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

BLOOD GLUCOSE INCREASED ( 3000 FDA reports)
NAUSEA ( 2504 FDA reports)
WEIGHT DECREASED ( 1972 FDA reports)
BLADDER CANCER ( 1704 FDA reports)
DYSPNOEA ( 1319 FDA reports)
OEDEMA PERIPHERAL ( 1205 FDA reports)
DIARRHOEA ( 1197 FDA reports)
VOMITING ( 1186 FDA reports)
DIZZINESS ( 1180 FDA reports)
WEIGHT INCREASED ( 1149 FDA reports)
DECREASED APPETITE ( 1132 FDA reports)
BLOOD GLUCOSE DECREASED ( 1125 FDA reports)
PAIN ( 1077 FDA reports)
FATIGUE ( 1058 FDA reports)
MYOCARDIAL INFARCTION ( 1058 FDA reports)
ASTHENIA ( 1039 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 915 FDA reports)
HEADACHE ( 864 FDA reports)
DRUG INEFFECTIVE ( 855 FDA reports)
FALL ( 834 FDA reports)
CHEST PAIN ( 816 FDA reports)
ANXIETY ( 795 FDA reports)
ANAEMIA ( 730 FDA reports)
DIABETES MELLITUS ( 713 FDA reports)
HYPERTENSION ( 707 FDA reports)
BACK PAIN ( 651 FDA reports)
HYPOGLYCAEMIA ( 639 FDA reports)
ABDOMINAL PAIN ( 625 FDA reports)
RENAL FAILURE ( 589 FDA reports)
DEPRESSION ( 581 FDA reports)
PNEUMONIA ( 576 FDA reports)
ARTHRALGIA ( 572 FDA reports)
MALAISE ( 566 FDA reports)
PAIN IN EXTREMITY ( 554 FDA reports)
RENAL FAILURE ACUTE ( 508 FDA reports)
TREMOR ( 494 FDA reports)
INSOMNIA ( 489 FDA reports)
PYREXIA ( 488 FDA reports)
DEHYDRATION ( 482 FDA reports)
CONSTIPATION ( 480 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 473 FDA reports)
CORONARY ARTERY DISEASE ( 459 FDA reports)
PANCREATITIS ( 459 FDA reports)
CEREBROVASCULAR ACCIDENT ( 449 FDA reports)
FEELING ABNORMAL ( 447 FDA reports)
INJURY ( 437 FDA reports)
PLEURAL EFFUSION ( 432 FDA reports)
CONDITION AGGRAVATED ( 429 FDA reports)
ATRIAL FIBRILLATION ( 397 FDA reports)
ABDOMINAL PAIN UPPER ( 395 FDA reports)
COUGH ( 395 FDA reports)
HYPERHIDROSIS ( 393 FDA reports)
TYPE 2 DIABETES MELLITUS ( 390 FDA reports)
MYALGIA ( 388 FDA reports)
HYPOTENSION ( 379 FDA reports)
URINARY TRACT INFECTION ( 375 FDA reports)
FLUSHING ( 372 FDA reports)
RASH ( 371 FDA reports)
OEDEMA ( 367 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 364 FDA reports)
ABDOMINAL DISTENSION ( 363 FDA reports)
LOSS OF CONSCIOUSNESS ( 358 FDA reports)
PRURITUS ( 355 FDA reports)
HYPOAESTHESIA ( 346 FDA reports)
MUSCLE SPASMS ( 339 FDA reports)
CARDIAC FAILURE ( 337 FDA reports)
DYSPEPSIA ( 336 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 335 FDA reports)
VISION BLURRED ( 332 FDA reports)
DEATH ( 313 FDA reports)
EMOTIONAL DISTRESS ( 312 FDA reports)
CARDIAC DISORDER ( 305 FDA reports)
CONFUSIONAL STATE ( 305 FDA reports)
HYPERGLYCAEMIA ( 302 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 300 FDA reports)
GAIT DISTURBANCE ( 296 FDA reports)
SOMNOLENCE ( 296 FDA reports)
BLOOD CREATININE INCREASED ( 291 FDA reports)
PALPITATIONS ( 288 FDA reports)
PARAESTHESIA ( 288 FDA reports)
RENAL IMPAIRMENT ( 281 FDA reports)
HAEMATURIA ( 280 FDA reports)
BLOOD PRESSURE INCREASED ( 277 FDA reports)
SWELLING ( 277 FDA reports)
NEUROPATHY PERIPHERAL ( 271 FDA reports)
ANOREXIA ( 269 FDA reports)
DRUG EFFECT DECREASED ( 269 FDA reports)
OSTEOARTHRITIS ( 266 FDA reports)
SYNCOPE ( 260 FDA reports)
CARDIOMEGALY ( 259 FDA reports)
ERYTHEMA ( 257 FDA reports)
INFECTION ( 257 FDA reports)
INJECTION SITE BRUISING ( 251 FDA reports)
JOINT SWELLING ( 251 FDA reports)
FLUID RETENTION ( 250 FDA reports)
BRONCHITIS ( 244 FDA reports)
INJECTION SITE PAIN ( 244 FDA reports)
HEART RATE INCREASED ( 242 FDA reports)
OSTEONECROSIS OF JAW ( 239 FDA reports)
CHEST DISCOMFORT ( 238 FDA reports)
ASTHMA ( 237 FDA reports)
HAEMOGLOBIN DECREASED ( 237 FDA reports)
RESPIRATORY FAILURE ( 237 FDA reports)
MUSCULAR WEAKNESS ( 235 FDA reports)
SINUSITIS ( 231 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 229 FDA reports)
DIABETIC NEUROPATHY ( 229 FDA reports)
ANGINA PECTORIS ( 228 FDA reports)
SEPSIS ( 227 FDA reports)
CONTUSION ( 226 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 225 FDA reports)
PULMONARY OEDEMA ( 225 FDA reports)
RENAL FAILURE CHRONIC ( 224 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 223 FDA reports)
CELLULITIS ( 222 FDA reports)
DRUG INTERACTION ( 222 FDA reports)
PANCREATITIS ACUTE ( 219 FDA reports)
INCORRECT DOSE ADMINISTERED ( 218 FDA reports)
CONVULSION ( 217 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 213 FDA reports)
NASOPHARYNGITIS ( 213 FDA reports)
BLOOD UREA INCREASED ( 208 FDA reports)
INJECTION SITE HAEMORRHAGE ( 206 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 203 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 202 FDA reports)
CHILLS ( 200 FDA reports)
STRESS ( 199 FDA reports)
VISUAL ACUITY REDUCED ( 199 FDA reports)
ANHEDONIA ( 198 FDA reports)
PLATELET COUNT DECREASED ( 195 FDA reports)
TREATMENT NONCOMPLIANCE ( 195 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 194 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 194 FDA reports)
DYSGEUSIA ( 193 FDA reports)
INTERSTITIAL LUNG DISEASE ( 193 FDA reports)
CHOLELITHIASIS ( 192 FDA reports)
ECONOMIC PROBLEM ( 192 FDA reports)
BLOOD PRESSURE DECREASED ( 187 FDA reports)
NERVOUSNESS ( 186 FDA reports)
OSTEOMYELITIS ( 186 FDA reports)
DYSPHAGIA ( 185 FDA reports)
UNEVALUABLE EVENT ( 185 FDA reports)
CATARACT ( 183 FDA reports)
HYPERLIPIDAEMIA ( 178 FDA reports)
ABDOMINAL DISCOMFORT ( 174 FDA reports)
NEPHROLITHIASIS ( 173 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 172 FDA reports)
MEDICATION ERROR ( 171 FDA reports)
THROMBOCYTOPENIA ( 171 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 170 FDA reports)
OBESITY ( 168 FDA reports)
PULMONARY EMBOLISM ( 167 FDA reports)
CORONARY ARTERY OCCLUSION ( 166 FDA reports)
DYSPNOEA EXERTIONAL ( 165 FDA reports)
GASTRITIS ( 165 FDA reports)
PANCYTOPENIA ( 165 FDA reports)
ARTERIOSCLEROSIS ( 163 FDA reports)
HYPERKALAEMIA ( 163 FDA reports)
DEEP VEIN THROMBOSIS ( 162 FDA reports)
POLLAKIURIA ( 161 FDA reports)
FEELING JITTERY ( 158 FDA reports)
RECTAL HAEMORRHAGE ( 158 FDA reports)
SLEEP APNOEA SYNDROME ( 158 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 158 FDA reports)
ARTHRITIS ( 157 FDA reports)
FLATULENCE ( 157 FDA reports)
MENTAL STATUS CHANGES ( 156 FDA reports)
RHABDOMYOLYSIS ( 155 FDA reports)
TACHYCARDIA ( 155 FDA reports)
CARDIAC ARREST ( 153 FDA reports)
ATELECTASIS ( 152 FDA reports)
BRADYCARDIA ( 151 FDA reports)
FEAR ( 151 FDA reports)
BALANCE DISORDER ( 150 FDA reports)
OFF LABEL USE ( 149 FDA reports)
DIABETIC RETINOPATHY ( 148 FDA reports)
HYPERSENSITIVITY ( 148 FDA reports)
OSTEOPOROSIS ( 148 FDA reports)
BONE DISORDER ( 147 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 146 FDA reports)
LIVER DISORDER ( 146 FDA reports)
DIVERTICULUM ( 144 FDA reports)
DRY MOUTH ( 144 FDA reports)
ERUCTATION ( 144 FDA reports)
FEELING HOT ( 143 FDA reports)
SUICIDAL IDEATION ( 143 FDA reports)
PAIN IN JAW ( 142 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 141 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 141 FDA reports)
MITRAL VALVE INCOMPETENCE ( 141 FDA reports)
RENAL DISORDER ( 141 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 140 FDA reports)
EXOSTOSIS ( 138 FDA reports)
ARRHYTHMIA ( 137 FDA reports)
SWELLING FACE ( 137 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 136 FDA reports)
MEMORY IMPAIRMENT ( 136 FDA reports)
MACULAR OEDEMA ( 135 FDA reports)
NECK PAIN ( 135 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 134 FDA reports)
ALOPECIA ( 133 FDA reports)
GENERALISED OEDEMA ( 133 FDA reports)
LETHARGY ( 133 FDA reports)
MYOCARDIAL ISCHAEMIA ( 133 FDA reports)
DEFORMITY ( 131 FDA reports)
MUSCULOSKELETAL PAIN ( 130 FDA reports)
SPINAL OSTEOARTHRITIS ( 129 FDA reports)
ABASIA ( 127 FDA reports)
ASCITES ( 126 FDA reports)
HYPOKALAEMIA ( 126 FDA reports)
HYPONATRAEMIA ( 126 FDA reports)
MULTIPLE INJURIES ( 125 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 124 FDA reports)
OVERDOSE ( 124 FDA reports)
DYSURIA ( 123 FDA reports)
PROSTATE CANCER ( 123 FDA reports)
AMNESIA ( 121 FDA reports)
CARDIO-RESPIRATORY ARREST ( 121 FDA reports)
DENTAL CARIES ( 118 FDA reports)
HEPATIC STEATOSIS ( 118 FDA reports)
PERICARDIAL EFFUSION ( 116 FDA reports)
ANGINA UNSTABLE ( 115 FDA reports)
URTICARIA ( 115 FDA reports)
ROAD TRAFFIC ACCIDENT ( 114 FDA reports)
THROMBOSIS ( 114 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 113 FDA reports)
HYPOXIA ( 113 FDA reports)
WHEEZING ( 113 FDA reports)
DISORIENTATION ( 112 FDA reports)
ERECTILE DYSFUNCTION ( 112 FDA reports)
CARDIOMYOPATHY ( 111 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 111 FDA reports)
AGITATION ( 110 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 110 FDA reports)
SPEECH DISORDER ( 110 FDA reports)
HAEMATOCRIT DECREASED ( 109 FDA reports)
HAEMORRHAGE ( 108 FDA reports)
VERTIGO ( 108 FDA reports)
HAEMORRHOIDS ( 107 FDA reports)
NASAL CONGESTION ( 107 FDA reports)
TOOTH ABSCESS ( 107 FDA reports)
ARTHROPATHY ( 106 FDA reports)
DRUG HYPERSENSITIVITY ( 106 FDA reports)
HYPOTHYROIDISM ( 106 FDA reports)
STOMACH DISCOMFORT ( 106 FDA reports)
TOOTH EXTRACTION ( 106 FDA reports)
CEREBRAL INFARCTION ( 105 FDA reports)
IMPAIRED HEALING ( 105 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 105 FDA reports)
FEELING COLD ( 104 FDA reports)
IRRITABILITY ( 104 FDA reports)
MOBILITY DECREASED ( 104 FDA reports)
HAEMATOCHEZIA ( 103 FDA reports)
HEART RATE IRREGULAR ( 103 FDA reports)
BURNING SENSATION ( 102 FDA reports)
RENAL INJURY ( 102 FDA reports)
EPISTAXIS ( 101 FDA reports)
RHINORRHOEA ( 101 FDA reports)
SINUS TACHYCARDIA ( 101 FDA reports)
STAPHYLOCOCCAL INFECTION ( 100 FDA reports)
DIABETIC KETOACIDOSIS ( 99 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 99 FDA reports)
LYMPHADENOPATHY ( 99 FDA reports)
ROTATOR CUFF SYNDROME ( 99 FDA reports)
SLEEP DISORDER ( 99 FDA reports)
LUNG DISORDER ( 98 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 98 FDA reports)
OSTEOPENIA ( 97 FDA reports)
PULMONARY CONGESTION ( 97 FDA reports)
PULMONARY HYPERTENSION ( 97 FDA reports)
OROPHARYNGEAL PAIN ( 96 FDA reports)
DIALYSIS ( 95 FDA reports)
URINARY RETENTION ( 94 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 93 FDA reports)
MULTIPLE MYELOMA ( 93 FDA reports)
INFLUENZA LIKE ILLNESS ( 92 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 92 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 92 FDA reports)
HYDRONEPHROSIS ( 91 FDA reports)
PATHOLOGICAL FRACTURE ( 91 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 91 FDA reports)
URINARY INCONTINENCE ( 91 FDA reports)
BLOOD POTASSIUM DECREASED ( 90 FDA reports)
TOOTHACHE ( 90 FDA reports)
DISCOMFORT ( 89 FDA reports)
GASTRIC ULCER ( 89 FDA reports)
SKIN ULCER ( 89 FDA reports)
ACUTE RESPIRATORY FAILURE ( 88 FDA reports)
CARDIOVASCULAR DISORDER ( 88 FDA reports)
FEMUR FRACTURE ( 88 FDA reports)
GOUT ( 88 FDA reports)
HIATUS HERNIA ( 88 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 88 FDA reports)
RESPIRATORY DISTRESS ( 88 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 88 FDA reports)
GALLBLADDER DISORDER ( 87 FDA reports)
OSTEONECROSIS ( 87 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 87 FDA reports)
RASH PRURITIC ( 87 FDA reports)
RENAL CYST ( 87 FDA reports)
VISUAL IMPAIRMENT ( 87 FDA reports)
COLD SWEAT ( 86 FDA reports)
FOOT FRACTURE ( 86 FDA reports)
HYPOPHAGIA ( 86 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 86 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 85 FDA reports)
MULTI-ORGAN FAILURE ( 85 FDA reports)
BLOOD BILIRUBIN INCREASED ( 84 FDA reports)
BLOOD POTASSIUM INCREASED ( 84 FDA reports)
CORONARY ARTERY STENOSIS ( 84 FDA reports)
HEART RATE DECREASED ( 84 FDA reports)
METASTASES TO BONE ( 84 FDA reports)
TYPE 1 DIABETES MELLITUS ( 84 FDA reports)
BONE PAIN ( 83 FDA reports)
CYSTITIS ( 83 FDA reports)
HALLUCINATION ( 83 FDA reports)
LUNG NEOPLASM ( 83 FDA reports)
DRUG DOSE OMISSION ( 81 FDA reports)
OSTEOLYSIS ( 81 FDA reports)
UNRESPONSIVE TO STIMULI ( 81 FDA reports)
DYSARTHRIA ( 80 FDA reports)
EARLY SATIETY ( 80 FDA reports)
GLAUCOMA ( 80 FDA reports)
HUMERUS FRACTURE ( 80 FDA reports)
INJECTION SITE ERYTHEMA ( 80 FDA reports)
SKIN DISCOLOURATION ( 80 FDA reports)
INFLUENZA ( 79 FDA reports)
MIGRAINE ( 79 FDA reports)
OESOPHAGITIS ( 79 FDA reports)
PRESYNCOPE ( 79 FDA reports)
STOMATITIS ( 79 FDA reports)
VISUAL DISTURBANCE ( 79 FDA reports)
MENTAL DISORDER ( 78 FDA reports)
PANCREATIC CARCINOMA ( 78 FDA reports)
SURGERY ( 78 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 77 FDA reports)
RETINAL HAEMORRHAGE ( 77 FDA reports)
SUICIDE ATTEMPT ( 77 FDA reports)
VENTRICULAR TACHYCARDIA ( 77 FDA reports)
HEPATIC FAILURE ( 76 FDA reports)
PRODUCT QUALITY ISSUE ( 76 FDA reports)
DISEASE PROGRESSION ( 75 FDA reports)
GASTROINTESTINAL DISORDER ( 75 FDA reports)
PROTEINURIA ( 75 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 74 FDA reports)
HUNGER ( 74 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 73 FDA reports)
BLISTER ( 73 FDA reports)
HYPERCHOLESTEROLAEMIA ( 73 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 73 FDA reports)
CARDIAC MURMUR ( 72 FDA reports)
DIVERTICULITIS ( 72 FDA reports)
DYSPHONIA ( 72 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 72 FDA reports)
PANIC ATTACK ( 72 FDA reports)
EMPHYSEMA ( 71 FDA reports)
FUNGAL INFECTION ( 71 FDA reports)
INJECTION SITE IRRITATION ( 71 FDA reports)
NEUTROPENIA ( 71 FDA reports)
COMA ( 70 FDA reports)
DEPRESSED MOOD ( 70 FDA reports)
DYSKINESIA ( 70 FDA reports)
ILL-DEFINED DISORDER ( 70 FDA reports)
JOINT DISLOCATION ( 70 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 70 FDA reports)
ORTHOSTATIC HYPOTENSION ( 70 FDA reports)
RETCHING ( 70 FDA reports)
ACCIDENTAL OVERDOSE ( 69 FDA reports)
DIABETIC NEPHROPATHY ( 69 FDA reports)
MOUTH ULCERATION ( 69 FDA reports)
TOOTH DISORDER ( 69 FDA reports)
GASTRIC DISORDER ( 68 FDA reports)
HAEMATEMESIS ( 68 FDA reports)
HYPOVOLAEMIA ( 68 FDA reports)
LEUKOCYTOSIS ( 68 FDA reports)
LEUKOPENIA ( 68 FDA reports)
METABOLIC ACIDOSIS ( 68 FDA reports)
NON-CARDIAC CHEST PAIN ( 68 FDA reports)
RIB FRACTURE ( 68 FDA reports)
TINNITUS ( 68 FDA reports)
TOOTH LOSS ( 68 FDA reports)
ATRIAL FLUTTER ( 67 FDA reports)
BONE LESION ( 67 FDA reports)
INCREASED APPETITE ( 67 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 67 FDA reports)
ACUTE PULMONARY OEDEMA ( 66 FDA reports)
BLOOD URINE PRESENT ( 66 FDA reports)
EXPOSED BONE IN JAW ( 66 FDA reports)
LUNG INFILTRATION ( 66 FDA reports)
OXYGEN SATURATION DECREASED ( 66 FDA reports)
CARPAL TUNNEL SYNDROME ( 65 FDA reports)
JAUNDICE ( 65 FDA reports)
JOINT STIFFNESS ( 65 FDA reports)
LUNG NEOPLASM MALIGNANT ( 65 FDA reports)
MELAENA ( 65 FDA reports)
PRODUCTIVE COUGH ( 65 FDA reports)
BLINDNESS ( 64 FDA reports)
FLANK PAIN ( 63 FDA reports)
GINGIVAL PAIN ( 63 FDA reports)
GOITRE ( 63 FDA reports)
UPPER LIMB FRACTURE ( 63 FDA reports)
ABNORMAL DREAMS ( 62 FDA reports)
ANKLE FRACTURE ( 62 FDA reports)
BLADDER NEOPLASM ( 62 FDA reports)
HEPATIC ENZYME INCREASED ( 62 FDA reports)
HERPES ZOSTER ( 62 FDA reports)
METASTASES TO LIVER ( 62 FDA reports)
MUCOSAL INFLAMMATION ( 62 FDA reports)
NEOPLASM MALIGNANT ( 62 FDA reports)
SCAR ( 62 FDA reports)
DECREASED INTEREST ( 61 FDA reports)
HEAD INJURY ( 61 FDA reports)
HEPATITIS ( 61 FDA reports)
HOT FLUSH ( 61 FDA reports)
VIRAL INFECTION ( 61 FDA reports)
DISABILITY ( 60 FDA reports)
GINGIVAL INFECTION ( 60 FDA reports)
PALLOR ( 60 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 59 FDA reports)
DIFFICULTY IN WALKING ( 59 FDA reports)
DRUG DISPENSING ERROR ( 59 FDA reports)
DRUG TOXICITY ( 59 FDA reports)
EYE DISORDER ( 59 FDA reports)
LIMB INJURY ( 59 FDA reports)
POST PROCEDURAL COMPLICATION ( 59 FDA reports)
SCIATICA ( 59 FDA reports)
SKIN LESION ( 59 FDA reports)
DISTURBANCE IN ATTENTION ( 58 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 58 FDA reports)
RASH GENERALISED ( 58 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 58 FDA reports)
RHEUMATOID ARTHRITIS ( 58 FDA reports)
SUDDEN DEATH ( 58 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 58 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 57 FDA reports)
BLADDER DISORDER ( 57 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 57 FDA reports)
BRONCHOPNEUMONIA ( 57 FDA reports)
EAR PAIN ( 57 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 57 FDA reports)
METASTASES TO LUNG ( 57 FDA reports)
RESTLESS LEGS SYNDROME ( 57 FDA reports)
SKIN EXFOLIATION ( 57 FDA reports)
ABDOMINAL PAIN LOWER ( 56 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 56 FDA reports)
AZOTAEMIA ( 56 FDA reports)
CAROTID ARTERY STENOSIS ( 56 FDA reports)
CHROMATURIA ( 56 FDA reports)
HAEMOPTYSIS ( 56 FDA reports)
HIP FRACTURE ( 56 FDA reports)
TARDIVE DYSKINESIA ( 56 FDA reports)
UTERINE LEIOMYOMA ( 56 FDA reports)
DRUG ERUPTION ( 55 FDA reports)
LIFE EXPECTANCY SHORTENED ( 55 FDA reports)
RESTLESSNESS ( 55 FDA reports)
SINUS DISORDER ( 55 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 54 FDA reports)
EJECTION FRACTION DECREASED ( 54 FDA reports)
