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

INFLAMMATORY BOWEL DISEASE ( 18224 FDA reports)
COLITIS ULCERATIVE ( 12844 FDA reports)
DEPRESSION ( 11815 FDA reports)
CROHN'S DISEASE ( 10848 FDA reports)
COLITIS ( 8181 FDA reports)
ANXIETY ( 7091 FDA reports)
IRRITABLE BOWEL SYNDROME ( 6745 FDA reports)
INTESTINAL HAEMORRHAGE ( 5874 FDA reports)
GASTROINTESTINAL DISORDER ( 5276 FDA reports)
RECTAL HAEMORRHAGE ( 5220 FDA reports)
DRY SKIN ( 5168 FDA reports)
LIP DRY ( 4483 FDA reports)
ANAEMIA ( 4471 FDA reports)
ARTHRALGIA ( 4202 FDA reports)
SUICIDAL IDEATION ( 3692 FDA reports)
MULTI-ORGAN DISORDER ( 3273 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3134 FDA reports)
HEADACHE ( 3042 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2954 FDA reports)
BACK PAIN ( 2935 FDA reports)
FATIGUE ( 2824 FDA reports)
INTESTINAL OBSTRUCTION ( 2803 FDA reports)
ABDOMINAL PAIN ( 2641 FDA reports)
INSOMNIA ( 2491 FDA reports)
HAEMORRHOIDS ( 2489 FDA reports)
ACNE ( 2442 FDA reports)
WEIGHT DECREASED ( 2409 FDA reports)
EPISTAXIS ( 2244 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2220 FDA reports)
ARTHRITIS ( 2216 FDA reports)
PROCTITIS ( 2077 FDA reports)
EMOTIONAL DISTRESS ( 2031 FDA reports)
NAUSEA ( 1983 FDA reports)
INJURY ( 1872 FDA reports)
GASTROINTESTINAL INJURY ( 1651 FDA reports)
PREGNANCY ( 1590 FDA reports)
MYALGIA ( 1557 FDA reports)
GASTRITIS ( 1547 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1527 FDA reports)
VOMITING ( 1524 FDA reports)
DRY EYE ( 1502 FDA reports)
ILEITIS ( 1492 FDA reports)
ANAL FISSURE ( 1473 FDA reports)
RASH ( 1459 FDA reports)
STRESS ( 1459 FDA reports)
ANAL FISTULA ( 1406 FDA reports)
CHEILITIS ( 1386 FDA reports)
PANIC ATTACK ( 1326 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1325 FDA reports)
HEPATIC ENZYME INCREASED ( 1245 FDA reports)
CHEST PAIN ( 1241 FDA reports)
PROCTITIS ULCERATIVE ( 1112 FDA reports)
PANCREATITIS ( 1110 FDA reports)
NO ADVERSE EFFECT ( 1099 FDA reports)
DIZZINESS ( 1088 FDA reports)
DEHYDRATION ( 1059 FDA reports)
DIARRHOEA ( 1053 FDA reports)
PAIN ( 1053 FDA reports)
GASTROENTERITIS ( 1026 FDA reports)
PYREXIA ( 1010 FDA reports)
PERIRECTAL ABSCESS ( 986 FDA reports)
SUICIDE ATTEMPT ( 979 FDA reports)
HYPERTENSION ( 971 FDA reports)
HAEMATOCHEZIA ( 955 FDA reports)
PHARYNGITIS ( 932 FDA reports)
POUCHITIS ( 903 FDA reports)
SINUSITIS ( 902 FDA reports)
CHAPPED LIPS ( 898 FDA reports)
NEPHROLITHIASIS ( 893 FDA reports)
CONSTIPATION ( 879 FDA reports)
DYSPEPSIA ( 877 FDA reports)
ECZEMA ( 875 FDA reports)
NIGHT BLINDNESS ( 872 FDA reports)
NASAL DRYNESS ( 858 FDA reports)
OSTEOPENIA ( 847 FDA reports)
ALOPECIA ( 842 FDA reports)
PEPTIC ULCER ( 816 FDA reports)
FOLLICULITIS ( 801 FDA reports)
CELLULITIS ( 792 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 775 FDA reports)
COLONIC POLYP ( 754 FDA reports)
OESOPHAGITIS ( 735 FDA reports)
BRONCHITIS ( 731 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 725 FDA reports)
ROAD TRAFFIC ACCIDENT ( 712 FDA reports)
ANHEDONIA ( 686 FDA reports)
SKIN PAPILLOMA ( 678 FDA reports)
DYSPNOEA ( 650 FDA reports)
VIRAL INFECTION ( 649 FDA reports)
ILL-DEFINED DISORDER ( 648 FDA reports)
ANGER ( 646 FDA reports)
VISION BLURRED ( 643 FDA reports)
BIPOLAR DISORDER ( 641 FDA reports)
TENDONITIS ( 638 FDA reports)
MAJOR DEPRESSION ( 635 FDA reports)
MOOD SWINGS ( 635 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 611 FDA reports)
DECREASED APPETITE ( 606 FDA reports)
XEROSIS ( 597 FDA reports)
CHRONIC FATIGUE SYNDROME ( 594 FDA reports)
ABDOMINAL PAIN UPPER ( 589 FDA reports)
ERYTHEMA ( 589 FDA reports)
PAIN IN EXTREMITY ( 584 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 580 FDA reports)
ORAL HERPES ( 580 FDA reports)
OEDEMA PERIPHERAL ( 569 FDA reports)
URINARY TRACT INFECTION ( 564 FDA reports)
PSEUDOPOLYP ( 555 FDA reports)
WEIGHT INCREASED ( 555 FDA reports)
FISTULA ( 554 FDA reports)
PSYCHOTIC DISORDER ( 554 FDA reports)
EMOTIONAL DISORDER ( 552 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 551 FDA reports)
POLYP ( 551 FDA reports)
FRACTURE ( 550 FDA reports)
SOMNOLENCE ( 549 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 543 FDA reports)
ASTHENIA ( 538 FDA reports)
OCULAR HYPERAEMIA ( 537 FDA reports)
PALPITATIONS ( 533 FDA reports)
SLEEP APNOEA SYNDROME ( 526 FDA reports)
HIATUS HERNIA ( 524 FDA reports)
ILEUS ( 522 FDA reports)
RHEUMATOID ARTHRITIS ( 521 FDA reports)
PROCTOCOLITIS ( 520 FDA reports)
ASTHMA ( 519 FDA reports)
BONE DISORDER ( 519 FDA reports)
APHTHOUS STOMATITIS ( 503 FDA reports)
COUGH ( 499 FDA reports)
DERMATITIS ( 497 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 496 FDA reports)
GASTRIC ULCER ( 495 FDA reports)
CHOLANGITIS SCLEROSING ( 490 FDA reports)
PNEUMONIA ( 490 FDA reports)
MENTAL DISORDER ( 482 FDA reports)
VISUAL DISTURBANCE ( 470 FDA reports)
PROCTALGIA ( 468 FDA reports)
ANAL ABSCESS ( 467 FDA reports)
CARDIAC DISORDER ( 466 FDA reports)
OSTEOARTHRITIS ( 461 FDA reports)
CHOLELITHIASIS ( 460 FDA reports)
PLEURAL EFFUSION ( 440 FDA reports)
RENAL DISORDER ( 439 FDA reports)
NECK INJURY ( 437 FDA reports)
DIVERTICULITIS ( 434 FDA reports)
HEPATIC STEATOSIS ( 433 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 428 FDA reports)
MIGRAINE ( 420 FDA reports)
PLATELET COUNT INCREASED ( 418 FDA reports)
MOOD ALTERED ( 416 FDA reports)
HAEMORRHAGE ( 407 FDA reports)
NECK PAIN ( 406 FDA reports)
PRURITUS ( 405 FDA reports)
MELANOCYTIC NAEVUS ( 399 FDA reports)
ILEAL STENOSIS ( 396 FDA reports)
DEPRESSED MOOD ( 393 FDA reports)
SCAR ( 388 FDA reports)
DUODENITIS ( 387 FDA reports)
CONVULSION ( 385 FDA reports)
DRUG INEFFECTIVE ( 385 FDA reports)
AGGRESSION ( 382 FDA reports)
CHILLS ( 379 FDA reports)
OVARIAN CYST ( 379 FDA reports)
LIVER DISORDER ( 378 FDA reports)
MUSCULOSKELETAL DISORDER ( 378 FDA reports)
AUTOIMMUNE DISORDER ( 376 FDA reports)
APPENDICITIS ( 374 FDA reports)
ANOREXIA ( 371 FDA reports)
DEEP VEIN THROMBOSIS ( 367 FDA reports)
LYMPHADENOPATHY ( 367 FDA reports)
SYNCOPE ( 365 FDA reports)
CYST ( 363 FDA reports)
GASTRIC DISORDER ( 360 FDA reports)
MUSCLE SPASMS ( 355 FDA reports)
ARTHROPATHY ( 350 FDA reports)
CONJUNCTIVITIS ( 350 FDA reports)
VISUAL ACUITY REDUCED ( 349 FDA reports)
DRUG HYPERSENSITIVITY ( 342 FDA reports)
MITRAL VALVE INCOMPETENCE ( 341 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 340 FDA reports)
DRY MOUTH ( 340 FDA reports)
ABDOMINAL ABSCESS ( 336 FDA reports)
ABSCESS ( 336 FDA reports)
IRRITABILITY ( 335 FDA reports)
ABDOMINAL DISCOMFORT ( 334 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 333 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 331 FDA reports)
CONDITION AGGRAVATED ( 328 FDA reports)
ABORTION INDUCED ( 322 FDA reports)
CHRONIC SINUSITIS ( 321 FDA reports)
HERPES SIMPLEX ( 321 FDA reports)
MALNUTRITION ( 313 FDA reports)
CANDIDIASIS ( 312 FDA reports)
HYPERGLYCAEMIA ( 311 FDA reports)
FEAR ( 308 FDA reports)
FALL ( 306 FDA reports)
EYE PAIN ( 305 FDA reports)
INTERNAL INJURY ( 304 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 304 FDA reports)
CERVICAL DYSPLASIA ( 301 FDA reports)
DYSURIA ( 297 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 295 FDA reports)
NIGHT SWEATS ( 295 FDA reports)
LARGE INTESTINE PERFORATION ( 294 FDA reports)
DISTURBANCE IN ATTENTION ( 292 FDA reports)
CLOSTRIDIAL INFECTION ( 290 FDA reports)
HERNIA ( 290 FDA reports)
THROMBOCYTOPENIA ( 290 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 289 FDA reports)
WOUND INFECTION ( 289 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 287 FDA reports)
HEPATOMEGALY ( 286 FDA reports)
HEPATITIS ( 283 FDA reports)
HAEMOGLOBIN DECREASED ( 282 FDA reports)
FIBROMYALGIA ( 281 FDA reports)
MUSCULAR WEAKNESS ( 280 FDA reports)
PULMONARY EMBOLISM ( 280 FDA reports)
SLEEP DISORDER ( 279 FDA reports)
HYPERHIDROSIS ( 276 FDA reports)
INGUINAL HERNIA ( 275 FDA reports)
ABORTION SPONTANEOUS ( 273 FDA reports)
HYPOAESTHESIA ( 272 FDA reports)
PERITONITIS ( 270 FDA reports)
RECTAL ABSCESS ( 270 FDA reports)
AGITATION ( 268 FDA reports)
LIGAMENT RUPTURE ( 264 FDA reports)
ASCITES ( 263 FDA reports)
CHOLECYSTITIS ( 263 FDA reports)
COMPLETED SUICIDE ( 263 FDA reports)
MUSCULOSKELETAL PAIN ( 263 FDA reports)
OSTEOPOROSIS ( 261 FDA reports)
TACHYCARDIA ( 260 FDA reports)
ANAL STENOSIS ( 258 FDA reports)
DYSPHAGIA ( 258 FDA reports)
SCOLIOSIS ( 258 FDA reports)
COSTOCHONDRITIS ( 256 FDA reports)
PILONIDAL CYST ( 256 FDA reports)
GALLBLADDER DISORDER ( 255 FDA reports)
AFFECT LABILITY ( 254 FDA reports)
DRUG DEPENDENCE ( 254 FDA reports)
ENDOMETRIOSIS ( 254 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 251 FDA reports)
ADJUSTMENT DISORDER ( 250 FDA reports)
LEUKOCYTOSIS ( 250 FDA reports)
ABDOMINAL DISTENSION ( 249 FDA reports)
INFLUENZA LIKE ILLNESS ( 249 FDA reports)
MITRAL VALVE PROLAPSE ( 249 FDA reports)
TESTICULAR TORSION ( 249 FDA reports)
HAEMATOCRIT DECREASED ( 247 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 246 FDA reports)
ABNORMAL BEHAVIOUR ( 240 FDA reports)
CONTUSION ( 240 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 240 FDA reports)
DIVERTICULUM ( 239 FDA reports)
GENERALISED ANXIETY DISORDER ( 239 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 239 FDA reports)
PARAESTHESIA ( 238 FDA reports)
CHEST DISCOMFORT ( 237 FDA reports)
SUNBURN ( 237 FDA reports)
JOINT SPRAIN ( 233 FDA reports)
RENAL FAILURE ( 232 FDA reports)
FAECES DISCOLOURED ( 231 FDA reports)
STAPHYLOCOCCAL INFECTION ( 231 FDA reports)
BURSITIS ( 230 FDA reports)
TREMOR ( 230 FDA reports)
HAEMANGIOMA ( 229 FDA reports)
TOOTHACHE ( 229 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 228 FDA reports)
NORMAL NEWBORN ( 228 FDA reports)
WRIST FRACTURE ( 228 FDA reports)
TENSION HEADACHE ( 227 FDA reports)
NASOPHARYNGITIS ( 226 FDA reports)
ERYTHEMA NODOSUM ( 225 FDA reports)
GASTROENTERITIS BACTERIAL ( 224 FDA reports)
COLON ADENOMA ( 223 FDA reports)
PHOTOSENSITIVITY REACTION ( 223 FDA reports)
FLANK PAIN ( 219 FDA reports)
PLEURISY ( 219 FDA reports)
SEPSIS ( 219 FDA reports)
BACK INJURY ( 218 FDA reports)
GASTROINTESTINAL PAIN ( 218 FDA reports)
DUODENAL ULCER ( 216 FDA reports)
RECTAL POLYP ( 216 FDA reports)
ENTEROCUTANEOUS FISTULA ( 215 FDA reports)
FUNGAL INFECTION ( 215 FDA reports)
PRURITUS ANI ( 215 FDA reports)
VISUAL IMPAIRMENT ( 215 FDA reports)
HYPERSENSITIVITY ( 213 FDA reports)
AFFECTIVE DISORDER ( 212 FDA reports)
LIMB INJURY ( 212 FDA reports)
RESTLESSNESS ( 211 FDA reports)
PELVIC ABSCESS ( 210 FDA reports)
HYDRONEPHROSIS ( 208 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 205 FDA reports)
ATELECTASIS ( 204 FDA reports)
CHOLECYSTECTOMY ( 204 FDA reports)
RIB FRACTURE ( 204 FDA reports)
STOMACH DISCOMFORT ( 202 FDA reports)
BLOOD GLUCOSE INCREASED ( 201 FDA reports)
SINUS TACHYCARDIA ( 201 FDA reports)
PROTEINURIA ( 200 FDA reports)
TYPE 1 DIABETES MELLITUS ( 200 FDA reports)
COAGULOPATHY ( 198 FDA reports)
ENTERITIS ( 197 FDA reports)
MICROCYTIC ANAEMIA ( 196 FDA reports)
HYPOKALAEMIA ( 195 FDA reports)
INTESTINAL STENOSIS ( 195 FDA reports)
MUSCLE TWITCHING ( 195 FDA reports)
SINUS BRADYCARDIA ( 194 FDA reports)
GASTROENTERITIS VIRAL ( 193 FDA reports)
LIVE BIRTH ( 193 FDA reports)
OESOPHAGEAL ULCER ( 193 FDA reports)
SPLENOMEGALY ( 190 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 190 FDA reports)
COELIAC DISEASE ( 189 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 189 FDA reports)
EATING DISORDER ( 188 FDA reports)
OROPHARYNGEAL PAIN ( 188 FDA reports)
ABSCESS INTESTINAL ( 185 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 185 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 184 FDA reports)
HAEMATURIA ( 182 FDA reports)
NASAL CONGESTION ( 182 FDA reports)
GROIN PAIN ( 181 FDA reports)
OTITIS MEDIA ( 181 FDA reports)
BULIMIA NERVOSA ( 180 FDA reports)
EAR INFECTION ( 180 FDA reports)
ONYCHOMYCOSIS ( 180 FDA reports)
ANKYLOSING SPONDYLITIS ( 178 FDA reports)
MENISCUS LESION ( 178 FDA reports)
PAIN OF SKIN ( 178 FDA reports)
SACROILIITIS ( 178 FDA reports)
FLATULENCE ( 177 FDA reports)
ARTHRITIS INFECTIVE ( 176 FDA reports)
PANCYTOPENIA ( 176 FDA reports)
TREATMENT NONCOMPLIANCE ( 176 FDA reports)
INFLUENZA ( 175 FDA reports)
FLIGHT OF IDEAS ( 173 FDA reports)
DISEASE RECURRENCE ( 171 FDA reports)
CALCULUS URETERIC ( 170 FDA reports)
PANIC DISORDER ( 170 FDA reports)
ABDOMINAL PAIN LOWER ( 169 FDA reports)
MENSTRUATION IRREGULAR ( 169 FDA reports)
HYPERTENSIVE CRISIS ( 167 FDA reports)
URTICARIA ( 167 FDA reports)
BREAST HYPERPLASIA ( 166 FDA reports)
ARTHRITIS ENTEROPATHIC ( 165 FDA reports)
INGROWING NAIL ( 165 FDA reports)
CRYING ( 164 FDA reports)
INFECTION ( 164 FDA reports)
NASAL DISORDER ( 164 FDA reports)
DELUSION ( 163 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 163 FDA reports)
NERVOUS SYSTEM DISORDER ( 163 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 163 FDA reports)
BLINDNESS ( 162 FDA reports)
BONE PAIN ( 162 FDA reports)
PYODERMA GANGRENOSUM ( 161 FDA reports)
CARDIAC MURMUR ( 160 FDA reports)
CYSTITIS ( 160 FDA reports)
LACERATION ( 160 FDA reports)
ARTERIOSCLEROSIS ( 159 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 159 FDA reports)
COLONIC STENOSIS ( 159 FDA reports)
DERMATITIS CONTACT ( 159 FDA reports)
UNEVALUABLE EVENT ( 159 FDA reports)
RECTAL FISSURE ( 157 FDA reports)
JOINT INJURY ( 155 FDA reports)
RHINITIS ALLERGIC ( 155 FDA reports)
INFLAMMATION ( 154 FDA reports)
SUBCUTANEOUS ABSCESS ( 154 FDA reports)
VIRAL PHARYNGITIS ( 154 FDA reports)
ANORECTAL DISORDER ( 153 FDA reports)
AUTOIMMUNE HEPATITIS ( 153 FDA reports)
DELIRIUM ( 153 FDA reports)
ERECTILE DYSFUNCTION ( 153 FDA reports)
THROMBOSIS ( 153 FDA reports)
PSORIASIS ( 151 FDA reports)
THERAPY NON-RESPONDER ( 150 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 150 FDA reports)
MEGACOLON ( 149 FDA reports)
NAIL DISORDER ( 149 FDA reports)
MOUTH ULCERATION ( 148 FDA reports)
RAYNAUD'S PHENOMENON ( 148 FDA reports)
LETHARGY ( 147 FDA reports)
NERVE COMPRESSION ( 147 FDA reports)
AGORAPHOBIA ( 146 FDA reports)
PARANOIA ( 146 FDA reports)
EYE IRRITATION ( 145 FDA reports)
HYPOTENSION ( 145 FDA reports)
LIPOMA ( 145 FDA reports)
POLYARTHRITIS ( 145 FDA reports)
PYELONEPHRITIS ( 145 FDA reports)
TONSILLITIS ( 145 FDA reports)
COLON INJURY ( 144 FDA reports)
NO ADVERSE DRUG EFFECT ( 144 FDA reports)
NO ADVERSE EVENT ( 144 FDA reports)
RADICULOPATHY ( 144 FDA reports)
ERUCTATION ( 143 FDA reports)
HEART INJURY ( 143 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 143 FDA reports)
MENORRHAGIA ( 143 FDA reports)
HAEMANGIOMA OF LIVER ( 141 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 141 FDA reports)
OTITIS EXTERNA ( 141 FDA reports)
SKIN ULCER ( 141 FDA reports)
FEELING ABNORMAL ( 139 FDA reports)
ANAL HAEMORRHAGE ( 138 FDA reports)
ANGIOPATHY ( 138 FDA reports)
JOINT STIFFNESS ( 137 FDA reports)
RENAL FAILURE ACUTE ( 137 FDA reports)
BLOOD PRESSURE INCREASED ( 136 FDA reports)
CONFUSIONAL STATE ( 136 FDA reports)
EPIDIDYMITIS ( 136 FDA reports)
HYPOGLYCAEMIA ( 136 FDA reports)
MUSCLE STRAIN ( 136 FDA reports)
ALOPECIA EFFLUVIUM ( 133 FDA reports)
DEAFNESS ( 133 FDA reports)
PENIS DISORDER ( 133 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 132 FDA reports)
EPISCLERITIS ( 132 FDA reports)
IMPETIGO ( 132 FDA reports)
CATARACT ( 131 FDA reports)
SELF-INJURIOUS IDEATION ( 131 FDA reports)
APPENDICECTOMY ( 130 FDA reports)
IMPAIRED WORK ABILITY ( 130 FDA reports)
INTESTINAL PERFORATION ( 130 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 130 FDA reports)
