports)
DYSPEPSIA ( 192 FDA reports)
PANCREATITIS ACUTE ( 191 FDA reports)
TREMOR ( 189 FDA reports)
DRUG INTERACTION ( 185 FDA reports)
DEATH ( 181 FDA reports)
NEUROPATHY PERIPHERAL ( 178 FDA reports)
RHABDOMYOLYSIS ( 175 FDA reports)
OSTEOARTHRITIS ( 174 FDA reports)
CHEST DISCOMFORT ( 171 FDA reports)
AMNESIA ( 169 FDA reports)
DEEP VEIN THROMBOSIS ( 164 FDA reports)
CONDITION AGGRAVATED ( 162 FDA reports)
BLOOD PRESSURE INCREASED ( 160 FDA reports)
ABDOMINAL DISTENSION ( 159 FDA reports)
SUICIDAL IDEATION ( 158 FDA reports)
DRY MOUTH ( 155 FDA reports)
HEPATIC ENZYME INCREASED ( 149 FDA reports)
DYSPHAGIA ( 148 FDA reports)
ABDOMINAL DISCOMFORT ( 146 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 146 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 146 FDA reports)
PULMONARY EMBOLISM ( 146 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 144 FDA reports)
FEELING HOT ( 144 FDA reports)
HYPERGLYCAEMIA ( 142 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 142 FDA reports)
URTICARIA ( 142 FDA reports)
CELLULITIS ( 140 FDA reports)
ANHEDONIA ( 139 FDA reports)
RENAL IMPAIRMENT ( 138 FDA reports)
UNEVALUABLE EVENT ( 138 FDA reports)
CONVULSION ( 137 FDA reports)
HEPATIC STEATOSIS ( 137 FDA reports)
NERVOUSNESS ( 137 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 136 FDA reports)
ECONOMIC PROBLEM ( 136 FDA reports)
OFF LABEL USE ( 136 FDA reports)
BALANCE DISORDER ( 134 FDA reports)
STRESS ( 134 FDA reports)
ANGINA PECTORIS ( 133 FDA reports)
ARTHRITIS ( 131 FDA reports)
PLEURAL EFFUSION ( 131 FDA reports)
ALOPECIA ( 127 FDA reports)
JOINT SWELLING ( 127 FDA reports)
NECK PAIN ( 127 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 126 FDA reports)
HYPOGLYCAEMIA ( 126 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 126 FDA reports)
BURNING SENSATION ( 122 FDA reports)
CORONARY ARTERY OCCLUSION ( 120 FDA reports)
SLEEP APNOEA SYNDROME ( 120 FDA reports)
CHILLS ( 119 FDA reports)
MUSCULOSKELETAL PAIN ( 119 FDA reports)
BRONCHITIS ( 118 FDA reports)
SINUSITIS ( 118 FDA reports)
SYNCOPE ( 118 FDA reports)
HYPERSENSITIVITY ( 117 FDA reports)
HAEMOGLOBIN DECREASED ( 116 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 116 FDA reports)
VERTIGO ( 115 FDA reports)
RENAL FAILURE CHRONIC ( 114 FDA reports)
DYSGEUSIA ( 113 FDA reports)
MEMORY IMPAIRMENT ( 113 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 111 FDA reports)
FEAR ( 111 FDA reports)
OBESITY ( 110 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 109 FDA reports)
HALLUCINATION ( 107 FDA reports)
THROMBOSIS ( 106 FDA reports)
CONTUSION ( 105 FDA reports)
OSTEONECROSIS OF JAW ( 105 FDA reports)
CARDIOMEGALY ( 104 FDA reports)
MULTIPLE INJURIES ( 104 FDA reports)
ARTERIOSCLEROSIS ( 103 FDA reports)
LETHARGY ( 103 FDA reports)
CATARACT ( 102 FDA reports)
HEART RATE INCREASED ( 102 FDA reports)
INJECTION SITE PAIN ( 102 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 102 FDA reports)
FLATULENCE ( 101 FDA reports)
RESPIRATORY FAILURE ( 100 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 99 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 96 FDA reports)
STAPHYLOCOCCAL INFECTION ( 95 FDA reports)
ABASIA ( 94 FDA reports)
OVERDOSE ( 94 FDA reports)
ASTHMA ( 92 FDA reports)
HYPOTHYROIDISM ( 92 FDA reports)
INFLUENZA LIKE ILLNESS ( 92 FDA reports)
MITRAL VALVE INCOMPETENCE ( 92 FDA reports)
DYSURIA ( 91 FDA reports)
MULTI-ORGAN FAILURE ( 91 FDA reports)
OSTEOMYELITIS ( 90 FDA reports)
AGITATION ( 89 FDA reports)
MOBILITY DECREASED ( 89 FDA reports)
BLOOD UREA INCREASED ( 88 FDA reports)
CARDIAC ARREST ( 88 FDA reports)
CARDIO-RESPIRATORY ARREST ( 88 FDA reports)
NASOPHARYNGITIS ( 88 FDA reports)
OEDEMA ( 87 FDA reports)
ABNORMAL DREAMS ( 86 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 86 FDA reports)
RENAL DISORDER ( 86 FDA reports)
SLEEP DISORDER ( 86 FDA reports)
MYOCARDIAL ISCHAEMIA ( 85 FDA reports)
SEPSIS ( 85 FDA reports)
NEPHROLITHIASIS ( 84 FDA reports)
RECTAL HAEMORRHAGE ( 84 FDA reports)
SKIN BURNING SENSATION ( 84 FDA reports)
BLOOD PRESSURE DECREASED ( 82 FDA reports)
DRUG DOSE OMISSION ( 82 FDA reports)
DRY SKIN ( 82 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 82 FDA reports)
ERECTILE DYSFUNCTION ( 81 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 81 FDA reports)
SWELLING ( 81 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 81 FDA reports)
DIABETIC NEUROPATHY ( 80 FDA reports)
EPISTAXIS ( 80 FDA reports)
HYPOKALAEMIA ( 80 FDA reports)
OSTEONECROSIS ( 80 FDA reports)
BONE DISORDER ( 79 FDA reports)
INCORRECT DOSE ADMINISTERED ( 79 FDA reports)
DIABETIC KETOACIDOSIS ( 78 FDA reports)
PULMONARY OEDEMA ( 78 FDA reports)
SKIN ULCER ( 78 FDA reports)
ANOREXIA ( 77 FDA reports)
DRUG HYPERSENSITIVITY ( 77 FDA reports)
HEART RATE IRREGULAR ( 77 FDA reports)
PRODUCT QUALITY ISSUE ( 77 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 77 FDA reports)
ANGER ( 76 FDA reports)
POLLAKIURIA ( 76 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 76 FDA reports)
INFECTION ( 75 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 74 FDA reports)
HEPATITIS ( 73 FDA reports)
IMPAIRED HEALING ( 73 FDA reports)
SCAR ( 73 FDA reports)
DISORIENTATION ( 72 FDA reports)
ROAD TRAFFIC ACCIDENT ( 72 FDA reports)
BRADYCARDIA ( 71 FDA reports)
GASTRITIS ( 71 FDA reports)
RENAL CYST ( 71 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 71 FDA reports)
SWELLING FACE ( 70 FDA reports)
DRUG EFFECT DECREASED ( 69 FDA reports)
DYSPNOEA EXERTIONAL ( 69 FDA reports)
HYPERCHOLESTEROLAEMIA ( 69 FDA reports)
MENTAL DISORDER ( 69 FDA reports)
MIGRAINE ( 69 FDA reports)
TREATMENT NONCOMPLIANCE ( 69 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 68 FDA reports)
ARRHYTHMIA ( 68 FDA reports)
HAEMORRHOIDS ( 68 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 68 FDA reports)
PANIC ATTACK ( 68 FDA reports)
RENAL INJURY ( 68 FDA reports)
THROMBOCYTOPENIA ( 68 FDA reports)
HEPATIC FAILURE ( 67 FDA reports)
RASH PRURITIC ( 67 FDA reports)
VISUAL IMPAIRMENT ( 67 FDA reports)
ANGINA UNSTABLE ( 66 FDA reports)
ATELECTASIS ( 66 FDA reports)
DENTAL CARIES ( 66 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 66 FDA reports)
HIATUS HERNIA ( 66 FDA reports)
GALLBLADDER DISORDER ( 65 FDA reports)
SPEECH DISORDER ( 65 FDA reports)
SPINAL OSTEOARTHRITIS ( 65 FDA reports)
TACHYCARDIA ( 65 FDA reports)
UNRESPONSIVE TO STIMULI ( 65 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 64 FDA reports)
RIB FRACTURE ( 64 FDA reports)
SKIN EXFOLIATION ( 64 FDA reports)
CARDIOMYOPATHY ( 63 FDA reports)
DYSLIPIDAEMIA ( 63 FDA reports)
HOT FLUSH ( 63 FDA reports)
HYPERKALAEMIA ( 63 FDA reports)
OROPHARYNGEAL PAIN ( 63 FDA reports)
SUICIDE ATTEMPT ( 63 FDA reports)
LYMPHADENOPATHY ( 62 FDA reports)
SURGERY ( 62 FDA reports)
ARTHROPATHY ( 61 FDA reports)
CARDIOVASCULAR DISORDER ( 61 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 61 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 61 FDA reports)
MENTAL STATUS CHANGES ( 61 FDA reports)
CARDIAC FAILURE ( 60 FDA reports)
IRRITABILITY ( 60 FDA reports)
NIGHTMARE ( 60 FDA reports)
DYSPHONIA ( 58 FDA reports)
GASTRIC DISORDER ( 58 FDA reports)
GASTROINTESTINAL DISORDER ( 58 FDA reports)
ILL-DEFINED DISORDER ( 58 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 58 FDA reports)
SKIN DISCOLOURATION ( 58 FDA reports)
BIPOLAR DISORDER ( 57 FDA reports)
HYPOXIA ( 57 FDA reports)
LIVER DISORDER ( 57 FDA reports)
MUSCLE STRAIN ( 57 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 57 FDA reports)
TOOTH EXTRACTION ( 57 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 57 FDA reports)
AGGRESSION ( 56 FDA reports)
EMOTIONAL DISORDER ( 56 FDA reports)
INFLUENZA ( 56 FDA reports)
ERUCTATION ( 55 FDA reports)
PAIN IN JAW ( 55 FDA reports)
VENTRICULAR TACHYCARDIA ( 55 FDA reports)
MEDICATION ERROR ( 54 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 54 FDA reports)
SWOLLEN TONGUE ( 54 FDA reports)
LUNG INFILTRATION ( 53 FDA reports)
PRURITUS GENERALISED ( 53 FDA reports)
ASCITES ( 52 FDA reports)
DEFORMITY ( 52 FDA reports)
DYSARTHRIA ( 52 FDA reports)
EJECTION FRACTION DECREASED ( 52 FDA reports)
FIBROMYALGIA ( 52 FDA reports)
HAEMATOCRIT DECREASED ( 52 FDA reports)
HAEMATURIA ( 52 FDA reports)
TYPE 1 DIABETES MELLITUS ( 52 FDA reports)
BREAST CANCER ( 51 FDA reports)
COLITIS ( 51 FDA reports)
FLANK PAIN ( 51 FDA reports)
HAEMATOCHEZIA ( 51 FDA reports)
PARANOIA ( 51 FDA reports)
RESTLESS LEGS SYNDROME ( 51 FDA reports)
COLONIC POLYP ( 50 FDA reports)
DISCOMFORT ( 50 FDA reports)
OSTEOPOROSIS ( 50 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 50 FDA reports)
BLOOD POTASSIUM DECREASED ( 49 FDA reports)
CARDIAC MURMUR ( 49 FDA reports)
CHOLECYSTITIS CHRONIC ( 49 FDA reports)
NASAL CONGESTION ( 49 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 48 FDA reports)
HAEMORRHAGE ( 48 FDA reports)
HERPES ZOSTER ( 48 FDA reports)
JOINT INJURY ( 48 FDA reports)
KIDNEY INFECTION ( 48 FDA reports)
PHOTOSENSITIVITY REACTION ( 48 FDA reports)
PULMONARY HYPERTENSION ( 48 FDA reports)
RHINORRHOEA ( 48 FDA reports)
ROTATOR CUFF SYNDROME ( 48 FDA reports)
WHEEZING ( 48 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 47 FDA reports)
CHROMATURIA ( 47 FDA reports)
CYSTITIS ( 47 FDA reports)
EAR PAIN ( 47 FDA reports)
HYPONATRAEMIA ( 47 FDA reports)
PSORIASIS ( 47 FDA reports)
VISUAL ACUITY REDUCED ( 47 FDA reports)
ADVERSE EVENT ( 46 FDA reports)
BLISTER ( 46 FDA reports)
MOVEMENT DISORDER ( 46 FDA reports)
NIGHT SWEATS ( 46 FDA reports)
SKIN TIGHTNESS ( 46 FDA reports)
TINNITUS ( 46 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 46 FDA reports)
BONE PAIN ( 45 FDA reports)
DRY EYE ( 45 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 45 FDA reports)
OXYGEN SATURATION DECREASED ( 45 FDA reports)
SINUS TACHYCARDIA ( 45 FDA reports)
CRYING ( 44 FDA reports)
DIPLOPIA ( 44 FDA reports)
DISTURBANCE IN ATTENTION ( 44 FDA reports)
DIVERTICULUM ( 44 FDA reports)
FLUID RETENTION ( 44 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 44 FDA reports)
MYOPATHY ( 44 FDA reports)
PLATELET COUNT DECREASED ( 44 FDA reports)
SINUS BRADYCARDIA ( 44 FDA reports)
URINARY INCONTINENCE ( 44 FDA reports)
BLINDNESS ( 43 FDA reports)
HEART RATE DECREASED ( 43 FDA reports)
HEPATOMEGALY ( 43 FDA reports)
IRON DEFICIENCY ANAEMIA ( 43 FDA reports)
IRRITABLE BOWEL SYNDROME ( 43 FDA reports)
OESOPHAGITIS ( 43 FDA reports)
PRESYNCOPE ( 43 FDA reports)
SKIN INDURATION ( 43 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 43 FDA reports)
AORTIC VALVE INCOMPETENCE ( 42 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 42 FDA reports)
DRUG DEPENDENCE ( 42 FDA reports)
EXCORIATION ( 42 FDA reports)
FEELING COLD ( 42 FDA reports)
INTESTINAL OBSTRUCTION ( 42 FDA reports)
LUNG DISORDER ( 42 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 42 FDA reports)
OSTEOPENIA ( 42 FDA reports)
RENAL PAIN ( 42 FDA reports)
ACUTE CORONARY SYNDROME ( 41 FDA reports)
BLOOD URINE PRESENT ( 41 FDA reports)
CHOLECYSTECTOMY ( 41 FDA reports)
FIBROSIS ( 41 FDA reports)
FOOT FRACTURE ( 41 FDA reports)
GOUT ( 41 FDA reports)
MEDICATION RESIDUE ( 41 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 41 FDA reports)
SOMNAMBULISM ( 41 FDA reports)
CEREBRAL INFARCTION ( 40 FDA reports)
COMA ( 40 FDA reports)
FEMUR FRACTURE ( 40 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 40 FDA reports)
LIP SWELLING ( 40 FDA reports)
LUNG NEOPLASM ( 40 FDA reports)
MOOD SWINGS ( 40 FDA reports)
PANCREATITIS CHRONIC ( 40 FDA reports)
RESPIRATORY DISTRESS ( 40 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 39 FDA reports)
CAROTID ARTERY STENOSIS ( 39 FDA reports)
CARPAL TUNNEL SYNDROME ( 39 FDA reports)
JAUNDICE ( 39 FDA reports)
PRODUCTIVE COUGH ( 39 FDA reports)
RESTLESSNESS ( 39 FDA reports)
ABNORMAL BEHAVIOUR ( 38 FDA reports)
BLOOD POTASSIUM INCREASED ( 38 FDA reports)
BURSITIS ( 38 FDA reports)
EYE DISORDER ( 38 FDA reports)
HAEMATOMA ( 38 FDA reports)
ABDOMINAL PAIN LOWER ( 37 FDA reports)
COAGULOPATHY ( 37 FDA reports)
COLD SWEAT ( 37 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 37 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 37 FDA reports)
HYPOVOLAEMIA ( 37 FDA reports)
IMPAIRED DRIVING ABILITY ( 37 FDA reports)
INJECTION SITE HAEMORRHAGE ( 37 FDA reports)
LABORATORY TEST ABNORMAL ( 37 FDA reports)
NEOPLASM MALIGNANT ( 37 FDA reports)
STOMACH DISCOMFORT ( 37 FDA reports)
TENDERNESS ( 37 FDA reports)
TOOTH ABSCESS ( 37 FDA reports)