GASTROENTERITIS ( 54 FDA reports)
IRRITABLE BOWEL SYNDROME ( 54 FDA reports)
JOINT INJURY ( 54 FDA reports)
PNEUMONIA ASPIRATION ( 54 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 54 FDA reports)
COLITIS ( 53 FDA reports)
EMOTIONAL DISORDER ( 53 FDA reports)
HAEMODIALYSIS ( 53 FDA reports)
HYPERSOMNIA ( 53 FDA reports)
NOCTURIA ( 53 FDA reports)
RESPIRATORY ARREST ( 53 FDA reports)
VENTRICULAR FIBRILLATION ( 53 FDA reports)
BLOOD MAGNESIUM DECREASED ( 52 FDA reports)
BLOOD SODIUM DECREASED ( 52 FDA reports)
BONE EROSION ( 52 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 52 FDA reports)
BURSITIS ( 52 FDA reports)
CHOLECYSTITIS ( 52 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 52 FDA reports)
LOCALISED INFECTION ( 52 FDA reports)
SEPTIC SHOCK ( 52 FDA reports)
ADVERSE EVENT ( 51 FDA reports)
DIVERTICULUM INTESTINAL ( 51 FDA reports)
DRY EYE ( 51 FDA reports)
FACE OEDEMA ( 51 FDA reports)
FAECES DISCOLOURED ( 51 FDA reports)
HEPATIC CIRRHOSIS ( 51 FDA reports)
INFLAMMATION ( 51 FDA reports)
JOINT SPRAIN ( 51 FDA reports)
LACTIC ACIDOSIS ( 51 FDA reports)
TOOTH FRACTURE ( 51 FDA reports)
ABNORMAL BEHAVIOUR ( 50 FDA reports)
AGGRESSION ( 50 FDA reports)
FLUID OVERLOAD ( 50 FDA reports)
HAEMATOMA ( 50 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 50 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 50 FDA reports)
SHOCK ( 50 FDA reports)
SKIN BURNING SENSATION ( 50 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 50 FDA reports)
THROAT TIGHTNESS ( 50 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 50 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 49 FDA reports)
DIABETIC COMA ( 49 FDA reports)
DYSLIPIDAEMIA ( 49 FDA reports)
EYE HAEMORRHAGE ( 49 FDA reports)
INJECTION SITE PRURITUS ( 49 FDA reports)
LUMBAR SPINAL STENOSIS ( 49 FDA reports)
PLATELET COUNT INCREASED ( 49 FDA reports)
COLONIC POLYP ( 48 FDA reports)
DEVICE FAILURE ( 48 FDA reports)
ILEUS ( 48 FDA reports)
PRURITUS GENERALISED ( 48 FDA reports)
RALES ( 48 FDA reports)
SWOLLEN TONGUE ( 48 FDA reports)
CRYING ( 47 FDA reports)
DYSSTASIA ( 47 FDA reports)
FAECAL INCONTINENCE ( 47 FDA reports)
HOSPITALISATION ( 47 FDA reports)
INCONTINENCE ( 47 FDA reports)
IRON DEFICIENCY ANAEMIA ( 47 FDA reports)
MENTAL IMPAIRMENT ( 47 FDA reports)
MOVEMENT DISORDER ( 47 FDA reports)
NEURALGIA ( 47 FDA reports)
POLYURIA ( 47 FDA reports)
PULMONARY FIBROSIS ( 47 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 47 FDA reports)
ANGIOEDEMA ( 46 FDA reports)
APPENDICITIS ( 46 FDA reports)
DRUG DEPENDENCE ( 46 FDA reports)
PERIODONTITIS ( 46 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 46 FDA reports)
VENTRICULAR HYPERTROPHY ( 46 FDA reports)
BREAST CANCER ( 45 FDA reports)
DEMENTIA ( 45 FDA reports)
EXCORIATION ( 45 FDA reports)
FEBRILE NEUTROPENIA ( 45 FDA reports)
INJECTION SITE HAEMATOMA ( 45 FDA reports)
KIDNEY INFECTION ( 45 FDA reports)
RESPIRATORY DISORDER ( 45 FDA reports)
RHINITIS ALLERGIC ( 45 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 44 FDA reports)
APHASIA ( 44 FDA reports)
ESCHERICHIA INFECTION ( 44 FDA reports)
EYE SWELLING ( 44 FDA reports)
GINGIVAL SWELLING ( 44 FDA reports)
GINGIVITIS ( 44 FDA reports)
INJECTION SITE URTICARIA ( 44 FDA reports)
NO THERAPEUTIC RESPONSE ( 44 FDA reports)
PSORIASIS ( 44 FDA reports)
STEVENS-JOHNSON SYNDROME ( 44 FDA reports)
DELIRIUM ( 43 FDA reports)
EYELID OEDEMA ( 43 FDA reports)
GASTROENTERITIS VIRAL ( 43 FDA reports)
HEMIPARESIS ( 43 FDA reports)
HYPOGLYCAEMIC COMA ( 43 FDA reports)
INTESTINAL OBSTRUCTION ( 43 FDA reports)
NIGHTMARE ( 43 FDA reports)
RETINOPATHY ( 43 FDA reports)
SINUS BRADYCARDIA ( 43 FDA reports)
SKIN INDURATION ( 43 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 43 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 43 FDA reports)
ANAPHYLACTIC REACTION ( 42 FDA reports)
BONE MARROW FAILURE ( 42 FDA reports)
COAGULOPATHY ( 42 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 42 FDA reports)
DRUG ADMINISTRATION ERROR ( 42 FDA reports)
FIBROMYALGIA ( 42 FDA reports)
GROIN PAIN ( 42 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 42 FDA reports)
OLIGURIA ( 42 FDA reports)
ORAL PAIN ( 42 FDA reports)
PELVIC FRACTURE ( 42 FDA reports)
SPINAL COMPRESSION FRACTURE ( 42 FDA reports)
THROAT IRRITATION ( 42 FDA reports)
VASCULITIS ( 42 FDA reports)
BLINDNESS UNILATERAL ( 41 FDA reports)
BLOOD CALCIUM DECREASED ( 41 FDA reports)
COLITIS ULCERATIVE ( 41 FDA reports)
DRY SKIN ( 41 FDA reports)
ENERGY INCREASED ( 41 FDA reports)
HAEMANGIOMA ( 41 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 41 FDA reports)
LIGAMENT SPRAIN ( 41 FDA reports)
PANCREATITIS CHRONIC ( 41 FDA reports)
PERIODONTAL DISEASE ( 41 FDA reports)
PLEURAL FIBROSIS ( 41 FDA reports)
THYROID NEOPLASM ( 41 FDA reports)
VITAMIN D DEFICIENCY ( 41 FDA reports)
BLOOD ALBUMIN DECREASED ( 40 FDA reports)
BREAST CANCER FEMALE ( 40 FDA reports)
CARDIAC FAILURE ACUTE ( 40 FDA reports)
HEART INJURY ( 40 FDA reports)
MOOD SWINGS ( 40 FDA reports)
MUSCLE TWITCHING ( 40 FDA reports)
NEUTROPHIL COUNT DECREASED ( 40 FDA reports)
RENAL CANCER ( 40 FDA reports)
SINUS CONGESTION ( 40 FDA reports)
STENT PLACEMENT ( 40 FDA reports)
BEDRIDDEN ( 39 FDA reports)
ENCEPHALOPATHY ( 39 FDA reports)
GASTRIC CANCER ( 39 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 39 FDA reports)
KNEE ARTHROPLASTY ( 39 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 39 FDA reports)
LOWER LIMB FRACTURE ( 39 FDA reports)
ONYCHOMYCOSIS ( 39 FDA reports)
SICK SINUS SYNDROME ( 39 FDA reports)
SPINAL COLUMN STENOSIS ( 39 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 38 FDA reports)
CEREBRAL ATROPHY ( 38 FDA reports)
EATING DISORDER ( 38 FDA reports)
ENTEROCOCCAL INFECTION ( 38 FDA reports)
FIBROSIS ( 38 FDA reports)
SNORING ( 38 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 38 FDA reports)
BLOOD AMYLASE INCREASED ( 37 FDA reports)
CATHETERISATION CARDIAC ( 37 FDA reports)
CHOLECYSTECTOMY ( 37 FDA reports)
COORDINATION ABNORMAL ( 37 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 37 FDA reports)
EYE PAIN ( 37 FDA reports)
GINGIVAL DISORDER ( 37 FDA reports)
METASTASES TO LYMPH NODES ( 37 FDA reports)
MUSCLE ATROPHY ( 37 FDA reports)
PERIPHERAL COLDNESS ( 37 FDA reports)
PROTHROMBIN TIME PROLONGED ( 37 FDA reports)
SPINAL FRACTURE ( 37 FDA reports)
SPONDYLOLISTHESIS ( 37 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 36 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 36 FDA reports)
EAR INFECTION ( 36 FDA reports)
HYPERKERATOSIS ( 36 FDA reports)
NEUROPATHY ( 36 FDA reports)
ORAL CANDIDIASIS ( 36 FDA reports)
SKIN DISORDER ( 36 FDA reports)
SKIN HYPERTROPHY ( 36 FDA reports)
BACK DISORDER ( 35 FDA reports)
BIPOLAR DISORDER ( 35 FDA reports)
CARDIOGENIC SHOCK ( 35 FDA reports)
DRUG PRESCRIBING ERROR ( 35 FDA reports)
ECZEMA ( 35 FDA reports)
ENDODONTIC PROCEDURE ( 35 FDA reports)
GRAND MAL CONVULSION ( 35 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 35 FDA reports)
PARANOIA ( 35 FDA reports)
PHOTOPHOBIA ( 35 FDA reports)
PRIMARY SEQUESTRUM ( 35 FDA reports)
PSYCHOTIC DISORDER ( 35 FDA reports)
RESPIRATORY TRACT INFECTION ( 35 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 34 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 34 FDA reports)
BODY HEIGHT DECREASED ( 34 FDA reports)
BONE FRAGMENTATION ( 34 FDA reports)
DEAFNESS ( 34 FDA reports)
DENTAL OPERATION ( 34 FDA reports)
DISEASE RECURRENCE ( 34 FDA reports)
GLOSSODYNIA ( 34 FDA reports)
HEPATOMEGALY ( 34 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 34 FDA reports)
INJECTION SITE RASH ( 34 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 34 FDA reports)
LYMPHOEDEMA ( 34 FDA reports)
LYMPHOMA ( 34 FDA reports)
METASTATIC NEOPLASM ( 34 FDA reports)
OSTEITIS ( 34 FDA reports)
POLYNEUROPATHY ( 34 FDA reports)
PYELONEPHRITIS ( 34 FDA reports)
RESPIRATORY TRACT CONGESTION ( 34 FDA reports)
TOOTH INJURY ( 34 FDA reports)
VITREOUS DETACHMENT ( 34 FDA reports)
BONE DEBRIDEMENT ( 33 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 33 FDA reports)
CORONARY ARTERY BYPASS ( 33 FDA reports)
DIABETIC COMPLICATION ( 33 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 33 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 33 FDA reports)
MASS ( 33 FDA reports)
NIGHT SWEATS ( 33 FDA reports)
PHARYNGEAL OEDEMA ( 33 FDA reports)
RENAL CELL CARCINOMA ( 33 FDA reports)
THINKING ABNORMAL ( 33 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 32 FDA reports)
CARDIAC FAILURE CHRONIC ( 32 FDA reports)
CEREBRAL HAEMORRHAGE ( 32 FDA reports)
DILATATION ATRIAL ( 32 FDA reports)
DIPLOPIA ( 32 FDA reports)
DRUG INTOLERANCE ( 32 FDA reports)
ELECTROLYTE IMBALANCE ( 32 FDA reports)
JAW FRACTURE ( 32 FDA reports)
ORTHOPNOEA ( 32 FDA reports)
PHOTOSENSITIVITY REACTION ( 32 FDA reports)
PITTING OEDEMA ( 32 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 32 FDA reports)
PROTEIN URINE PRESENT ( 32 FDA reports)
PURPURA ( 32 FDA reports)
RENAL COLIC ( 32 FDA reports)
SCLERODERMA ( 32 FDA reports)
THIRST ( 32 FDA reports)
WEGENER'S GRANULOMATOSIS ( 32 FDA reports)
ADVERSE DRUG REACTION ( 31 FDA reports)
ANURIA ( 31 FDA reports)
CARDIAC PACEMAKER INSERTION ( 31 FDA reports)
DIABETIC GASTROPARESIS ( 31 FDA reports)
FAILURE TO THRIVE ( 31 FDA reports)
LACRIMATION INCREASED ( 31 FDA reports)
LIPASE INCREASED ( 31 FDA reports)
MITRAL VALVE PROLAPSE ( 31 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 31 FDA reports)
PELVIC PAIN ( 31 FDA reports)
PHARYNGITIS ( 31 FDA reports)
PULSE ABSENT ( 31 FDA reports)
RASH ERYTHEMATOUS ( 31 FDA reports)
STRESS FRACTURE ( 31 FDA reports)
TACHYPNOEA ( 31 FDA reports)
THYROID DISORDER ( 31 FDA reports)
TIBIA FRACTURE ( 31 FDA reports)
AGEUSIA ( 30 FDA reports)
ANAPHYLACTIC SHOCK ( 30 FDA reports)
ANGER ( 30 FDA reports)
AORTIC STENOSIS ( 30 FDA reports)
AORTIC VALVE INCOMPETENCE ( 30 FDA reports)
BACK INJURY ( 30 FDA reports)
BODY TEMPERATURE INCREASED ( 30 FDA reports)
DIASTOLIC DYSFUNCTION ( 30 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 30 FDA reports)
FIBULA FRACTURE ( 30 FDA reports)
FRACTURE ( 30 FDA reports)
HYPOMAGNESAEMIA ( 30 FDA reports)
INGUINAL HERNIA ( 30 FDA reports)
ISCHAEMIC STROKE ( 30 FDA reports)
MENISCUS LESION ( 30 FDA reports)
OCULAR HYPERAEMIA ( 30 FDA reports)
THROMBOCYTOSIS ( 30 FDA reports)
TOOTH INFECTION ( 30 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 30 FDA reports)
URINE OUTPUT DECREASED ( 30 FDA reports)
VENTRICULAR HYPOKINESIA ( 30 FDA reports)
ACUTE CORONARY SYNDROME ( 29 FDA reports)
AORTIC CALCIFICATION ( 29 FDA reports)
APTYALISM ( 29 FDA reports)
BLOOD IRON DECREASED ( 29 FDA reports)
BRONCHOSPASM ( 29 FDA reports)
CARDIAC FLUTTER ( 29 FDA reports)
CHOLESTASIS ( 29 FDA reports)
COLON CANCER ( 29 FDA reports)
CYANOSIS ( 29 FDA reports)
DILATATION VENTRICULAR ( 29 FDA reports)
ENTERITIS ( 29 FDA reports)
EYE IRRITATION ( 29 FDA reports)
FACIAL NEURALGIA ( 29 FDA reports)
FAMILY STRESS ( 29 FDA reports)
HEPATITIS C ( 29 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 29 FDA reports)
LACERATION ( 29 FDA reports)
MEDICATION RESIDUE ( 29 FDA reports)
MUSCLE STRAIN ( 29 FDA reports)
RENAL TUBULAR NECROSIS ( 29 FDA reports)
SENSORY LOSS ( 29 FDA reports)
SKIN LACERATION ( 29 FDA reports)
TENDONITIS ( 29 FDA reports)
THERAPY NON-RESPONDER ( 29 FDA reports)
ULCER ( 29 FDA reports)
WEIGHT FLUCTUATION ( 29 FDA reports)
WOUND ( 29 FDA reports)
ABDOMINAL TENDERNESS ( 28 FDA reports)
APPETITE DISORDER ( 28 FDA reports)
ATRIOVENTRICULAR BLOCK ( 28 FDA reports)
BACTERIAL INFECTION ( 28 FDA reports)
CONJUNCTIVITIS ( 28 FDA reports)
LABORATORY TEST ABNORMAL ( 28 FDA reports)
MALOCCLUSION ( 28 FDA reports)
MOOD ALTERED ( 28 FDA reports)
MYOPATHY ( 28 FDA reports)
NERVOUS SYSTEM DISORDER ( 28 FDA reports)
OSTEITIS DEFORMANS ( 28 FDA reports)
PEPTIC ULCER ( 28 FDA reports)
PETECHIAE ( 28 FDA reports)
PHLEBITIS ( 28 FDA reports)
PHYSICAL DISABILITY ( 28 FDA reports)
POLYDIPSIA ( 28 FDA reports)
POOR DENTAL CONDITION ( 28 FDA reports)
PULPITIS DENTAL ( 28 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 28 FDA reports)
WRIST FRACTURE ( 28 FDA reports)
ANEURYSM ( 27 FDA reports)
BASAL CELL CARCINOMA ( 27 FDA reports)
BREATH ODOUR ( 27 FDA reports)
CANDIDIASIS ( 27 FDA reports)
DIZZINESS POSTURAL ( 27 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 27 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 27 FDA reports)
HYPERTENSIVE HEART DISEASE ( 27 FDA reports)
HYPOCALCAEMIA ( 27 FDA reports)
HYSTERECTOMY ( 27 FDA reports)
IMPAIRED WORK ABILITY ( 27 FDA reports)
INJECTION SITE NODULE ( 27 FDA reports)
KETOACIDOSIS ( 27 FDA reports)
LOCAL SWELLING ( 27 FDA reports)
MICTURITION URGENCY ( 27 FDA reports)
PNEUMONITIS ( 27 FDA reports)
PRESCRIBED OVERDOSE ( 27 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 27 FDA reports)
RESPIRATORY RATE INCREASED ( 27 FDA reports)
SCAB ( 27 FDA reports)
ABSCESS ( 26 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 26 FDA reports)
CAROTID ARTERY OCCLUSION ( 26 FDA reports)
EXTRASYSTOLES ( 26 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 26 FDA reports)
HYPERCALCAEMIA ( 26 FDA reports)
INTENTIONAL DRUG MISUSE ( 26 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 26 FDA reports)
OPEN WOUND ( 26 FDA reports)
PARAESTHESIA ORAL ( 26 FDA reports)
PROCTALGIA ( 26 FDA reports)
RASH MACULAR ( 26 FDA reports)
RASH MACULO-PAPULAR ( 26 FDA reports)
ADRENAL INSUFFICIENCY ( 25 FDA reports)
APPENDICECTOMY ( 25 FDA reports)
BRONCHITIS CHRONIC ( 25 FDA reports)
CATARACT OPERATION ( 25 FDA reports)
DECUBITUS ULCER ( 25 FDA reports)
DUODENAL ULCER ( 25 FDA reports)
DUODENITIS ( 25 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 25 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 25 FDA reports)
FAECALOMA ( 25 FDA reports)
FRACTURED SACRUM ( 25 FDA reports)
HYPOAESTHESIA ORAL ( 25 FDA reports)
MUSCLE TIGHTNESS ( 25 FDA reports)
MYELODYSPLASTIC SYNDROME ( 25 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 25 FDA reports)
OCCULT BLOOD POSITIVE ( 25 FDA reports)
OCULAR ICTERUS ( 25 FDA reports)
RECTAL CANCER ( 25 FDA reports)
SKIN CANCER ( 25 FDA reports)
SPINAL COLUMN INJURY ( 25 FDA reports)
SYNOVIAL CYST ( 25 FDA reports)
AORTIC ANEURYSM ( 24 FDA reports)
ARTHROPOD BITE ( 24 FDA reports)
BACTERAEMIA ( 24 FDA reports)
BLOOD CREATINE INCREASED ( 24 FDA reports)
BONE OPERATION ( 24 FDA reports)
BREAST MASS ( 24 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 24 FDA reports)
CHOKING SENSATION ( 24 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 24 FDA reports)
CREPITATIONS ( 24 FDA reports)
DEVICE MALFUNCTION ( 24 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 24 FDA reports)
DIABETIC FOOT ( 24 FDA reports)
EXPIRED DRUG ADMINISTERED ( 24 FDA reports)
GANGRENE ( 24 FDA reports)
GASTROINTESTINAL PAIN ( 24 FDA reports)
HEARING IMPAIRED ( 24 FDA reports)
HYPOKINESIA ( 24 FDA reports)
HYPOVENTILATION ( 24 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 24 FDA reports)
INSULIN RESISTANCE ( 24 FDA reports)
INTERMITTENT CLAUDICATION ( 24 FDA reports)
JAW DISORDER ( 24 FDA reports)
MAJOR DEPRESSION ( 24 FDA reports)
MASTICATION DISORDER ( 24 FDA reports)
MUSCLE DISORDER ( 24 FDA reports)
NEPHROGENIC ANAEMIA ( 24 FDA reports)
NERVE INJURY ( 24 FDA reports)
PERITONITIS ( 24 FDA reports)
PNEUMOTHORAX ( 24 FDA reports)
SNEEZING ( 24 FDA reports)
UROSEPSIS ( 24 FDA reports)
ACIDOSIS ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 23 FDA reports)
CHEST X-RAY ABNORMAL ( 23 FDA reports)
CHOLECYSTITIS CHRONIC ( 23 FDA reports)
CIRCULATORY COLLAPSE ( 23 FDA reports)
GASTRIC HAEMORRHAGE ( 23 FDA reports)
HIP ARTHROPLASTY ( 23 FDA reports)
JOINT EFFUSION ( 23 FDA reports)
LIMB DISCOMFORT ( 23 FDA reports)
LIVER INJURY ( 23 FDA reports)
NEOPLASM ( 23 FDA reports)
NO ADVERSE EVENT ( 23 FDA reports)
ORAL DISORDER ( 23 FDA reports)
OTITIS EXTERNA ( 23 FDA reports)
PARKINSON'S DISEASE ( 23 FDA reports)
PROSTATOMEGALY ( 23 FDA reports)
PULMONARY MASS ( 23 FDA reports)
RADICULOPATHY ( 23 FDA reports)
RETINAL DETACHMENT ( 23 FDA reports)
RETINAL EXUDATES ( 23 FDA reports)
SKIN FIBROSIS ( 23 FDA reports)
SKIN FISSURES ( 23 FDA reports)
VENOUS THROMBOSIS LIMB ( 23 FDA reports)
VITREOUS HAEMORRHAGE ( 23 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 22 FDA reports)
ANGIOMYOLIPOMA ( 22 FDA reports)
ANGIOPATHY ( 22 FDA reports)
APLASIA PURE RED CELL ( 22 FDA reports)
CARDIAC VALVE DISEASE ( 22 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 22 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 22 FDA reports)
ESSENTIAL HYPERTENSION ( 22 FDA reports)
FACET JOINT SYNDROME ( 22 FDA reports)
FACIAL PALSY ( 22 FDA reports)
FOOT DEFORMITY ( 22 FDA reports)
GASTRODUODENITIS ( 22 FDA reports)
HERNIA ( 22 FDA reports)
HILAR LYMPHADENOPATHY ( 22 FDA reports)
KYPHOSIS ( 22 FDA reports)
LIP SWELLING ( 22 FDA reports)
MEDICAL DEVICE COMPLICATION ( 22 FDA reports)
MULTIPLE SCLEROSIS ( 22 FDA reports)
OROANTRAL FISTULA ( 22 FDA reports)