SINUS CONGESTION ( 130 FDA reports)
ARRHYTHMIA ( 129 FDA reports)
HYPERLIPIDAEMIA ( 129 FDA reports)
IMPULSE-CONTROL DISORDER ( 129 FDA reports)
ADVERSE EVENT ( 128 FDA reports)
ASTEATOSIS ( 128 FDA reports)
CARDIOMEGALY ( 128 FDA reports)
COLITIS ISCHAEMIC ( 128 FDA reports)
BLOOD BILIRUBIN INCREASED ( 127 FDA reports)
HYDROCELE ( 127 FDA reports)
IMPAIRED HEALING ( 127 FDA reports)
PNEUMONITIS ( 126 FDA reports)
POLYTRAUMATISM ( 125 FDA reports)
VERTIGO ( 125 FDA reports)
EROSIVE OESOPHAGITIS ( 124 FDA reports)
OEDEMA ( 124 FDA reports)
TINNITUS ( 123 FDA reports)
DERMAL CYST ( 122 FDA reports)
NEURALGIA ( 122 FDA reports)
INTESTINAL FISTULA ( 121 FDA reports)
BLOOD ALBUMIN DECREASED ( 120 FDA reports)
EAR PAIN ( 120 FDA reports)
MASS ( 120 FDA reports)
NASAL SEPTUM DEVIATION ( 119 FDA reports)
PNEUMOTHORAX ( 119 FDA reports)
PSEUDOPOLYPOSIS ( 119 FDA reports)
RENAL CYST ( 119 FDA reports)
VIITH NERVE PARALYSIS ( 119 FDA reports)
DEPERSONALISATION ( 118 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 118 FDA reports)
ECONOMIC PROBLEM ( 118 FDA reports)
HERPES ZOSTER ( 118 FDA reports)
ILEUS PARALYTIC ( 118 FDA reports)
OESOPHAGEAL DISORDER ( 118 FDA reports)
SPINAL OSTEOARTHRITIS ( 118 FDA reports)
ANGINA PECTORIS ( 117 FDA reports)
DEFAECATION URGENCY ( 117 FDA reports)
LUNG NEOPLASM ( 117 FDA reports)
LIMB DISCOMFORT ( 116 FDA reports)
MALAISE ( 116 FDA reports)
OESOPHAGEAL STENOSIS ( 116 FDA reports)
UMBILICAL HERNIA ( 116 FDA reports)
HEPATIC CIRRHOSIS ( 115 FDA reports)
MEMORY IMPAIRMENT ( 115 FDA reports)
PARONYCHIA ( 115 FDA reports)
TONSILLECTOMY ( 115 FDA reports)
AUTOIMMUNE THYROIDITIS ( 113 FDA reports)
CERVICITIS ( 113 FDA reports)
FOOT FRACTURE ( 113 FDA reports)
JOINT SWELLING ( 112 FDA reports)
VITAMIN B12 DEFICIENCY ( 112 FDA reports)
ACCIDENTAL EXPOSURE ( 111 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 111 FDA reports)
DEATH ( 110 FDA reports)
HEPATIC FAILURE ( 110 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 110 FDA reports)
TESTICULAR PAIN ( 110 FDA reports)
HYPERAESTHESIA ( 109 FDA reports)
LOSS OF CONSCIOUSNESS ( 109 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 109 FDA reports)
STOMATITIS ( 109 FDA reports)
ULCER ( 109 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 108 FDA reports)
AMNESIA ( 108 FDA reports)
ANEURYSMAL BONE CYST ( 108 FDA reports)
HAEMATEMESIS ( 108 FDA reports)
MYOCARDIAL INFARCTION ( 108 FDA reports)
DIABETES MELLITUS ( 107 FDA reports)
HYPOTHYROIDISM ( 107 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 107 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 107 FDA reports)
VARICELLA ( 107 FDA reports)
ABDOMINAL ADHESIONS ( 106 FDA reports)
BLEPHARITIS ( 106 FDA reports)
FEELING GUILTY ( 106 FDA reports)
PROSTATITIS ( 106 FDA reports)
CORONARY ARTERY DISEASE ( 105 FDA reports)
FACIAL PALSY ( 105 FDA reports)
LIP EXFOLIATION ( 105 FDA reports)
LOCALISED INFECTION ( 105 FDA reports)
SKIN HYPERPIGMENTATION ( 105 FDA reports)
ALCOHOL USE ( 104 FDA reports)
FEELING OF DESPAIR ( 104 FDA reports)
INFERTILITY ( 104 FDA reports)
RHINORRHOEA ( 104 FDA reports)
SEBORRHOEIC DERMATITIS ( 104 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 103 FDA reports)
BURNING SENSATION ( 103 FDA reports)
LEUKOPENIA ( 103 FDA reports)
MULTIPLE SCLEROSIS ( 103 FDA reports)
MUSCLE INJURY ( 103 FDA reports)
OBESITY ( 103 FDA reports)
VASCULITIS ( 103 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 102 FDA reports)
SKIN EXFOLIATION ( 102 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 101 FDA reports)
BILIARY DYSKINESIA ( 101 FDA reports)
DRUG ABUSER ( 101 FDA reports)
MYOCARDIAL ISCHAEMIA ( 101 FDA reports)
EPIPHYSES PREMATURE FUSION ( 100 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 100 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 100 FDA reports)
PHOBIA ( 100 FDA reports)
PNEUMATOSIS INTESTINALIS ( 100 FDA reports)
SPONDYLOARTHROPATHY ( 100 FDA reports)
TINEA PEDIS ( 100 FDA reports)
COLONIC FISTULA ( 99 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 99 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 98 FDA reports)
CHOLECYSTITIS CHRONIC ( 98 FDA reports)
EYE PRURITUS ( 98 FDA reports)
HEAD INJURY ( 98 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 98 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 98 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 98 FDA reports)
DRUG EFFECT DECREASED ( 97 FDA reports)
HYPERKERATOSIS ( 97 FDA reports)
JOINT EFFUSION ( 97 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 97 FDA reports)
SKIN LACERATION ( 97 FDA reports)
HEPATIC CYST ( 96 FDA reports)
JOINT DISLOCATION ( 96 FDA reports)
PAPILLOMA VIRAL INFECTION ( 96 FDA reports)
BARRETT'S OESOPHAGUS ( 95 FDA reports)
HEPATOCELLULAR DAMAGE ( 95 FDA reports)
OSTEOMYELITIS ( 95 FDA reports)
SHOULDER PAIN ( 95 FDA reports)
VARICOCELE ( 95 FDA reports)
ANKLE FRACTURE ( 94 FDA reports)
CALCINOSIS ( 94 FDA reports)
SYNCOPE VASOVAGAL ( 94 FDA reports)
COLON CANCER ( 93 FDA reports)
PSOAS ABSCESS ( 93 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 92 FDA reports)
PELVIC PAIN ( 92 FDA reports)
RHINITIS ( 92 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 92 FDA reports)
COLITIS COLLAGENOUS ( 91 FDA reports)
OVERDOSE ( 91 FDA reports)
SWELLING ( 91 FDA reports)
ABDOMINAL HERNIA ( 90 FDA reports)
CHRONIC HEPATIC FAILURE ( 90 FDA reports)
DISCOMFORT ( 90 FDA reports)
NERVOUSNESS ( 90 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 89 FDA reports)
GASTRITIS EROSIVE ( 89 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 89 FDA reports)
INTESTINAL POLYP ( 89 FDA reports)
UVEITIS ( 89 FDA reports)
ANASTOMOTIC STENOSIS ( 88 FDA reports)
CAESAREAN SECTION ( 88 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 88 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 88 FDA reports)
MYOSITIS ( 88 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 88 FDA reports)
EYE HAEMORRHAGE ( 87 FDA reports)
RECTAL TENESMUS ( 87 FDA reports)
SKIN DISORDER ( 87 FDA reports)
ARTHROPOD BITE ( 86 FDA reports)
DYSTHYMIC DISORDER ( 86 FDA reports)
HEPATOTOXICITY ( 86 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 85 FDA reports)
RESPIRATORY TRACT CONGESTION ( 85 FDA reports)
VENTRICULAR HYPERTROPHY ( 85 FDA reports)
HALLUCINATION ( 84 FDA reports)
BREAST MASS ( 83 FDA reports)
ENTEROCOLITIS ( 83 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 83 FDA reports)
SCIATICA ( 83 FDA reports)
TOOTH DISORDER ( 83 FDA reports)
VAGINAL HAEMORRHAGE ( 83 FDA reports)
CARPAL TUNNEL SYNDROME ( 82 FDA reports)
DIVERTICULUM INTESTINAL ( 82 FDA reports)
DYSMENORRHOEA ( 81 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 81 FDA reports)
TINEA INFECTION ( 81 FDA reports)
VAGINITIS BACTERIAL ( 81 FDA reports)
FACIAL BONES FRACTURE ( 80 FDA reports)
REFRACTION DISORDER ( 80 FDA reports)
SINUS HEADACHE ( 80 FDA reports)
BASAL CELL CARCINOMA ( 79 FDA reports)
BLOOD CALCIUM DECREASED ( 79 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 79 FDA reports)
GOUT ( 79 FDA reports)
HIDRADENITIS ( 79 FDA reports)
HOT FLUSH ( 79 FDA reports)
NEUTROPHIL COUNT INCREASED ( 79 FDA reports)
ORAL CANDIDIASIS ( 79 FDA reports)
POST PROCEDURAL COMPLICATION ( 79 FDA reports)
ROTATOR CUFF SYNDROME ( 79 FDA reports)
ABNORMAL FAECES ( 78 FDA reports)
ANGIOKERATOMA ( 78 FDA reports)
CERVICOBRACHIAL SYNDROME ( 78 FDA reports)
GASTRIC HAEMORRHAGE ( 78 FDA reports)
GRANULOMA ( 78 FDA reports)
RASH PRURITIC ( 78 FDA reports)
SELF ESTEEM DECREASED ( 78 FDA reports)
EPICONDYLITIS ( 77 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 77 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 77 FDA reports)
PHARYNGEAL ULCERATION ( 77 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 77 FDA reports)
SPONDYLITIS ( 77 FDA reports)
ECCHYMOSIS ( 76 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 76 FDA reports)
IMPULSIVE BEHAVIOUR ( 76 FDA reports)
RASH PAPULAR ( 76 FDA reports)
SEASONAL ALLERGY ( 76 FDA reports)
VARICOSE VEIN ( 76 FDA reports)
BLOOD IRON DECREASED ( 75 FDA reports)
GLOMERULOSCLEROSIS ( 75 FDA reports)
HYDROCEPHALUS ( 75 FDA reports)
INTENTIONAL SELF-INJURY ( 75 FDA reports)
LABORATORY TEST ABNORMAL ( 75 FDA reports)
LACTOSE INTOLERANCE ( 75 FDA reports)
PRODUCTIVE COUGH ( 75 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 75 FDA reports)
TIBIA FRACTURE ( 75 FDA reports)
ULCERATIVE KERATITIS ( 75 FDA reports)
WINGED SCAPULA ( 75 FDA reports)
BLOOD URINE PRESENT ( 74 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 74 FDA reports)
LIBIDO DECREASED ( 74 FDA reports)
ODYNOPHAGIA ( 74 FDA reports)
PERSONALITY DISORDER ( 74 FDA reports)
PLATELET COUNT DECREASED ( 74 FDA reports)
VITAMIN D DEFICIENCY ( 74 FDA reports)
ACNE CYSTIC ( 73 FDA reports)
ANAEMIA MACROCYTIC ( 73 FDA reports)
AORTIC VALVE INCOMPETENCE ( 73 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 73 FDA reports)
ECZEMA NUMMULAR ( 73 FDA reports)
HYPOALBUMINAEMIA ( 73 FDA reports)
OSTEONECROSIS ( 73 FDA reports)
POSTPARTUM DEPRESSION ( 73 FDA reports)
SWEAT GLAND INFECTION ( 73 FDA reports)
TENDON CALCIFICATION ( 73 FDA reports)
THROAT TIGHTNESS ( 73 FDA reports)
BLOOD POTASSIUM DECREASED ( 72 FDA reports)
HAEMATOMA ( 72 FDA reports)
LARGE INTESTINAL ULCER ( 72 FDA reports)
LIGAMENT CALCIFICATION ( 72 FDA reports)
MALLORY-WEISS SYNDROME ( 72 FDA reports)
ALCOHOL ABUSE ( 71 FDA reports)
ALCOHOLISM ( 71 FDA reports)
BIPOLAR II DISORDER ( 71 FDA reports)
CARDIOMYOPATHY ( 71 FDA reports)
PAINFUL DEFAECATION ( 71 FDA reports)
PARALYSIS ( 71 FDA reports)
PHOTOPHOBIA ( 71 FDA reports)
SKIN LESION ( 71 FDA reports)
ADHESION ( 70 FDA reports)
ANGINA UNSTABLE ( 70 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 70 FDA reports)
DEAFNESS UNILATERAL ( 70 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 70 FDA reports)
ESSENTIAL HYPERTENSION ( 70 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 70 FDA reports)
INTERSTITIAL LUNG DISEASE ( 70 FDA reports)
MICTURITION URGENCY ( 70 FDA reports)
MYOPIA ( 70 FDA reports)
SINUS DISORDER ( 70 FDA reports)
TENDERNESS ( 70 FDA reports)
ENCEPHALOPATHY ( 69 FDA reports)
ILEAL PERFORATION ( 69 FDA reports)
RENAL FAILURE CHRONIC ( 69 FDA reports)
ATHEROSCLEROSIS ( 68 FDA reports)
CUSHINGOID ( 68 FDA reports)
HYPERCOAGULATION ( 68 FDA reports)
IMMUNE SYSTEM DISORDER ( 68 FDA reports)
NASAL DISCOMFORT ( 68 FDA reports)
URINARY RETENTION ( 68 FDA reports)
MUCOUS STOOLS ( 67 FDA reports)
THIRST ( 67 FDA reports)
HUNGER ( 66 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 66 FDA reports)
MULTIPLE ALLERGIES ( 66 FDA reports)
SYNOVIAL CYST ( 66 FDA reports)
VITREOUS FLOATERS ( 66 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 65 FDA reports)
ORAL PAIN ( 65 FDA reports)
POLYCYSTIC OVARIES ( 65 FDA reports)
BODY DYSMORPHIC DISORDER ( 64 FDA reports)
CEREBROVASCULAR ACCIDENT ( 64 FDA reports)
FEELING JITTERY ( 64 FDA reports)
RED BLOOD CELLS SEMEN POSITIVE ( 64 FDA reports)
SJOGREN'S SYNDROME ( 64 FDA reports)
WEIGHT FLUCTUATION ( 64 FDA reports)
EXCORIATION ( 63 FDA reports)
RADICULITIS BRACHIAL ( 63 FDA reports)
CLAVICLE FRACTURE ( 62 FDA reports)
EYE DISORDER ( 62 FDA reports)
HIRSUTISM ( 62 FDA reports)
PERICARDITIS ( 62 FDA reports)
RECTAL DISCHARGE ( 62 FDA reports)
STITCH ABSCESS ( 62 FDA reports)
THYROID DISORDER ( 62 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 62 FDA reports)
VAGINAL DISCHARGE ( 62 FDA reports)
ANAL DISCOMFORT ( 61 FDA reports)
AORTIC ANEURYSM ( 61 FDA reports)
HERPES VIRUS INFECTION ( 61 FDA reports)
INTUSSUSCEPTION ( 61 FDA reports)
LYMPHADENITIS ( 61 FDA reports)
MALABSORPTION ( 61 FDA reports)
NEUTROPENIA ( 61 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 61 FDA reports)
PERINEAL ABSCESS ( 61 FDA reports)
ACROCHORDON ( 60 FDA reports)
ADENOMA BENIGN ( 60 FDA reports)
ALOPECIA AREATA ( 60 FDA reports)
BLOOD POTASSIUM INCREASED ( 60 FDA reports)
COMA ( 60 FDA reports)
FURUNCLE ( 60 FDA reports)
PERICARDIAL EFFUSION ( 60 FDA reports)
SEROSITIS ( 60 FDA reports)
BONE DENSITY DECREASED ( 59 FDA reports)
COLITIS MICROSCOPIC ( 59 FDA reports)
CYSTITIS INTERSTITIAL ( 59 FDA reports)
DERMOID CYST ( 59 FDA reports)
GIARDIASIS ( 59 FDA reports)
HEART RATE IRREGULAR ( 59 FDA reports)
LIPIDS INCREASED ( 59 FDA reports)
MENTAL STATUS CHANGES ( 59 FDA reports)
PERNICIOUS ANAEMIA ( 59 FDA reports)
PREMENSTRUAL SYNDROME ( 59 FDA reports)
SKIN FISSURES ( 59 FDA reports)
UTERINE POLYP ( 59 FDA reports)
ACID FAST BACILLI INFECTION ( 58 FDA reports)
ARTHRITIS REACTIVE ( 58 FDA reports)
BRONCHOSPASM ( 58 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 58 FDA reports)
CONGENITAL ANOMALY ( 58 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 58 FDA reports)
HYPOGONADISM ( 58 FDA reports)
INFECTED CYST ( 58 FDA reports)
OVARIAN CYST RUPTURED ( 58 FDA reports)
PORTAL VEIN THROMBOSIS ( 58 FDA reports)
RASH PUSTULAR ( 58 FDA reports)
BLOOD GLUCOSE DECREASED ( 57 FDA reports)
DYSKINESIA OESOPHAGEAL ( 57 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 57 FDA reports)
GOITRE ( 57 FDA reports)
JUGULAR VEIN THROMBOSIS ( 57 FDA reports)
NO ADVERSE REACTION ( 57 FDA reports)
PANCREATITIS ACUTE ( 57 FDA reports)
REFLUX OESOPHAGITIS ( 57 FDA reports)
SALIVARY GLAND MASS ( 57 FDA reports)
VOLVULUS ( 57 FDA reports)
WOUND ( 57 FDA reports)
ABSCESS LIMB ( 56 FDA reports)
ECZEMA ASTEATOTIC ( 56 FDA reports)
MORBID THOUGHTS ( 56 FDA reports)
NEUROPATHY PERIPHERAL ( 56 FDA reports)
OSTEOCHONDROSIS ( 56 FDA reports)
SCHIZOPHRENIA ( 56 FDA reports)
SPINAL DISORDER ( 56 FDA reports)
ENDODONTIC PROCEDURE ( 55 FDA reports)
EYE INFLAMMATION ( 55 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 55 FDA reports)
GENERALISED OEDEMA ( 55 FDA reports)
HEPATIC CONGESTION ( 55 FDA reports)
LACRIMATION INCREASED ( 55 FDA reports)
NERVE INJURY ( 55 FDA reports)
RENAL LIPOMATOSIS ( 55 FDA reports)
RESPIRATORY TRACT INFECTION ( 55 FDA reports)
SYNOVITIS ( 55 FDA reports)
THROMBOPHLEBITIS ( 55 FDA reports)
UTERINE LEIOMYOMA ( 55 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 54 FDA reports)
BLOOD DISORDER ( 54 FDA reports)
ENTEROCOLONIC FISTULA ( 54 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 54 FDA reports)
HOMICIDAL IDEATION ( 54 FDA reports)
HORDEOLUM ( 54 FDA reports)
SCROTAL CYST ( 54 FDA reports)
ANXIETY DISORDER ( 53 FDA reports)
DYSPHONIA ( 53 FDA reports)
LUNG INFILTRATION ( 53 FDA reports)
SUBSTANCE ABUSE ( 53 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 53 FDA reports)
TRIGEMINAL NEURALGIA ( 53 FDA reports)
URETERIC OBSTRUCTION ( 53 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 52 FDA reports)
FACIAL PAIN ( 52 FDA reports)
HAND FRACTURE ( 52 FDA reports)
HELICOBACTER INFECTION ( 52 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 52 FDA reports)
NIGHTMARE ( 52 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 52 FDA reports)
POLLAKIURIA ( 52 FDA reports)
PROTEIN TOTAL DECREASED ( 52 FDA reports)
SINUS ARRHYTHMIA ( 52 FDA reports)
SNEEZING ( 52 FDA reports)
THYROID NEOPLASM ( 52 FDA reports)
ANGIOEDEMA ( 51 FDA reports)
FIBROADENOMA OF BREAST ( 51 FDA reports)
FRUSTRATION ( 51 FDA reports)
HYPOTRICHOSIS ( 51 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 51 FDA reports)
METRORRHAGIA ( 51 FDA reports)
PALLOR ( 51 FDA reports)
POSTNASAL DRIP ( 51 FDA reports)
POSTOPERATIVE INFECTION ( 51 FDA reports)
VARICES OESOPHAGEAL ( 51 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 50 FDA reports)
BUTTOCK PAIN ( 50 FDA reports)
FEELINGS OF WORTHLESSNESS ( 50 FDA reports)