TOOTHACHE ( 37 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 36 FDA reports)
CYST ( 36 FDA reports)
DIVERTICULUM INTESTINAL ( 36 FDA reports)
FLUID OVERLOAD ( 36 FDA reports)
HEART INJURY ( 36 FDA reports)
LIMB INJURY ( 36 FDA reports)
METASTASES TO BONE ( 36 FDA reports)
MIDDLE INSOMNIA ( 36 FDA reports)
MUSCLE ATROPHY ( 36 FDA reports)
MUSCLE TWITCHING ( 36 FDA reports)
NERVE COMPRESSION ( 36 FDA reports)
RASH GENERALISED ( 36 FDA reports)
SKIN LESION ( 36 FDA reports)
SPINAL COLUMN STENOSIS ( 36 FDA reports)
SUBDURAL HAEMATOMA ( 36 FDA reports)
THYROID DISORDER ( 36 FDA reports)
TOOTH FRACTURE ( 36 FDA reports)
ACUTE RESPIRATORY FAILURE ( 35 FDA reports)
ADVERSE DRUG REACTION ( 35 FDA reports)
CARDIAC PACEMAKER INSERTION ( 35 FDA reports)
DRUG TOXICITY ( 35 FDA reports)
DYSKINESIA ( 35 FDA reports)
GASTROENTERITIS ( 35 FDA reports)
INCREASED APPETITE ( 35 FDA reports)
INJECTION SITE BRUISING ( 35 FDA reports)
INJECTION SITE HAEMATOMA ( 35 FDA reports)
INTENTIONAL DRUG MISUSE ( 35 FDA reports)
MENISCUS LESION ( 35 FDA reports)
ORTHOSTATIC HYPOTENSION ( 35 FDA reports)
RHINITIS ALLERGIC ( 35 FDA reports)
SCIATICA ( 35 FDA reports)
SKIN HYPERTROPHY ( 35 FDA reports)
SPLENOMEGALY ( 35 FDA reports)
TENDONITIS ( 35 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 35 FDA reports)
TOOTH DISORDER ( 35 FDA reports)
BASAL CELL CARCINOMA ( 34 FDA reports)
BIPOLAR I DISORDER ( 34 FDA reports)
DIABETIC RETINOPATHY ( 34 FDA reports)
DRUG ADMINISTRATION ERROR ( 34 FDA reports)
EYE SWELLING ( 34 FDA reports)
GINGIVAL DISORDER ( 34 FDA reports)
LEUKOCYTOSIS ( 34 FDA reports)
LIPASE INCREASED ( 34 FDA reports)
MYOSITIS ( 34 FDA reports)
TOOTH LOSS ( 34 FDA reports)
VIRAL INFECTION ( 34 FDA reports)
ACNE ( 33 FDA reports)
DIVERTICULITIS ( 33 FDA reports)
DYSSTASIA ( 33 FDA reports)
EATING DISORDER ( 33 FDA reports)
HYPERSOMNIA ( 33 FDA reports)
INJECTION SITE ERYTHEMA ( 33 FDA reports)
MULTIPLE MYELOMA ( 33 FDA reports)
MUSCLE DISORDER ( 33 FDA reports)
PERICARDIAL EFFUSION ( 33 FDA reports)
POST PROCEDURAL COMPLICATION ( 33 FDA reports)
QUALITY OF LIFE DECREASED ( 33 FDA reports)
SPINAL COMPRESSION FRACTURE ( 33 FDA reports)
THROAT IRRITATION ( 33 FDA reports)
ANGIOEDEMA ( 32 FDA reports)
BLOOD BILIRUBIN INCREASED ( 32 FDA reports)
DRUG ABUSE ( 32 FDA reports)
FEELING JITTERY ( 32 FDA reports)
HEAD INJURY ( 32 FDA reports)
HEMIPARESIS ( 32 FDA reports)
HYPOPHAGIA ( 32 FDA reports)
IMPAIRED WORK ABILITY ( 32 FDA reports)
INTERSTITIAL LUNG DISEASE ( 32 FDA reports)
JOINT SPRAIN ( 32 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 32 FDA reports)
PALLOR ( 32 FDA reports)
PSYCHOTIC DISORDER ( 32 FDA reports)
THINKING ABNORMAL ( 32 FDA reports)
URINARY RETENTION ( 32 FDA reports)
ATRIAL FLUTTER ( 31 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 31 FDA reports)
BLADDER DISORDER ( 31 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 31 FDA reports)
EMPHYSEMA ( 31 FDA reports)
GINGIVAL BLEEDING ( 31 FDA reports)
MOUTH ULCERATION ( 31 FDA reports)
MUSCLE TIGHTNESS ( 31 FDA reports)
ONYCHOMYCOSIS ( 31 FDA reports)
SENSORY LOSS ( 31 FDA reports)
SKIN CANCER ( 31 FDA reports)
SKIN DISORDER ( 31 FDA reports)
SLEEP TALKING ( 31 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 30 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 30 FDA reports)
COORDINATION ABNORMAL ( 30 FDA reports)
DISEASE PROGRESSION ( 30 FDA reports)
GASTRIC ULCER ( 30 FDA reports)
MAJOR DEPRESSION ( 30 FDA reports)
OVARIAN CYST ( 30 FDA reports)
PELVIC PAIN ( 30 FDA reports)
PHARYNGEAL OEDEMA ( 30 FDA reports)
PRIMARY SEQUESTRUM ( 30 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 30 FDA reports)
STENT PLACEMENT ( 30 FDA reports)
VISUAL DISTURBANCE ( 30 FDA reports)
AORTIC ANEURYSM ( 29 FDA reports)
AZOTAEMIA ( 29 FDA reports)
CHOLECYSTITIS ( 29 FDA reports)
DIFFICULTY IN WALKING ( 29 FDA reports)
FUNGAL INFECTION ( 29 FDA reports)
GINGIVITIS ( 29 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 29 FDA reports)
GLOSSODYNIA ( 29 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 29 FDA reports)
METASTASES TO LUNG ( 29 FDA reports)
NOCTURIA ( 29 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 29 FDA reports)
PANCYTOPENIA ( 29 FDA reports)
SPINAL DISORDER ( 29 FDA reports)
TARDIVE DYSKINESIA ( 29 FDA reports)
APHTHOUS STOMATITIS ( 28 FDA reports)
BLOOD SODIUM DECREASED ( 28 FDA reports)
CORONARY ARTERY STENOSIS ( 28 FDA reports)
EYE IRRITATION ( 28 FDA reports)
EYE PRURITUS ( 28 FDA reports)
GROIN PAIN ( 28 FDA reports)
HIP FRACTURE ( 28 FDA reports)
KNEE ARTHROPLASTY ( 28 FDA reports)
LACERATION ( 28 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 28 FDA reports)
LEUKOPENIA ( 28 FDA reports)
LYMPHOMA ( 28 FDA reports)
RASH MACULAR ( 28 FDA reports)
SENSORY DISTURBANCE ( 28 FDA reports)
AGEUSIA ( 27 FDA reports)
CANDIDIASIS ( 27 FDA reports)
COGNITIVE DISORDER ( 27 FDA reports)
DIABETIC FOOT ( 27 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 27 FDA reports)
GASTROINTESTINAL PAIN ( 27 FDA reports)
HEPATIC CIRRHOSIS ( 27 FDA reports)
INJECTION SITE PRURITUS ( 27 FDA reports)
JOINT DISLOCATION ( 27 FDA reports)
MANIA ( 27 FDA reports)
METASTASES TO LIVER ( 27 FDA reports)
METASTASES TO LYMPH NODES ( 27 FDA reports)
NODULE ( 27 FDA reports)
PEPTIC ULCER ( 27 FDA reports)
POLYNEUROPATHY ( 27 FDA reports)
RHEUMATOID ARTHRITIS ( 27 FDA reports)
SEPTIC SHOCK ( 27 FDA reports)
ANAPHYLACTIC REACTION ( 26 FDA reports)
BLINDNESS UNILATERAL ( 26 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 26 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 26 FDA reports)
DRUG INTOLERANCE ( 26 FDA reports)
FAECAL INCONTINENCE ( 26 FDA reports)
INFLAMMATION ( 26 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 26 FDA reports)
LUMBAR SPINAL STENOSIS ( 26 FDA reports)
PROTHROMBIN TIME PROLONGED ( 26 FDA reports)
RETCHING ( 26 FDA reports)
STOMATITIS ( 26 FDA reports)
ACUTE SINUSITIS ( 25 FDA reports)
APHASIA ( 25 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 25 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 25 FDA reports)
DEMENTIA ( 25 FDA reports)
DEPRESSED MOOD ( 25 FDA reports)
ENDODONTIC PROCEDURE ( 25 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 25 FDA reports)
HYPOMAGNESAEMIA ( 25 FDA reports)
LIMB DISCOMFORT ( 25 FDA reports)
LOCALISED INFECTION ( 25 FDA reports)
MENTAL IMPAIRMENT ( 25 FDA reports)
METABOLIC ACIDOSIS ( 25 FDA reports)
ORAL DISCOMFORT ( 25 FDA reports)
POLYP ( 25 FDA reports)
PULMONARY CONGESTION ( 25 FDA reports)
RASH ERYTHEMATOUS ( 25 FDA reports)
RASH PAPULAR ( 25 FDA reports)
RENAL TUBULAR NECROSIS ( 25 FDA reports)
RESPIRATORY ARREST ( 25 FDA reports)
SENSATION OF HEAVINESS ( 25 FDA reports)
SICK SINUS SYNDROME ( 25 FDA reports)
SKIN FIBROSIS ( 25 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 25 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 25 FDA reports)
URINARY TRACT DISORDER ( 25 FDA reports)
UTERINE LEIOMYOMA ( 25 FDA reports)
VENTRICULAR HYPOKINESIA ( 25 FDA reports)
ANXIETY DISORDER ( 24 FDA reports)
CEREBRAL ATROPHY ( 24 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 24 FDA reports)
DECREASED INTEREST ( 24 FDA reports)
DIALYSIS ( 24 FDA reports)
DIASTOLIC DYSFUNCTION ( 24 FDA reports)
ENCEPHALOPATHY ( 24 FDA reports)
GENERALISED OEDEMA ( 24 FDA reports)
HAEMOPTYSIS ( 24 FDA reports)
MACULAR DEGENERATION ( 24 FDA reports)
METABOLIC SYNDROME ( 24 FDA reports)
NEURALGIA ( 24 FDA reports)
NEUTROPENIA ( 24 FDA reports)
ORAL PAIN ( 24 FDA reports)
PANCREATITIS NECROTISING ( 24 FDA reports)
WITHDRAWAL SYNDROME ( 24 FDA reports)
ATRIOVENTRICULAR BLOCK ( 23 FDA reports)
BACK INJURY ( 23 FDA reports)
BLOOD CALCIUM INCREASED ( 23 FDA reports)
BREAST MASS ( 23 FDA reports)
COMPRESSION FRACTURE ( 23 FDA reports)
DERMATITIS ( 23 FDA reports)
EYE PAIN ( 23 FDA reports)
HAEMATEMESIS ( 23 FDA reports)
HUMERUS FRACTURE ( 23 FDA reports)
HYPOKINESIA ( 23 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 23 FDA reports)
INCONTINENCE ( 23 FDA reports)
INTERMITTENT CLAUDICATION ( 23 FDA reports)
METASTASES TO SPINE ( 23 FDA reports)
NERVOUS SYSTEM DISORDER ( 23 FDA reports)
PERIODONTAL DISEASE ( 23 FDA reports)
PERSONALITY CHANGE ( 23 FDA reports)
PHOTOPHOBIA ( 23 FDA reports)
PNEUMONIA ASPIRATION ( 23 FDA reports)
PROTEINURIA ( 23 FDA reports)
THROAT TIGHTNESS ( 23 FDA reports)
URINE OUTPUT DECREASED ( 23 FDA reports)
VENTRICULAR FIBRILLATION ( 23 FDA reports)
VENTRICULAR HYPERTROPHY ( 23 FDA reports)
WOUND ( 23 FDA reports)
ANKLE FRACTURE ( 22 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 22 FDA reports)
BONE LESION ( 22 FDA reports)
CEREBROVASCULAR DISORDER ( 22 FDA reports)
CERVICOBRACHIAL SYNDROME ( 22 FDA reports)
CHRONIC SINUSITIS ( 22 FDA reports)
DENTAL OPERATION ( 22 FDA reports)
FISTULA ( 22 FDA reports)
FOOT DEFORMITY ( 22 FDA reports)
GOITRE ( 22 FDA reports)
HALLUCINATION, VISUAL ( 22 FDA reports)
HEPATIC CYST ( 22 FDA reports)
ILEUS ( 22 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 22 FDA reports)
ORTHOPNOEA ( 22 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 22 FDA reports)
SHOCK ( 22 FDA reports)
SKELETAL INJURY ( 22 FDA reports)
SKIN LACERATION ( 22 FDA reports)
THIRST ( 22 FDA reports)
TONGUE DISORDER ( 22 FDA reports)
VISUAL FIELD DEFECT ( 22 FDA reports)
APPENDICITIS ( 21 FDA reports)
BLOOD CALCIUM DECREASED ( 21 FDA reports)
CATHETERISATION CARDIAC ( 21 FDA reports)
CONCUSSION ( 21 FDA reports)
CROHN'S DISEASE ( 21 FDA reports)
DIABETIC NEPHROPATHY ( 21 FDA reports)
FAILURE TO THRIVE ( 21 FDA reports)
GENERALISED ERYTHEMA ( 21 FDA reports)
GRAND MAL CONVULSION ( 21 FDA reports)
HALLUCINATION, AUDITORY ( 21 FDA reports)
LOOSE TOOTH ( 21 FDA reports)
MALNUTRITION ( 21 FDA reports)
PROSTATE CANCER ( 21 FDA reports)
RADICULOPATHY ( 21 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 21 FDA reports)
APHAGIA ( 20 FDA reports)
BLOOD DISORDER ( 20 FDA reports)
BODY TEMPERATURE INCREASED ( 20 FDA reports)
CARDIAC VALVE DISEASE ( 20 FDA reports)
CHOKING ( 20 FDA reports)
DEAFNESS ( 20 FDA reports)
DENTAL DISCOMFORT ( 20 FDA reports)
ECCHYMOSIS ( 20 FDA reports)
FACIAL PALSY ( 20 FDA reports)
GASTRITIS EROSIVE ( 20 FDA reports)
HAEMODIALYSIS ( 20 FDA reports)
HYPERCALCAEMIA ( 20 FDA reports)
HYPOACUSIS ( 20 FDA reports)
JOINT STIFFNESS ( 20 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 20 FDA reports)
MUSCLE INJURY ( 20 FDA reports)
PHARYNGITIS ( 20 FDA reports)
POOR QUALITY SLEEP ( 20 FDA reports)
PULMONARY FIBROSIS ( 20 FDA reports)
STEVENS-JOHNSON SYNDROME ( 20 FDA reports)
THYROID NEOPLASM ( 20 FDA reports)
UPPER LIMB FRACTURE ( 20 FDA reports)
VAGINAL HAEMORRHAGE ( 20 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 19 FDA reports)
AORTIC STENOSIS ( 19 FDA reports)
BREAST CANCER FEMALE ( 19 FDA reports)
CARDIAC FLUTTER ( 19 FDA reports)
DIABETIC COMA ( 19 FDA reports)
HYDRONEPHROSIS ( 19 FDA reports)
INFUSION RELATED REACTION ( 19 FDA reports)
JAW DISORDER ( 19 FDA reports)
KYPHOSCOLIOSIS ( 19 FDA reports)
LIFE EXPECTANCY SHORTENED ( 19 FDA reports)
LUNG NEOPLASM MALIGNANT ( 19 FDA reports)
MELAENA ( 19 FDA reports)
MOOD ALTERED ( 19 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 19 FDA reports)
NON-CARDIAC CHEST PAIN ( 19 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 19 FDA reports)
PERIPHERAL COLDNESS ( 19 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 19 FDA reports)
PROCEDURAL PAIN ( 19 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 19 FDA reports)
SKIN GRAFT ( 19 FDA reports)
SNEEZING ( 19 FDA reports)
TOOTH INFECTION ( 19 FDA reports)
VITAMIN B12 DEFICIENCY ( 19 FDA reports)
ACTINOMYCOSIS ( 18 FDA reports)
ADRENAL ADENOMA ( 18 FDA reports)
ANAPHYLACTIC SHOCK ( 18 FDA reports)
ANEURYSM ( 18 FDA reports)
BLOOD IRON DECREASED ( 18 FDA reports)
BREAST PAIN ( 18 FDA reports)
CATARACT OPERATION ( 18 FDA reports)
CEREBRAL HAEMORRHAGE ( 18 FDA reports)
CEREBRAL ISCHAEMIA ( 18 FDA reports)
CORONARY ARTERY BYPASS ( 18 FDA reports)
COSTOCHONDRITIS ( 18 FDA reports)
DILATATION ATRIAL ( 18 FDA reports)
EATING DISORDER SYMPTOM ( 18 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 18 FDA reports)
HEPATITIS C ( 18 FDA reports)
HEPATOTOXICITY ( 18 FDA reports)
HIP ARTHROPLASTY ( 18 FDA reports)
HUNGER ( 18 FDA reports)
LIGAMENT SPRAIN ( 18 FDA reports)
LIPOMA ( 18 FDA reports)
LIVER INJURY ( 18 FDA reports)
LOBAR PNEUMONIA ( 18 FDA reports)
LYMPHOEDEMA ( 18 FDA reports)
MULTIPLE FRACTURES ( 18 FDA reports)
MUSCLE SPASTICITY ( 18 FDA reports)
NECK INJURY ( 18 FDA reports)