PHOTOPSIA ( 22 FDA reports)
QUALITY OF LIFE DECREASED ( 22 FDA reports)
SPLENOMEGALY ( 22 FDA reports)
URETERIC CANCER ( 22 FDA reports)
VIITH NERVE PARALYSIS ( 22 FDA reports)
VITREOUS FLOATERS ( 22 FDA reports)
AGRANULOCYTOSIS ( 21 FDA reports)
CHOLANGITIS ( 21 FDA reports)
CHOLECYSTITIS ACUTE ( 21 FDA reports)
EYE LASER SURGERY ( 21 FDA reports)
GASTRIC BYPASS ( 21 FDA reports)
HEPATIC ENCEPHALOPATHY ( 21 FDA reports)
HICCUPS ( 21 FDA reports)
HYPOACUSIS ( 21 FDA reports)
INTENTIONAL OVERDOSE ( 21 FDA reports)
NECK INJURY ( 21 FDA reports)
NERVE COMPRESSION ( 21 FDA reports)
ORAL DISCOMFORT ( 21 FDA reports)
OSTEOMALACIA ( 21 FDA reports)
OTITIS MEDIA ( 21 FDA reports)
PARONYCHIA ( 21 FDA reports)
PERSONALITY CHANGE ( 21 FDA reports)
RASH PAPULAR ( 21 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 21 FDA reports)
SKIN ATROPHY ( 21 FDA reports)
TENDERNESS ( 21 FDA reports)
VAGINAL HAEMORRHAGE ( 21 FDA reports)
VARICOSE VEIN ( 21 FDA reports)
ACUTE SINUSITIS ( 20 FDA reports)
APLASTIC ANAEMIA ( 20 FDA reports)
BLADDER CANCER RECURRENT ( 20 FDA reports)
BLOOD URIC ACID INCREASED ( 20 FDA reports)
BONE NEOPLASM ( 20 FDA reports)
BRONCHIECTASIS ( 20 FDA reports)
COGNITIVE DISORDER ( 20 FDA reports)
CYST ( 20 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 20 FDA reports)
GYNAECOMASTIA ( 20 FDA reports)
HYPERTHYROIDISM ( 20 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 20 FDA reports)
INGROWING NAIL ( 20 FDA reports)
INJECTION SITE EXTRAVASATION ( 20 FDA reports)
INJECTION SITE SWELLING ( 20 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 20 FDA reports)
ISCHAEMIA ( 20 FDA reports)
LIPOMA ( 20 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 20 FDA reports)
MACULAR DEGENERATION ( 20 FDA reports)
MALNUTRITION ( 20 FDA reports)
METASTASES TO ADRENALS ( 20 FDA reports)
ORAL INTAKE REDUCED ( 20 FDA reports)
PANCREATITIS NECROTISING ( 20 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 20 FDA reports)
SELF-MEDICATION ( 20 FDA reports)
SENSORY DISTURBANCE ( 20 FDA reports)
SUBDURAL HAEMATOMA ( 20 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 20 FDA reports)
VASCULAR CALCIFICATION ( 20 FDA reports)
VENTRICULAR DYSFUNCTION ( 20 FDA reports)
VISUAL FIELD DEFECT ( 20 FDA reports)
WHEELCHAIR USER ( 20 FDA reports)
ACUTE PRERENAL FAILURE ( 19 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 19 FDA reports)
APNOEA ( 19 FDA reports)
BONE NEOPLASM MALIGNANT ( 19 FDA reports)
CALCULUS BLADDER ( 19 FDA reports)
CARDIAC TAMPONADE ( 19 FDA reports)
CAROTID BRUIT ( 19 FDA reports)
CEREBRAL ISCHAEMIA ( 19 FDA reports)
DERMATITIS CONTACT ( 19 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 19 FDA reports)
GLUCOSE URINE PRESENT ( 19 FDA reports)
HAND FRACTURE ( 19 FDA reports)
HEPATITIS ACUTE ( 19 FDA reports)
HYPERURICAEMIA ( 19 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 19 FDA reports)
IRITIS ( 19 FDA reports)
KNEE OPERATION ( 19 FDA reports)
LACUNAR INFARCTION ( 19 FDA reports)
LEG AMPUTATION ( 19 FDA reports)
LOOSE TOOTH ( 19 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 19 FDA reports)
MYELITIS TRANSVERSE ( 19 FDA reports)
OVERWEIGHT ( 19 FDA reports)
PANCREATIC DISORDER ( 19 FDA reports)
PANIC REACTION ( 19 FDA reports)
PAROSMIA ( 19 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 19 FDA reports)
POOR QUALITY SLEEP ( 19 FDA reports)
SCHIZOPHRENIA ( 19 FDA reports)
SEDATION ( 19 FDA reports)
SINUS HEADACHE ( 19 FDA reports)
SKIN HYPERPIGMENTATION ( 19 FDA reports)
SKIN IRRITATION ( 19 FDA reports)
SKIN TIGHTNESS ( 19 FDA reports)
TRANSAMINASES INCREASED ( 19 FDA reports)
APATHY ( 18 FDA reports)
BONE DENSITY DECREASED ( 18 FDA reports)
BRONCHITIS ACUTE ( 18 FDA reports)
CAROTID ARTERY DISEASE ( 18 FDA reports)
CEREBROVASCULAR DISORDER ( 18 FDA reports)
CHRONIC FATIGUE SYNDROME ( 18 FDA reports)
DEBRIDEMENT ( 18 FDA reports)
DEVELOPMENTAL DELAY ( 18 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 18 FDA reports)
ECCHYMOSIS ( 18 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 18 FDA reports)
EXERCISE TOLERANCE DECREASED ( 18 FDA reports)
FALLOT'S TETRALOGY ( 18 FDA reports)
FISTULA ( 18 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 18 FDA reports)
HYPERTENSIVE CRISIS ( 18 FDA reports)
INADEQUATE ANALGESIA ( 18 FDA reports)
LIPIDS INCREASED ( 18 FDA reports)
MANIA ( 18 FDA reports)
MIDDLE INSOMNIA ( 18 FDA reports)
NEPHROPATHY ( 18 FDA reports)
NEURITIS ( 18 FDA reports)
PROSTATITIS ( 18 FDA reports)
PROTEIN TOTAL DECREASED ( 18 FDA reports)
PULMONARY ARTERY ATRESIA ( 18 FDA reports)
RADIUS FRACTURE ( 18 FDA reports)
RIGHT VENTRICULAR FAILURE ( 18 FDA reports)
SCAN BONE MARROW ABNORMAL ( 18 FDA reports)
SEXUAL DYSFUNCTION ( 18 FDA reports)
SPINAL CORD COMPRESSION ( 18 FDA reports)
SPONDYLITIS ( 18 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 18 FDA reports)
SYNOVITIS ( 18 FDA reports)
UTERINE ENLARGEMENT ( 18 FDA reports)
VASCULAR GRAFT OCCLUSION ( 18 FDA reports)
VASCULAR OCCLUSION ( 18 FDA reports)
VASODILATATION ( 18 FDA reports)
WOUND COMPLICATION ( 18 FDA reports)
ANGIONEUROTIC OEDEMA ( 17 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 17 FDA reports)
BODY TEMPERATURE DECREASED ( 17 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 17 FDA reports)
EOSINOPHIL COUNT INCREASED ( 17 FDA reports)
EPILEPSY ( 17 FDA reports)
HAEMOLYSIS ( 17 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 17 FDA reports)
HALLUCINATION, VISUAL ( 17 FDA reports)
HEPATIC LESION ( 17 FDA reports)
HEPATOTOXICITY ( 17 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 17 FDA reports)
HYPERBILIRUBINAEMIA ( 17 FDA reports)
IMPAIRED DRIVING ABILITY ( 17 FDA reports)
INCOHERENT ( 17 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 17 FDA reports)
INITIAL INSOMNIA ( 17 FDA reports)
INJECTION SITE INDURATION ( 17 FDA reports)
INJECTION SITE REACTION ( 17 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 17 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 17 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 17 FDA reports)
MACULOPATHY ( 17 FDA reports)
MALIGNANT MELANOMA ( 17 FDA reports)
METABOLIC SYNDROME ( 17 FDA reports)
OESOPHAGEAL DISORDER ( 17 FDA reports)
ONYCHOCLASIS ( 17 FDA reports)
ORGAN FAILURE ( 17 FDA reports)
PANCREATIC MASS ( 17 FDA reports)
PARKINSONISM ( 17 FDA reports)
PERICARDITIS ( 17 FDA reports)
POLYP ( 17 FDA reports)
PROCEDURAL COMPLICATION ( 17 FDA reports)
RENAL MASS ( 17 FDA reports)
RHINITIS ( 17 FDA reports)
SHOULDER PAIN ( 17 FDA reports)
SOCIAL PROBLEM ( 17 FDA reports)
TESTICULAR PAIN ( 17 FDA reports)
TONGUE DISORDER ( 17 FDA reports)
WITHDRAWAL SYNDROME ( 17 FDA reports)
WOUND DRAINAGE ( 17 FDA reports)
ACNE ( 16 FDA reports)
ACROCHORDON ( 16 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 16 FDA reports)
BILE DUCT OBSTRUCTION ( 16 FDA reports)
BLEPHARITIS ( 16 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 16 FDA reports)
BONE LOSS ( 16 FDA reports)
BREAST CANCER METASTATIC ( 16 FDA reports)
BREATH SOUNDS ABNORMAL ( 16 FDA reports)
CARDIAC ENZYMES INCREASED ( 16 FDA reports)
CARDIAC OPERATION ( 16 FDA reports)
CERVICOBRACHIAL SYNDROME ( 16 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 16 FDA reports)
COSTOCHONDRITIS ( 16 FDA reports)
DERMAL CYST ( 16 FDA reports)
DERMATITIS EXFOLIATIVE ( 16 FDA reports)
DEVICE RELATED INFECTION ( 16 FDA reports)
ENDOTRACHEAL INTUBATION ( 16 FDA reports)
FACIAL BONES FRACTURE ( 16 FDA reports)
FOOD CRAVING ( 16 FDA reports)
FORMICATION ( 16 FDA reports)
GOUTY ARTHRITIS ( 16 FDA reports)
INJECTION SITE MASS ( 16 FDA reports)
LOBAR PNEUMONIA ( 16 FDA reports)
LUNG CONSOLIDATION ( 16 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 16 FDA reports)
MONOPLEGIA ( 16 FDA reports)
PERIARTHRITIS ( 16 FDA reports)
PERIRECTAL ABSCESS ( 16 FDA reports)
PIGMENTATION DISORDER ( 16 FDA reports)
PNEUMONIA BACTERIAL ( 16 FDA reports)
PROCEDURAL PAIN ( 16 FDA reports)
PSEUDOMONAS INFECTION ( 16 FDA reports)
RENAL ARTERY STENOSIS ( 16 FDA reports)
RENAL NEOPLASM ( 16 FDA reports)
RETINAL DISORDER ( 16 FDA reports)
SERUM FERRITIN INCREASED ( 16 FDA reports)
SLUGGISHNESS ( 16 FDA reports)
SOMNAMBULISM ( 16 FDA reports)
SQUAMOUS CELL CARCINOMA ( 16 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 16 FDA reports)
TENDON RUPTURE ( 16 FDA reports)
TENSION ( 16 FDA reports)
UTERINE CANCER ( 16 FDA reports)
VITAMIN B12 DEFICIENCY ( 16 FDA reports)
VOCAL CORD PARALYSIS ( 16 FDA reports)
WALKING AID USER ( 16 FDA reports)
WRONG DRUG ADMINISTERED ( 16 FDA reports)
ALCOHOL USE ( 15 FDA reports)
ANAL FISTULA ( 15 FDA reports)
BLOOD CHLORIDE DECREASED ( 15 FDA reports)
BUNDLE BRANCH BLOCK ( 15 FDA reports)
CALCULUS URETERIC ( 15 FDA reports)
COMPRESSION FRACTURE ( 15 FDA reports)
COR PULMONALE CHRONIC ( 15 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 15 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 15 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 15 FDA reports)
EJECTION FRACTION ABNORMAL ( 15 FDA reports)
EXTREMITY CONTRACTURE ( 15 FDA reports)
GASTRITIS EROSIVE ( 15 FDA reports)
GRANULOCYTOPENIA ( 15 FDA reports)
HEPATIC NECROSIS ( 15 FDA reports)
HEPATITIS B ( 15 FDA reports)
HYPERVENTILATION ( 15 FDA reports)
HYPOAESTHESIA FACIAL ( 15 FDA reports)
HYPOALBUMINAEMIA ( 15 FDA reports)
INTESTINAL PERFORATION ( 15 FDA reports)
IRON DEFICIENCY ( 15 FDA reports)
JAUNDICE CHOLESTATIC ( 15 FDA reports)
LEFT ATRIAL DILATATION ( 15 FDA reports)
MUSCLE HAEMORRHAGE ( 15 FDA reports)
NEUROGENIC BLADDER ( 15 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 15 FDA reports)
ORAL INFECTION ( 15 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 15 FDA reports)
REFLUX OESOPHAGITIS ( 15 FDA reports)
RESPIRATORY ACIDOSIS ( 15 FDA reports)
SKIN HAEMORRHAGE ( 15 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 15 FDA reports)
URINE ABNORMALITY ( 15 FDA reports)
URINE FLOW DECREASED ( 15 FDA reports)
UVEITIS ( 15 FDA reports)
VARICES OESOPHAGEAL ( 15 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 15 FDA reports)
WEIGHT LOSS POOR ( 15 FDA reports)
ABORTION SPONTANEOUS ( 14 FDA reports)
ABSCESS JAW ( 14 FDA reports)
ACCIDENTAL NEEDLE STICK ( 14 FDA reports)
ACUTE HEPATIC FAILURE ( 14 FDA reports)
ADENOCARCINOMA ( 14 FDA reports)
AORTIC DILATATION ( 14 FDA reports)
ASPIRATION ( 14 FDA reports)
BILIARY DILATATION ( 14 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 14 FDA reports)
BLOOD CALCIUM INCREASED ( 14 FDA reports)
BREAST PAIN ( 14 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 14 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 14 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 14 FDA reports)
CULTURE URINE POSITIVE ( 14 FDA reports)
DECREASED ACTIVITY ( 14 FDA reports)
DERMATOMYOSITIS ( 14 FDA reports)
DIABETIC EYE DISEASE ( 14 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 14 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 14 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 14 FDA reports)
GALLBLADDER POLYP ( 14 FDA reports)
GASTRIC POLYPS ( 14 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 14 FDA reports)
GRIP STRENGTH DECREASED ( 14 FDA reports)
HELICOBACTER INFECTION ( 14 FDA reports)
HEMIPLEGIA ( 14 FDA reports)
HEPATIC CYST ( 14 FDA reports)
HEPATOCELLULAR DAMAGE ( 14 FDA reports)
HYPERCHLORHYDRIA ( 14 FDA reports)
HYPERPHAGIA ( 14 FDA reports)
IMMUNE SYSTEM DISORDER ( 14 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 14 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 14 FDA reports)
JOINT CONTRACTURE ( 14 FDA reports)
LOCALISED OEDEMA ( 14 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 14 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 14 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 14 FDA reports)
MICROALBUMINURIA ( 14 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 14 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 14 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 14 FDA reports)
MYOSITIS ( 14 FDA reports)
NEPHRITIS ( 14 FDA reports)
OPTIC NEURITIS ( 14 FDA reports)
ORAL HERPES ( 14 FDA reports)
OSTEOSCLEROSIS ( 14 FDA reports)
PANCREATIC NEOPLASM ( 14 FDA reports)
PAPILLOEDEMA ( 14 FDA reports)
PARALYSIS ( 14 FDA reports)
PECTUS EXCAVATUM ( 14 FDA reports)
PLASMACYTOMA ( 14 FDA reports)
POOR PERIPHERAL CIRCULATION ( 14 FDA reports)
POST LAMINECTOMY SYNDROME ( 14 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 14 FDA reports)
PROSTATE CANCER METASTATIC ( 14 FDA reports)
PULMONARY THROMBOSIS ( 14 FDA reports)
RASH PUSTULAR ( 14 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 14 FDA reports)
RETINAL OEDEMA ( 14 FDA reports)
RETINITIS ( 14 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 14 FDA reports)
SHOCK HAEMORRHAGIC ( 14 FDA reports)
SOFT TISSUE DISORDER ( 14 FDA reports)
SOFT TISSUE MASS ( 14 FDA reports)
SPONDYLOLYSIS ( 14 FDA reports)
SPUTUM PURULENT ( 14 FDA reports)
TENDON DISORDER ( 14 FDA reports)
TOE AMPUTATION ( 14 FDA reports)
UNDERDOSE ( 14 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 14 FDA reports)
VASCULAR PSEUDOANEURYSM ( 14 FDA reports)
WOUND INFECTION ( 14 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 13 FDA reports)
AUTOIMMUNE HEPATITIS ( 13 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 13 FDA reports)
BLOOD PRESSURE ABNORMAL ( 13 FDA reports)
CHANGE OF BOWEL HABIT ( 13 FDA reports)
CHOKING ( 13 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 13 FDA reports)
CONCUSSION ( 13 FDA reports)
DELUSION ( 13 FDA reports)
EAR DISCOMFORT ( 13 FDA reports)
GLYCOSURIA ( 13 FDA reports)
GRANULOMA ( 13 FDA reports)
HAEMODYNAMIC INSTABILITY ( 13 FDA reports)
HISTOPLASMOSIS ( 13 FDA reports)
HYPERCAPNIA ( 13 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 13 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 13 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 13 FDA reports)
INJECTION SITE DISCOMFORT ( 13 FDA reports)
INTESTINAL ISCHAEMIA ( 13 FDA reports)
LARGE INTESTINE CARCINOMA ( 13 FDA reports)
LIVEDO RETICULARIS ( 13 FDA reports)
MACULAR HOLE ( 13 FDA reports)
MYASTHENIA GRAVIS ( 13 FDA reports)
NODAL RHYTHM ( 13 FDA reports)
OPEN ANGLE GLAUCOMA ( 13 FDA reports)
OSTEORADIONECROSIS ( 13 FDA reports)
PANCREATIC PSEUDOCYST ( 13 FDA reports)
PERITONITIS BACTERIAL ( 13 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 13 FDA reports)
PREGNANCY ( 13 FDA reports)
PROSTATE INFECTION ( 13 FDA reports)
QUADRIPARESIS ( 13 FDA reports)
RADIOTHERAPY ( 13 FDA reports)
RENAL PAIN ( 13 FDA reports)
RETINAL ANEURYSM ( 13 FDA reports)
ROSACEA ( 13 FDA reports)
SEASONAL ALLERGY ( 13 FDA reports)
SPINAL FUSION SURGERY ( 13 FDA reports)
TUMOUR LYSIS SYNDROME ( 13 FDA reports)
ULNA FRACTURE ( 13 FDA reports)
URINE ODOUR ABNORMAL ( 13 FDA reports)
XEROSIS ( 13 FDA reports)
ABDOMINAL HERNIA ( 12 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 12 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 12 FDA reports)
ADNEXA UTERI MASS ( 12 FDA reports)
AMMONIA INCREASED ( 12 FDA reports)
ANGIOPLASTY ( 12 FDA reports)
ANOSMIA ( 12 FDA reports)
AORTIC VALVE SCLEROSIS ( 12 FDA reports)
APPARENT DEATH ( 12 FDA reports)
APPENDICITIS PERFORATED ( 12 FDA reports)
APPLICATION SITE ERYTHEMA ( 12 FDA reports)
BLOOD CREATININE DECREASED ( 12 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 12 FDA reports)
BLOOD TEST ABNORMAL ( 12 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 12 FDA reports)
CLOSTRIDIAL INFECTION ( 12 FDA reports)
COMMUNICATION DISORDER ( 12 FDA reports)
CONDUCTION DISORDER ( 12 FDA reports)
DEMYELINATION ( 12 FDA reports)
DIABETIC RETINAL OEDEMA ( 12 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 12 FDA reports)
DRUG EFFECT INCREASED ( 12 FDA reports)
DRUG SCREEN POSITIVE ( 12 FDA reports)
DRY THROAT ( 12 FDA reports)
DUODENAL ULCER PERFORATION ( 12 FDA reports)
DYSTONIA ( 12 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 12 FDA reports)
EYE DISCHARGE ( 12 FDA reports)
EYE OEDEMA ( 12 FDA reports)
EYELID PTOSIS ( 12 FDA reports)
FEELING DRUNK ( 12 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 12 FDA reports)
HAEMATOCRIT INCREASED ( 12 FDA reports)
HALLUCINATION, AUDITORY ( 12 FDA reports)
HEART RATE ABNORMAL ( 12 FDA reports)
HEPATITIS TOXIC ( 12 FDA reports)
HOMICIDAL IDEATION ( 12 FDA reports)
HYPERAESTHESIA ( 12 FDA reports)
HYPERCOAGULATION ( 12 FDA reports)
HYPOTONIA ( 12 FDA reports)
ILIAC ARTERY STENOSIS ( 12 FDA reports)
INFUSION RELATED REACTION ( 12 FDA reports)
KLEBSIELLA INFECTION ( 12 FDA reports)
LOW TURNOVER OSTEOPATHY ( 12 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
LUNG INFECTION ( 12 FDA reports)
METABOLIC ENCEPHALOPATHY ( 12 FDA reports)
METASTASES TO NECK ( 12 FDA reports)
MITRAL VALVE DISEASE ( 12 FDA reports)
MUCOSAL ULCERATION ( 12 FDA reports)
MULTIPLE FRACTURES ( 12 FDA reports)
NAIL INFECTION ( 12 FDA reports)
NASAL DISCOMFORT ( 12 FDA reports)
NECROSIS ( 12 FDA reports)
PAINFUL DEFAECATION ( 12 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 12 FDA reports)
