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

DEPRESSION ( 2274 FDA reports)
ANXIETY ( 2146 FDA reports)
NAUSEA ( 2051 FDA reports)
DRUG INEFFECTIVE ( 1772 FDA reports)
PAIN ( 1741 FDA reports)
HEADACHE ( 1653 FDA reports)
FATIGUE ( 1548 FDA reports)
INSOMNIA ( 1533 FDA reports)
DIZZINESS ( 1519 FDA reports)
CONVULSION ( 1291 FDA reports)
DYSPNOEA ( 1278 FDA reports)
VOMITING ( 1278 FDA reports)
WEIGHT INCREASED ( 1174 FDA reports)
BACK PAIN ( 1021 FDA reports)
DIARRHOEA ( 1008 FDA reports)
DIABETES MELLITUS ( 973 FDA reports)
CHEST PAIN ( 966 FDA reports)
TREMOR ( 965 FDA reports)
SUICIDAL IDEATION ( 963 FDA reports)
FALL ( 958 FDA reports)
WEIGHT DECREASED ( 928 FDA reports)
ASTHENIA ( 902 FDA reports)
HYPERTENSION ( 897 FDA reports)
ARTHRALGIA ( 879 FDA reports)
FEELING ABNORMAL ( 879 FDA reports)
PAIN IN EXTREMITY ( 866 FDA reports)
PYREXIA ( 750 FDA reports)
ABDOMINAL PAIN ( 726 FDA reports)
RASH ( 724 FDA reports)
OEDEMA PERIPHERAL ( 700 FDA reports)
SOMNOLENCE ( 669 FDA reports)
CONSTIPATION ( 659 FDA reports)
ABDOMINAL PAIN UPPER ( 647 FDA reports)
INJURY ( 629 FDA reports)
MYOCARDIAL INFARCTION ( 624 FDA reports)
SUICIDE ATTEMPT ( 604 FDA reports)
TYPE 2 DIABETES MELLITUS ( 604 FDA reports)
PNEUMONIA ( 603 FDA reports)
CONFUSIONAL STATE ( 602 FDA reports)
HYPOAESTHESIA ( 588 FDA reports)
ANAEMIA ( 576 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 566 FDA reports)
HYPERHIDROSIS ( 564 FDA reports)
VISION BLURRED ( 561 FDA reports)
PARAESTHESIA ( 558 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 554 FDA reports)
COUGH ( 533 FDA reports)
EMOTIONAL DISTRESS ( 530 FDA reports)
AMNESIA ( 515 FDA reports)
OVERDOSE ( 515 FDA reports)
MALAISE ( 503 FDA reports)
AGITATION ( 493 FDA reports)
MUSCLE SPASMS ( 490 FDA reports)
LOSS OF CONSCIOUSNESS ( 485 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 480 FDA reports)
DEHYDRATION ( 478 FDA reports)
GAIT DISTURBANCE ( 467 FDA reports)
PRURITUS ( 463 FDA reports)
CEREBROVASCULAR ACCIDENT ( 446 FDA reports)
DRUG INTERACTION ( 442 FDA reports)
MEMORY IMPAIRMENT ( 442 FDA reports)
PULMONARY EMBOLISM ( 441 FDA reports)
CONDITION AGGRAVATED ( 438 FDA reports)
OSTEONECROSIS OF JAW ( 427 FDA reports)
MYALGIA ( 422 FDA reports)
HYPOTENSION ( 420 FDA reports)
IRRITABILITY ( 414 FDA reports)
OSTEOARTHRITIS ( 412 FDA reports)
SINUSITIS ( 412 FDA reports)
HALLUCINATION ( 405 FDA reports)
URINARY TRACT INFECTION ( 392 FDA reports)
DECREASED APPETITE ( 390 FDA reports)
DEEP VEIN THROMBOSIS ( 386 FDA reports)
ROAD TRAFFIC ACCIDENT ( 383 FDA reports)
BLOOD PRESSURE INCREASED ( 381 FDA reports)
PANCREATITIS ( 377 FDA reports)
MIGRAINE ( 374 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 373 FDA reports)
DISTURBANCE IN ATTENTION ( 369 FDA reports)
ALOPECIA ( 365 FDA reports)
NEUROPATHY PERIPHERAL ( 364 FDA reports)
CHOLELITHIASIS ( 361 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 360 FDA reports)
URTICARIA ( 352 FDA reports)
BLOOD GLUCOSE INCREASED ( 351 FDA reports)
BRONCHITIS ( 349 FDA reports)
ANGER ( 346 FDA reports)
PALPITATIONS ( 341 FDA reports)
NECK PAIN ( 340 FDA reports)
RENAL FAILURE ( 337 FDA reports)
CHEST DISCOMFORT ( 331 FDA reports)
DYSPEPSIA ( 331 FDA reports)
DRY MOUTH ( 327 FDA reports)
AGGRESSION ( 323 FDA reports)
COMPLETED SUICIDE ( 323 FDA reports)
ANHEDONIA ( 322 FDA reports)
BONE DISORDER ( 320 FDA reports)
MENTAL DISORDER ( 320 FDA reports)