GAIT DISTURBANCE ( 50 FDA reports)
GASTROINTESTINAL NEOPLASM ( 50 FDA reports)
KERATOSIS PILARIS ( 50 FDA reports)
KIDNEY INFECTION ( 50 FDA reports)
KLEBSIELLA INFECTION ( 50 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 50 FDA reports)
TENOSYNOVITIS STENOSANS ( 50 FDA reports)
AMENORRHOEA ( 49 FDA reports)
ANAL SKIN TAGS ( 49 FDA reports)
FAECAL INCONTINENCE ( 49 FDA reports)
HYPERTROPHIC ANAL PAPILLA ( 49 FDA reports)
HYPOMAGNESAEMIA ( 49 FDA reports)
ILEAL ULCER ( 49 FDA reports)
LYMPHOCYTIC INFILTRATION ( 49 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 49 FDA reports)
PANCREATITIS CHRONIC ( 49 FDA reports)
RECTAL ULCER ( 49 FDA reports)
SEMINAL VESICULITIS ( 49 FDA reports)
SOCIAL FEAR ( 49 FDA reports)
SPEECH DISORDER ( 49 FDA reports)
TESTICULAR DISORDER ( 49 FDA reports)
ABDOMINAL SEPSIS ( 48 FDA reports)
ABDOMINAL TENDERNESS ( 48 FDA reports)
BRONCHITIS CHRONIC ( 48 FDA reports)
CHEMICAL EYE INJURY ( 48 FDA reports)
CHOLANGITIS ( 48 FDA reports)
DRUG INTOLERANCE ( 48 FDA reports)
INGROWN HAIR ( 48 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 48 FDA reports)
SKIN DISCOLOURATION ( 48 FDA reports)
THINKING ABNORMAL ( 48 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 47 FDA reports)
AUTOMATISM ( 47 FDA reports)
EDUCATIONAL PROBLEM ( 47 FDA reports)
GRAND MAL CONVULSION ( 47 FDA reports)
HEPATITIS C ( 47 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 47 FDA reports)
HYPOACUSIS ( 47 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 47 FDA reports)
KETOACIDOSIS ( 47 FDA reports)
PITYRIASIS ALBA ( 47 FDA reports)
PNEUMOPERITONEUM ( 47 FDA reports)
PREMATURE LABOUR ( 47 FDA reports)
SERUM FERRITIN INCREASED ( 47 FDA reports)
VESTIBULAR NEURONITIS ( 47 FDA reports)
ARTHROSCOPY ( 46 FDA reports)
BLOOD OESTROGEN DECREASED ( 46 FDA reports)
CONTACT LENS INTOLERANCE ( 46 FDA reports)
DYSPNOEA EXERTIONAL ( 46 FDA reports)
EXTRASYSTOLES ( 46 FDA reports)
PLEURITIC PAIN ( 46 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 46 FDA reports)
PSYCHOMOTOR RETARDATION ( 46 FDA reports)
THROMBOCYTHAEMIA ( 46 FDA reports)
VAGINAL CANDIDIASIS ( 46 FDA reports)
ADENOIDECTOMY ( 45 FDA reports)
DEMYELINATION ( 45 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 45 FDA reports)
HYPOPHOSPHATAEMIA ( 45 FDA reports)
INCREASED APPETITE ( 45 FDA reports)
JAW DISORDER ( 45 FDA reports)
NEUTROPHIL COUNT DECREASED ( 45 FDA reports)
OBSESSIVE THOUGHTS ( 45 FDA reports)
SACRAL PAIN ( 45 FDA reports)
SKIN IRRITATION ( 45 FDA reports)
THALASSAEMIA TRAIT ( 45 FDA reports)
VAGINAL INFECTION ( 45 FDA reports)
BLOOD SODIUM DECREASED ( 44 FDA reports)
CARTILAGE INJURY ( 44 FDA reports)
FLUSHING ( 44 FDA reports)
INCISION SITE COMPLICATION ( 44 FDA reports)
INTENTIONAL DRUG MISUSE ( 44 FDA reports)
LOWER LIMB FRACTURE ( 44 FDA reports)
RHEUMATIC FEVER ( 44 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 44 FDA reports)
SMEAR CERVIX ABNORMAL ( 44 FDA reports)
STREPTOCOCCAL INFECTION ( 44 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 44 FDA reports)
BLOOD ALBUMIN INCREASED ( 43 FDA reports)
DUODENAL STENOSIS ( 43 FDA reports)
GASTROINTESTINAL ULCER ( 43 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 43 FDA reports)
MULTI-ORGAN FAILURE ( 43 FDA reports)
NEUROPATHY ( 43 FDA reports)
NODULE ( 43 FDA reports)
OPTIC DISC DRUSEN ( 43 FDA reports)
PAPILLOEDEMA ( 43 FDA reports)
POOR QUALITY SLEEP ( 43 FDA reports)
SEBORRHOEIC KERATOSIS ( 43 FDA reports)
WEGENER'S GRANULOMATOSIS ( 43 FDA reports)
BLOOD CALCIUM INCREASED ( 42 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 42 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 42 FDA reports)
FAMILY STRESS ( 42 FDA reports)
HEART RATE INCREASED ( 42 FDA reports)
LUPUS NEPHRITIS ( 42 FDA reports)
MENIERE'S DISEASE ( 42 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 42 FDA reports)
PREMATURE BABY ( 42 FDA reports)
ROSACEA ( 42 FDA reports)
SUICIDAL BEHAVIOUR ( 42 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 41 FDA reports)
ARTHRODESIS ( 41 FDA reports)
ENDOCARDITIS BACTERIAL ( 41 FDA reports)
ENTEROCOCCAL INFECTION ( 41 FDA reports)
EYE INFECTION ( 41 FDA reports)
FIBROADENOMA ( 41 FDA reports)
FIBROUS HISTIOCYTOMA ( 41 FDA reports)
FIBULA FRACTURE ( 41 FDA reports)
GLOMERULONEPHRITIS ( 41 FDA reports)
LARYNGITIS ( 41 FDA reports)
LOWER EXTREMITY MASS ( 41 FDA reports)
NEURODERMATITIS ( 41 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 41 FDA reports)
SINUS OPERATION ( 41 FDA reports)
SKIN STRIAE ( 41 FDA reports)
SOCIAL PROBLEM ( 41 FDA reports)
WHEEZING ( 41 FDA reports)
ABORTION THREATENED ( 40 FDA reports)
ACRODERMATITIS ( 40 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 40 FDA reports)
ACUTE PRERENAL FAILURE ( 40 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 40 FDA reports)
CARTILAGE NEOPLASM ( 40 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 40 FDA reports)
DIVERTICULAR PERFORATION ( 40 FDA reports)
FOREARM FRACTURE ( 40 FDA reports)
GALLBLADDER POLYP ( 40 FDA reports)
HALLUCINATION, AUDITORY ( 40 FDA reports)
HYPERMOBILITY SYNDROME ( 40 FDA reports)
LEFT ATRIAL DILATATION ( 40 FDA reports)
LONG QT SYNDROME ( 40 FDA reports)
MYOCLONUS ( 40 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 40 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 40 FDA reports)
UTERINE PROLAPSE ( 40 FDA reports)
UVULOPALATOPHARYNGOPLASTY ( 40 FDA reports)
ATRIAL FIBRILLATION ( 39 FDA reports)
BALANCE DISORDER ( 39 FDA reports)
CLOSTRIDIUM COLITIS ( 39 FDA reports)
EOSINOPHILIA ( 39 FDA reports)
FEELING HOT ( 39 FDA reports)
FOOD POISONING ( 39 FDA reports)
GUN SHOT WOUND ( 39 FDA reports)
HYPERTRICHOSIS ( 39 FDA reports)
HYPONATRAEMIA ( 39 FDA reports)
MALIGNANT MELANOMA ( 39 FDA reports)
OBSTRUCTION GASTRIC ( 39 FDA reports)
OSTEOCHONDROMA ( 39 FDA reports)
SNORING ( 39 FDA reports)
SPORTS INJURY ( 39 FDA reports)
SWELLING FACE ( 39 FDA reports)
TENSION ( 39 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 39 FDA reports)
EYELID PAIN ( 38 FDA reports)
GASTROENTERITIS SALMONELLA ( 38 FDA reports)
OSCILLOPSIA ( 38 FDA reports)
OSTEITIS ( 38 FDA reports)
POSTOPERATIVE ILEUS ( 38 FDA reports)
THERMAL BURN ( 38 FDA reports)
WOUND DEHISCENCE ( 38 FDA reports)
BLISTER ( 37 FDA reports)
DECREASED INTEREST ( 37 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 37 FDA reports)
HEPATIC LESION ( 37 FDA reports)
RADIUS FRACTURE ( 37 FDA reports)
RASH MACULAR ( 37 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 37 FDA reports)
RENAL TRANSPLANT ( 37 FDA reports)
STRESS AT WORK ( 37 FDA reports)
TENDON INJURY ( 37 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 37 FDA reports)
ACUTE SINUSITIS ( 36 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 36 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 36 FDA reports)
CHOLANGITIS SUPPURATIVE ( 36 FDA reports)
CYSTITIS HAEMORRHAGIC ( 36 FDA reports)
DERMATITIS EXFOLIATIVE ( 36 FDA reports)
ESCHERICHIA INFECTION ( 36 FDA reports)
HAEMOPTYSIS ( 36 FDA reports)
HAMARTOMA ( 36 FDA reports)
OESOPHAGITIS ULCERATIVE ( 36 FDA reports)
PHLEBITIS ( 36 FDA reports)
PRECANCEROUS CELLS PRESENT ( 36 FDA reports)
SKIN NODULE ( 36 FDA reports)
ANORECTAL STENOSIS ( 35 FDA reports)
BODY TEMPERATURE INCREASED ( 35 FDA reports)
CHANGE OF BOWEL HABIT ( 35 FDA reports)
DIARRHOEA INFECTIOUS ( 35 FDA reports)
DYSPAREUNIA ( 35 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 35 FDA reports)
GASTRITIS VIRAL ( 35 FDA reports)
INCONTINENCE ( 35 FDA reports)
LENTIGO ( 35 FDA reports)
LIGAMENT SPRAIN ( 35 FDA reports)
MEASLES ( 35 FDA reports)
MENOMETRORRHAGIA ( 35 FDA reports)
MUCOSAL INFLAMMATION ( 35 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 35 FDA reports)
ORAL INTAKE REDUCED ( 35 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 35 FDA reports)
ADNEXA UTERI MASS ( 34 FDA reports)
ANAL ULCER ( 34 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 34 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 34 FDA reports)
BLOOD CREATININE INCREASED ( 34 FDA reports)
BUNDLE BRANCH BLOCK ( 34 FDA reports)
EAR MALFORMATION ( 34 FDA reports)
ENTEROVESICAL FISTULA ( 34 FDA reports)
GALLBLADDER OPERATION ( 34 FDA reports)
HEPATITIS ACUTE ( 34 FDA reports)
OPPORTUNISTIC INFECTION ( 34 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 34 FDA reports)
SEXUAL DYSFUNCTION ( 34 FDA reports)
SOCIAL PHOBIA ( 34 FDA reports)
SUPRAPUBIC PAIN ( 34 FDA reports)
VAGINAL FISTULA ( 34 FDA reports)
BIPOLAR I DISORDER ( 33 FDA reports)
DEVELOPMENTAL DELAY ( 33 FDA reports)
DYSARTHRIA ( 33 FDA reports)
FIBROSIS ( 33 FDA reports)
FOOT DEFORMITY ( 33 FDA reports)
GASTROINTESTINAL NECROSIS ( 33 FDA reports)
GASTROINTESTINAL PERFORATION ( 33 FDA reports)
HAEMOGLOBIN INCREASED ( 33 FDA reports)
HAEMOLYTIC ANAEMIA ( 33 FDA reports)
HYPOVOLAEMIA ( 33 FDA reports)
INFECTED VARICOSE VEIN ( 33 FDA reports)
LEARNING DISORDER ( 33 FDA reports)
MENINGITIS VIRAL ( 33 FDA reports)
PELVIC INFECTION ( 33 FDA reports)
PERINEAL LACERATION ( 33 FDA reports)
POSTOPERATIVE ABSCESS ( 33 FDA reports)
POSTPARTUM HAEMORRHAGE ( 33 FDA reports)
PROTHROMBIN TIME PROLONGED ( 33 FDA reports)
RETROPERITONEAL ABSCESS ( 33 FDA reports)
SKIN NECROSIS ( 33 FDA reports)
TENOSYNOVITIS ( 33 FDA reports)
BLOOD UREA DECREASED ( 32 FDA reports)
BONE MARROW FAILURE ( 32 FDA reports)
CYCLOTHYMIC DISORDER ( 32 FDA reports)
DERMATITIS ATOPIC ( 32 FDA reports)
GASTRIC PERFORATION ( 32 FDA reports)
JAUNDICE ( 32 FDA reports)
PULMONARY OEDEMA ( 32 FDA reports)
SEBORRHOEA ( 32 FDA reports)
SHOCK ( 32 FDA reports)
TRICHOTILLOMANIA ( 32 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 31 FDA reports)
CULTURE STOOL POSITIVE ( 31 FDA reports)
ECTOPIC PREGNANCY ( 31 FDA reports)
HORMONE LEVEL ABNORMAL ( 31 FDA reports)
HYPOPROTEINAEMIA ( 31 FDA reports)
INTESTINAL ISCHAEMIA ( 31 FDA reports)
IRITIS ( 31 FDA reports)
LIVER INJURY ( 31 FDA reports)
MANIA ( 31 FDA reports)
PARTNER STRESS ( 31 FDA reports)
PELVIC HAEMATOMA ( 31 FDA reports)
PERSONALITY CHANGE ( 31 FDA reports)
PSYCHIATRIC SYMPTOM ( 31 FDA reports)
PULMONARY CONGESTION ( 31 FDA reports)
RESTLESS LEGS SYNDROME ( 31 FDA reports)
STILLBIRTH ( 31 FDA reports)
TOOTH ABSCESS ( 31 FDA reports)
ULNA FRACTURE ( 31 FDA reports)
VITILIGO ( 31 FDA reports)
ACUTE RESPIRATORY FAILURE ( 30 FDA reports)
AUTOIMMUNE INNER EAR DISEASE ( 30 FDA reports)
BALANITIS ( 30 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 30 FDA reports)
BRADYCARDIA ( 30 FDA reports)
CHROMATURIA ( 30 FDA reports)
COGNITIVE DISORDER ( 30 FDA reports)
CONCUSSION ( 30 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 30 FDA reports)
ELECTROLYTE IMBALANCE ( 30 FDA reports)
EXTERNAL EAR CELLULITIS ( 30 FDA reports)
GASTRIC POLYPS ( 30 FDA reports)
GROWTH RETARDATION ( 30 FDA reports)
HALO VISION ( 30 FDA reports)
HYDROURETER ( 30 FDA reports)
HYSTERECTOMY ( 30 FDA reports)
INFUSION RELATED REACTION ( 30 FDA reports)
MUSCLE DISORDER ( 30 FDA reports)
PERIANAL ABSCESS ( 30 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 30 FDA reports)
TRAUMATIC BRAIN INJURY ( 30 FDA reports)
BREAST NEOPLASM ( 29 FDA reports)
DIALYSIS ( 29 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 29 FDA reports)
EAR DISCOMFORT ( 29 FDA reports)
EYE SWELLING ( 29 FDA reports)
FACE INJURY ( 29 FDA reports)
FAILURE TO THRIVE ( 29 FDA reports)
GALLBLADDER INJURY ( 29 FDA reports)
GENITAL BURNING SENSATION ( 29 FDA reports)
HAIR TEXTURE ABNORMAL ( 29 FDA reports)
LIP BLISTER ( 29 FDA reports)
METAPLASIA ( 29 FDA reports)
OCCULT BLOOD POSITIVE ( 29 FDA reports)
PENILE DISCHARGE ( 29 FDA reports)
PORTAL HYPERTENSION ( 29 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 29 FDA reports)
PURPURA ( 29 FDA reports)
SMALL INTESTINAL PERFORATION ( 29 FDA reports)
VENTRICULAR TACHYCARDIA ( 29 FDA reports)
ACCIDENT AT WORK ( 28 FDA reports)
APPENDICITIS PERFORATED ( 28 FDA reports)
APPENDIX DISORDER ( 28 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 28 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 28 FDA reports)
DEFORMITY ( 28 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 28 FDA reports)
HYPERSOMNIA ( 28 FDA reports)
INTERNAL HERNIA ( 28 FDA reports)
MOUTH CYST ( 28 FDA reports)
OLIGOMENORRHOEA ( 28 FDA reports)
PERITONITIS BACTERIAL ( 28 FDA reports)
QUALITY OF LIFE DECREASED ( 28 FDA reports)
SPONDYLOLISTHESIS ( 28 FDA reports)
TYPE 2 DIABETES MELLITUS ( 28 FDA reports)
ALLERGY TO CHEMICALS ( 27 FDA reports)
BACTERIA STOOL IDENTIFIED ( 27 FDA reports)
CLOSED HEAD INJURY ( 27 FDA reports)
CLOSTRIDIUM TEST ( 27 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 27 FDA reports)
EROSIVE DUODENITIS ( 27 FDA reports)
EYE INJURY ( 27 FDA reports)
GESTATIONAL HYPERTENSION ( 27 FDA reports)
ILEAL FISTULA ( 27 FDA reports)
KIDNEY FIBROSIS ( 27 FDA reports)
LIP SWELLING ( 27 FDA reports)
METABOLIC SYNDROME ( 27 FDA reports)
NEUROTOXICITY ( 27 FDA reports)
UTERINE DILATION AND CURETTAGE ( 27 FDA reports)
ANDROGENETIC ALOPECIA ( 26 FDA reports)
ANOGENITAL WARTS ( 26 FDA reports)
ATRIAL SEPTAL DEFECT ( 26 FDA reports)
BREAST CANCER ( 26 FDA reports)
CARDIAC TAMPONADE ( 26 FDA reports)
CONVERSION DISORDER ( 26 FDA reports)
DIFFICULTY IN WALKING ( 26 FDA reports)
DILATATION ATRIAL ( 26 FDA reports)
EOSINOPHIL COUNT INCREASED ( 26 FDA reports)
FUNGAL SKIN INFECTION ( 26 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 26 FDA reports)
LIP PAIN ( 26 FDA reports)
NEOPLASM MALIGNANT ( 26 FDA reports)
PAPILLOMA ( 26 FDA reports)
PERITONEAL ABSCESS ( 26 FDA reports)
PULMONARY HAEMATOMA ( 26 FDA reports)
PULMONARY VASCULITIS ( 26 FDA reports)
PYLORIC STENOSIS ( 26 FDA reports)
RECTAL PROLAPSE ( 26 FDA reports)
SPOUSAL ABUSE ( 26 FDA reports)
TRANSFUSION REACTION ( 26 FDA reports)
WEIGHT GAIN POOR ( 26 FDA reports)
ACCIDENT ( 25 FDA reports)
BACTERIAL CULTURE POSITIVE ( 25 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 25 FDA reports)
BLOOD UREA INCREASED ( 25 FDA reports)
EXOSTOSIS ( 25 FDA reports)
GENITAL DISCHARGE ( 25 FDA reports)
GENITAL HERPES ( 25 FDA reports)
HELICOBACTER GASTRITIS ( 25 FDA reports)
HUMERUS FRACTURE ( 25 FDA reports)
HYPERCHOLESTEROLAEMIA ( 25 FDA reports)
LUNG INJURY ( 25 FDA reports)
MARITAL PROBLEM ( 25 FDA reports)
MIDDLE INSOMNIA ( 25 FDA reports)
OOPHORECTOMY ( 25 FDA reports)
RESPIRATORY FAILURE ( 25 FDA reports)
SKULL FRACTURE ( 25 FDA reports)
TEMPERATURE INTOLERANCE ( 25 FDA reports)
TENDON RUPTURE ( 25 FDA reports)
URINE KETONE BODY PRESENT ( 25 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 25 FDA reports)
ACOUSTIC NEUROMA ( 24 FDA reports)
BLADDER DISORDER ( 24 FDA reports)
BLEPHARITIS ALLERGIC ( 24 FDA reports)
CEREBRAL HAEMATOMA ( 24 FDA reports)
DYSPHORIA ( 24 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 24 FDA reports)
FUCHS' SYNDROME ( 24 FDA reports)
GASTROINTESTINAL INFECTION ( 24 FDA reports)
GASTROOESOPHAGITIS ( 24 FDA reports)
GESTATIONAL DIABETES ( 24 FDA reports)
HAEMOTHORAX ( 24 FDA reports)
LOSS OF EMPLOYMENT ( 24 FDA reports)
MENTAL IMPAIRMENT ( 24 FDA reports)
OLIGURIA ( 24 FDA reports)
PAROVARIAN CYST ( 24 FDA reports)
PELVIC FRACTURE ( 24 FDA reports)
PULMONARY ARTERY ATRESIA ( 24 FDA reports)
PURULENT DISCHARGE ( 24 FDA reports)
SKIN INFECTION ( 24 FDA reports)
SKIN REACTION ( 24 FDA reports)
SMALL INTESTINAL STENOSIS ( 24 FDA reports)
SPUTUM DISCOLOURED ( 24 FDA reports)
STRESS URINARY INCONTINENCE ( 24 FDA reports)
SYRINGOMYELIA ( 24 FDA reports)
TESTICULAR HAEMORRHAGE ( 24 FDA reports)
TONSILLAR HYPERTROPHY ( 24 FDA reports)
UROGENITAL PROLAPSE ( 24 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 23 FDA reports)
