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

PAIN ( 3506 FDA reports)
NAUSEA ( 2588 FDA reports)
ANXIETY ( 2421 FDA reports)
DYSPNOEA ( 1993 FDA reports)
FATIGUE ( 1887 FDA reports)
BACK PAIN ( 1771 FDA reports)
VOMITING ( 1743 FDA reports)
HEADACHE ( 1622 FDA reports)
DEPRESSION ( 1603 FDA reports)
ARTHRALGIA ( 1560 FDA reports)
ASTHENIA ( 1551 FDA reports)
DIARRHOEA ( 1524 FDA reports)
FALL ( 1475 FDA reports)
PAIN IN EXTREMITY ( 1456 FDA reports)
DIZZINESS ( 1426 FDA reports)
ANAEMIA ( 1406 FDA reports)
OEDEMA PERIPHERAL ( 1373 FDA reports)
CHEST PAIN ( 1362 FDA reports)
CONSTIPATION ( 1261 FDA reports)
INJURY ( 1253 FDA reports)
PNEUMONIA ( 1244 FDA reports)
WEIGHT DECREASED ( 1234 FDA reports)
ABDOMINAL PAIN ( 1230 FDA reports)
INSOMNIA ( 1204 FDA reports)
OSTEONECROSIS OF JAW ( 1162 FDA reports)
DRUG INEFFECTIVE ( 1161 FDA reports)
HYPERTENSION ( 1114 FDA reports)
PYREXIA ( 1100 FDA reports)
HYPOAESTHESIA ( 960 FDA reports)
DEHYDRATION ( 923 FDA reports)
OSTEOARTHRITIS ( 902 FDA reports)
BONE DISORDER ( 901 FDA reports)
OSTEOMYELITIS ( 869 FDA reports)
HYPOTENSION ( 811 FDA reports)
EMOTIONAL DISTRESS ( 806 FDA reports)
CONFUSIONAL STATE ( 798 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 782 FDA reports)
PLEURAL EFFUSION ( 780 FDA reports)
PULMONARY EMBOLISM ( 774 FDA reports)
GAIT DISTURBANCE ( 773 FDA reports)
DEEP VEIN THROMBOSIS ( 757 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 748 FDA reports)
MYOCARDIAL INFARCTION ( 735 FDA reports)
PAIN IN JAW ( 733 FDA reports)
URINARY TRACT INFECTION ( 729 FDA reports)
DECREASED APPETITE ( 719 FDA reports)
MALAISE ( 716 FDA reports)
NEUROPATHY PERIPHERAL ( 716 FDA reports)
MUSCLE SPASMS ( 700 FDA reports)
INFECTION ( 686 FDA reports)
ANHEDONIA ( 680 FDA reports)
RASH ( 669 FDA reports)
SPINAL OSTEOARTHRITIS ( 665 FDA reports)
SOMNOLENCE ( 663 FDA reports)
ABDOMINAL PAIN UPPER ( 663 FDA reports)
WEIGHT INCREASED ( 661 FDA reports)
BONE PAIN ( 656 FDA reports)
COUGH ( 655 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 643 FDA reports)
RENAL FAILURE ( 641 FDA reports)
PARAESTHESIA ( 639 FDA reports)
SINUSITIS ( 620 FDA reports)
TOOTH EXTRACTION ( 610 FDA reports)
OSTEONECROSIS ( 608 FDA reports)
CHOLELITHIASIS ( 595 FDA reports)
LOSS OF CONSCIOUSNESS ( 595 FDA reports)
CELLULITIS ( 593 FDA reports)
MUSCULAR WEAKNESS ( 590 FDA reports)
HYPERHIDROSIS ( 582 FDA reports)
MYALGIA ( 579 FDA reports)
BRONCHITIS ( 578 FDA reports)
DYSPHAGIA ( 568 FDA reports)
NECK PAIN ( 552 FDA reports)
ERYTHEMA ( 549 FDA reports)
TREMOR ( 546 FDA reports)
DRUG DEPENDENCE ( 545 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 544 FDA reports)
VISION BLURRED ( 540 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 536 FDA reports)
DEATH ( 529 FDA reports)
PRURITUS ( 520 FDA reports)
FEELING ABNORMAL ( 519 FDA reports)
SYNCOPE ( 517 FDA reports)
RENAL FAILURE ACUTE ( 514 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 511 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 511 FDA reports)
IMPAIRED HEALING ( 508 FDA reports)
ATELECTASIS ( 507 FDA reports)
SWELLING ( 505 FDA reports)
DEFORMITY ( 498 FDA reports)
HYPOKALAEMIA ( 492 FDA reports)
ATRIAL FIBRILLATION ( 490 FDA reports)
CONVULSION ( 483 FDA reports)
MUSCULOSKELETAL PAIN ( 482 FDA reports)
CEREBROVASCULAR ACCIDENT ( 471 FDA reports)
OSTEOPOROSIS ( 468 FDA reports)
THROMBOCYTOPENIA ( 464 FDA reports)
DENTAL CARIES ( 463 FDA reports)
METASTASES TO BONE ( 463 FDA reports)
HAEMOGLOBIN DECREASED ( 461 FDA reports)
ARTHRITIS ( 457 FDA reports)
CHILLS ( 449 FDA reports)
OVERDOSE ( 448 FDA reports)
SEPSIS ( 446 FDA reports)
TOOTH DISORDER ( 444 FDA reports)
OSTEOPENIA ( 438 FDA reports)
DYSPEPSIA ( 436 FDA reports)
CONTUSION ( 434 FDA reports)
DIABETES MELLITUS ( 431 FDA reports)
CORONARY ARTERY DISEASE ( 418 FDA reports)
BLOOD GLUCOSE INCREASED ( 408 FDA reports)
SUICIDAL IDEATION ( 406 FDA reports)
MEMORY IMPAIRMENT ( 400 FDA reports)
MITRAL VALVE INCOMPETENCE ( 396 FDA reports)
MENTAL STATUS CHANGES ( 392 FDA reports)
RIB FRACTURE ( 392 FDA reports)
PALPITATIONS ( 389 FDA reports)
DYSURIA ( 381 FDA reports)
HYPERLIPIDAEMIA ( 380 FDA reports)
HERPES ZOSTER ( 378 FDA reports)
CONDITION AGGRAVATED ( 376 FDA reports)
TOOTHACHE ( 375 FDA reports)
JOINT SWELLING ( 373 FDA reports)
SWELLING FACE ( 358 FDA reports)
BLOOD PRESSURE INCREASED ( 353 FDA reports)
PANCYTOPENIA ( 351 FDA reports)
TOOTH LOSS ( 351 FDA reports)
AMNESIA ( 346 FDA reports)
RESPIRATORY FAILURE ( 344 FDA reports)
CARDIOMEGALY ( 341 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 340 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 338 FDA reports)
HAEMORRHOIDS ( 337 FDA reports)
CHEST DISCOMFORT ( 334 FDA reports)
OEDEMA ( 334 FDA reports)
ASTHMA ( 331 FDA reports)
CATARACT ( 329 FDA reports)
LYMPHADENOPATHY ( 327 FDA reports)
BONE LESION ( 323 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 323 FDA reports)
DECREASED INTEREST ( 322 FDA reports)
DIVERTICULUM ( 319 FDA reports)
MIGRAINE ( 317 FDA reports)
NEOPLASM MALIGNANT ( 317 FDA reports)
MULTIPLE MYELOMA ( 316 FDA reports)
HIATUS HERNIA ( 314 FDA reports)
CHOLECYSTITIS CHRONIC ( 308 FDA reports)
HAEMATURIA ( 308 FDA reports)
GASTRITIS ( 306 FDA reports)
THROMBOSIS ( 303 FDA reports)
NEPHROLITHIASIS ( 300 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 298 FDA reports)
ABDOMINAL DISCOMFORT ( 294 FDA reports)
ARTHROPATHY ( 290 FDA reports)
SLEEP APNOEA SYNDROME ( 290 FDA reports)
TACHYCARDIA ( 290 FDA reports)
LETHARGY ( 288 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 287 FDA reports)
DRY MOUTH ( 286 FDA reports)
BLOOD CREATININE INCREASED ( 284 FDA reports)
DYSPNOEA EXERTIONAL ( 283 FDA reports)
HYPOPHAGIA ( 279 FDA reports)
AGITATION ( 275 FDA reports)
ORAL PAIN ( 275 FDA reports)
RECTAL HAEMORRHAGE ( 272 FDA reports)
HAEMATOCRIT DECREASED ( 271 FDA reports)
NEUTROPENIA ( 271 FDA reports)
OROPHARYNGEAL PAIN ( 269 FDA reports)
TOOTH ABSCESS ( 265 FDA reports)
ROTATOR CUFF SYNDROME ( 263 FDA reports)
SCOLIOSIS ( 262 FDA reports)
HALLUCINATION ( 261 FDA reports)
HEART RATE INCREASED ( 261 FDA reports)
HYPOXIA ( 261 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 260 FDA reports)
ROAD TRAFFIC ACCIDENT ( 260 FDA reports)
BALANCE DISORDER ( 256 FDA reports)
GALLBLADDER DISORDER ( 255 FDA reports)
URINARY RETENTION ( 255 FDA reports)
STRESS ( 254 FDA reports)
LUNG NEOPLASM ( 254 FDA reports)
MENTAL DISORDER ( 254 FDA reports)
HYPERSENSITIVITY ( 253 FDA reports)
GINGIVITIS ( 252 FDA reports)
ABDOMINAL DISTENSION ( 251 FDA reports)
MASTICATION DISORDER ( 251 FDA reports)
EXOSTOSIS ( 250 FDA reports)
LUNG INFILTRATION ( 249 FDA reports)
RENAL FAILURE CHRONIC ( 248 FDA reports)
FIBROMYALGIA ( 247 FDA reports)
STAPHYLOCOCCAL INFECTION ( 247 FDA reports)
COMPRESSION FRACTURE ( 245 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 245 FDA reports)
SPINAL COMPRESSION FRACTURE ( 244 FDA reports)
URINARY INCONTINENCE ( 242 FDA reports)
POLLAKIURIA ( 242 FDA reports)
PRIMARY SEQUESTRUM ( 242 FDA reports)
DYSARTHRIA ( 241 FDA reports)
DYSGEUSIA ( 239 FDA reports)
PRODUCT QUALITY ISSUE ( 238 FDA reports)
SLEEP DISORDER ( 238 FDA reports)
BURSITIS ( 236 FDA reports)
PULMONARY OEDEMA ( 236 FDA reports)
PANCREATITIS ( 233 FDA reports)
HEPATIC STEATOSIS ( 232 FDA reports)
ALOPECIA ( 231 FDA reports)
HAEMATOCHEZIA ( 231 FDA reports)
DRUG HYPERSENSITIVITY ( 230 FDA reports)
HYPERGLYCAEMIA ( 230 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 229 FDA reports)
TOOTH FRACTURE ( 229 FDA reports)
STOMATITIS ( 227 FDA reports)
URTICARIA ( 227 FDA reports)
DISABILITY ( 227 FDA reports)
NERVOUSNESS ( 226 FDA reports)
SKIN ULCER ( 226 FDA reports)
DRUG DOSE OMISSION ( 225 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 225 FDA reports)
HYPONATRAEMIA ( 224 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 223 FDA reports)
ARTERIOSCLEROSIS ( 221 FDA reports)
INFLAMMATION ( 219 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 219 FDA reports)
CARDIAC DISORDER ( 217 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 216 FDA reports)
RENAL CYST ( 216 FDA reports)
OSTEOLYSIS ( 215 FDA reports)
ABSCESS ( 212 FDA reports)
SINUS TACHYCARDIA ( 212 FDA reports)
VISUAL IMPAIRMENT ( 212 FDA reports)
INFLUENZA LIKE ILLNESS ( 211 FDA reports)
LEUKOPENIA ( 210 FDA reports)
DRUG ABUSER ( 209 FDA reports)
DRUG INTERACTION ( 209 FDA reports)
EAR PAIN ( 208 FDA reports)
IRRITABILITY ( 208 FDA reports)
SKIN LESION ( 208 FDA reports)
MASS ( 207 FDA reports)
ANOREXIA ( 205 FDA reports)
LOOSE TOOTH ( 204 FDA reports)
ARRHYTHMIA ( 203 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 203 FDA reports)
EPISTAXIS ( 202 FDA reports)
INADEQUATE ANALGESIA ( 202 FDA reports)
INJECTION SITE PAIN ( 202 FDA reports)
SUICIDE ATTEMPT ( 202 FDA reports)
VERTIGO ( 201 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 201 FDA reports)
KYPHOSIS ( 201 FDA reports)
BLOOD PRESSURE DECREASED ( 200 FDA reports)
GINGIVAL PAIN ( 200 FDA reports)
DISTURBANCE IN ATTENTION ( 198 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 198 FDA reports)
CHRONIC SINUSITIS ( 196 FDA reports)
SPINAL COLUMN STENOSIS ( 196 FDA reports)
CARDIAC ARREST ( 195 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 195 FDA reports)
MOUTH ULCERATION ( 195 FDA reports)
PERIODONTAL DISEASE ( 194 FDA reports)
SCAR ( 194 FDA reports)
WHEEZING ( 194 FDA reports)
CARDIOMYOPATHY ( 193 FDA reports)
DEBRIDEMENT ( 193 FDA reports)
FISTULA ( 193 FDA reports)
ORAL DISORDER ( 193 FDA reports)
PERIODONTITIS ( 192 FDA reports)
PLATELET COUNT DECREASED ( 192 FDA reports)
HOT FLUSH ( 191 FDA reports)
WITHDRAWAL SYNDROME ( 190 FDA reports)
SURGERY ( 189 FDA reports)
LUMBAR SPINAL STENOSIS ( 189 FDA reports)
DRUG TOXICITY ( 188 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 186 FDA reports)
EXPOSED BONE IN JAW ( 186 FDA reports)
DRUG EFFECT DECREASED ( 185 FDA reports)
FOOT FRACTURE ( 185 FDA reports)
MOBILITY DECREASED ( 185 FDA reports)
ORAL INFECTION ( 185 FDA reports)
TYPE 2 DIABETES MELLITUS ( 185 FDA reports)
HAEMORRHAGE ( 184 FDA reports)
CARDIAC MURMUR ( 183 FDA reports)
CARDIO-RESPIRATORY ARREST ( 183 FDA reports)
EMPHYSEMA ( 183 FDA reports)
FEBRILE NEUTROPENIA ( 183 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 183 FDA reports)
ERECTILE DYSFUNCTION ( 182 FDA reports)
CYST ( 179 FDA reports)
NIGHT SWEATS ( 178 FDA reports)
PERICARDIAL EFFUSION ( 178 FDA reports)
LUNG DISORDER ( 177 FDA reports)
MUCOSAL INFLAMMATION ( 175 FDA reports)
BURNING SENSATION ( 174 FDA reports)
OFF LABEL USE ( 174 FDA reports)
PANIC ATTACK ( 174 FDA reports)
NEURALGIA ( 172 FDA reports)
PATHOLOGICAL FRACTURE ( 172 FDA reports)
HIP FRACTURE ( 171 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 170 FDA reports)
BONE DEBRIDEMENT ( 170 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 170 FDA reports)
BONE DENSITY DECREASED ( 169 FDA reports)
DISEASE PROGRESSION ( 169 FDA reports)
HAEMATOMA ( 169 FDA reports)
JAW OPERATION ( 169 FDA reports)
GINGIVAL SWELLING ( 168 FDA reports)
HYPERCHOLESTEROLAEMIA ( 168 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 167 FDA reports)
COLONIC POLYP ( 167 FDA reports)
DEPRESSED MOOD ( 167 FDA reports)
DISCOMFORT ( 167 FDA reports)
PURULENT DISCHARGE ( 166 FDA reports)
TREATMENT NONCOMPLIANCE ( 166 FDA reports)
SPINAL FRACTURE ( 165 FDA reports)
JAW DISORDER ( 165 FDA reports)
NASAL CONGESTION ( 165 FDA reports)
ABASIA ( 164 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 164 FDA reports)
RENAL DISORDER ( 164 FDA reports)
UNEVALUABLE EVENT ( 164 FDA reports)
DRUG ABUSE ( 163 FDA reports)
LEUKOCYTOSIS ( 163 FDA reports)
IRRITABLE BOWEL SYNDROME ( 162 FDA reports)
METASTASES TO LIVER ( 162 FDA reports)
RESTLESS LEGS SYNDROME ( 162 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 161 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 161 FDA reports)
RHEUMATOID ARTHRITIS ( 161 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 160 FDA reports)
DIVERTICULUM INTESTINAL ( 160 FDA reports)
HAEMOPTYSIS ( 160 FDA reports)
ANGER ( 159 FDA reports)
ANGINA PECTORIS ( 159 FDA reports)
BRADYCARDIA ( 158 FDA reports)
COMA ( 158 FDA reports)
METASTASES TO SPINE ( 158 FDA reports)
OBESITY ( 158 FDA reports)
CHOLECYSTITIS ( 157 FDA reports)
DYSPHONIA ( 157 FDA reports)
HYPOTHYROIDISM ( 157 FDA reports)
OESOPHAGITIS ( 157 FDA reports)
BLOOD UREA INCREASED ( 156 FDA reports)
ENDODONTIC PROCEDURE ( 155 FDA reports)
PARANOIA ( 155 FDA reports)
RASH PRURITIC ( 155 FDA reports)
GASTROINTESTINAL DISORDER ( 154 FDA reports)
SINUS DISORDER ( 154 FDA reports)
BLOOD CALCIUM DECREASED ( 153 FDA reports)
EJECTION FRACTION DECREASED ( 153 FDA reports)
JAW FRACTURE ( 153 FDA reports)
TENDERNESS ( 153 FDA reports)
SPINAL DISORDER ( 151 FDA reports)
FEAR ( 150 FDA reports)
MALNUTRITION ( 150 FDA reports)
RESPIRATORY ARREST ( 150 FDA reports)
HAEMATEMESIS ( 149 FDA reports)
PRODUCTIVE COUGH ( 149 FDA reports)
TOOTH INFECTION ( 149 FDA reports)
UNRESPONSIVE TO STIMULI ( 149 FDA reports)
LIFE EXPECTANCY SHORTENED ( 148 FDA reports)
CRYING ( 147 FDA reports)
ONYCHOMYCOSIS ( 147 FDA reports)
DISORIENTATION ( 146 FDA reports)
HYPERKALAEMIA ( 146 FDA reports)
HYPOGLYCAEMIA ( 145 FDA reports)
PHYSICAL DISABILITY ( 145 FDA reports)
PULMONARY CONGESTION ( 145 FDA reports)
SCIATICA ( 145 FDA reports)
INCORRECT DOSE ADMINISTERED ( 144 FDA reports)
PRESYNCOPE ( 144 FDA reports)
CROHN'S DISEASE ( 143 FDA reports)
RESPIRATORY DISTRESS ( 143 FDA reports)
GINGIVAL BLEEDING ( 142 FDA reports)
ACTINOMYCOSIS ( 141 FDA reports)
LIMB INJURY ( 141 FDA reports)
CARPAL TUNNEL SYNDROME ( 140 FDA reports)
HEAD INJURY ( 140 FDA reports)
JOINT EFFUSION ( 140 FDA reports)
METASTASES TO LUNG ( 140 FDA reports)
OSTEITIS ( 140 FDA reports)
GINGIVAL INFECTION ( 139 FDA reports)
AGGRESSION ( 138 FDA reports)
FLANK PAIN ( 138 FDA reports)
SPEECH DISORDER ( 138 FDA reports)
SKIN DISCOLOURATION ( 137 FDA reports)
DIVERTICULITIS ( 137 FDA reports)
COLITIS ( 136 FDA reports)
DENTURE WEARER ( 136 FDA reports)
DIPLOPIA ( 136 FDA reports)
NIGHTMARE ( 136 FDA reports)
PNEUMOTHORAX ( 135 FDA reports)
ECONOMIC PROBLEM ( 134 FDA reports)
MEDICATION ERROR ( 134 FDA reports)
NASOPHARYNGITIS ( 134 FDA reports)
PULMONARY HYPERTENSION ( 134 FDA reports)
RADICULOPATHY ( 134 FDA reports)
VISUAL ACUITY REDUCED ( 134 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 133 FDA reports)
BLOOD POTASSIUM DECREASED ( 132 FDA reports)
DEAFNESS ( 132 FDA reports)
FLUSHING ( 132 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 132 FDA reports)
ORTHOSTATIC HYPOTENSION ( 132 FDA reports)
NOCTURIA ( 131 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 131 FDA reports)
ILEUS ( 130 FDA reports)
GINGIVAL DISORDER ( 129 FDA reports)
HYPERSOMNIA ( 129 FDA reports)
LUMBAR RADICULOPATHY ( 129 FDA reports)
TENDONITIS ( 129 FDA reports)
WOUND DEHISCENCE ( 128 FDA reports)
SEQUESTRECTOMY ( 128 FDA reports)
MICTURITION URGENCY ( 127 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 127 FDA reports)
ASCITES ( 126 FDA reports)
INTENTIONAL OVERDOSE ( 126 FDA reports)
JOINT INJURY ( 126 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 126 FDA reports)
PULMONARY FIBROSIS ( 126 FDA reports)
AZOTAEMIA ( 125 FDA reports)
EATING DISORDER ( 125 FDA reports)
FLUID OVERLOAD ( 125 FDA reports)
PROTHROMBIN TIME PROLONGED ( 125 FDA reports)
BLOOD GLUCOSE DECREASED ( 124 FDA reports)
CYSTITIS ( 124 FDA reports)
DRUG PRESCRIBING ERROR ( 123 FDA reports)
GLAUCOMA ( 123 FDA reports)
GROIN PAIN ( 123 FDA reports)
INTENTIONAL DRUG MISUSE ( 123 FDA reports)
BASAL CELL CARCINOMA ( 122 FDA reports)
INFLUENZA ( 122 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 121 FDA reports)
HEPATOMEGALY ( 121 FDA reports)
MOOD SWINGS ( 121 FDA reports)
RASH MACULAR ( 121 FDA reports)
EMOTIONAL DISORDER ( 120 FDA reports)
FAECAL INCONTINENCE ( 120 FDA reports)
LEFT ATRIAL DILATATION ( 120 FDA reports)
SEPTIC SHOCK ( 120 FDA reports)
SPONDYLOLISTHESIS ( 120 FDA reports)
SPINAL CORD COMPRESSION ( 119 FDA reports)
FLATULENCE ( 119 FDA reports)
OSTEOSCLEROSIS ( 119 FDA reports)
ABSCESS JAW ( 118 FDA reports)
CHOLECYSTECTOMY ( 118 FDA reports)
EYE PAIN ( 118 FDA reports)
HYDRONEPHROSIS ( 118 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 118 FDA reports)
BLOOD SODIUM DECREASED ( 117 FDA reports)
COORDINATION ABNORMAL ( 117 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 117 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 116 FDA reports)
METASTATIC NEOPLASM ( 116 FDA reports)
SPLENOMEGALY ( 116 FDA reports)
GOITRE ( 115 FDA reports)
POST PROCEDURAL COMPLICATION ( 115 FDA reports)
RHINORRHOEA ( 115 FDA reports)
ABDOMINAL PAIN LOWER ( 114 FDA reports)
BACK DISORDER ( 114 FDA reports)
GENERALISED OEDEMA ( 114 FDA reports)
PANCREATITIS ACUTE ( 114 FDA reports)
PLASMACYTOMA ( 113 FDA reports)
SKIN EXFOLIATION ( 113 FDA reports)
COLITIS ULCERATIVE ( 112 FDA reports)
HEPATIC FAILURE ( 112 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 112 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 112 FDA reports)
COGNITIVE DISORDER ( 111 FDA reports)
DRY EYE ( 111 FDA reports)
DYSKINESIA ( 111 FDA reports)
LYMPHOEDEMA ( 111 FDA reports)
MUSCLE TWITCHING ( 111 FDA reports)
ANKLE FRACTURE ( 110 FDA reports)
JOINT STIFFNESS ( 110 FDA reports)
NERVOUS SYSTEM DISORDER ( 110 FDA reports)
RENAL IMPAIRMENT ( 110 FDA reports)
TINNITUS ( 110 FDA reports)
FACIAL PAIN ( 109 FDA reports)
FEELING HOT ( 109 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 109 FDA reports)
CANDIDIASIS ( 108 FDA reports)
VENTRICULAR HYPERTROPHY ( 108 FDA reports)
MULTIPLE SCLEROSIS ( 107 FDA reports)
SEDATION ( 107 FDA reports)
LIBIDO DECREASED ( 106 FDA reports)
DECUBITUS ULCER ( 105 FDA reports)
INFUSION RELATED REACTION ( 105 FDA reports)
NEOPLASM PROGRESSION ( 105 FDA reports)
STEM CELL TRANSPLANT ( 105 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 104 FDA reports)
BLISTER ( 104 FDA reports)
CEREBRAL ATROPHY ( 104 FDA reports)
HEART RATE IRREGULAR ( 104 FDA reports)
OPEN WOUND ( 104 FDA reports)
BLINDNESS ( 103 FDA reports)
DELIRIUM ( 103 FDA reports)
FEELING COLD ( 103 FDA reports)
IRON DEFICIENCY ANAEMIA ( 103 FDA reports)
OXYGEN SATURATION DECREASED ( 103 FDA reports)
PHARYNGEAL OEDEMA ( 103 FDA reports)
RETCHING ( 103 FDA reports)
VAGINAL HAEMORRHAGE ( 103 FDA reports)
SYNOVIAL CYST ( 102 FDA reports)
UTERINE LEIOMYOMA ( 102 FDA reports)
VENTRICULAR TACHYCARDIA ( 102 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 102 FDA reports)
DRY SKIN ( 102 FDA reports)
EXCORIATION ( 102 FDA reports)
JOINT DISLOCATION ( 102 FDA reports)
MULTIPLE DRUG OVERDOSE ( 102 FDA reports)
RADIOTHERAPY ( 102 FDA reports)
AORTIC VALVE INCOMPETENCE ( 101 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 101 FDA reports)
DIABETIC NEUROPATHY ( 101 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 101 FDA reports)
ECCHYMOSIS ( 101 FDA reports)
FLUID RETENTION ( 101 FDA reports)
BONE LOSS ( 100 FDA reports)
DYSLIPIDAEMIA ( 100 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 100 FDA reports)
VASCULITIS ( 100 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 99 FDA reports)
ANGINA UNSTABLE ( 99 FDA reports)
BACK INJURY ( 99 FDA reports)
COAGULOPATHY ( 99 FDA reports)
GASTROENTERITIS ( 99 FDA reports)
HEPATIC CYST ( 99 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 99 FDA reports)
RESTLESSNESS ( 99 FDA reports)
CERVICAL SPINAL STENOSIS ( 98 FDA reports)
ENCEPHALOPATHY ( 98 FDA reports)
FEMUR FRACTURE ( 98 FDA reports)
HYPERCALCAEMIA ( 98 FDA reports)
HYPOCALCAEMIA ( 98 FDA reports)
METABOLIC ACIDOSIS ( 98 FDA reports)
SKIN DISORDER ( 98 FDA reports)
ULCER ( 97 FDA reports)
ABNORMAL BEHAVIOUR ( 97 FDA reports)
CAROTID ARTERY STENOSIS ( 97 FDA reports)
BODY TEMPERATURE INCREASED ( 96 FDA reports)
GASTRIC ULCER ( 96 FDA reports)
POLYSUBSTANCE ABUSE ( 96 FDA reports)
ABNORMAL DREAMS ( 95 FDA reports)
DRUG ADMINISTRATION ERROR ( 95 FDA reports)
FAILURE TO THRIVE ( 95 FDA reports)
LACERATION ( 95 FDA reports)
MENTAL IMPAIRMENT ( 95 FDA reports)
SUBSTANCE ABUSE ( 95 FDA reports)
MAJOR DEPRESSION ( 94 FDA reports)
ORAL CANDIDIASIS ( 94 FDA reports)
SINUS BRADYCARDIA ( 94 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 93 FDA reports)
HYPOMAGNESAEMIA ( 93 FDA reports)
LUNG NEOPLASM MALIGNANT ( 93 FDA reports)
PERONEAL NERVE PALSY ( 93 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 93 FDA reports)
APHASIA ( 92 FDA reports)
BACTERIAL INFECTION ( 91 FDA reports)
BLOOD ALBUMIN DECREASED ( 91 FDA reports)
CYANOSIS ( 91 FDA reports)
DENTAL OPERATION ( 91 FDA reports)
FIBROSIS ( 91 FDA reports)
GYNAECOMASTIA ( 91 FDA reports)
MENISCUS LESION ( 91 FDA reports)
PULMONARY MASS ( 91 FDA reports)
GINGIVAL ULCERATION ( 90 FDA reports)
ILL-DEFINED DISORDER ( 90 FDA reports)
ORAL SURGERY ( 90 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 90 FDA reports)
RHINITIS ALLERGIC ( 90 FDA reports)
BLOOD BILIRUBIN INCREASED ( 89 FDA reports)
GASTRIC DISORDER ( 89 FDA reports)
HIP ARTHROPLASTY ( 89 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 89 FDA reports)
ATRIAL FLUTTER ( 88 FDA reports)
CEREBRAL ISCHAEMIA ( 88 FDA reports)
ESCHERICHIA INFECTION ( 88 FDA reports)
INJECTION SITE ERYTHEMA ( 88 FDA reports)
MULTI-ORGAN FAILURE ( 88 FDA reports)
PELVIC PAIN ( 88 FDA reports)
DERMATITIS ( 87 FDA reports)
EAR INFECTION ( 87 FDA reports)
HEPATIC ENZYME INCREASED ( 87 FDA reports)
UPPER LIMB FRACTURE ( 87 FDA reports)
VARICOSE VEIN ( 86 FDA reports)
ACCIDENTAL OVERDOSE ( 86 FDA reports)
AORTIC ANEURYSM ( 86 FDA reports)
FUNGAL INFECTION ( 86 FDA reports)
METASTASES TO LYMPH NODES ( 86 FDA reports)
PROCEDURAL PAIN ( 86 FDA reports)
PURULENCE ( 86 FDA reports)
ACUTE RESPIRATORY FAILURE ( 85 FDA reports)
CARDIAC FAILURE ( 85 FDA reports)
CEREBRAL INFARCTION ( 85 FDA reports)
INGUINAL HERNIA ( 85 FDA reports)
PSYCHOTIC DISORDER ( 85 FDA reports)
THROAT TIGHTNESS ( 85 FDA reports)
COMPLETED SUICIDE ( 84 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 84 FDA reports)
HYPERKERATOSIS ( 84 FDA reports)
HYPOVOLAEMIA ( 84 FDA reports)
OSTEORADIONECROSIS ( 84 FDA reports)
RHABDOMYOLYSIS ( 84 FDA reports)
GINGIVAL EROSION ( 83 FDA reports)
GOUT ( 83 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 83 FDA reports)
PLEURAL FIBROSIS ( 83 FDA reports)
WALKING AID USER ( 83 FDA reports)
THINKING ABNORMAL ( 82 FDA reports)
THYROID NEOPLASM ( 82 FDA reports)
VITREOUS FLOATERS ( 82 FDA reports)
DIASTOLIC DYSFUNCTION ( 82 FDA reports)
ENTEROCOCCAL INFECTION ( 82 FDA reports)