NERVOUSNESS ( 318 FDA reports)
CRYING ( 316 FDA reports)
HYPERLIPIDAEMIA ( 316 FDA reports)
CORONARY ARTERY DISEASE ( 314 FDA reports)
MEDICATION ERROR ( 314 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 303 FDA reports)
OSTEOMYELITIS ( 302 FDA reports)
PANIC ATTACK ( 301 FDA reports)
STRESS ( 301 FDA reports)
CONTUSION ( 298 FDA reports)
PAIN IN JAW ( 296 FDA reports)
SYNCOPE ( 295 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 291 FDA reports)
OBESITY ( 291 FDA reports)
HYPERSENSITIVITY ( 287 FDA reports)
GRAND MAL CONVULSION ( 286 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 282 FDA reports)
DYSGEUSIA ( 281 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 281 FDA reports)
CELLULITIS ( 279 FDA reports)
MUSCULAR WEAKNESS ( 279 FDA reports)
ABNORMAL BEHAVIOUR ( 278 FDA reports)
HYPERGLYCAEMIA ( 278 FDA reports)
TINNITUS ( 278 FDA reports)
BALANCE DISORDER ( 276 FDA reports)
ASTHMA ( 273 FDA reports)
SLEEP APNOEA SYNDROME ( 267 FDA reports)
SPINAL OSTEOARTHRITIS ( 264 FDA reports)
SLEEP DISORDER ( 263 FDA reports)
TACHYCARDIA ( 260 FDA reports)
ERYTHEMA ( 259 FDA reports)
ARTHRITIS ( 257 FDA reports)
CHILLS ( 256 FDA reports)
INFECTION ( 254 FDA reports)
DYSPHAGIA ( 252 FDA reports)
MUSCULOSKELETAL PAIN ( 250 FDA reports)
CHOLECYSTITIS CHRONIC ( 249 FDA reports)
HEART RATE INCREASED ( 249 FDA reports)
HOT FLUSH ( 247 FDA reports)
DEATH ( 243 FDA reports)
CARDIAC DISORDER ( 241 FDA reports)
DRUG DEPENDENCE ( 241 FDA reports)
NIGHTMARE ( 240 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 234 FDA reports)
TARDIVE DYSKINESIA ( 231 FDA reports)
ABDOMINAL DISTENSION ( 230 FDA reports)
ERECTILE DYSFUNCTION ( 228 FDA reports)
DYSKINESIA ( 225 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 224 FDA reports)
MOOD SWINGS ( 223 FDA reports)
FLUSHING ( 221 FDA reports)
IMPAIRED HEALING ( 220 FDA reports)
PARANOIA ( 220 FDA reports)
BIPOLAR DISORDER ( 217 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 216 FDA reports)
OSTEOPOROSIS ( 214 FDA reports)
GALLBLADDER DISORDER ( 213 FDA reports)
RENAL FAILURE ACUTE ( 211 FDA reports)
ANOREXIA ( 210 FDA reports)
LETHARGY ( 210 FDA reports)
INJECTION SITE PAIN ( 209 FDA reports)
OSTEONECROSIS ( 208 FDA reports)
INTENTIONAL OVERDOSE ( 206 FDA reports)
MENTAL STATUS CHANGES ( 205 FDA reports)
OEDEMA ( 205 FDA reports)
INFLUENZA LIKE ILLNESS ( 204 FDA reports)
ABDOMINAL DISCOMFORT ( 203 FDA reports)
ABNORMAL DREAMS ( 203 FDA reports)
BONE PAIN ( 203 FDA reports)
SWELLING ( 203 FDA reports)
GASTRITIS ( 201 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 199 FDA reports)
FEAR ( 198 FDA reports)
ATELECTASIS ( 197 FDA reports)
TREATMENT NONCOMPLIANCE ( 196 FDA reports)
DRUG DOSE OMISSION ( 195 FDA reports)
SPEECH DISORDER ( 193 FDA reports)
LYMPHADENOPATHY ( 192 FDA reports)
JOINT SWELLING ( 191 FDA reports)
VERTIGO ( 191 FDA reports)
DEPRESSED MOOD ( 190 FDA reports)
HIATUS HERNIA ( 190 FDA reports)
WITHDRAWAL SYNDROME ( 189 FDA reports)
TOOTH EXTRACTION ( 188 FDA reports)
DENTAL CARIES ( 188 FDA reports)
PLEURAL EFFUSION ( 188 FDA reports)
HYPOKALAEMIA ( 185 FDA reports)
RIB FRACTURE ( 185 FDA reports)
MANIA ( 184 FDA reports)
SWELLING FACE ( 184 FDA reports)
PSYCHOTIC DISORDER ( 183 FDA reports)
DECREASED INTEREST ( 182 FDA reports)
NASOPHARYNGITIS ( 182 FDA reports)
LIBIDO DECREASED ( 180 FDA reports)