BLOOD MAGNESIUM DECREASED ( 23 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 23 FDA reports)
CHONDROMALACIA ( 23 FDA reports)
DRUG DOSE OMISSION ( 23 FDA reports)
DRUG INTERACTION ( 23 FDA reports)
DRUG TOXICITY ( 23 FDA reports)
DYSKINESIA ( 23 FDA reports)
FAT NECROSIS ( 23 FDA reports)
MENINGIOMA ( 23 FDA reports)
MENINGITIS ( 23 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 23 FDA reports)
MONOCYTE COUNT INCREASED ( 23 FDA reports)
ORTHOSTATIC HYPOTENSION ( 23 FDA reports)
POLYURIA ( 23 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 23 FDA reports)
RESPIRATORY DISORDER ( 23 FDA reports)
TINEA CRURIS ( 23 FDA reports)
VAGINAL MYCOSIS ( 23 FDA reports)
ABDOMINAL WALL MASS ( 22 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 22 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 22 FDA reports)
APATHY ( 22 FDA reports)
APHASIA ( 22 FDA reports)
APPETITE DISORDER ( 22 FDA reports)
CONGENITAL EYE DISORDER ( 22 FDA reports)
DIPLOPIA ( 22 FDA reports)
DUODENAL OBSTRUCTION ( 22 FDA reports)
EYELID OEDEMA ( 22 FDA reports)
FACTOR V LEIDEN MUTATION ( 22 FDA reports)
FLUID RETENTION ( 22 FDA reports)
FRACTURE NONUNION ( 22 FDA reports)
IMMUNODEFICIENCY ( 22 FDA reports)
LIVER TRANSPLANT ( 22 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 22 FDA reports)
MUCOUS MEMBRANE DISORDER ( 22 FDA reports)
MUSCLE ABSCESS ( 22 FDA reports)
OVERGROWTH BACTERIAL ( 22 FDA reports)
PAIN IN JAW ( 22 FDA reports)
PAPILLITIS ( 22 FDA reports)
PLEUROPERICARDITIS ( 22 FDA reports)
PREGNANCY TEST POSITIVE ( 22 FDA reports)
PSYCHOTIC BEHAVIOUR ( 22 FDA reports)
RETCHING ( 22 FDA reports)
SIGMOIDITIS ( 22 FDA reports)
SPLENIC CYST ( 22 FDA reports)
TELANGIECTASIA ( 22 FDA reports)
TOOTH EXTRACTION ( 22 FDA reports)
UTERINE CANCER ( 22 FDA reports)
VENOUS INSUFFICIENCY ( 22 FDA reports)
VULVAL DISORDER ( 22 FDA reports)
WOUND INFECTION FUNGAL ( 22 FDA reports)
ABORTION MISSED ( 21 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 21 FDA reports)
BACTERIAL INFECTION ( 21 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 21 FDA reports)
BRAIN CONTUSION ( 21 FDA reports)
BRONCHITIS ACUTE ( 21 FDA reports)
CALCULUS URINARY ( 21 FDA reports)
CARCINOID TUMOUR ( 21 FDA reports)
FLAT FEET ( 21 FDA reports)
GASTROINTESTINAL OEDEMA ( 21 FDA reports)
HYPERPLASIA ( 21 FDA reports)
HYPOAESTHESIA FACIAL ( 21 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 21 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 21 FDA reports)
OPTIC ATROPHY ( 21 FDA reports)
PERITONSILLAR ABSCESS ( 21 FDA reports)
PITUITARY TUMOUR BENIGN ( 21 FDA reports)
PLANTAR FASCIITIS ( 21 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 21 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 21 FDA reports)
SCAB ( 21 FDA reports)
STREPTOCOCCAL SEPSIS ( 21 FDA reports)
SUPERFICIAL INJURY OF EYE ( 21 FDA reports)
UMBILICAL CORD AROUND NECK ( 21 FDA reports)
UNINTENDED PREGNANCY ( 21 FDA reports)
URGE INCONTINENCE ( 21 FDA reports)
VENOUS THROMBOSIS ( 21 FDA reports)
WHITE BLOOD CELL DISORDER ( 21 FDA reports)
ANKYLOGLOSSIA ACQUIRED ( 20 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 20 FDA reports)
BLOOD CREATININE DECREASED ( 20 FDA reports)
BREAST PAIN ( 20 FDA reports)
BURNS SECOND DEGREE ( 20 FDA reports)
CYST RUPTURE ( 20 FDA reports)
DEREALISATION ( 20 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 20 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 20 FDA reports)
HEPATIC ENCEPHALOPATHY ( 20 FDA reports)
HYPERBILIRUBINAEMIA ( 20 FDA reports)
IRON DEFICIENCY ( 20 FDA reports)
IUCD COMPLICATION ( 20 FDA reports)
METABOLIC ENCEPHALOPATHY ( 20 FDA reports)
MULTIPLE INJURIES ( 20 FDA reports)
NEONATAL DISORDER ( 20 FDA reports)
NO THERAPEUTIC RESPONSE ( 20 FDA reports)
PANCREATIC INJURY ( 20 FDA reports)
POSTOPERATIVE ADHESION ( 20 FDA reports)
SELF ESTEEM INFLATED ( 20 FDA reports)
SKIN HAEMORRHAGE ( 20 FDA reports)
SPERM COUNT DECREASED ( 20 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 20 FDA reports)
ABNORMAL DREAMS ( 19 FDA reports)
ADENOIDAL HYPERTROPHY ( 19 FDA reports)
BREAST DISCHARGE ( 19 FDA reports)
COLECTOMY ( 19 FDA reports)
CONGENITAL HYDROCEPHALUS ( 19 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 19 FDA reports)
EJECTION FRACTION DECREASED ( 19 FDA reports)
ENCOPRESIS ( 19 FDA reports)
EPIDERMAL NAEVUS ( 19 FDA reports)
FACE OEDEMA ( 19 FDA reports)
FOOD ALLERGY ( 19 FDA reports)
FOOD INTOLERANCE ( 19 FDA reports)
HAEMATOCRIT INCREASED ( 19 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 19 FDA reports)
HYPERTHYROIDISM ( 19 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 19 FDA reports)
INCREASED TENDENCY TO BRUISE ( 19 FDA reports)
KYPHOSIS ( 19 FDA reports)
LIGAMENT DISORDER ( 19 FDA reports)
LOCALISED EXFOLIATION ( 19 FDA reports)
LYMPHOMA ( 19 FDA reports)
NEPHROPATHY ( 19 FDA reports)
PANCREATIC CARCINOMA ( 19 FDA reports)
PETIT MAL EPILEPSY ( 19 FDA reports)
SPINAL COMPRESSION FRACTURE ( 19 FDA reports)
URINE ANALYSIS ABNORMAL ( 19 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 18 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 18 FDA reports)
APPENDICEAL ABSCESS ( 18 FDA reports)
BILIARY DILATATION ( 18 FDA reports)
BONE INFARCTION ( 18 FDA reports)
BOWEL SOUNDS ABNORMAL ( 18 FDA reports)
BURNING MOUTH SYNDROME ( 18 FDA reports)
CARDIOVASCULAR DISORDER ( 18 FDA reports)
CATATONIA ( 18 FDA reports)
CERVICAL SPINE FLATTENING ( 18 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 18 FDA reports)
CHOLECYSTITIS ACUTE ( 18 FDA reports)
COLLAPSE OF LUNG ( 18 FDA reports)
COORDINATION ABNORMAL ( 18 FDA reports)
DIVERTICULAR HERNIA ( 18 FDA reports)
DIZZINESS POSTURAL ( 18 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 18 FDA reports)
ELBOW OPERATION ( 18 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 18 FDA reports)
GALACTORRHOEA ( 18 FDA reports)
GLOSSODYNIA ( 18 FDA reports)
GYNAECOMASTIA ( 18 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 18 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 18 FDA reports)
INCISION SITE INFECTION ( 18 FDA reports)
INTESTINAL ULCER ( 18 FDA reports)
LIGAMENT INJURY ( 18 FDA reports)
LIPOMA EXCISION ( 18 FDA reports)
MICROGNATHIA ( 18 FDA reports)
PELVIC ADHESIONS ( 18 FDA reports)
PERIPHERAL COLDNESS ( 18 FDA reports)
POLYCYTHAEMIA VERA ( 18 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 18 FDA reports)
PROCEDURAL PAIN ( 18 FDA reports)
PROTEIN TOTAL INCREASED ( 18 FDA reports)
PROTEIN URINE PRESENT ( 18 FDA reports)
PURULENCE ( 18 FDA reports)
SCROTAL DISORDER ( 18 FDA reports)
SMALL INTESTINE ULCER ( 18 FDA reports)
TESTIS CANCER ( 18 FDA reports)
ACQUIRED NIGHT BLINDNESS ( 17 FDA reports)
ACTINIC KERATOSIS ( 17 FDA reports)
ANION GAP INCREASED ( 17 FDA reports)
ATROPHY ( 17 FDA reports)
AUTISM ( 17 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 17 FDA reports)
BLEEDING TIME PROLONGED ( 17 FDA reports)
BREECH PRESENTATION ( 17 FDA reports)
CAT SCRATCH DISEASE ( 17 FDA reports)
CEREBRAL PALSY ( 17 FDA reports)
CHOLESTEROSIS ( 17 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 17 FDA reports)
COLONIC OBSTRUCTION ( 17 FDA reports)
COMPLICATION OF PREGNANCY ( 17 FDA reports)
CONNECTIVE TISSUE DISORDER ( 17 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 17 FDA reports)
DYSPLASIA ( 17 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 17 FDA reports)
EYELID PTOSIS ( 17 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 17 FDA reports)
HAEMATOSPERMIA ( 17 FDA reports)
HAEMORRHAGIC ANAEMIA ( 17 FDA reports)
HEPATOSPLENOMEGALY ( 17 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 17 FDA reports)
HYPOKINESIA ( 17 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 17 FDA reports)
INJECTION SITE PAIN ( 17 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 17 FDA reports)
LOBAR PNEUMONIA ( 17 FDA reports)
NAIL INFECTION ( 17 FDA reports)
NEURITIS ( 17 FDA reports)
OPTIC NEURITIS ( 17 FDA reports)
PRESYNCOPE ( 17 FDA reports)
RECTAL PERFORATION ( 17 FDA reports)
SPINAL COLUMN STENOSIS ( 17 FDA reports)
STEVENS-JOHNSON SYNDROME ( 17 FDA reports)
TOOTH INJURY ( 17 FDA reports)
VAGINAL BURNING SENSATION ( 17 FDA reports)
VENOUS THROMBOSIS LIMB ( 17 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 17 FDA reports)
ABSCESS ORAL ( 16 FDA reports)
ALOPECIA SCARRING ( 16 FDA reports)
ANORECTAL ULCER ( 16 FDA reports)
BONE METABOLISM DISORDER ( 16 FDA reports)
BREAST CYST ( 16 FDA reports)
BRONCHOPNEUMONIA ( 16 FDA reports)
CAECITIS ( 16 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 16 FDA reports)
CAROTIDYNIA ( 16 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 16 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 16 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 16 FDA reports)
CONJUNCTIVITIS VIRAL ( 16 FDA reports)
DIVORCED ( 16 FDA reports)
DYSGEUSIA ( 16 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 16 FDA reports)
ENAMEL ANOMALY ( 16 FDA reports)
EPIGASTRIC DISCOMFORT ( 16 FDA reports)
GINGIVAL HYPERPLASIA ( 16 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 16 FDA reports)
HALLUCINATION, VISUAL ( 16 FDA reports)
HAND DERMATITIS ( 16 FDA reports)
HEPATIC VEIN THROMBOSIS ( 16 FDA reports)
HIV INFECTION ( 16 FDA reports)
HYPOTONIA ( 16 FDA reports)
INFARCTION ( 16 FDA reports)
INSULIN RESISTANCE ( 16 FDA reports)
INTESTINAL MASS ( 16 FDA reports)
INTRA-UTERINE DEATH ( 16 FDA reports)
JUVENILE ARTHRITIS ( 16 FDA reports)
KIDNEY ENLARGEMENT ( 16 FDA reports)
LABYRINTHITIS ( 16 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 16 FDA reports)
LUNG DISORDER ( 16 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 16 FDA reports)
MEAN CELL VOLUME DECREASED ( 16 FDA reports)
MELAENA ( 16 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 16 FDA reports)
MICROCYTOSIS ( 16 FDA reports)
MUSCLE ATROPHY ( 16 FDA reports)
MYELOPATHY ( 16 FDA reports)
NEPHRITIS INTERSTITIAL ( 16 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 16 FDA reports)
PENIS DEVIATION ( 16 FDA reports)
PETECHIAE ( 16 FDA reports)
RETINAL DEGENERATION ( 16 FDA reports)
SCREAMING ( 16 FDA reports)
SEMINAL VESICULAR DISORDER ( 16 FDA reports)
SEXUAL ASSAULT VICTIM ( 16 FDA reports)
SQUAMOUS CELL CARCINOMA ( 16 FDA reports)
STRABISMUS ( 16 FDA reports)
SURGERY ( 16 FDA reports)
THROMBOCYTOSIS ( 16 FDA reports)
ABDOMINAL WALL ABSCESS ( 15 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 15 FDA reports)
ANAL POLYP ( 15 FDA reports)
APGAR SCORE LOW ( 15 FDA reports)
BACK DISORDER ( 15 FDA reports)
BODY TINEA ( 15 FDA reports)
CARDIAC VALVE DISEASE ( 15 FDA reports)
CATHETER RELATED COMPLICATION ( 15 FDA reports)
CERUMEN IMPACTION ( 15 FDA reports)
CHORIOAMNIONITIS ( 15 FDA reports)
CHORIORETINOPATHY ( 15 FDA reports)
CONDYLOMA ACUMINATUM ( 15 FDA reports)
CORONARY ARTERY STENOSIS ( 15 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 15 FDA reports)
EAR DISORDER ( 15 FDA reports)
FACIAL DYSMORPHISM ( 15 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 15 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 15 FDA reports)
HAEMORRHAGIC CYST ( 15 FDA reports)
HERNIA REPAIR ( 15 FDA reports)
HYPOVOLAEMIC SHOCK ( 15 FDA reports)
INFECTION PARASITIC ( 15 FDA reports)
INFECTIOUS PERITONITIS ( 15 FDA reports)
MILIA ( 15 FDA reports)
MUCOSAL DRYNESS ( 15 FDA reports)
NITRITE URINE PRESENT ( 15 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 15 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 15 FDA reports)
OTITIS MEDIA CHRONIC ( 15 FDA reports)
PALINDROMIC RHEUMATISM ( 15 FDA reports)
PERFORMANCE FEAR ( 15 FDA reports)
POST CONCUSSION SYNDROME ( 15 FDA reports)
PRE-ECLAMPSIA ( 15 FDA reports)
PROCEDURAL COMPLICATION ( 15 FDA reports)
PYOGENIC GRANULOMA ( 15 FDA reports)
RADICULITIS ( 15 FDA reports)
RASH MACULO-PAPULAR ( 15 FDA reports)
SEDATION ( 15 FDA reports)
SELF-MEDICATION ( 15 FDA reports)
SKULL MALFORMATION ( 15 FDA reports)
SLUGGISHNESS ( 15 FDA reports)
SPINAL DEFORMITY ( 15 FDA reports)
VENTRICULAR DYSFUNCTION ( 15 FDA reports)
VESICOURETERIC REFLUX ( 15 FDA reports)
WISDOM TEETH REMOVAL ( 15 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 14 FDA reports)
ARTERITIS ( 14 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 14 FDA reports)
CARBON DIOXIDE DECREASED ( 14 FDA reports)
CHRONIC TONSILLITIS ( 14 FDA reports)
CONGENITAL NOSE MALFORMATION ( 14 FDA reports)
CONTRAST MEDIA REACTION ( 14 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 14 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 14 FDA reports)
DYSHIDROSIS ( 14 FDA reports)
FAECES HARD ( 14 FDA reports)
FEEDING DISORDER ( 14 FDA reports)
GASTRODUODENITIS ( 14 FDA reports)
IMPINGEMENT SYNDROME ( 14 FDA reports)
INFANT ( 14 FDA reports)
INTENTIONAL OVERDOSE ( 14 FDA reports)
INTESTINAL ANASTOMOSIS ( 14 FDA reports)
INTESTINAL RESECTION ( 14 FDA reports)
JAUNDICE NEONATAL ( 14 FDA reports)
PERIARTHRITIS ( 14 FDA reports)
PLACENTAL DISORDER ( 14 FDA reports)
SKIN CHAPPED ( 14 FDA reports)
SLEEP TERROR ( 14 FDA reports)
THALASSAEMIA ( 14 FDA reports)
TWIN PREGNANCY ( 14 FDA reports)
URINE ODOUR ABNORMAL ( 14 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 14 FDA reports)
VERTIGO POSITIONAL ( 14 FDA reports)
ADRENAL CYST ( 13 FDA reports)
ARTERIAL RESTENOSIS ( 13 FDA reports)
BACTERAEMIA ( 13 FDA reports)
BIOPSY COLON ABNORMAL ( 13 FDA reports)
BRACHIAL PLEXUS INJURY ( 13 FDA reports)
BREAST CANCER IN SITU ( 13 FDA reports)
BRUXISM ( 13 FDA reports)
CARBON DIOXIDE INCREASED ( 13 FDA reports)
CARDIAC ARREST ( 13 FDA reports)
CARDIAC FAILURE ( 13 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 13 FDA reports)
CERVICAL SPINAL STENOSIS ( 13 FDA reports)
CHOKING ( 13 FDA reports)
CHONDROPATHY ( 13 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 13 FDA reports)
DERMATITIS ALLERGIC ( 13 FDA reports)
DRUG SCREEN POSITIVE ( 13 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 13 FDA reports)
ERYSIPELAS ( 13 FDA reports)
FALLOPIAN TUBE DISORDER ( 13 FDA reports)
FOETAL MOVEMENTS DECREASED ( 13 FDA reports)
FORCEPS DELIVERY ( 13 FDA reports)
GASTRIC STENOSIS ( 13 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 13 FDA reports)
GINGIVAL DISORDER ( 13 FDA reports)
HAEMATOMA INFECTION ( 13 FDA reports)
HEPATIC NECROSIS ( 13 FDA reports)
HERNIA OBSTRUCTIVE ( 13 FDA reports)
HYPERKALAEMIA ( 13 FDA reports)
HYPOPHAGIA ( 13 FDA reports)
INCISIONAL HERNIA ( 13 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 13 FDA reports)
LIMB CRUSHING INJURY ( 13 FDA reports)
LOSS OF LIBIDO ( 13 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 13 FDA reports)
MUCOSAL ULCERATION ( 13 FDA reports)
MUSCLE TIGHTNESS ( 13 FDA reports)
MYOCARDITIS ( 13 FDA reports)
MYOFASCITIS ( 13 FDA reports)
NASAL OEDEMA ( 13 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 13 FDA reports)
OILY SKIN ( 13 FDA reports)
POLYP COLORECTAL ( 13 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 13 FDA reports)
PYURIA ( 13 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 13 FDA reports)
SEPTIC SHOCK ( 13 FDA reports)
SHOULDER OPERATION ( 13 FDA reports)
SKIN HYPOPIGMENTATION ( 13 FDA reports)
SOFT TISSUE DISORDER ( 13 FDA reports)
SPLENIC INFARCTION ( 13 FDA reports)
STEATORRHOEA ( 13 FDA reports)
TEARFULNESS ( 13 FDA reports)
THROAT IRRITATION ( 13 FDA reports)
UROGENITAL DISORDER ( 13 FDA reports)
WOUND SECRETION ( 13 FDA reports)
ABORTION ( 12 FDA reports)
ACIDOSIS ( 12 FDA reports)
AMBLYOPIA ( 12 FDA reports)
AMOEBIC DYSENTERY ( 12 FDA reports)
ANAL PRURITUS ( 12 FDA reports)
ANDROGEN DEFICIENCY ( 12 FDA reports)