FAECALOMA ( 82 FDA reports)
FOOT DEFORMITY ( 82 FDA reports)
ORAL CAVITY FISTULA ( 82 FDA reports)
SENSITIVITY OF TEETH ( 82 FDA reports)
ABDOMINAL HERNIA ( 81 FDA reports)
BONE FRAGMENTATION ( 81 FDA reports)
BREAST CANCER ( 81 FDA reports)
BREAST CANCER RECURRENT ( 81 FDA reports)
MYOCARDIAL ISCHAEMIA ( 81 FDA reports)
PALLOR ( 81 FDA reports)
PELVIC FRACTURE ( 81 FDA reports)
SQUAMOUS CELL CARCINOMA ( 81 FDA reports)
VISUAL DISTURBANCE ( 81 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 80 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 80 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 80 FDA reports)
BIPOLAR DISORDER ( 80 FDA reports)
CHOLECYSTITIS ACUTE ( 80 FDA reports)
DRUG TOLERANCE ( 80 FDA reports)
HEPATIC LESION ( 80 FDA reports)
IMPAIRED WORK ABILITY ( 80 FDA reports)
ADVERSE DRUG REACTION ( 79 FDA reports)
BONE EROSION ( 79 FDA reports)
INTERSTITIAL LUNG DISEASE ( 79 FDA reports)
POLYURIA ( 79 FDA reports)
PROTEINURIA ( 79 FDA reports)
BONE NEOPLASM MALIGNANT ( 78 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 78 FDA reports)
PHARYNGITIS ( 78 FDA reports)
BREAST PAIN ( 77 FDA reports)
ECZEMA ( 77 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 77 FDA reports)
RHINITIS ( 77 FDA reports)
SKIN CANCER ( 77 FDA reports)
SNORING ( 76 FDA reports)
HEPATITIS ( 76 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 76 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 76 FDA reports)
PLATELET COUNT INCREASED ( 76 FDA reports)
MULTIPLE INJURIES ( 75 FDA reports)
ORAL DISCOMFORT ( 75 FDA reports)
VIRAL INFECTION ( 75 FDA reports)
TENDON DISORDER ( 74 FDA reports)
APPENDICITIS ( 74 FDA reports)
LYMPHOMA ( 74 FDA reports)
OTITIS MEDIA ( 74 FDA reports)
QUALITY OF LIFE DECREASED ( 74 FDA reports)
DEVICE RELATED INFECTION ( 73 FDA reports)
DRUG INTOLERANCE ( 73 FDA reports)
DRUG SCREEN POSITIVE ( 73 FDA reports)
INTESTINAL OBSTRUCTION ( 73 FDA reports)
NERVE INJURY ( 73 FDA reports)
PSEUDOMONAS INFECTION ( 73 FDA reports)
RASH GENERALISED ( 73 FDA reports)
BACTERAEMIA ( 72 FDA reports)
BONE SCAN ABNORMAL ( 72 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 72 FDA reports)
DIFFICULTY IN WALKING ( 72 FDA reports)
INCONTINENCE ( 72 FDA reports)
NODULE ( 72 FDA reports)
PRODUCT ADHESION ISSUE ( 72 FDA reports)
RASH ERYTHEMATOUS ( 72 FDA reports)
ADVERSE EVENT ( 71 FDA reports)
HYPOAESTHESIA ORAL ( 71 FDA reports)
LOCAL SWELLING ( 71 FDA reports)
MUSCLE ATROPHY ( 71 FDA reports)
ODYNOPHAGIA ( 71 FDA reports)
SENSORY LOSS ( 71 FDA reports)
VAGINAL INFECTION ( 71 FDA reports)
WOUND INFECTION ( 71 FDA reports)
SWOLLEN TONGUE ( 70 FDA reports)
DEPENDENCE ( 70 FDA reports)
MELAENA ( 70 FDA reports)
PLEURITIC PAIN ( 70 FDA reports)
BREAST TENDERNESS ( 69 FDA reports)
DEAFNESS NEUROSENSORY ( 69 FDA reports)
IMPAIRED DRIVING ABILITY ( 69 FDA reports)
PNEUMONIA ASPIRATION ( 69 FDA reports)
RENAL TUBULAR NECROSIS ( 69 FDA reports)
ABSCESS DRAINAGE ( 68 FDA reports)
DILATATION VENTRICULAR ( 68 FDA reports)
MOVEMENT DISORDER ( 68 FDA reports)
PARAESTHESIA ORAL ( 68 FDA reports)
PEPTIC ULCER ( 68 FDA reports)
PHLEBITIS ( 68 FDA reports)
PYELONEPHRITIS ( 68 FDA reports)
RESPIRATORY DISORDER ( 68 FDA reports)
THIRST ( 68 FDA reports)
THROAT IRRITATION ( 67 FDA reports)
BREAST MASS ( 67 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 67 FDA reports)
LACRIMATION INCREASED ( 67 FDA reports)
MOOD ALTERED ( 67 FDA reports)
GINGIVAL RECESSION ( 66 FDA reports)
HEART RATE DECREASED ( 66 FDA reports)
KNEE ARTHROPLASTY ( 66 FDA reports)
SEBORRHOEIC KERATOSIS ( 66 FDA reports)
SKIN INDURATION ( 66 FDA reports)
SKIN LACERATION ( 65 FDA reports)
STOMACH DISCOMFORT ( 65 FDA reports)
BEDRIDDEN ( 65 FDA reports)
CARDIOVASCULAR DISORDER ( 65 FDA reports)
COLITIS ISCHAEMIC ( 65 FDA reports)
DERMATITIS CONTACT ( 65 FDA reports)
DYSSTASIA ( 65 FDA reports)
EUPHORIC MOOD ( 65 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 65 FDA reports)
KIDNEY INFECTION ( 65 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 65 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 65 FDA reports)
ACTINIC KERATOSIS ( 64 FDA reports)
AORTIC VALVE SCLEROSIS ( 64 FDA reports)
ASPIRATION ( 64 FDA reports)
BONE OPERATION ( 64 FDA reports)
BRONCHOPNEUMONIA ( 64 FDA reports)
COLD SWEAT ( 64 FDA reports)
DUODENITIS ( 64 FDA reports)
FACET JOINT SYNDROME ( 64 FDA reports)
HAEMANGIOMA ( 64 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 64 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 64 FDA reports)
DIABETIC KETOACIDOSIS ( 63 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 63 FDA reports)
GLOSSODYNIA ( 63 FDA reports)
HOSPITALISATION ( 63 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 63 FDA reports)
SKIN TIGHTNESS ( 63 FDA reports)
TOOTH INJURY ( 63 FDA reports)
VASCULAR CALCIFICATION ( 63 FDA reports)
VENOUS INSUFFICIENCY ( 63 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 62 FDA reports)
ATAXIA ( 62 FDA reports)
BLOOD URINE PRESENT ( 62 FDA reports)
CLOSTRIDIAL INFECTION ( 62 FDA reports)
FRACTURE ( 62 FDA reports)
JOINT SPRAIN ( 62 FDA reports)
POOR QUALITY SLEEP ( 62 FDA reports)
PROSTATE CANCER ( 62 FDA reports)
RESPIRATORY DEPRESSION ( 62 FDA reports)
BILIARY DYSKINESIA ( 61 FDA reports)
GASTROENTERITIS VIRAL ( 61 FDA reports)
LOBAR PNEUMONIA ( 61 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 60 FDA reports)
CORONARY ARTERY STENOSIS ( 60 FDA reports)
HALLUCINATION, AUDITORY ( 60 FDA reports)
HAND FRACTURE ( 60 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 60 FDA reports)
UMBILICAL HERNIA ( 60 FDA reports)
VITAMIN D DEFICIENCY ( 60 FDA reports)
TENDON RUPTURE ( 59 FDA reports)
VERTEBROPLASTY ( 59 FDA reports)
BLOOD POTASSIUM INCREASED ( 59 FDA reports)
BREATH ODOUR ( 59 FDA reports)
CONJUNCTIVITIS ( 59 FDA reports)
HUMERUS FRACTURE ( 59 FDA reports)
LIVER DISORDER ( 59 FDA reports)
OVARIAN CYST ( 59 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 59 FDA reports)
ACCIDENT ( 58 FDA reports)
ANAPHYLACTIC REACTION ( 58 FDA reports)
APPLICATION SITE PRURITUS ( 58 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 58 FDA reports)
DEVICE MALFUNCTION ( 58 FDA reports)
FEELING OF DESPAIR ( 58 FDA reports)
HEARING IMPAIRED ( 58 FDA reports)
MUSCLE TIGHTNESS ( 58 FDA reports)
NON-CARDIAC CHEST PAIN ( 58 FDA reports)
PULMONARY INFARCTION ( 58 FDA reports)
RENAL INJURY ( 58 FDA reports)
WRIST FRACTURE ( 58 FDA reports)
AFFECTIVE DISORDER ( 57 FDA reports)
ISCHAEMIA ( 57 FDA reports)
LOWER LIMB FRACTURE ( 57 FDA reports)
MYOSITIS ( 57 FDA reports)
PERSONALITY CHANGE ( 57 FDA reports)
RENAL ATROPHY ( 57 FDA reports)
SCAB ( 57 FDA reports)
CEREBRAL HAEMORRHAGE ( 56 FDA reports)
EYE DISORDER ( 56 FDA reports)
FACE OEDEMA ( 56 FDA reports)
HEMIPARESIS ( 56 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 56 FDA reports)
MULTIPLE ALLERGIES ( 56 FDA reports)
MUSCLE STRAIN ( 56 FDA reports)
OCULAR HYPERAEMIA ( 56 FDA reports)
ORAL INTAKE REDUCED ( 56 FDA reports)
OTITIS EXTERNA ( 56 FDA reports)
TARDIVE DYSKINESIA ( 56 FDA reports)
URINARY HESITATION ( 56 FDA reports)
ANGIOPATHY ( 55 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 55 FDA reports)
CATHETER PLACEMENT ( 55 FDA reports)
CERVICOBRACHIAL SYNDROME ( 55 FDA reports)
EYE SWELLING ( 55 FDA reports)
GRAND MAL CONVULSION ( 55 FDA reports)
LIGAMENT SPRAIN ( 55 FDA reports)
PHOTOPHOBIA ( 55 FDA reports)
SICK SINUS SYNDROME ( 55 FDA reports)
APPLICATION SITE ERYTHEMA ( 54 FDA reports)
ATRIOVENTRICULAR BLOCK ( 54 FDA reports)
BLADDER DISORDER ( 54 FDA reports)
CERUMEN IMPACTION ( 54 FDA reports)
FAECES DISCOLOURED ( 54 FDA reports)
HEPATITIS C ( 54 FDA reports)
INJECTION SITE HAEMORRHAGE ( 54 FDA reports)
LIPOMA ( 54 FDA reports)
LOCALISED INFECTION ( 54 FDA reports)
ORTHOPNOEA ( 54 FDA reports)
OVERWEIGHT ( 54 FDA reports)
PROSTATOMEGALY ( 54 FDA reports)
PRURITUS GENERALISED ( 54 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 54 FDA reports)
SKELETAL INJURY ( 54 FDA reports)
COSTOCHONDRITIS ( 53 FDA reports)
DYSAESTHESIA ( 53 FDA reports)
GINGIVAL ERYTHEMA ( 53 FDA reports)
GRANULOMA ( 53 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 53 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 53 FDA reports)
PNEUMONITIS ( 53 FDA reports)
PROSTATE CANCER METASTATIC ( 53 FDA reports)
PULPITIS DENTAL ( 53 FDA reports)
STRESS URINARY INCONTINENCE ( 53 FDA reports)
SKIN HYPERTROPHY ( 52 FDA reports)
SPINAL FUSION SURGERY ( 52 FDA reports)
VENTRICULAR HYPOKINESIA ( 52 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 52 FDA reports)
BREAST CANCER METASTATIC ( 52 FDA reports)
INCREASED TENDENCY TO BRUISE ( 52 FDA reports)
JAUNDICE ( 52 FDA reports)
NEUTROPHIL COUNT DECREASED ( 52 FDA reports)
PLASMACYTOSIS ( 52 FDA reports)
APATHY ( 51 FDA reports)
APPENDICECTOMY ( 51 FDA reports)
BONE MARROW TRANSPLANT ( 51 FDA reports)
CARDIAC VALVE DISEASE ( 51 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 51 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 51 FDA reports)
HYPERTENSIVE HEART DISEASE ( 51 FDA reports)
HYPOKINESIA ( 51 FDA reports)
MENINGIOMA ( 51 FDA reports)
PETECHIAE ( 51 FDA reports)
PSORIASIS ( 51 FDA reports)
TOOTH DEPOSIT ( 51 FDA reports)
SOFT TISSUE DISORDER ( 50 FDA reports)
SPONDYLITIS ( 50 FDA reports)
SUBCUTANEOUS ABSCESS ( 50 FDA reports)
SUBDURAL HAEMATOMA ( 50 FDA reports)
THROMBOPHLEBITIS ( 50 FDA reports)
THYROID DISORDER ( 50 FDA reports)
UROSEPSIS ( 50 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 50 FDA reports)
BLINDNESS UNILATERAL ( 50 FDA reports)
CATHETERISATION CARDIAC ( 50 FDA reports)
DERMAL CYST ( 50 FDA reports)
DEVICE FAILURE ( 50 FDA reports)
GASTRITIS EROSIVE ( 50 FDA reports)
HYPOACUSIS ( 50 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 50 FDA reports)
CHONDROMALACIA ( 49 FDA reports)
CORONARY ARTERY OCCLUSION ( 49 FDA reports)
DIABETIC RETINOPATHY ( 49 FDA reports)
FEELING JITTERY ( 49 FDA reports)
INJECTION SITE HAEMATOMA ( 49 FDA reports)
INTERMITTENT CLAUDICATION ( 49 FDA reports)
OEDEMA MOUTH ( 49 FDA reports)
PULMONARY GRANULOMA ( 49 FDA reports)
RECTAL POLYP ( 49 FDA reports)
SENSORY DISTURBANCE ( 49 FDA reports)
SKIN BURNING SENSATION ( 49 FDA reports)
SYNOVITIS ( 49 FDA reports)
TRISMUS ( 49 FDA reports)
VISUAL FIELD DEFECT ( 48 FDA reports)
BLOOD IRON DECREASED ( 48 FDA reports)
DEMENTIA ( 48 FDA reports)
ENTERITIS ( 48 FDA reports)
EXOPHTHALMOS ( 48 FDA reports)
LARYNGITIS ( 48 FDA reports)
MITRAL VALVE PROLAPSE ( 48 FDA reports)
PERICARDITIS ( 48 FDA reports)
PERITONITIS ( 48 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 48 FDA reports)
POLYP ( 48 FDA reports)
PULSE ABSENT ( 48 FDA reports)
RESPIRATORY RATE INCREASED ( 48 FDA reports)
ABSCESS ORAL ( 47 FDA reports)
AORTIC STENOSIS ( 47 FDA reports)
APPLICATION SITE RASH ( 47 FDA reports)
CAESAREAN SECTION ( 47 FDA reports)
CATARACT OPERATION ( 47 FDA reports)
CHROMATURIA ( 47 FDA reports)
HYDROCEPHALUS ( 47 FDA reports)
INJECTION SITE REACTION ( 47 FDA reports)
ORAL HERPES ( 47 FDA reports)
THYROID CANCER ( 47 FDA reports)
TIBIA FRACTURE ( 47 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 47 FDA reports)
WOUND ( 47 FDA reports)
WOUND DRAINAGE ( 47 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 46 FDA reports)
TEARFULNESS ( 46 FDA reports)
VENTRICULAR FIBRILLATION ( 46 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 46 FDA reports)
BACTERIAL DISEASE CARRIER ( 46 FDA reports)
BARRETT'S OESOPHAGUS ( 46 FDA reports)
BILIARY COLIC ( 46 FDA reports)
BODY HEIGHT DECREASED ( 46 FDA reports)
CACHEXIA ( 46 FDA reports)
DENTAL CARE ( 46 FDA reports)
HYPERPLASIA ( 46 FDA reports)
LUNG INFECTION ( 46 FDA reports)
MIDDLE INSOMNIA ( 46 FDA reports)
MUCOSAL ULCERATION ( 46 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 46 FDA reports)
PROCTALGIA ( 46 FDA reports)
RASH PAPULAR ( 46 FDA reports)
BONE CYST ( 45 FDA reports)
BONE MARROW FAILURE ( 45 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 45 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 45 FDA reports)
FIBULA FRACTURE ( 45 FDA reports)
HERPES SIMPLEX ( 45 FDA reports)
MALOCCLUSION ( 45 FDA reports)
MAXILLOFACIAL OPERATION ( 45 FDA reports)
NEURODERMATITIS ( 45 FDA reports)
OSTEOMYELITIS CHRONIC ( 45 FDA reports)
RASH MACULO-PAPULAR ( 45 FDA reports)
ABDOMINAL TENDERNESS ( 44 FDA reports)
APPLICATION SITE IRRITATION ( 44 FDA reports)
BIOPSY ( 44 FDA reports)
BRAIN INJURY ( 44 FDA reports)
BRUXISM ( 44 FDA reports)
COLON CANCER ( 44 FDA reports)
DENTAL FISTULA ( 44 FDA reports)
INTENTIONAL MISUSE ( 44 FDA reports)
MENORRHAGIA ( 44 FDA reports)
MYOPATHY ( 44 FDA reports)
NEUROGENIC BLADDER ( 44 FDA reports)
ORTHOSIS USER ( 44 FDA reports)
PARALYSIS ( 44 FDA reports)
PERIPHERAL COLDNESS ( 44 FDA reports)
RADICULAR PAIN ( 44 FDA reports)
SEXUAL DYSFUNCTION ( 44 FDA reports)
SINUS CONGESTION ( 44 FDA reports)
TOOTH REPAIR ( 44 FDA reports)
URINE OUTPUT DECREASED ( 44 FDA reports)
VITREOUS DETACHMENT ( 44 FDA reports)
TENOSYNOVITIS ( 43 FDA reports)
ACUTE SINUSITIS ( 43 FDA reports)
BRONCHOSPASM ( 43 FDA reports)
DIALYSIS ( 43 FDA reports)
GANGRENE ( 43 FDA reports)
GASTRODUODENITIS ( 43 FDA reports)
INCISIONAL DRAINAGE ( 43 FDA reports)
MELANOCYTIC NAEVUS ( 43 FDA reports)
MOUTH HAEMORRHAGE ( 43 FDA reports)
PLANTAR FASCIITIS ( 43 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 42 FDA reports)
ADRENAL INSUFFICIENCY ( 42 FDA reports)
APNOEA ( 42 FDA reports)
CHOKING ( 42 FDA reports)
ELECTROLYTE IMBALANCE ( 42 FDA reports)
HODGKIN'S DISEASE ( 42 FDA reports)
INCREASED APPETITE ( 42 FDA reports)
LIMB DISCOMFORT ( 42 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 42 FDA reports)
METABOLIC ENCEPHALOPATHY ( 42 FDA reports)
METASTASIS ( 42 FDA reports)
NECK INJURY ( 42 FDA reports)
NEPHROGENIC ANAEMIA ( 42 FDA reports)
NEURITIS ( 42 FDA reports)
PERIPHERAL ISCHAEMIA ( 42 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 42 FDA reports)
TRANSFUSION ( 42 FDA reports)
ANIMAL BITE ( 41 FDA reports)
DILATATION ATRIAL ( 41 FDA reports)
GALLBLADDER INJURY ( 41 FDA reports)
HAEMODIALYSIS ( 41 FDA reports)
HOMICIDAL IDEATION ( 41 FDA reports)
LACUNAR INFARCTION ( 41 FDA reports)
MYOCLONUS ( 41 FDA reports)
NASAL SEPTUM DEVIATION ( 41 FDA reports)
OESOPHAGEAL DISORDER ( 41 FDA reports)
OLIGURIA ( 41 FDA reports)
PANCREATITIS CHRONIC ( 41 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 41 FDA reports)
SERUM FERRITIN INCREASED ( 41 FDA reports)
BLOOD CHLORIDE DECREASED ( 40 FDA reports)
BLOOD MAGNESIUM DECREASED ( 40 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 40 FDA reports)
CEREBROVASCULAR DISORDER ( 40 FDA reports)
DEVICE BREAKAGE ( 40 FDA reports)
NECROSIS ( 40 FDA reports)
PANIC DISORDER ( 40 FDA reports)
PRESBYOPIA ( 40 FDA reports)
RETINAL HAEMORRHAGE ( 40 FDA reports)
RHONCHI ( 40 FDA reports)
SACROILIITIS ( 40 FDA reports)
SHOCK ( 40 FDA reports)
APHAGIA ( 39 FDA reports)
CREPITATIONS ( 39 FDA reports)
DISEASE RECURRENCE ( 39 FDA reports)
HAEMANGIOMA OF LIVER ( 39 FDA reports)
HYDROCELE ( 39 FDA reports)
MANIA ( 39 FDA reports)
MASTECTOMY ( 39 FDA reports)
OESOPHAGEAL ULCER ( 39 FDA reports)
OSTEOMYELITIS ACUTE ( 39 FDA reports)
POOR DENTAL CONDITION ( 39 FDA reports)
PREGNANCY ( 39 FDA reports)
RADIUS FRACTURE ( 39 FDA reports)
SKIN PAPILLOMA ( 39 FDA reports)
TACHYPNOEA ( 39 FDA reports)
TYPE 1 DIABETES MELLITUS ( 39 FDA reports)
STRESS FRACTURE ( 38 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 38 FDA reports)
TROPONIN INCREASED ( 38 FDA reports)
ACUTE CORONARY SYNDROME ( 38 FDA reports)
APTYALISM ( 38 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 38 FDA reports)
DELUSION ( 38 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 38 FDA reports)
HYPOALBUMINAEMIA ( 38 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 38 FDA reports)
ISCHAEMIC STROKE ( 38 FDA reports)
METAPLASIA ( 38 FDA reports)
MITRAL VALVE CALCIFICATION ( 38 FDA reports)
MYELOPATHY ( 38 FDA reports)
PLEURISY ( 38 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 37 FDA reports)
AORTIC CALCIFICATION ( 37 FDA reports)
ASPIRATION PLEURAL CAVITY ( 37 FDA reports)
BLEPHARITIS ( 37 FDA reports)
BONE GRAFT ( 37 FDA reports)
CLAVICLE FRACTURE ( 37 FDA reports)
DUODENAL ULCER ( 37 FDA reports)
ERUCTATION ( 37 FDA reports)
FACIAL BONES FRACTURE ( 37 FDA reports)
HIGH FREQUENCY ABLATION ( 37 FDA reports)
HYPOVENTILATION ( 37 FDA reports)
INJECTION SITE IRRITATION ( 37 FDA reports)
MEDICAL DEVICE COMPLICATION ( 37 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 37 FDA reports)
PAIN OF SKIN ( 37 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 36 FDA reports)
ATRIAL SEPTAL DEFECT ( 36 FDA reports)
CALCULUS URETERIC ( 36 FDA reports)
COLON ADENOMA ( 36 FDA reports)
FEELING DRUNK ( 36 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 36 FDA reports)
HERNIA ( 36 FDA reports)
HYPERAESTHESIA ( 36 FDA reports)
HYPOPHOSPHATAEMIA ( 36 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 36 FDA reports)
LUNG CONSOLIDATION ( 36 FDA reports)
METABOLIC DISORDER ( 36 FDA reports)
NO THERAPEUTIC RESPONSE ( 36 FDA reports)
PELVIC ABSCESS ( 36 FDA reports)
RENAL PAIN ( 36 FDA reports)
RESPIRATORY TRACT CONGESTION ( 36 FDA reports)
SOFT TISSUE INFLAMMATION ( 36 FDA reports)
SPINAL LAMINECTOMY ( 36 FDA reports)
STENT PLACEMENT ( 36 FDA reports)
SKIN NEOPLASM EXCISION ( 35 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 35 FDA reports)
SUDDEN DEATH ( 35 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 35 FDA reports)
WHEELCHAIR USER ( 35 FDA reports)
AFFECT LABILITY ( 35 FDA reports)
APPENDICITIS PERFORATED ( 35 FDA reports)
BIPOLAR I DISORDER ( 35 FDA reports)
CORONARY ARTERY BYPASS ( 35 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 35 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 35 FDA reports)
DYSPHEMIA ( 35 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 35 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 35 FDA reports)
INJECTION SITE SWELLING ( 35 FDA reports)
MACULAR DEGENERATION ( 35 FDA reports)
MYELODYSPLASTIC SYNDROME ( 35 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 34 FDA reports)
BONE SWELLING ( 34 FDA reports)
CHANGE OF BOWEL HABIT ( 34 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 34 FDA reports)
GASTROINTESTINAL PAIN ( 34 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 34 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 34 FDA reports)
HALLUCINATION, VISUAL ( 34 FDA reports)
HEPATIC CIRRHOSIS ( 34 FDA reports)
HYPERMETABOLISM ( 34 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 34 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 34 FDA reports)
MENINGITIS ( 34 FDA reports)
MYELOMA RECURRENCE ( 34 FDA reports)
NASAL MUCOSAL DISORDER ( 34 FDA reports)
NECK MASS ( 34 FDA reports)
NEUROPATHY ( 34 FDA reports)
OSTEITIS DEFORMANS ( 34 FDA reports)
PYELOCALIECTASIS ( 34 FDA reports)
RAYNAUD'S PHENOMENON ( 34 FDA reports)
RESPIRATORY TRACT INFECTION ( 34 FDA reports)
SCLERODERMA ( 34 FDA reports)
TEMPERATURE INTOLERANCE ( 34 FDA reports)
THERMAL BURN ( 34 FDA reports)
TOXIC ENCEPHALOPATHY ( 34 FDA reports)
VITAMIN B12 DEFICIENCY ( 34 FDA reports)
SKIN ATROPHY ( 33 FDA reports)
SKIN HYPERPIGMENTATION ( 33 FDA reports)
ACETABULUM FRACTURE ( 33 FDA reports)
ACNE ( 33 FDA reports)
ALCOHOL USE ( 33 FDA reports)
ANGIOEDEMA ( 33 FDA reports)
BLINDNESS TRANSIENT ( 33 FDA reports)
BLOOD UREA DECREASED ( 33 FDA reports)
CEREBRAL ARTERY STENOSIS ( 33 FDA reports)
EYE IRRITATION ( 33 FDA reports)
HYPERTHYROIDISM ( 33 FDA reports)
HYPERTONIC BLADDER ( 33 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 33 FDA reports)
JOINT CONTRACTURE ( 33 FDA reports)
MONOCLONAL GAMMOPATHY ( 33 FDA reports)
PHOTOPSIA ( 33 FDA reports)
SINUS OPERATION ( 33 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 32 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 32 FDA reports)
BILE DUCT STONE ( 32 FDA reports)
BILIARY DILATATION ( 32 FDA reports)
BIOPSY BONE MARROW ( 32 FDA reports)
BRONCHITIS CHRONIC ( 32 FDA reports)
CHEST WALL PAIN ( 32 FDA reports)
CHEST X-RAY ABNORMAL ( 32 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 32 FDA reports)
EPICONDYLITIS ( 32 FDA reports)
FLAT AFFECT ( 32 FDA reports)
INCOHERENT ( 32 FDA reports)
LABORATORY TEST ABNORMAL ( 32 FDA reports)
NARCOTIC INTOXICATION ( 32 FDA reports)
PROCEDURAL COMPLICATION ( 32 FDA reports)
RENAL CANCER ( 32 FDA reports)
SINUS HEADACHE ( 32 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 32 FDA reports)
THROMBOCYTOSIS ( 32 FDA reports)
VENOUS OCCLUSION ( 32 FDA reports)
VENOUS THROMBOSIS ( 32 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 31 FDA reports)
THERAPY NON-RESPONDER ( 31 FDA reports)
TREATMENT FAILURE ( 31 FDA reports)
TRIGGER FINGER ( 31 FDA reports)
VIITH NERVE PARALYSIS ( 31 FDA reports)
AORTIC DILATATION ( 31 FDA reports)
BLADDER PROLAPSE ( 31 FDA reports)
DRUG DISPENSING ERROR ( 31 FDA reports)
DYSPAREUNIA ( 31 FDA reports)
DYSTHYMIC DISORDER ( 31 FDA reports)
ESSENTIAL HYPERTENSION ( 31 FDA reports)
NYSTAGMUS ( 31 FDA reports)
PSYCHIATRIC SYMPTOM ( 31 FDA reports)
RALES ( 31 FDA reports)
ALVEOLAR OSTEITIS ( 30 FDA reports)
ALVEOLOPLASTY ( 30 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 30 FDA reports)
BONE MARROW DISORDER ( 30 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 30 FDA reports)
FISTULA REPAIR ( 30 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 30 FDA reports)
HYPERCOAGULATION ( 30 FDA reports)
MACROGLOSSIA ( 30 FDA reports)
MUSCLE HAEMORRHAGE ( 30 FDA reports)
NERVE COMPRESSION ( 30 FDA reports)
OCCULT BLOOD POSITIVE ( 30 FDA reports)
OESOPHAGEAL PAIN ( 30 FDA reports)
OPEN REDUCTION OF FRACTURE ( 30 FDA reports)
OVARIAN MASS ( 30 FDA reports)
POSTNASAL DRIP ( 30 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 30 FDA reports)
STEVENS-JOHNSON SYNDROME ( 30 FDA reports)
TENDON INJURY ( 30 FDA reports)
SOMNAMBULISM ( 29 FDA reports)
TOOTH IMPACTED ( 29 FDA reports)
VENA CAVA THROMBOSIS ( 29 FDA reports)
VENTRICULAR DYSFUNCTION ( 29 FDA reports)
WOUND SECRETION ( 29 FDA reports)
ANAEMIA POSTOPERATIVE ( 29 FDA reports)
ANEURYSM ( 29 FDA reports)
APHTHOUS STOMATITIS ( 29 FDA reports)
APPLICATION SITE REACTION ( 29 FDA reports)
BILE DUCT OBSTRUCTION ( 29 FDA reports)
BLADDER SPASM ( 29 FDA reports)
CYSTOCELE ( 29 FDA reports)
EMBOLISM ( 29 FDA reports)
JUGULAR VEIN THROMBOSIS ( 29 FDA reports)
LIGAMENT RUPTURE ( 29 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 29 FDA reports)
NEPHROPATHY ( 29 FDA reports)
NO ADVERSE EVENT ( 29 FDA reports)
OESOPHAGEAL STENOSIS ( 29 FDA reports)