DISORIENTATION ( 179 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 178 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 177 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 177 FDA reports)
DIABETIC NEUROPATHY ( 174 FDA reports)
DIVERTICULUM ( 174 FDA reports)
MITRAL VALVE INCOMPETENCE ( 172 FDA reports)
MUSCLE TWITCHING ( 171 FDA reports)
DRUG EFFECT DECREASED ( 170 FDA reports)
DRUG HYPERSENSITIVITY ( 170 FDA reports)
DIABETIC KETOACIDOSIS ( 169 FDA reports)
HYPOGLYCAEMIA ( 169 FDA reports)
THROMBOSIS ( 169 FDA reports)
ATRIAL FIBRILLATION ( 168 FDA reports)
NEPHROLITHIASIS ( 168 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 167 FDA reports)
EMOTIONAL DISORDER ( 167 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 167 FDA reports)
DEFORMITY ( 166 FDA reports)
COGNITIVE DISORDER ( 165 FDA reports)
CARDIAC ARREST ( 164 FDA reports)
INCORRECT DOSE ADMINISTERED ( 164 FDA reports)
METASTASES TO BONE ( 163 FDA reports)
URINARY INCONTINENCE ( 162 FDA reports)
APHASIA ( 161 FDA reports)
CARDIOMEGALY ( 161 FDA reports)
ADVERSE EVENT ( 160 FDA reports)
DYSARTHRIA ( 160 FDA reports)
HEPATIC STEATOSIS ( 160 FDA reports)
OFF LABEL USE ( 160 FDA reports)
SEPSIS ( 158 FDA reports)
HAEMOGLOBIN DECREASED ( 157 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 155 FDA reports)
NASAL CONGESTION ( 155 FDA reports)
DYSURIA ( 154 FDA reports)
TOOTH ABSCESS ( 154 FDA reports)
VISUAL IMPAIRMENT ( 153 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 153 FDA reports)
ARTHROPATHY ( 153 FDA reports)
RECTAL HAEMORRHAGE ( 152 FDA reports)
HAEMORRHOIDS ( 151 FDA reports)
THINKING ABNORMAL ( 151 FDA reports)
TOOTH FRACTURE ( 151 FDA reports)
ARTERIOSCLEROSIS ( 150 FDA reports)
HEAD INJURY ( 150 FDA reports)
HERPES ZOSTER ( 150 FDA reports)
CATARACT ( 149 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 148 FDA reports)
EMPHYSEMA ( 148 FDA reports)
RESPIRATORY FAILURE ( 147 FDA reports)
POLLAKIURIA ( 146 FDA reports)
HAEMATURIA ( 145 FDA reports)
HEPATIC ENZYME INCREASED ( 145 FDA reports)
HYPOTHYROIDISM ( 145 FDA reports)
UNEVALUABLE EVENT ( 145 FDA reports)
TOOTHACHE ( 144 FDA reports)
OROPHARYNGEAL PAIN ( 144 FDA reports)
RESTLESSNESS ( 144 FDA reports)
HALLUCINATION, AUDITORY ( 143 FDA reports)
BURNING SENSATION ( 142 FDA reports)
VISUAL ACUITY REDUCED ( 142 FDA reports)
WHEEZING ( 142 FDA reports)
TOOTH LOSS ( 141 FDA reports)
MAJOR DEPRESSION ( 141 FDA reports)
DIPLOPIA ( 140 FDA reports)
HAEMATOCHEZIA ( 139 FDA reports)
TOOTH DISORDER ( 139 FDA reports)
MULTIPLE SCLEROSIS ( 138 FDA reports)
FLATULENCE ( 136 FDA reports)
HYPOXIA ( 136 FDA reports)
EAR PAIN ( 135 FDA reports)
HYPONATRAEMIA ( 135 FDA reports)
CHOLECYSTITIS ( 129 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 129 FDA reports)
RENAL CYST ( 129 FDA reports)
SINUS DISORDER ( 129 FDA reports)
HYPERCHOLESTEROLAEMIA ( 127 FDA reports)
ILL-DEFINED DISORDER ( 127 FDA reports)
EXOSTOSIS ( 126 FDA reports)
ORAL PAIN ( 126 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 125 FDA reports)
IRRITABLE BOWEL SYNDROME ( 124 FDA reports)
BREAST CANCER ( 123 FDA reports)
HYPERSOMNIA ( 123 FDA reports)
RESTLESS LEGS SYNDROME ( 123 FDA reports)
FIBROMYALGIA ( 122 FDA reports)
NEOPLASM MALIGNANT ( 121 FDA reports)
NIGHT SWEATS ( 121 FDA reports)
CROHN'S DISEASE ( 120 FDA reports)
DYSPHONIA ( 120 FDA reports)
HALLUCINATION, VISUAL ( 120 FDA reports)
LUNG NEOPLASM ( 120 FDA reports)