PANCREATIC ENZYMES INCREASED ( 12 FDA reports)
PERIORBITAL OEDEMA ( 12 FDA reports)
PO2 DECREASED ( 12 FDA reports)
PORTAL HYPERTENSION ( 12 FDA reports)
PSORIATIC ARTHROPATHY ( 12 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 12 FDA reports)
PURULENCE ( 12 FDA reports)
PURULENT DISCHARGE ( 12 FDA reports)
RENAL ATROPHY ( 12 FDA reports)
SENSATION OF FOREIGN BODY ( 12 FDA reports)
SEQUESTRECTOMY ( 12 FDA reports)
SERONEGATIVE ARTHRITIS ( 12 FDA reports)
STAPHYLOMA ( 12 FDA reports)
STREPTOCOCCAL INFECTION ( 12 FDA reports)
TENSION HEADACHE ( 12 FDA reports)
TINEA CRURIS ( 12 FDA reports)
TRACHEAL DEVIATION ( 12 FDA reports)
TROPONIN INCREASED ( 12 FDA reports)
VENTRICULAR ARRHYTHMIA ( 12 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 12 FDA reports)
ACTINIC KERATOSIS ( 11 FDA reports)
AORTIC VALVE STENOSIS ( 11 FDA reports)
ARTERIOVENOUS MALFORMATION ( 11 FDA reports)
ASPIRATION JOINT ( 11 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 11 FDA reports)
BILE DUCT STONE ( 11 FDA reports)
BLEEDING TIME PROLONGED ( 11 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 11 FDA reports)
BLOOD COUNT ABNORMAL ( 11 FDA reports)
BLOOD DISORDER ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 11 FDA reports)
BRAIN OEDEMA ( 11 FDA reports)
BREAST OEDEMA ( 11 FDA reports)
CARDIAC HYPERTROPHY ( 11 FDA reports)
CARDIAC SEPTAL DEFECT ( 11 FDA reports)
CELL MARKER INCREASED ( 11 FDA reports)
CHONDROCALCINOSIS ( 11 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 11 FDA reports)
DENTAL DISCOMFORT ( 11 FDA reports)
DENTURE WEARER ( 11 FDA reports)
DERMATITIS ( 11 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 11 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 11 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 11 FDA reports)
EOSINOPHILIC PNEUMONIA ( 11 FDA reports)
EPIGASTRIC DISCOMFORT ( 11 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 11 FDA reports)
EYE INFECTION ( 11 FDA reports)
EYE PRURITUS ( 11 FDA reports)
FIBRIN D DIMER INCREASED ( 11 FDA reports)
FOOD ALLERGY ( 11 FDA reports)
GENERALISED ERYTHEMA ( 11 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 11 FDA reports)
HYDROCELE ( 11 FDA reports)
HYDROCEPHALUS ( 11 FDA reports)
INFARCTION ( 11 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 11 FDA reports)
JOINT CREPITATION ( 11 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 11 FDA reports)
LISTLESS ( 11 FDA reports)
LUNG HYPERINFLATION ( 11 FDA reports)
LYMPHADENECTOMY ( 11 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 11 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 11 FDA reports)
MELANOCYTIC NAEVUS ( 11 FDA reports)
MYELITIS ( 11 FDA reports)
NAIL DISORDER ( 11 FDA reports)
NASAL ULCER ( 11 FDA reports)
NODULE ( 11 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 11 FDA reports)
NYSTAGMUS ( 11 FDA reports)
ODYNOPHAGIA ( 11 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 11 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 11 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 11 FDA reports)
PNEUMOPERITONEUM ( 11 FDA reports)
POLYMYALGIA RHEUMATICA ( 11 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 11 FDA reports)
POSTRENAL FAILURE ( 11 FDA reports)
RED BLOOD CELL ABNORMALITY ( 11 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 11 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 11 FDA reports)
SCRATCH ( 11 FDA reports)
SCREAMING ( 11 FDA reports)
SENSATION OF HEAVINESS ( 11 FDA reports)
SEROTONIN SYNDROME ( 11 FDA reports)
SHOULDER ARTHROPLASTY ( 11 FDA reports)
SINUS OPERATION ( 11 FDA reports)
SPLEEN DISORDER ( 11 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 11 FDA reports)
SUDDEN CARDIAC DEATH ( 11 FDA reports)
SUDDEN HEARING LOSS ( 11 FDA reports)
THYROID CANCER ( 11 FDA reports)
TOBACCO USER ( 11 FDA reports)
ULCER HAEMORRHAGE ( 11 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 11 FDA reports)
URETERAL NEOPLASM ( 11 FDA reports)
URINE CYTOLOGY ABNORMAL ( 11 FDA reports)
URINE OUTPUT INCREASED ( 11 FDA reports)
VENOUS INSUFFICIENCY ( 11 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 11 FDA reports)
VITAMIN D DECREASED ( 11 FDA reports)
ABNORMAL SENSATION IN EYE ( 10 FDA reports)
ABSCESS LIMB ( 10 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 10 FDA reports)
ADENOCARCINOMA PANCREAS ( 10 FDA reports)
ALBUMIN URINE PRESENT ( 10 FDA reports)
ANORECTAL DISORDER ( 10 FDA reports)
ANOXIC ENCEPHALOPATHY ( 10 FDA reports)
ANXIETY DISORDER ( 10 FDA reports)
APHONIA ( 10 FDA reports)
ATRIAL TACHYCARDIA ( 10 FDA reports)
BLOOD CULTURE POSITIVE ( 10 FDA reports)
BOWEL SOUNDS ABNORMAL ( 10 FDA reports)
CORONARY ARTERY RESTENOSIS ( 10 FDA reports)
CROHN'S DISEASE ( 10 FDA reports)
DEFAECATION URGENCY ( 10 FDA reports)
DERMOID CYST ( 10 FDA reports)
DRUG ABUSE ( 10 FDA reports)
DYSPNOEA EXACERBATED ( 10 FDA reports)
EAR HAEMORRHAGE ( 10 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 10 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 10 FDA reports)
ENDOCARDITIS ( 10 FDA reports)
FAECES HARD ( 10 FDA reports)
FEMORAL NECK FRACTURE ( 10 FDA reports)
FOLLICULITIS ( 10 FDA reports)
FOOD AVERSION ( 10 FDA reports)
FRACTURE DELAYED UNION ( 10 FDA reports)
FURUNCLE ( 10 FDA reports)
FUSOBACTERIUM INFECTION ( 10 FDA reports)
GASTRITIS ATROPHIC ( 10 FDA reports)
GINGIVAL BLEEDING ( 10 FDA reports)
HAEMOLYTIC ANAEMIA ( 10 FDA reports)
HAEMORRHAGIC STROKE ( 10 FDA reports)
HEAD DISCOMFORT ( 10 FDA reports)
HEART VALVE INCOMPETENCE ( 10 FDA reports)
HODGKIN'S DISEASE ( 10 FDA reports)
HYPOPHOSPHATAEMIA ( 10 FDA reports)
IMMUNOSUPPRESSION ( 10 FDA reports)
INCISIONAL HERNIA ( 10 FDA reports)
INFECTIOUS PERITONITIS ( 10 FDA reports)
INJECTION SITE DISCOLOURATION ( 10 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 10 FDA reports)
INTRACARDIAC THROMBUS ( 10 FDA reports)
INTRACRANIAL HYPOTENSION ( 10 FDA reports)
LUMBAR RADICULOPATHY ( 10 FDA reports)
LUNG CANCER METASTATIC ( 10 FDA reports)
LYMPHANGITIS ( 10 FDA reports)
MALIGNANT HYPERTENSION ( 10 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 10 FDA reports)
MEAN CELL VOLUME INCREASED ( 10 FDA reports)
MECHANICAL VENTILATION ( 10 FDA reports)
METASTASES TO SPINE ( 10 FDA reports)
MITRAL VALVE CALCIFICATION ( 10 FDA reports)
MONOCLONAL GAMMOPATHY ( 10 FDA reports)
MUSCULOSKELETAL DISORDER ( 10 FDA reports)
MYDRIASIS ( 10 FDA reports)
NEPHROPATHY TOXIC ( 10 FDA reports)
NEUTROPHIL COUNT INCREASED ( 10 FDA reports)
OCCULT BLOOD ( 10 FDA reports)
ORAL SURGERY ( 10 FDA reports)
ORAL TORUS ( 10 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 10 FDA reports)
OVARIAN MASS ( 10 FDA reports)
PANCREATITIS RELAPSING ( 10 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 10 FDA reports)
PARAPLEGIA ( 10 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 10 FDA reports)
RASH VESICULAR ( 10 FDA reports)
SCOLIOSIS ( 10 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 10 FDA reports)
SINUS RHYTHM ( 10 FDA reports)
SKIN INFECTION ( 10 FDA reports)
SKIN WARM ( 10 FDA reports)
SLEEP TALKING ( 10 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 10 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 10 FDA reports)
SPUTUM DISCOLOURED ( 10 FDA reports)
TEMPERATURE INTOLERANCE ( 10 FDA reports)
TENDON PAIN ( 10 FDA reports)
TORSADE DE POINTES ( 10 FDA reports)
TRANSPLANT FAILURE ( 10 FDA reports)
URINARY BLADDER POLYP ( 10 FDA reports)
URINARY TRACT OBSTRUCTION ( 10 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 10 FDA reports)
ABDOMINAL MASS ( 9 FDA reports)
ACCIDENT ( 9 FDA reports)
ACCIDENTAL EXPOSURE ( 9 FDA reports)
ADRENAL ADENOMA ( 9 FDA reports)
ADRENAL MASS ( 9 FDA reports)
ALCOHOL ABUSE ( 9 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 9 FDA reports)
ANAL FISSURE ( 9 FDA reports)
ANAL INJURY ( 9 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 9 FDA reports)
AUTONOMIC NEUROPATHY ( 9 FDA reports)
BEREAVEMENT REACTION ( 9 FDA reports)
BLADDER CANCER STAGE II ( 9 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE III ( 9 FDA reports)
BLOOD BLISTER ( 9 FDA reports)
BULLOUS LUNG DISEASE ( 9 FDA reports)
CALCINOSIS ( 9 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 9 FDA reports)
CERVICAL MYELOPATHY ( 9 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 9 FDA reports)
CLAVICLE FRACTURE ( 9 FDA reports)
COMPLETED SUICIDE ( 9 FDA reports)
CYSTITIS NONINFECTIVE ( 9 FDA reports)
DRUG LEVEL INCREASED ( 9 FDA reports)
DYSPHEMIA ( 9 FDA reports)
EDENTULOUS ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 9 FDA reports)
EPICONDYLITIS ( 9 FDA reports)
ERYTHEMA MULTIFORME ( 9 FDA reports)
EYE INJURY ( 9 FDA reports)
FACIAL PAIN ( 9 FDA reports)
FACTOR V LEIDEN MUTATION ( 9 FDA reports)
FAT NECROSIS ( 9 FDA reports)
GASTROENTERITIS RADIATION ( 9 FDA reports)
HAEMORRHAGIC DIATHESIS ( 9 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 9 FDA reports)
HYDROURETER ( 9 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 9 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 9 FDA reports)
JOINT ANKYLOSIS ( 9 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 9 FDA reports)
LIBIDO DECREASED ( 9 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 9 FDA reports)
LIPID METABOLISM DISORDER ( 9 FDA reports)
LOWER EXTREMITY MASS ( 9 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 9 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 9 FDA reports)
MICROCYTIC ANAEMIA ( 9 FDA reports)
MOTOR DYSFUNCTION ( 9 FDA reports)
MULTIPLE ALLERGIES ( 9 FDA reports)
MUSCLE INJURY ( 9 FDA reports)
MYELOPATHY ( 9 FDA reports)
NEOPLASM PROGRESSION ( 9 FDA reports)
NEPHRITIS INTERSTITIAL ( 9 FDA reports)
NEPHROSCLEROSIS ( 9 FDA reports)
NEUTROPENIC INFECTION ( 9 FDA reports)
NOCTURNAL DYSPNOEA ( 9 FDA reports)
OEDEMA MOUTH ( 9 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 9 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 9 FDA reports)
PEMPHIGOID ( 9 FDA reports)
PENILE INFECTION ( 9 FDA reports)
PERSONALITY DISORDER ( 9 FDA reports)
PHARYNGEAL ULCERATION ( 9 FDA reports)
PNEUMONIA LEGIONELLA ( 9 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 9 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 9 FDA reports)
POSTNASAL DRIP ( 9 FDA reports)
PRESBYACUSIS ( 9 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 9 FDA reports)
PROSTATECTOMY ( 9 FDA reports)
PULSE PRESSURE DECREASED ( 9 FDA reports)
QRS AXIS ABNORMAL ( 9 FDA reports)
REFLUX GASTRITIS ( 9 FDA reports)
SCOTOMA ( 9 FDA reports)
SCROTAL IRRITATION ( 9 FDA reports)
SEBORRHOEIC KERATOSIS ( 9 FDA reports)
SKELETAL INJURY ( 9 FDA reports)
SPINAL DISORDER ( 9 FDA reports)
STRIDOR ( 9 FDA reports)
THYROID CYST ( 9 FDA reports)
URETHRAL OBSTRUCTION ( 9 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 9 FDA reports)
URINE KETONE BODY PRESENT ( 9 FDA reports)
UTERINE MASS ( 9 FDA reports)
VASCULAR GRAFT ( 9 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 9 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 9 FDA reports)
ABDOMINAL RIGIDITY ( 8 FDA reports)
ABNORMAL FAECES ( 8 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 8 FDA reports)
APPLICATION SITE PRURITUS ( 8 FDA reports)
ARTERIAL STENOSIS ( 8 FDA reports)
ARTERIOSPASM CORONARY ( 8 FDA reports)
ARTHRITIS BACTERIAL ( 8 FDA reports)
ATRIAL SEPTAL DEFECT ( 8 FDA reports)
BILE DUCT CANCER ( 8 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 8 FDA reports)
BLADDER OBSTRUCTION ( 8 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE II ( 8 FDA reports)
BLOOD LACTIC ACID INCREASED ( 8 FDA reports)
BRAIN NEOPLASM ( 8 FDA reports)
BRAIN STEM INFARCTION ( 8 FDA reports)
BRONCHIAL SECRETION RETENTION ( 8 FDA reports)
CAUDA EQUINA SYNDROME ( 8 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 8 FDA reports)
COLORECTAL CANCER ( 8 FDA reports)
COMMINUTED FRACTURE ( 8 FDA reports)
CONGENITAL ANOMALY ( 8 FDA reports)
CORONARY ANGIOPLASTY ( 8 FDA reports)
DERMATITIS ACNEIFORM ( 8 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 8 FDA reports)
DUODENAL OBSTRUCTION ( 8 FDA reports)
ENTEROCOLITIS ( 8 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 8 FDA reports)
ERYTHEMA OF EYELID ( 8 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 8 FDA reports)
FLUID INTAKE REDUCED ( 8 FDA reports)
FUNGAL SKIN INFECTION ( 8 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 8 FDA reports)
HAEMORRHAGIC ANAEMIA ( 8 FDA reports)
HAIR GROWTH ABNORMAL ( 8 FDA reports)
HEART DISEASE CONGENITAL ( 8 FDA reports)
HEPATIC CANCER METASTATIC ( 8 FDA reports)
HEPATIC ENZYME ABNORMAL ( 8 FDA reports)
HEPATITIS A ( 8 FDA reports)
HERPES SIMPLEX ( 8 FDA reports)
HERPES VIRUS INFECTION ( 8 FDA reports)
HIDRADENITIS ( 8 FDA reports)
HYPERAMMONAEMIA ( 8 FDA reports)
HYPOVOLAEMIC SHOCK ( 8 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 8 FDA reports)
IMMOBILE ( 8 FDA reports)
INCISION SITE HAEMORRHAGE ( 8 FDA reports)
INJECTION SITE ABSCESS ( 8 FDA reports)
INJECTION SITE WARMTH ( 8 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 8 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 8 FDA reports)
KIDNEY ENLARGEMENT ( 8 FDA reports)
LARYNGITIS ( 8 FDA reports)
LEUKAEMIA ( 8 FDA reports)
LOCALISED OSTEOARTHRITIS ( 8 FDA reports)
LOSS OF EMPLOYMENT ( 8 FDA reports)
MALIGNANT ASCITES ( 8 FDA reports)
METABOLIC DISORDER ( 8 FDA reports)
MICTURITION DISORDER ( 8 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 8 FDA reports)
MULTI-ORGAN DISORDER ( 8 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 8 FDA reports)
MYOCLONUS ( 8 FDA reports)
NEOPLASM RECURRENCE ( 8 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 8 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 8 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 8 FDA reports)
OBSTRUCTION ( 8 FDA reports)
OESOPHAGITIS ULCERATIVE ( 8 FDA reports)
ORAL FUNGAL INFECTION ( 8 FDA reports)
OVARIAN CANCER ( 8 FDA reports)
PAIN OF SKIN ( 8 FDA reports)
PCO2 INCREASED ( 8 FDA reports)
PELVIC MASS ( 8 FDA reports)
PNEUMONIA VIRAL ( 8 FDA reports)
POLYCYSTIC OVARIES ( 8 FDA reports)
PROSTATIC OPERATION ( 8 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 8 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 8 FDA reports)
READING DISORDER ( 8 FDA reports)
RESUSCITATION ( 8 FDA reports)
SERUM FERRITIN DECREASED ( 8 FDA reports)
SINUS ARRHYTHMIA ( 8 FDA reports)
SJOGREN'S SYNDROME ( 8 FDA reports)
SKIN GRAFT ( 8 FDA reports)
SKIN PAPILLOMA ( 8 FDA reports)
SOFT TISSUE INJURY ( 8 FDA reports)
SPUTUM CULTURE POSITIVE ( 8 FDA reports)
SYRINGOMYELIA ( 8 FDA reports)
TACHYARRHYTHMIA ( 8 FDA reports)
TELANGIECTASIA ( 8 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 8 FDA reports)
TONGUE DISCOLOURATION ( 8 FDA reports)
TONSILLITIS ( 8 FDA reports)
TRIGGER FINGER ( 8 FDA reports)
VAGINAL INFECTION ( 8 FDA reports)
ABDOMINAL ADHESIONS ( 7 FDA reports)
ADHESION ( 7 FDA reports)
AFFECTIVE DISORDER ( 7 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 7 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 7 FDA reports)
AORTIC BYPASS ( 7 FDA reports)
AORTIC VALVE DISEASE ( 7 FDA reports)
APHAGIA ( 7 FDA reports)
AREFLEXIA ( 7 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 7 FDA reports)
ATAXIA ( 7 FDA reports)
BLINDNESS TRANSIENT ( 7 FDA reports)
BLOOD CHLORIDE INCREASED ( 7 FDA reports)
BLOOD PH DECREASED ( 7 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 7 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 7 FDA reports)
BLOODY DISCHARGE ( 7 FDA reports)
BONE MARROW TRANSPLANT ( 7 FDA reports)
BRADYARRHYTHMIA ( 7 FDA reports)
BRAIN SCAN ABNORMAL ( 7 FDA reports)
BREAST TENDERNESS ( 7 FDA reports)
CAESAREAN SECTION ( 7 FDA reports)
CATARACT NUCLEAR ( 7 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 7 FDA reports)
COLLAPSE OF LUNG ( 7 FDA reports)
COR PULMONALE ( 7 FDA reports)
CYTOLYTIC HEPATITIS ( 7 FDA reports)
DEAFNESS UNILATERAL ( 7 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 7 FDA reports)
DERMATITIS ALLERGIC ( 7 FDA reports)
DRUG LEVEL DECREASED ( 7 FDA reports)
DYSAESTHESIA ( 7 FDA reports)
DYSPLASIA ( 7 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 7 FDA reports)
EOSINOPHILIA ( 7 FDA reports)
ERECTION INCREASED ( 7 FDA reports)
ESCHAR ( 7 FDA reports)
EXERCISE TEST ABNORMAL ( 7 FDA reports)
FAT EMBOLISM ( 7 FDA reports)
FEELING GUILTY ( 7 FDA reports)
FEMORAL ARTERY OCCLUSION ( 7 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 7 FDA reports)
FOREIGN BODY TRAUMA ( 7 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 7 FDA reports)
GASTROINTESTINAL INFECTION ( 7 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 7 FDA reports)
GINGIVAL ERYTHEMA ( 7 FDA reports)
HELICOBACTER GASTRITIS ( 7 FDA reports)
HEPATIC FIBROSIS ( 7 FDA reports)
HEPATITIS CHOLESTATIC ( 7 FDA reports)
HOSTILITY ( 7 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 7 FDA reports)
HYPOMETABOLISM ( 7 FDA reports)
HYPOTHERMIA ( 7 FDA reports)
IMPAIRED SELF-CARE ( 7 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 7 FDA reports)