ONYCHOCLASIS ( 29 FDA reports)
PHOTOSENSITIVITY REACTION ( 29 FDA reports)
RENAL MASS ( 29 FDA reports)
RIGHT ATRIAL DILATATION ( 29 FDA reports)
ABDOMINAL ABSCESS ( 28 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 28 FDA reports)
ADENOCARCINOMA ( 28 FDA reports)
AMAUROSIS FUGAX ( 28 FDA reports)
AXILLARY MASS ( 28 FDA reports)
BLADDER CANCER ( 28 FDA reports)
BLOOD PRESSURE ABNORMAL ( 28 FDA reports)
BUNION ( 28 FDA reports)
CARDIAC PACEMAKER INSERTION ( 28 FDA reports)
CAROTID BRUIT ( 28 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 28 FDA reports)
DIABETIC FOOT ( 28 FDA reports)
DRUG EFFECT INCREASED ( 28 FDA reports)
DYSMENORRHOEA ( 28 FDA reports)
EXTRASYSTOLES ( 28 FDA reports)
EYELID PTOSIS ( 28 FDA reports)
FACIAL NEURALGIA ( 28 FDA reports)
FAT NECROSIS ( 28 FDA reports)
FEMORAL ARTERY OCCLUSION ( 28 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 28 FDA reports)
HYSTERECTOMY ( 28 FDA reports)
IMMUNODEFICIENCY ( 28 FDA reports)
KELOID SCAR ( 28 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 28 FDA reports)
REFLUX LARYNGITIS ( 28 FDA reports)
RESORPTION BONE INCREASED ( 28 FDA reports)
RESPIRATORY RATE DECREASED ( 28 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 28 FDA reports)
TINEA PEDIS ( 28 FDA reports)
WEGENER'S GRANULOMATOSIS ( 28 FDA reports)
ADJUSTMENT DISORDER ( 27 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 27 FDA reports)
BODY TEMPERATURE DECREASED ( 27 FDA reports)
CATHETER RELATED COMPLICATION ( 27 FDA reports)
CATHETER REMOVAL ( 27 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 27 FDA reports)
DENTAL DISCOMFORT ( 27 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 27 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 27 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 27 FDA reports)
FAMILY STRESS ( 27 FDA reports)
FISTULA DISCHARGE ( 27 FDA reports)
FOOT OPERATION ( 27 FDA reports)
GUN SHOT WOUND ( 27 FDA reports)
INITIAL INSOMNIA ( 27 FDA reports)
INTESTINAL PERFORATION ( 27 FDA reports)
LIP SWELLING ( 27 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 27 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 27 FDA reports)
OESOPHAGEAL SPASM ( 27 FDA reports)
PIGMENTATION DISORDER ( 27 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 27 FDA reports)
SELF-MEDICATION ( 27 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 26 FDA reports)
APPLICATION SITE VESICLES ( 26 FDA reports)
BRAIN OEDEMA ( 26 FDA reports)
BREATH SOUNDS ABNORMAL ( 26 FDA reports)
CARDIAC FLUTTER ( 26 FDA reports)
COLLAPSE OF LUNG ( 26 FDA reports)
DYSTONIA ( 26 FDA reports)
EPIDIDYMITIS ( 26 FDA reports)
FORMICATION ( 26 FDA reports)
FRACTURE NONUNION ( 26 FDA reports)
GENERALISED ANXIETY DISORDER ( 26 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 26 FDA reports)
HYPERPARATHYROIDISM ( 26 FDA reports)
HYPERPHAGIA ( 26 FDA reports)
ILEUS PARALYTIC ( 26 FDA reports)
INTRACRANIAL ANEURYSM ( 26 FDA reports)
LIPASE INCREASED ( 26 FDA reports)
MOTOR DYSFUNCTION ( 26 FDA reports)
POLYNEUROPATHY ( 26 FDA reports)
POST LAMINECTOMY SYNDROME ( 26 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 26 FDA reports)
PROSTATIC OBSTRUCTION ( 26 FDA reports)
RENAL CELL CARCINOMA ( 26 FDA reports)
SEASONAL ALLERGY ( 26 FDA reports)
TALIPES ( 26 FDA reports)
TONGUE INJURY ( 26 FDA reports)
TRAUMATIC BRAIN INJURY ( 26 FDA reports)
UTERINE CANCER ( 26 FDA reports)
STREPTOCOCCAL INFECTION ( 25 FDA reports)
TACHYARRHYTHMIA ( 25 FDA reports)
UMBILICAL CORD ABNORMALITY ( 25 FDA reports)
BLOOD BICARBONATE INCREASED ( 25 FDA reports)
BLOOD TEST ABNORMAL ( 25 FDA reports)
BRONCHIECTASIS ( 25 FDA reports)
CERVICAL CORD COMPRESSION ( 25 FDA reports)
EATING DISORDER SYMPTOM ( 25 FDA reports)
ENDOTRACHEAL INTUBATION ( 25 FDA reports)
EROSIVE OESOPHAGITIS ( 25 FDA reports)
FLUID INTAKE REDUCED ( 25 FDA reports)
GASTRITIS HAEMORRHAGIC ( 25 FDA reports)
HAEMORRHAGIC STROKE ( 25 FDA reports)
HAEMOTHORAX ( 25 FDA reports)
HEPATIC NECROSIS ( 25 FDA reports)
HYPOTONIA ( 25 FDA reports)
INGROWING NAIL ( 25 FDA reports)
KLEBSIELLA INFECTION ( 25 FDA reports)
LABYRINTHITIS ( 25 FDA reports)
LIP DRY ( 25 FDA reports)
MITRAL VALVE DISEASE ( 25 FDA reports)
NERVE BLOCK ( 25 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 25 FDA reports)
PARAPLEGIA ( 25 FDA reports)
PATHOLOGICAL GAMBLING ( 25 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 25 FDA reports)
SINUS ANTROSTOMY ( 25 FDA reports)
ACCIDENTAL DEATH ( 24 FDA reports)
ACIDOSIS ( 24 FDA reports)
ADRENAL DISORDER ( 24 FDA reports)
ANXIETY DISORDER ( 24 FDA reports)
BLADDER DYSFUNCTION ( 24 FDA reports)
BLOOD CALCIUM INCREASED ( 24 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 24 FDA reports)
BONE MARROW OEDEMA ( 24 FDA reports)
BREAST LUMP REMOVAL ( 24 FDA reports)
BRONCHITIS ACUTE ( 24 FDA reports)
BULLOUS LUNG DISEASE ( 24 FDA reports)
CARDIOGENIC SHOCK ( 24 FDA reports)
CHOLESTEROSIS ( 24 FDA reports)
CYSTITIS HAEMORRHAGIC ( 24 FDA reports)
DECREASED ACTIVITY ( 24 FDA reports)
EMPYEMA ( 24 FDA reports)
ENCEPHALOMALACIA ( 24 FDA reports)
GALLBLADDER ENLARGEMENT ( 24 FDA reports)
HOSTILITY ( 24 FDA reports)
HYPERBILIRUBINAEMIA ( 24 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 24 FDA reports)
MENOPAUSE ( 24 FDA reports)
MUSCLE DISORDER ( 24 FDA reports)
MUSCLE SPASTICITY ( 24 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 24 FDA reports)
POLYPECTOMY ( 24 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 24 FDA reports)
RETINOPATHY ( 24 FDA reports)
SKIN FIBROSIS ( 24 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 24 FDA reports)
TELANGIECTASIA ( 24 FDA reports)
URINARY TRACT DISORDER ( 24 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 24 FDA reports)
VITAMIN D DECREASED ( 24 FDA reports)
VULVOVAGINAL DRYNESS ( 24 FDA reports)
SNEEZING ( 23 FDA reports)
TEMPORAL ARTERITIS ( 23 FDA reports)
THROMBOSIS IN DEVICE ( 23 FDA reports)
URETERIC OBSTRUCTION ( 23 FDA reports)
VOCAL CORD PARALYSIS ( 23 FDA reports)
WOUND COMPLICATION ( 23 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 23 FDA reports)
DIABETIC NEPHROPATHY ( 23 FDA reports)
FOREIGN BODY ( 23 FDA reports)
GINGIVAL ABSCESS ( 23 FDA reports)
GINGIVAL OPERATION ( 23 FDA reports)
HEPATITIS ACUTE ( 23 FDA reports)
HYPERURICAEMIA ( 23 FDA reports)
HYPOGONADISM ( 23 FDA reports)
INCISIONAL HERNIA ( 23 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 23 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 23 FDA reports)
LIMB OPERATION ( 23 FDA reports)
MARROW HYPERPLASIA ( 23 FDA reports)
MASS EXCISION ( 23 FDA reports)
MASTITIS ( 23 FDA reports)
MENINGITIS ASEPTIC ( 23 FDA reports)
MENSTRUATION IRREGULAR ( 23 FDA reports)
METRORRHAGIA ( 23 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 23 FDA reports)
NEPHROTIC SYNDROME ( 23 FDA reports)
OBSTRUCTIVE UROPATHY ( 23 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 23 FDA reports)
PANNICULITIS ( 23 FDA reports)
PAPILLOEDEMA ( 23 FDA reports)
PAPILLOMA ( 23 FDA reports)
PERFORMANCE STATUS DECREASED ( 23 FDA reports)
PERIARTHRITIS ( 23 FDA reports)
POLYMYALGIA RHEUMATICA ( 23 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 23 FDA reports)
RADIATION INJURY ( 23 FDA reports)
SCRATCH ( 23 FDA reports)
SENSATION OF FOREIGN BODY ( 23 FDA reports)
SHOULDER OPERATION ( 23 FDA reports)
ACCIDENT AT WORK ( 22 FDA reports)
APPARENT DEATH ( 22 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 22 FDA reports)
CAUDA EQUINA SYNDROME ( 22 FDA reports)
CHOLECYSTITIS INFECTIVE ( 22 FDA reports)
CLAUSTROPHOBIA ( 22 FDA reports)
COLECTOMY ( 22 FDA reports)
DEPRESSIVE SYMPTOM ( 22 FDA reports)
DRUG DIVERSION ( 22 FDA reports)
DRUG TOLERANCE INCREASED ( 22 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 22 FDA reports)
ENTEROVESICAL FISTULA ( 22 FDA reports)
FEMORAL NECK FRACTURE ( 22 FDA reports)
FIBROUS HISTIOCYTOMA ( 22 FDA reports)
HEPATIC NEOPLASM ( 22 FDA reports)
HEPATIC PAIN ( 22 FDA reports)
LACTOSE INTOLERANCE ( 22 FDA reports)
METASTASES TO MENINGES ( 22 FDA reports)
METASTATIC PAIN ( 22 FDA reports)
MONOCYTE COUNT INCREASED ( 22 FDA reports)
MULTIPLE FRACTURES ( 22 FDA reports)
NERVE ROOT COMPRESSION ( 22 FDA reports)
PERIODONTAL INFECTION ( 22 FDA reports)
POOR PERSONAL HYGIENE ( 22 FDA reports)
POUCHITIS ( 22 FDA reports)
PRESCRIBED OVERDOSE ( 22 FDA reports)
PULMONARY THROMBOSIS ( 22 FDA reports)
PULMONARY VASCULAR DISORDER ( 22 FDA reports)
PURPURA ( 22 FDA reports)
SEROTONIN SYNDROME ( 22 FDA reports)
SKIN SWELLING ( 22 FDA reports)
SPINAL COLUMN INJURY ( 22 FDA reports)
TENSION ( 22 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 22 FDA reports)
SPINAL CORPECTOMY ( 21 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 21 FDA reports)
TOOTH EROSION ( 21 FDA reports)
TRANSAMINASES INCREASED ( 21 FDA reports)
UTERINE HAEMORRHAGE ( 21 FDA reports)
VASODILATATION ( 21 FDA reports)
WRONG DRUG ADMINISTERED ( 21 FDA reports)
ABORTION SPONTANEOUS ( 21 FDA reports)
ADENOMA BENIGN ( 21 FDA reports)
ADRENAL MASS ( 21 FDA reports)
AGRANULOCYTOSIS ( 21 FDA reports)
ARTHRITIS BACTERIAL ( 21 FDA reports)
ARTHROSCOPIC SURGERY ( 21 FDA reports)
BREAKTHROUGH PAIN ( 21 FDA reports)
BREAST CALCIFICATIONS ( 21 FDA reports)
CARDIAC ANEURYSM ( 21 FDA reports)
CARDIAC ENZYMES INCREASED ( 21 FDA reports)
CARTILAGE INJURY ( 21 FDA reports)
CIRCULATORY COLLAPSE ( 21 FDA reports)
COLONOSCOPY ABNORMAL ( 21 FDA reports)
CORNEAL ABRASION ( 21 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 21 FDA reports)
CUSHINGOID ( 21 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 21 FDA reports)
DYSGRAPHIA ( 21 FDA reports)
EXTERNAL EAR DISORDER ( 21 FDA reports)
EYE LASER SURGERY ( 21 FDA reports)
EYE MOVEMENT DISORDER ( 21 FDA reports)
FEELING GUILTY ( 21 FDA reports)
FRUSTRATION ( 21 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 21 FDA reports)
HAMARTOMA ( 21 FDA reports)
HYPERNATRAEMIA ( 21 FDA reports)
HYPOAESTHESIA FACIAL ( 21 FDA reports)
INJECTION SITE RASH ( 21 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 21 FDA reports)
INTRAOCULAR LENS IMPLANT ( 21 FDA reports)
LEG AMPUTATION ( 21 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 21 FDA reports)
LYMPHADENECTOMY ( 21 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 21 FDA reports)
MUSCULOSKELETAL DISORDER ( 21 FDA reports)
ORAL FUNGAL INFECTION ( 21 FDA reports)
OVARIAN CANCER ( 21 FDA reports)
PERIPHERAL EMBOLISM ( 21 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 21 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 21 FDA reports)
POOR VENOUS ACCESS ( 21 FDA reports)
PREMATURE BABY ( 21 FDA reports)
PROSTATE CANCER RECURRENT ( 21 FDA reports)
PROTEIN URINE PRESENT ( 21 FDA reports)
PSEUDOPOLYP ( 21 FDA reports)
REFLUX GASTRITIS ( 21 FDA reports)
REFLUX OESOPHAGITIS ( 21 FDA reports)
RETINAL TEAR ( 21 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 20 FDA reports)
ANAPHYLACTIC SHOCK ( 20 FDA reports)
ARACHNOIDITIS ( 20 FDA reports)
ATRIAL TACHYCARDIA ( 20 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 20 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 20 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 20 FDA reports)
BONE DEFORMITY ( 20 FDA reports)
BONE TRIMMING ( 20 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 20 FDA reports)
COMMUNICATION DISORDER ( 20 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 20 FDA reports)
DUODENAL ULCER PERFORATION ( 20 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 20 FDA reports)
FOOD POISONING ( 20 FDA reports)
GASTRIC HAEMORRHAGE ( 20 FDA reports)
GLOMERULONEPHRITIS ( 20 FDA reports)
GRAFT VERSUS HOST DISEASE ( 20 FDA reports)
HAEMOLYSIS ( 20 FDA reports)
HAEMORRHAGIC ANAEMIA ( 20 FDA reports)
HEMIPLEGIA ( 20 FDA reports)
HEPATOTOXICITY ( 20 FDA reports)
HICCUPS ( 20 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 20 FDA reports)
INTENTIONAL SELF-INJURY ( 20 FDA reports)
INTRACARDIAC THROMBUS ( 20 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 20 FDA reports)
KNEE OPERATION ( 20 FDA reports)
MELANOSIS COLI ( 20 FDA reports)
MENSTRUAL DISORDER ( 20 FDA reports)
MYDRIASIS ( 20 FDA reports)
MYELITIS TRANSVERSE ( 20 FDA reports)
ORGAN FAILURE ( 20 FDA reports)
PAROTID GLAND ENLARGEMENT ( 20 FDA reports)
PAROTITIS ( 20 FDA reports)
PELVIC INFECTION ( 20 FDA reports)
PERIODONTAL OPERATION ( 20 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 20 FDA reports)
PHARYNGEAL ERYTHEMA ( 20 FDA reports)
PROCEDURAL NAUSEA ( 20 FDA reports)
PROSTATITIS ( 20 FDA reports)
PROTEIN TOTAL DECREASED ( 20 FDA reports)
PULSE ABNORMAL ( 20 FDA reports)
PYURIA ( 20 FDA reports)
RADICULITIS BRACHIAL ( 20 FDA reports)
SCAN BONE MARROW ABNORMAL ( 20 FDA reports)
SPUTUM DISCOLOURED ( 20 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 20 FDA reports)
THYROID CYST ( 20 FDA reports)
THYROXINE FREE DECREASED ( 20 FDA reports)
TONGUE DISCOLOURATION ( 20 FDA reports)
UTERINE ENLARGEMENT ( 20 FDA reports)
STAPHYLOMA ( 19 FDA reports)
TOBACCO ABUSE ( 19 FDA reports)
TOBACCO USER ( 19 FDA reports)
TONGUE COATED ( 19 FDA reports)
TRACHEAL DEVIATION ( 19 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 19 FDA reports)
ADRENAL ADENOMA ( 19 FDA reports)
ANOXIC ENCEPHALOPATHY ( 19 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 19 FDA reports)
APPLICATION SITE PAIN ( 19 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 19 FDA reports)
ASEPTIC NECROSIS BONE ( 19 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 19 FDA reports)
BONE FISTULA ( 19 FDA reports)
CALCULUS URINARY ( 19 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 19 FDA reports)
DENTAL PROSTHESIS USER ( 19 FDA reports)
DIABETIC GASTROPARESIS ( 19 FDA reports)
DIAPHRAGMATIC HERNIA ( 19 FDA reports)
EFFUSION ( 19 FDA reports)
ENDOMETRIOSIS ( 19 FDA reports)
EPILEPSY ( 19 FDA reports)
FACIAL PARESIS ( 19 FDA reports)
FIBRIN D DIMER INCREASED ( 19 FDA reports)
FRACTURE DISPLACEMENT ( 19 FDA reports)
FURUNCLE ( 19 FDA reports)
GASTROINTESTINAL PERFORATION ( 19 FDA reports)
GINGIVAL HYPERTROPHY ( 19 FDA reports)
GINGIVAL OEDEMA ( 19 FDA reports)
GRIP STRENGTH DECREASED ( 19 FDA reports)
HEART DISEASE CONGENITAL ( 19 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 19 FDA reports)
HUNGER ( 19 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 19 FDA reports)
HYPERVENTILATION ( 19 FDA reports)
HYPERVISCOSITY SYNDROME ( 19 FDA reports)
INJECTION SITE PRURITUS ( 19 FDA reports)
JOINT CREPITATION ( 19 FDA reports)
LARYNGOCELE ( 19 FDA reports)
MENINGEAL NEOPLASM ( 19 FDA reports)
MENOPAUSAL SYMPTOMS ( 19 FDA reports)
NASAL POLYPS ( 19 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 19 FDA reports)
ORAL PRURITUS ( 19 FDA reports)
PAIN EXACERBATED ( 19 FDA reports)
PARKINSON'S DISEASE ( 19 FDA reports)
PELVIC MASS ( 19 FDA reports)
PULMONARY HAEMORRHAGE ( 19 FDA reports)
RADICULITIS ( 19 FDA reports)
RENAL ISCHAEMIA ( 19 FDA reports)
RENAL TUBULAR ACIDOSIS ( 19 FDA reports)
SEBORRHOEIC DERMATITIS ( 19 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 18 FDA reports)
AORTIC VALVE STENOSIS ( 18 FDA reports)
APPLICATION SITE URTICARIA ( 18 FDA reports)
ASTROCYTOMA ( 18 FDA reports)
ATROPHIC VULVOVAGINITIS ( 18 FDA reports)
BLADDER DILATATION ( 18 FDA reports)
BLADDER DISCOMFORT ( 18 FDA reports)
BRAIN SCAN ABNORMAL ( 18 FDA reports)
BRONCHOPLEURAL FISTULA ( 18 FDA reports)
BUTTOCK PAIN ( 18 FDA reports)
CARDIAC VALVE ABSCESS ( 18 FDA reports)
CHORIOAMNIONITIS ( 18 FDA reports)
COR PULMONALE CHRONIC ( 18 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 18 FDA reports)
DEVICE DISLOCATION ( 18 FDA reports)
DISORDER OF ORBIT ( 18 FDA reports)
DISSOCIATION ( 18 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 18 FDA reports)
EYE DISCHARGE ( 18 FDA reports)
EYE HAEMORRHAGE ( 18 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 18 FDA reports)
FRACTURED SACRUM ( 18 FDA reports)
GLOSSITIS ( 18 FDA reports)
HEARING AID USER ( 18 FDA reports)
HEPATIC ENZYME ABNORMAL ( 18 FDA reports)
HYDROPNEUMOTHORAX ( 18 FDA reports)
INCISION SITE COMPLICATION ( 18 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 18 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 18 FDA reports)
LARYNGOSPASM ( 18 FDA reports)
LIGAMENT INJURY ( 18 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 18 FDA reports)
LIVER INJURY ( 18 FDA reports)
LOGORRHOEA ( 18 FDA reports)
MALIGNANT HYPERTENSION ( 18 FDA reports)
MEDICAL DEVICE REMOVAL ( 18 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 18 FDA reports)
MUSCLE CRAMP ( 18 FDA reports)
MUSCLE INJURY ( 18 FDA reports)
NASAL NECROSIS ( 18 FDA reports)
PAINFUL RESPIRATION ( 18 FDA reports)
PALATAL OEDEMA ( 18 FDA reports)
PANCREATIC DISORDER ( 18 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 18 FDA reports)
PERIODONTAL DESTRUCTION ( 18 FDA reports)
PHYSIOTHERAPY ( 18 FDA reports)
PIRIFORMIS SYNDROME ( 18 FDA reports)
PLACENTAL INSUFFICIENCY ( 18 FDA reports)
PULMONARY RADIATION INJURY ( 18 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 18 FDA reports)
ROTATOR CUFF REPAIR ( 18 FDA reports)
SCOTOMA ( 18 FDA reports)
SEROMA ( 18 FDA reports)
SIGMOIDITIS ( 18 FDA reports)
SINUS ARRHYTHMIA ( 18 FDA reports)
SKIN FISSURES ( 18 FDA reports)
SKIN ODOUR ABNORMAL ( 18 FDA reports)
SKIN WARM ( 18 FDA reports)
STASIS DERMATITIS ( 18 FDA reports)
TESTICULAR PAIN ( 18 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 18 FDA reports)
THORACOTOMY ( 18 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 18 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 18 FDA reports)
TRICUSPID VALVE DISEASE ( 18 FDA reports)
TUBERCULOSIS ( 18 FDA reports)
ULNA FRACTURE ( 18 FDA reports)
VAGINAL DISCHARGE ( 18 FDA reports)
SPINAL DEFORMITY ( 17 FDA reports)
TENSION HEADACHE ( 17 FDA reports)
THERAPEUTIC PROCEDURE ( 17 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 17 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 17 FDA reports)
URINE ANALYSIS ABNORMAL ( 17 FDA reports)
UTEROVAGINAL PROLAPSE ( 17 FDA reports)
VASCULAR INSUFFICIENCY ( 17 FDA reports)
VEIN DISORDER ( 17 FDA reports)
VERTEBRAL WEDGING ( 17 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 17 FDA reports)
X-RAY ABNORMAL ( 17 FDA reports)
ABSCESS LIMB ( 17 FDA reports)
ACINETOBACTER INFECTION ( 17 FDA reports)
ADHESION ( 17 FDA reports)
ALCOHOLISM ( 17 FDA reports)
BLADDER CATHETERISATION ( 17 FDA reports)
BLADDER OPERATION ( 17 FDA reports)
BLOOD COUNT ABNORMAL ( 17 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 17 FDA reports)
BREAST RECONSTRUCTION ( 17 FDA reports)
CARDIAC OUTPUT DECREASED ( 17 FDA reports)
CHEST TUBE INSERTION ( 17 FDA reports)
COMMINUTED FRACTURE ( 17 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 17 FDA reports)
DEMYELINATION ( 17 FDA reports)
DENTAL TREATMENT ( 17 FDA reports)
DROP ATTACKS ( 17 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 17 FDA reports)
ENDOCARDITIS ( 17 FDA reports)
FASCIITIS ( 17 FDA reports)
FOREIGN BODY REACTION ( 17 FDA reports)
HEPATIC CONGESTION ( 17 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 17 FDA reports)
JAW LESION EXCISION ( 17 FDA reports)
LUNG HYPERINFLATION ( 17 FDA reports)
MASTOCYTOSIS ( 17 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 17 FDA reports)
MITRAL VALVE SCLEROSIS ( 17 FDA reports)
NEUROENDOCRINE CARCINOMA ( 17 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 17 FDA reports)
ORAL DISCHARGE ( 17 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 17 FDA reports)
PALATAL DISORDER ( 17 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 17 FDA reports)
PITUITARY ENLARGEMENT ( 17 FDA reports)
QRS AXIS ABNORMAL ( 17 FDA reports)
RASH VESICULAR ( 17 FDA reports)
RETINAL INFARCTION ( 17 FDA reports)
SCREAMING ( 17 FDA reports)
ABDOMINAL MASS ( 16 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 16 FDA reports)
AMBLYOPIA ( 16 FDA reports)
APPETITE DISORDER ( 16 FDA reports)
APPLICATION SITE EROSION ( 16 FDA reports)
ARTERIAL BYPASS OPERATION ( 16 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 16 FDA reports)
BLOOD CHLORIDE INCREASED ( 16 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 16 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 16 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 16 FDA reports)
BLOODY DISCHARGE ( 16 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 16 FDA reports)
CAROTID ARTERY DISEASE ( 16 FDA reports)
CATHETER RELATED INFECTION ( 16 FDA reports)
CEREBELLAR ATROPHY ( 16 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 16 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 16 FDA reports)
DEVICE OCCLUSION ( 16 FDA reports)
DRUG ERUPTION ( 16 FDA reports)
DRUG LEVEL INCREASED ( 16 FDA reports)
ECZEMA ASTEATOTIC ( 16 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 16 FDA reports)
EXPIRED DRUG ADMINISTERED ( 16 FDA reports)
FACIAL OPERATION ( 16 FDA reports)
FALLOPIAN TUBE DISORDER ( 16 FDA reports)
FEELING HOT AND COLD ( 16 FDA reports)
FULL BLOOD COUNT DECREASED ( 16 FDA reports)
GASTROENTERITIS RADIATION ( 16 FDA reports)
GASTROSTOMY TUBE INSERTION ( 16 FDA reports)
ICHTHYOSIS ( 16 FDA reports)
INJURY CORNEAL ( 16 FDA reports)
IRON DEFICIENCY ( 16 FDA reports)
LIP DISCOLOURATION ( 16 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 16 FDA reports)
LUDWIG ANGINA ( 16 FDA reports)
MACROCYTOSIS ( 16 FDA reports)
MICTURITION DISORDER ( 16 FDA reports)
MONOCYTOSIS ( 16 FDA reports)
MORTON'S NEUROMA ( 16 FDA reports)
NAIL DYSTROPHY ( 16 FDA reports)
NASAL OBSTRUCTION ( 16 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 16 FDA reports)
OESOPHAGITIS ULCERATIVE ( 16 FDA reports)
ORAL FIBROMA ( 16 FDA reports)
ORAL MUCOSA ATROPHY ( 16 FDA reports)
ORAL TORUS ( 16 FDA reports)
ORTHODONTIC APPLIANCE USER ( 16 FDA reports)
OSTEOSYNTHESIS ( 16 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 16 FDA reports)
PITTING OEDEMA ( 16 FDA reports)
PLACENTAL INFARCTION ( 16 FDA reports)
PROCEDURAL HYPERTENSION ( 16 FDA reports)
PROCTITIS ( 16 FDA reports)
PUPIL FIXED ( 16 FDA reports)
RASH PUSTULAR ( 16 FDA reports)
SCHIZOPHRENIA ( 16 FDA reports)
SELF-INJURIOUS IDEATION ( 16 FDA reports)
SKIN INJURY ( 16 FDA reports)
SOFT TISSUE INFECTION ( 16 FDA reports)
SPLEEN CONGESTION ( 16 FDA reports)
SUBCUTANEOUS NODULE ( 16 FDA reports)
TENOSYNOVITIS STENOSANS ( 16 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 16 FDA reports)
TIC ( 16 FDA reports)
VOMITING PROJECTILE ( 16 FDA reports)
SKIN IRRITATION ( 15 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 15 FDA reports)
TEETH BRITTLE ( 15 FDA reports)