SEDATION ( 120 FDA reports)
BACK INJURY ( 119 FDA reports)
COLONIC POLYP ( 119 FDA reports)
ECONOMIC PROBLEM ( 119 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 119 FDA reports)
MOOD ALTERED ( 119 FDA reports)
FEELING JITTERY ( 118 FDA reports)
MOUTH ULCERATION ( 118 FDA reports)
PANCREATITIS ACUTE ( 118 FDA reports)
SINUS TACHYCARDIA ( 118 FDA reports)
ANGINA PECTORIS ( 117 FDA reports)
SEXUAL DYSFUNCTION ( 117 FDA reports)
VISUAL DISTURBANCE ( 117 FDA reports)
DISABILITY ( 116 FDA reports)
PRODUCT QUALITY ISSUE ( 116 FDA reports)
ADVERSE DRUG REACTION ( 115 FDA reports)
CARDIOMYOPATHY ( 115 FDA reports)
GASTROINTESTINAL DISORDER ( 115 FDA reports)
IMPAIRED DRIVING ABILITY ( 115 FDA reports)
INFLUENZA ( 115 FDA reports)
RETCHING ( 115 FDA reports)
EPISTAXIS ( 114 FDA reports)
FEELING HOT ( 114 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 114 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 114 FDA reports)
BRUXISM ( 113 FDA reports)
HYPOPHAGIA ( 113 FDA reports)
STAPHYLOCOCCAL INFECTION ( 113 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 112 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 112 FDA reports)
HAEMORRHAGE ( 112 FDA reports)
INTENTIONAL DRUG MISUSE ( 112 FDA reports)
THROMBOCYTOPENIA ( 112 FDA reports)
URINARY RETENTION ( 111 FDA reports)
CANDIDIASIS ( 111 FDA reports)
COMA ( 110 FDA reports)
OSTEOPENIA ( 110 FDA reports)
SCAR ( 110 FDA reports)
STOMATITIS ( 110 FDA reports)
DEAFNESS ( 109 FDA reports)
DYSPNOEA EXERTIONAL ( 109 FDA reports)
MASTICATION DISORDER ( 109 FDA reports)
PULMONARY HYPERTENSION ( 109 FDA reports)
DRUG SCREEN POSITIVE ( 108 FDA reports)
EJECTION FRACTION DECREASED ( 108 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 108 FDA reports)
INCREASED APPETITE ( 106 FDA reports)
LACERATION ( 106 FDA reports)
CYST ( 105 FDA reports)
SURGERY ( 105 FDA reports)
THYROID DISORDER ( 105 FDA reports)
TYPE 1 DIABETES MELLITUS ( 104 FDA reports)
FACIAL PAIN ( 104 FDA reports)
LEUKOCYTOSIS ( 104 FDA reports)
MOVEMENT DISORDER ( 103 FDA reports)
DELUSION ( 102 FDA reports)
INJECTION SITE ERYTHEMA ( 102 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 102 FDA reports)
ARRHYTHMIA ( 101 FDA reports)
MUSCLE STRAIN ( 101 FDA reports)
PERIODONTITIS ( 101 FDA reports)
BURSITIS ( 100 FDA reports)
CORONARY ARTERY OCCLUSION ( 100 FDA reports)
COLITIS ( 99 FDA reports)
RASH PRURITIC ( 99 FDA reports)
RHEUMATOID ARTHRITIS ( 99 FDA reports)
ROTATOR CUFF SYNDROME ( 99 FDA reports)
BLOOD POTASSIUM DECREASED ( 98 FDA reports)
EYE PAIN ( 98 FDA reports)
IMPAIRED WORK ABILITY ( 98 FDA reports)
PANCYTOPENIA ( 98 FDA reports)
HAEMATOCRIT DECREASED ( 97 FDA reports)
PLATELET COUNT DECREASED ( 97 FDA reports)
SKIN DISCOLOURATION ( 96 FDA reports)
VAGINAL HAEMORRHAGE ( 96 FDA reports)
BONE LESION ( 95 FDA reports)
CARDIAC MURMUR ( 95 FDA reports)
EATING DISORDER ( 95 FDA reports)
JOINT INJURY ( 95 FDA reports)
NEUTROPENIA ( 95 FDA reports)
PULMONARY OEDEMA ( 95 FDA reports)
SCOLIOSIS ( 95 FDA reports)
HOMICIDAL IDEATION ( 94 FDA reports)
INFLAMMATION ( 94 FDA reports)
INJECTION SITE REACTION ( 94 FDA reports)
CARPAL TUNNEL SYNDROME ( 93 FDA reports)
DRUG ABUSE ( 93 FDA reports)
EXCORIATION ( 93 FDA reports)
GINGIVAL DISORDER ( 93 FDA reports)
LOOSE TOOTH ( 93 FDA reports)
UTERINE LEIOMYOMA ( 93 FDA reports)
TENDERNESS ( 92 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 92 FDA reports)