APHONIA ( 12 FDA reports)
ASPHYXIA ( 12 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 12 FDA reports)
BLEPHAROSPASM ( 12 FDA reports)
BLOOD URIC ACID DECREASED ( 12 FDA reports)
BONE GRAFT ( 12 FDA reports)
CARBUNCLE ( 12 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 12 FDA reports)
CULTURE THROAT POSITIVE ( 12 FDA reports)
CUSHING'S SYNDROME ( 12 FDA reports)
DIAPHRAGMATIC INJURY ( 12 FDA reports)
DIAPHRAGMATIC RUPTURE ( 12 FDA reports)
DISTRACTIBILITY ( 12 FDA reports)
DRUG LEVEL DECREASED ( 12 FDA reports)
EOSINOPHIL COUNT DECREASED ( 12 FDA reports)
EXTREMITY NECROSIS ( 12 FDA reports)
FACIAL PARESIS ( 12 FDA reports)
FEMUR FRACTURE ( 12 FDA reports)
FLAT AFFECT ( 12 FDA reports)
GASTRIC ULCER PERFORATION ( 12 FDA reports)
GLAUCOMA ( 12 FDA reports)
GRANULOCYTOPENIA ( 12 FDA reports)
HEARING IMPAIRED ( 12 FDA reports)
HEPATITIS B ( 12 FDA reports)
HYPERSPLENISM ( 12 FDA reports)
HYPOCOMPLEMENTAEMIA ( 12 FDA reports)
HYPOXIA ( 12 FDA reports)
INDURATION ( 12 FDA reports)
INITIAL INSOMNIA ( 12 FDA reports)
INJURY ASPHYXIATION ( 12 FDA reports)
LABORATORY TEST INTERFERENCE ( 12 FDA reports)
MALIGNANT NEOPLASM OF UTERINE ADNEXA ( 12 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 12 FDA reports)
MEDICATION ERROR ( 12 FDA reports)
MENINGOCOCCAL BACTERAEMIA ( 12 FDA reports)
MENSTRUAL DISORDER ( 12 FDA reports)
NORMAL DELIVERY ( 12 FDA reports)
OESOPHAGEAL ACHALASIA ( 12 FDA reports)
ORAL DISORDER ( 12 FDA reports)
ORGAN FAILURE ( 12 FDA reports)
PANCREATIC CYST ( 12 FDA reports)
PHARYNGEAL OEDEMA ( 12 FDA reports)
PIGMENTATION DISORDER ( 12 FDA reports)
PITYRIASIS ( 12 FDA reports)
PITYRIASIS ROSEA ( 12 FDA reports)
PLACENTA PRAEVIA ( 12 FDA reports)
PSORIATIC ARTHROPATHY ( 12 FDA reports)
PYLOROSPASM ( 12 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 12 FDA reports)
REPETITIVE STRAIN INJURY ( 12 FDA reports)
SELF MUTILATION ( 12 FDA reports)
SPINA BIFIDA OCCULTA ( 12 FDA reports)
SPLINTER ( 12 FDA reports)
TENDON DISORDER ( 12 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 12 FDA reports)
THYROID CANCER ( 12 FDA reports)
TINEA VERSICOLOUR ( 12 FDA reports)
TORTICOLLIS ( 12 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 12 FDA reports)
UMBILICAL HERNIA REPAIR ( 12 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
URINARY INCONTINENCE ( 12 FDA reports)
UTERINE DISORDER ( 12 FDA reports)
UTERINE HAEMORRHAGE ( 12 FDA reports)
VAGINAL ABSCESS ( 12 FDA reports)
VITREOUS DEGENERATION ( 12 FDA reports)
ACCIDENTAL OVERDOSE ( 11 FDA reports)
ANAEMIA MEGALOBLASTIC ( 11 FDA reports)
ANAPHYLACTIC REACTION ( 11 FDA reports)
ANGIONEUROTIC OEDEMA ( 11 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 11 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 11 FDA reports)
BILE DUCT STENOSIS ( 11 FDA reports)
BLINDNESS CORTICAL ( 11 FDA reports)
BLOOD AMYLASE INCREASED ( 11 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 11 FDA reports)
BREAST TENDERNESS ( 11 FDA reports)
BREECH DELIVERY ( 11 FDA reports)
CERVICAL POLYP ( 11 FDA reports)
CONDUCTION DISORDER ( 11 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 11 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 11 FDA reports)
DACTYLITIS ( 11 FDA reports)
DERMATITIS DIAPER ( 11 FDA reports)
DISEASE PROGRESSION ( 11 FDA reports)
DRUG ABUSE ( 11 FDA reports)
DYSMORPHISM ( 11 FDA reports)
DYSSOMNIA ( 11 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 11 FDA reports)
ENDOMETRITIS ( 11 FDA reports)
EPIPHYSEAL INJURY ( 11 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 11 FDA reports)
GRAFT VERSUS HOST DISEASE ( 11 FDA reports)
HAIR DISORDER ( 11 FDA reports)
HEART DISEASE CONGENITAL ( 11 FDA reports)
HEMIPARESIS ( 11 FDA reports)
HEPATIC FIBROSIS ( 11 FDA reports)
HODGKIN'S DISEASE ( 11 FDA reports)
HYPERTROPHIC SCAR ( 11 FDA reports)
INCISION SITE HAEMORRHAGE ( 11 FDA reports)
INCORRECT DOSE ADMINISTERED ( 11 FDA reports)
INTERTRIGO ( 11 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 11 FDA reports)
KIDNEY SMALL ( 11 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 11 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 11 FDA reports)
METHAEMOGLOBINAEMIA ( 11 FDA reports)
MILK ALLERGY ( 11 FDA reports)
MONOCYTE COUNT DECREASED ( 11 FDA reports)
MONONUCLEOSIS SYNDROME ( 11 FDA reports)
MOTOR DYSFUNCTION ( 11 FDA reports)
MOVEMENT DISORDER ( 11 FDA reports)
NECROTISING COLITIS ( 11 FDA reports)
ORCHITIS ( 11 FDA reports)
PERITONEAL INFECTION ( 11 FDA reports)
PHOTOPSIA ( 11 FDA reports)
POLYDIPSIA ( 11 FDA reports)
PRURITUS GENERALISED ( 11 FDA reports)
PULMONARY HYPERTENSION ( 11 FDA reports)
PULMONARY THROMBOSIS ( 11 FDA reports)
RADICULITIS LUMBOSACRAL ( 11 FDA reports)
RASH ERYTHEMATOUS ( 11 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 11 FDA reports)
SEMEN VOLUME DECREASED ( 11 FDA reports)
SKELETAL INJURY ( 11 FDA reports)
SMALL FOR DATES BABY ( 11 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 11 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 11 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 11 FDA reports)
URETHRITIS ( 11 FDA reports)
VAGINAL DISORDER ( 11 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 11 FDA reports)
ABASIA ( 10 FDA reports)
ANION GAP DECREASED ( 10 FDA reports)
AORTIC VALVE DISEASE ( 10 FDA reports)
AXILLARY MASS ( 10 FDA reports)
BACTEROIDES INFECTION ( 10 FDA reports)
BILE DUCT OBSTRUCTION ( 10 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 10 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 10 FDA reports)
BLINDNESS TRANSIENT ( 10 FDA reports)
BLOOD CHLORIDE DECREASED ( 10 FDA reports)
BLOOD PRESSURE ABNORMAL ( 10 FDA reports)
BLOOD PRESSURE DECREASED ( 10 FDA reports)
BONE MARROW TRANSPLANT ( 10 FDA reports)
BONE SWELLING ( 10 FDA reports)
BRONCHITIS VIRAL ( 10 FDA reports)
CIRCULATORY COLLAPSE ( 10 FDA reports)
CORNEAL ABRASION ( 10 FDA reports)
CORRECTIVE LENS USER ( 10 FDA reports)
DECREASED ACTIVITY ( 10 FDA reports)
DENTAL CARIES ( 10 FDA reports)
DERMATITIS BULLOUS ( 10 FDA reports)
DRUG ERUPTION ( 10 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 10 FDA reports)
ENCHONDROMA ( 10 FDA reports)
FACET JOINT SYNDROME ( 10 FDA reports)
FEAR OF DISEASE ( 10 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 10 FDA reports)
HAEMOGLOBINOPATHY ( 10 FDA reports)
HYPOTONIA NEONATAL ( 10 FDA reports)
IMMUNOSUPPRESSION ( 10 FDA reports)
INTERTRIGO CANDIDA ( 10 FDA reports)
KERATITIS ( 10 FDA reports)
LEGAL PROBLEM ( 10 FDA reports)
LIP HAEMORRHAGE ( 10 FDA reports)
LIP ULCERATION ( 10 FDA reports)
LOW SET EARS ( 10 FDA reports)
MICROALBUMINURIA ( 10 FDA reports)
MIGRAINE WITH AURA ( 10 FDA reports)
MYCOPLASMA INFECTION ( 10 FDA reports)
MYOCLONIC EPILEPSY ( 10 FDA reports)
NEURILEMMOMA ( 10 FDA reports)
OEDEMA MOUTH ( 10 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 10 FDA reports)
PERINEAL FISTULA ( 10 FDA reports)
PNEUMONIA HERPES VIRAL ( 10 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 10 FDA reports)
POLYSUBSTANCE ABUSE ( 10 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 10 FDA reports)
PULMONARY FIBROSIS ( 10 FDA reports)
PULMONARY MASS ( 10 FDA reports)
SERUM FERRITIN DECREASED ( 10 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 10 FDA reports)
SPINAL FRACTURE ( 10 FDA reports)
SPINE MALFORMATION ( 10 FDA reports)
SPONDYLOLYSIS ( 10 FDA reports)
STOMA SITE ABSCESS ( 10 FDA reports)
STRESS FRACTURE ( 10 FDA reports)
SYNOVIAL DISORDER ( 10 FDA reports)
TONGUE ULCERATION ( 10 FDA reports)
TOOTH IMPACTED ( 10 FDA reports)
TRANSPLANT REJECTION ( 10 FDA reports)
VASCULAR RUPTURE ( 10 FDA reports)
VENTRICULAR HYPOKINESIA ( 10 FDA reports)
WOUND ABSCESS ( 10 FDA reports)
ACNE FULMINANS ( 9 FDA reports)
ACUTE PSYCHOSIS ( 9 FDA reports)
ADENOCARCINOMA ( 9 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 9 FDA reports)
AMOEBIASIS ( 9 FDA reports)
ANAL ATRESIA ( 9 FDA reports)
ANTICHOLINERGIC SYNDROME ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 9 FDA reports)
BARTHOLIN'S ABSCESS ( 9 FDA reports)
BASEDOW'S DISEASE ( 9 FDA reports)
BILIARY COLIC ( 9 FDA reports)
BLOOD CHLORIDE INCREASED ( 9 FDA reports)
BRAIN HERNIATION ( 9 FDA reports)
BREAST INFECTION ( 9 FDA reports)
BRONCHIAL HYPERACTIVITY ( 9 FDA reports)
BUNION OPERATION ( 9 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 9 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 9 FDA reports)
DEAFNESS NEUROSENSORY ( 9 FDA reports)
DEVICE RELATED INFECTION ( 9 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 9 FDA reports)
EPIDIDYMAL CYST ( 9 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 9 FDA reports)
EYE DISCHARGE ( 9 FDA reports)
EYELID DISORDER ( 9 FDA reports)
EYELID PTOSIS CONGENITAL ( 9 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 9 FDA reports)
GALLBLADDER NECROSIS ( 9 FDA reports)
GASTRIC VARICES ( 9 FDA reports)
GINGIVAL PAIN ( 9 FDA reports)
HAEMOPHILUS INFECTION ( 9 FDA reports)
HAIR GROWTH ABNORMAL ( 9 FDA reports)
HEPATIC ENZYME ABNORMAL ( 9 FDA reports)
HYPERAEMIA ( 9 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 9 FDA reports)
INTESTINAL MALROTATION ( 9 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 9 FDA reports)
JOINT INSTABILITY ( 9 FDA reports)
KELOID SCAR ( 9 FDA reports)
LOCAL SWELLING ( 9 FDA reports)
LUNG CONSOLIDATION ( 9 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 9 FDA reports)
MALE PATTERN BALDNESS ( 9 FDA reports)
MERALGIA PARAESTHETICA ( 9 FDA reports)
MONONEUROPATHY ( 9 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 9 FDA reports)
MYDRIASIS ( 9 FDA reports)
NECROSIS ( 9 FDA reports)
NERVE ROOT INJURY ( 9 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 9 FDA reports)
OEDEMA MUCOSAL ( 9 FDA reports)
OESOPHAGEAL PAIN ( 9 FDA reports)
ONYCHOCLASIS ( 9 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 9 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 9 FDA reports)
POST HERPETIC NEURALGIA ( 9 FDA reports)
POST PROCEDURAL DIARRHOEA ( 9 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 9 FDA reports)
PSEUDOMONAS INFECTION ( 9 FDA reports)
PULMONARY INFARCTION ( 9 FDA reports)
SCOTOMA ( 9 FDA reports)
SENSORY DISTURBANCE ( 9 FDA reports)
SEPSIS SYNDROME ( 9 FDA reports)
SKIN BURNING SENSATION ( 9 FDA reports)
SKIN TEST POSITIVE ( 9 FDA reports)
STRESS SYMPTOMS ( 9 FDA reports)
TRANSAMINASES INCREASED ( 9 FDA reports)
UPPER LIMB FRACTURE ( 9 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 9 FDA reports)
VAGINAL POLYP ( 9 FDA reports)
VAGINITIS GARDNERELLA ( 9 FDA reports)
VASCULITIS CEREBRAL ( 9 FDA reports)
VASECTOMY ( 9 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 9 FDA reports)
VULVOVAGINAL DRYNESS ( 9 FDA reports)
ABORTION INCOMPLETE ( 8 FDA reports)
ADENOMYOSIS ( 8 FDA reports)
ANAL CHLAMYDIA INFECTION ( 8 FDA reports)
ANISOCYTOSIS ( 8 FDA reports)
ARTHROPOD STING ( 8 FDA reports)
ASTIGMATISM ( 8 FDA reports)
BACTERIA URINE ( 8 FDA reports)
BEZOAR ( 8 FDA reports)
BLIGHTED OVUM ( 8 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 8 FDA reports)
BONE MARROW DISORDER ( 8 FDA reports)
BREAST ABSCESS ( 8 FDA reports)
BREAST LUMP REMOVAL ( 8 FDA reports)
BREAST PROSTHESIS REMOVAL ( 8 FDA reports)
BUNION ( 8 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 8 FDA reports)
CD4/CD8 RATIO DECREASED ( 8 FDA reports)
CEREBRAL ISCHAEMIA ( 8 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 8 FDA reports)
CULTURE URINE POSITIVE ( 8 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 8 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 8 FDA reports)
DERMATOMYOSITIS ( 8 FDA reports)
DIABETIC ULCER ( 8 FDA reports)
DRY THROAT ( 8 FDA reports)
EARLY SATIETY ( 8 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 8 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 8 FDA reports)
EYE MOVEMENT DISORDER ( 8 FDA reports)
FAECAL FAT INCREASED ( 8 FDA reports)
FAT TISSUE INCREASED ( 8 FDA reports)
FOETAL DISORDER ( 8 FDA reports)
FOREIGN BODY IN EYE ( 8 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 8 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 8 FDA reports)
GENITAL PRURITUS FEMALE ( 8 FDA reports)
GROIN ABSCESS ( 8 FDA reports)
HEAD DEFORMITY ( 8 FDA reports)
HEPATIC INFARCTION ( 8 FDA reports)
HORSESHOE KIDNEY ( 8 FDA reports)
HYPERPARATHYROIDISM ( 8 FDA reports)
HYPERREFLEXIA ( 8 FDA reports)
HYPOCALCAEMIA ( 8 FDA reports)
HYPOVENTILATION ( 8 FDA reports)
HYPOVITAMINOSIS ( 8 FDA reports)
IIIRD NERVE DISORDER ( 8 FDA reports)
INTESTINAL SPASM ( 8 FDA reports)
JUDGEMENT IMPAIRED ( 8 FDA reports)
JUVENILE CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 8 FDA reports)
KNEE OPERATION ( 8 FDA reports)
LEGIONELLA INFECTION ( 8 FDA reports)
LIGAMENT OPERATION ( 8 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
LUNG INFECTION ( 8 FDA reports)
MALIGNANT NEOPLASM OF CORNEA ( 8 FDA reports)
METASTASES TO LYMPH NODES ( 8 FDA reports)
MOLE EXCISION ( 8 FDA reports)
ONYCHOGRYPHOSIS ( 8 FDA reports)
ORAL SOFT TISSUE DISORDER ( 8 FDA reports)
PARAKERATOSIS ( 8 FDA reports)
PERIUMBILICAL ABSCESS ( 8 FDA reports)
PHIMOSIS ( 8 FDA reports)
PIGMENTED NAEVUS ( 8 FDA reports)
PNEUMONIA ASPIRATION ( 8 FDA reports)
POST-TRAUMATIC PAIN ( 8 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 8 FDA reports)
PREGNANCY OF PARTNER ( 8 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 8 FDA reports)
PRODUCT QUALITY ISSUE ( 8 FDA reports)
PTERYGIUM COLLI ( 8 FDA reports)
RASH SCALY ( 8 FDA reports)
RATHKE'S CLEFT CYST ( 8 FDA reports)
RENAL HYPERTROPHY ( 8 FDA reports)
RETINAL DETACHMENT ( 8 FDA reports)
RIB DEFORMITY ( 8 FDA reports)
SALMONELLOSIS ( 8 FDA reports)
SKIN ATROPHY ( 8 FDA reports)
SKIN CANCER ( 8 FDA reports)
SKIN DEPIGMENTATION ( 8 FDA reports)
SMOKER ( 8 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 8 FDA reports)
TALIPES ( 8 FDA reports)
THEFT ( 8 FDA reports)
THREATENED LABOUR ( 8 FDA reports)
ULNAR NERVE PALSY ( 8 FDA reports)
UPPER EXTREMITY MASS ( 8 FDA reports)
URETHRAL DISORDER ( 8 FDA reports)
URINE OUTPUT DECREASED ( 8 FDA reports)
VASCULAR HEADACHE ( 8 FDA reports)
VESTIBULAR DISORDER ( 8 FDA reports)
VULVAL ABSCESS ( 8 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 8 FDA reports)
ABDOMINAL INJURY ( 7 FDA reports)
ACUTE TONSILLITIS ( 7 FDA reports)
ADNEXA UTERI PAIN ( 7 FDA reports)
ALLERGIC COLITIS ( 7 FDA reports)
ANIMAL BITE ( 7 FDA reports)
ANOSMIA ( 7 FDA reports)
ANOVULATORY CYCLE ( 7 FDA reports)
AREFLEXIA ( 7 FDA reports)
BACTERIURIA ( 7 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 7 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 7 FDA reports)
BRACHIAL PLEXOPATHY ( 7 FDA reports)
BRAIN OEDEMA ( 7 FDA reports)
CALCIUM DEFICIENCY ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
CEREBROVASCULAR DISORDER ( 7 FDA reports)
CHEST WALL ABSCESS ( 7 FDA reports)
CITROBACTER INFECTION ( 7 FDA reports)
CONGENITAL CEREBELLAR AGENESIS ( 7 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 7 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 7 FDA reports)
DISABILITY ( 7 FDA reports)
DISORIENTATION ( 7 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 7 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 7 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 7 FDA reports)
EAR DEFORMITY ACQUIRED ( 7 FDA reports)
ENCEPHALOMALACIA ( 7 FDA reports)
ENTERITIS INFECTIOUS ( 7 FDA reports)
EXFOLIATIVE RASH ( 7 FDA reports)
FLUID OVERLOAD ( 7 FDA reports)
FOETAL HEART RATE DECELERATION ( 7 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 7 FDA reports)
GILBERT'S SYNDROME ( 7 FDA reports)