TESTICULAR SWELLING ( 15 FDA reports)
TINEA INFECTION ( 15 FDA reports)
TONGUE DISORDER ( 15 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 15 FDA reports)
VASCULAR INJURY ( 15 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 15 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 15 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 15 FDA reports)
ACUTE PRERENAL FAILURE ( 15 FDA reports)
AKATHISIA ( 15 FDA reports)
ALOPECIA AREATA ( 15 FDA reports)
ARTERIAL DISORDER ( 15 FDA reports)
ARTHROPOD BITE ( 15 FDA reports)
BACTERIAL TEST POSITIVE ( 15 FDA reports)
BLADDER PAIN ( 15 FDA reports)
BLOOD DISORDER ( 15 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 15 FDA reports)
BRADYPHRENIA ( 15 FDA reports)
BRAIN MASS ( 15 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 15 FDA reports)
BREAST FIBROSIS ( 15 FDA reports)
CANCER PAIN ( 15 FDA reports)
CARDIAC TAMPONADE ( 15 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 15 FDA reports)
CLUMSINESS ( 15 FDA reports)
CORONARY ARTERY REOCCLUSION ( 15 FDA reports)
CYSTITIS INTERSTITIAL ( 15 FDA reports)
DIZZINESS POSTURAL ( 15 FDA reports)
DYSPHORIA ( 15 FDA reports)
EAR DISCOMFORT ( 15 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 15 FDA reports)
ENTHESOPATHY ( 15 FDA reports)
EPIGASTRIC DISCOMFORT ( 15 FDA reports)
EXTRADURAL ABSCESS ( 15 FDA reports)
FIBROMA ( 15 FDA reports)
FOOD CRAVING ( 15 FDA reports)
GALLOP RHYTHM PRESENT ( 15 FDA reports)
GRANULOCYTOPENIA ( 15 FDA reports)
HAEMORRHOID OPERATION ( 15 FDA reports)
HEPATIC MASS ( 15 FDA reports)
HEPATOSPLENOMEGALY ( 15 FDA reports)
HERNIA REPAIR ( 15 FDA reports)
HISTOPLASMOSIS ( 15 FDA reports)
HYPOTHERMIA ( 15 FDA reports)
ILIAC ARTERY THROMBOSIS ( 15 FDA reports)
IMPULSIVE BEHAVIOUR ( 15 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 15 FDA reports)
INTESTINAL HAEMORRHAGE ( 15 FDA reports)
ISCHAEMIC HEPATITIS ( 15 FDA reports)
LERICHE SYNDROME ( 15 FDA reports)
LIPOMA EXCISION ( 15 FDA reports)
LOSS OF LIBIDO ( 15 FDA reports)
LYMPHADENITIS ( 15 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 15 FDA reports)
LYMPHOPENIA ( 15 FDA reports)
MALIGNANT MELANOMA IN SITU ( 15 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 15 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 15 FDA reports)
NEOPLASM ( 15 FDA reports)
NEUROMA ( 15 FDA reports)
NEUTROPENIC COLITIS ( 15 FDA reports)
PANCREATIC CYST ( 15 FDA reports)
PARAPROTEINAEMIA ( 15 FDA reports)
PLASMAPHERESIS ( 15 FDA reports)
POLYARTHRITIS ( 15 FDA reports)
POLYDIPSIA ( 15 FDA reports)
PORTAL VEIN THROMBOSIS ( 15 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 15 FDA reports)
POSTOPERATIVE INFECTION ( 15 FDA reports)
PREMATURE LABOUR ( 15 FDA reports)
RENAL COLIC ( 15 FDA reports)
RENAL OSTEODYSTROPHY ( 15 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 15 FDA reports)
SINUS POLYP DEGENERATION ( 15 FDA reports)
ACROCHORDON ( 14 FDA reports)
ACUTE PULMONARY OEDEMA ( 14 FDA reports)
AGEUSIA ( 14 FDA reports)
ANGIOLIPOMA ( 14 FDA reports)
ANOGENITAL WARTS ( 14 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 14 FDA reports)
ARRESTED LABOUR ( 14 FDA reports)
ARTHROPOD STING ( 14 FDA reports)
ATROPHY ( 14 FDA reports)
BASEDOW'S DISEASE ( 14 FDA reports)
BIOPSY CHEST WALL ABNORMAL ( 14 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 14 FDA reports)
BLOOD PROLACTIN INCREASED ( 14 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 14 FDA reports)
BLOOD URIC ACID INCREASED ( 14 FDA reports)
BREAST CELLULITIS ( 14 FDA reports)
BREAST NECROSIS ( 14 FDA reports)
BUNDLE BRANCH BLOCK ( 14 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 14 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 14 FDA reports)
COELIAC ARTERY COMPRESSION SYNDROME ( 14 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 14 FDA reports)
CONCUSSION ( 14 FDA reports)
CONVERSION DISORDER ( 14 FDA reports)
CORONARY ARTERY THROMBOSIS ( 14 FDA reports)
CULTURE URINE POSITIVE ( 14 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 14 FDA reports)
EAR DISORDER ( 14 FDA reports)
FORAMEN MAGNUM STENOSIS ( 14 FDA reports)
GASTRIC POLYPS ( 14 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 14 FDA reports)
GENERALISED ERYTHEMA ( 14 FDA reports)
HEPATITIS B ( 14 FDA reports)
HOMOCYSTINAEMIA ( 14 FDA reports)
IMPAIRED REASONING ( 14 FDA reports)
IMPETIGO ( 14 FDA reports)
INJECTION SITE BRUISING ( 14 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 14 FDA reports)
INTERCOSTAL NEURALGIA ( 14 FDA reports)
INTERVERTEBRAL DISCITIS ( 14 FDA reports)
JUDGEMENT IMPAIRED ( 14 FDA reports)
LEUKAEMIA ( 14 FDA reports)
LIP DISORDER ( 14 FDA reports)
LYMPH GLAND INFECTION ( 14 FDA reports)
LYMPHOHISTIOCYTOSIS ( 14 FDA reports)
MACULE ( 14 FDA reports)
MECHANICAL VENTILATION ( 14 FDA reports)
MEDICATION RESIDUE ( 14 FDA reports)
MENINGITIS VIRAL ( 14 FDA reports)
MERALGIA PARAESTHETICA ( 14 FDA reports)
NAIL DISORDER ( 14 FDA reports)
NASAL DISORDER ( 14 FDA reports)
NEPHROSCLEROSIS ( 14 FDA reports)
NEUROFIBROMA ( 14 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 14 FDA reports)
NEUTROPHIL COUNT INCREASED ( 14 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 14 FDA reports)
ORCHITIS ( 14 FDA reports)
PANCREATIC ATROPHY ( 14 FDA reports)
PANCREATIC DUCT DILATATION ( 14 FDA reports)
PANIC REACTION ( 14 FDA reports)
PARAPARESIS ( 14 FDA reports)
PAROSMIA ( 14 FDA reports)
PELVIC DISCOMFORT ( 14 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 14 FDA reports)
POLYARTERITIS NODOSA ( 14 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 14 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 14 FDA reports)
PULMONARY AIR LEAKAGE ( 14 FDA reports)
RADIATION OESOPHAGITIS ( 14 FDA reports)
RADICULITIS LUMBOSACRAL ( 14 FDA reports)
RESPIRATORY ACIDOSIS ( 14 FDA reports)
RETINAL ARTERY OCCLUSION ( 14 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 14 FDA reports)
SARCOIDOSIS ( 14 FDA reports)
SENSATION OF HEAVINESS ( 14 FDA reports)
SEROSITIS ( 14 FDA reports)
SHOULDER ARTHROPLASTY ( 14 FDA reports)
SKULL MALFORMATION ( 14 FDA reports)
SLEEP TERROR ( 14 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 14 FDA reports)
STENT OCCLUSION ( 14 FDA reports)
STREPTOCOCCAL SEPSIS ( 14 FDA reports)
STUPOR ( 14 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 14 FDA reports)
TONGUE PARALYSIS ( 14 FDA reports)
TONGUE ULCERATION ( 14 FDA reports)
TUMOUR MARKER INCREASED ( 14 FDA reports)
VENTRICULAR ARRHYTHMIA ( 14 FDA reports)
VERTIGO POSITIONAL ( 14 FDA reports)
SKIN CANDIDA ( 13 FDA reports)
SKIN INFECTION ( 13 FDA reports)
STEAL SYNDROME ( 13 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 13 FDA reports)
TRACHEOBRONCHITIS ( 13 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 13 FDA reports)
UTERINE DISORDER ( 13 FDA reports)
VARICELLA ( 13 FDA reports)
VENOUS THROMBOSIS LIMB ( 13 FDA reports)
VESTIBULAR DISORDER ( 13 FDA reports)
ACANTHOMA ( 13 FDA reports)
ACUTE HEPATIC FAILURE ( 13 FDA reports)
ADNEXA UTERI MASS ( 13 FDA reports)
ALCOHOL POISONING ( 13 FDA reports)
AMYLOIDOSIS ( 13 FDA reports)
ANAL FISTULA ( 13 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 13 FDA reports)
AUTOIMMUNE THYROIDITIS ( 13 FDA reports)
BACTERIAL TEST ( 13 FDA reports)
BENCE JONES PROTEINURIA ( 13 FDA reports)
BIOPSY GINGIVAL ( 13 FDA reports)
BLOOD CULTURE POSITIVE ( 13 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 13 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 13 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 13 FDA reports)
BRACHIAL PLEXOPATHY ( 13 FDA reports)
BREAST DISCHARGE ( 13 FDA reports)
CALCULUS URETHRAL ( 13 FDA reports)
CATHETER SITE HAEMATOMA ( 13 FDA reports)
CHEST INJURY ( 13 FDA reports)
CHONDROCALCINOSIS ( 13 FDA reports)
CHRONIC FATIGUE SYNDROME ( 13 FDA reports)
COLON OPERATION ( 13 FDA reports)
CONNECTIVE TISSUE DISORDER ( 13 FDA reports)
CRANIOTOMY ( 13 FDA reports)
DENTAL PLAQUE ( 13 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 13 FDA reports)
DERMATOMYOSITIS ( 13 FDA reports)
DIURETIC THERAPY ( 13 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 13 FDA reports)
ENCEPHALITIS ( 13 FDA reports)
ERYTHEMA NODOSUM ( 13 FDA reports)
EYELID OEDEMA ( 13 FDA reports)
GINGIVAL GRAFT ( 13 FDA reports)
HAND DEFORMITY ( 13 FDA reports)
HELICOBACTER INFECTION ( 13 FDA reports)
HEMIANOPIA ( 13 FDA reports)
HILAR LYMPHADENOPATHY ( 13 FDA reports)
HIP SURGERY ( 13 FDA reports)
HYPERTENSIVE CRISIS ( 13 FDA reports)
HYPOPNOEA ( 13 FDA reports)
HYPOREFLEXIA ( 13 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 13 FDA reports)
IMMUNOSUPPRESSION ( 13 FDA reports)
INTESTINAL POLYP ( 13 FDA reports)
IRITIS ( 13 FDA reports)
LABILE HYPERTENSION ( 13 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 13 FDA reports)
LUPUS-LIKE SYNDROME ( 13 FDA reports)
MAMMOPLASTY ( 13 FDA reports)
METASTASES TO LARGE INTESTINE ( 13 FDA reports)
MUMPS ( 13 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 13 FDA reports)
NARCOLEPSY ( 13 FDA reports)
NEOPLASM SKIN ( 13 FDA reports)
NEPHRECTOMY ( 13 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 13 FDA reports)
ONYCHALGIA ( 13 FDA reports)
OOPHORECTOMY ( 13 FDA reports)
OROPHARYNGEAL PLAQUE ( 13 FDA reports)
OSTEOCHONDROSIS ( 13 FDA reports)
PANCREATIC MASS ( 13 FDA reports)
PANCREATITIS RELAPSING ( 13 FDA reports)
PCO2 DECREASED ( 13 FDA reports)
PERINEURIAL CYST ( 13 FDA reports)
PERIORBITAL OEDEMA ( 13 FDA reports)
PLASTIC SURGERY TO THE FACE ( 13 FDA reports)
PNEUMONIA VIRAL ( 13 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 13 FDA reports)
POSTOPERATIVE ILEUS ( 13 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 13 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 13 FDA reports)
PSYCHOLOGICAL TRAUMA ( 13 FDA reports)
PYELONEPHRITIS ACUTE ( 13 FDA reports)
RECTOCELE ( 13 FDA reports)
RETINAL ISCHAEMIA ( 13 FDA reports)
SCROTAL SWELLING ( 13 FDA reports)
SENSATION OF PRESSURE ( 13 FDA reports)
SHOULDER PAIN ( 13 FDA reports)
ABORTION INDUCED ( 12 FDA reports)
ABSCESS NECK ( 12 FDA reports)
ACCELERATED HYPERTENSION ( 12 FDA reports)
ACCIDENTAL EXPOSURE ( 12 FDA reports)
ACUTE LEUKAEMIA ( 12 FDA reports)
ALLERGY TO ANIMAL ( 12 FDA reports)
ANAL FISSURE ( 12 FDA reports)
ANGIONEUROTIC OEDEMA ( 12 FDA reports)
ANOSMIA ( 12 FDA reports)
APHONIA ( 12 FDA reports)
AUTOIMMUNE DISORDER ( 12 FDA reports)
AXILLARY PAIN ( 12 FDA reports)
BACTERIAL SEPSIS ( 12 FDA reports)
BACTERIAL TEST NEGATIVE ( 12 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 12 FDA reports)
BLEEDING TIME ABNORMAL ( 12 FDA reports)
BLOOD BICARBONATE DECREASED ( 12 FDA reports)
BLOOD CREATINE INCREASED ( 12 FDA reports)
BREAST OPERATION ( 12 FDA reports)
BREAST SWELLING ( 12 FDA reports)
BURNS SECOND DEGREE ( 12 FDA reports)
CALCIUM METABOLISM DISORDER ( 12 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 12 FDA reports)
CELLULITIS ORBITAL ( 12 FDA reports)
CEREBRAL DISORDER ( 12 FDA reports)
CHARLES BONNET SYNDROME ( 12 FDA reports)
CHLAMYDIAL INFECTION ( 12 FDA reports)
CLUSTER HEADACHE ( 12 FDA reports)
COLON NEOPLASM ( 12 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 12 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 12 FDA reports)
CONGENITAL ANOMALY ( 12 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 12 FDA reports)
DIABETIC COMPLICATION ( 12 FDA reports)
DIFFUSE VASCULITIS ( 12 FDA reports)
DRY THROAT ( 12 FDA reports)
EAR NEOPLASM ( 12 FDA reports)
EARLY SATIETY ( 12 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 12 FDA reports)
EDENTULOUS ( 12 FDA reports)
FOLLICULITIS ( 12 FDA reports)
GASTRIC CANCER ( 12 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 12 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 12 FDA reports)
GLOMERULOSCLEROSIS ( 12 FDA reports)
GRAVITATIONAL OEDEMA ( 12 FDA reports)
HAEMOLYTIC ANAEMIA ( 12 FDA reports)
HALLUCINATIONS, MIXED ( 12 FDA reports)
HEAD DISCOMFORT ( 12 FDA reports)
HEART RATE ABNORMAL ( 12 FDA reports)
HORNER'S SYNDROME ( 12 FDA reports)
HYPERREFLEXIA ( 12 FDA reports)
HYPOMANIA ( 12 FDA reports)
IMMUNE SYSTEM DISORDER ( 12 FDA reports)
INCISION SITE INFECTION ( 12 FDA reports)
INJECTION SITE INFECTION ( 12 FDA reports)
IRIS DISORDER ( 12 FDA reports)
JOINT LOCK ( 12 FDA reports)
LASER THERAPY ( 12 FDA reports)
LEUKOENCEPHALOPATHY ( 12 FDA reports)
LYMPH NODE CALCIFICATION ( 12 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 12 FDA reports)
MASTOIDITIS ( 12 FDA reports)
MEDIASTINAL DISORDER ( 12 FDA reports)
MEGACOLON ( 12 FDA reports)
METASTASES TO PELVIS ( 12 FDA reports)
MUSCLE SWELLING ( 12 FDA reports)
NEURAL TUBE DEFECT ( 12 FDA reports)
NEUROLOGICAL SYMPTOM ( 12 FDA reports)
OCCULT BLOOD ( 12 FDA reports)
ONYCHOLYSIS ( 12 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 12 FDA reports)
ORAL LICHEN PLANUS ( 12 FDA reports)
OROPHARYNGEAL BLISTERING ( 12 FDA reports)
PANCOAST'S TUMOUR ( 12 FDA reports)
PARATHYROID TUMOUR BENIGN ( 12 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 12 FDA reports)
PELVIC PROLAPSE ( 12 FDA reports)
PERIPHERAL NERVE INJURY ( 12 FDA reports)
PERIVASCULAR DERMATITIS ( 12 FDA reports)
PERSONALITY DISORDER ( 12 FDA reports)
PHLEBOLITH ( 12 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 12 FDA reports)
POLYCHROMASIA ( 12 FDA reports)
PORTAL HYPERTENSION ( 12 FDA reports)
POST HERPETIC NEURALGIA ( 12 FDA reports)
POST THROMBOTIC SYNDROME ( 12 FDA reports)
PROTEIN TOTAL INCREASED ( 12 FDA reports)
PSORIATIC ARTHROPATHY ( 12 FDA reports)
REACTIVE PSYCHOSIS ( 12 FDA reports)
RED BLOOD CELLS URINE ( 12 FDA reports)
RENAL STONE REMOVAL ( 12 FDA reports)
RESUSCITATION ( 12 FDA reports)
RETINAL DETACHMENT ( 12 FDA reports)
RETROPERITONEAL HAEMATOMA ( 12 FDA reports)
RIGHT VENTRICULAR FAILURE ( 12 FDA reports)
RUBELLA ( 12 FDA reports)
SCARLET FEVER ( 12 FDA reports)
SKIN REACTION ( 12 FDA reports)
SPINAL CORD INJURY ( 12 FDA reports)
SPLENIC LESION ( 12 FDA reports)
SPUTUM PURULENT ( 12 FDA reports)
STENOTROPHOMONAS INFECTION ( 12 FDA reports)
STRABISMUS ( 12 FDA reports)
TESTICULAR ATROPHY ( 12 FDA reports)
THROAT CANCER ( 12 FDA reports)
TOE AMPUTATION ( 12 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 12 FDA reports)
ULCER HAEMORRHAGE ( 12 FDA reports)
URINE ANALYSIS ( 12 FDA reports)
VENTRICULAR DYSKINESIA ( 12 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 12 FDA reports)
WHITE BLOOD CELL COUNT ( 12 FDA reports)
SKIN HAEMORRHAGE ( 11 FDA reports)
SKIN STRIAE ( 11 FDA reports)
SPINA BIFIDA ( 11 FDA reports)
SPINAL DECOMPRESSION ( 11 FDA reports)
SPINAL OPERATION ( 11 FDA reports)
SPONDYLOLYSIS ( 11 FDA reports)
SPUTUM CULTURE POSITIVE ( 11 FDA reports)
THORACIC OPERATION ( 11 FDA reports)
THYROIDITIS ( 11 FDA reports)
TOE DEFORMITY ( 11 FDA reports)
TONGUE BITING ( 11 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 11 FDA reports)
TRIGEMINAL NEURALGIA ( 11 FDA reports)
VENA CAVA FILTER INSERTION ( 11 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 11 FDA reports)
WEIGHT BEARING DIFFICULTY ( 11 FDA reports)
WEIGHT FLUCTUATION ( 11 FDA reports)
ABNORMAL SENSATION IN EYE ( 11 FDA reports)
ADVERSE REACTION ( 11 FDA reports)
ANISOCYTOSIS ( 11 FDA reports)
ANKYLOSING SPONDYLITIS ( 11 FDA reports)
APLASIA PURE RED CELL ( 11 FDA reports)
APPLICATION SITE ULCER ( 11 FDA reports)
AREFLEXIA ( 11 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 11 FDA reports)
BICYTOPENIA ( 11 FDA reports)
BLOOD BLISTER ( 11 FDA reports)
BLOOD CREATININE DECREASED ( 11 FDA reports)
BONE CANCER METASTATIC ( 11 FDA reports)
BRADYARRHYTHMIA ( 11 FDA reports)
BREAST CANCER FEMALE ( 11 FDA reports)
BRONCHOSTENOSIS ( 11 FDA reports)
CALCINOSIS ( 11 FDA reports)
CARDIOPULMONARY FAILURE ( 11 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 11 FDA reports)
CHONDROPATHY ( 11 FDA reports)
CLOSTRIDIUM COLITIS ( 11 FDA reports)
COLONIC OBSTRUCTION ( 11 FDA reports)
COLOSTOMY ( 11 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 11 FDA reports)
DEAFNESS UNILATERAL ( 11 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 11 FDA reports)
DERMATITIS ACNEIFORM ( 11 FDA reports)
DIABETIC COMA ( 11 FDA reports)
DISSEMINATED TUBERCULOSIS ( 11 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 11 FDA reports)
ENDOMETRIAL CANCER ( 11 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 11 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 11 FDA reports)
ERYTHEMA MULTIFORME ( 11 FDA reports)
EXERCISE TOLERANCE DECREASED ( 11 FDA reports)
EXTRASKELETAL OSSIFICATION ( 11 FDA reports)
EYE PRURITUS ( 11 FDA reports)
FACIAL PALSY ( 11 FDA reports)
FAT TISSUE INCREASED ( 11 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 11 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 11 FDA reports)
GOUTY ARTHRITIS ( 11 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 11 FDA reports)
HEPATIC ENCEPHALOPATHY ( 11 FDA reports)
HYPERSEXUALITY ( 11 FDA reports)
IMMOBILE ( 11 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 11 FDA reports)
INAPPROPRIATE AFFECT ( 11 FDA reports)
INFUSION SITE PAIN ( 11 FDA reports)
INJECTION SITE URTICARIA ( 11 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 11 FDA reports)
JOINT ARTHROPLASTY ( 11 FDA reports)
LIGHT CHAIN DISEASE ( 11 FDA reports)
LIP PAIN ( 11 FDA reports)
LOWER EXTREMITY MASS ( 11 FDA reports)
MALIGNANT MELANOMA ( 11 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 11 FDA reports)
METATARSALGIA ( 11 FDA reports)
MICROCYTOSIS ( 11 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 11 FDA reports)
MUCOSAL EROSION ( 11 FDA reports)
MUSCLE CONTRACTURE ( 11 FDA reports)
MUSCLE RIGIDITY ( 11 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 11 FDA reports)
NEPHRITIC SYNDROME ( 11 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 11 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 11 FDA reports)
OBSTRUCTION GASTRIC ( 11 FDA reports)
PARATHYROIDECTOMY ( 11 FDA reports)
PELVIC VENOUS THROMBOSIS ( 11 FDA reports)
RECTAL PROLAPSE ( 11 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 11 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 11 FDA reports)
RETINAL DISORDER ( 11 FDA reports)
RHEUMATIC FEVER ( 11 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 11 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 11 FDA reports)
SEBACEOUS GLAND DISORDER ( 11 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 10 FDA reports)
ALCOHOL ABUSE ( 10 FDA reports)
ANAL CANCER ( 10 FDA reports)
ANAL CANDIDIASIS ( 10 FDA reports)
ANAL SPHINCTER ATONY ( 10 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 10 FDA reports)
AORTIC VALVE CALCIFICATION ( 10 FDA reports)
ATHEROSCLEROSIS ( 10 FDA reports)
BACTEROIDES TEST POSITIVE ( 10 FDA reports)
BIFIDOBACTERIUM TEST POSITIVE ( 10 FDA reports)
BLADDER HYPERTROPHY ( 10 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 10 FDA reports)
BLEPHAROSPASM ( 10 FDA reports)
BLOOD AMYLASE INCREASED ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 10 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 10 FDA reports)
BLOOD PH DECREASED ( 10 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 10 FDA reports)
BRAIN STEM INFARCTION ( 10 FDA reports)
BREAST INFECTION ( 10 FDA reports)
BRONCHIOLITIS ( 10 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 10 FDA reports)
CATARACT NUCLEAR ( 10 FDA reports)
CEREBELLAR SYNDROME ( 10 FDA reports)
CHOKING SENSATION ( 10 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 10 FDA reports)
CLONUS ( 10 FDA reports)
DENTAL NECROSIS ( 10 FDA reports)
DEPRESSION SUICIDAL ( 10 FDA reports)
DEVICE LEAKAGE ( 10 FDA reports)
DRUG DETOXIFICATION ( 10 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 10 FDA reports)
DUODENAL POLYP ( 10 FDA reports)
ENERGY INCREASED ( 10 FDA reports)
ENTEROCUTANEOUS FISTULA ( 10 FDA reports)
EPIDURAL LIPOMATOSIS ( 10 FDA reports)
EXCESSIVE EYE BLINKING ( 10 FDA reports)
EYE INFECTION ( 10 FDA reports)
FACE INJURY ( 10 FDA reports)
FEELINGS OF WORTHLESSNESS ( 10 FDA reports)
FOETAL GROWTH RETARDATION ( 10 FDA reports)
FOOD INTOLERANCE ( 10 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 10 FDA reports)
GAMMOPATHY ( 10 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 10 FDA reports)
H1N1 INFLUENZA ( 10 FDA reports)
HEART SOUNDS ABNORMAL ( 10 FDA reports)
HYPERACUSIS ( 10 FDA reports)
HYPERPHOSPHATAEMIA ( 10 FDA reports)
ILEITIS ( 10 FDA reports)
IMPRISONMENT ( 10 FDA reports)
INFARCTION ( 10 FDA reports)
INJECTION SITE NECROSIS ( 10 FDA reports)
INJECTION SITE NODULE ( 10 FDA reports)
INTESTINAL PROLAPSE ( 10 FDA reports)
JAUNDICE NEONATAL ( 10 FDA reports)
LARGE INTESTINE PERFORATION ( 10 FDA reports)
LARYNGEAL OEDEMA ( 10 FDA reports)
LEUKAEMIA PLASMACYTIC ( 10 FDA reports)
LITHOTRIPSY ( 10 FDA reports)
LOSS OF CONTROL OF LEGS ( 10 FDA reports)
LOW TURNOVER OSTEOPATHY ( 10 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 10 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 10 FDA reports)
MEDIASTINUM NEOPLASM ( 10 FDA reports)
MENINGITIS HERPES ( 10 FDA reports)
MENINGOMYELOCELE ( 10 FDA reports)
MICROCYTIC ANAEMIA ( 10 FDA reports)
MIGRAINE WITH AURA ( 10 FDA reports)
MIXED DEAFNESS ( 10 FDA reports)
MONONEUROPATHY MULTIPLEX ( 10 FDA reports)
MONOPARESIS ( 10 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 10 FDA reports)
NEPHROPATHY TOXIC ( 10 FDA reports)
NODULE ON EXTREMITY ( 10 FDA reports)
OBSTRUCTION ( 10 FDA reports)
OCULAR ICTERUS ( 10 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 10 FDA reports)
OSTEOGENESIS IMPERFECTA ( 10 FDA reports)
OSTEOMALACIA ( 10 FDA reports)
OSTEOTOMY ( 10 FDA reports)
OVARIAN ABSCESS ( 10 FDA reports)
PAINFUL DEFAECATION ( 10 FDA reports)
PANCREATIC CARCINOMA ( 10 FDA reports)
PARONYCHIA ( 10 FDA reports)
PHYSICAL ASSAULT ( 10 FDA reports)
PILOERECTION ( 10 FDA reports)
PNEUMONIA BACTERIAL ( 10 FDA reports)
POST PROCEDURAL INFECTION ( 10 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 10 FDA reports)
PUBIS FRACTURE ( 10 FDA reports)
QUADRIPARESIS ( 10 FDA reports)
RENAL ARTERY STENOSIS ( 10 FDA reports)
RENAL INFARCT ( 10 FDA reports)
RENAL LIPOMATOSIS ( 10 FDA reports)
RESPIRATORY TRACT OEDEMA ( 10 FDA reports)
SALIVARY GLAND DISORDER ( 10 FDA reports)
SALIVARY HYPERSECRETION ( 10 FDA reports)
SCAPULA FRACTURE ( 10 FDA reports)
SCAR EXCISION ( 10 FDA reports)
SKIN NODULE ( 10 FDA reports)
SOMATISATION DISORDER ( 10 FDA reports)
SPONDYLITIC MYELOPATHY ( 10 FDA reports)
SPONDYLOARTHROPATHY ( 10 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 10 FDA reports)
TERATOMA BENIGN ( 10 FDA reports)