ABASIA ( 92 FDA reports)
JAW DISORDER ( 92 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 92 FDA reports)
PSORIASIS ( 92 FDA reports)
SEROTONIN SYNDROME ( 92 FDA reports)
LUNG DISORDER ( 91 FDA reports)
PRODUCTIVE COUGH ( 91 FDA reports)
SPINAL COMPRESSION FRACTURE ( 91 FDA reports)
BLOOD PRESSURE DECREASED ( 90 FDA reports)
FLANK PAIN ( 90 FDA reports)
FOOT FRACTURE ( 90 FDA reports)
MALNUTRITION ( 90 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 90 FDA reports)
PERIODONTAL DISEASE ( 90 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 90 FDA reports)
SINUS CONGESTION ( 90 FDA reports)
MENISCUS LESION ( 89 FDA reports)
ABSCESS ( 88 FDA reports)
BONE DENSITY DECREASED ( 88 FDA reports)
CARDIO-RESPIRATORY ARREST ( 88 FDA reports)
MENTAL IMPAIRMENT ( 88 FDA reports)
SPINAL COLUMN STENOSIS ( 88 FDA reports)
BLINDNESS ( 87 FDA reports)
DELIRIUM ( 87 FDA reports)
DEVICE FAILURE ( 87 FDA reports)
DRUG ABUSER ( 87 FDA reports)
DRUG ADMINISTRATION ERROR ( 87 FDA reports)
ENDODONTIC PROCEDURE ( 87 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 87 FDA reports)
SKIN LACERATION ( 87 FDA reports)
MIDDLE INSOMNIA ( 86 FDA reports)
PRIMARY SEQUESTRUM ( 86 FDA reports)
PURULENT DISCHARGE ( 86 FDA reports)
SKIN LESION ( 86 FDA reports)
FUNGAL INFECTION ( 85 FDA reports)
LIMB INJURY ( 85 FDA reports)
TENDONITIS ( 85 FDA reports)
DIABETIC COMA ( 84 FDA reports)
DIVERTICULITIS ( 84 FDA reports)
BLOOD GLUCOSE DECREASED ( 83 FDA reports)
CHOLECYSTECTOMY ( 83 FDA reports)
DRUG TOXICITY ( 83 FDA reports)
MOBILITY DECREASED ( 83 FDA reports)
MULTIPLE MYELOMA ( 83 FDA reports)
RHINORRHOEA ( 83 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 83 FDA reports)
VENTRICULAR TACHYCARDIA ( 83 FDA reports)
JAW OPERATION ( 82 FDA reports)
MUSCLE TIGHTNESS ( 82 FDA reports)
CYSTITIS ( 81 FDA reports)
DRY SKIN ( 81 FDA reports)
HAEMOPTYSIS ( 81 FDA reports)
PERSONALITY CHANGE ( 81 FDA reports)
PHARYNGEAL OEDEMA ( 81 FDA reports)
SKIN DISORDER ( 81 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 80 FDA reports)
FISTULA ( 80 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 79 FDA reports)
RASH GENERALISED ( 79 FDA reports)
COLITIS ULCERATIVE ( 78 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 78 FDA reports)
MENORRHAGIA ( 78 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 78 FDA reports)
RESPIRATORY ARREST ( 78 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 77 FDA reports)
PRESYNCOPE ( 77 FDA reports)
CHRONIC SINUSITIS ( 76 FDA reports)
DEBRIDEMENT ( 76 FDA reports)
DISCOMFORT ( 76 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 76 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 76 FDA reports)
ACTINOMYCOSIS ( 75 FDA reports)
BLISTER ( 75 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 75 FDA reports)
COORDINATION ABNORMAL ( 75 FDA reports)
OESOPHAGITIS ( 75 FDA reports)
RESPIRATORY DISTRESS ( 75 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 74 FDA reports)
DRY EYE ( 74 FDA reports)
PALLOR ( 74 FDA reports)
PELVIC PAIN ( 74 FDA reports)
SENSORY DISTURBANCE ( 74 FDA reports)
SWOLLEN TONGUE ( 74 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 73 FDA reports)
PREGNANCY ( 73 FDA reports)
RENAL FAILURE CHRONIC ( 73 FDA reports)
BLOOD CREATININE INCREASED ( 72 FDA reports)
EYE SWELLING ( 72 FDA reports)
RENAL IMPAIRMENT ( 72 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 71 FDA reports)