OCULAR ICTERUS ( 18 FDA reports)
ORAL INFECTION ( 18 FDA reports)
PYELONEPHRITIS ( 18 FDA reports)
RESPIRATORY DISORDER ( 18 FDA reports)
SCOLIOSIS ( 18 FDA reports)
SPINAL FRACTURE ( 18 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 18 FDA reports)
VENOUS INSUFFICIENCY ( 18 FDA reports)
ABDOMINAL HERNIA ( 17 FDA reports)
ACUTE PRERENAL FAILURE ( 17 FDA reports)
BLOOD AMYLASE INCREASED ( 17 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 17 FDA reports)
BLOOD MAGNESIUM DECREASED ( 17 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 17 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 17 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 17 FDA reports)
CARDIOGENIC SHOCK ( 17 FDA reports)
CAROTID ARTERY OCCLUSION ( 17 FDA reports)
DISABILITY ( 17 FDA reports)
EARLY SATIETY ( 17 FDA reports)
ELECTROLYTE IMBALANCE ( 17 FDA reports)
FAECES DISCOLOURED ( 17 FDA reports)
FRACTURE NONUNION ( 17 FDA reports)
GINGIVAL RECESSION ( 17 FDA reports)
GINGIVAL SWELLING ( 17 FDA reports)
GRANULOCYTOPENIA ( 17 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 17 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 17 FDA reports)
HYPERTENSIVE CRISIS ( 17 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 17 FDA reports)
JOINT CONTRACTURE ( 17 FDA reports)
KYPHOSIS ( 17 FDA reports)
LACUNAR INFARCTION ( 17 FDA reports)
METABOLIC ENCEPHALOPATHY ( 17 FDA reports)
MULTIPLE SCLEROSIS ( 17 FDA reports)
POOR PERSONAL HYGIENE ( 17 FDA reports)
PRESCRIBED OVERDOSE ( 17 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 17 FDA reports)
PULMONARY MASS ( 17 FDA reports)
RETINAL DETACHMENT ( 17 FDA reports)
SKIN PLAQUE ( 17 FDA reports)
ADRENAL DISORDER ( 16 FDA reports)
ASTIGMATISM ( 16 FDA reports)
BACK DISORDER ( 16 FDA reports)
BILIARY DYSKINESIA ( 16 FDA reports)
BLINDNESS TRANSIENT ( 16 FDA reports)
CAROTID ARTERY DISEASE ( 16 FDA reports)
DILATATION VENTRICULAR ( 16 FDA reports)
DYSPHORIA ( 16 FDA reports)
ECZEMA ( 16 FDA reports)
EXOSTOSIS ( 16 FDA reports)
EXPIRED DRUG ADMINISTERED ( 16 FDA reports)
FEELING DRUNK ( 16 FDA reports)
FLAT AFFECT ( 16 FDA reports)
GLAUCOMA ( 16 FDA reports)
HEPATIC LESION ( 16 FDA reports)
HERNIA ( 16 FDA reports)
HOSPITALISATION ( 16 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 16 FDA reports)
INJECTION SITE REACTION ( 16 FDA reports)
INTENTIONAL OVERDOSE ( 16 FDA reports)
MACULAR OEDEMA ( 16 FDA reports)
MALIGNANT HYPERTENSION ( 16 FDA reports)
NERVE INJURY ( 16 FDA reports)
NEUROPATHY ( 16 FDA reports)
OSTEORADIONECROSIS ( 16 FDA reports)
PERIODONTITIS ( 16 FDA reports)
PERONEAL NERVE PALSY ( 16 FDA reports)
PHYSICAL DISABILITY ( 16 FDA reports)
PLATELET COUNT INCREASED ( 16 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 16 FDA reports)
SPINAL CLAUDICATION ( 16 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 16 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 16 FDA reports)
TENDON INJURY ( 16 FDA reports)
TIBIA FRACTURE ( 16 FDA reports)
TOBACCO ABUSE ( 16 FDA reports)
VASOCONSTRICTION ( 16 FDA reports)
VITAMIN D DECREASED ( 16 FDA reports)
ATHEROSCLEROSIS ( 15 FDA reports)
ATROPHY ( 15 FDA reports)
BLADDER CANCER ( 15 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 15 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 15 FDA reports)
CARDIAC OPERATION ( 15 FDA reports)
CERVICAL DYSPLASIA ( 15 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 15 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 15 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 15 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 15 FDA reports)
DRUG ERUPTION ( 15 FDA reports)
EAR INFECTION ( 15 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 15 FDA reports)
FACIAL PAIN ( 15 FDA reports)
GASTROENTERITIS VIRAL ( 15 FDA reports)
GRAFT VERSUS HOST DISEASE ( 15 FDA reports)
HYPERTONIC BLADDER ( 15 FDA reports)
INTESTINAL DILATATION ( 15 FDA reports)
ISCHAEMIA ( 15 FDA reports)
LACRIMATION INCREASED ( 15 FDA reports)
LOCAL SWELLING ( 15 FDA reports)
LUMBAR RADICULOPATHY ( 15 FDA reports)
OCULAR HYPERAEMIA ( 15 FDA reports)
PANCREATITIS RELAPSING ( 15 FDA reports)
PERITONITIS ( 15 FDA reports)
PRESBYOPIA ( 15 FDA reports)
SEXUAL DYSFUNCTION ( 15 FDA reports)
SINUS CONGESTION ( 15 FDA reports)
SNORING ( 15 FDA reports)
TENDON RUPTURE ( 15 FDA reports)
TONGUE OEDEMA ( 15 FDA reports)
VAGINAL INFECTION ( 15 FDA reports)
VULVOVAGINAL PRURITUS ( 15 FDA reports)
ABDOMINAL ADHESIONS ( 14 FDA reports)
ACIDOSIS ( 14 FDA reports)
APPLICATION SITE ERYTHEMA ( 14 FDA reports)
AUTONOMIC NEUROPATHY ( 14 FDA reports)
BIOPSY CHEST WALL ABNORMAL ( 14 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 14 FDA reports)
CERVICAL SPINAL STENOSIS ( 14 FDA reports)
CHOLECYSTITIS ACUTE ( 14 FDA reports)
DIABETIC GASTROPARESIS ( 14 FDA reports)
DIZZINESS POSTURAL ( 14 FDA reports)
DRUG PRESCRIBING ERROR ( 14 FDA reports)
DRUG TOLERANCE ( 14 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 14 FDA reports)
DYSTHYMIC DISORDER ( 14 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 14 FDA reports)
ESSENTIAL HYPERTENSION ( 14 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 14 FDA reports)
EXERCISE TOLERANCE DECREASED ( 14 FDA reports)
EXPOSED BONE IN JAW ( 14 FDA reports)
FEBRILE NEUTROPENIA ( 14 FDA reports)
HAND FRACTURE ( 14 FDA reports)
HEPATOCELLULAR DAMAGE ( 14 FDA reports)
HERNIA REPAIR ( 14 FDA reports)
HILAR LYMPHADENOPATHY ( 14 FDA reports)
INITIAL INSOMNIA ( 14 FDA reports)
INTESTINAL PERFORATION ( 14 FDA reports)
JAUNDICE CHOLESTATIC ( 14 FDA reports)
LACTIC ACIDOSIS ( 14 FDA reports)
LUNG INFECTION ( 14 FDA reports)
MALIGNANT MELANOMA ( 14 FDA reports)
MUSCLE CRAMP ( 14 FDA reports)
NEPHRITIS INTERSTITIAL ( 14 FDA reports)
NO ADVERSE EVENT ( 14 FDA reports)
PARALYSIS ( 14 FDA reports)
PNEUMONITIS ( 14 FDA reports)
PRODUCT ADHESION ISSUE ( 14 FDA reports)
RALES ( 14 FDA reports)
SPONDYLOLISTHESIS ( 14 FDA reports)
STRIDOR ( 14 FDA reports)
TENDON DISORDER ( 14 FDA reports)
URINE COLOUR ABNORMAL ( 14 FDA reports)
VAGINAL DISCHARGE ( 14 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 14 FDA reports)
ABDOMINAL TENDERNESS ( 13 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 13 FDA reports)
ANOSMIA ( 13 FDA reports)
APHONIA ( 13 FDA reports)
BREAST CANCER METASTATIC ( 13 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 13 FDA reports)
DRUG DISPENSING ERROR ( 13 FDA reports)
DRY THROAT ( 13 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 13 FDA reports)
EYE HAEMORRHAGE ( 13 FDA reports)
FEAR OF DEATH ( 13 FDA reports)
GINGIVAL ULCERATION ( 13 FDA reports)
HOMICIDAL IDEATION ( 13 FDA reports)
HYPOCALCAEMIA ( 13 FDA reports)
INADEQUATE ANALGESIA ( 13 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 13 FDA reports)
INJECTION SITE EXTRAVASATION ( 13 FDA reports)
INJECTION SITE IRRITATION ( 13 FDA reports)
INJECTION SITE SWELLING ( 13 FDA reports)
LIPIDS INCREASED ( 13 FDA reports)
LOW TURNOVER OSTEOPATHY ( 13 FDA reports)
LOWER LIMB FRACTURE ( 13 FDA reports)
ORAL INTAKE REDUCED ( 13 FDA reports)
PAIN OF SKIN ( 13 FDA reports)
PARAESTHESIA ORAL ( 13 FDA reports)
PAROSMIA ( 13 FDA reports)
PATHOLOGICAL FRACTURE ( 13 FDA reports)
PATHOLOGICAL GAMBLING ( 13 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 13 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 13 FDA reports)
SEPSIS SYNDROME ( 13 FDA reports)
SICCA SYNDROME ( 13 FDA reports)
SINUS DISORDER ( 13 FDA reports)
SPINAL DEFORMITY ( 13 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 13 FDA reports)
VASCULITIS ( 13 FDA reports)
VIITH NERVE PARALYSIS ( 13 FDA reports)
ACCIDENT ( 12 FDA reports)
AKATHISIA ( 12 FDA reports)
BARTHOLIN'S ABSCESS ( 12 FDA reports)
BARTHOLIN'S CYST ( 12 FDA reports)
BILE DUCT OBSTRUCTION ( 12 FDA reports)
BLOOD CULTURE POSITIVE ( 12 FDA reports)
BLOOD PRESSURE ABNORMAL ( 12 FDA reports)
BODY HEIGHT DECREASED ( 12 FDA reports)
BONE MARROW FAILURE ( 12 FDA reports)
BRONCHOSPASM ( 12 FDA reports)
CARDIAC ANEURYSM ( 12 FDA reports)
CATHETER SITE INFECTION ( 12 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 12 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 12 FDA reports)
CIRCULATORY COLLAPSE ( 12 FDA reports)
DEAFNESS UNILATERAL ( 12 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 12 FDA reports)
DEPENDENCE ( 12 FDA reports)
DEVICE MALFUNCTION ( 12 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 12 FDA reports)
DUODENITIS ( 12 FDA reports)
EAR DISORDER ( 12 FDA reports)
EMBOLISM ( 12 FDA reports)
FACE OEDEMA ( 12 FDA reports)
FACET JOINT SYNDROME ( 12 FDA reports)
FACIAL BONES FRACTURE ( 12 FDA reports)
FIBULA FRACTURE ( 12 FDA reports)
GENITAL HERPES ( 12 FDA reports)
GINGIVAL OPERATION ( 12 FDA reports)
HAEMORRHAGIC STROKE ( 12 FDA reports)
HEAD DISCOMFORT ( 12 FDA reports)
HEMIPLEGIA ( 12 FDA reports)
HEPATIC FIBROSIS ( 12 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 12 FDA reports)
IMMUNE SYSTEM DISORDER ( 12 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 12 FDA reports)
INTRACARDIAC THROMBUS ( 12 FDA reports)
ISCHAEMIC STROKE ( 12 FDA reports)
JAW FRACTURE ( 12 FDA reports)
LEFT ATRIAL DILATATION ( 12 FDA reports)
LIBIDO DECREASED ( 12 FDA reports)
METASTATIC NEOPLASM ( 12 FDA reports)
MITRAL VALVE CALCIFICATION ( 12 FDA reports)
MITRAL VALVE DISEASE ( 12 FDA reports)
OPEN ANGLE GLAUCOMA ( 12 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 12 FDA reports)
PHOTOPSIA ( 12 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 12 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 12 FDA reports)
PROSTATE INFECTION ( 12 FDA reports)
PROSTATOMEGALY ( 12 FDA reports)
PURULENT DISCHARGE ( 12 FDA reports)
SCAB ( 12 FDA reports)
SEDATION ( 12 FDA reports)
SLUGGISHNESS ( 12 FDA reports)
STASIS DERMATITIS ( 12 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 12 FDA reports)
TACHYPHRENIA ( 12 FDA reports)
TENSION HEADACHE ( 12 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 12 FDA reports)
TRAUMATIC BRAIN INJURY ( 12 FDA reports)
ULCER ( 12 FDA reports)
UMBILICAL HERNIA ( 12 FDA reports)
VASCULAR GRAFT ( 12 FDA reports)
VENTRICULAR DYSFUNCTION ( 12 FDA reports)
VITAMIN D DEFICIENCY ( 12 FDA reports)
ABDOMINAL MASS ( 11 FDA reports)
ABSCESS ( 11 FDA reports)
ACCELERATED HYPERTENSION ( 11 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 11 FDA reports)
BACTERIAL INFECTION ( 11 FDA reports)
BLOOD CREATINE INCREASED ( 11 FDA reports)
BONE CYST ( 11 FDA reports)
BONE LOSS ( 11 FDA reports)
BRONCHIECTASIS ( 11 FDA reports)
BRUXISM ( 11 FDA reports)
CAROTIDYNIA ( 11 FDA reports)
CHEST X-RAY ABNORMAL ( 11 FDA reports)
COLITIS ISCHAEMIC ( 11 FDA reports)
COLON ADENOMA ( 11 FDA reports)
DEBRIDEMENT ( 11 FDA reports)
DECREASED ACTIVITY ( 11 FDA reports)
DEMYELINATION ( 11 FDA reports)
DEVICE FAILURE ( 11 FDA reports)
EPICONDYLITIS ( 11 FDA reports)
ESCHERICHIA INFECTION ( 11 FDA reports)
EXTRASYSTOLES ( 11 FDA reports)
GROIN ABSCESS ( 11 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 11 FDA reports)
HEPATITIS ACUTE ( 11 FDA reports)
HYPERTHYROIDISM ( 11 FDA reports)
HYPOAESTHESIA ORAL ( 11 FDA reports)
MYOPIA ( 11 FDA reports)
NASAL SEPTUM DEVIATION ( 11 FDA reports)
NEPHROPATHY ( 11 FDA reports)
NEUTROPHIL COUNT DECREASED ( 11 FDA reports)
NON-SMALL CELL LUNG CANCER ( 11 FDA reports)
OTITIS MEDIA ( 11 FDA reports)
PERSONALITY DISORDER ( 11 FDA reports)
PLEURISY ( 11 FDA reports)
PROCEDURAL COMPLICATION ( 11 FDA reports)
PURPURA ( 11 FDA reports)
REFLUX OESOPHAGITIS ( 11 FDA reports)
RENAL CELL CARCINOMA ( 11 FDA reports)
RETINAL HAEMORRHAGE ( 11 FDA reports)
SCHIZOPHRENIA ( 11 FDA reports)
SEASONAL ALLERGY ( 11 FDA reports)
SENSATION OF FOREIGN BODY ( 11 FDA reports)
SHOULDER PAIN ( 11 FDA reports)
SKIN HAEMORRHAGE ( 11 FDA reports)
TENSION ( 11 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 11 FDA reports)
TOE AMPUTATION ( 11 FDA reports)
WEIGHT FLUCTUATION ( 11 FDA reports)
WRIST FRACTURE ( 11 FDA reports)
ACCIDENTAL OVERDOSE ( 10 FDA reports)
ACUTE HEPATIC FAILURE ( 10 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 10 FDA reports)
ACUTE PULMONARY OEDEMA ( 10 FDA reports)
ADRENAL MASS ( 10 FDA reports)
AFFECTIVE DISORDER ( 10 FDA reports)
ALCOHOL USE ( 10 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 10 FDA reports)
ANGIOPATHY ( 10 FDA reports)
APPLICATION SITE IRRITATION ( 10 FDA reports)
APPLICATION SITE PRURITUS ( 10 FDA reports)
BACTERIAL DISEASE CARRIER ( 10 FDA reports)
BLOOD ALBUMIN DECREASED ( 10 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 10 FDA reports)