THERAPY CESSATION ( 10 FDA reports)
THROMBOCYTHAEMIA ( 10 FDA reports)
THROMBOSED VARICOSE VEIN ( 10 FDA reports)
TOXIC SHOCK SYNDROME ( 10 FDA reports)
UNDERDOSE ( 10 FDA reports)
URINE OUTPUT ( 10 FDA reports)
UTERINE MASS ( 10 FDA reports)
VASCULAR COMPRESSION ( 10 FDA reports)
VASCULAR STENOSIS ( 10 FDA reports)
WOUND TREATMENT ( 10 FDA reports)
YELLOW SKIN ( 10 FDA reports)
SLEEP TALKING ( 9 FDA reports)
SPINAL CORD DISORDER ( 9 FDA reports)
SPINAL PAIN ( 9 FDA reports)
SPONDYLOSIS ( 9 FDA reports)
STRESS ULCER ( 9 FDA reports)
SUTURE RELATED COMPLICATION ( 9 FDA reports)
TOOTH RESORPTION ( 9 FDA reports)
TRACHEAL OBSTRUCTION ( 9 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 9 FDA reports)
TUMOUR LYSIS SYNDROME ( 9 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 9 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 9 FDA reports)
VASCULAR GRAFT ( 9 FDA reports)
VITAMIN K DEFICIENCY ( 9 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 9 FDA reports)
WOUND HAEMORRHAGE ( 9 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 9 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 9 FDA reports)
ALLODYNIA ( 9 FDA reports)
ANAEMIA MACROCYTIC ( 9 FDA reports)
APLASTIC ANAEMIA ( 9 FDA reports)
APPLICATION SITE SCAR ( 9 FDA reports)
ARTERIAL STENOSIS ( 9 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 9 FDA reports)
ASBESTOSIS ( 9 FDA reports)
ATRIAL THROMBOSIS ( 9 FDA reports)
AURICULAR SWELLING ( 9 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 9 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 9 FDA reports)
BINGE EATING ( 9 FDA reports)
BIOPSY BONE ( 9 FDA reports)
BIOPSY BREAST ( 9 FDA reports)
BLADDER NECK OPERATION ( 9 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 9 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 9 FDA reports)
BRAIN DAMAGE ( 9 FDA reports)
BRAIN HERNIATION ( 9 FDA reports)
BRAIN HYPOXIA ( 9 FDA reports)
BUNION OPERATION ( 9 FDA reports)
CARDIAC ABLATION ( 9 FDA reports)
CEREBELLAR ISCHAEMIA ( 9 FDA reports)
CHOLESTASIS ( 9 FDA reports)
CHORIORETINAL DISORDER ( 9 FDA reports)
CHORIORETINOPATHY ( 9 FDA reports)
COLON POLYPECTOMY ( 9 FDA reports)
COLONIC STENOSIS ( 9 FDA reports)
COR PULMONALE ( 9 FDA reports)
CRANIAL NERVE DISORDER ( 9 FDA reports)
CSF TEST ABNORMAL ( 9 FDA reports)
CULTURE STOOL POSITIVE ( 9 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 9 FDA reports)
DETOXIFICATION ( 9 FDA reports)
DEVICE RELATED SEPSIS ( 9 FDA reports)
DIABETIC VASCULAR DISORDER ( 9 FDA reports)
DROOLING ( 9 FDA reports)
DYSPLASIA ( 9 FDA reports)
EAR TUBE INSERTION ( 9 FDA reports)
EJECTION FRACTION ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 9 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 9 FDA reports)
ENEMA ADMINISTRATION ( 9 FDA reports)
EOSINOPHILIA ( 9 FDA reports)
FACIAL NERVE DISORDER ( 9 FDA reports)
FAECES HARD ( 9 FDA reports)
FEAR OF DEATH ( 9 FDA reports)
FEMALE STERILISATION ( 9 FDA reports)
FUNGAL OESOPHAGITIS ( 9 FDA reports)
GALLBLADDER POLYP ( 9 FDA reports)
GASTROINTESTINAL INFECTION ( 9 FDA reports)
GASTROINTESTINAL INJURY ( 9 FDA reports)
GRIMACING ( 9 FDA reports)
HAEMOGLOBIN ABNORMAL ( 9 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 9 FDA reports)
HEART INJURY ( 9 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 9 FDA reports)
HYPOCHROMASIA ( 9 FDA reports)
IMPAIRED FASTING GLUCOSE ( 9 FDA reports)
INFECTED SKIN ULCER ( 9 FDA reports)
INFUSION SITE ERYTHEMA ( 9 FDA reports)
INGUINAL HERNIA REPAIR ( 9 FDA reports)
INJECTION SITE MASS ( 9 FDA reports)
INTESTINAL ISCHAEMIA ( 9 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 9 FDA reports)
INTRA-UTERINE DEATH ( 9 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 9 FDA reports)
KLEBSIELLA TEST POSITIVE ( 9 FDA reports)
LIVEDO RETICULARIS ( 9 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 9 FDA reports)
MEDIASTINAL MASS ( 9 FDA reports)
MENIERE'S DISEASE ( 9 FDA reports)
METASTASES TO BONE MARROW ( 9 FDA reports)
METASTASES TO OVARY ( 9 FDA reports)
METASTASES TO PERITONEUM ( 9 FDA reports)
METATARSUS PRIMUS VARUS ( 9 FDA reports)
MIOSIS ( 9 FDA reports)
MYOPIA ( 9 FDA reports)
NAIL DISCOLOURATION ( 9 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 9 FDA reports)
NODAL RHYTHM ( 9 FDA reports)
NON-SMALL CELL LUNG CANCER ( 9 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 9 FDA reports)
OROANTRAL FISTULA ( 9 FDA reports)
OTITIS MEDIA ACUTE ( 9 FDA reports)
OTORRHOEA ( 9 FDA reports)
PATELLA FRACTURE ( 9 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 9 FDA reports)
PERIRECTAL ABSCESS ( 9 FDA reports)
PETIT MAL EPILEPSY ( 9 FDA reports)
PHANTOM PAIN ( 9 FDA reports)
PO2 DECREASED ( 9 FDA reports)
POST CONCUSSION SYNDROME ( 9 FDA reports)
POSTERIOR CAPSULOTOMY ( 9 FDA reports)
POSTURING ( 9 FDA reports)
PROSTHESIS IMPLANTATION ( 9 FDA reports)
PULMONARY VALVE STENOSIS ( 9 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 9 FDA reports)
RETINAL VEIN OCCLUSION ( 9 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 9 FDA reports)
ROSACEA ( 9 FDA reports)
ROULEAUX FORMATION ( 9 FDA reports)
SCROTAL CYST ( 9 FDA reports)
SCROTAL IRRITATION ( 9 FDA reports)
SENILE OSTEOPOROSIS ( 9 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 8 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 8 FDA reports)
ADRENAL HAEMORRHAGE ( 8 FDA reports)
ADRENAL NEOPLASM ( 8 FDA reports)
AMENORRHOEA ( 8 FDA reports)
ANTISOCIAL BEHAVIOUR ( 8 FDA reports)
AORTIC ATHEROSCLEROSIS ( 8 FDA reports)
APPLICATION SITE EXFOLIATION ( 8 FDA reports)
ARTHRITIS INFECTIVE ( 8 FDA reports)
AUTONOMIC NEUROPATHY ( 8 FDA reports)
BELLIGERENCE ( 8 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 8 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 8 FDA reports)
BILE DUCT STENOSIS ( 8 FDA reports)
BIOPSY THYMUS GLAND ABNORMAL ( 8 FDA reports)
BLINDNESS CORTICAL ( 8 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 8 FDA reports)
CAECITIS ( 8 FDA reports)
CARBON DIOXIDE INCREASED ( 8 FDA reports)
CATHETERISATION VENOUS ( 8 FDA reports)
CEREBELLAR INFARCTION ( 8 FDA reports)
CEREBRAL THROMBOSIS ( 8 FDA reports)
CERVIX INFLAMMATION ( 8 FDA reports)
CHAPPED LIPS ( 8 FDA reports)
CHEILITIS ( 8 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 8 FDA reports)
COGWHEEL RIGIDITY ( 8 FDA reports)
COLON CANCER STAGE III ( 8 FDA reports)
CONDUCTION DISORDER ( 8 FDA reports)
CONDUCTIVE DEAFNESS ( 8 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 8 FDA reports)
CONJUNCTIVITIS VIRAL ( 8 FDA reports)
CORONARY ARTERY RESTENOSIS ( 8 FDA reports)
CRYOTHERAPY ( 8 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 8 FDA reports)
DERMATITIS BULLOUS ( 8 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 8 FDA reports)
DUODENAL OBSTRUCTION ( 8 FDA reports)
DYSPNOEA EXACERBATED ( 8 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 8 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 8 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 8 FDA reports)
ERYTHEMA OF EYELID ( 8 FDA reports)
ETHMOID SINUS SURGERY ( 8 FDA reports)
FEEDING TUBE COMPLICATION ( 8 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 8 FDA reports)
FOREIGN BODY TRAUMA ( 8 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 8 FDA reports)
GALACTORRHOEA ( 8 FDA reports)
GALLBLADDER PAIN ( 8 FDA reports)
GASTRIC CANCER RECURRENT ( 8 FDA reports)
GASTROSTOMY ( 8 FDA reports)
GRAFT THROMBOSIS ( 8 FDA reports)
GROUP B STREPTOCOCCUS NEONATAL SEPSIS ( 8 FDA reports)
GUILLAIN-BARRE SYNDROME ( 8 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 8 FDA reports)
INCISION SITE PAIN ( 8 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 8 FDA reports)
INJECTION SITE WARMTH ( 8 FDA reports)
JUGULAR VEIN DISTENSION ( 8 FDA reports)
KIDNEY ENLARGEMENT ( 8 FDA reports)
KYPHOSCOLIOSIS ( 8 FDA reports)
LIPOATROPHY ( 8 FDA reports)
LUNG CANCER METASTATIC ( 8 FDA reports)
LUNG OPERATION ( 8 FDA reports)
LYMPHOCYTOSIS ( 8 FDA reports)
MENINGITIS NEONATAL ( 8 FDA reports)
METASTASES TO MOUTH ( 8 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 8 FDA reports)
MONARTHRITIS ( 8 FDA reports)
MONOPLEGIA ( 8 FDA reports)
MURPHY'S SIGN POSITIVE ( 8 FDA reports)
NAIL BED TENDERNESS ( 8 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 8 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 8 FDA reports)
ODONTOGENIC CYST ( 8 FDA reports)
OPTIC NEURITIS ( 8 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 8 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 8 FDA reports)
PANCREATIC NEOPLASM ( 8 FDA reports)
PARVOVIRUS INFECTION ( 8 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 8 FDA reports)
PERIORBITAL HAEMATOMA ( 8 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 8 FDA reports)
PERITONITIS BACTERIAL ( 8 FDA reports)
PHIMOSIS ( 8 FDA reports)
PLATELET TRANSFUSION ( 8 FDA reports)
PLEURAL CALCIFICATION ( 8 FDA reports)
POISONING ( 8 FDA reports)
POOR PERIPHERAL CIRCULATION ( 8 FDA reports)
POSITIVE ROMBERGISM ( 8 FDA reports)
POST PROCEDURAL CELLULITIS ( 8 FDA reports)
POSTURE ABNORMAL ( 8 FDA reports)
PROSTATISM ( 8 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 8 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 8 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 8 FDA reports)
PYODERMA GANGRENOSUM ( 8 FDA reports)
RADIATION SKIN INJURY ( 8 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 8 FDA reports)
RECTAL CANCER ( 8 FDA reports)
RECTAL FISSURE ( 8 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 8 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 8 FDA reports)
RIB DEFORMITY ( 8 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 8 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 8 FDA reports)
SARCOMA ( 8 FDA reports)
SECRETION DISCHARGE ( 8 FDA reports)
SERRATIA BACTERAEMIA ( 8 FDA reports)
SKIN NECROSIS ( 8 FDA reports)
SKIN PLAQUE ( 8 FDA reports)
SKIN TURGOR DECREASED ( 8 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 8 FDA reports)
SOFT TISSUE INJURY ( 8 FDA reports)
SPLENIC CYST ( 8 FDA reports)
SPLENIC INFARCTION ( 8 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 8 FDA reports)
SUDDEN CARDIAC DEATH ( 8 FDA reports)
THEFT ( 8 FDA reports)
TONGUE OEDEMA ( 8 FDA reports)
TRAUMATIC HAEMATOMA ( 8 FDA reports)
TRIGONITIS ( 8 FDA reports)
UMBILICAL HERNIA REPAIR ( 8 FDA reports)
URINE ODOUR ABNORMAL ( 8 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 8 FDA reports)
UVEITIS ( 8 FDA reports)
VAGINITIS BACTERIAL ( 8 FDA reports)
VASCULAR PSEUDOANEURYSM ( 8 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 8 FDA reports)
WOUND DEBRIDEMENT ( 8 FDA reports)
SKIN CHAPPED ( 7 FDA reports)
SKIN GRAFT ( 7 FDA reports)
SLEEP WALKING ( 7 FDA reports)
SLUGGISHNESS ( 7 FDA reports)
SOCIAL PROBLEM ( 7 FDA reports)
SPLEEN DISORDER ( 7 FDA reports)
SPUTUM ABNORMAL ( 7 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 7 FDA reports)
STARING ( 7 FDA reports)
STATUS EPILEPTICUS ( 7 FDA reports)
STERNAL FRACTURE ( 7 FDA reports)
STILLBIRTH ( 7 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 7 FDA reports)
SUPERINFECTION ( 7 FDA reports)
SUPRAPUBIC PAIN ( 7 FDA reports)
TINEA CRURIS ( 7 FDA reports)
TONSIL CANCER ( 7 FDA reports)
TRANSPLANT REJECTION ( 7 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 7 FDA reports)
TRAUMATIC ARTHRITIS ( 7 FDA reports)
TUMOUR PAIN ( 7 FDA reports)
TURNER'S SYNDROME ( 7 FDA reports)
URETHRAL DILATATION ( 7 FDA reports)
URETHRAL OBSTRUCTION ( 7 FDA reports)
URINARY TRACT OBSTRUCTION ( 7 FDA reports)
URTICARIA GENERALISED ( 7 FDA reports)
VAGINAL DISORDER ( 7 FDA reports)
VAGINAL PAIN ( 7 FDA reports)
VAGOTOMY ( 7 FDA reports)
VASCULAR GRAFT OCCLUSION ( 7 FDA reports)
VITAMIN B12 INCREASED ( 7 FDA reports)
VOCAL CORD DISORDER ( 7 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 7 FDA reports)
WALKING DISABILITY ( 7 FDA reports)
ABDOMINAL INFECTION ( 7 FDA reports)
ACANTHOLYSIS ( 7 FDA reports)
ADENOMYOSIS ( 7 FDA reports)
ADNEXA UTERI PAIN ( 7 FDA reports)
ALCOHOL PROBLEM ( 7 FDA reports)
ALLERGIC SINUSITIS ( 7 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 7 FDA reports)
ANGIOPLASTY ( 7 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 7 FDA reports)
ANURIA ( 7 FDA reports)
AORTIC VALVE DISEASE ( 7 FDA reports)
APPLICATION SITE DERMATITIS ( 7 FDA reports)
BEREAVEMENT REACTION ( 7 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 7 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 7 FDA reports)
BLOOD SODIUM INCREASED ( 7 FDA reports)
BRAIN NEOPLASM ( 7 FDA reports)
BREAST HYPERPLASIA ( 7 FDA reports)
CARBON DIOXIDE DECREASED ( 7 FDA reports)
CARDIAC VALVE VEGETATION ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 7 FDA reports)
CAROTID ARTERY OCCLUSION ( 7 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 7 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 7 FDA reports)
CERVICAL DYSPLASIA ( 7 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 7 FDA reports)
CHONDROLYSIS ( 7 FDA reports)
CHROMATOPSIA ( 7 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 7 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 7 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 7 FDA reports)
CONGENITAL GASTRIC ANOMALY ( 7 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 7 FDA reports)
CONJUNCTIVAL OEDEMA ( 7 FDA reports)
CRANIOCEREBRAL INJURY ( 7 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 7 FDA reports)
DELIRIUM TREMENS ( 7 FDA reports)
DENTAL IMPLANTATION ( 7 FDA reports)
DIABETIC ULCER ( 7 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 7 FDA reports)
DIVERTICULAR PERFORATION ( 7 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 7 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 7 FDA reports)
EMBOLIC STROKE ( 7 FDA reports)
ENDARTERECTOMY ( 7 FDA reports)
ENDOMETRIAL DISORDER ( 7 FDA reports)
EPIGLOTTITIS ( 7 FDA reports)
ESCHAR ( 7 FDA reports)
EYELID CYST ( 7 FDA reports)
FIBROUS DYSPLASIA OF JAW ( 7 FDA reports)
GALLBLADDER OPERATION ( 7 FDA reports)
GASTRECTOMY ( 7 FDA reports)
GASTRIC INFECTION ( 7 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 7 FDA reports)
HEART VALVE INCOMPETENCE ( 7 FDA reports)
HELICOBACTER TEST POSITIVE ( 7 FDA reports)
HIDRADENITIS ( 7 FDA reports)
HOSPICE CARE ( 7 FDA reports)
HYPERCAPNIA ( 7 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 7 FDA reports)
INTESTINAL RESECTION ( 7 FDA reports)
IUD MIGRATION ( 7 FDA reports)
JOINT SURGERY ( 7 FDA reports)
LACTIC ACIDOSIS ( 7 FDA reports)
LARYNGEAL REPAIR ( 7 FDA reports)
LIGAMENT DISORDER ( 7 FDA reports)
LISTLESS ( 7 FDA reports)
LOSS OF EMPLOYMENT ( 7 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 7 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 7 FDA reports)
MACULAR SCAR ( 7 FDA reports)
MACULOPATHY ( 7 FDA reports)
MAMMARY DUCT ECTASIA ( 7 FDA reports)
MARITAL PROBLEM ( 7 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 7 FDA reports)
METASTASES TO PLEURA ( 7 FDA reports)
MYELITIS ( 7 FDA reports)
NASAL DISCOMFORT ( 7 FDA reports)
NASAL SEPTAL OPERATION ( 7 FDA reports)
NASAL TURBINATE ABNORMALITY ( 7 FDA reports)
NEUROPATHIC ARTHROPATHY ( 7 FDA reports)
OPERATIVE HAEMORRHAGE ( 7 FDA reports)
OPHTHALMOPLEGIA ( 7 FDA reports)
OPPORTUNISTIC INFECTION ( 7 FDA reports)
ORGANISING PNEUMONIA ( 7 FDA reports)
PARKINSONISM ( 7 FDA reports)
PCO2 INCREASED ( 7 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 7 FDA reports)
PENILE HAEMORRHAGE ( 7 FDA reports)
PENIS DISORDER ( 7 FDA reports)
PERIPHERAL BLOOD STEM CELL APHERESIS ( 7 FDA reports)
PEYRONIE'S DISEASE ( 7 FDA reports)
PICKWICKIAN SYNDROME ( 7 FDA reports)
PITUITARY TUMOUR BENIGN ( 7 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 7 FDA reports)
POLYTRAUMATISM ( 7 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE II ( 7 FDA reports)
PROSTATECTOMY ( 7 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 7 FDA reports)
PTERYGIUM ( 7 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 7 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 7 FDA reports)
PYOGENIC GRANULOMA ( 7 FDA reports)
RASH MORBILLIFORM ( 7 FDA reports)
REGURGITATION ( 7 FDA reports)
REHABILITATION THERAPY ( 7 FDA reports)
RENAL HAEMATOMA ( 7 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 7 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
SALMONELLA BACTERAEMIA ( 7 FDA reports)
SCAN ABNORMAL ( 7 FDA reports)
SECONDARY SEQUESTRUM ( 7 FDA reports)
SELF MUTILATION ( 7 FDA reports)
SHOULDER DEFORMITY ( 7 FDA reports)
SINUS ARREST ( 7 FDA reports)
SJOGREN'S SYNDROME ( 7 FDA reports)
ABDOMINAL OPERATION ( 6 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 6 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 6 FDA reports)
ADRENOMEGALY ( 6 FDA reports)
AMMONIA INCREASED ( 6 FDA reports)
ANAL ABSCESS ( 6 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 6 FDA reports)
ANTERIOR DISPLACED ANUS ( 6 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 6 FDA reports)
AORTIC DISORDER ( 6 FDA reports)
APNOEIC ATTACK ( 6 FDA reports)
APPLICATION SITE BURN ( 6 FDA reports)
ARTERIOSPASM CORONARY ( 6 FDA reports)
ARTHRODESIS ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 6 FDA reports)
ASPIRATION BREAST ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 6 FDA reports)
BILIARY CYST ( 6 FDA reports)
BIOPSY BREAST ABNORMAL ( 6 FDA reports)
BIOPSY ENDOMETRIUM ( 6 FDA reports)
BLADDER OBSTRUCTION ( 6 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 6 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 6 FDA reports)
BLOOD PRESSURE ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 6 FDA reports)
BLOOD URINE ( 6 FDA reports)
BONE MARROW DEPRESSION ( 6 FDA reports)
BRAIN CONTUSION ( 6 FDA reports)
BREAST CYST ( 6 FDA reports)
BREAST DISORDER ( 6 FDA reports)
BREAST DISORDER FEMALE ( 6 FDA reports)
BREAST HAEMATOMA ( 6 FDA reports)
CALCULUS BLADDER ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 6 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 6 FDA reports)
CEREBRAL HAEMATOMA ( 6 FDA reports)
CERVICITIS ( 6 FDA reports)
CHOLANGITIS ( 6 FDA reports)
CHYLOTHORAX ( 6 FDA reports)
CLUBBING ( 6 FDA reports)
COLON CANCER METASTATIC ( 6 FDA reports)
COLONOSCOPY ( 6 FDA reports)
CONGENITAL ECTOPIC BLADDER ( 6 FDA reports)
CONGENITAL URETERIC ANOMALY ( 6 FDA reports)
CONJUNCTIVAL ABRASION ( 6 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 6 FDA reports)
CORONARY ANGIOPLASTY ( 6 FDA reports)
CYSTITIS NONINFECTIVE ( 6 FDA reports)
DEFAECATION URGENCY ( 6 FDA reports)
DERMATITIS EXFOLIATIVE ( 6 FDA reports)
DEVELOPMENTAL DELAY ( 6 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 6 FDA reports)
DRUG ADDICT ( 6 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 6 FDA reports)
DRUG SCREEN NEGATIVE ( 6 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 6 FDA reports)
ELECTROPHORESIS ABNORMAL ( 6 FDA reports)
EMBOLISM VENOUS ( 6 FDA reports)
ENCEPHALITIS HERPES ( 6 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 6 FDA reports)
ENTEROCOCCAL SEPSIS ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
EXFOLIATIVE RASH ( 6 FDA reports)
EXOMPHALOS ( 6 FDA reports)
EYE INFECTION VIRAL ( 6 FDA reports)
EYE INFLAMMATION ( 6 FDA reports)
EYE ROLLING ( 6 FDA reports)
EYELID OPERATION ( 6 FDA reports)
FINGER AMPUTATION ( 6 FDA reports)
FOREIGN BODY ASPIRATION ( 6 FDA reports)
GASTRIC PERFORATION ( 6 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 6 FDA reports)
GASTROINTESTINAL FISTULA ( 6 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 6 FDA reports)
GENERAL SYMPTOM ( 6 FDA reports)
GENITAL HERPES ( 6 FDA reports)
GENITALIA EXTERNAL AMBIGUOUS ( 6 FDA reports)
GIANT CELL EPULIS ( 6 FDA reports)
GRANULOCYTES MATURATION ARREST ( 6 FDA reports)
HAEMATOCRIT ABNORMAL ( 6 FDA reports)
HAEMOGLOBIN INCREASED ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HANGOVER ( 6 FDA reports)
HEAT EXHAUSTION ( 6 FDA reports)
HEPATIC FIBROSIS ( 6 FDA reports)
HEPATITIS C POSITIVE ( 6 FDA reports)
HEPATITIS TOXIC ( 6 FDA reports)
HEPATOCELLULAR DAMAGE ( 6 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 6 FDA reports)
HORDEOLUM ( 6 FDA reports)
HYDROMETRA ( 6 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 6 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 6 FDA reports)
HYPERTONIA ( 6 FDA reports)
HYPOCHROMIC ANAEMIA ( 6 FDA reports)
HYPOTONIA NEONATAL ( 6 FDA reports)
IATROGENIC INJURY ( 6 FDA reports)
ILEAL STENOSIS ( 6 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 6 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
INJECTION SITE DISCOLOURATION ( 6 FDA reports)
INJECTION SITE EXTRAVASATION ( 6 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 6 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 6 FDA reports)
KIDNEY MALROTATION ( 6 FDA reports)
KLEBSIELLA BACTERAEMIA ( 6 FDA reports)
KLEBSIELLA SEPSIS ( 6 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LARGE INTESTINAL ULCER ( 6 FDA reports)
LEGAL PROBLEM ( 6 FDA reports)
LIMB CRUSHING INJURY ( 6 FDA reports)
LIVER TENDERNESS ( 6 FDA reports)
LIVER TRANSPLANT ( 6 FDA reports)
LOCALISED OEDEMA ( 6 FDA reports)
LYME DISEASE ( 6 FDA reports)
LYMPHATIC OBSTRUCTION ( 6 FDA reports)
LYMPHOCYTIC INFILTRATION ( 6 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 6 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 6 FDA reports)
MEAN CELL VOLUME DECREASED ( 6 FDA reports)
MEDIASTINAL BIOPSY ( 6 FDA reports)
MEDICATION TAMPERING ( 6 FDA reports)
METABOLIC SYNDROME ( 6 FDA reports)
MICROANGIOPATHY ( 6 FDA reports)
MIDDLE EAR EFFUSION ( 6 FDA reports)
MOANING ( 6 FDA reports)
MUSCLE FLAP OPERATION ( 6 FDA reports)
MUSCLE RUPTURE ( 6 FDA reports)
NEONATAL TACHYPNOEA ( 6 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 6 FDA reports)
NIGHT BLINDNESS ( 6 FDA reports)
NONSPECIFIC REACTION ( 6 FDA reports)
OESTRADIOL DECREASED ( 6 FDA reports)
OPTIC ATROPHY ( 6 FDA reports)
OVARIAN DISORDER ( 6 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 6 FDA reports)
PANCREATITIS NECROTISING ( 6 FDA reports)
PARANEOPLASTIC SYNDROME ( 6 FDA reports)
PEAU D'ORANGE ( 6 FDA reports)
PELVIC HAEMATOMA ( 6 FDA reports)
PERIORBITAL HAEMORRHAGE ( 6 FDA reports)
PERITONEAL DIALYSIS ( 6 FDA reports)
PERITONEAL HAEMORRHAGE ( 6 FDA reports)
PHONOPHOBIA ( 6 FDA reports)
PLACENTAL DISORDER ( 6 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 6 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 6 FDA reports)
POST PROCEDURAL HAEMATOMA ( 6 FDA reports)
POSTICTAL STATE ( 6 FDA reports)
POSTMENOPAUSE ( 6 FDA reports)