INADEQUATE ANALGESIA ( 71 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 71 FDA reports)
ULCER ( 71 FDA reports)
VIRAL INFECTION ( 70 FDA reports)
FEMUR FRACTURE ( 70 FDA reports)
HAEMATOMA ( 70 FDA reports)
JAUNDICE ( 70 FDA reports)
RENAL DISORDER ( 70 FDA reports)
ANGINA UNSTABLE ( 69 FDA reports)
CERVICAL SPINAL STENOSIS ( 69 FDA reports)
DRUG TOLERANCE ( 69 FDA reports)
DYSLIPIDAEMIA ( 69 FDA reports)
DYSPHEMIA ( 69 FDA reports)
GOUT ( 69 FDA reports)
MYOCARDIAL ISCHAEMIA ( 69 FDA reports)
NERVOUS SYSTEM DISORDER ( 69 FDA reports)
APATHY ( 68 FDA reports)
GASTRIC DISORDER ( 68 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 68 FDA reports)
LIVER DISORDER ( 68 FDA reports)
METRORRHAGIA ( 68 FDA reports)
ABDOMINAL PAIN LOWER ( 67 FDA reports)
BONE LOSS ( 67 FDA reports)
FLUID RETENTION ( 67 FDA reports)
HEPATOMEGALY ( 67 FDA reports)
JOINT EFFUSION ( 67 FDA reports)
LYMPHOEDEMA ( 67 FDA reports)
SKIN ULCER ( 67 FDA reports)
EUPHORIC MOOD ( 66 FDA reports)
INJECTION SITE HAEMATOMA ( 66 FDA reports)
IRON DEFICIENCY ANAEMIA ( 66 FDA reports)
NEOPLASM PROGRESSION ( 66 FDA reports)
OSTEITIS ( 66 FDA reports)
SKIN EXFOLIATION ( 66 FDA reports)
ANAPHYLACTIC REACTION ( 65 FDA reports)
ATAXIA ( 65 FDA reports)
CHOLECYSTITIS ACUTE ( 65 FDA reports)
GINGIVAL BLEEDING ( 65 FDA reports)
HEPATIC CYST ( 65 FDA reports)
HOSTILITY ( 65 FDA reports)
PATHOLOGICAL FRACTURE ( 65 FDA reports)
RADICULOPATHY ( 65 FDA reports)
SPONDYLOLISTHESIS ( 65 FDA reports)
ACCIDENTAL OVERDOSE ( 64 FDA reports)
BACK DISORDER ( 64 FDA reports)
BONE DEBRIDEMENT ( 64 FDA reports)
NEURALGIA ( 64 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 64 FDA reports)
GINGIVAL PAIN ( 63 FDA reports)
INCONTINENCE ( 63 FDA reports)
BILIARY DYSKINESIA ( 62 FDA reports)
ECZEMA ( 62 FDA reports)
ENCEPHALOPATHY ( 62 FDA reports)
JOINT SPRAIN ( 62 FDA reports)
OTITIS MEDIA ( 62 FDA reports)
ATRIAL SEPTAL DEFECT ( 61 FDA reports)
BLADDER DISORDER ( 61 FDA reports)
DEMENTIA ( 61 FDA reports)
INITIAL INSOMNIA ( 61 FDA reports)
INJECTION SITE HAEMORRHAGE ( 61 FDA reports)
SCIATICA ( 61 FDA reports)
STOMACH DISCOMFORT ( 61 FDA reports)
ILEUS ( 60 FDA reports)
INTENTIONAL SELF-INJURY ( 60 FDA reports)
LUNG NEOPLASM MALIGNANT ( 60 FDA reports)
PERICARDIAL EFFUSION ( 60 FDA reports)
RHABDOMYOLYSIS ( 60 FDA reports)
RHINITIS ( 60 FDA reports)
TEARFULNESS ( 60 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 59 FDA reports)
GASTROENTERITIS VIRAL ( 59 FDA reports)
HIP FRACTURE ( 59 FDA reports)
PANIC DISORDER ( 59 FDA reports)
PNEUMOTHORAX ( 59 FDA reports)
TENSION ( 59 FDA reports)
VENTRICULAR HYPERTROPHY ( 59 FDA reports)
CARDIAC FAILURE ( 58 FDA reports)
FLUID OVERLOAD ( 58 FDA reports)
GASTROENTERITIS ( 58 FDA reports)
HEPATITIS C ( 58 FDA reports)
LUNG INFILTRATION ( 58 FDA reports)
MENSTRUATION IRREGULAR ( 58 FDA reports)
ORAL CANDIDIASIS ( 58 FDA reports)
PHYSICAL DISABILITY ( 58 FDA reports)
PNEUMONIA ASPIRATION ( 58 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 58 FDA reports)
BARRETT'S OESOPHAGUS ( 57 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 57 FDA reports)
CEREBRAL ISCHAEMIA ( 57 FDA reports)
GINGIVAL RECESSION ( 57 FDA reports)
LEUKOPENIA ( 57 FDA reports)
LIFE EXPECTANCY SHORTENED ( 57 FDA reports)
MUCOSAL INFLAMMATION ( 57 FDA reports)
ORAL CAVITY FISTULA ( 57 FDA reports)