HEART RATE DECREASED ( 7 FDA reports)
HIGH RISK PREGNANCY ( 7 FDA reports)
HOMICIDE ( 7 FDA reports)
HYPERMETROPIA ( 7 FDA reports)
HYPERVENTILATION ( 7 FDA reports)
ILEOSTOMY ( 7 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 7 FDA reports)
INCOHERENT ( 7 FDA reports)
INTENTIONAL MISUSE ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 7 FDA reports)
LARGE INTESTINAL STRICTURE ( 7 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 7 FDA reports)
LUPUS-LIKE SYNDROME ( 7 FDA reports)
MARFAN'S SYNDROME ( 7 FDA reports)
MENINGOMYELOCELE ( 7 FDA reports)
MENOPAUSE ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
METAL POISONING ( 7 FDA reports)
NAIL TINEA ( 7 FDA reports)
OPTIC NERVE DISORDER ( 7 FDA reports)
PCO2 DECREASED ( 7 FDA reports)
PELVIC SEPSIS ( 7 FDA reports)
PERIORBITAL HAEMATOMA ( 7 FDA reports)
PITTING OEDEMA ( 7 FDA reports)
POISONING ( 7 FDA reports)
POLYHYDRAMNIOS ( 7 FDA reports)
POST PROCEDURAL NAUSEA ( 7 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 7 FDA reports)
PSEUDOMENINGOCELE ( 7 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 7 FDA reports)
PYELONEPHRITIS ACUTE ( 7 FDA reports)
RENAL CANCER ( 7 FDA reports)
RENAL COLIC ( 7 FDA reports)
RESPIRATORY DISTRESS ( 7 FDA reports)
RETINOPATHY ( 7 FDA reports)
SALPINGITIS ( 7 FDA reports)
SENSATION OF PRESSURE ( 7 FDA reports)
SHORT-BOWEL SYNDROME ( 7 FDA reports)
SPLEEN DISORDER ( 7 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 7 FDA reports)
STARGARDT'S DISEASE ( 7 FDA reports)
STRABISMUS CONGENITAL ( 7 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 7 FDA reports)
TRACHEOBRONCHITIS ( 7 FDA reports)
TROPONIN INCREASED ( 7 FDA reports)
UMBILICAL CORD ABNORMALITY ( 7 FDA reports)
URINARY SEDIMENT PRESENT ( 7 FDA reports)
UTERINE TENDERNESS ( 7 FDA reports)
VAGINAL PAIN ( 7 FDA reports)
VAGINAL ULCERATION ( 7 FDA reports)
VAGUS NERVE DISORDER ( 7 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 7 FDA reports)
VOCAL CORD CYST ( 7 FDA reports)
VOLVULUS OF SMALL BOWEL ( 7 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 7 FDA reports)
YERSINIA INFECTION ( 7 FDA reports)
ACROCHORDON EXCISION ( 6 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
ADRENAL HAEMORRHAGE ( 6 FDA reports)
AGEUSIA ( 6 FDA reports)
AGNOSIA ( 6 FDA reports)
AKATHISIA ( 6 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 6 FDA reports)
ANASTOMOTIC COMPLICATION ( 6 FDA reports)
ANASTOMOTIC ULCER ( 6 FDA reports)
ANENCEPHALY ( 6 FDA reports)
ANOTIA ( 6 FDA reports)
ARTERIAL DISORDER ( 6 FDA reports)
ASTHMA EXERCISE INDUCED ( 6 FDA reports)
BACTERIA URINE IDENTIFIED ( 6 FDA reports)
BEHCET'S SYNDROME ( 6 FDA reports)
BILE DUCT STONE ( 6 FDA reports)
BLADDER OBSTRUCTION ( 6 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 6 FDA reports)
BODY HEIGHT DECREASED ( 6 FDA reports)
BRADYCARDIA FOETAL ( 6 FDA reports)
BRAIN NEOPLASM ( 6 FDA reports)
BREAST DISCOMFORT ( 6 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 6 FDA reports)
CATHETER SITE INFECTION ( 6 FDA reports)
CEREBRAL DISORDER ( 6 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 6 FDA reports)
CHEILOSIS ( 6 FDA reports)
CHEST WALL PAIN ( 6 FDA reports)
CHEST X-RAY ABNORMAL ( 6 FDA reports)
CLEFT PALATE ( 6 FDA reports)
COITAL BLEEDING ( 6 FDA reports)
COLD SWEAT ( 6 FDA reports)
COLON NEOPLASM ( 6 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 6 FDA reports)
CONGENITAL JAW MALFORMATION ( 6 FDA reports)
CONGENITAL MUSCLE ABSENCE ( 6 FDA reports)
CRANIAL NERVE DISORDER ( 6 FDA reports)
CRYPTORCHISM ( 6 FDA reports)
CULTURE POSITIVE ( 6 FDA reports)
CYSTOCELE ( 6 FDA reports)
DACRYOADENITIS ACQUIRED ( 6 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 6 FDA reports)
DIABETIC FOOT ( 6 FDA reports)
DISINHIBITION ( 6 FDA reports)
DUPUYTREN'S CONTRACTURE ( 6 FDA reports)
EAR CANAL INJURY ( 6 FDA reports)
EMPHYSEMA ( 6 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 6 FDA reports)
ENTEROBACTER INFECTION ( 6 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 6 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 6 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 6 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 6 FDA reports)
FOETAL GROWTH RETARDATION ( 6 FDA reports)
FULL BLOOD COUNT DECREASED ( 6 FDA reports)
GANGLION ( 6 FDA reports)
GASTROINTESTINAL MUCOSITIS ( 6 FDA reports)
GIANT PAPILLARY CONJUNCTIVITIS ( 6 FDA reports)
GINGIVAL BLEEDING ( 6 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 6 FDA reports)
GRANULOCYTE COUNT INCREASED ( 6 FDA reports)
HEAD DISCOMFORT ( 6 FDA reports)
HEMIHYPERTROPHY ( 6 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 6 FDA reports)
HISTOPLASMOSIS ( 6 FDA reports)
HYPERTELORISM OF ORBIT ( 6 FDA reports)
HYPERTONIC BLADDER ( 6 FDA reports)
HYPOMANIA ( 6 FDA reports)
HYPOMENORRHOEA ( 6 FDA reports)
INADEQUATE ANALGESIA ( 6 FDA reports)
INGUINAL HERNIA REPAIR ( 6 FDA reports)
INTELLIGENCE TEST ABNORMAL ( 6 FDA reports)
INTESTINAL DILATATION ( 6 FDA reports)
ISCHAEMIC HEPATITIS ( 6 FDA reports)
KIDNEY MALFORMATION ( 6 FDA reports)
LACTATION DISORDER ( 6 FDA reports)
LEIOMYOMA ( 6 FDA reports)
LEUKOPLAKIA ( 6 FDA reports)
LIMB MALFORMATION ( 6 FDA reports)
LIPASE INCREASED ( 6 FDA reports)
LOCHIA MALODOUROUS ( 6 FDA reports)
LUMBAR RADICULOPATHY ( 6 FDA reports)
LUNG HYPERINFLATION ( 6 FDA reports)
LUNG TRANSPLANT REJECTION ( 6 FDA reports)
LUPUS VASCULITIS ( 6 FDA reports)
MEDICATION RESIDUE ( 6 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 6 FDA reports)
METABOLIC DISORDER ( 6 FDA reports)
MICROCEPHALY ( 6 FDA reports)
MICROTIA ( 6 FDA reports)
MOTION SICKNESS ( 6 FDA reports)
MUSCLE FATIGUE ( 6 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 6 FDA reports)
NASAL POLYPS ( 6 FDA reports)
NEGATIVE THOUGHTS ( 6 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
NEOPLASM ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
OSTEOMA ( 6 FDA reports)
OTORRHOEA ( 6 FDA reports)
OVARIAN CANCER ( 6 FDA reports)
OVERWEIGHT ( 6 FDA reports)
PARANASAL SINUS DISCOMFORT ( 6 FDA reports)
PARVOVIRUS INFECTION ( 6 FDA reports)
PCO2 INCREASED ( 6 FDA reports)
PECTUS EXCAVATUM ( 6 FDA reports)
PERITONEAL DIALYSIS ( 6 FDA reports)
PHLEBOLITH ( 6 FDA reports)
PICKWICKIAN SYNDROME ( 6 FDA reports)
PLACENTAL NECROSIS ( 6 FDA reports)
PLATELET DISORDER ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
POLYMENORRHOEA ( 6 FDA reports)
POST PROCEDURAL VOMITING ( 6 FDA reports)
PROCEDURAL SITE REACTION ( 6 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 6 FDA reports)
RENAL ABSCESS ( 6 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 6 FDA reports)
SENSORY LOSS ( 6 FDA reports)
SEROMA ( 6 FDA reports)
SPINA BIFIDA ( 6 FDA reports)
SPINAL COLUMN INJURY ( 6 FDA reports)
SPINAL X-RAY ABNORMAL ( 6 FDA reports)
STENT PLACEMENT ( 6 FDA reports)
SYSTOLIC HYPERTENSION ( 6 FDA reports)
TARDIVE DYSKINESIA ( 6 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
TOBACCO ABUSE ( 6 FDA reports)
TONGUE DISCOLOURATION ( 6 FDA reports)
TONSILLAR DISORDER ( 6 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 6 FDA reports)
TRICHOMONIASIS ( 6 FDA reports)
TRISOMY 13 ( 6 FDA reports)
URINARY HESITATION ( 6 FDA reports)
VESTIBULITIS ( 6 FDA reports)
VICTIM OF SPOUSAL ABUSE ( 6 FDA reports)
VIRAEMIA ( 6 FDA reports)
VISUAL FIELD DEFECT ( 6 FDA reports)
VITAMIN B12 DECREASED ( 6 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 6 FDA reports)
ABDOMINAL MASS ( 5 FDA reports)
ADNEXA UTERI CYST ( 5 FDA reports)
ADVERSE DRUG REACTION ( 5 FDA reports)
ALCOHOL POISONING ( 5 FDA reports)
ALVEOLITIS ALLERGIC ( 5 FDA reports)
ANAL INFECTION ( 5 FDA reports)
ANOMALY OF MIDDLE EAR CONGENITAL ( 5 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 5 FDA reports)
AORTIC BRUIT ( 5 FDA reports)
APPLICATION SITE MASS ( 5 FDA reports)
ARTERY DISSECTION ( 5 FDA reports)
BACILLUS INFECTION ( 5 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 5 FDA reports)
BLOOD CULTURE POSITIVE ( 5 FDA reports)
BLOOD ETHANOL INCREASED ( 5 FDA reports)
BLOOD OSMOLARITY DECREASED ( 5 FDA reports)
BLOOD SODIUM INCREASED ( 5 FDA reports)
BONE CYST ( 5 FDA reports)
BRAIN DAMAGE ( 5 FDA reports)
BREAST FIBROSIS ( 5 FDA reports)
CARDIAC ENZYMES INCREASED ( 5 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 5 FDA reports)
CATHETERISATION CARDIAC ( 5 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CEREBRAL THROMBOSIS ( 5 FDA reports)
CERVICAL CYST ( 5 FDA reports)
CHOLESTEATOMA ( 5 FDA reports)
CHONDRITIS ( 5 FDA reports)
CLUSTER HEADACHE ( 5 FDA reports)
COLONOSCOPY ABNORMAL ( 5 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 5 FDA reports)
CONGENITAL SCOLIOSIS ( 5 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 5 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 5 FDA reports)
CORONARY ARTERY DILATATION ( 5 FDA reports)
CREATININE URINE INCREASED ( 5 FDA reports)
CULTURE WOUND POSITIVE ( 5 FDA reports)
CUTANEOUS VASCULITIS ( 5 FDA reports)
DANDRUFF ( 5 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 5 FDA reports)
DIABETIC KETOACIDOSIS ( 5 FDA reports)
DROWNING ( 5 FDA reports)
DYSPHEMIA ( 5 FDA reports)
EAR CONGESTION ( 5 FDA reports)
EAR OPERATION ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
ENDOMETRIAL DISORDER ( 5 FDA reports)
ENTHESOPATHY ( 5 FDA reports)
EPILEPSY ( 5 FDA reports)
EYE REDNESS ( 5 FDA reports)
FASCIA RELEASE ( 5 FDA reports)
FEAR OF WEIGHT GAIN ( 5 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 5 FDA reports)
GASTROENTERITIS ADENOVIRUS ( 5 FDA reports)
GASTROINTESTINAL FISTULA ( 5 FDA reports)
GAZE PALSY ( 5 FDA reports)
GINGIVAL RECESSION ( 5 FDA reports)
GLUCOSE URINE PRESENT ( 5 FDA reports)
HEMIVERTEBRA ( 5 FDA reports)
HERPANGINA ( 5 FDA reports)
HOSPITALISATION ( 5 FDA reports)
HOSTILITY ( 5 FDA reports)
HYPERACUSIS ( 5 FDA reports)
HYPOCHROMASIA ( 5 FDA reports)
HYPOCHROMIC ANAEMIA ( 5 FDA reports)
HYPOTHERMIA ( 5 FDA reports)
IGA NEPHROPATHY ( 5 FDA reports)
ILEORECTAL FISTULA ( 5 FDA reports)
IMPAIRED DRIVING ABILITY ( 5 FDA reports)
IMPLANT SITE RASH ( 5 FDA reports)
INTESTINAL TRANSPOSITION ( 5 FDA reports)
LEFT VENTRICULAR FAILURE ( 5 FDA reports)
LIMB REDUCTION DEFECT ( 5 FDA reports)
LIP DISORDER ( 5 FDA reports)
LIVER ABSCESS ( 5 FDA reports)
LOOSE STOOLS ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 5 FDA reports)
LUMBAR SPINAL STENOSIS ( 5 FDA reports)
MEAN CELL VOLUME INCREASED ( 5 FDA reports)
MELANODERMIA ( 5 FDA reports)
MUSCLE CRAMP ( 5 FDA reports)
MUSCLE HYPERTROPHY ( 5 FDA reports)
MYCOTIC ALLERGY ( 5 FDA reports)
NAIL DISCOLOURATION ( 5 FDA reports)
NERVE ROOT COMPRESSION ( 5 FDA reports)
NEUROMYOPATHY ( 5 FDA reports)
NOCTURIA ( 5 FDA reports)
OPTIC NERVE CUP/DISC RATIO INCREASED ( 5 FDA reports)
PANCREATIC DISORDER ( 5 FDA reports)
PARASITE BLOOD TEST POSITIVE ( 5 FDA reports)
PENILE ULCERATION ( 5 FDA reports)
PITUITARY ENLARGEMENT ( 5 FDA reports)
PITYRIASIS LICHENOIDES ET VARIOLIFORMIS ACUTA ( 5 FDA reports)
POSTURE ABNORMAL ( 5 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 5 FDA reports)
PULMONARY ARTERY DILATATION ( 5 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 5 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 5 FDA reports)
PULSE PRESSURE DECREASED ( 5 FDA reports)
PUPILS UNEQUAL ( 5 FDA reports)
RECURRING SKIN BOILS ( 5 FDA reports)
REMOVAL OF FOREIGN BODY ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
RETINAL DISORDER ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
RETROGRADE EJACULATION ( 5 FDA reports)
SCAR EXCISION ( 5 FDA reports)
SCROTAL SWELLING ( 5 FDA reports)
SEPTIC EMBOLUS ( 5 FDA reports)
SHOULDER DYSTOCIA ( 5 FDA reports)
SICCA SYNDROME ( 5 FDA reports)
SOFT TISSUE INJURY ( 5 FDA reports)
SPINAL CORD DISORDER ( 5 FDA reports)
STOOL ANALYSIS ABNORMAL ( 5 FDA reports)
SUBACUTE ENDOCARDITIS ( 5 FDA reports)
SUTURE RELATED COMPLICATION ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 5 FDA reports)
THYROIDECTOMY ( 5 FDA reports)
TIC ( 5 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 5 FDA reports)
TRISOMY 21 ( 5 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 5 FDA reports)
VEIN DISORDER ( 5 FDA reports)
VICTIM OF ABUSE ( 5 FDA reports)
VICTIM OF CRIME ( 5 FDA reports)
VICTIM OF SEXUAL ABUSE ( 5 FDA reports)
VOMITING IN PREGNANCY ( 5 FDA reports)
VULVAL ULCERATION ( 5 FDA reports)
VULVITIS ( 5 FDA reports)
ABDOMINAL HERNIA REPAIR ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 4 FDA reports)
ALCOHOLIC PSYCHOSIS ( 4 FDA reports)
AMNIOTIC CAVITY DISORDER ( 4 FDA reports)
ANAL SPHINCTER ATONY ( 4 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 4 FDA reports)
ANGELMAN'S SYNDROME ( 4 FDA reports)
ANORECTAL DISCOMFORT ( 4 FDA reports)
ANORECTAL INFECTION ( 4 FDA reports)
AORTIC DILATATION ( 4 FDA reports)
ARTHROFIBROSIS ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
AUTOANTIBODY POSITIVE ( 4 FDA reports)
BILIARY TRACT DISORDER ( 4 FDA reports)
BILIRUBIN URINE ( 4 FDA reports)
BITE ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 4 FDA reports)
BLOOD LUTEINISING HORMONE INCREASED ( 4 FDA reports)
BLOOD PH INCREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BODY HEIGHT BELOW NORMAL ( 4 FDA reports)
BONE LESION ( 4 FDA reports)
BOREDOM ( 4 FDA reports)
CAROTID ARTERY STENOSIS ( 4 FDA reports)
CATHETER SITE PAIN ( 4 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 4 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
CEREBRAL CYST ( 4 FDA reports)
CERVIX CARCINOMA ( 4 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 4 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 4 FDA reports)
CONGENITAL BRAIN DAMAGE ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 4 FDA reports)
COXSACKIE VIRAL INFECTION ( 4 FDA reports)
CRYOGLOBULINAEMIA ( 4 FDA reports)
DEAFNESS CONGENITAL ( 4 FDA reports)
DELIVERY ( 4 FDA reports)
DENTAL PLAQUE ( 4 FDA reports)
DEPRESSION SUICIDAL ( 4 FDA reports)
DEPRESSIVE SYMPTOM ( 4 FDA reports)
DEVICE DISLOCATION ( 4 FDA reports)
DILATATION VENTRICULAR ( 4 FDA reports)
DISSOCIATION ( 4 FDA reports)
DISTAL ILEAL OBSTRUCTION SYNDROME ( 4 FDA reports)
DYSGRAPHIA ( 4 FDA reports)
EJACULATION DISORDER ( 4 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 4 FDA reports)
ENDOCRINE DISORDER ( 4 FDA reports)
EPIDIDYMAL ENLARGEMENT ( 4 FDA reports)
EPIPHYSEAL DISORDER ( 4 FDA reports)
EXERCISE CAPACITY DECREASED ( 4 FDA reports)
EXERCISE LACK OF ( 4 FDA reports)
EXPOSURE TO ALLERGEN ( 4 FDA reports)
EXPOSURE TO TOXIC AGENT ( 4 FDA reports)
EYELID CYST ( 4 FDA reports)
EYELID MARGIN CRUSTING ( 4 FDA reports)
FACIAL SPASM ( 4 FDA reports)
FAECALOMA ( 4 FDA reports)
FALLOT'S TETRALOGY ( 4 FDA reports)
FEEDING DISORDER NEONATAL ( 4 FDA reports)
GENERAL NUTRITION DISORDER ( 4 FDA reports)
HAEMOPHILIA ( 4 FDA reports)
HEPATIC ADENOMA ( 4 FDA reports)
HERNIA PAIN ( 4 FDA reports)
HIP SWELLING ( 4 FDA reports)
HOARSENESS ( 4 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 4 FDA reports)
HYPERINSULINAEMIA ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPOCHLORAEMIA ( 4 FDA reports)
HYPOREFLEXIA ( 4 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 4 FDA reports)
INCISION SITE PAIN ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 4 FDA reports)
INFERTILITY MALE ( 4 FDA reports)
INFESTATION ( 4 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
INJECTION SITE THROMBOSIS ( 4 FDA reports)
INNER EAR DISORDER ( 4 FDA reports)
INTESTINAL STOMA COMPLICATION ( 4 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE INSERTION ( 4 FDA reports)
INTRANEURAL CYST ( 4 FDA reports)