POSTOPERATIVE ADHESION ( 6 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 6 FDA reports)
PROLAPSE REPAIR ( 6 FDA reports)
PROTRUSION TONGUE ( 6 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 6 FDA reports)
RADIATION NECROSIS ( 6 FDA reports)
RENAL APLASIA ( 6 FDA reports)
RENAL NEOPLASM ( 6 FDA reports)
RESIDUAL URINE VOLUME ( 6 FDA reports)
RETINAL SCAR ( 6 FDA reports)
SALIVARY GLAND MASS ( 6 FDA reports)
SCINTILLATING SCOTOMA ( 6 FDA reports)
SKIN MASS ( 6 FDA reports)
SKIN WRINKLING ( 6 FDA reports)
SMALL FOR DATES BABY ( 6 FDA reports)
SOFT TISSUE MASS ( 6 FDA reports)
SOFT TISSUE NECROSIS ( 6 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 6 FDA reports)
SPLENECTOMY ( 6 FDA reports)
STRESS INCONTINENCE ( 6 FDA reports)
STRESS SYMPTOMS ( 6 FDA reports)
SUBDURAL HAEMORRHAGE ( 6 FDA reports)
SUBRETINAL FIBROSIS ( 6 FDA reports)
SUICIDAL BEHAVIOUR ( 6 FDA reports)
SWOLLEN TEAR DUCT ( 6 FDA reports)
SYNCOPE VASOVAGAL ( 6 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 6 FDA reports)
TACHYPHRENIA ( 6 FDA reports)
THERAPY REGIMEN CHANGED ( 6 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 6 FDA reports)
THYROID GLAND CANCER ( 6 FDA reports)
TONGUE BLISTERING ( 6 FDA reports)
TONSILLAR DISORDER ( 6 FDA reports)
TOOTH DISCOLOURATION ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
TUMOUR EXCISION ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
URETHRAL DISORDER ( 6 FDA reports)
URETHRAL PROLAPSE ( 6 FDA reports)
UTERINE MALPOSITION ( 6 FDA reports)
UTERINE POLYP ( 6 FDA reports)
VASCULAR OCCLUSION ( 6 FDA reports)
VITAMIN B12 DECREASED ( 6 FDA reports)
VITREOUS DEGENERATION ( 6 FDA reports)
VULVOVAGINAL PAIN ( 6 FDA reports)
WOUND DECOMPOSITION ( 6 FDA reports)
XEROSIS ( 6 FDA reports)
SKIN CANCER METASTATIC ( 5 FDA reports)
SKIN HYPOPIGMENTATION ( 5 FDA reports)
SKIN LESION EXCISION ( 5 FDA reports)
SKIN OEDEMA ( 5 FDA reports)
SMEAR CERVIX ABNORMAL ( 5 FDA reports)
SPINAL CORD INFECTION ( 5 FDA reports)
SPLENIC GRANULOMA ( 5 FDA reports)
SPLENIC INJURY ( 5 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 5 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 5 FDA reports)
SUPERINFECTION BACTERIAL ( 5 FDA reports)
SUSPICIOUSNESS ( 5 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 5 FDA reports)
THYROID MASS ( 5 FDA reports)
TORSADE DE POINTES ( 5 FDA reports)
TRAUMATIC LUNG INJURY ( 5 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 5 FDA reports)
UMBILICAL CORD AROUND NECK ( 5 FDA reports)
URETHRAL FISTULA ( 5 FDA reports)
URETHRAL STENOSIS ( 5 FDA reports)
URINARY SEDIMENT PRESENT ( 5 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 5 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
URINARY TRACT OPERATION ( 5 FDA reports)
URINE CALCIUM DECREASED ( 5 FDA reports)
URINE COLOUR ABNORMAL ( 5 FDA reports)
VAGINAL OPERATION ( 5 FDA reports)
VASCULAR OPERATION ( 5 FDA reports)
VASOCONSTRICTION ( 5 FDA reports)
VENOUS INJURY ( 5 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
VESTIBULOPLASTY ( 5 FDA reports)
VITREOUS HAEMORRHAGE ( 5 FDA reports)
VOLVULUS ( 5 FDA reports)
WEIGHT ( 5 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
ABDOMINAL ADHESIONS ( 5 FDA reports)
ABDOMINAL NEOPLASM ( 5 FDA reports)
ABNORMAL FAECES ( 5 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 5 FDA reports)
ACARODERMATITIS ( 5 FDA reports)
ADDISON'S DISEASE ( 5 FDA reports)
AGORAPHOBIA ( 5 FDA reports)
ALLERGY TEST POSITIVE ( 5 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 5 FDA reports)
ANAESTHETIC COMPLICATION ( 5 FDA reports)
ANAL HAEMORRHAGE ( 5 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
ANASTOMOTIC LEAK ( 5 FDA reports)
ANDROGEN DEFICIENCY ( 5 FDA reports)
ANION GAP DECREASED ( 5 FDA reports)
ANKLE OPERATION ( 5 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
APPENDIX DISORDER ( 5 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 5 FDA reports)
ARTERIOVENOUS MALFORMATION ( 5 FDA reports)
ARTERITIS ( 5 FDA reports)
BACTERIA URINE IDENTIFIED ( 5 FDA reports)
BACTEROIDES INFECTION ( 5 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 5 FDA reports)
BICUSPID AORTIC VALVE ( 5 FDA reports)
BILE DUCT CANCER ( 5 FDA reports)
BILIARY CIRRHOSIS ( 5 FDA reports)
BILIARY TRACT DISORDER ( 5 FDA reports)
BLOOD ALCOHOL INCREASED ( 5 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 5 FDA reports)
BLOOD FOLATE INCREASED ( 5 FDA reports)
BLOOD OSMOLARITY DECREASED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 5 FDA reports)
BLOOD TESTOSTERONE FREE DECREASED ( 5 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 5 FDA reports)
BLOOD URIC ACID DECREASED ( 5 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 5 FDA reports)
BRAIN CANCER METASTATIC ( 5 FDA reports)
BREAST OEDEMA ( 5 FDA reports)
BRONCHIAL NEOPLASM ( 5 FDA reports)
BRONCHIAL SECRETION RETENTION ( 5 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 5 FDA reports)
BURNING MOUTH SYNDROME ( 5 FDA reports)
CARCINOMA IN SITU OF EYE ( 5 FDA reports)
CARDIAC DISCOMFORT ( 5 FDA reports)
CARDIAC OPERATION ( 5 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 5 FDA reports)
CATATONIA ( 5 FDA reports)
CELL DEATH ( 5 FDA reports)
CENTRAL LINE INFECTION ( 5 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 5 FDA reports)
COARCTATION OF THE AORTA ( 5 FDA reports)
COELIAC DISEASE ( 5 FDA reports)
COLON CANCER RECURRENT ( 5 FDA reports)
COLOUR BLINDNESS ( 5 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 5 FDA reports)
CONTRAST MEDIA REACTION ( 5 FDA reports)
CSF PROTEIN INCREASED ( 5 FDA reports)
CULTURE WOUND POSITIVE ( 5 FDA reports)
CYCLOTHYMIC DISORDER ( 5 FDA reports)
DEATH OF RELATIVE ( 5 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 5 FDA reports)
DERMOID CYST ( 5 FDA reports)
DEVICE ADHESION ISSUE ( 5 FDA reports)
DEVICE COMPONENT ISSUE ( 5 FDA reports)
DEVICE ISSUE ( 5 FDA reports)
DIAPHRAGMATIC DISORDER ( 5 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 5 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 5 FDA reports)
DRUG EFFECT DELAYED ( 5 FDA reports)
DRUG LEVEL DECREASED ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
DRUG TOLERANCE DECREASED ( 5 FDA reports)
DUANE'S SYNDROME ( 5 FDA reports)
DUPUYTREN'S CONTRACTURE ( 5 FDA reports)
EAR CONGESTION ( 5 FDA reports)
EAR PRURITUS ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 5 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 5 FDA reports)
EXTREMITY CONTRACTURE ( 5 FDA reports)
EXTREMITY NECROSIS ( 5 FDA reports)
EYE INJURY ( 5 FDA reports)
EYELID DISORDER ( 5 FDA reports)
FANCONI SYNDROME ACQUIRED ( 5 FDA reports)
FAT INTOLERANCE ( 5 FDA reports)
FEEDING DISORDER ( 5 FDA reports)
FLATBACK SYNDROME ( 5 FDA reports)
FOOD ALLERGY ( 5 FDA reports)
FUNGAL SKIN INFECTION ( 5 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 5 FDA reports)
GASTRIC ULCER PERFORATION ( 5 FDA reports)
GESTATIONAL DIABETES ( 5 FDA reports)
GLIOSIS ( 5 FDA reports)
GLOBULINS INCREASED ( 5 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 5 FDA reports)
GLYCOSURIA ( 5 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 5 FDA reports)
HAEMODYNAMIC INSTABILITY ( 5 FDA reports)
HAEMORRHAGIC DISORDER ( 5 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 5 FDA reports)
HEPATIC CANCER METASTATIC ( 5 FDA reports)
HEPATIC HAEMORRHAGE ( 5 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 5 FDA reports)
HEREDITARY ANGIOEDEMA ( 5 FDA reports)
HERPES VIRUS INFECTION ( 5 FDA reports)
HYALOSIS ASTEROID ( 5 FDA reports)
HYPERMETROPIA ( 5 FDA reports)
HYPERPROLACTINAEMIA ( 5 FDA reports)
IMPAIRED SELF-CARE ( 5 FDA reports)
IMPLANT SITE INDURATION ( 5 FDA reports)
IMPULSE-CONTROL DISORDER ( 5 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
INDURATION ( 5 FDA reports)
INFECTIOUS PERITONITIS ( 5 FDA reports)
INFUSION SITE REACTION ( 5 FDA reports)
INJECTION SITE INDURATION ( 5 FDA reports)
INJECTION SITE PAPULE ( 5 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 5 FDA reports)
INTESTINAL DILATATION ( 5 FDA reports)
INTRACRANIAL HYPOTENSION ( 5 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 5 FDA reports)
JAUNDICE CHOLESTATIC ( 5 FDA reports)
KERATITIS ( 5 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 5 FDA reports)
LEUKOPLAKIA ORAL ( 5 FDA reports)
LIBIDO INCREASED ( 5 FDA reports)
LIVE BIRTH ( 5 FDA reports)
LOCALISED OSTEOARTHRITIS ( 5 FDA reports)
LUNG ABSCESS ( 5 FDA reports)
LUNG TRANSPLANT ( 5 FDA reports)
MACULAR OEDEMA ( 5 FDA reports)
MALABSORPTION ( 5 FDA reports)
MEDIASTINAL CYST ( 5 FDA reports)
MENINGITIS BACTERIAL ( 5 FDA reports)
METASTASES TO SKIN ( 5 FDA reports)
MITRAL VALVE REPLACEMENT ( 5 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 5 FDA reports)
NAIL INFECTION ( 5 FDA reports)
NECK DEFORMITY ( 5 FDA reports)
NECROTISING FASCIITIS ( 5 FDA reports)
NEPHRITIS ( 5 FDA reports)
NEURALGIC AMYOTROPHY ( 5 FDA reports)
NICOTINE DEPENDENCE ( 5 FDA reports)
NIPPLE DISORDER ( 5 FDA reports)
NITRITE URINE PRESENT ( 5 FDA reports)
NORMAL NEWBORN ( 5 FDA reports)
OBSESSIVE THOUGHTS ( 5 FDA reports)
OESOPHAGEAL ACHALASIA ( 5 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 5 FDA reports)
OLIGOMENORRHOEA ( 5 FDA reports)
OPTIC NEUROPATHY ( 5 FDA reports)
ORAL BACTERIAL INFECTION ( 5 FDA reports)
ORAL MUCOSAL BLISTERING ( 5 FDA reports)
ORBITAL OEDEMA ( 5 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 5 FDA reports)
ORTHOSTATIC INTOLERANCE ( 5 FDA reports)
OSTEOPOROTIC FRACTURE ( 5 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 5 FDA reports)
PARASITE BLOOD TEST POSITIVE ( 5 FDA reports)
PARESIS ( 5 FDA reports)
PELVIC ADHESIONS ( 5 FDA reports)
PELVIC FLUID COLLECTION ( 5 FDA reports)
PEMPHIGUS ( 5 FDA reports)
PENILE PAIN ( 5 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 5 FDA reports)
PNEUMOCEPHALUS ( 5 FDA reports)
POLYCYTHAEMIA ( 5 FDA reports)
POLYP COLORECTAL ( 5 FDA reports)
POSTOPERATIVE CONSTIPATION ( 5 FDA reports)
POSTOPERATIVE FEVER ( 5 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 5 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 5 FDA reports)
PRESSURE OF SPEECH ( 5 FDA reports)
PROCEDURAL VOMITING ( 5 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 5 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 5 FDA reports)
PSEUDARTHROSIS ( 5 FDA reports)
PULMONARY ARTERY ATRESIA ( 5 FDA reports)
PULMONARY MYCOSIS ( 5 FDA reports)
REBOUND EFFECT ( 5 FDA reports)
RECTAL ABSCESS ( 5 FDA reports)
RECURRENT CANCER ( 5 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
RENAL HYPERTROPHY ( 5 FDA reports)
RHYTHM IDIOVENTRICULAR ( 5 FDA reports)
RICKETTSIOSIS ( 5 FDA reports)
SCROTAL OEDEMA ( 5 FDA reports)
SEPSIS SYNDROME ( 5 FDA reports)
SERUM SICKNESS ( 5 FDA reports)
SINUS TARSI SYNDROME ( 5 FDA reports)
ABDOMINAL INJURY ( 4 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 4 FDA reports)
ABNORMAL WEIGHT GAIN ( 4 FDA reports)
ABSCESS INTESTINAL ( 4 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 4 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 4 FDA reports)
ACUTE POLYNEUROPATHY ( 4 FDA reports)
ALCOHOL INTERACTION ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
ANAL ATRESIA ( 4 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 4 FDA reports)
ANOVULATORY CYCLE ( 4 FDA reports)
ANOXIA ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
AORTIC VALVE REPLACEMENT ( 4 FDA reports)
APGAR SCORE LOW ( 4 FDA reports)
APPLICATION SITE INFECTION ( 4 FDA reports)
APPLICATION SITE INFLAMMATION ( 4 FDA reports)
APPLICATION SITE SWELLING ( 4 FDA reports)
ARTERIAL INJURY ( 4 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 4 FDA reports)
ARTHROSCOPY ( 4 FDA reports)
BENIGN BONE NEOPLASM ( 4 FDA reports)
BENIGN TUMOUR EXCISION ( 4 FDA reports)
BLADDER INJURY ( 4 FDA reports)
BLADDER MASS ( 4 FDA reports)
BLADDER NEOPLASM ( 4 FDA reports)
BLADDER PAPILLOMA ( 4 FDA reports)
BLOOD BILIRUBIN DECREASED ( 4 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 4 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 4 FDA reports)
BLOOD KETONE BODY ( 4 FDA reports)
BLOOD MAGNESIUM INCREASED ( 4 FDA reports)
BLOOD PH INCREASED ( 4 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 4 FDA reports)
BONE DENSITY INCREASED ( 4 FDA reports)
BONE NEOPLASM ( 4 FDA reports)
BORDERLINE GLAUCOMA ( 4 FDA reports)
BRADYCARDIA NEONATAL ( 4 FDA reports)
BREAST CANCER IN SITU ( 4 FDA reports)
CANDIDURIA ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CATHETER SITE HAEMORRHAGE ( 4 FDA reports)
CAUDAL REGRESSION SYNDROME ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 4 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 4 FDA reports)
CEREBRAL CYST ( 4 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 4 FDA reports)
CHONDROPLASTY ( 4 FDA reports)
CLEFT PALATE ( 4 FDA reports)
CLOSED HEAD INJURY ( 4 FDA reports)
COCCIDIOIDOMYCOSIS ( 4 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 4 FDA reports)
COLON INJURY ( 4 FDA reports)
COMPLEX PARTIAL SEIZURES ( 4 FDA reports)
COMPULSIVE SHOPPING ( 4 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 4 FDA reports)
CONUS MEDULLARIS SYNDROME ( 4 FDA reports)
CORNEAL DYSTROPHY ( 4 FDA reports)
CORONARY BYPASS THROMBOSIS ( 4 FDA reports)
CRACKLES LUNG ( 4 FDA reports)
CUSHING'S SYNDROME ( 4 FDA reports)
CYANOPSIA ( 4 FDA reports)
CYSTITIS RADIATION ( 4 FDA reports)
CYSTOCELE REPAIR ( 4 FDA reports)
CYSTOSCOPY ( 4 FDA reports)
DACRYOCYSTITIS INFECTIVE ( 4 FDA reports)
DACRYOCYSTORHINOSTOMY ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DEPERSONALISATION ( 4 FDA reports)
DERMATITIS ALLERGIC ( 4 FDA reports)
DIABETES INSIPIDUS ( 4 FDA reports)
DIABETIC EYE DISEASE ( 4 FDA reports)
DIABETIC FOOT INFECTION ( 4 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 4 FDA reports)
DIPLEGIA ( 4 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 4 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 4 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 4 FDA reports)
DRY GANGRENE ( 4 FDA reports)
EJACULATION FAILURE ( 4 FDA reports)
ELECTRIC SHOCK ( 4 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 4 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 4 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 4 FDA reports)
ENDOSCOPY ( 4 FDA reports)
ENURESIS ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
EYE ABSCESS ( 4 FDA reports)
FACIAL SPASM ( 4 FDA reports)
FALLOT'S TETRALOGY ( 4 FDA reports)
FEAR OF DISEASE ( 4 FDA reports)
FEELING OF RELAXATION ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
FOOT CRUSHING ( 4 FDA reports)
FOREARM FRACTURE ( 4 FDA reports)
FRACTURE DELAYED UNION ( 4 FDA reports)
FRACTURE TREATMENT ( 4 FDA reports)
GAIT SPASTIC ( 4 FDA reports)
GASTRIC DILATATION ( 4 FDA reports)
GASTRIC MUCOSAL LESION ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 4 FDA reports)
GASTROINTESTINAL EROSION ( 4 FDA reports)
GASTROINTESTINAL ULCER ( 4 FDA reports)
GAZE PALSY ( 4 FDA reports)
GENITAL HAEMORRHAGE ( 4 FDA reports)
GLUCOSE URINE PRESENT ( 4 FDA reports)
GRIEF REACTION ( 4 FDA reports)
HAEMORRHAGE URINARY TRACT ( 4 FDA reports)
HAIR GROWTH ABNORMAL ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 4 FDA reports)
HERNIA OBSTRUCTIVE ( 4 FDA reports)
HYDROURETER ( 4 FDA reports)
HYPEROSMOLAR STATE ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
HYPERTRANSAMINASAEMIA ( 4 FDA reports)
HYPERTROPHY BREAST ( 4 FDA reports)
HYPOGEUSIA ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
ILEOSTOMY ( 4 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 4 FDA reports)
IMPLANT SITE EXTRAVASATION ( 4 FDA reports)
IMPLANT SITE INFECTION ( 4 FDA reports)
INCISION SITE HAEMORRHAGE ( 4 FDA reports)
INFANTILE APNOEIC ATTACK ( 4 FDA reports)
INFECTED BITES ( 4 FDA reports)
INFECTED DERMAL CYST ( 4 FDA reports)
INFUSION SITE OEDEMA ( 4 FDA reports)
INFUSION SITE SWELLING ( 4 FDA reports)
INJECTION SITE ABSCESS ( 4 FDA reports)
INJECTION SITE DISCOMFORT ( 4 FDA reports)
INTERCEPTED MEDICATION ERROR ( 4 FDA reports)
JOINT DESTRUCTION ( 4 FDA reports)
JOINT INSTABILITY ( 4 FDA reports)
KETOACIDOSIS ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 4 FDA reports)
LACRIMAL DUCT PROCEDURE ( 4 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 4 FDA reports)
LICHENIFICATION ( 4 FDA reports)
LIGAMENT OPERATION ( 4 FDA reports)
LIMB DEFORMITY ( 4 FDA reports)
LISTERIOSIS ( 4 FDA reports)
LIVIDITY ( 4 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 4 FDA reports)
LUNG TRANSPLANT REJECTION ( 4 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 4 FDA reports)
MADAROSIS ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 4 FDA reports)
MEDICAL DEVICE PAIN ( 4 FDA reports)
MENISCUS REMOVAL ( 4 FDA reports)
MESENTERITIS ( 4 FDA reports)
METABOLIC ALKALOSIS ( 4 FDA reports)
METASTASES TO STOMACH ( 4 FDA reports)
MITRAL VALVE STENOSIS ( 4 FDA reports)
MIXED LIVER INJURY ( 4 FDA reports)
MOLE EXCISION ( 4 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MULTI-ORGAN DISORDER ( 4 FDA reports)
MYCOBACTERIAL INFECTION ( 4 FDA reports)
MYELOFIBROSIS ( 4 FDA reports)
MYOCARDIAL FIBROSIS ( 4 FDA reports)
NAIL GROWTH ABNORMAL ( 4 FDA reports)
NAIL HYPERTROPHY ( 4 FDA reports)
NASAL DRYNESS ( 4 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 4 FDA reports)
NEGATIVE THOUGHTS ( 4 FDA reports)
NEONATAL HYPOTENSION ( 4 FDA reports)
NEUROPATHIC PAIN ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
NODAL ARRHYTHMIA ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 4 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 4 FDA reports)
NOSOCOMIAL INFECTION ( 4 FDA reports)
OCCIPITAL NEURALGIA ( 4 FDA reports)
OCULAR VASCULAR DISORDER ( 4 FDA reports)
OEDEMA MUCOSAL ( 4 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 4 FDA reports)
OESTROGEN DEFICIENCY ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
OSTEODYSTROPHY ( 4 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 4 FDA reports)
OXYGEN SUPPLEMENTATION ( 4 FDA reports)
PAINFUL ERECTION ( 4 FDA reports)
PANCREATIC INJURY ( 4 FDA reports)
PANCREATIC PSEUDOCYST ( 4 FDA reports)
PAPULE ( 4 FDA reports)
PARACENTESIS ( 4 FDA reports)
PARTNER STRESS ( 4 FDA reports)
PEDAL PULSE DECREASED ( 4 FDA reports)
PELVIC HAEMORRHAGE ( 4 FDA reports)
PEPTIC ULCER PERFORATION ( 4 FDA reports)
PERICARDIAL CYST ( 4 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 4 FDA reports)
PERIRENAL HAEMATOMA ( 4 FDA reports)
PERSISTENT CLOACA ( 4 FDA reports)
PHARYNGEAL ULCERATION ( 4 FDA reports)
PLATELET COUNT ABNORMAL ( 4 FDA reports)
PLATELET DISORDER ( 4 FDA reports)
PLEURAL DISORDER ( 4 FDA reports)
PNEUMOCONIOSIS ( 4 FDA reports)
POST PROCEDURAL DISCOMFORT ( 4 FDA reports)
POST-TRAUMATIC PAIN ( 4 FDA reports)
POTENTIATING DRUG INTERACTION ( 4 FDA reports)
PRE-ECLAMPSIA ( 4 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 4 FDA reports)
PROLONGED EXPIRATION ( 4 FDA reports)
PROSTATIC ACID PHOSPHATASE INCREASED ( 4 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 4 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 4 FDA reports)
PUPILS UNEQUAL ( 4 FDA reports)
RASH SCALY ( 4 FDA reports)
RENAL ARTERIOSCLEROSIS ( 4 FDA reports)
RENAL SURGERY ( 4 FDA reports)
RESPIRATION ABNORMAL ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
RHEUMATOID FACTOR INCREASED ( 4 FDA reports)
ROTAVIRUS TEST POSITIVE ( 4 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 4 FDA reports)
SCROTAL INFECTION ( 4 FDA reports)
SEIZURE LIKE PHENOMENA ( 4 FDA reports)
SEPTIC EMBOLUS ( 4 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 4 FDA reports)
SHOCK HYPOGLYCAEMIC ( 4 FDA reports)
SKIN EROSION ( 4 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 4 FDA reports)
SMALL INTESTINAL RESECTION ( 4 FDA reports)
SMOKER ( 4 FDA reports)
SOCIAL PHOBIA ( 4 FDA reports)
SPLEEN SCAN ABNORMAL ( 4 FDA reports)
SPLENIC VEIN THROMBOSIS ( 4 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE NEONATAL ( 4 FDA reports)
SUBDURAL HAEMORRHAGE NEONATAL ( 4 FDA reports)
SYRINGOMYELIA ( 4 FDA reports)
TACHYCARDIA PAROXYSMAL ( 4 FDA reports)
TAENIASIS ( 4 FDA reports)
THOUGHT BLOCKING ( 4 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
TONSILLAR HYPERTROPHY ( 4 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 4 FDA reports)
TOXOPLASMOSIS ( 4 FDA reports)
TRANSPLANT FAILURE ( 4 FDA reports)
TUMOUR FLARE ( 4 FDA reports)
TUMOUR HAEMORRHAGE ( 4 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 4 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 4 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 4 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
URETERAL DISORDER ( 4 FDA reports)
URETERAL STENT INSERTION ( 4 FDA reports)
URETHRAL STENT INSERTION ( 4 FDA reports)
UTERINE ATROPHY ( 4 FDA reports)
UTERINE FIBROSIS ( 4 FDA reports)
VACTERL SYNDROME ( 4 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 4 FDA reports)
VAGINAL FISTULA ( 4 FDA reports)
VASCULAR BYPASS GRAFT ( 4 FDA reports)
VASCULAR DEMENTIA ( 4 FDA reports)
VEIN PAIN ( 4 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 4 FDA reports)
VENOUS STASIS ( 4 FDA reports)
VESICOURETERIC REFLUX ( 4 FDA reports)
VULVAL ABSCESS ( 4 FDA reports)
VULVAL DISORDER ( 4 FDA reports)
VULVAR DYSPLASIA ( 4 FDA reports)
SKIN TOXICITY ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
SOMATOFORM DISORDER ( 3 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 3 FDA reports)
SPINAL FUSION ACQUIRED ( 3 FDA reports)
STATUS ASTHMATICUS ( 3 FDA reports)
STICKY SKIN ( 3 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 3 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 3 FDA reports)
STRESS AT WORK ( 3 FDA reports)
SUBSTANCE USE ( 3 FDA reports)
SUDDEN ONSET OF SLEEP ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
SURGICAL FAILURE ( 3 FDA reports)
TENDON CALCIFICATION ( 3 FDA reports)
THALAMUS HAEMORRHAGE ( 3 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 3 FDA reports)
THYMUS DISORDER ( 3 FDA reports)
THYROIDECTOMY ( 3 FDA reports)
TORTICOLLIS ( 3 FDA reports)
TRACHEOMALACIA ( 3 FDA reports)
TRAUMATIC ARTHROPATHY ( 3 FDA reports)
TRICHOMONIASIS ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
UNDERWEIGHT ( 3 FDA reports)
URATE NEPHROPATHY ( 3 FDA reports)
URETHRAL MEATUS STENOSIS ( 3 FDA reports)
URGE INCONTINENCE ( 3 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
URINE AMPHETAMINE POSITIVE ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
UTERINE CERVIX STENOSIS ( 3 FDA reports)
UTERINE SPASM ( 3 FDA reports)
VAGINAL CANDIDIASIS ( 3 FDA reports)