VITREOUS FLOATERS ( 57 FDA reports)
THROAT TIGHTNESS ( 56 FDA reports)
BREAST MASS ( 56 FDA reports)
COLD SWEAT ( 56 FDA reports)
HEART RATE DECREASED ( 56 FDA reports)
ONYCHOMYCOSIS ( 56 FDA reports)
ORAL DISORDER ( 56 FDA reports)
ABORTION SPONTANEOUS ( 55 FDA reports)
AFFECTIVE DISORDER ( 55 FDA reports)
ANGIOPATHY ( 55 FDA reports)
BONE EROSION ( 55 FDA reports)
BRADYCARDIA ( 55 FDA reports)
DYSSTASIA ( 55 FDA reports)
GASTRIC ULCER ( 55 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 55 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 55 FDA reports)
HEART RATE IRREGULAR ( 55 FDA reports)
HYSTERECTOMY ( 55 FDA reports)
INTERSTITIAL LUNG DISEASE ( 55 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 55 FDA reports)
LOCAL SWELLING ( 55 FDA reports)
MULTIPLE INJURIES ( 55 FDA reports)
PANIC REACTION ( 55 FDA reports)
SCREAMING ( 55 FDA reports)
SPINAL FRACTURE ( 55 FDA reports)
TENDON RUPTURE ( 55 FDA reports)
TOOTH INFECTION ( 55 FDA reports)
LACRIMATION INCREASED ( 54 FDA reports)
MICTURITION URGENCY ( 54 FDA reports)
NICOTINE DEPENDENCE ( 54 FDA reports)
POST PROCEDURAL COMPLICATION ( 54 FDA reports)
PRESCRIBED OVERDOSE ( 54 FDA reports)
RADIOTHERAPY ( 54 FDA reports)
RASH ERYTHEMATOUS ( 54 FDA reports)
STEVENS-JOHNSON SYNDROME ( 54 FDA reports)
BLOOD SODIUM DECREASED ( 53 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 53 FDA reports)
DEPENDENCE ( 53 FDA reports)
DISEASE PROGRESSION ( 53 FDA reports)
HYPERKALAEMIA ( 53 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 53 FDA reports)
METASTASES TO LUNG ( 53 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 52 FDA reports)
DENTAL FISTULA ( 52 FDA reports)
DYSTONIA ( 52 FDA reports)
EXPOSED BONE IN JAW ( 52 FDA reports)
JAW FRACTURE ( 52 FDA reports)
SINUS BRADYCARDIA ( 52 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 52 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 52 FDA reports)
DIFFICULTY IN WALKING ( 51 FDA reports)
ECCHYMOSIS ( 51 FDA reports)
HAEMATEMESIS ( 51 FDA reports)
INTESTINAL OBSTRUCTION ( 51 FDA reports)
NOCTURIA ( 51 FDA reports)
PULMONARY FIBROSIS ( 51 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 50 FDA reports)
DERMATITIS ( 50 FDA reports)
DYSTHYMIC DISORDER ( 50 FDA reports)
FAECAL INCONTINENCE ( 50 FDA reports)
GROIN PAIN ( 50 FDA reports)
INTERMITTENT CLAUDICATION ( 50 FDA reports)
LARYNGITIS ( 50 FDA reports)
LEFT ATRIAL DILATATION ( 50 FDA reports)
UNRESPONSIVE TO STIMULI ( 50 FDA reports)
WOUND DEHISCENCE ( 50 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 49 FDA reports)
BREAST TENDERNESS ( 49 FDA reports)
CONJUNCTIVITIS ( 49 FDA reports)
HYPOVOLAEMIA ( 49 FDA reports)
LUMBAR SPINAL STENOSIS ( 49 FDA reports)
MASS ( 49 FDA reports)
POLYURIA ( 49 FDA reports)
PROTHROMBIN TIME PROLONGED ( 49 FDA reports)
SOMNAMBULISM ( 49 FDA reports)
ACNE ( 48 FDA reports)
AFFECT LABILITY ( 48 FDA reports)
BRAIN INJURY ( 48 FDA reports)
HYDRONEPHROSIS ( 48 FDA reports)
NON-CARDIAC CHEST PAIN ( 48 FDA reports)
SENSITIVITY OF TEETH ( 48 FDA reports)
ACUTE RESPIRATORY FAILURE ( 47 FDA reports)
AMENORRHOEA ( 47 FDA reports)
ANKLE FRACTURE ( 47 FDA reports)
BASAL CELL CARCINOMA ( 47 FDA reports)
CYANOSIS ( 47 FDA reports)
GLOSSODYNIA ( 47 FDA reports)
HYPOCALCAEMIA ( 47 FDA reports)
LIP SWELLING ( 47 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 47 FDA reports)
MULTIPLE DRUG OVERDOSE ( 47 FDA reports)