BODY TEMPERATURE DECREASED ( 10 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 10 FDA reports)
BUNDLE BRANCH BLOCK ( 10 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 10 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 10 FDA reports)
CERUMEN IMPACTION ( 10 FDA reports)
CHANGE OF BOWEL HABIT ( 10 FDA reports)
CHOLESTASIS ( 10 FDA reports)
CLUMSINESS ( 10 FDA reports)
DELUSION ( 10 FDA reports)
DIABETIC COMPLICATION ( 10 FDA reports)
DYSPAREUNIA ( 10 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 10 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 10 FDA reports)
ENTEROCOCCAL INFECTION ( 10 FDA reports)
EXTREMITY CONTRACTURE ( 10 FDA reports)
EYE INFECTION ( 10 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 10 FDA reports)
GYNAECOMASTIA ( 10 FDA reports)
HEPATIC ENZYME ABNORMAL ( 10 FDA reports)
HEPATIC MASS ( 10 FDA reports)
HYPERBILIRUBINAEMIA ( 10 FDA reports)
HYPERCHLORHYDRIA ( 10 FDA reports)
HYPOALBUMINAEMIA ( 10 FDA reports)
HYPOVITAMINOSIS ( 10 FDA reports)
INJECTION SITE RASH ( 10 FDA reports)
LABILE HYPERTENSION ( 10 FDA reports)
METRORRHAGIA ( 10 FDA reports)
MITRAL VALVE PROLAPSE ( 10 FDA reports)
MUSCULOSKELETAL DISORDER ( 10 FDA reports)
NO THERAPEUTIC RESPONSE ( 10 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 10 FDA reports)
ORAL CANDIDIASIS ( 10 FDA reports)
OSTEOLYSIS ( 10 FDA reports)
OVARIAN ADHESION ( 10 FDA reports)
PELVIC ADHESIONS ( 10 FDA reports)
PERITONITIS BACTERIAL ( 10 FDA reports)
POLYURIA ( 10 FDA reports)
PROCTALGIA ( 10 FDA reports)
PULMONARY THROMBOSIS ( 10 FDA reports)
SALPINGITIS ( 10 FDA reports)
SEQUESTRECTOMY ( 10 FDA reports)
SINUS HEADACHE ( 10 FDA reports)
SUNBURN ( 10 FDA reports)
SYNOVIAL CYST ( 10 FDA reports)
TRANSAMINASES INCREASED ( 10 FDA reports)
URETHRAL STENOSIS ( 10 FDA reports)
VASCULAR GRAFT OCCLUSION ( 10 FDA reports)
WALKING AID USER ( 10 FDA reports)
ADENOMYOSIS ( 9 FDA reports)
APPLICATION SITE PAIN ( 9 FDA reports)
ATRIAL SEPTAL DEFECT ( 9 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 9 FDA reports)
AUTOIMMUNE HEPATITIS ( 9 FDA reports)
BLOOD CHLORIDE DECREASED ( 9 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 9 FDA reports)
BULIMIA NERVOSA ( 9 FDA reports)
CALCINOSIS ( 9 FDA reports)
CARDIAC ENZYMES INCREASED ( 9 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 9 FDA reports)
COELIAC DISEASE ( 9 FDA reports)
CONDUCTION DISORDER ( 9 FDA reports)
CUTIS LAXA ( 9 FDA reports)
DELIRIUM ( 9 FDA reports)
DENTAL PLAQUE ( 9 FDA reports)
DIABETIC ULCER ( 9 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 9 FDA reports)
DRUG LEVEL INCREASED ( 9 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 9 FDA reports)
EAR DISCOMFORT ( 9 FDA reports)
EPIGASTRIC DISCOMFORT ( 9 FDA reports)
EYELID DISORDER ( 9 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 9 FDA reports)
FIBRIN D DIMER INCREASED ( 9 FDA reports)
FORMICATION ( 9 FDA reports)
FRACTURE ( 9 FDA reports)
FURUNCLE ( 9 FDA reports)
GRIEF REACTION ( 9 FDA reports)
HAEMORRHAGE URINARY TRACT ( 9 FDA reports)
HEARING IMPAIRED ( 9 FDA reports)
HEPATITIS CHOLESTATIC ( 9 FDA reports)
INCREASED TENDENCY TO BRUISE ( 9 FDA reports)
LARYNGITIS ( 9 FDA reports)
LOSS OF EMPLOYMENT ( 9 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 9 FDA reports)
MEIBOMIANITIS ( 9 FDA reports)
MELANOCYTIC NAEVUS ( 9 FDA reports)
MICTURITION URGENCY ( 9 FDA reports)
MIOSIS ( 9 FDA reports)
NEURODERMATITIS ( 9 FDA reports)
NOCTURNAL DYSPNOEA ( 9 FDA reports)
OCCULT BLOOD POSITIVE ( 9 FDA reports)
ODYNOPHAGIA ( 9 FDA reports)
OEDEMA MOUTH ( 9 FDA reports)
OESOPHAGEAL RUPTURE ( 9 FDA reports)
OPEN WOUND ( 9 FDA reports)
OTITIS MEDIA ACUTE ( 9 FDA reports)
OVERWEIGHT ( 9 FDA reports)
PAINFUL DEFAECATION ( 9 FDA reports)
PANCREATIC DISORDER ( 9 FDA reports)
PAPILLOEDEMA ( 9 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 9 FDA reports)
PETECHIAE ( 9 FDA reports)
PINGUECULA ( 9 FDA reports)
PITTING OEDEMA ( 9 FDA reports)
PROTEIN URINE PRESENT ( 9 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 9 FDA reports)
SERUM FERRITIN INCREASED ( 9 FDA reports)
SKIN FISSURES ( 9 FDA reports)
SPINAL CORD COMPRESSION ( 9 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 9 FDA reports)
STRESS FRACTURE ( 9 FDA reports)
SUDDEN DEATH ( 9 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 9 FDA reports)
TELANGIECTASIA ( 9 FDA reports)
TINEA PEDIS ( 9 FDA reports)
TOBACCO USER ( 9 FDA reports)
TOE DEFORMITY ( 9 FDA reports)
TONGUE DISCOLOURATION ( 9 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 9 FDA reports)
UTERINE HAEMORRHAGE ( 9 FDA reports)
VASCULAR DEMENTIA ( 9 FDA reports)
VENA CAVA THROMBOSIS ( 9 FDA reports)
VITREOUS DETACHMENT ( 9 FDA reports)
WOUND INFECTION ( 9 FDA reports)
ABNORMAL FAECES ( 8 FDA reports)
AFFECT LABILITY ( 8 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 8 FDA reports)
AORTIC THROMBOSIS ( 8 FDA reports)
AORTIC VALVE CALCIFICATION ( 8 FDA reports)
APATHY ( 8 FDA reports)
APPENDICITIS PERFORATED ( 8 FDA reports)
APPLICATION SITE RASH ( 8 FDA reports)
ARTHROPOD BITE ( 8 FDA reports)
BILE DUCT STONE ( 8 FDA reports)
BLADDER PAIN ( 8 FDA reports)
BLEPHARITIS ( 8 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 8 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 8 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 8 FDA reports)
BONE DENSITY DECREASED ( 8 FDA reports)
BONE SWELLING ( 8 FDA reports)
BRAIN OEDEMA ( 8 FDA reports)
CAROTID INTIMA-MEDIA THICKNESS INCREASED ( 8 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 8 FDA reports)
CHONDROMALACIA ( 8 FDA reports)
COLITIS ULCERATIVE ( 8 FDA reports)
COLON CANCER ( 8 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 8 FDA reports)
DEFAECATION URGENCY ( 8 FDA reports)
DENTAL CARE ( 8 FDA reports)
DEPERSONALISATION ( 8 FDA reports)
DERMATITIS CONTACT ( 8 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 8 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 8 FDA reports)
EMBOLIC STROKE ( 8 FDA reports)
EMPTY SELLA SYNDROME ( 8 FDA reports)
EYE DISCHARGE ( 8 FDA reports)
EYE INJURY ( 8 FDA reports)
FACE INJURY ( 8 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 8 FDA reports)
FOLLICULITIS ( 8 FDA reports)
GALLBLADDER OPERATION ( 8 FDA reports)
HERPES SIMPLEX ( 8 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 8 FDA reports)
HYPERKERATOSIS ( 8 FDA reports)
HYPERPARATHYROIDISM ( 8 FDA reports)
HYPERVENTILATION ( 8 FDA reports)
INGUINAL HERNIA ( 8 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 8 FDA reports)
LABYRINTHITIS ( 8 FDA reports)
LIP BLISTER ( 8 FDA reports)
LOSS OF LIBIDO ( 8 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 8 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 8 FDA reports)
MASTECTOMY ( 8 FDA reports)
METABOLIC DISORDER ( 8 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 8 FDA reports)
METASTASES TO SKIN ( 8 FDA reports)
MOTOR DYSFUNCTION ( 8 FDA reports)
MYCOSIS FUNGOIDES ( 8 FDA reports)
MYELODYSPLASTIC SYNDROME ( 8 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 8 FDA reports)
NEOPLASM PROGRESSION ( 8 FDA reports)
NYSTAGMUS ( 8 FDA reports)
OPTIC NEURITIS ( 8 FDA reports)
ORAL DISORDER ( 8 FDA reports)
OTITIS EXTERNA ( 8 FDA reports)
OVARIAN MASS ( 8 FDA reports)
PERIARTHRITIS ( 8 FDA reports)
PERICARDIAL CALCIFICATION ( 8 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 8 FDA reports)
PLEURAL CALCIFICATION ( 8 FDA reports)
POLYDIPSIA ( 8 FDA reports)
POLYMYALGIA RHEUMATICA ( 8 FDA reports)
POSTMENOPAUSE ( 8 FDA reports)
PRODUCT ODOUR ABNORMAL ( 8 FDA reports)
PRODUCT TASTE ABNORMAL ( 8 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 8 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 8 FDA reports)
PROSTATITIS ( 8 FDA reports)
PSEUDOCYST ( 8 FDA reports)
PSORIATIC ARTHROPATHY ( 8 FDA reports)
PULSE ABSENT ( 8 FDA reports)
RASH PUSTULAR ( 8 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 8 FDA reports)
RENAL ATROPHY ( 8 FDA reports)
RESPIRATORY TRACT CONGESTION ( 8 FDA reports)
SCRATCH ( 8 FDA reports)
SPINAL FUSION SURGERY ( 8 FDA reports)
STREPTOCOCCAL INFECTION ( 8 FDA reports)
STRESS INCONTINENCE ( 8 FDA reports)
STRESS URINARY INCONTINENCE ( 8 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 8 FDA reports)
T-CELL LYMPHOMA ( 8 FDA reports)
TACHYPNOEA ( 8 FDA reports)
THROAT LESION ( 8 FDA reports)
TROPONIN INCREASED ( 8 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
URINARY TRACT OBSTRUCTION ( 8 FDA reports)
URINE ODOUR ABNORMAL ( 8 FDA reports)
VASCULAR OCCLUSION ( 8 FDA reports)
VITAMIN B12 DECREASED ( 8 FDA reports)
VITREOUS HAEMORRHAGE ( 8 FDA reports)
WRONG DRUG ADMINISTERED ( 8 FDA reports)
YELLOW SKIN ( 8 FDA reports)
ABORTION SPONTANEOUS ( 7 FDA reports)
ADRENAL INSUFFICIENCY ( 7 FDA reports)
ADVERSE REACTION ( 7 FDA reports)
ALCOHOLIC LIVER DISEASE ( 7 FDA reports)
AMENORRHOEA ( 7 FDA reports)
ANGIOMYOLIPOMA ( 7 FDA reports)
ANGIONEUROTIC OEDEMA ( 7 FDA reports)
AORTIC CALCIFICATION ( 7 FDA reports)
AORTIC VALVE SCLEROSIS ( 7 FDA reports)
ARTERIAL INSUFFICIENCY ( 7 FDA reports)
ATAXIA ( 7 FDA reports)
ATROPHIC VULVOVAGINITIS ( 7 FDA reports)
AUTOIMMUNE THYROIDITIS ( 7 FDA reports)
BILIARY DILATATION ( 7 FDA reports)
BLOOD CHLORIDE INCREASED ( 7 FDA reports)
BLOOD CREATININE DECREASED ( 7 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 7 FDA reports)
BLOOD TEST ABNORMAL ( 7 FDA reports)
COLLAPSE OF LUNG ( 7 FDA reports)
CONJUNCTIVITIS ( 7 FDA reports)
CORONARY ARTERY THROMBOSIS ( 7 FDA reports)
CULTURE URINE POSITIVE ( 7 FDA reports)
DECUBITUS ULCER ( 7 FDA reports)
DEPRESSIVE SYMPTOM ( 7 FDA reports)
DROOLING ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 7 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 7 FDA reports)
ENTERITIS ( 7 FDA reports)
EUPHORIC MOOD ( 7 FDA reports)
EYE OPERATION ( 7 FDA reports)
FACTOR V LEIDEN MUTATION ( 7 FDA reports)
FAECALOMA ( 7 FDA reports)
FAECES HARD ( 7 FDA reports)
FAMILY STRESS ( 7 FDA reports)
GALLBLADDER INJURY ( 7 FDA reports)
GINGIVAL INFECTION ( 7 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 7 FDA reports)
GRAFT DYSFUNCTION ( 7 FDA reports)
HAEMANGIOMA ( 7 FDA reports)
HANGOVER ( 7 FDA reports)
HEART RATE ABNORMAL ( 7 FDA reports)
HODGKIN'S DISEASE ( 7 FDA reports)
HYDROCEPHALUS ( 7 FDA reports)
HYPERAESTHESIA ( 7 FDA reports)
HYPERPROLACTINAEMIA ( 7 FDA reports)
HYSTERECTOMY ( 7 FDA reports)
IMPAIRED SELF-CARE ( 7 FDA reports)
INGROWING NAIL ( 7 FDA reports)
KNEE OPERATION ( 7 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 7 FDA reports)
LICHENOID KERATOSIS ( 7 FDA reports)
LIVER SCAN ABNORMAL ( 7 FDA reports)
LOCALISED OEDEMA ( 7 FDA reports)
LYMPHOPENIA ( 7 FDA reports)
MASS ( 7 FDA reports)
MEDICAL DEVICE COMPLICATION ( 7 FDA reports)
MENORRHAGIA ( 7 FDA reports)
MUSCLE HAEMORRHAGE ( 7 FDA reports)
MYDRIASIS ( 7 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 7 FDA reports)
NEUTROPHIL COUNT INCREASED ( 7 FDA reports)
NICOTINE DEPENDENCE ( 7 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 7 FDA reports)
OESOPHAGEAL ULCER ( 7 FDA reports)
ORGAN FAILURE ( 7 FDA reports)
PANCREATIC PSEUDOCYST ( 7 FDA reports)
PERIPHERAL ISCHAEMIA ( 7 FDA reports)
PLANTAR FASCIITIS ( 7 FDA reports)
POLYP COLORECTAL ( 7 FDA reports)
POLYTRAUMATISM ( 7 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 7 FDA reports)
PULMONARY HAEMORRHAGE ( 7 FDA reports)
PUPIL FIXED ( 7 FDA reports)
RESPIRATORY RATE INCREASED ( 7 FDA reports)
RESPIRATORY TRACT INFECTION ( 7 FDA reports)
RETINOPATHY ( 7 FDA reports)
RHINITIS ( 7 FDA reports)
RIGHT ATRIAL DILATATION ( 7 FDA reports)
ROTATOR CUFF REPAIR ( 7 FDA reports)
SCOTOMA ( 7 FDA reports)
SEROMA ( 7 FDA reports)
SKIN INFECTION ( 7 FDA reports)
SKIN NECROSIS ( 7 FDA reports)
SKIN NODULE ( 7 FDA reports)
SOCIAL PROBLEM ( 7 FDA reports)
SPINAL CORD DISORDER ( 7 FDA reports)
SPUTUM DISCOLOURED ( 7 FDA reports)
STENT OCCLUSION ( 7 FDA reports)
SUICIDAL BEHAVIOUR ( 7 FDA reports)
TEETH BRITTLE ( 7 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 7 FDA reports)
THERMAL BURN ( 7 FDA reports)
THYROID CANCER ( 7 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 7 FDA reports)
TORSADE DE POINTES ( 7 FDA reports)
TRACHEAL DEVIATION ( 7 FDA reports)
ULCER HAEMORRHAGE ( 7 FDA reports)
ULCERATIVE KERATITIS ( 7 FDA reports)
VENTRICULAR ARRHYTHMIA ( 7 FDA reports)
VERTIGO POSITIONAL ( 7 FDA reports)
WOUND INFECTION BACTERIAL ( 7 FDA reports)
ABDOMINAL INFECTION ( 6 FDA reports)