VAGINAL ODOUR ( 3 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 3 FDA reports)
VARICES OESOPHAGEAL ( 3 FDA reports)
VARICOSE VEIN OPERATION ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 3 FDA reports)
VENTRICULOPERITONEAL SHUNT MALFUNCTION ( 3 FDA reports)
VICTIM OF CRIME ( 3 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 3 FDA reports)
VISCERAL OEDEMA ( 3 FDA reports)
VOCAL CORD NEOPLASM ( 3 FDA reports)
VULVAL CANCER STAGE I ( 3 FDA reports)
VULVAR EROSION ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
WEANING FAILURE ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WHITE BLOOD CELLS URINE ( 3 FDA reports)
WISDOM TEETH REMOVAL ( 3 FDA reports)
WOUND NECROSIS ( 3 FDA reports)
XANTHOGRANULOMA ( 3 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 3 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ABSCESS RUPTURE ( 3 FDA reports)
ACTINIC ELASTOSIS ( 3 FDA reports)
ACUTE LUNG INJURY ( 3 FDA reports)
ACUTE PSYCHOSIS ( 3 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
ADENOTONSILLECTOMY ( 3 FDA reports)
ALCOHOL INDUCED PERSISTING DEMENTIA ( 3 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 3 FDA reports)
AMPUTATION OF PENIS ( 3 FDA reports)
ANAL DISCOMFORT ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANORECTAL DISCOMFORT ( 3 FDA reports)
ANTI-PLATELET ANTIBODY ( 3 FDA reports)
ANTIANDROGEN THERAPY ( 3 FDA reports)
ANTIBODY TEST POSITIVE ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
APPLICATION SITE BLEEDING ( 3 FDA reports)
ARCUS LIPOIDES ( 3 FDA reports)
ARM AMPUTATION ( 3 FDA reports)
ARTERIAL RUPTURE ( 3 FDA reports)
ARTERIAL THROMBOSIS ( 3 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ASTIGMATISM ( 3 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 3 FDA reports)
BACTERIA STOOL IDENTIFIED ( 3 FDA reports)
BLADDER IRRITATION ( 3 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 3 FDA reports)
BLEEDING PERIPARTUM ( 3 FDA reports)
BLINDNESS TRAUMATIC ( 3 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 3 FDA reports)
BLOOD CREATINE ABNORMAL ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 3 FDA reports)
BLUE TOE SYNDROME ( 3 FDA reports)
BLUNTED AFFECT ( 3 FDA reports)
BONE INFARCTION ( 3 FDA reports)
BONE METABOLISM DISORDER ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
BRAIN COMPRESSION ( 3 FDA reports)
BREAST CANCER STAGE I ( 3 FDA reports)
BREAST CANCER STAGE III ( 3 FDA reports)
BREAST PROSTHESIS USER ( 3 FDA reports)
BREATH SOUNDS DECREASED ( 3 FDA reports)
BURNS THIRD DEGREE ( 3 FDA reports)
BUTTERFLY RASH ( 3 FDA reports)
CALCIUM IONISED ( 3 FDA reports)
CANDIDA TEST POSITIVE ( 3 FDA reports)
CAPILLARY LEAK SYNDROME ( 3 FDA reports)
CARCINOID TUMOUR ( 3 FDA reports)
CARDIAC DEATH ( 3 FDA reports)
CARDIAC FAILURE CHRONIC ( 3 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CATHETER SEPSIS ( 3 FDA reports)
CATHETER SITE ERYTHEMA ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CATHETER SITE PAIN ( 3 FDA reports)
CD4/CD8 RATIO DECREASED ( 3 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 3 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 3 FDA reports)
CERVICAL MYELOPATHY ( 3 FDA reports)
CERVIX CARCINOMA ( 3 FDA reports)
CHOLANGITIS ACUTE ( 3 FDA reports)
CHOREA ( 3 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 3 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 3 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COITAL BLEEDING ( 3 FDA reports)
COLECTOMY TOTAL ( 3 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CUBITAL TUNNEL SYNDROME ( 3 FDA reports)
CUTANEOUS CONTOUR DEFORMITY ( 3 FDA reports)
CYSTOPEXY ( 3 FDA reports)
CYTOREDUCTIVE SURGERY ( 3 FDA reports)
DECREASED VIBRATORY SENSE ( 3 FDA reports)
DEPRESSION POSTOPERATIVE ( 3 FDA reports)
DERMATITIS PSORIASIFORM ( 3 FDA reports)
DEVICE MISUSE ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DISEASE COMPLICATION ( 3 FDA reports)
DISLOCATION OF VERTEBRA ( 3 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 3 FDA reports)
DYSENTERY ( 3 FDA reports)
DYSTROPHIC CALCIFICATION ( 3 FDA reports)
EAR HAEMORRHAGE ( 3 FDA reports)
ENCHONDROMA ( 3 FDA reports)
ENDOCRINE DISORDER ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
ESSENTIAL TREMOR ( 3 FDA reports)
EUSTACHIAN TUBE DISORDER ( 3 FDA reports)
EXPOSURE TO TOXIC AGENT ( 3 FDA reports)
EYE EXCISION ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
FAILED INDUCTION OF LABOUR ( 3 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 3 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 3 FDA reports)
FLASHBACK ( 3 FDA reports)
FLIGHT OF IDEAS ( 3 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 3 FDA reports)
FOETAL HEART RATE ABNORMAL ( 3 FDA reports)
FRACTURE MALUNION ( 3 FDA reports)
FUNGAL PARONYCHIA ( 3 FDA reports)
GAMBLING ( 3 FDA reports)
GASTRIC PH DECREASED ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
HAEMARTHROSIS ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMOCHROMATOSIS ( 3 FDA reports)
HAEMORRHAGIC CYST ( 3 FDA reports)
HAIR TEXTURE ABNORMAL ( 3 FDA reports)
HEAD AND NECK CANCER ( 3 FDA reports)
HEAD DEFORMITY ( 3 FDA reports)
HEAD TITUBATION ( 3 FDA reports)
HEAT RASH ( 3 FDA reports)
HELICOBACTER GASTRITIS ( 3 FDA reports)
HEMIANOPIA HOMONYMOUS ( 3 FDA reports)
HEMISENSORY NEGLECT ( 3 FDA reports)
HEPATIC INFECTION ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HERPES ZOSTER DISSEMINATED ( 3 FDA reports)
HIV INFECTION ( 3 FDA reports)
HYDROTHORAX ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPERGLOBULINAEMIA ( 3 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 3 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 3 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 3 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 3 FDA reports)
HYPOCHONDRIASIS ( 3 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOPHOSPHATASIA ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
HYPOVITAMINOSIS ( 3 FDA reports)
ILEOSTOMY CLOSURE ( 3 FDA reports)
IMMUNOGLOBULINS INCREASED ( 3 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 3 FDA reports)
INCORRECT PRODUCT STORAGE ( 3 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
INFUSION SITE DISCOMFORT ( 3 FDA reports)
INHALATION THERAPY ( 3 FDA reports)
INJECTION SITE STINGING ( 3 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 3 FDA reports)
INTERNAL HERNIA ( 3 FDA reports)
INTESTINAL MALROTATION ( 3 FDA reports)
INTESTINAL STENOSIS ( 3 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
INTUBATION ( 3 FDA reports)
IRON OVERLOAD ( 3 FDA reports)
ISCHAEMIC ULCER ( 3 FDA reports)
IUCD COMPLICATION ( 3 FDA reports)
JAW CYST ( 3 FDA reports)
JOINT WARMTH ( 3 FDA reports)
KETONURIA ( 3 FDA reports)
KNEE DEFORMITY ( 3 FDA reports)
LAGOPHTHALMOS ( 3 FDA reports)
LATEX ALLERGY ( 3 FDA reports)
LENTIGO ( 3 FDA reports)
LESION EXCISION ( 3 FDA reports)
LIMB ASYMMETRY ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 3 FDA reports)
LUTEAL PHASE DEFICIENCY ( 3 FDA reports)
LYMPHADENITIS BACTERIAL ( 3 FDA reports)
LYMPHANGITIS ( 3 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 3 FDA reports)
MAMMOGRAM ABNORMAL ( 3 FDA reports)
MANDIBULECTOMY ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 3 FDA reports)
MENINGEAL DISORDER ( 3 FDA reports)
MENINGITIS CHEMICAL ( 3 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 3 FDA reports)
METASTASES TO ADRENALS ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 3 FDA reports)
MICROVASCULAR ANGINA ( 3 FDA reports)
MICTURITION FREQUENCY DECREASED ( 3 FDA reports)
MINERAL METABOLISM DISORDER ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MORGANELLA INFECTION ( 3 FDA reports)
MORPHOEA ( 3 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 3 FDA reports)
MUCOSAL DRYNESS ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
MUSCLE ABSCESS ( 3 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 3 FDA reports)
MYELOID LEUKAEMIA ( 3 FDA reports)
MYOCARDIAL CALCIFICATION ( 3 FDA reports)
MYOPATHY STEROID ( 3 FDA reports)
MYOSCLEROSIS ( 3 FDA reports)
MYRINGOTOMY ( 3 FDA reports)
NASAL CYST ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NASOPHARYNGEAL DISORDER ( 3 FDA reports)
NECROTISING COLITIS ( 3 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NERVE ROOT LESION ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 3 FDA reports)
NON-CONSUMMATION ( 3 FDA reports)
OBTURATOR HERNIA ( 3 FDA reports)
OCULAR DISCOMFORT ( 3 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
OESOPHAGEAL RUPTURE ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
ORBITAL INFECTION ( 3 FDA reports)
OSTEOCHONDROMA ( 3 FDA reports)
OVARIAN CYST RUPTURED ( 3 FDA reports)
OVARIAN FAILURE ( 3 FDA reports)
PACHYMENINGITIS ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PECTUS EXCAVATUM ( 3 FDA reports)
PELVIC NEOPLASM ( 3 FDA reports)
PENILE PROSTHESIS INSERTION ( 3 FDA reports)
PERICARDIAL DRAINAGE ( 3 FDA reports)
PERICARDIAL EXCISION ( 3 FDA reports)
PERICARDIAL FIBROSIS ( 3 FDA reports)
PERICORONITIS ( 3 FDA reports)
PERINEPHRIC COLLECTION ( 3 FDA reports)
PERIPHERAL NERVE LESION ( 3 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERITONEAL ADHESIONS ( 3 FDA reports)
PERITONEAL EFFUSION ( 3 FDA reports)
PHOBIA ( 3 FDA reports)
PILONIDAL CYST ( 3 FDA reports)
PLEOCYTOSIS ( 3 FDA reports)
PNEUMONECTOMY ( 3 FDA reports)
PNEUMONIA KLEBSIELLA ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
POLYCYSTIC LIVER DISEASE ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
POST PROCEDURAL CONSTIPATION ( 3 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 3 FDA reports)
PRECANCEROUS CELLS PRESENT ( 3 FDA reports)
PROCEDURAL DIZZINESS ( 3 FDA reports)
PROCEDURAL HYPOTENSION ( 3 FDA reports)
PROCEDURAL SITE REACTION ( 3 FDA reports)
PRODUCT CONTAMINATION ( 3 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 3 FDA reports)
PRODUCT TAMPERING ( 3 FDA reports)
PRODUCT TASTE ABNORMAL ( 3 FDA reports)
PROSTATIC DISORDER ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PSEUDOCYST ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PSYCHOMOTOR RETARDATION ( 3 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PULMONARY CALCIFICATION ( 3 FDA reports)
PULMONARY TOXICITY ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PUPILLARY DISORDER ( 3 FDA reports)
PURPURA SENILE ( 3 FDA reports)
RADIATION NEUROPATHY ( 3 FDA reports)
RASH PAPULOSQUAMOUS ( 3 FDA reports)
RECTAL ADENOMA ( 3 FDA reports)
RECTAL DISCHARGE ( 3 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 3 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 3 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 3 FDA reports)
REGURGITATION OF FOOD ( 3 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 3 FDA reports)
RENAL NECROSIS ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RESPIRATORY TRACT IRRITATION ( 3 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 3 FDA reports)
RHINALGIA ( 3 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 3 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 3 FDA reports)
SEROCONVERSION TEST POSITIVE ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SHUNT INFECTION ( 3 FDA reports)
SHUNT MALFUNCTION ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACCIDENT AT HOME ( 2 FDA reports)
ACNE CYSTIC ( 2 FDA reports)
ACTINOMYCES TEST POSITIVE ( 2 FDA reports)
ADHESIOLYSIS ( 2 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
AMNIORRHOEA ( 2 FDA reports)
AMPULLA OF VATER STENOSIS ( 2 FDA reports)
ANAL INJURY ( 2 FDA reports)
ANAL SKIN TAGS ( 2 FDA reports)
ANAL STENOSIS ( 2 FDA reports)
ANALGESIC THERAPY ( 2 FDA reports)
ANEURYSM REPAIR ( 2 FDA reports)
ANGIOMYOLIPOMA ( 2 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANORECTAL INFECTION ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
AORTIC OCCLUSION ( 2 FDA reports)
AORTITIS ( 2 FDA reports)
APPLICATION SITE HAEMATOMA ( 2 FDA reports)
APPLICATION SITE PUSTULES ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 2 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ATRIAL HYPERTROPHY ( 2 FDA reports)
ATRIAL PRESSURE INCREASED ( 2 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BALANITIS CANDIDA ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BENIGN NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 2 FDA reports)
BILE DUCT CANCER STAGE IV ( 2 FDA reports)
BILIRUBIN URINE ( 2 FDA reports)
BIOPSY ARTERY ( 2 FDA reports)
BIOPSY BONE ABNORMAL ( 2 FDA reports)
BIOPSY COLON ABNORMAL ( 2 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BIOPSY STOMACH ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 2 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD ETHANOL INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLOOD SODIUM ABNORMAL ( 2 FDA reports)
BLOOD UREA ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BONE TUBERCULOSIS ( 2 FDA reports)
BOTULISM ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYCARDIA FOETAL ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN MIDLINE SHIFT ( 2 FDA reports)
BRAIN OPERATION ( 2 FDA reports)
BRAIN STEM AUDITORY EVOKED RESPONSE ABNORMAL ( 2 FDA reports)
BRAIN STEM STROKE ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BREAST MICROCALCIFICATION ( 2 FDA reports)
BREATH SOUNDS ABSENT ( 2 FDA reports)
BREECH PRESENTATION ( 2 FDA reports)
BRONCHIAL HYPERACTIVITY ( 2 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 2 FDA reports)
BRONCHIAL IRRITATION ( 2 FDA reports)
BRONCHITIS BACTERIAL ( 2 FDA reports)
CAPILLARY DISORDER ( 2 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 2 FDA reports)
CARCINOMA ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CAUSTIC INJURY ( 2 FDA reports)
CELLULITIS GANGRENOUS ( 2 FDA reports)
CEREBRAL HAEMANGIOMA ( 2 FDA reports)
CERULOPLASMIN DECREASED ( 2 FDA reports)
CERVICAL DISCHARGE ( 2 FDA reports)
CERVIX CARCINOMA STAGE III ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CHALAZION ( 2 FDA reports)
CHEILOSIS ( 2 FDA reports)
CHEMICAL INJURY ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHOLANGITIS SCLEROSING ( 2 FDA reports)
CHOLECYSTOSTOMY ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHONDRECTOMY ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
CLEFT LIP AND PALATE ( 2 FDA reports)
COLECTOMY PARTIAL ( 2 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 2 FDA reports)
COMPULSIONS ( 2 FDA reports)
COMPULSIVE LIP BITING ( 2 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 2 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
CONJUNCTIVOCHALASIS ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
CONVULSION NEONATAL ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CORNEAL PERFORATION ( 2 FDA reports)
CORONARY ARTERY EMBOLISM ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CRUSH INJURY ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CULTURE THROAT POSITIVE ( 2 FDA reports)
CYST RUPTURE ( 2 FDA reports)
CYSTITIS ESCHERICHIA ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DEAFNESS TRANSITORY ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC CHEIROPATHY ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 2 FDA reports)
DRESSLER'S SYNDROME ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 2 FDA reports)
DUODENAL STENOSIS ( 2 FDA reports)
DYSKINESIA OESOPHAGEAL ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
EAR INJURY ( 2 FDA reports)
EAR OPERATION ( 2 FDA reports)
EBSTEIN'S ANOMALY ( 2 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELEPHANTIASIS NOSTRAS VERRUCOSA ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
EMBOLISM ARTERIAL ( 2 FDA reports)
ENAMEL ANOMALY ( 2 FDA reports)
ENCHONDROMATOSIS ( 2 FDA reports)
ENTEROBACTER SEPSIS ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPULIS ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EUTHYROID SICK SYNDROME ( 2 FDA reports)
EXSANGUINATION ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EYE INFECTION BACTERIAL ( 2 FDA reports)
EYEBALL RUPTURE ( 2 FDA reports)
FACTOR VII DEFICIENCY ( 2 FDA reports)
FACTOR VIII DEFICIENCY ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FAILURE OF IMPLANT ( 2 FDA reports)
FANCONI SYNDROME ( 2 FDA reports)
FEAR OF PREGNANCY ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FEMORAL ARTERY ANEURYSM ( 2 FDA reports)
FOETAL DISORDER ( 2 FDA reports)
FOETAL HEART RATE DECREASED ( 2 FDA reports)
FOETAL MOVEMENTS DECREASED ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
FREEZING PHENOMENON ( 2 FDA reports)
GANGLION ( 2 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 2 FDA reports)
GASTRIC OCCULT BLOOD POSITIVE ( 2 FDA reports)
GASTRITIS FUNGAL ( 2 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 2 FDA reports)
GENITAL BURNING SENSATION ( 2 FDA reports)
GENITAL DISCOMFORT ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GENITAL DISORDER MALE ( 2 FDA reports)
GENITAL ERYTHEMA ( 2 FDA reports)
GENITAL PAIN ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GINGIVAL BLISTER ( 2 FDA reports)
GINGIVAL DISCOLOURATION ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLOMUS TUMOUR ( 2 FDA reports)
GOUTY TOPHUS ( 2 FDA reports)
GRAFT HAEMORRHAGE ( 2 FDA reports)
GRAFT INFECTION ( 2 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 2 FDA reports)
HAEMOGLOBIN ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HALO VISION ( 2 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 2 FDA reports)
HEART BLOCK CONGENITAL ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATIC ISCHAEMIA ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HERPES ZOSTER OTICUS ( 2 FDA reports)
HIP DEFORMITY ( 2 FDA reports)
HISTAMINE ABNORMAL ( 2 FDA reports)
HISTONE ANTIBODY POSITIVE ( 2 FDA reports)
HOUSE DUST ALLERGY ( 2 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPERDYNAMIC PRECORDIUM ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
HYPERVOLAEMIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 2 FDA reports)
HYPOMENORRHOEA ( 2 FDA reports)
HYPOPROTHROMBINAEMIA ( 2 FDA reports)
HYPOURICAEMIA ( 2 FDA reports)
ILEAL FISTULA ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
IMPLANT SITE HAEMATOMA ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCISION SITE ERYTHEMA ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INDIFFERENCE ( 2 FDA reports)
INFECTED SEBACEOUS CYST ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFERTILITY ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INFUSION SITE URTICARIA ( 2 FDA reports)
INFUSION SITE WARMTH ( 2 FDA reports)
INGROWN HAIR ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTESTINAL ULCER PERFORATION ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
ISCHAEMIC NEPHROPATHY ( 2 FDA reports)
JOINT HYPEREXTENSION ( 2 FDA reports)
JOINT IRRIGATION ( 2 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 2 FDA reports)
LACRIMAL GLAND ENLARGEMENT ( 2 FDA reports)
LACRIMATION DECREASED ( 2 FDA reports)
LAPAROTOMY ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LEARNING DISORDER ( 2 FDA reports)
LEUKAEMIC INFILTRATION ( 2 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 2 FDA reports)
LICE INFESTATION ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIPOSARCOMA ( 2 FDA reports)
LOSS OF PROPRIOCEPTION ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE II ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 2 FDA reports)
MACULAR ISCHAEMIA ( 2 FDA reports)
MALE SEXUAL DYSFUNCTION ( 2 FDA reports)
MALIGNANT ASCITES ( 2 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 2 FDA reports)
MARASMUS ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 2 FDA reports)
MENINGITIS COCCIDIOIDES ( 2 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 2 FDA reports)
MENSTRUATION DELAYED ( 2 FDA reports)
MENTAL DISABILITY ( 2 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 2 FDA reports)
METASTASES TO CHEST WALL ( 2 FDA reports)
METASTASES TO HEART ( 2 FDA reports)
METASTASES TO KIDNEY ( 2 FDA reports)
METASTASES TO NASAL SINUSES ( 2 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 2 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MOTOR NEURONE DISEASE ( 2 FDA reports)
NAIL TINEA ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NEUROFIBROMATOSIS ( 2 FDA reports)
NEUROGENIC BOWEL ( 2 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NEUTROPHIL COUNT ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NONINFECTIOUS PERITONITIS ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OESOPHAGEAL INJURY ( 2 FDA reports)
OESOPHAGEAL OEDEMA ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 2 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 2 FDA reports)
OILY SKIN ( 2 FDA reports)
OPEN ANGLE GLAUCOMA ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
OPTIC NERVE INJURY ( 2 FDA reports)
OPTIC NERVE NEOPLASM ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
ORAL MUCOSAL PETECHIAE ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 2 FDA reports)
ORGASM ABNORMAL ( 2 FDA reports)
OROPHARYNGEAL NEOPLASM BENIGN ( 2 FDA reports)
OSCILLOPSIA ( 2 FDA reports)
OVARIAN ADENOMA ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
PAIN THRESHOLD DECREASED ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATIC NECROSIS ( 2 FDA reports)
PARANOID PERSONALITY DISORDER ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 2 FDA reports)
PARENT-CHILD PROBLEM ( 2 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 2 FDA reports)
PENILE OPERATION ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PERFORATED ULCER ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PERNICIOUS ANAEMIA ( 2 FDA reports)
PERSEVERATION ( 2 FDA reports)
PHARYNGEAL CANDIDIASIS ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHLEBOSCLEROSIS ( 2 FDA reports)
PHOTODERMATOSIS ( 2 FDA reports)
PHRENIC NERVE PARALYSIS ( 2 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMOCOCCAL INFECTION ( 2 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 2 FDA reports)
POIKILOCYTOSIS ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POST POLIO SYNDROME ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
POSTPARTUM HAEMORRHAGE ( 2 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA ( 2 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 2 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 2 FDA reports)
PREMENSTRUAL SYNDROME ( 2 FDA reports)
PRESBYOESOPHAGUS ( 2 FDA reports)
PRODUCT COLOUR ISSUE ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
PROSTATIC ABSCESS ( 2 FDA reports)
PROSTATIC OPERATION ( 2 FDA reports)