INJECTION SITE VESICLES ( 7 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 7 FDA reports)
JUGULAR VEIN DISTENSION ( 7 FDA reports)
LARGE INTESTINE PERFORATION ( 7 FDA reports)
LAZINESS ( 7 FDA reports)
LIBIDO INCREASED ( 7 FDA reports)
LIP BLISTER ( 7 FDA reports)
MEGACOLON ( 7 FDA reports)
MENORRHAGIA ( 7 FDA reports)
METAPLASIA ( 7 FDA reports)
METASTASES TO THE MEDIASTINUM ( 7 FDA reports)
METRORRHAGIA ( 7 FDA reports)
MOUTH HAEMORRHAGE ( 7 FDA reports)
MUSCLE RIGIDITY ( 7 FDA reports)
MYOCARDITIS ( 7 FDA reports)
NEUROGLYCOPENIA ( 7 FDA reports)
NEUROPATHIC ARTHROPATHY ( 7 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 7 FDA reports)
OCULAR DISCOMFORT ( 7 FDA reports)
OESOPHAGEAL SPASM ( 7 FDA reports)
OESOPHAGEAL STENOSIS ( 7 FDA reports)
ORTHOSIS USER ( 7 FDA reports)
OSTEOCHONDROSIS ( 7 FDA reports)
PARTNER STRESS ( 7 FDA reports)
PEAU D'ORANGE ( 7 FDA reports)
PHARYNGEAL ERYTHEMA ( 7 FDA reports)
PHYSIOTHERAPY ( 7 FDA reports)
PLEURISY ( 7 FDA reports)
PRODUCT ADHESION ISSUE ( 7 FDA reports)
PSYCHIATRIC SYMPTOM ( 7 FDA reports)
PULMONARY GRANULOMA ( 7 FDA reports)
PULMONARY HILUM MASS ( 7 FDA reports)
REGURGITATION ( 7 FDA reports)
RENAL HAEMORRHAGE ( 7 FDA reports)
RETINAL VEIN OCCLUSION ( 7 FDA reports)
RHONCHI ( 7 FDA reports)
SALIVARY HYPERSECRETION ( 7 FDA reports)
SCROTAL OEDEMA ( 7 FDA reports)
SEBORRHOEIC DERMATITIS ( 7 FDA reports)
SECRETION DISCHARGE ( 7 FDA reports)
SENSATION OF PRESSURE ( 7 FDA reports)
SENSITIVITY OF TEETH ( 7 FDA reports)
SKIN MASS ( 7 FDA reports)
SKULL FRACTURED BASE ( 7 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 7 FDA reports)
SPINAL CORPECTOMY ( 7 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 7 FDA reports)
STERNAL FRACTURE ( 7 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 7 FDA reports)
TEARFULNESS ( 7 FDA reports)
TENOSYNOVITIS ( 7 FDA reports)
THORACIC OPERATION ( 7 FDA reports)
THROMBOCYTHAEMIA ( 7 FDA reports)
THROMBOSIS IN DEVICE ( 7 FDA reports)
THYROIDITIS ( 7 FDA reports)
TOE DEFORMITY ( 7 FDA reports)
TONGUE BLACK HAIRY ( 7 FDA reports)
UMBILICAL HERNIA ( 7 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 7 FDA reports)
VARICOSE VEIN RUPTURED ( 7 FDA reports)
VEIN DISORDER ( 7 FDA reports)
VERTEBROPLASTY ( 7 FDA reports)
WOUND SECRETION ( 7 FDA reports)
ADNEXA UTERI CYST ( 6 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 6 FDA reports)
ANAL SPHINCTER ATONY ( 6 FDA reports)
AORTIC DISORDER ( 6 FDA reports)
APPENDIX DISORDER ( 6 FDA reports)
APPLICATION SITE RASH ( 6 FDA reports)
APPLICATION SITE REACTION ( 6 FDA reports)
ARTERIAL DISORDER ( 6 FDA reports)
ASTHENOPIA ( 6 FDA reports)
ATROPHY ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
B-CELL LYMPHOMA STAGE I ( 6 FDA reports)
BACTERIA URINE IDENTIFIED ( 6 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 6 FDA reports)
BIPOLAR I DISORDER ( 6 FDA reports)
BLADDER CANCER STAGE III ( 6 FDA reports)
BLADDER MASS ( 6 FDA reports)
BLOOD BICARBONATE DECREASED ( 6 FDA reports)
BLOOD BICARBONATE INCREASED ( 6 FDA reports)
BLOOD GLUCOSE ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 6 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 6 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 6 FDA reports)
BONE MARROW DEPRESSION ( 6 FDA reports)
BRADYPHRENIA ( 6 FDA reports)
BRAIN HERNIATION ( 6 FDA reports)
BRAIN INJURY ( 6 FDA reports)
CALCULUS URINARY ( 6 FDA reports)
CANCER PAIN ( 6 FDA reports)
CARCINOMA IN SITU ( 6 FDA reports)
CARDIAC DEATH ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 6 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 6 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 6 FDA reports)
CHEST WALL MASS ( 6 FDA reports)
CHONDROPATHY ( 6 FDA reports)
COAGULATION TIME PROLONGED ( 6 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 6 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 6 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 6 FDA reports)
DEVICE DISLOCATION ( 6 FDA reports)
DIABETES INSIPIDUS ( 6 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 6 FDA reports)
DISSOCIATION ( 6 FDA reports)
DIVERTICULAR PERFORATION ( 6 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 6 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 6 FDA reports)
EMBOLISM VENOUS ( 6 FDA reports)
ENCEPHALITIS ( 6 FDA reports)
ENDOCARDITIS BACTERIAL ( 6 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 6 FDA reports)
ERYSIPELAS ( 6 FDA reports)
ESCHERICHIA BACTERAEMIA ( 6 FDA reports)
EUPHORIC MOOD ( 6 FDA reports)
FACE INJURY ( 6 FDA reports)
FAECES PALE ( 6 FDA reports)
FAT TISSUE INCREASED ( 6 FDA reports)
FEAR OF DEATH ( 6 FDA reports)
FISTULA REPAIR ( 6 FDA reports)
FLAT AFFECT ( 6 FDA reports)
FOLATE DEFICIENCY ( 6 FDA reports)
FULL BLOOD COUNT DECREASED ( 6 FDA reports)
GALLBLADDER OPERATION ( 6 FDA reports)
GASTRIC OPERATION ( 6 FDA reports)
GENERALISED ANXIETY DISORDER ( 6 FDA reports)
GINGIVAL EROSION ( 6 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 6 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 6 FDA reports)
HAIR TEXTURE ABNORMAL ( 6 FDA reports)
HEART VALVE REPLACEMENT ( 6 FDA reports)
HEPATITIS FULMINANT ( 6 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 6 FDA reports)
HYPERMETABOLISM ( 6 FDA reports)
HYPERPARATHYROIDISM ( 6 FDA reports)
HYPERTONIC BLADDER ( 6 FDA reports)
HYPHAEMA ( 6 FDA reports)
HYPOTRICHOSIS ( 6 FDA reports)
INCISION SITE COMPLICATION ( 6 FDA reports)
INCISION SITE INFECTION ( 6 FDA reports)
INCREASED TENDENCY TO BRUISE ( 6 FDA reports)
INDURATION ( 6 FDA reports)
INJECTION SITE BURNING ( 6 FDA reports)
INTENTIONAL SELF-INJURY ( 6 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 6 FDA reports)
INTESTINAL RESECTION ( 6 FDA reports)
INTRAOCULAR LENS IMPLANT ( 6 FDA reports)
JAW OPERATION ( 6 FDA reports)
LIGAMENT RUPTURE ( 6 FDA reports)
LIP EXFOLIATION ( 6 FDA reports)
LIPOMA EXCISION ( 6 FDA reports)
LOGORRHOEA ( 6 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 6 FDA reports)
MENOMETRORRHAGIA ( 6 FDA reports)
METASTASIS ( 6 FDA reports)
METASTATIC PAIN ( 6 FDA reports)
MITRAL VALVE SCLEROSIS ( 6 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 6 FDA reports)
MUSCLE RUPTURE ( 6 FDA reports)
MYELOMA RECURRENCE ( 6 FDA reports)
NASAL DRYNESS ( 6 FDA reports)
NASAL SEPTAL OPERATION ( 6 FDA reports)
NECK MASS ( 6 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 6 FDA reports)
NEPHROTIC SYNDROME ( 6 FDA reports)
NEUROLOGICAL SYMPTOM ( 6 FDA reports)
NO ADVERSE EFFECT ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER ( 6 FDA reports)
OESOPHAGEAL DILATATION ( 6 FDA reports)
OPEN REDUCTION OF FRACTURE ( 6 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 6 FDA reports)
OROPHARYNGEAL BLISTERING ( 6 FDA reports)
OVARIAN CYST ( 6 FDA reports)
PANCREATIC ENLARGEMENT ( 6 FDA reports)
PAROTID GLAND ENLARGEMENT ( 6 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 6 FDA reports)
PENILE PAIN ( 6 FDA reports)
PERIPHERAL EMBOLISM ( 6 FDA reports)
PERITONEAL DIALYSIS ( 6 FDA reports)
PHARYNGEAL DISORDER ( 6 FDA reports)
PLATELET COUNT ABNORMAL ( 6 FDA reports)
POST-THORACOTOMY PAIN SYNDROME ( 6 FDA reports)
POSTOPERATIVE INFECTION ( 6 FDA reports)
PREAURICULAR CYST ( 6 FDA reports)
PRODUCT ODOUR ABNORMAL ( 6 FDA reports)
PROSTATIC DISORDER ( 6 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 6 FDA reports)
PULMONARY VASCULAR DISORDER ( 6 FDA reports)
PYLORIC STENOSIS ( 6 FDA reports)
RENAL SURGERY ( 6 FDA reports)
RENAL TUBULAR DISORDER ( 6 FDA reports)
RESPIRATORY TRACT IRRITATION ( 6 FDA reports)
RETINAL ISCHAEMIA ( 6 FDA reports)
RETINAL MICROANEURYSMS ( 6 FDA reports)
RIGHT ATRIAL DILATATION ( 6 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 6 FDA reports)
SEPTOPLASTY ( 6 FDA reports)
SEROMA ( 6 FDA reports)
SPINAL HAEMANGIOMA ( 6 FDA reports)
STRESS ULCER ( 6 FDA reports)
SUBCUTANEOUS NODULE ( 6 FDA reports)
SUBILEUS ( 6 FDA reports)
SUFFOCATION FEELING ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 6 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 6 FDA reports)
THYROID MASS ( 6 FDA reports)
TONSILLAR DISORDER ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
TRACHEOSTOMY ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
TREATMENT FAILURE ( 6 FDA reports)
TUBERCULOSIS ( 6 FDA reports)
UMBILICAL CORD AROUND NECK ( 6 FDA reports)
URETERIC DILATATION ( 6 FDA reports)
URINARY TRACT DISORDER ( 6 FDA reports)
VASCULAR INSUFFICIENCY ( 6 FDA reports)
VERTIGO POSITIONAL ( 6 FDA reports)
VITAMIN B12 DECREASED ( 6 FDA reports)
VITH NERVE PARALYSIS ( 6 FDA reports)
ABSCESS BACTERIAL ( 5 FDA reports)
ACCIDENT AT WORK ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
ALDOLASE INCREASED ( 5 FDA reports)
AMBLYOPIA ( 5 FDA reports)
AMNESTIC DISORDER ( 5 FDA reports)
ANAEMIA MACROCYTIC ( 5 FDA reports)
ANIMAL BITE ( 5 FDA reports)
AORTIC ATHEROSCLEROSIS ( 5 FDA reports)
AORTIC VALVE CALCIFICATION ( 5 FDA reports)
APNOEIC ATTACK ( 5 FDA reports)
BACTERIA URINE ( 5 FDA reports)
BARRETT'S OESOPHAGUS ( 5 FDA reports)
BENIGN ANORECTAL NEOPLASM ( 5 FDA reports)
BILIARY DYSKINESIA ( 5 FDA reports)
BLADDER TAMPONADE ( 5 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE 0 ( 5 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 5 FDA reports)
BLOOD COPPER DECREASED ( 5 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 5 FDA reports)
BLOOD SODIUM INCREASED ( 5 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 5 FDA reports)
BLOOD URIC ACID ABNORMAL ( 5 FDA reports)
BREAST ABSCESS ( 5 FDA reports)
BREAST CANCER RECURRENT ( 5 FDA reports)
BREAST DISCHARGE ( 5 FDA reports)
BREAST HYPERPLASIA ( 5 FDA reports)
BREAST SWELLING ( 5 FDA reports)
BRUXISM ( 5 FDA reports)
CACHEXIA ( 5 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 5 FDA reports)
CARCINOID TUMOUR ( 5 FDA reports)
CARDIAC ASTHMA ( 5 FDA reports)
CARDIOPULMONARY FAILURE ( 5 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 5 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 5 FDA reports)
CAROTID ENDARTERECTOMY ( 5 FDA reports)
CEREBELLAR ATROPHY ( 5 FDA reports)
CEREBRAL DISORDER ( 5 FDA reports)
CEREBRAL HAEMATOMA ( 5 FDA reports)
CHOLECYSTITIS INFECTIVE ( 5 FDA reports)
CHROMATOPSIA ( 5 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 5 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 5 FDA reports)
COLON CANCER STAGE I ( 5 FDA reports)
CORONARY ARTERY SURGERY ( 5 FDA reports)
CORONARY ARTERY THROMBOSIS ( 5 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 5 FDA reports)
CREATININE URINE INCREASED ( 5 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 5 FDA reports)
DEVICE LEAKAGE ( 5 FDA reports)
DEVICE OCCLUSION ( 5 FDA reports)
DIABETIC CARDIOMYOPATHY ( 5 FDA reports)
DIABETIC VASCULAR DISORDER ( 5 FDA reports)
DUODENAL STENOSIS ( 5 FDA reports)
DYSCHEZIA ( 5 FDA reports)
EAR DISORDER ( 5 FDA reports)
EFFUSION ( 5 FDA reports)
EMBOLISM ( 5 FDA reports)
ENURESIS ( 5 FDA reports)
ENZYME ABNORMALITY ( 5 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 5 FDA reports)
EROSIVE DUODENITIS ( 5 FDA reports)
ERYSIPELOID ( 5 FDA reports)
EYE BURNS ( 5 FDA reports)
EYE ROLLING ( 5 FDA reports)
EYELIDS PRURITUS ( 5 FDA reports)
FEELING HOT AND COLD ( 5 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 5 FDA reports)
FOOD POISONING ( 5 FDA reports)
FRACTURED COCCYX ( 5 FDA reports)
FRUSTRATION ( 5 FDA reports)
FUNGAL OESOPHAGITIS ( 5 FDA reports)
GALLBLADDER FISTULA ( 5 FDA reports)
GALLBLADDER PAIN ( 5 FDA reports)
GALLBLADDER PERFORATION ( 5 FDA reports)
GASTROINTESTINAL PERFORATION ( 5 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 5 FDA reports)
GASTROINTESTINAL ULCER ( 5 FDA reports)
GASTROOESOPHAGEAL CANCER ( 5 FDA reports)
GESTATIONAL DIABETES ( 5 FDA reports)
GLOMERULONEPHRITIS ( 5 FDA reports)
GLOSSITIS ( 5 FDA reports)
HAEMOGLOBIN INCREASED ( 5 FDA reports)
HEART SOUNDS ABNORMAL ( 5 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 5 FDA reports)
HEMIANOPIA HOMONYMOUS ( 5 FDA reports)
HEPATIC NEOPLASM ( 5 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 5 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 5 FDA reports)
HYPERPHOSPHATAEMIA ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
HYPOCHLORAEMIA ( 5 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 5 FDA reports)
INCORRECT STORAGE OF DRUG ( 5 FDA reports)
INFECTED SKIN ULCER ( 5 FDA reports)
INTERCEPTED MEDICATION ERROR ( 5 FDA reports)
JOINT ARTHROPLASTY ( 5 FDA reports)
KETOSIS ( 5 FDA reports)
LEFT VENTRICULAR FAILURE ( 5 FDA reports)
LICHEN PLANUS ( 5 FDA reports)
LIGAMENT INJURY ( 5 FDA reports)
LIP DRY ( 5 FDA reports)
LOSS OF CONTROL OF LEGS ( 5 FDA reports)
LOSS OF LIBIDO ( 5 FDA reports)
MALABSORPTION ( 5 FDA reports)
MALIGNANT NEOPLASM OF RENAL PELVIS ( 5 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 5 FDA reports)
MAMMOGRAM ABNORMAL ( 5 FDA reports)
MANTLE CELL LYMPHOMA ( 5 FDA reports)
MENINGIOMA ( 5 FDA reports)
MENINGITIS ( 5 FDA reports)
MENINGITIS VIRAL ( 5 FDA reports)
MENSTRUAL DISORDER ( 5 FDA reports)
METASTASES TO PERITONEUM ( 5 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 5 FDA reports)
MICROANGIOPATHY ( 5 FDA reports)
MONOCYTE COUNT INCREASED ( 5 FDA reports)
MOUTH INJURY ( 5 FDA reports)
MYCOSIS FUNGOIDES ( 5 FDA reports)
NASAL SEPTUM DEVIATION ( 5 FDA reports)
NEUROPATHIC PAIN ( 5 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 5 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 5 FDA reports)
OEDEMA MUCOSAL ( 5 FDA reports)
OPTIC ATROPHY ( 5 FDA reports)
OSTEOMYELITIS CHRONIC ( 5 FDA reports)
PANCREAS INFECTION ( 5 FDA reports)
PANCREATIC CYST ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PATELLA FRACTURE ( 5 FDA reports)
PATHOLOGICAL GAMBLING ( 5 FDA reports)
PEMPHIGUS ( 5 FDA reports)
PENILE OEDEMA ( 5 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 5 FDA reports)
PLANTAR FASCIITIS ( 5 FDA reports)
PLEURITIC PAIN ( 5 FDA reports)
PNEUMONIA FUNGAL ( 5 FDA reports)
PNEUMONIA KLEBSIELLA ( 5 FDA reports)
POST PROCEDURAL INFECTION ( 5 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 5 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 5 FDA reports)
PRECANCEROUS SKIN LESION ( 5 FDA reports)
PRODUCT TASTE ABNORMAL ( 5 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 5 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 5 FDA reports)
PSEUDOMONAL SEPSIS ( 5 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 5 FDA reports)
PULSE ABNORMAL ( 5 FDA reports)
PYELONEPHRITIS ACUTE ( 5 FDA reports)
RECTAL POLYP ( 5 FDA reports)
RESPIRATION ABNORMAL ( 5 FDA reports)
RESPIRATORY DEPRESSION ( 5 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 5 FDA reports)
RETINAL NEOVASCULARISATION ( 5 FDA reports)
RETROPERITONEAL FIBROSIS ( 5 FDA reports)
SACROILIITIS ( 5 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 5 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 5 FDA reports)
SEPSIS SYNDROME ( 5 FDA reports)
SKIN NECROSIS ( 5 FDA reports)
SKIN ODOUR ABNORMAL ( 5 FDA reports)
SKIN REACTION ( 5 FDA reports)
SODIUM RETENTION ( 5 FDA reports)
SPERMATOCELE ( 5 FDA reports)
STASIS DERMATITIS ( 5 FDA reports)
STEM CELL TRANSPLANT ( 5 FDA reports)
STRESS SYMPTOMS ( 5 FDA reports)
SUBDURAL HAEMORRHAGE ( 5 FDA reports)
SUNBURN ( 5 FDA reports)
TEETH BRITTLE ( 5 FDA reports)
THERMAL BURN ( 5 FDA reports)
TINEA PEDIS ( 5 FDA reports)
TONGUE OEDEMA ( 5 FDA reports)
TOOTH DISCOLOURATION ( 5 FDA reports)
TORTICOLLIS ( 5 FDA reports)
TRICHORRHEXIS ( 5 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 5 FDA reports)
ULCERATIVE KERATITIS ( 5 FDA reports)
URETERIC OBSTRUCTION ( 5 FDA reports)
URINE ANALYSIS ABNORMAL ( 5 FDA reports)
VASCULAR DEMENTIA ( 5 FDA reports)
VENOUS STASIS ( 5 FDA reports)
WEIGHT ABNORMAL ( 5 FDA reports)
WOUND DEHISCENCE ( 5 FDA reports)
ABORTION ( 4 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
ABSCESS DRAINAGE ( 4 FDA reports)
ACCELERATED HYPERTENSION ( 4 FDA reports)
ACQUIRED NIGHT BLINDNESS ( 4 FDA reports)
ALCOHOL POISONING ( 4 FDA reports)
ALCOHOLIC LIVER DISEASE ( 4 FDA reports)
ALVEOLOPLASTY ( 4 FDA reports)
AMENORRHOEA ( 4 FDA reports)
ANOTIA ( 4 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
APPLICATION SITE IRRITATION ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
B-CELL LYMPHOMA ( 4 FDA reports)
BACTERIAL SEPSIS ( 4 FDA reports)
BASEDOW'S DISEASE ( 4 FDA reports)
BENIGN RENAL NEOPLASM ( 4 FDA reports)
BILIARY TRACT DISORDER ( 4 FDA reports)
BIOPSY ( 4 FDA reports)
BIOPSY SKIN ( 4 FDA reports)
BLADDER ADENOCARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
BLADDER CANCER STAGE I, WITHOUT CANCER IN SITU ( 4 FDA reports)
BLADDER INJURY ( 4 FDA reports)
BLADDER PAIN ( 4 FDA reports)
BLAST CELL COUNT INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 4 FDA reports)
BLOOD CREATININE ( 4 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 4 FDA reports)
BLOOD OSMOLARITY DECREASED ( 4 FDA reports)
BLOOD PH INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 4 FDA reports)
BLOOD URIC ACID DECREASED ( 4 FDA reports)
BODY TINEA ( 4 FDA reports)