JOINT CREPITATION ( 4 FDA reports)
KERATOSIS FOLLICULAR ( 4 FDA reports)
KETONURIA ( 4 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 4 FDA reports)
LICHEN SCLEROSUS ( 4 FDA reports)
LIVEDO RETICULARIS ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 4 FDA reports)
MELANOSIS COLI ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
METATARSALGIA ( 4 FDA reports)
MIDDLE EAR EFFUSION ( 4 FDA reports)
MONARTHRITIS ( 4 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
MUSCLE SPASTICITY ( 4 FDA reports)
MYASTHENIA GRAVIS ( 4 FDA reports)
MYELOFIBROSIS ( 4 FDA reports)
NAIL DYSTROPHY ( 4 FDA reports)
NECK MASS ( 4 FDA reports)
NEPHRITIC SYNDROME ( 4 FDA reports)
NERVE STIMULATION TEST ( 4 FDA reports)
NEUROBLASTOMA ( 4 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 4 FDA reports)
NEUROSIS ( 4 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 4 FDA reports)
NYSTAGMUS ( 4 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 4 FDA reports)
OTITIS MEDIA ACUTE ( 4 FDA reports)
PANCREATIC INSUFFICIENCY ( 4 FDA reports)
PARANOID PERSONALITY DISORDER ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PAROSMIA ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PHARYNGEAL LESION ( 4 FDA reports)
PILONIDAL SINUS REPAIR ( 4 FDA reports)
PNEUMATURIA ( 4 FDA reports)
PORPHYRIA ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
POSTOPERATIVE FEVER ( 4 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 4 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 4 FDA reports)
PRESCRIBED OVERDOSE ( 4 FDA reports)
PROTEUS INFECTION ( 4 FDA reports)
PRURITUS GENITAL ( 4 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 4 FDA reports)
RADICULAR PAIN ( 4 FDA reports)
RADICULITIS CERVICAL ( 4 FDA reports)
RALES ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 4 FDA reports)
RETROPERITONEAL OEDEMA ( 4 FDA reports)
RHINITIS SEASONAL ( 4 FDA reports)
RHONCHI ( 4 FDA reports)
SALPINGO-OOPHORECTOMY ( 4 FDA reports)
SCHOOL REFUSAL ( 4 FDA reports)
SICK RELATIVE ( 4 FDA reports)
SKIN INJURY ( 4 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
SPERMATOCELE ( 4 FDA reports)
SPIDER NAEVUS ( 4 FDA reports)
SPINAL FUSION SURGERY ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 4 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 4 FDA reports)
STOMA SITE REACTION ( 4 FDA reports)
STOOLS WATERY ( 4 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 4 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 4 FDA reports)
TEMPERATURE REGULATION DISORDER ( 4 FDA reports)
THORACIC OUTLET SYNDROME ( 4 FDA reports)
THROAT LESION ( 4 FDA reports)
THYROID GLAND CANCER ( 4 FDA reports)
TONGUE DISORDER ( 4 FDA reports)
TOOTH FRACTURE ( 4 FDA reports)
TRANSVERSE PRESENTATION ( 4 FDA reports)
TREATMENT FAILURE ( 4 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 4 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
URETHRAL DISCHARGE ( 4 FDA reports)
URINARY BLADDER ABSCESS ( 4 FDA reports)
URINARY TRACT DISORDER ( 4 FDA reports)
URINE ABNORMALITY ( 4 FDA reports)
URINE FLOW DECREASED ( 4 FDA reports)
UROBILIN URINE PRESENT ( 4 FDA reports)
UTERINE CYST ( 4 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 4 FDA reports)
VAGINAL LACERATION ( 4 FDA reports)
VIRAL RASH ( 4 FDA reports)
VITREOUS OPACITIES ( 4 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 4 FDA reports)
XANTHOMA ( 4 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ABO INCOMPATIBILITY ( 3 FDA reports)
ACID FAST STAIN POSITIVE ( 3 FDA reports)
ACNE PUSTULAR ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 3 FDA reports)
ANAL FUNGAL INFECTION ( 3 FDA reports)
ANASTOMOTIC LEAK ( 3 FDA reports)
ANORECTAL CELLULITIS ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
ARRESTED LABOUR ( 3 FDA reports)
ARTHROPOD INFESTATION ( 3 FDA reports)
AUTOIMMUNE PANCREATITIS ( 3 FDA reports)
AVOIDANT PERSONALITY DISORDER ( 3 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 3 FDA reports)
BACTERIA WOUND IDENTIFIED ( 3 FDA reports)
BACTERIAL FOOD POISONING ( 3 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 3 FDA reports)
BILIARY CIRRHOSIS ( 3 FDA reports)
BIOPSY RECTUM ABNORMAL ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD CREATINE DECREASED ( 3 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 3 FDA reports)
BLOOD IRON ABNORMAL ( 3 FDA reports)
BONE SCAN ABNORMAL ( 3 FDA reports)
BRAIN STEM SYNDROME ( 3 FDA reports)
BREAST PROSTHESIS USER ( 3 FDA reports)
BREATH ODOUR ( 3 FDA reports)
BRONCHIAL DISORDER ( 3 FDA reports)
CALCULUS BLADDER ( 3 FDA reports)
CAROTID ARTERY DISEASE ( 3 FDA reports)
CATARACT SUBCAPSULAR ( 3 FDA reports)
CEREBELLAR HYPOPLASIA ( 3 FDA reports)
CERVIX DISORDER ( 3 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
CHLAMYDIAL INFECTION ( 3 FDA reports)
CHROMOSOMAL MUTATION ( 3 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 3 FDA reports)
COLON CANCER METASTATIC ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 3 FDA reports)
CONDUCTIVE DEAFNESS ( 3 FDA reports)
CONGENITAL ENDOCRINE ANOMALY ( 3 FDA reports)
CONGENITAL EYELID MALFORMATION ( 3 FDA reports)
CONGENITAL OPTIC NERVE ANOMALY ( 3 FDA reports)
CONGENITAL TORTICOLLIS ( 3 FDA reports)
CONJUNCTIVAL ABRASION ( 3 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 3 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 3 FDA reports)
CORNEAL ULCER ( 3 FDA reports)
CROUP INFECTIOUS ( 3 FDA reports)
CSF PRESSURE INCREASED ( 3 FDA reports)
CYSTIC LYMPHANGIOMA ( 3 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
DACRYOSTENOSIS CONGENITAL ( 3 FDA reports)
DEATH OF RELATIVE ( 3 FDA reports)
DECOMPRESSION SICKNESS ( 3 FDA reports)
DELAYED FONTANELLE CLOSURE ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DERMATILLOMANIA ( 3 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 3 FDA reports)
EAR CANAL STENOSIS ( 3 FDA reports)
ECHINOCOCCIASIS ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 3 FDA reports)
ERGOT POISONING ( 3 FDA reports)
ERYTHEMA OF EYELID ( 3 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 3 FDA reports)
EXOPHTHALMOS ( 3 FDA reports)
EXTERNAL EAR DISORDER ( 3 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 3 FDA reports)
EYELID BLEEDING ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
FAECALITH ( 3 FDA reports)
FASCIITIS ( 3 FDA reports)
FEAR OF OPEN SPACES ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FONTANELLE BULGING ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
FUNGUS STOOL IDENTIFIED ( 3 FDA reports)
GALACTOSE INTOLERANCE ( 3 FDA reports)
GASTRIC ATONY ( 3 FDA reports)
GASTRITIS ALCOHOLIC ( 3 FDA reports)
GASTRITIS ATROPHIC ( 3 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 3 FDA reports)
GASTROINTESTINAL EROSION ( 3 FDA reports)
GINGIVITIS ULCERATIVE ( 3 FDA reports)
GLYCOSURIA ( 3 FDA reports)
GONORRHOEA ( 3 FDA reports)
GYNAECOLOGICAL CHLAMYDIA INFECTION ( 3 FDA reports)
H1N1 INFLUENZA ( 3 FDA reports)
HAEMORRHAGIC DISORDER ( 3 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
HEPATIC ATROPHY ( 3 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HERPES OPHTHALMIC ( 3 FDA reports)
HIGH RISK SEXUAL BEHAVIOUR ( 3 FDA reports)
HILAR LYMPHADENOPATHY ( 3 FDA reports)
HOMELESS ( 3 FDA reports)
HYPERALBUMINAEMIA ( 3 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 3 FDA reports)
HYPERVITAMINOSIS ( 3 FDA reports)
HYPERVITAMINOSIS A ( 3 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 3 FDA reports)
IATROGENIC INJURY ( 3 FDA reports)
IMPAIRED SELF-CARE ( 3 FDA reports)
IMPRISONMENT ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INBORN ERROR OF METABOLISM ( 3 FDA reports)
INGUINAL MASS ( 3 FDA reports)
INTRACRANIAL HYPOTENSION ( 3 FDA reports)
INTRACRANIAL INJURY ( 3 FDA reports)
JOB DISSATISFACTION ( 3 FDA reports)
LACRIMATION DECREASED ( 3 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 3 FDA reports)
LAZINESS ( 3 FDA reports)
LEARNING DISABILITY ( 3 FDA reports)
LIPASE DECREASED ( 3 FDA reports)
LIPOPROTEIN (A) INCREASED ( 3 FDA reports)
LIPOSARCOMA ( 3 FDA reports)
LOWER LIMB DEFORMITY ( 3 FDA reports)
LYMPHADENITIS BACTERIAL ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MALIGNANT MELANOMA IN SITU ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MASTOIDITIS ( 3 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 3 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 3 FDA reports)
MERYCISM ( 3 FDA reports)
MICROPHTHALMOS ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 3 FDA reports)
MURPHY'S SIGN POSITIVE ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
NEPHRITIS ( 3 FDA reports)
NEPHROCALCINOSIS ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NOSE DEFORMITY ( 3 FDA reports)
OBSTRUCTION ( 3 FDA reports)
OESTRIOL INCREASED ( 3 FDA reports)
OOPHORECTOMY BILATERAL ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
OVARIAN ADENOMA ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 3 FDA reports)
PENILE PAIN ( 3 FDA reports)
PERINEAL PAIN ( 3 FDA reports)
PERITONEAL DISORDER ( 3 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 3 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 3 FDA reports)
PHYSICAL DISABILITY ( 3 FDA reports)
PLASMACYTOSIS ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
POLYCHONDRITIS ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
POSTOPERATIVE STITCH SINUS ( 3 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 3 FDA reports)
PROLONGED LABOUR ( 3 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 3 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 3 FDA reports)
PRURIGO ( 3 FDA reports)
PSOAS SIGN ( 3 FDA reports)
PYODERMA ( 3 FDA reports)
PYROMANIA ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RECTAL SPASM ( 3 FDA reports)
RECTOCELE ( 3 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 3 FDA reports)
REFLUX GASTRITIS ( 3 FDA reports)
RELATIONSHIP BREAKDOWN ( 3 FDA reports)
RENAL HAEMORRHAGE ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
RHINALGIA ( 3 FDA reports)
RHINITIS PERENNIAL ( 3 FDA reports)
ROSAI-DORFMAN SYNDROME ( 3 FDA reports)
RUBELLA IN PREGNANCY ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 3 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 3 FDA reports)
SHUNT MALFUNCTION ( 3 FDA reports)
SKIN FRAGILITY ( 3 FDA reports)
SKIN HYPERTROPHY ( 3 FDA reports)
SKIN ODOUR ABNORMAL ( 3 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SPERMATOZOA MORPHOLOGY ABNORMAL ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
STAPHYLOCOCCAL IMPETIGO ( 3 FDA reports)
STARING ( 3 FDA reports)
STREPTOBACILLUS INFECTION ( 3 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 3 FDA reports)
SYNDACTYLY ( 3 FDA reports)
TACHYPHRENIA ( 3 FDA reports)
TERMINAL INSOMNIA ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
TOBACCO USER ( 3 FDA reports)
TOOTH INFECTION ( 3 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 3 FDA reports)
TRICHORRHEXIS ( 3 FDA reports)
TRISOMY 18 ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 3 FDA reports)
TUBO-OVARIAN ABSCESS ( 3 FDA reports)
TUMOUR NECROSIS ( 3 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UNDERWEIGHT ( 3 FDA reports)
URETERAL DISORDER ( 3 FDA reports)
URETHROPERINEAL FISTULA ( 3 FDA reports)
UTERINE ENLARGEMENT ( 3 FDA reports)
UTERINE MALPOSITION ( 3 FDA reports)
VAGINAL PROLAPSE ( 3 FDA reports)
VENA CAVA THROMBOSIS ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VULVAL CANCER ( 3 FDA reports)
VULVOVAGINAL ULCERATION ( 3 FDA reports)
WHITE BLOOD CELLS URINE ( 3 FDA reports)
WOUND NECROSIS ( 3 FDA reports)
ABORTION COMPLETE ( 2 FDA reports)
ABORTION SPONTANEOUS INCOMPLETE ( 2 FDA reports)
ABSCESS DRAINAGE ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
ALLERGIC COUGH ( 2 FDA reports)
ALLERGY TEST POSITIVE ( 2 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 2 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 2 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANO-RECTAL ULCER ( 2 FDA reports)
ANOREXIA AND BULIMIA SYNDROME ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ASHERMAN'S SYNDROME ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
ATROPHIC GLOSSITIS ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
BANKRUPTCY ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BILIARY ADENOMA ( 2 FDA reports)
BINGE EATING ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD FOLATE INCREASED ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD GASTRIN INCREASED ( 2 FDA reports)
BLOOD KETONE BODY INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
BUDD-CHIARI SYNDROME ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 2 FDA reports)
CASTLEMAN'S DISEASE ( 2 FDA reports)
CATHETER BACTERAEMIA ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
CHLOASMA ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 2 FDA reports)
CLEFT LIP AND PALATE ( 2 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMEDONE ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPULSIVE HOARDING ( 2 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 2 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 2 FDA reports)
CONGENITAL MEGAURETER ( 2 FDA reports)
CONVULSION NEONATAL ( 2 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CRUSH INJURY ( 2 FDA reports)
CRYSTAL URINE PRESENT ( 2 FDA reports)
CSF TEST ABNORMAL ( 2 FDA reports)
CUBITAL TUNNEL SYNDROME ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DENTAL IMPLANTATION ( 2 FDA reports)
DENTAL PROSTHESIS USER ( 2 FDA reports)
DEXTROCARDIA ( 2 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 2 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DIVERTICULITIS MECKEL'S ( 2 FDA reports)
DIVORCED PARENTS ( 2 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DRY SOCKET ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ELLIPTOCYTOSIS ( 2 FDA reports)
ENCEPHALOPATHY NEONATAL ( 2 FDA reports)
ENDOMETRIAL ATROPHY ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEMALE SEXUAL AROUSAL DISORDER ( 2 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FISTULA REPAIR ( 2 FDA reports)
FOETAL CARDIAC DISORDER ( 2 FDA reports)
FOETAL HEART RATE ABNORMAL ( 2 FDA reports)
FOETAL HEART RATE INCREASED ( 2 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 2 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 2 FDA reports)
GASTROENTERITIS HELICOBACTER ( 2 FDA reports)
GASTROENTERITIS YERSINIA ( 2 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL STENOSIS ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL INFECTION ( 2 FDA reports)
GENITAL INFECTION FUNGAL ( 2 FDA reports)
GENITAL LESION ( 2 FDA reports)
GENITAL ULCERATION ( 2 FDA reports)
GINGIVAL CYST ( 2 FDA reports)
GLIOBLASTOMA ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GRANDIOSITY ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
GREIG'S SYNDROME ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMORRHOID INFECTION ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HEAD CIRCUMFERENCE ABNORMAL ( 2 FDA reports)
HEAT EXHAUSTION ( 2 FDA reports)
HEAT STROKE ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERCHROMASIA ( 2 FDA reports)
HYPERCHROMIC ANAEMIA ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPOGONADISM MALE ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCISION SITE OEDEMA ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTESTINAL FISTULA INFECTION ( 2 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 2 FDA reports)
INTESTINAL ULCER PERFORATION ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
JEJUNAL ULCER ( 2 FDA reports)