PROTEUS INFECTION ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
PULMONARY HILUM MASS ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RECTAL LESION ( 2 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 2 FDA reports)
RENAL ANEURYSM ( 2 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 2 FDA reports)
RENAL CYST HAEMORRHAGE ( 2 FDA reports)
RENAL EMBOLISM ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
RETINAL ARTERY THROMBOSIS ( 2 FDA reports)
RETINAL VASCULAR OCCLUSION ( 2 FDA reports)
RETINOIC ACID SYNDROME ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 2 FDA reports)
SALIVARY GLAND RESECTION ( 2 FDA reports)
SALPINGO-OOPHORECTOMY ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SEPTOPLASTY ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SERUM FERRITIN ABNORMAL ( 2 FDA reports)
SEXUAL ASSAULT VICTIM ( 2 FDA reports)
SHIFT TO THE LEFT ( 2 FDA reports)
SHOULDER DYSTOCIA ( 2 FDA reports)
SICKLE CELL ANAEMIA ( 2 FDA reports)
SIGMOIDECTOMY ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 2 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN DISCOMFORT ( 2 FDA reports)
SKIN GRAFT INFECTION ( 2 FDA reports)
SKIN OPERATION ( 2 FDA reports)
SKULL FRACTURE ( 2 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
SLOW RESPONSE TO STIMULI ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SOFT TISSUE NEOPLASM ( 2 FDA reports)
SPINAL CORD INJURY CERVICAL ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SPLINT APPLICATION ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 2 FDA reports)
STEREOTYPY ( 2 FDA reports)
STOOLS WATERY ( 2 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SWEAT GLAND INFECTION ( 2 FDA reports)
SYMBOLIC DYSFUNCTION ( 2 FDA reports)
SYSTOLIC DYSFUNCTION ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
TABLET PHYSICAL ISSUE ( 2 FDA reports)
TACHYCARDIA FOETAL ( 2 FDA reports)
TARSAL TUNNEL SYNDROME ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
TERTIARY SYPHILIS ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 2 FDA reports)
THERAPY NAIVE ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
THYROIDITIS SUBACUTE ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
TOE OPERATION ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TORULOPSIS INFECTION ( 2 FDA reports)
TRACHEAL DISORDER ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSPLANT ( 2 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 2 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 2 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 2 FDA reports)
TRICHIASIS ( 2 FDA reports)
TRICHOSPORON INFECTION ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TUMOUR ASSOCIATED FEVER ( 2 FDA reports)
TUMOUR NECROSIS ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
ULNAR NEURITIS ( 2 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 2 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 2 FDA reports)
URETERAL SPASM ( 2 FDA reports)
URINARY TRACT PAIN ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 2 FDA reports)
UTERINE OPERATION ( 2 FDA reports)
VAGINAL DYSPLASIA ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 2 FDA reports)
VASCULAR PUNCTURE SITE SEALING ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VENOUS STENOSIS ( 2 FDA reports)
VERTEBRAL COLUMN MASS ( 2 FDA reports)
VICTIM OF SEXUAL ABUSE ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VITAL CAPACITY DECREASED ( 2 FDA reports)
VOCAL CORD POLYP ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 2 FDA reports)
WHITE CLOT SYNDROME ( 2 FDA reports)
WITHDRAWAL BLEED ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
WOUND SEPSIS ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPINA BIFIDA OCCULTA ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL CORD PARALYSIS ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STOMACH SCAN ABNORMAL ( 1 FDA reports)
STOMATOCOCCUS TEST POSITIVE ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STRESS POLYCYTHAEMIA ( 1 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 1 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SWEATING FEVER ( 1 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
TANNING ( 1 FDA reports)
TEAR DISCOLOURATION ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TERMINAL DRIBBLING ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TESTIS CANCER ( 1 FDA reports)
TETANUS IMMUNISATION ( 1 FDA reports)
TETANY ( 1 FDA reports)
THALASSAEMIA ( 1 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 1 FDA reports)
THYROID ATROPHY ( 1 FDA reports)
THYROID CANCER METASTATIC ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
THYROXINE ABNORMAL ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TONGUE PRURITUS ( 1 FDA reports)
TONSILLAR HAEMORRHAGE ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC LIVER INJURY ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TROPICAL ULCER ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR THROMBOSIS ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
ULTRAFILTRATION FAILURE ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UNEQUAL LIMB LENGTH ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URETERAL NEOPLASM ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE CANNABINOIDS INCREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO ABNORMAL ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UTERINE RUPTURE ( 1 FDA reports)
UTERINE STENOSIS ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGINAL ABSCESS ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL CELLULITIS ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL WALL CONGESTION ( 1 FDA reports)
VANISHING TWIN SYNDROME ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASOPRESSIVE THERAPY ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERBALLY ABUSED ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VICTIM OF SPOUSAL ABUSE ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVA INJURY ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
WALKING DISTANCE TEST ABNORMAL ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WHITE BLOOD CELLS STOOL ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)
YAWNING ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL WALL MASS ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACQUIRED CLAW TOE ( 1 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADENOVIRAL CONJUNCTIVITIS ( 1 FDA reports)
ADMINISTRATION SITE PAIN ( 1 FDA reports)
ADNEXA UTERI CYST ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
ALBUMIN CSF INCREASED ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 1 FDA reports)
ALLERGY TO VACCINE ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANAEMIA OF PREGNANCY ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAL SPASM ( 1 FDA reports)
ANALGESIC DRUG LEVEL ( 1 FDA reports)
ANALGESIC EFFECT ( 1 FDA reports)
ANDROGENS DECREASED ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANORECTAL INFECTION BACTERIAL ( 1 FDA reports)
ANORECTAL STENOSIS ( 1 FDA reports)
ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 1 FDA reports)
ANTI-HBS ANTIBODY ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC DISSECTION RUPTURE ( 1 FDA reports)
AORTIC ELONGATION ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
AORTIC VALVE ATRESIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE DISCHARGE ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE MASS ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
APPLICATION SITE PHOTOSENSITIVITY REACTION ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMORRHAGE ( 1 FDA reports)
ARTHROPOD INFESTATION ( 1 FDA reports)
ARTIFICIAL MENOPAUSE ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ASTHMA EXERCISE INDUCED ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AUTOMATIC BLADDER ( 1 FDA reports)
AVERSION ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BALANOPOSTHITIS ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BENIGN UTERINE NEOPLASM ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BIOPSY BRONCHUS ABNORMAL ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER NECK SUSPENSION ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLAST CELL CRISIS ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALCOHOL ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD CAFFEINE INCREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GROWTH HORMONE DECREASED ( 1 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC INCREASED ( 1 FDA reports)
BLOOD PROLACTIN ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BORDERLINE MENTAL IMPAIRMENT ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BURNING FEET SYNDROME ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
CALCIFICATION PANCREATIC DUCT ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM IONISED INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC TELEMETRY ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CAREGIVER ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ASPERGILLOSIS ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 1 FDA reports)
CEREBROSPINAL FISTULA ( 1 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 1 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVIX CARCINOMA STAGE II ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHARGE SYNDROME ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHOLANGIOGRAM ABNORMAL ( 1 FDA reports)
CHOROID MELANOMA ( 1 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 1 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLEFT LIP ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COMPLICATED FRACTURE ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 1 FDA reports)
CONGENITAL TORTICOLLIS ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
CORNEAL DEGENERATION ( 1 FDA reports)
CORNEAL NEOVASCULARISATION ( 1 FDA reports)
CORNEAL STAPHYLOMA ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF IMMUNOGLOBULIN INCREASED ( 1 FDA reports)
CSF LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
CSF NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYANOSIS NEONATAL ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH OF CHILD ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF PET ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELINQUENCY ( 1 FDA reports)
DELUSION OF REFERENCE ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DEVICE DEPLOYMENT ISSUE ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DEVICE INTERACTION ( 1 FDA reports)
DEVICE INTOLERANCE ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE PSYCHOGENIC COMPLICATION ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC ENCEPHALOPATHY ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIFFUSE AXONAL INJURY ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
DIPHTHERIA IMMUNISATION ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG REHABILITATION ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE OPERATION ( 1 FDA reports)
DYSAESTHESIA PHARYNX ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSHIDROSIS ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELBOW DEFORMITY ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
EMERGENCY CARE ( 1 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOCARDITIS VIRAL ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ABNORMAL ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENOPHTHALMOS ( 1 FDA reports)
ENTEROCLYSIS ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPENDYMOMA ( 1 FDA reports)
EPENDYMOMA MALIGNANT ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIDURAL ANAESTHESIA ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXERCISE CAPACITY DECREASED ( 1 FDA reports)
EXHIBITIONISM ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPLORATORY OPERATION ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE LUXATION ( 1 FDA reports)
EYE MUSCLE OPERATION ( 1 FDA reports)
EYE PROSTHESIS INSERTION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID VASCULAR DISORDER ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAECAL DISIMPACTION ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAMILIAL PERIODIC PARALYSIS ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEAR OF WEIGHT GAIN ( 1 FDA reports)
FEMORAL ARTERY EMBOLISM ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FEMORAL NERVE INJURY ( 1 FDA reports)
FEVER NEONATAL ( 1 FDA reports)
FIBRILLARY GLOMERULONEPHRITIS ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FIBRINOLYSIS INCREASED ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FRACTURE REDUCTION ( 1 FDA reports)
FROSTBITE ( 1 FDA reports)
FUNDOSCOPY ABNORMAL ( 1 FDA reports)
FUNGAL CYSTITIS ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
GAIT DEVIATION ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GAS GANGRENE ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC LAVAGE ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRITIS VIRAL ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GASTROSCHISIS ( 1 FDA reports)
GENITAL INFECTION BACTERIAL ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GINGIVAL CANCER ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOSSOPHARYNGEAL NEURALGIA ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
HAEMATURIA TRAUMATIC ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMODIALYSIS COMPLICATION ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGE SUBEPIDERMAL ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HALLUCINATION, OLFACTORY ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATITIS A IMMUNISATION ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEREDITARY HAEMOCHROMATOSIS ( 1 FDA reports)
HEREDITARY SPHEROCYTOSIS ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERNIAL EVENTRATION ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HIV ANTIBODY POSITIVE ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HOMANS' SIGN ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HUMAN CHORIONIC GONADOTROPIN DECREASED ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYSTEROSCOPY ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILEUS SPASTIC ( 1 FDA reports)
ILIAC ARTERY EMBOLISM ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMMUNOGLOBULIN THERAPY ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPLANT SITE DISCHARGE ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANT SITE RASH ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTION MASKED ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTION PROTOZOAL ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFERTILITY FEMALE ( 1 FDA reports)
INFESTATION ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFUSION ( 1 FDA reports)
INFUSION SITE ABSCESS ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INFUSION SITE INFLAMMATION ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE SCAR ( 1 FDA reports)
INFUSION SITE THROMBOSIS ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INJECTED LIMB MOBILITY DECREASED ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE JOINT REDNESS ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PARAESTHESIA ( 1 FDA reports)
INJECTION SITE RECALL REACTION ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INSTILLATION SITE ERYTHEMA ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN RESISTANCE SYNDROME ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERNAL FIXATION OF SPINE ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL CONGESTION ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 1 FDA reports)
INTRA-CEREBRAL ANEURYSM OPERATION ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE INSERTION ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
ISCHAEMIC LIMB PAIN ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KARNOFSKY SCALE WORSENED ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KYPHOSIS CONGENITAL ( 1 FDA reports)
LABELLED DRUG-DISEASE INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABIA ENLARGED ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LABOUR ONSET DELAYED ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE OPERATION ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGEAL MASS ( 1 FDA reports)
LARYNGEAL NEOPLASM ( 1 FDA reports)
LARYNGEAL POLYP ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGOMALACIA ( 1 FDA reports)
LDL/HDL RATIO DECREASED ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LIGAMENT LAXITY ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 1 FDA reports)
LIPOSUCTION ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MAGNESIUM DEFICIENCY ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALIGNANT NEOPLASM OF ORBIT ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MAY-THURNER SYNDROME ( 1 FDA reports)
MEAN CELL VOLUME ( 1 FDA reports)
MEAN PLATELET VOLUME ABNORMAL ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MEDIAN NERVE INJURY ( 1 FDA reports)
MEDIASTINAL FIBROSIS ( 1 FDA reports)
MEDICAL DEVICE CHANGE ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO RECTUM ( 1 FDA reports)
METASTASES TO RETROPERITONEUM ( 1 FDA reports)
METASTASES TO THORAX ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METATARSAL EXCISION ( 1 FDA reports)
MICROSPORUM INFECTION ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MILIA ( 1 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MOUTH CYST ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOCUTANEOUS FLAP OPERATION ( 1 FDA reports)
MUCOCUTANEOUS ULCERATION ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUNCHAUSEN'S SYNDROME ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELOID METAPLASIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOMECTOMY ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NASOPHARYNGEAL CANCER ( 1 FDA reports)
NEAR DROWNING ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING FASCIITIS STAPHYLOCOCCAL ( 1 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEEDLE TRACK MARKS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NEURECTOMY ( 1 FDA reports)
NEUROCYSTICERCOSIS ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NO ADVERSE DRUG REACTION ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL OPERATION ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
OPIATES ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
OROPHARYNGEAL NEOPLASM ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSTEOCHONDRITIS ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OSTEOSARCOMA METASTATIC ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
OVARIAN RUPTURE ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATECTOMY ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC LEAK ( 1 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 1 FDA reports)
PANCREATIC SPHINCTEROTOMY ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PAPILLARY SEROUS ENDOMETRIAL CARCINOMA ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PATIENT RESTRAINT ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENILE PROSTHESIS USER ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PENILE VASCULAR DISORDER ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERFUME SENSITIVITY ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PERTUSSIS IMMUNISATION ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHAGOPHOBIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARMACOPHOBIA ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGEAL NECROSIS ( 1 FDA reports)
PHARYNGEAL NEOPLASM ( 1 FDA reports)
PHARYNGEAL NEOPLASM BENIGN ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHOBIA OF DRIVING ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PICA ( 1 FDA reports)
PIGMENTATION LIP ( 1 FDA reports)
PINEAL GLAND CYST ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLANTAR ERYTHEMA ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATYBASIA ( 1 FDA reports)
PLEURAL MESOTHELIOMA ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMOPERICARDIUM ( 1 FDA reports)
POLYCHONDRITIS ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
PORENCEPHALY ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
PORTAL TRIADITIS ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST PROCEDURAL STROKE ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTINFARCTION ANGINA ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREHYPERTENSION ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT EXPIRATION DATE ISSUE ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROLONGED LABOUR ( 1 FDA reports)
PROSTATE CANCER STAGE IV ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATE TENDERNESS ( 1 FDA reports)
PROSTATIC CALCIFICATION ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSEUDOMENINGOCELE ( 1 FDA reports)
PSEUDOPAPILLOEDEMA ( 1 FDA reports)
PSEUDOPARALYSIS ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PSYCHOPATHIC PERSONALITY ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PULMONARY AMYLOIDOSIS ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY FISTULA ( 1 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 1 FDA reports)
PULMONARY PNEUMATOCELE ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELONEPHRITIS FUNGAL ( 1 FDA reports)
RADIATION MUCOSITIS ( 1 FDA reports)
RADICAL MASTECTOMY ( 1 FDA reports)
RADICAL NECK DISSECTION ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
RADICULAR SYNDROME ( 1 FDA reports)
RASH MACULOVESICULAR ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
RELAPSING FEVER ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
REMOVAL OF FOREIGN BODY FROM NOSE ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL CYST INFECTION ( 1 FDA reports)
RENAL GRAFT LOSS ( 1 FDA reports)
RENAL LYMPHOCELE ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETICULOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
RETICULOCYTOPENIA ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETROPHARYNGEAL ABSCESS ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
RIFT VALLEY FEVER ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALPINGECTOMY ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SARCOMA METASTATIC ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER DEPRESSIVE TYPE ( 1 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 1 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL CYST ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEROLOGY POSITIVE ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SEXUAL ACTIVITY INCREASED ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINUS POLYP ( 1 FDA reports)