ABDOMINAL NEOPLASM ( 6 FDA reports)
ABSCESS DRAINAGE ( 6 FDA reports)
ADNEXA UTERI MASS ( 6 FDA reports)
AGORAPHOBIA ( 6 FDA reports)
ALVEOLITIS ALLERGIC ( 6 FDA reports)
AMMONIA INCREASED ( 6 FDA reports)
ANAL HAEMORRHAGE ( 6 FDA reports)
ANGIOPLASTY ( 6 FDA reports)
APLASIA PURE RED CELL ( 6 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 6 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 6 FDA reports)
ARTHROPOD STING ( 6 FDA reports)
ASPIRATION ( 6 FDA reports)
ASTERIXIS ( 6 FDA reports)
BEDRIDDEN ( 6 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 6 FDA reports)
BLADDER SPASM ( 6 FDA reports)
BONE CANCER METASTATIC ( 6 FDA reports)
BONE GRAFT ( 6 FDA reports)
BRAIN COMPRESSION ( 6 FDA reports)
BREAST HYPERPLASIA ( 6 FDA reports)
BRONCHIAL SECRETION RETENTION ( 6 FDA reports)
BRONCHITIS CHRONIC ( 6 FDA reports)
BRONCHOPNEUMONIA ( 6 FDA reports)
CAESAREAN SECTION ( 6 FDA reports)
CARBON DIOXIDE DECREASED ( 6 FDA reports)
CARDIAC ABLATION ( 6 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 6 FDA reports)
CHOLECYSTITIS INFECTIVE ( 6 FDA reports)
CIRRHOSIS ALCOHOLIC ( 6 FDA reports)
COCCYDYNIA ( 6 FDA reports)
COMPLETED SUICIDE ( 6 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 6 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 6 FDA reports)
CONNECTIVE TISSUE DISORDER ( 6 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 6 FDA reports)
CUSHINGOID ( 6 FDA reports)
DEATH OF RELATIVE ( 6 FDA reports)
DERMATITIS ATOPIC ( 6 FDA reports)
DERMATITIS BULLOUS ( 6 FDA reports)
DERMATITIS EXFOLIATIVE ( 6 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 6 FDA reports)
DISEASE RECURRENCE ( 6 FDA reports)
DRUG LEVEL FLUCTUATING ( 6 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 6 FDA reports)
ENERGY INCREASED ( 6 FDA reports)
EPIDERMAL NAEVUS ( 6 FDA reports)
ERYTHEMA OF EYELID ( 6 FDA reports)
EYELID OEDEMA ( 6 FDA reports)
FANCONI SYNDROME ACQUIRED ( 6 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 6 FDA reports)
GASTRIC POLYPS ( 6 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 6 FDA reports)
GENERALISED ANXIETY DISORDER ( 6 FDA reports)
GINGIVAL PAIN ( 6 FDA reports)
GRAFT THROMBOSIS ( 6 FDA reports)
GRAM STAIN ( 6 FDA reports)
GRANULOMA ANNULARE ( 6 FDA reports)
GRIP STRENGTH DECREASED ( 6 FDA reports)
HAEMOLYTIC ANAEMIA ( 6 FDA reports)
HAEMORRHAGIC ANAEMIA ( 6 FDA reports)
HAIR COLOUR CHANGES ( 6 FDA reports)
HEART VALVE INCOMPETENCE ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 6 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 6 FDA reports)
HYPERTENSIVE HEART DISEASE ( 6 FDA reports)
HYPOVOLAEMIC SHOCK ( 6 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 6 FDA reports)
IATROGENIC INJURY ( 6 FDA reports)
IMPAIRED FASTING GLUCOSE ( 6 FDA reports)
IMPLANT SITE DISCHARGE ( 6 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 6 FDA reports)
IMPULSIVE BEHAVIOUR ( 6 FDA reports)
INCISION SITE PAIN ( 6 FDA reports)
INJECTION SITE INDURATION ( 6 FDA reports)
INJECTION SITE MASS ( 6 FDA reports)
INJECTION SITE URTICARIA ( 6 FDA reports)
INSULIN RESISTANCE ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 6 FDA reports)
INTESTINAL ISCHAEMIA ( 6 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 6 FDA reports)
JOINT CREPITATION ( 6 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 6 FDA reports)
KETOACIDOSIS ( 6 FDA reports)
KNEE DEFORMITY ( 6 FDA reports)
LICHEN PLANUS ( 6 FDA reports)
LIGAMENT RUPTURE ( 6 FDA reports)
LIP OEDEMA ( 6 FDA reports)
LISTLESS ( 6 FDA reports)
LOWER EXTREMITY MASS ( 6 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
LUNG LOBECTOMY ( 6 FDA reports)
MALIGNANT MELANOMA IN SITU ( 6 FDA reports)
MENSTRUAL DISORDER ( 6 FDA reports)
MICROALBUMINURIA ( 6 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 6 FDA reports)
MUSCLE RUPTURE ( 6 FDA reports)
MYODESOPSIA ( 6 FDA reports)
NAIL DISORDER ( 6 FDA reports)
NASAL ULCER ( 6 FDA reports)
NEOPLASM ( 6 FDA reports)
NEPHROSCLEROSIS ( 6 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 6 FDA reports)
NODAL OSTEOARTHRITIS ( 6 FDA reports)
OBSTRUCTION GASTRIC ( 6 FDA reports)
OESOPHAGEAL SPASM ( 6 FDA reports)
ONYCHALGIA ( 6 FDA reports)
OPERATIVE HAEMORRHAGE ( 6 FDA reports)
OPTIC NERVE DISORDER ( 6 FDA reports)
ORAL CAVITY FISTULA ( 6 FDA reports)
OSTEOSCLEROSIS ( 6 FDA reports)
PANCREATIC CARCINOMA ( 6 FDA reports)
PAROTID GLAND ENLARGEMENT ( 6 FDA reports)
PARTNER STRESS ( 6 FDA reports)
PERFORMANCE STATUS DECREASED ( 6 FDA reports)
PERNICIOUS ANAEMIA ( 6 FDA reports)
PHYSICAL ASSAULT ( 6 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 6 FDA reports)
PNEUMOTHORAX ( 6 FDA reports)
POLYCYTHAEMIA ( 6 FDA reports)
POOR DENTAL CONDITION ( 6 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 6 FDA reports)
POST PROCEDURAL HAEMATOMA ( 6 FDA reports)
POSTOPERATIVE ILEUS ( 6 FDA reports)
PROCEDURAL SITE REACTION ( 6 FDA reports)
PSYCHOMOTOR RETARDATION ( 6 FDA reports)
QRS AXIS ABNORMAL ( 6 FDA reports)
RASH MACULO-PAPULAR ( 6 FDA reports)
READING DISORDER ( 6 FDA reports)
RECTAL POLYP ( 6 FDA reports)
RENAL ARTERY STENOSIS ( 6 FDA reports)
RENAL CANCER ( 6 FDA reports)
RENAL COLIC ( 6 FDA reports)
RETINAL TEAR ( 6 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 6 FDA reports)
SACRALISATION ( 6 FDA reports)
SACROILIITIS ( 6 FDA reports)
SINUS OPERATION ( 6 FDA reports)
SKULL FRACTURED BASE ( 6 FDA reports)
SUBCUTANEOUS ABSCESS ( 6 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 6 FDA reports)
TENDON PAIN ( 6 FDA reports)
TESTICULAR MASS ( 6 FDA reports)
URETHRITIS ( 6 FDA reports)
VISUAL MIDLINE SHIFT SYNDROME ( 6 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 5 FDA reports)
ACCIDENTAL EXPOSURE ( 5 FDA reports)
ALCOHOLIC PANCREATITIS ( 5 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 5 FDA reports)
ANORECTAL DISORDER ( 5 FDA reports)
APNOEA ( 5 FDA reports)
APPARENT DEATH ( 5 FDA reports)
APPENDICECTOMY ( 5 FDA reports)
ARTERIAL STENOSIS ( 5 FDA reports)
ARTERIOSPASM CORONARY ( 5 FDA reports)
ARTHRITIS INFECTIVE ( 5 FDA reports)
ASEPTIC NECROSIS BONE ( 5 FDA reports)
ATRIAL TACHYCARDIA ( 5 FDA reports)
AUTOIMMUNE DISORDER ( 5 FDA reports)
BILIARY CIRRHOSIS ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 5 FDA reports)
BLOOD COUNT ABNORMAL ( 5 FDA reports)
BLOOD UREA DECREASED ( 5 FDA reports)
BLOOD URIC ACID INCREASED ( 5 FDA reports)
BLOODY DISCHARGE ( 5 FDA reports)
BORDERLINE GLAUCOMA ( 5 FDA reports)
BRAIN NEOPLASM ( 5 FDA reports)
BRAIN STEM INFARCTION ( 5 FDA reports)
BREAKTHROUGH PAIN ( 5 FDA reports)
BREAST CALCIFICATIONS ( 5 FDA reports)
BREAST CANCER IN SITU ( 5 FDA reports)
CARDIAC FAILURE CHRONIC ( 5 FDA reports)
CAROTID BRUIT ( 5 FDA reports)
CATARACT DIABETIC ( 5 FDA reports)
CATHETER RELATED INFECTION ( 5 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 5 FDA reports)
CHEST WALL PAIN ( 5 FDA reports)
CHRONIC FATIGUE SYNDROME ( 5 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 5 FDA reports)
CLAUSTROPHOBIA ( 5 FDA reports)
CLAVICLE FRACTURE ( 5 FDA reports)
CLOSTRIDIAL INFECTION ( 5 FDA reports)
CONTRACEPTION ( 5 FDA reports)
CREPITATIONS ( 5 FDA reports)
CYST RUPTURE ( 5 FDA reports)
CYTOLYTIC HEPATITIS ( 5 FDA reports)
DIABETIC EYE DISEASE ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
DRUG SCREEN POSITIVE ( 5 FDA reports)
DYSMENORRHOEA ( 5 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 5 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 5 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 5 FDA reports)
EMBOLISM ARTERIAL ( 5 FDA reports)
ENDARTERECTOMY ( 5 FDA reports)
ENDOMETRIOSIS ( 5 FDA reports)
ENURESIS ( 5 FDA reports)
EOSINOPHIL COUNT INCREASED ( 5 FDA reports)
EXFOLIATIVE RASH ( 5 FDA reports)
EYE OEDEMA ( 5 FDA reports)
FAECES PALE ( 5 FDA reports)
FALLOPIAN TUBE OPERATION ( 5 FDA reports)
FOOD INTOLERANCE ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 5 FDA reports)
GASTROINTESTINAL ULCER ( 5 FDA reports)
GRAFT COMPLICATION ( 5 FDA reports)
HAEMOCHROMATOSIS ( 5 FDA reports)
HAEMODYNAMIC INSTABILITY ( 5 FDA reports)
HELICOBACTER GASTRITIS ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HEPATIC PAIN ( 5 FDA reports)
HEPATITIS TOXIC ( 5 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
HYPERCOAGULATION ( 5 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 5 FDA reports)
HYPERINSULINAEMIA ( 5 FDA reports)
HYPOPITUITARISM ( 5 FDA reports)
HYPOTRICHOSIS ( 5 FDA reports)
ILEUS PARALYTIC ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 5 FDA reports)
INCORRECT STORAGE OF DRUG ( 5 FDA reports)
INJECTION SITE NODULE ( 5 FDA reports)
INJECTION SITE WARMTH ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 5 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 5 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 5 FDA reports)
INTRACRANIAL ANEURYSM ( 5 FDA reports)
IRON DEFICIENCY ( 5 FDA reports)
KERATOACANTHOMA ( 5 FDA reports)
KIDNEY FIBROSIS ( 5 FDA reports)
KLEBSIELLA INFECTION ( 5 FDA reports)
LIBIDO INCREASED ( 5 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 5 FDA reports)
LUNG CANCER METASTATIC ( 5 FDA reports)
LUNG CONSOLIDATION ( 5 FDA reports)
MEGAKARYOCYTES INCREASED ( 5 FDA reports)
MENINGIOMA ( 5 FDA reports)
MENINGITIS ASEPTIC ( 5 FDA reports)
MENINGITIS VIRAL ( 5 FDA reports)
MICROCYTIC ANAEMIA ( 5 FDA reports)
MOUTH INJURY ( 5 FDA reports)
MUCOSAL INFLAMMATION ( 5 FDA reports)
NASAL OEDEMA ( 5 FDA reports)
NEPHROCALCINOSIS ( 5 FDA reports)
NO ADVERSE EFFECT ( 5 FDA reports)
NODAL ARRHYTHMIA ( 5 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 5 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 5 FDA reports)
OCULAR VASCULAR DISORDER ( 5 FDA reports)
OESOPHAGEAL DISORDER ( 5 FDA reports)
OESOPHAGEAL PAIN ( 5 FDA reports)
OLIGURIA ( 5 FDA reports)
ORAL HERPES ( 5 FDA reports)
PANCREATIC ENZYMES INCREASED ( 5 FDA reports)
PAPILLARY THYROID CANCER ( 5 FDA reports)
PARKINSON'S DISEASE ( 5 FDA reports)
PARKINSONISM ( 5 FDA reports)
PELVIC ABSCESS ( 5 FDA reports)
PERIDIVERTICULAR ABSCESS ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 5 FDA reports)
POLYCYSTIC OVARIES ( 5 FDA reports)
POSTNASAL DRIP ( 5 FDA reports)
POSTPARTUM HAEMORRHAGE ( 5 FDA reports)
POSTURE ABNORMAL ( 5 FDA reports)
POSTURING ( 5 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 5 FDA reports)
PROSTATIC DISORDER ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 5 FDA reports)
PULMONARY INFARCTION ( 5 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 5 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 5 FDA reports)
RECTOCELE ( 5 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 5 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
RESPIRATORY RATE DECREASED ( 5 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 5 FDA reports)
RETICULOCYTOSIS ( 5 FDA reports)
RETINAL ARTERY OCCLUSION ( 5 FDA reports)
RIGHT VENTRICULAR FAILURE ( 5 FDA reports)
ROSACEA ( 5 FDA reports)
SJOGREN'S SYNDROME ( 5 FDA reports)
SKIN IRRITATION ( 5 FDA reports)
SKIN REACTION ( 5 FDA reports)
SKIN WARM ( 5 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 5 FDA reports)
SOFT TISSUE INFECTION ( 5 FDA reports)
SPLENIC ABSCESS ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
SUDDEN CARDIAC DEATH ( 5 FDA reports)
TACHYARRHYTHMIA ( 5 FDA reports)
THYROID MASS ( 5 FDA reports)
TONSIL CANCER ( 5 FDA reports)
TONSILLAR HYPERTROPHY ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
TRANSFUSION ( 5 FDA reports)
TRIGEMINAL NEURALGIA ( 5 FDA reports)
UMBILICAL CORD ABNORMALITY ( 5 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 5 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 5 FDA reports)
VAGINITIS BACTERIAL ( 5 FDA reports)
VENOUS THROMBOSIS ( 5 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 5 FDA reports)
VULVAL DISORDER ( 5 FDA reports)
VULVOVAGINAL DRYNESS ( 5 FDA reports)
WOUND DRAINAGE ( 5 FDA reports)
ABSCESS INTESTINAL ( 4 FDA reports)
ACCIDENT AT WORK ( 4 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 4 FDA reports)
ACUTE LUNG INJURY ( 4 FDA reports)
ADDISON'S DISEASE ( 4 FDA reports)
ADHESION ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ALCOHOL ABUSE ( 4 FDA reports)
ALCOHOLISM ( 4 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 4 FDA reports)
ANOXIC ENCEPHALOPATHY ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
APPLICATION SITE URTICARIA ( 4 FDA reports)
APPLICATION SITE VESICLES ( 4 FDA reports)
ARTERIAL BYPASS OPERATION ( 4 FDA reports)
ARTERIAL DISORDER ( 4 FDA reports)