KERATOMILEUSIS ( 2 FDA reports)
KLEBSIELLA BACTERAEMIA ( 2 FDA reports)
KYPHOSIS CONGENITAL ( 2 FDA reports)
LABOUR ONSET DELAYED ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LARYNGITIS VIRAL ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LIPOSUCTION ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
MACROCYTOSIS ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MAMMOPLASTY ( 2 FDA reports)
MATERNAL EXPOSURE DURING DELIVERY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MECHANICAL URTICARIA ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
MIGRAINE WITHOUT AURA ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
NAIL AVULSION ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NERVE STIMULATION TEST ABNORMAL ( 2 FDA reports)
NEURAL TUBE DEFECT ( 2 FDA reports)
NEUROLOGICAL EYELID DISORDER ( 2 FDA reports)
NITRITE URINE ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
OCULOMOTOR STUDY ABNORMAL ( 2 FDA reports)
OESOPHAGEAL ATRESIA ( 2 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 2 FDA reports)
ORAL SURGERY ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PELVIC HAEMORRHAGE ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERITONEAL CYST ( 2 FDA reports)
PES CAVUS ( 2 FDA reports)
PEYRONIE'S DISEASE ( 2 FDA reports)
PH URINE INCREASED ( 2 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 2 FDA reports)
PHOBIC AVOIDANCE ( 2 FDA reports)
PHONOPHOBIA ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PIRIFORMIS SYNDROME ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PLACENTAL INFARCTION ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POOR SUCKING REFLEX ( 2 FDA reports)
PORENCEPHALY ( 2 FDA reports)
POSTPARTUM VAGINAL LACERATION ( 2 FDA reports)
PROLONGED PREGNANCY ( 2 FDA reports)
PROSTATIC PAIN ( 2 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 2 FDA reports)
PTERYGIUM ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY GRANULOMA ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PUS IN STOOL ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RECTAL STENOSIS ( 2 FDA reports)
RECTOVAGINAL SEPTUM ABSCESS ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
RENAL AGENESIS ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RENAL VEIN THROMBOSIS ( 2 FDA reports)
REPRODUCTIVE TRACT HYPOPLASIA, MALE ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RETINOIC ACID SYNDROME ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
SCARLET FEVER ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
SELF-INDUCED VOMITING ( 2 FDA reports)
SEMEN ABNORMAL ( 2 FDA reports)
SEMEN VOLUME ABNORMAL ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 2 FDA reports)
SINUS PAIN ( 2 FDA reports)
SINUSITIS BACTERIAL ( 2 FDA reports)
SKIN CYST EXCISION ( 2 FDA reports)
SKIN FIBROSIS ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SPECIAL SENSES CONGENITAL ANOMALY ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
STAPHYLOMA ( 2 FDA reports)
TATTOO ( 2 FDA reports)
TEMPORAL LOBE EPILEPSY ( 2 FDA reports)
TERATOGENICITY ( 2 FDA reports)
TESTICULAR NEOPLASM ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THIRD TRIMESTER PREGNANCY ( 2 FDA reports)
THOUGHT BLOCKING ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
THYROXINE INCREASED ( 2 FDA reports)
TONGUE BLACK HAIRY ( 2 FDA reports)
TONGUE GEOGRAPHIC ( 2 FDA reports)
TOOTH MALFORMATION ( 2 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRAUMATIC FRACTURE ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
ULNAR NERVE INJURY ( 2 FDA reports)
ULTRASOUND SCAN VAGINA ABNORMAL ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
UNWANTED PREGNANCY ( 2 FDA reports)
URETHRAL FISTULA ( 2 FDA reports)
URETHRAL POLYP ( 2 FDA reports)
URETHRAL STENOSIS ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY TRACT MALFORMATION ( 2 FDA reports)
URINE BILIRUBIN INCREASED ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VERBALLY ABUSED ( 2 FDA reports)
VIRAL LOAD ( 2 FDA reports)
VITAMIN A DEFICIENCY ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
WART EXCISION ( 2 FDA reports)
WEIGHT CONTROL ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WITHDRAWAL BLEED ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABNORMAL LABOUR AFFECTING FOETUS ( 1 FDA reports)
ABNORMAL PALMAR/PLANTAR CREASES ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACROPHOBIA ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADENOTONSILLECTOMY ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED DISTURBANCE OF EMOTION AND CONDUCT ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AEROMONA INFECTION ( 1 FDA reports)
ALCOHOLIC ( 1 FDA reports)
ALLERGIC RESPIRATORY DISEASE ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMOEBIC COLITIS ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANOVULVAR FISTULA ( 1 FDA reports)
ANTI-THYROID ANTIBODY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTHRITIS VIRAL ( 1 FDA reports)
ASCARIASIS ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BATTERED WIFE ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN HYDATIDIFORM MOLE ( 1 FDA reports)
BENIGN SMALL INTESTINAL NEOPLASM ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE OUTPUT INCREASED ( 1 FDA reports)
BILIARY FIBROSIS ( 1 FDA reports)
BILOMA ( 1 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLEEDING ANOVULATORY ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CHOLESTEROL NORMAL ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD DONOR ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BULLOUS IMPETIGO ( 1 FDA reports)
BURKITT'S LYMPHOMA ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
CALCIFICATION OF MUSCLE ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CERVICAL STRICTURE ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLORADO TICK FEVER ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONDUCT DISORDER ( 1 FDA reports)
CONGENITAL ANOMALIES OF EAR OSSICLES ( 1 FDA reports)
CONGENITAL ANOMALY OF INNER EAR ( 1 FDA reports)
CONGENITAL AORTIC ANOMALY ( 1 FDA reports)
CONGENITAL AORTIC ATRESIA ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CONGENITAL BLADDER ANOMALY ( 1 FDA reports)
CONGENITAL CEREBRAL CYST ( 1 FDA reports)
CONGENITAL GASTRIC ANOMALY ( 1 FDA reports)
CONGENITAL IRIS ANOMALY ( 1 FDA reports)
CONGENITAL KNEE DEFORMITY ( 1 FDA reports)
CONGENITAL MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
CONGENITAL NEUROLOGICAL DISORDER ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONGENITAL OESOPHAGEAL ANOMALY ( 1 FDA reports)
CONGENITAL RENAL DISORDER ( 1 FDA reports)
CONGENITAL TERATOMA ( 1 FDA reports)
CONJUNCTIVAL IRRITATION ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTACT LENS COMPLICATION ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORNEAL THINNING ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CRIME ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 1 FDA reports)
DANDY-WALKER SYNDROME ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DERMOGRAPHISM ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DYSPRAXIA ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
ECTOPIC PREGNANCY WITH INTRAUTERINE DEVICE ( 1 FDA reports)
ECZEMA HERPETICUM ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOMETRIAL HYPOPLASIA ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE OPERATION COMPLICATION ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
FACTOR V INHIBITION ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FAILED EXAMINATIONS ( 1 FDA reports)
FAILED INDUCTION OF LABOUR ( 1 FDA reports)
FEEDING PROBLEM IN CHILD ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOETAL CYSTIC HYGROMA ( 1 FDA reports)
FOETAL MACROSOMIA ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FORAMEN MAGNUM STENOSIS ( 1 FDA reports)
FULL BLOOD COUNT ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRO-INTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL DYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROINTESTINAL ULCER PERFORATION ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITAL INFECTION VIRAL ( 1 FDA reports)
GENITOURINARY TRACT NEOPLASM ( 1 FDA reports)
GINGIVAL GRAFT ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLARE ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
HAEMANGIOMA CONGENITAL ( 1 FDA reports)
HAEMANGIOMA OF SPLEEN ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE IN PREGNANCY ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAIR TRANSPLANT ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEAD LAG ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS A ANTIBODY ( 1 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 1 FDA reports)
HIGH ARCHED PALATE ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYSTEROSCOPY ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INADEQUATE LUBRICATION ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INFECTED SEBACEOUS CYST ( 1 FDA reports)
INFERTILITY FEMALE ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERRUPTION OF AORTIC ARCH ( 1 FDA reports)
INTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL VILLI ATROPHY ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IRIS HYPERPIGMENTATION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JEJUNAL PERFORATION ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LACTOSE TOLERANCE TEST ABNORMAL ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LAXATIVE SUPPORTIVE CARE ( 1 FDA reports)
LEPTOSPIROSIS ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LID LAG ( 1 FDA reports)
LIMB HYPOPLASIA CONGENITAL ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER STAGE 0 ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MACULAR CYST ( 1 FDA reports)
MACULAR SCAR ( 1 FDA reports)
MALIGNANT HISTIOCYTOSIS ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MAY-THURNER SYNDROME ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MECONIUM ABNORMAL ( 1 FDA reports)
MECONIUM INCREASED ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDIASTINAL HAEMATOMA ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENOPAUSAL DISORDER ( 1 FDA reports)
MENTAL DISABILITY ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICROGRAPHIA ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MOROSE ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL ATROPHY ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MULTIPLE CARDIAC DEFECTS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE ENZYME ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
MYRINGOTOMY ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NERVE ROOT INJURY LUMBAR ( 1 FDA reports)
NEUROECTODERMAL NEOPLASM ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROPSYCHOLOGICAL TEST ABNORMAL ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
OCCUPATIONAL EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OLFACTORY NERVE DISORDER ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPTIC NERVE HYPOPLASIA ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL VIRAL INFECTION ( 1 FDA reports)
ORCHIDOPEXY ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
OSTEOGENESIS IMPERFECTA ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
OVULATION PAIN ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PENICILLIOSIS ( 1 FDA reports)
PENILE VASCULAR DISORDER ( 1 FDA reports)
PERIANAL FUNGAL INFECTION ( 1 FDA reports)
PERINEAL OPERATION ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIPHERAL OEDEMA NEONATAL ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGOLARYNGEAL ABSCESS ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHYSICAL ABUSE ( 1 FDA reports)
PITUITARY HYPOPLASIA ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 1 FDA reports)
POST LAMINECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL URINE LEAK ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY WITH INJECTABLE CONTRACEPTIVE ( 1 FDA reports)
PREMATURE AGEING ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTOCOLECTOMY ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROMINENT EPICANTHAL FOLDS ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PSEUDOPAPILLOEDEMA ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY MALFORMATION ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURGING ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL CRAMPS ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL HYPOPLASIA ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESIDUAL OVARY SYNDROME ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RICKETTSIOSIS ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
SAPHO SYNDROME ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCROTAL INFECTION ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELECTIVE IGA IMMUNODEFICIENCY ( 1 FDA reports)
SEMEN VOLUME INCREASED ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
SEVER'S DISEASE ( 1 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 1 FDA reports)
SHARED PSYCHOTIC DISORDER ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN MALFORMATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL INTESTINAL BACTERIAL OVERGROWTH ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPERMATORRHOEA ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPLENITIS ( 1 FDA reports)
SPUTUM CULTURE ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STOMATOCYTES PRESENT ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 1 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 1 FDA reports)
SUBACUTE SCLEROSING PANENCEPHALITIS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE NEONATAL ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUBSTANCE USE ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUPERNUMERARY NIPPLE ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TESTICULAR CANCER METASTATIC ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
TESTICULAR EMBRYONAL CARCINOMA ( 1 FDA reports)
TESTICULAR GERM CELL TUMOUR MIXED STAGE I ( 1 FDA reports)
TESTICULAR INFARCTION ( 1 FDA reports)
TESTICULAR MASS ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROID GLAND SCAN ABNORMAL ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLAR NEOPLASM BENIGN ( 1 FDA reports)
TONSILLAR ULCER ( 1 FDA reports)
TOURETTE'S DISORDER ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE DECREASED ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TRUANCY ( 1 FDA reports)
TULARAEMIA ( 1 FDA reports)
TYPHOID FEVER ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UMBILICAL CORD PROLAPSE ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER LIMB DEFORMITY ( 1 FDA reports)
URETHRAL ATROPHY ( 1 FDA reports)
URETHRAL CYST ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE CERVIX HYPOPLASIA ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UVULECTOMY ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VAGINITIS ( 1 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 1 FDA reports)
VARICOCELE REPAIR ( 1 FDA reports)
VARICOSE VEIN OPERATION ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR HYPOPLASIA ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
VIOLENT IDEATION ( 1 FDA reports)
VIRAL OESOPHAGITIS ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
VITAMIN A INCREASED ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN C DEFICIENCY ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELLS STOOL ( 1 FDA reports)
WITHDRAWAL BLEEDING IRREGULAR ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
YELLOW NAIL SYNDROME ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use