BONE GRAFT ( 4 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 4 FDA reports)
BREAST CANCER IN SITU ( 4 FDA reports)
BULIMIA NERVOSA ( 4 FDA reports)
BURNS SECOND DEGREE ( 4 FDA reports)
BURSA DISORDER ( 4 FDA reports)
CARDIAC ANEURYSM ( 4 FDA reports)
CARDIAC VALVE VEGETATION ( 4 FDA reports)
CATHETER RELATED COMPLICATION ( 4 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
CEREBRAL CYST ( 4 FDA reports)
CEREBRAL MICROANGIOPATHY ( 4 FDA reports)
CEREBRAL THROMBOSIS ( 4 FDA reports)
CERVICAL SPINAL STENOSIS ( 4 FDA reports)
CHAPPED LIPS ( 4 FDA reports)
CHEST INJURY ( 4 FDA reports)
CLUBBING ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COELIAC DISEASE ( 4 FDA reports)
COLECTOMY ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
COLITIS MICROSCOPIC ( 4 FDA reports)
COLONIC OBSTRUCTION ( 4 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 4 FDA reports)
CONJUNCTIVAL ABRASION ( 4 FDA reports)
CORNEAL ABRASION ( 4 FDA reports)
CORNEAL REFLEX DECREASED ( 4 FDA reports)
CRUSH INJURY ( 4 FDA reports)
CUSHING'S SYNDROME ( 4 FDA reports)
CYSTITIS HAEMORRHAGIC ( 4 FDA reports)
DEATH OF RELATIVE ( 4 FDA reports)
DENTAL CARE ( 4 FDA reports)
DENTAL FISTULA ( 4 FDA reports)
DEREALISATION ( 4 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 4 FDA reports)
DIABETIC GANGRENE ( 4 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 4 FDA reports)
DISLOCATION OF VERTEBRA ( 4 FDA reports)
DYSLALIA ( 4 FDA reports)
DYSPNOEA AT REST ( 4 FDA reports)
EAR CONGESTION ( 4 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 4 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 4 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 4 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 4 FDA reports)
EXERCISE LACK OF ( 4 FDA reports)
EYE OPERATION COMPLICATION ( 4 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 4 FDA reports)
FOOT OPERATION ( 4 FDA reports)
FRACTURE DISPLACEMENT ( 4 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 4 FDA reports)
GASTRIC VARICES ( 4 FDA reports)
GASTROINTESTINAL CARCINOMA ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
GASTROINTESTINAL SURGERY ( 4 FDA reports)
GENERAL SYMPTOM ( 4 FDA reports)
GILBERT'S SYNDROME ( 4 FDA reports)
GINGIVAL DISCOLOURATION ( 4 FDA reports)
GLARE ( 4 FDA reports)
GROWTH HORMONE DEFICIENCY ( 4 FDA reports)
HAEMATOMA INFECTION ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HALLUCINATIONS, MIXED ( 4 FDA reports)
HANGOVER ( 4 FDA reports)
HEAD AND NECK CANCER ( 4 FDA reports)
HEPATIC ATROPHY ( 4 FDA reports)
HEPATIC MASS ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
HIP SURGERY ( 4 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 4 FDA reports)
HYDROCHOLECYSTIS ( 4 FDA reports)
HYPERPROLACTINAEMIA ( 4 FDA reports)
HYPERREFLEXIA ( 4 FDA reports)
HYPOCHOLESTEROLAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 4 FDA reports)
HYPOPROTEINAEMIA ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
IMPETIGO ( 4 FDA reports)
INAPPROPRIATE AFFECT ( 4 FDA reports)
INCISION SITE PAIN ( 4 FDA reports)
INCLUSION BODY MYOSITIS ( 4 FDA reports)
INJECTION SITE INFECTION ( 4 FDA reports)
INJECTION SITE INFLAMMATION ( 4 FDA reports)
INJECTION SITE INJURY ( 4 FDA reports)
INJURY ASPHYXIATION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 4 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 4 FDA reports)
KERATOACANTHOMA ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
LABILE HYPERTENSION ( 4 FDA reports)
LARGE INTESTINAL ULCER ( 4 FDA reports)
LARYNGEAL DISORDER ( 4 FDA reports)
LEUKOPLAKIA ORAL ( 4 FDA reports)
LICHEN SCLEROSUS ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
LUNG ABSCESS ( 4 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 4 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 4 FDA reports)
MAMMARY DUCT ECTASIA ( 4 FDA reports)
MASTOIDITIS ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
METASTASES TO KIDNEY ( 4 FDA reports)
METASTATIC LYMPHOMA ( 4 FDA reports)
MIDDLE EAR EFFUSION ( 4 FDA reports)
MITRAL VALVE STENOSIS ( 4 FDA reports)
MOTION SICKNESS ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
MUSCLE FATIGUE ( 4 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 4 FDA reports)
MYOSCLEROSIS ( 4 FDA reports)
NAIL HYPERTROPHY ( 4 FDA reports)
NECROTISING COLITIS ( 4 FDA reports)
NEUROGENIC BOWEL ( 4 FDA reports)
NEUROMA ( 4 FDA reports)
NEUROSIS ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 4 FDA reports)
OCULAR HYPERTENSION ( 4 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 4 FDA reports)
OESOPHAGEAL PAIN ( 4 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 4 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 4 FDA reports)
ORTHOPEDIC PROCEDURE ( 4 FDA reports)
PAINFUL RESPIRATION ( 4 FDA reports)
PAROTITIS ( 4 FDA reports)
PCO2 DECREASED ( 4 FDA reports)
PERICARDIAL HAEMORRHAGE ( 4 FDA reports)
PERINEURIAL CYST ( 4 FDA reports)
PERSECUTORY DELUSION ( 4 FDA reports)
PETIT MAL EPILEPSY ( 4 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 4 FDA reports)
PITUITARY TUMOUR BENIGN ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PNEUMOCOCCAL INFECTION ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
PNEUMONIA NECROTISING ( 4 FDA reports)
POLYCYTHAEMIA ( 4 FDA reports)
PORTAL VEIN THROMBOSIS ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
POST PROCEDURAL HAEMATURIA ( 4 FDA reports)
POSTOPERATIVE FEVER ( 4 FDA reports)
PREMATURE LABOUR ( 4 FDA reports)
PRESSURE OF SPEECH ( 4 FDA reports)
PRIAPISM ( 4 FDA reports)
PROTHROMBIN TIME SHORTENED ( 4 FDA reports)
PULMONARY HYPOPLASIA ( 4 FDA reports)
PYURIA ( 4 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 4 FDA reports)
RECTAL CANCER STAGE III ( 4 FDA reports)
RECTOCELE ( 4 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 4 FDA reports)
RENAL FAILURE NEONATAL ( 4 FDA reports)
RENAL OSTEODYSTROPHY ( 4 FDA reports)
RENAL TRANSPLANT ( 4 FDA reports)
RESIDUAL URINE ( 4 FDA reports)
RETINAL ARTERY OCCLUSION ( 4 FDA reports)
RETINAL ARTERY THROMBOSIS ( 4 FDA reports)
RETINAL TEAR ( 4 FDA reports)
RETROGRADE AMNESIA ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 4 FDA reports)
SERRATIA BACTERAEMIA ( 4 FDA reports)
SERRATIA SEPSIS ( 4 FDA reports)
SKIN CANDIDA ( 4 FDA reports)
SKIN PLAQUE ( 4 FDA reports)
SOCIAL PHOBIA ( 4 FDA reports)
SOFT TISSUE INFECTION ( 4 FDA reports)
SPINAL CORD DISORDER ( 4 FDA reports)
SPINAL CORD INJURY ( 4 FDA reports)
STENT OCCLUSION ( 4 FDA reports)
STENT-GRAFT MALFUNCTION ( 4 FDA reports)
STRESS URINARY INCONTINENCE ( 4 FDA reports)
STUPOR ( 4 FDA reports)
SUBCUTANEOUS ABSCESS ( 4 FDA reports)
SUICIDAL BEHAVIOUR ( 4 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 4 FDA reports)
THERAPY CESSATION ( 4 FDA reports)
TONGUE BITING ( 4 FDA reports)
TONGUE COATED ( 4 FDA reports)
TONGUE HAEMORRHAGE ( 4 FDA reports)
TOOTH REPAIR ( 4 FDA reports)
TOXIC NODULAR GOITRE ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TRACHEAL STENOSIS ( 4 FDA reports)
TUBERCULIN TEST POSITIVE ( 4 FDA reports)
TUBERCULOUS PLEURISY ( 4 FDA reports)
UPPER EXTREMITY MASS ( 4 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 4 FDA reports)
URETHRAL PAIN ( 4 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 4 FDA reports)
URINE COLOUR ABNORMAL ( 4 FDA reports)
UTERINE POLYP ( 4 FDA reports)
VAGINAL DISCHARGE ( 4 FDA reports)
VAGINITIS ( 4 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 4 FDA reports)
VENOUS OCCLUSION ( 4 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 4 FDA reports)
VIRAL PERICARDITIS ( 4 FDA reports)
VISUAL BRIGHTNESS ( 4 FDA reports)
VOMITING PROJECTILE ( 4 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 4 FDA reports)
WHITE BLOOD CELL COUNT ( 4 FDA reports)
X-RAY ABNORMAL ( 4 FDA reports)
YELLOW SKIN ( 4 FDA reports)
ZINC DEFICIENCY ( 4 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 3 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 3 FDA reports)
ACCOMMODATION DISORDER ( 3 FDA reports)
ACHLORHYDRIA ( 3 FDA reports)
ACQUIRED MACROGLOSSIA ( 3 FDA reports)
ACROMEGALY ( 3 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ACUTE LUNG INJURY ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
ACUTE PSYCHOSIS ( 3 FDA reports)
ADRENAL NEOPLASM ( 3 FDA reports)
AGORAPHOBIA ( 3 FDA reports)
AKINESIA ( 3 FDA reports)
ALBUMINURIA ( 3 FDA reports)
ALVEOLITIS ALLERGIC ( 3 FDA reports)
ANAEMIA MEGALOBLASTIC ( 3 FDA reports)
ANAL FUNGAL INFECTION ( 3 FDA reports)
ANENCEPHALY ( 3 FDA reports)
ANEURYSM RUPTURED ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
ANORECTAL DISCOMFORT ( 3 FDA reports)
ANOXIA ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
AORTIC VALVE REPLACEMENT ( 3 FDA reports)
APLASIA ( 3 FDA reports)
APPLICATION SITE DERMATITIS ( 3 FDA reports)
APPLICATION SITE PAIN ( 3 FDA reports)
ARTERIOVENOUS FISTULA ( 3 FDA reports)
ASEPTIC NECROSIS BONE ( 3 FDA reports)
ATHERECTOMY ( 3 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 3 FDA reports)
AUTOIMMUNE PANCREATITIS ( 3 FDA reports)
AXILLARY MASS ( 3 FDA reports)
BACTERIAL TEST POSITIVE ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 3 FDA reports)
BILIARY FIBROSIS ( 3 FDA reports)
BIOPSY BILE DUCT ABNORMAL ( 3 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 3 FDA reports)
BIOPSY BREAST ( 3 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 3 FDA reports)
BLADDER CATHETERISATION ( 3 FDA reports)
BLADDER DISCOMFORT ( 3 FDA reports)
BLADDER DYSFUNCTION ( 3 FDA reports)
BLADDER PROLAPSE ( 3 FDA reports)
BLADDER SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD CALCIUM ABNORMAL ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD ELASTASE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 3 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 3 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 3 FDA reports)
BLOOD PRESSURE ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
BONE CANCER METASTATIC ( 3 FDA reports)
BONE FISSURE ( 3 FDA reports)
BONE MARROW DISORDER ( 3 FDA reports)
BONE MARROW TOXICITY ( 3 FDA reports)
BORDERLINE GLAUCOMA ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BRAIN STEM STROKE ( 3 FDA reports)
BREAKTHROUGH PAIN ( 3 FDA reports)
BREAST DISCOMFORT ( 3 FDA reports)
BREAST DISORDER ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BUNION ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARBUNCLE ( 3 FDA reports)
CARCINOID TUMOUR OF THE PANCREAS ( 3 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 3 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
CEREBELLAR SYNDROME ( 3 FDA reports)
CEREBRAL ARTERIOVENOUS MALFORMATION HAEMORRHAGIC ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CEREBROVASCULAR STENOSIS ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CHEST WALL PAIN ( 3 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 3 FDA reports)
CHONDROMALACIA ( 3 FDA reports)
CHOREA ( 3 FDA reports)
CLAUSTROPHOBIA ( 3 FDA reports)
CLONUS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 3 FDA reports)
COLON ADENOMA ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 3 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 3 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 3 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 3 FDA reports)
CONTRAST MEDIA ALLERGY ( 3 FDA reports)
CORNEAL OPACITY ( 3 FDA reports)
CORYNEBACTERIUM INFECTION ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
CUBITAL TUNNEL SYNDROME ( 3 FDA reports)
CULTURE WOUND POSITIVE ( 3 FDA reports)
CUTANEOUS VASCULITIS ( 3 FDA reports)
CYSTOCELE ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DECREASED INSULIN REQUIREMENT ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DERMATITIS ATOPIC ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 3 FDA reports)
DIABETIC GASTROENTEROPATHY ( 3 FDA reports)
DIABETIC GASTROPATHY ( 3 FDA reports)
DIABETIC ULCER ( 3 FDA reports)
DIET REFUSAL ( 3 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DRUG TOLERANCE DECREASED ( 3 FDA reports)
DYSPAREUNIA ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
DYSTHYMIC DISORDER ( 3 FDA reports)
EAR CANAL ABRASION ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 3 FDA reports)
EMPYEMA ( 3 FDA reports)
ENCEPHALOMALACIA ( 3 FDA reports)
ENDOMETRIAL CANCER ( 3 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 3 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 3 FDA reports)
EPIDIDYMITIS ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
ESSENTIAL TREMOR ( 3 FDA reports)
EXCITABILITY ( 3 FDA reports)
EXFOLIATIVE RASH ( 3 FDA reports)
EXTRADURAL HAEMATOMA ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
FACIAL WASTING ( 3 FDA reports)
FEAR OF DISEASE ( 3 FDA reports)
FEBRILE BONE MARROW APLASIA ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
FOOD INTOLERANCE ( 3 FDA reports)
FOREARM FRACTURE ( 3 FDA reports)
FRACTURE NONUNION ( 3 FDA reports)
GALLBLADDER ENLARGEMENT ( 3 FDA reports)
GALLBLADDER INJURY ( 3 FDA reports)
GASTROINTESTINAL EROSION ( 3 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 3 FDA reports)
GENITAL HAEMORRHAGE ( 3 FDA reports)
GIGANTISM ( 3 FDA reports)
GLOBULINS INCREASED ( 3 FDA reports)
GLOMERULOSCLEROSIS ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMOGLOBIN ( 3 FDA reports)
HAEMORRHAGE URINARY TRACT ( 3 FDA reports)
HAIR COLOUR CHANGES ( 3 FDA reports)
HANTAVIRAL INFECTION ( 3 FDA reports)
HEPATIC CALCIFICATION ( 3 FDA reports)
HEPATIC CONGESTION ( 3 FDA reports)
HEPATIC HAEMORRHAGE ( 3 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HIP SWELLING ( 3 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPERINSULINAEMIA ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPERLACTACIDAEMIA ( 3 FDA reports)
HYPEROSMOLAR STATE ( 3 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 3 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 3 FDA reports)
HYPERTENSIVE EMERGENCY ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPOCHROMIC ANAEMIA ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
INTESTINAL HAEMATOMA ( 3 FDA reports)
INTESTINAL HAEMORRHAGE ( 3 FDA reports)
ISCHAEMIC HEPATITIS ( 3 FDA reports)
KIDNEY FIBROSIS ( 3 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 3 FDA reports)
LARYNGEAL CANCER ( 3 FDA reports)
LIGAMENT DISORDER ( 3 FDA reports)
LIMB CRUSHING INJURY ( 3 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 3 FDA reports)
LIPIDS ABNORMAL ( 3 FDA reports)
LIPOMATOSIS ( 3 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LOSS OF PROPRIOCEPTION ( 3 FDA reports)
LUNG ADENOCARCINOMA ( 3 FDA reports)
LYME DISEASE ( 3 FDA reports)
LYMPHADENITIS ( 3 FDA reports)
MACULAR ISCHAEMIA ( 3 FDA reports)
MACULAR PSEUDOHOLE ( 3 FDA reports)
MEDIASTINAL MASS ( 3 FDA reports)
MEDICAL DEVICE REMOVAL ( 3 FDA reports)
MENIERE'S DISEASE ( 3 FDA reports)
MENOPAUSAL SYMPTOMS ( 3 FDA reports)
METATARSALGIA ( 3 FDA reports)
MICTURITION FREQUENCY DECREASED ( 3 FDA reports)
MIGRAINE WITH AURA ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MONOPARESIS ( 3 FDA reports)
MOUTH BREATHING ( 3 FDA reports)
MUCOSA VESICLE ( 3 FDA reports)
MUCOSAL DRYNESS ( 3 FDA reports)
MUCOUS STOOLS ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MUSCLE MASS ( 3 FDA reports)
MUSCLE NECROSIS ( 3 FDA reports)
MUSCLE SPASTICITY ( 3 FDA reports)
MYOGLOBIN URINE PRESENT ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NASAL SINUS DRAINAGE ( 3 FDA reports)
NASOPHARYNGEAL DISORDER ( 3 FDA reports)
NEGATIVISM ( 3 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
NEOVASCULARISATION ( 3 FDA reports)
NEPHRITIS ALLERGIC ( 3 FDA reports)
NEPHROCALCINOSIS ( 3 FDA reports)
NEUROENDOCRINE CARCINOMA ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUTROPHIL COUNT ( 3 FDA reports)
NIGHT BLINDNESS ( 3 FDA reports)
NO ADVERSE REACTION ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
OCULAR NEOPLASM ( 3 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 3 FDA reports)
OLIGOMENORRHOEA ( 3 FDA reports)
OPTIC DISC DISORDER ( 3 FDA reports)
OPTIC NEUROPATHY ( 3 FDA reports)
OROPHARYNGEAL SWELLING ( 3 FDA reports)
OVARIAN ABSCESS ( 3 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PAIN EXACERBATED ( 3 FDA reports)
PANCREATIC ABSCESS ( 3 FDA reports)
PANCREATIC CALCIFICATION ( 3 FDA reports)
PANCREATIC INJURY ( 3 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 3 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 3 FDA reports)
PANOPHTHALMITIS ( 3 FDA reports)
PELVIC NEOPLASM ( 3 FDA reports)
PERICARDIAL DISEASE ( 3 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 3 FDA reports)
PHYSICAL ASSAULT ( 3 FDA reports)
PLATELET COUNT ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
PNEUMOMEDIASTINUM ( 3 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 3 FDA reports)
PNEUMONIA MYCOPLASMAL ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
POLYP COLORECTAL ( 3 FDA reports)
POLYTRAUMATISM ( 3 FDA reports)
POST PROCEDURAL DIARRHOEA ( 3 FDA reports)
POST PROCEDURAL PAIN ( 3 FDA reports)