ASTHENOPIA ( 4 FDA reports)
BARRETT'S OESOPHAGUS ( 4 FDA reports)
BASEDOW'S DISEASE ( 4 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 4 FDA reports)
BILIARY TRACT DISORDER ( 4 FDA reports)
BLADDER CATHETERISATION ( 4 FDA reports)
BLADDER DYSFUNCTION ( 4 FDA reports)
BLADDER NEOPLASM ( 4 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 4 FDA reports)
BLEEDING TIME PROLONGED ( 4 FDA reports)
BLEPHAROSPASM ( 4 FDA reports)
BLOOD CALCIUM ABNORMAL ( 4 FDA reports)
BLOOD IRON INCREASED ( 4 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 4 FDA reports)
BLOOD PRESSURE ( 4 FDA reports)
BLOOD SODIUM INCREASED ( 4 FDA reports)
BONE DEBRIDEMENT ( 4 FDA reports)
BONE NEOPLASM MALIGNANT ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
BRAIN INJURY ( 4 FDA reports)
BREAST DISORDER ( 4 FDA reports)
BREAST INFECTION ( 4 FDA reports)
BREAST TENDERNESS ( 4 FDA reports)
BRONCHITIS ACUTE ( 4 FDA reports)
BUNION ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
CARDIOPULMONARY FAILURE ( 4 FDA reports)
CAROTID ARTERY THROMBOSIS ( 4 FDA reports)
CAROTID ENDARTERECTOMY ( 4 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CEREBRAL DISORDER ( 4 FDA reports)
CEREBRAL HAEMATOMA ( 4 FDA reports)
CERVICAL CORD COMPRESSION ( 4 FDA reports)
CHEST EXPANSION DECREASED ( 4 FDA reports)
CHOLESTEROSIS ( 4 FDA reports)
CHOREA ( 4 FDA reports)
COLON CANCER STAGE I ( 4 FDA reports)
CORNEAL OPACITY ( 4 FDA reports)
CORNEAL SCAR ( 4 FDA reports)
CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
CORONARY ARTERY SURGERY ( 4 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
CYSTOCELE ( 4 FDA reports)
DEVICE RELATED INFECTION ( 4 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 4 FDA reports)
DISSOCIATION ( 4 FDA reports)
DIVERTICULAR PERFORATION ( 4 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 4 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 4 FDA reports)
DYSPHEMIA ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
ERYTHEMA NODOSUM ( 4 FDA reports)
EXCESSIVE EYE BLINKING ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FIBROUS HISTIOCYTOMA ( 4 FDA reports)
FOOD ALLERGY ( 4 FDA reports)
FRUSTRATION ( 4 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 4 FDA reports)
FUNGAEMIA ( 4 FDA reports)
GALLBLADDER PAIN ( 4 FDA reports)
GALLBLADDER PERFORATION ( 4 FDA reports)
GALLOP RHYTHM PRESENT ( 4 FDA reports)
GANGRENE ( 4 FDA reports)
GASTRIC PERFORATION ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 4 FDA reports)
GOUTY ARTHRITIS ( 4 FDA reports)
GRANDIOSITY ( 4 FDA reports)
HAEMANGIOMA OF SKIN ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
HAIR DISORDER ( 4 FDA reports)
HAND DEFORMITY ( 4 FDA reports)
HELICOBACTER INFECTION ( 4 FDA reports)
HEPATECTOMY ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATIC INFARCTION ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
HISTOPLASMOSIS ( 4 FDA reports)
HYPERMETROPIA ( 4 FDA reports)
HYPERPHAGIA ( 4 FDA reports)
HYPOVENTILATION ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 4 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
INCISION SITE ERYTHEMA ( 4 FDA reports)
INFUSION SITE ERYTHEMA ( 4 FDA reports)
INJECTION SITE INFLAMMATION ( 4 FDA reports)
INJECTION SITE INJURY ( 4 FDA reports)
INJECTION SITE SCAR ( 4 FDA reports)
INTENTION TREMOR ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 4 FDA reports)
JAW OPERATION ( 4 FDA reports)
JOINT LOCK ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
LARGE INTESTINE PERFORATION ( 4 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LIP EXFOLIATION ( 4 FDA reports)
LIVER CARCINOMA RUPTURED ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 4 FDA reports)
LYMPHADENITIS ( 4 FDA reports)
MALABSORPTION ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MASTICATION DISORDER ( 4 FDA reports)
MASTITIS ( 4 FDA reports)
MEDIASTINITIS ( 4 FDA reports)
METASTASES TO SOFT TISSUE ( 4 FDA reports)
MOUTH HAEMORRHAGE ( 4 FDA reports)
MUCOUS STOOLS ( 4 FDA reports)
MUSCLE FLAP OPERATION ( 4 FDA reports)
MUSCULAR DYSTROPHY ( 4 FDA reports)
MYELOMALACIA ( 4 FDA reports)
NASAL DRYNESS ( 4 FDA reports)
NECK MASS ( 4 FDA reports)
NECROTISING COLITIS ( 4 FDA reports)
NERVE ROOT COMPRESSION ( 4 FDA reports)
NEUROMA ( 4 FDA reports)
OBSTRUCTIVE UROPATHY ( 4 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 4 FDA reports)
OESOPHAGEAL MASS ( 4 FDA reports)
ONYCHOCLASIS ( 4 FDA reports)
OPTIC NERVE INJURY ( 4 FDA reports)
OPTIC NEUROPATHY ( 4 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 4 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 4 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 4 FDA reports)
PANIC DISORDER ( 4 FDA reports)
PANIC REACTION ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PERITONEAL ADHESIONS ( 4 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 4 FDA reports)
PITUITARY TUMOUR ( 4 FDA reports)
PLASMACYTOMA ( 4 FDA reports)
PNEUMATOSIS ( 4 FDA reports)
PNEUMOCONIOSIS ( 4 FDA reports)
POOR PERIPHERAL CIRCULATION ( 4 FDA reports)
POST PROCEDURAL SWELLING ( 4 FDA reports)
PRESBYOESOPHAGUS ( 4 FDA reports)
PRODUCT PHYSICAL ISSUE ( 4 FDA reports)
PROGRESSIVE MASSIVE FIBROSIS ( 4 FDA reports)
PROTEIN TOTAL DECREASED ( 4 FDA reports)
PROTHROMBIN TIME SHORTENED ( 4 FDA reports)
PTERYGIUM ( 4 FDA reports)
PULSE ABNORMAL ( 4 FDA reports)
RASH VESICULAR ( 4 FDA reports)
RECTAL CANCER STAGE III ( 4 FDA reports)
RENAL ANEURYSM ( 4 FDA reports)
RENAL TUBULAR ATROPHY ( 4 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 4 FDA reports)
SALIVARY HYPERSECRETION ( 4 FDA reports)
SALPINGECTOMY ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 4 FDA reports)
SENSATION OF PRESSURE ( 4 FDA reports)
SERUM SICKNESS ( 4 FDA reports)
SHOCK HYPOGLYCAEMIC ( 4 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 4 FDA reports)
SINUS ARRHYTHMIA ( 4 FDA reports)
SKIN HYPERPIGMENTATION ( 4 FDA reports)
SKIN SWELLING ( 4 FDA reports)
SKIN WRINKLING ( 4 FDA reports)
SMALL INTESTINAL RESECTION ( 4 FDA reports)
SOFT TISSUE DISORDER ( 4 FDA reports)
SPINAL CORD HERNIATION ( 4 FDA reports)
SPINAL VASCULAR DISORDER ( 4 FDA reports)
SPLEEN DISORDER ( 4 FDA reports)
SPLENECTOMY ( 4 FDA reports)
SPLENIC INFARCTION ( 4 FDA reports)
SPLENIC LESION ( 4 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 4 FDA reports)
STEM CELL TRANSPLANT ( 4 FDA reports)
STEROID THERAPY ( 4 FDA reports)
SUPERINFECTION ( 4 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 4 FDA reports)
SYNCOPE VASOVAGAL ( 4 FDA reports)
TABLET PHYSICAL ISSUE ( 4 FDA reports)
TEARFULNESS ( 4 FDA reports)
TESTICULAR ATROPHY ( 4 FDA reports)
TONGUE BITING ( 4 FDA reports)
TONGUE ULCERATION ( 4 FDA reports)
TRICHORRHEXIS ( 4 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 4 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
URINE ANALYSIS ABNORMAL ( 4 FDA reports)
URINE OUTPUT INCREASED ( 4 FDA reports)
UTERINE DISORDER ( 4 FDA reports)
UTERINE POLYP ( 4 FDA reports)
VAGINAL REMOVAL OF INTRAUTERINE FOREIGN BODY ( 4 FDA reports)
VASCULAR RUPTURE ( 4 FDA reports)
VERTEBROPLASTY ( 4 FDA reports)
VITREOUS FLOATERS ( 4 FDA reports)
WHITE CLOT SYNDROME ( 4 FDA reports)
WOUND DEHISCENCE ( 4 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
WOUND SECRETION ( 4 FDA reports)
X-RAY ABNORMAL ( 4 FDA reports)
YAWNING ( 4 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ACQUIRED CLAW TOE ( 3 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 3 FDA reports)
ADENOCARCINOMA ( 3 FDA reports)
ADJUSTMENT DISORDER ( 3 FDA reports)
AKINESIA ( 3 FDA reports)
ALLERGY TEST POSITIVE ( 3 FDA reports)
ALLERGY TO CHEMICALS ( 3 FDA reports)
ALVEOLAR PROTEINOSIS ( 3 FDA reports)
ANAESTHETIC COMPLICATION ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
ANHIDROSIS ( 3 FDA reports)
ANORECTAL DISCOMFORT ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC DILATATION ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
APPETITE DISORDER ( 3 FDA reports)
ARTHROSCOPIC SURGERY ( 3 FDA reports)
ATRIAL THROMBOSIS ( 3 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 3 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 3 FDA reports)
B-CELL LYMPHOMA ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BACTERIAL TEST POSITIVE ( 3 FDA reports)
BALANITIS CANDIDA ( 3 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
BLADDER INJURY ( 3 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
BLOOD CHOLESTEROL ( 3 FDA reports)
BLOOD CREATINE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 3 FDA reports)
BOWEL SOUNDS ABNORMAL ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
BRONCHITIS FUNGAL ( 3 FDA reports)
BURNS SECOND DEGREE ( 3 FDA reports)
CALCIUM DEFICIENCY ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CALCULUS URETHRAL ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARCINOID SYNDROME ( 3 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
CARDIOVERSION ( 3 FDA reports)
CATARACT NUCLEAR ( 3 FDA reports)
CATHETER RELATED COMPLICATION ( 3 FDA reports)
CATHETER SEPSIS ( 3 FDA reports)
CENTRAL LINE INFECTION ( 3 FDA reports)
CENTRAL OBESITY ( 3 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 3 FDA reports)
CERVIX DISORDER ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CHEST INJURY ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHOLELITHOTOMY ( 3 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 3 FDA reports)
COLON CANCER STAGE III ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
COMPARTMENT SYNDROME ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 3 FDA reports)
COMPULSIVE SHOPPING ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
CORONARY ANGIOPLASTY ( 3 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 3 FDA reports)
CUSHING'S SYNDROME ( 3 FDA reports)
CYCLOTHYMIC DISORDER ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DANDRUFF ( 3 FDA reports)
DEAFNESS NEUROSENSORY ( 3 FDA reports)
DELUSION OF GRANDEUR ( 3 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 3 FDA reports)
DENTAL IMPLANTATION ( 3 FDA reports)
DENTAL TREATMENT ( 3 FDA reports)
DEREALISATION ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DEVICE OCCLUSION ( 3 FDA reports)
DRUG EFFECT DELAYED ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 3 FDA reports)
DUODENAL STENOSIS ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DYSAESTHESIA ( 3 FDA reports)
ECTOPIC PREGNANCY ( 3 FDA reports)
EJECTION FRACTION ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
ENDOPHTHALMITIS ( 3 FDA reports)
EPIGLOTTIC CARCINOMA ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 3 FDA reports)
EXTERNAL EAR CELLULITIS ( 3 FDA reports)
EYE INFECTION FUNGAL ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
FACTOR V DEFICIENCY ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FEMORAL ARTERY OCCLUSION ( 3 FDA reports)
FLASHBACK ( 3 FDA reports)
FOOD CRAVING ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
FRACTURE DELAYED UNION ( 3 FDA reports)
FRACTURED COCCYX ( 3 FDA reports)
FULL BLOOD COUNT DECREASED ( 3 FDA reports)
GALACTORRHOEA ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GALLBLADDER POLYP ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTROENTERITIS RADIATION ( 3 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 3 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 3 FDA reports)
GASTROINTESTINAL INJURY ( 3 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
GENITAL RASH ( 3 FDA reports)
GINGIVAL ATROPHY ( 3 FDA reports)
GLOMERULONEPHRITIS ( 3 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 3 FDA reports)
GLYCOSURIA ( 3 FDA reports)
GRIMACING ( 3 FDA reports)
H1N1 INFLUENZA ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMOGLOBIN ABNORMAL ( 3 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 3 FDA reports)
HEART DISEASE CONGENITAL ( 3 FDA reports)
HEPATIC CANCER METASTATIC ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HERNIA OBSTRUCTIVE ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPERLACTACIDAEMIA ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOAESTHESIA FACIAL ( 3 FDA reports)
HYPOMETABOLISM ( 3 FDA reports)
INCISION SITE INFECTION ( 3 FDA reports)
INFERTILITY FEMALE ( 3 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
INJECTION SITE BURNING ( 3 FDA reports)
INJECTION SITE OEDEMA ( 3 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 3 FDA reports)
INTERVERTEBRAL DISC INJURY ( 3 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 3 FDA reports)
ISCHAEMIC HEPATITIS ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