POSTMENOPAUSE ( 3 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PREMENSTRUAL SYNDROME ( 3 FDA reports)
PROCEDURAL SITE REACTION ( 3 FDA reports)
PROSTATIC OBSTRUCTION ( 3 FDA reports)
PROTEUS INFECTION ( 3 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
PSYCHOMOTOR RETARDATION ( 3 FDA reports)
PUBIC RAMI FRACTURE ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 3 FDA reports)
PUPIL FIXED ( 3 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
RECTAL CANCER METASTATIC ( 3 FDA reports)
RECTAL FISTULA REPAIR ( 3 FDA reports)
RECTAL TENESMUS ( 3 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
RENAL ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL ISCHAEMIA ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
REPETITIVE SPEECH ( 3 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
RETINAL ARTERY EMBOLISM ( 3 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 3 FDA reports)
SALIVARY GLAND NEOPLASM ( 3 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 3 FDA reports)
SCLERITIS ( 3 FDA reports)
SCROTAL PAIN ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SEPTIC EMBOLUS ( 3 FDA reports)
SHOULDER OPERATION ( 3 FDA reports)
SIGMOIDECTOMY ( 3 FDA reports)
SINOATRIAL BLOCK ( 3 FDA reports)
SINUS POLYP ( 3 FDA reports)
SKIN CHAPPED ( 3 FDA reports)
SKIN DESQUAMATION ( 3 FDA reports)
SLEEP WALKING ( 3 FDA reports)
SOMATOFORM DISORDER ( 3 FDA reports)
SPINAL OPERATION ( 3 FDA reports)
SPLENIC INFARCTION ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 3 FDA reports)
STARING ( 3 FDA reports)
STATUS ASTHMATICUS ( 3 FDA reports)
STRESS AT WORK ( 3 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
TENDON OPERATION ( 3 FDA reports)
TESTICULAR DISORDER ( 3 FDA reports)
TESTICULAR SWELLING ( 3 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 3 FDA reports)
THERAPY REGIMEN CHANGED ( 3 FDA reports)
THROAT LESION ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
THYROID ADENOMA ( 3 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 3 FDA reports)
TOBACCO ABUSE ( 3 FDA reports)
TONGUE PARALYSIS ( 3 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 3 FDA reports)
TRANSFUSION ( 3 FDA reports)
TRANSITIONAL CELL CANCER OF THE RENAL PELVIS AND URETER ( 3 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 3 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
TUMOUR COMPRESSION ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
URETHRAL CANCER ( 3 FDA reports)
URETHRAL MEATUS STENOSIS ( 3 FDA reports)
URETHRAL STENOSIS ( 3 FDA reports)
URINARY TRACT NEOPLASM ( 3 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 3 FDA reports)
VALVULOPLASTY CARDIAC ( 3 FDA reports)
VERTEBRAL INJURY ( 3 FDA reports)
VESTIBULAR DISORDER ( 3 FDA reports)
VESTIBULAR NEURONITIS ( 3 FDA reports)
VIRAL LOAD INCREASED ( 3 FDA reports)
VIRAL PHARYNGITIS ( 3 FDA reports)
VITRECTOMY ( 3 FDA reports)
VOLVULUS ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ABDOMINOPLASTY ( 2 FDA reports)
ACCESSORY NAVICULAR SYNDROME ( 2 FDA reports)
ACETONAEMIA ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADENOMYOSIS ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADJUSTMENT DISORDER ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ADRENAL HAEMORRHAGE ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
ALBUMIN URINE ( 2 FDA reports)
ALCOHOLIC PANCREATITIS ( 2 FDA reports)
ALLERGENIC DESENSITISATION PROCEDURE ( 2 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
AMAUROSIS ( 2 FDA reports)
AMPUTATION ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
AMYOTROPHY ( 2 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANDROGEN DEFICIENCY ( 2 FDA reports)
ANIMAL SCRATCH ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
ANXIETY POSTOPERATIVE ( 2 FDA reports)
AORTIC OCCLUSION ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTERIAL RESTENOSIS ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASTIGMATISM ( 2 FDA reports)
ATHETOSIS ( 2 FDA reports)
ATROPHIC VULVOVAGINITIS ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AVULSION FRACTURE ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACILLUS TEST POSITIVE ( 2 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BENIGN CARDIAC NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BILE DUCT STENT INSERTION ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BILIRUBIN URINE ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER CANCER STAGE IV ( 2 FDA reports)
BLADDER DYSPLASIA ( 2 FDA reports)
BLADDER HYPERTROPHY ( 2 FDA reports)
BLADDER PAPILLOMA ( 2 FDA reports)
BLADDER SPASM ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA RECURRENT ( 2 FDA reports)
BLISTER INFECTED ( 2 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 2 FDA reports)
BLOOD AMYLASE ( 2 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD GALACTOSE ABNORMAL ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD GROWTH HORMONE DECREASED ( 2 FDA reports)
BLOOD KETONE BODY ( 2 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 2 FDA reports)
BLOOD SODIUM ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 2 FDA reports)
BODY MASS INDEX INCREASED ( 2 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BREAST HAEMATOMA ( 2 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
CALCIUM METABOLISM DISORDER ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CAPILLARY DISORDER ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
CARBON DIOXIDE ABNORMAL ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARCINOMA ( 2 FDA reports)
CARDIAC DISCOMFORT ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 2 FDA reports)
CARDITIS ( 2 FDA reports)
CAROTID ARTERY DISSECTION ( 2 FDA reports)
CAROTID ARTERY STENT INSERTION ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CATATONIA ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CERVICAL CORD COMPRESSION ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CHLOROPSIA ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 2 ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
CITROBACTER TEST POSITIVE ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COITAL BLEEDING ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 2 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
COMPULSIONS ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
CONFUSION POSTOPERATIVE ( 2 FDA reports)
CONGENITAL ABSENCE OF CRANIAL VAULT ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORONARY ARTERY EMBOLISM ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 2 FDA reports)
COXSACKIE VIRUS TEST POSITIVE ( 2 FDA reports)
CRACKLES LUNG ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 2 FDA reports)
CRYSTAL ARTHROPATHY ( 2 FDA reports)
CSF CELL COUNT INCREASED ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
CYSTOSCOPY ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DAWN PHENOMENON ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DELUSION OF GRANDEUR ( 2 FDA reports)
DELUSIONAL DISORDER, EROTOMANIC TYPE ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DIABETIC BLINDNESS ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIASTOLIC HYPERTENSION ( 2 FDA reports)
DISSOCIATIVE AMNESIA ( 2 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DUODENAL POLYP ( 2 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 2 FDA reports)
ECZEMA ASTEATOTIC ( 2 FDA reports)
EJACULATION DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EPULIS ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
EXCESSIVE EXERCISE ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
EXPOSURE TO CONTAMINATED AIR ( 2 FDA reports)
EYE ALLERGY ( 2 FDA reports)
EYE INFECTION FUNGAL ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYELID IRRITATION ( 2 FDA reports)
FACIAL SPASM ( 2 FDA reports)
FACTITIOUS DISORDER ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FAECAL VOLUME DECREASED ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FAT REDISTRIBUTION ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 2 FDA reports)
FEMORAL ARTERY ANEURYSM ( 2 FDA reports)
FEMORAL NERVE INJURY ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FLOPPY IRIS SYNDROME ( 2 FDA reports)
FOETAL GROWTH RESTRICTION ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
GALLSTONE ILEUS ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTRODUODENAL HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
GINGIVAL RECESSION ( 2 FDA reports)
GLOMUS TUMOUR ( 2 FDA reports)
GRAFT COMPLICATION ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GRANULOCYTOSIS ( 2 FDA reports)
GRANULOMA ANNULARE ( 2 FDA reports)
GREENSTICK FRACTURE ( 2 FDA reports)
GRIEF REACTION ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HALLUCINATION, OLFACTORY ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART VALVE CALCIFICATION ( 2 FDA reports)
HEAT ILLNESS ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEPATIC ENZYME DECREASED ( 2 FDA reports)
HEPATIC INFECTION ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 2 FDA reports)
HEPATIC PAIN ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HEPATITIS C POSITIVE ( 2 FDA reports)
HEPATOJUGULAR REFLUX ( 2 FDA reports)
HERPES OESOPHAGITIS ( 2 FDA reports)
HERPES PHARYNGITIS ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HOSPICE CARE ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPOALDOSTERONISM ( 2 FDA reports)
HYPOCHONDRIASIS ( 2 FDA reports)
HYPOURICAEMIA ( 2 FDA reports)
HYPOVITAMINOSIS ( 2 FDA reports)
IGA NEPHROPATHY ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
ILLITERACY ( 2 FDA reports)
IMMOBILISATION PROLONGED ( 2 FDA reports)
IMMUNOGLOBULINS INCREASED ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
IMPLANT SITE PAIN ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INCISION SITE ABSCESS ( 2 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFECTIVE GLOSSITIS ( 2 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 2 FDA reports)
INJECTION SITE PARAESTHESIA ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INSULIN C-PEPTIDE DECREASED ( 2 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 2 FDA reports)
INTENSIVE CARE ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTERVERTEBRAL DISC CALCIFICATION ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 2 FDA reports)
IODINE ALLERGY ( 2 FDA reports)
ISCHAEMIC NEUROPATHY ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LIBIDO DISORDER ( 2 FDA reports)
LID LAG ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LIP INJURY ( 2 FDA reports)
LIPIDOSIS ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LITHOTRIPSY ( 2 FDA reports)
LIVER TENDERNESS ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 2 FDA reports)
LOWER LIMB DEFORMITY ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
MAGNESIUM DEFICIENCY ( 2 FDA reports)
MALIGNANT NEOPLASM OF LACRIMAL DUCT ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MAMMOPLASTY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MEDIASTINUM NEOPLASM ( 2 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 2 FDA reports)
MENISCUS REMOVAL ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MENTAL DISABILITY ( 2 FDA reports)
MERALGIA PARAESTHETICA ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METASTASES TO PANCREAS ( 2 FDA reports)
METASTASES TO RETROPERITONEUM ( 2 FDA reports)
METASTASES TO SKIN ( 2 FDA reports)
MIXED HYPERLIPIDAEMIA ( 2 FDA reports)
MIXED RECEPTIVE-EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
MOANING ( 2 FDA reports)
MONONEUROPATHY MULTIPLEX ( 2 FDA reports)
MONONUCLEOSIS SYNDROME ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MUSCLE ENZYME INCREASED ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYOCARDIAL STRAIN ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
MYOPIA ( 2 FDA reports)
NAIL DYSTROPHY ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NEAR DROWNING ( 2 FDA reports)
NEEDLE ISSUE ( 2 FDA reports)
NEONATAL ASPHYXIA ( 2 FDA reports)
NEONATAL HYPOXIA ( 2 FDA reports)
NERVE ROOT INJURY LUMBAR ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OCULAR MYASTHENIA ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OLIGOHYDRAMNIOS ( 2 FDA reports)
ONYCHALGIA ( 2 FDA reports)
ONYCHOMADESIS ( 2 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
ORAL CAVITY FISTULA ( 2 FDA reports)
ORAL FIBROMA ( 2 FDA reports)
ORAL LICHEN PLANUS ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
ORTHOSTATIC HYPERTENSION ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
OTITIS MEDIA CHRONIC ( 2 FDA reports)
OVARIAN NEOPLASM ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PALLANAESTHESIA ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PANCREATIC CARCINOMA RECURRENT ( 2 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 2 FDA reports)
PANCREATIC NECROSIS ( 2 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 2 FDA reports)
PAPILLITIS ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARATHYROID TUMOUR BENIGN ( 2 FDA reports)
PARATHYROIDECTOMY ( 2 FDA reports)
PARKINSONIAN REST TREMOR ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIDIVERTICULAR ABSCESS ( 2 FDA reports)
PERIODONTAL OPERATION ( 2 FDA reports)
PERIPHERAL NERVE OPERATION ( 2 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PERITONEAL TUBERCULOSIS ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PHANTOM PAIN ( 2 FDA reports)
PHIMOSIS ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PICKWICKIAN SYNDROME ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLACENTAL INSUFFICIENCY ( 2 FDA reports)
PNEUMATURIA ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POST PROCEDURAL OEDEMA ( 2 FDA reports)
POST-TRAUMATIC HEADACHE ( 2 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PRECANCEROUS CELLS PRESENT ( 2 FDA reports)
PRESENILE DEMENTIA ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
PROSTATE CANCER STAGE II ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSEUDOCYST ( 2 FDA reports)
PSEUDOENDOPHTHALMITIS ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 2 FDA reports)
PUTAMEN HAEMORRHAGE ( 2 FDA reports)
PYOTHORAX ( 2 FDA reports)
RADIATION INJURY ( 2 FDA reports)
RADIATION OESOPHAGITIS ( 2 FDA reports)
RADICULITIS ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RECTOSIGMOID CANCER ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED BLOOD CELL ELLIPTOCYTES PRESENT ( 2 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL CANCER METASTATIC ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
RESORPTION BONE INCREASED ( 2 FDA reports)
RESPIRATORY FATIGUE ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
RETINOPATHY BACKGROUND ( 2 FDA reports)
RETINOPATHY PROLIFERATIVE ( 2 FDA reports)
RHEUMATIC HEART DISEASE ( 2 FDA reports)
RIFT VALLEY FEVER ( 2 FDA reports)
SALPINGO-OOPHORITIS ( 2 FDA reports)
SCAN ABDOMEN ABNORMAL ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 2 FDA reports)
SCAR EXCISION ( 2 FDA reports)
SCIATIC NERVE NEUROPATHY ( 2 FDA reports)
SCLERODACTYLIA ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SEMEN VOLUME DECREASED ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
SHOPLIFTING ( 2 FDA reports)
SKIN DISCOMFORT ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
SKIN TEST POSITIVE ( 2 FDA reports)
SKIN TURGOR DECREASED ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SOFT TISSUE NECROSIS ( 2 FDA reports)
SPERM COUNT DECREASED ( 2 FDA reports)
SPINAL CORD INJURY CERVICAL ( 2 FDA reports)
SPINAL CORD NEOPLASM ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPINAL LAMINECTOMY ( 2 FDA reports)
SPINOCEREBELLAR DISORDER ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
STENT RELATED INFECTION ( 2 FDA reports)
STOMACH MASS ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUBSTANCE ABUSE ( 2 FDA reports)
SUDDEN ONSET OF SLEEP ( 2 FDA reports)
SUPERFICIAL INJURY OF EYE ( 2 FDA reports)
SURGICAL FAILURE ( 2 FDA reports)
SWEAT GLAND DISORDER ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
TALIPES ( 2 FDA reports)
TENDON INJURY ( 2 FDA reports)
TENOSYNOVITIS STENOSANS ( 2 FDA reports)
TESTICULAR MASS ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THALAMUS HAEMORRHAGE ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 2 FDA reports)
THIRST DECREASED ( 2 FDA reports)
THROAT CANCER ( 2 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 2 FDA reports)
TINEA INFECTION ( 2 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 2 FDA reports)
TOE WALKING ( 2 FDA reports)
TONGUE GEOGRAPHIC ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TRAUMATIC AMPUTATION ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TUMOUR FLARE ( 2 FDA reports)
TUMOUR INVASION ( 2 FDA reports)
TUMOUR PAIN ( 2 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
URINARY TRACT PAIN ( 2 FDA reports)
URTICARIA GENERALISED ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
UTERINE SPASM ( 2 FDA reports)
VAGINAL BURNING SENSATION ( 2 FDA reports)
VAGINAL CYST ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VASCULAR BYPASS GRAFT ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 2 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