JOINT WARMTH ( 3 FDA reports)
JUDGEMENT IMPAIRED ( 3 FDA reports)
LABORATORY TEST INTERFERENCE ( 3 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 3 FDA reports)
LACRIMATION DECREASED ( 3 FDA reports)
LAZINESS ( 3 FDA reports)
LENTIGO ( 3 FDA reports)
LIP ULCERATION ( 3 FDA reports)
LIPIDS ABNORMAL ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
LYMPH NODE PAIN ( 3 FDA reports)
LYMPHADENECTOMY ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MACULOPATHY ( 3 FDA reports)
MALFORMATION VENOUS ( 3 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 3 FDA reports)
MASTOIDITIS ( 3 FDA reports)
MENIERE'S DISEASE ( 3 FDA reports)
MENSTRUATION IRREGULAR ( 3 FDA reports)
MENTAL DISABILITY ( 3 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 3 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
METATARSAL EXCISION ( 3 FDA reports)
MITRAL VALVE SCLEROSIS ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MUSCLE ENZYME INCREASED ( 3 FDA reports)
MUSCLE MASS ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
MYOPATHY TOXIC ( 3 FDA reports)
NASAL DISORDER ( 3 FDA reports)
NEAR DROWNING ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NEUROENDOCRINE CARCINOMA ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
NIPPLE PAIN ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
OBSTRUCTION ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
ORAL SURGERY ( 3 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 3 FDA reports)
OROPHARYNGEAL BLISTERING ( 3 FDA reports)
ORTHOSTATIC HYPERTENSION ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
OVARIAN DISORDER ( 3 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 3 FDA reports)
PANCREATIC CYST ( 3 FDA reports)
PANCREATIC ENLARGEMENT ( 3 FDA reports)
PANCREATIC INJURY ( 3 FDA reports)
PANCREATIC NEOPLASM ( 3 FDA reports)
PARADOXICAL DRUG REACTION ( 3 FDA reports)
PARAKERATOSIS ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PELVIC FRACTURE ( 3 FDA reports)
PENIS DISORDER ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PERIVASCULAR DERMATITIS ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PHLEBITIS SUPERFICIAL ( 3 FDA reports)
PHONOPHOBIA ( 3 FDA reports)
PILOERECTION ( 3 FDA reports)
PLASMA CELLS INCREASED ( 3 FDA reports)
PLEURAL FIBROSIS ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
POLYARTHRITIS ( 3 FDA reports)
POST PROCEDURAL PAIN ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
POTENTIATING DRUG INTERACTION ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PRESSURE OF SPEECH ( 3 FDA reports)
PROSTATE CANCER STAGE I ( 3 FDA reports)
PROTEIN C INCREASED ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 3 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 3 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
PURULENCE ( 3 FDA reports)
PYELONEPHRITIS ACUTE ( 3 FDA reports)
QUADRIPARESIS ( 3 FDA reports)
RADIOTHERAPY ( 3 FDA reports)
RECTAL CANCER ( 3 FDA reports)
REFLUX GASTRITIS ( 3 FDA reports)
REGURGITATION ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RENAL TUBULAR ACIDOSIS ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RESORPTION BONE INCREASED ( 3 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 3 FDA reports)
RETINAL ARTERY THROMBOSIS ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SCAPULA FRACTURE ( 3 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SCROTAL HAEMATOCOELE ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SINUS ARREST ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
SPINAL HAEMANGIOMA ( 3 FDA reports)
SPLINTER HAEMORRHAGES ( 3 FDA reports)
SPONDYLITIS ( 3 FDA reports)
STARING ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
STATUS MIGRAINOSUS ( 3 FDA reports)
SUBRETINAL FIBROSIS ( 3 FDA reports)
SYNOVITIS ( 3 FDA reports)
SYRINGOMYELIA ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 3 FDA reports)
TENOSYNOVITIS ( 3 FDA reports)
TESTICULAR PAIN ( 3 FDA reports)
THERAPEUTIC PROCEDURE ( 3 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 3 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THERAPY REGIMEN CHANGED ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
THYROIDITIS ( 3 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 3 FDA reports)
TONGUE COATED ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TONSILLAR DISORDER ( 3 FDA reports)
TOOTH REPAIR ( 3 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 3 FDA reports)
TRACHEAL DISORDER ( 3 FDA reports)
TRACHEAL FISTULA ( 3 FDA reports)
TRACHEAL STENOSIS ( 3 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
UNINTENDED PREGNANCY ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
URETHRAL PAIN ( 3 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 3 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 3 FDA reports)
VASCULAR BYPASS GRAFT ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
VOCAL CORD PARALYSIS ( 3 FDA reports)
VULVAL ULCERATION ( 3 FDA reports)
WEIGHT LOSS POOR ( 3 FDA reports)
WHEELCHAIR USER ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 2 FDA reports)
ABDOMINAL WALL DISORDER ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ALCOHOL DETOXIFICATION ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
ALLERGIC OEDEMA ( 2 FDA reports)
ALLERGY TO ANIMAL ( 2 FDA reports)
ANAL CANDIDIASIS ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANAL PRURITUS ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-SS-B ANTIBODY POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
APPLICATION SITE ULCER ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTERIOGRAM CORONARY ( 2 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ASPIRATION JOINT ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
B-CELL LYMPHOMA STAGE II ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BALANITIS ( 2 FDA reports)
BANDAEMIA ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BENIGN UTERINE NEOPLASM ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BIOPSY ENDOMETRIUM ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD COPPER ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD IRON ABNORMAL ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BREAST CANCER RECURRENT ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
BREAST MALFORMATION ( 2 FDA reports)
BREAST RECONSTRUCTION ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 2 FDA reports)
BUNION OPERATION ( 2 FDA reports)
BUTTERFLY RASH ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CARBON DIOXIDE ABNORMAL ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 2 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CAROTID ARTERY STENT INSERTION ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CATHETER PLACEMENT ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 2 FDA reports)
CERVIX CARCINOMA ( 2 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC LEFT VENTRICULAR FAILURE ( 2 FDA reports)
CLOSED HEAD INJURY ( 2 FDA reports)
COLON CANCER STAGE 0 ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
COMPLICATED MIGRAINE ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONFUSION POSTOPERATIVE ( 2 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
CONTRAST MEDIA ALLERGY ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CORONARY ARTERY EMBOLISM ( 2 FDA reports)
CORONARY REVASCULARISATION ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 2 FDA reports)
CYSTITIS RADIATION ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DELUSIONAL DISORDER, EROTOMANIC TYPE ( 2 FDA reports)
DELUSIONAL PERCEPTION ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 2 FDA reports)
DIAPHRAGMATIC DISORDER ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DIZZINESS EXERTIONAL ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 2 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
EAR HAEMORRHAGE ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
EJACULATION DISORDER ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
ELECTRIC SHOCK ( 2 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 2 FDA reports)
ENDOMETRIAL ABLATION ( 2 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 2 FDA reports)
ENDOSCOPY ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EOSINOPHILS URINE PRESENT ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
EPIDURAL ANAESTHESIA ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERYTHROMELALGIA ( 2 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 2 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EXPLORATIVE LAPAROTOMY ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EYE INFECTION VIRAL ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYEBALL RUPTURE ( 2 FDA reports)
FAT NECROSIS ( 2 FDA reports)
FOOD AVERSION ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FRACTURED SACRUM ( 2 FDA reports)
FUSOBACTERIUM INFECTION ( 2 FDA reports)
GALLBLADDER ENLARGEMENT ( 2 FDA reports)
GALLBLADDER FISTULA ( 2 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GENE MUTATION ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GINGIVAL DISCOLOURATION ( 2 FDA reports)
GINGIVAL EROSION ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GRAFT INFECTION ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMATOCRIT ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART TRANSPLANT ( 2 FDA reports)
HEART VALVE STENOSIS ( 2 FDA reports)
HEAT STROKE ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HOUSE DUST ALLERGY ( 2 FDA reports)
HYPERALDOSTERONISM ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERLIPASAEMIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPOCHONDRIASIS ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOHIDROSIS ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
IGA NEPHROPATHY ( 2 FDA reports)
ILIAC ARTERY THROMBOSIS ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCISION SITE HYPOAESTHESIA ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INCLUSION BODY MYOSITIS ( 2 FDA reports)
INCORRECT PRODUCT STORAGE ( 2 FDA reports)
INCREASED INSULIN REQUIREMENT ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFECTIVE GLOSSITIS ( 2 FDA reports)
INFUSION SITE SWELLING ( 2 FDA reports)
INJECTION SITE STREAKING ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INSULIN RESISTANT DIABETES ( 2 FDA reports)
INTERCOSTAL NEURALGIA ( 2 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL ANGINA ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTESTINAL MASS ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
INTRAOCULAR LENS IMPLANT ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
IRITIS ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LACRIMAL DISORDER ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LESION EXCISION ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
LIBIDO DISORDER ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIPASE DECREASED ( 2 FDA reports)
LIPOMA EXCISION ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 2 FDA reports)
LOCALISED OSTEOARTHRITIS ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LUNG INFILTRATION MALIGNANT ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
MAMMOGRAM ( 2 FDA reports)
MEDIASTINAL HAEMATOMA ( 2 FDA reports)
MEIGE'S SYNDROME ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
METASTATIC UTERINE CANCER ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MICTURITION FREQUENCY DECREASED ( 2 FDA reports)
MIXED HYPERLIPIDAEMIA ( 2 FDA reports)
MONONEURITIS ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MUMPS ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE FATIGUE ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
MYOSCLEROSIS ( 2 FDA reports)
MYOTONIC DYSTROPHY ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NIGHT CRAMPS ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OCCIPITAL NEURALGIA ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
ONCOLOGIC COMPLICATION ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
ORAL BACTERIAL INFECTION ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OSTEOCHONDROSIS ( 2 FDA reports)
PAIN THRESHOLD DECREASED ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARANOID PERSONALITY DISORDER ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PELVIC MASS ( 2 FDA reports)
PENILE OEDEMA ( 2 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PHLEBOTHROMBOSIS ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PITUITARY ENLARGEMENT ( 2 FDA reports)
PITUITARY TUMOUR RECURRENT ( 2 FDA reports)
PLASTIC SURGERY TO THE FACE ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
PORTAL VENOUS GAS ( 2 FDA reports)
POST CONCUSSION SYNDROME ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POST PROCEDURAL OEDEMA ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE MENOPAUSE ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTATISM ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTEUS INFECTION ( 2 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PRURITUS ALLERGIC ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PSEUDODEMENTIA ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PURGING ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RASH PAPULOSQUAMOUS ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RECTAL CANCER STAGE 0 ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RED BLOOD CELL ROULEAUX FORMATION PRESENT ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
REHABILITATION THERAPY ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 2 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
RENOVASCULAR HYPERTENSION ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL ISCHAEMIA ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 2 FDA reports)
RETROGRADE EJACULATION ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SALIVARY GLAND CANCER ( 2 FDA reports)
SCAN ABDOMEN ABNORMAL ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 2 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 2 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 2 FDA reports)
SCHIZOPHRENIA, UNDIFFERENTIATED TYPE ( 2 FDA reports)
SCLERITIS ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SCROTAL VARICOSE VEINS ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SELF-INDUCED VOMITING ( 2 FDA reports)
SEMEN VOLUME DECREASED ( 2 FDA reports)
SENILE OSTEOPOROSIS ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SHOULDER ARTHROPLASTY ( 2 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SKIN FRAGILITY ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SLEEP TERROR ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SMOKER ( 2 FDA reports)
SODIUM RETENTION ( 2 FDA reports)
SPINAL CORD INJURY ( 2 FDA reports)
SPLENIC GRANULOMA ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPONTANEOUS PENILE ERECTION ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 2 FDA reports)
SUBSTANCE ABUSE ( 2 FDA reports)
SUDDEN ONSET OF SLEEP ( 2 FDA reports)
SUPERINFECTION BACTERIAL ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SURGICAL FAILURE ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
TEMPORAL ARTERITIS ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
TESTIS CANCER ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THYROIDITIS CHRONIC ( 2 FDA reports)
TINEA VERSICOLOUR ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TOTAL BILE ACIDS INCREASED ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TOXICOLOGIC TEST ( 2 FDA reports)
TRACHEAL INJURY ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
TUMOUR ASSOCIATED FEVER ( 2 FDA reports)
TUMOUR FLARE ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 2 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
UPPER EXTREMITY MASS ( 2 FDA reports)
URETERAL DISORDER ( 2 FDA reports)
URETHRAL INJURY ( 2 FDA reports)
URGE INCONTINENCE ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY HESITATION ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
UTERINE STENOSIS ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VAGINAL DISORDER ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM ( 2 FDA reports)
VENA CAVA FILTER INSERTION ( 2 FDA reports)
VENOM POISONING ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VIRAL LOAD DECREASED ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VITAMIN K DEFICIENCY ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
X-RAY LIMB ABNORMAL ( 2 FDA reports)
XANTHOMA ( 2 FDA reports)
5Q MINUS SYNDROME ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADENOVIRUS TEST POSITIVE ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
ALBUMIN URINE ABSENT ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
AORTOGRAM ABNORMAL ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE DISCHARGE ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPERMIA ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTOPSY ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BEREAVEMENT ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BIOPSY BRAIN ABNORMAL ( 1 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 1 FDA reports)
BIOPSY PANCREAS ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER CYST ( 1 FDA reports)
BLADDER FIBROSIS ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLADDER TUMOUR RESECTION ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD HIV RNA INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID ABNORMAL ( 1 FDA reports)
BLOOD LUTEINISING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST DISORDER MALE ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREAST OEDEMA ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL NEOPLASM ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHITIS ACUTE VIRAL ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNS FOURTH DEGREE ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CAPSULAR CONTRACTURE ASSOCIATED WITH BREAST IMPLANT ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 1 FDA reports)
CARDIAC ENZYMES ( 1 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ANEURYSM RUPTURE ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL AMYLOID ANGIOPATHY ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL SPINE FLATTENING ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHOROIDAL DETACHMENT ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION FACTOR V LEVEL ABNORMAL ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COLON CANCER RECURRENT ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COLPORRHAPHY ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DEFORMITY THORAX ( 1 FDA reports)
DEHYDROEPIANDROSTERONE DECREASED ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEMENTIA WITH LEWY BODIES ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DISSOCIATIVE AMNESIA ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSAESTHESIA PHARYNX ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR CANAL STENOSIS ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENTERITIS NECROTICANS ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EPINEPHRINE INCREASED ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHEMA INDURATUM ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCESSIVE MASTURBATION ( 1 FDA reports)
EXCESSIVE SEXUAL FANTASIES ( 1 FDA reports)
EXERCISE CAPACITY DECREASED ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EXPOSURE TO EXTREME TEMPERATURE ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYE OPERATION COMPLICATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID OPERATION ( 1 FDA reports)
EYELID VASCULAR DISORDER ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLOPPY IRIS SYNDROME ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FORCED EXPIRATORY VOLUME INCREASED ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALACTOSTASIS ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC HYPOMOTILITY ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL PROLAPSE ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL HYPOPLASIA ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOGLOBIN URINE ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAND DERMATITIS ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC ARTERY ANEURYSM ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS A VIRUS TEST ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HORMONE THERAPY ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERCALCAEMIC NEPHROPATHY ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERMAGNESAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPHARYNGEAL CANCER ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IDIOSYNCRATIC ALCOHOL INTOXICATION ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE DISCOLOURATION ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERNAL FIXATION OF SPINE ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
IODINE UPTAKE DECREASED ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 1 FDA reports)
ITCHING SCAR ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
KERATOSIS OBTURANS ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
LACRIMAL DUCT PROCEDURE ( 1 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LENS DISLOCATION ( 1 FDA reports)
LERICHE SYNDROME ( 1 FDA reports)
LEUKAEMIA GRANULOCYTIC ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKAEMIC LYMPHOMA ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIPIDOSIS ( 1 FDA reports)
LIPOPROTEIN (A) ABNORMAL ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVER SARCOIDOSIS ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOCYTIC HYPOPHYSITIS ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MAMMOPLASTY ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENOPAUSE DELAYED ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL BED INFECTION FUNGAL ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NECK EXPLORATION ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NIPPLE SWELLING ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OESTRADIOL ABNORMAL ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
ONYCHOGRYPHOSIS ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
OPTIC NERVE CUP/DISC RATIO DECREASED ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
ORGASMIC SENSATION DECREASED ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVARIAN ADENOMA ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PASTEURELLA INFECTION ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENILE PROSTHESIS USER ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL MEMBRANE FAILURE ( 1 FDA reports)
PERITONEAL NEOPLASM ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PHYSIOTHERAPY ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLICA SYNDROME ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POST LAMINECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL STROKE ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 1 FDA reports)
PREGNANCY TEST NEGATIVE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PRODUCT CLOSURE ISSUE ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PRODUCT TAMPERING ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PSEUDOANGINA ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RADICULITIS LUMBOSACRAL ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL SCAR ( 1 FDA reports)
RETINAL TRANSPLANT ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCLEROTHERAPY ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SERUM FERRITIN ABNORMAL ( 1 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
SMOKING CESSATION THERAPY ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SOMOGYI PHENOMENON ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPINAL CORD INJURY CERVICAL ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
SPONDYLITIC MYELOPATHY ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STENT EMBOLISATION ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STERNAL INJURY ( 1 FDA reports)
STITCH ABSCESS ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
THYROID GLAND SCAN ABNORMAL ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRANSIENT PSYCHOSIS ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPE IV HYPERLIPIDAEMIA ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
ULTRASOUND SCAN ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URETERAL POLYP ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URETHRAL MEATUS STENOSIS ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE CALCIUM ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE VISCOSITY INCREASED ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE CYST ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR MALFORMATION PERIPHERAL ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASOMOTOR RHINITIS ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITREOUS ADHESIONS ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VULVAL ABSCESS ( 1 FDA reports)
VULVAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WINGED SCAPULA ( 1 FDA reports)
WISDOM TEETH REMOVAL ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)