VITAL CAPACITY DECREASED ( 2 FDA reports)
VULVAL ABSCESS ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
WEIGHT ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WHITE CLOT SYNDROME ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
X-RAY LIMB ABNORMAL ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABORTION THREATENED ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABSCESS OF EXTERNAL AUDITORY MEATUS ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACQUIRED CLAW TOE ( 1 FDA reports)
ACQUIRED PHIMOSIS ( 1 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ADENOIDAL HYPERTROPHY ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
AEROMONA INFECTION ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALKALOSIS HYPOCHLORAEMIC ( 1 FDA reports)
ALLERGIC BRONCHITIS ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALVEOLAR PROTEINOSIS ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMMONIA ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANALGESIA ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANDROGEN INSENSITIVITY SYNDROME ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOGRAM PULMONARY ABNORMAL ( 1 FDA reports)
ANGIOSARCOMA ( 1 FDA reports)
ANOGENITAL DYSPLASIA ( 1 FDA reports)
ANORECTAL INFECTION BACTERIAL ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTI-HBC IGM ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTIC BIFURCATION GRAFT ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTOGRAM ABNORMAL ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE DESQUAMATION ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE ODOUR ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE PUSTULES ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARRHYTHMIA NEONATAL ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL GRAFT ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASPERMIA ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA WOUND IDENTIFIED ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BARIUM SWALLOW ABNORMAL ( 1 FDA reports)
BARREL CHEST ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BASILAR ARTERY STENOSIS ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 1 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 1 FDA reports)
BENIGN TUMOUR EXCISION ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIOPSY BONE ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 1 FDA reports)
BIOPSY UTERUS ABNORMAL ( 1 FDA reports)
BISEXUALITY ( 1 FDA reports)
BLADDER CANCER STAGE I, WITH CANCER IN SITU ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER IRRITATION ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLADDER SPHINCTER ATONY ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA METASTATIC ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CALCITONIN ABNORMAL ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD GASTRIN INCREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD INSULIN ABNORMAL ( 1 FDA reports)
BLOOD INSULIN DECREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD KETONE BODY INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE FREE INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE CALLUS EXCESSIVE ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW OEDEMA SYNDROME ( 1 FDA reports)
BONE METABOLISM DISORDER ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BOWEL PREPARATION ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN MALFORMATION ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST DISORDER MALE ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 1 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BULLOUS IMPETIGO ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CALCIUM IONISED ABNORMAL ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 1 FDA reports)
CARDIAC PACEMAKER REVISION ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC SARCOIDOSIS ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC STRESS TEST NORMAL ( 1 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ABNORMAL ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 1 FDA reports)
CAROTID ARTERY BYPASS ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATARACT TRAUMATIC ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEPHALHAEMATOMA ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHORDOMA ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHROMOSOMAL MUTATION ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 1 FDA reports)
CLEFT LIP ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON CANCER RECURRENT ( 1 FDA reports)
COLON CANCER STAGE III ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVAL NEOPLASM ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COPROLALIA ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 1 FDA reports)
CORNEAL STAPHYLOMA ( 1 FDA reports)
CORNEAL STRIAE ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYSTITIS INTERSTITIAL ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYSTOSTOMY ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMABRASION ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DERMOGRAPHISM ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE DEPLOYMENT ISSUE ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETES COMPLICATING PREGNANCY ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DISUSE SYNDROME ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSHIDROSIS ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
EAR CANAL INJURY ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROCARDIOGRAM U-WAVE ABNORMALITY ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPIDIDYMAL CYST ( 1 FDA reports)
EPIDURAL INJECTION ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPINEPHRINE INCREASED ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHROBLAST COUNT DECREASED ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EX-SMOKER ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE IRRIGATION ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELID RETRACTION ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FASCIOTOMY ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FIBROMATOSIS ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FOLLICULAR THYROID CANCER ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FREE FATTY ACIDS INCREASED ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL CYSTITIS ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLBLADDER CANCER METASTATIC ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC CANCER STAGE III ( 1 FDA reports)
GASTRIC CANCER STAGE IV WITH METASTASES ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRITIS VIRAL ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST NEGATIVE ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GINGIVAL CYST ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPATIC ADENOMA ( 1 FDA reports)
HEPATIC CANCER STAGE IV ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS A POSITIVE ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HERNIA GANGRENOUS ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES SIMPLEX DNA TEST POSITIVE ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HORSESHOE KIDNEY ( 1 FDA reports)
HTLV-2 TEST POSITIVE ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERMAGNESAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPO HDL CHOLESTEROLAEMIA ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOGONADISM MALE ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPAIRED INSULIN SECRETION ( 1 FDA reports)
IMPLANT SITE ERYTHEMA ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISIONAL HERNIA GANGRENOUS ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCREASED INSULIN REQUIREMENT ( 1 FDA reports)
INCREASED VENTRICULAR PRELOAD ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTIVE SPONDYLITIS ( 1 FDA reports)
INFLUENZA B VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE ECZEMA ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PUSTULE ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJURY CORNEAL ( 1 FDA reports)
INSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INSULINOMA ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERTRIGO CANDIDA ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IODINE UPTAKE DECREASED ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
JEJUNAL PERFORATION ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KIDNEY MALFORMATION ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL ERYTHEMA ( 1 FDA reports)
LASEGUE'S TEST NEGATIVE ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LENS DISLOCATION ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LEPTOSPIROSIS ( 1 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOCYTE ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOEDEMA ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVER OPERATION ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LUMBAR HERNIA ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE I ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LYMPH NODE ABSCESS ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTIC HYPOPHYSITIS ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MACROANGIOPATHY ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACULAR SCAR ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALE PATTERN BALDNESS ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MASTOCYTOSIS ( 1 FDA reports)
MAXILLOFACIAL SINUS NEOPLASM ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEIBOMIANITIS ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGOCELE ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 1 FDA reports)
MESENTERIC PANNICULITIS ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO MUSCLE ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO PROSTATE ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
METATARSAL EXCISION ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MILIA ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MIXED DEAFNESS ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOCYTOPENIA ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MORAXELLA TEST POSITIVE ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE OPERATION ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYELOID METAPLASIA ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOFASCITIS ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NAIL BED INFECTION FUNGAL ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEONATAL TACHYPNOEA ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROLOGICAL INFECTION ( 1 FDA reports)
NEUROSENSORY HYPOACUSIS ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NIPPLE EXUDATE BLOODY ( 1 FDA reports)
NIPPLE SWELLING ( 1 FDA reports)
NO ADVERSE DRUG REACTION ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE I ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCCUPATIONAL PROBLEM ENVIRONMENTAL ( 1 FDA reports)
OCHLOPHOBIA ( 1 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL INJURY ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL VARICEAL LIGATION ( 1 FDA reports)
OESOPHAGITIS CHEMICAL ( 1 FDA reports)
OESTRADIOL INCREASED ( 1 FDA reports)
OLFACTORY NERVE DISORDER ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
ONCOCYTOMA ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NERVE OPERATION ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORAL PUSTULE ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC CARCINOMA NON-RESECTABLE ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PANCREATIC DUCT STENOSIS ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCREATIC PHLEGMON ( 1 FDA reports)
PANCREATICODUODENECTOMY ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARATHYROID HORMONE-RELATED PROTEIN INCREASED ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PENILE ERYTHEMA ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPHERAL REVASCULARISATION ( 1 FDA reports)
PERIPORTAL SINUS DILATATION ( 1 FDA reports)
PERIPROCTITIS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGEAL OPERATION ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PIERRE ROBIN SYNDROME ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITUITARY CYST ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLATELET DESTRUCTION INCREASED ( 1 FDA reports)
PLICA SYNDROME ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA ADENOVIRAL ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORTAL VEIN PHLEBITIS ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL URINE LEAK ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTOPERATIVE CONSTIPATION ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PREDISPOSITION TO DISEASE ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PROCEDURAL DIZZINESS ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTITIS HAEMORRHAGIC ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATE CANCER STAGE IV ( 1 FDA reports)
PROSTATE EXAMINATION ( 1 FDA reports)
PROSTATE INDURATION ( 1 FDA reports)
PROSTATE TENDERNESS ( 1 FDA reports)
PROSTATIC CALCIFICATION ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN INDUCED BY VITAMIN K ABSENCE OR ANTAGONIST II INCREASED ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOANGINA ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOPOLYP ( 1 FDA reports)
PSYCHIATRIC EVALUATION ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY VALVE DISEASE ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
RADICAL PROSTATECTOMY ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL CANCER STAGE IV ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RECURRING SKIN BOILS ( 1 FDA reports)
RED BLOOD CELL BURR CELLS PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL CANCER STAGE I ( 1 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL ONCOCYTOMA ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL LASER COAGULATION ( 1 FDA reports)
RETINAL OPERATION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHINOTRACHEITIS ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SARCOMA METASTATIC ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 1 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERAL HYPERAEMIA ( 1 FDA reports)
SCLEROEDEMA ( 1 FDA reports)
SECONDARY HYPERTHYROIDISM ( 1 FDA reports)
SECONDARY HYPOGONADISM ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SENSATION OF BLOCK IN EAR ( 1 FDA reports)
SEPTAL PANNICULITIS ( 1 FDA reports)
SEPTIC ENCEPHALOPATHY ( 1 FDA reports)
SEPTIC PHLEBITIS ( 1 FDA reports)
SEXUAL ACTIVITY INCREASED ( 1 FDA reports)
SHUNT INFECTION ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SIGNET-RING CELL CARCINOMA ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINGLE UMBILICAL ARTERY ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SMOKING CESSATION THERAPY ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SPINAL CORD INFARCTION ( 1 FDA reports)
SPINAL CORD INFECTION ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENT MALFUNCTION ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUBMAXILLARY GLAND ENLARGEMENT ( 1 FDA reports)
SUBRETINAL FIBROSIS ( 1 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TESTICULAR HAEMORRHAGE ( 1 FDA reports)
TETANY ( 1 FDA reports)
TETHERED CORD SYNDROME ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYROID CANCER METASTATIC ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROIDITIS SUBACUTE ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR HAEMORRHAGE ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA METASTATIC ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRIFASCICULAR BLOCK ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TUMOUR RUPTURE ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
TYPHOID FEVER ( 1 FDA reports)
UBIQUINONE DECREASED ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URETERAL POLYP ( 1 FDA reports)
URETERAL STENT REMOVAL ( 1 FDA reports)
URETERIC CANCER LOCAL ( 1 FDA reports)
URETERIC CANCER METASTATIC ( 1 FDA reports)
URETEROSCOPY ( 1 FDA reports)
URETHRAL CANCER METASTATIC ( 1 FDA reports)
URETHRAL MEATOTOMY ( 1 FDA reports)
URETHRAL PAPILLOMA ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY CALCULUS REMOVAL ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINARY TRACT INFLAMMATION ( 1 FDA reports)
URINE AMYLASE INCREASED ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE COPPER DECREASED ( 1 FDA reports)
URINE ELECTROPHORESIS ABNORMAL ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VAGINAL CANCER ( 1 FDA reports)
VAGINAL CANCER STAGE III ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VARICOSE VEIN OPERATION ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULAR CAUTERISATION ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN D ABNORMAL ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VULVAL CANCER ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEST NILE VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)

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