PNEUMONITIS ( 47 FDA reports)
VITAMIN B12 DEFICIENCY ( 47 FDA reports)
BONE NEOPLASM MALIGNANT ( 46 FDA reports)
DIABETIC NEPHROPATHY ( 46 FDA reports)
DRUG INTOLERANCE ( 46 FDA reports)
GINGIVAL INFECTION ( 46 FDA reports)
HEMIPARESIS ( 46 FDA reports)
METABOLIC DISORDER ( 46 FDA reports)
MUSCULOSKELETAL DISORDER ( 46 FDA reports)
PATHOLOGICAL GAMBLING ( 46 FDA reports)
POLYDIPSIA ( 46 FDA reports)
BLOOD CALCIUM DECREASED ( 45 FDA reports)
ENERGY INCREASED ( 45 FDA reports)
HOSPITALISATION ( 45 FDA reports)
MITRAL VALVE PROLAPSE ( 45 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 45 FDA reports)
ORTHOSTATIC HYPOTENSION ( 45 FDA reports)
OSTEOSCLEROSIS ( 45 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 45 FDA reports)
POOR QUALITY SLEEP ( 45 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 45 FDA reports)
PULMONARY CONGESTION ( 45 FDA reports)
RHINITIS ALLERGIC ( 45 FDA reports)
STEM CELL TRANSPLANT ( 45 FDA reports)
TIBIA FRACTURE ( 45 FDA reports)
WOUND ( 45 FDA reports)
TONGUE BITING ( 44 FDA reports)
VENTRICULAR FIBRILLATION ( 44 FDA reports)
AKATHISIA ( 44 FDA reports)
BACTERAEMIA ( 44 FDA reports)
BACTERIAL INFECTION ( 44 FDA reports)
DIVERTICULUM INTESTINAL ( 44 FDA reports)
FEELING COLD ( 44 FDA reports)
HYPERKERATOSIS ( 44 FDA reports)
HYPERPHAGIA ( 44 FDA reports)
KYPHOSIS ( 44 FDA reports)
METASTASES TO SPINE ( 44 FDA reports)
MOTOR DYSFUNCTION ( 44 FDA reports)
MYOPATHY ( 44 FDA reports)
PARAESTHESIA ORAL ( 44 FDA reports)
PROCEDURAL PAIN ( 44 FDA reports)
CAROTID ARTERY STENOSIS ( 43 FDA reports)
EAR DISCOMFORT ( 43 FDA reports)
HYPOMAGNESAEMIA ( 43 FDA reports)
OSTEOLYSIS ( 43 FDA reports)
SEASONAL ALLERGY ( 43 FDA reports)
SELF-INJURIOUS IDEATION ( 43 FDA reports)
TESTICULAR PAIN ( 43 FDA reports)
THROAT IRRITATION ( 43 FDA reports)
VISUAL FIELD DEFECT ( 43 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 42 FDA reports)
ANXIETY DISORDER ( 42 FDA reports)
BIPOLAR I DISORDER ( 42 FDA reports)
BLOOD UREA INCREASED ( 42 FDA reports)
CEREBRAL INFARCTION ( 42 FDA reports)
DIABETIC RETINOPATHY ( 42 FDA reports)
DISSOCIATION ( 42 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 42 FDA reports)
EYE IRRITATION ( 42 FDA reports)
FEELING OF DESPAIR ( 42 FDA reports)
GENERALISED ANXIETY DISORDER ( 42 FDA reports)
HYPOACUSIS ( 42 FDA reports)
HYPOKINESIA ( 42 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 42 FDA reports)
INJECTION SITE PRURITUS ( 42 FDA reports)
KNEE ARTHROPLASTY ( 42 FDA reports)
LOCALISED INFECTION ( 42 FDA reports)
MYOCLONUS ( 42 FDA reports)
PARALYSIS ( 42 FDA reports)
RASH MACULAR ( 42 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 42 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 42 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 41 FDA reports)
DERMATITIS CONTACT ( 41 FDA reports)
DEVICE RELATED INFECTION ( 41 FDA reports)
DIABETIC COMPLICATION ( 41 FDA reports)
FEELING DRUNK ( 41 FDA reports)
HEARING IMPAIRED ( 41 FDA reports)
HUNGER ( 41 FDA reports)
HYPOAESTHESIA ORAL ( 41 FDA reports)
INFUSION RELATED REACTION ( 41 FDA reports)
TENDON DISORDER ( 41 FDA reports)
WHEELCHAIR USER ( 41 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 40 FDA reports)
VULVOVAGINAL DRYNESS ( 40 FDA reports)
ALCOHOLISM ( 40 FDA reports)
BODY TEMPERATURE INCREASED ( 40 FDA reports)
CERUMEN IMPACTION ( 40 FDA reports)
COAGULOPATHY ( 40 FDA reports)
DENTURE WEARER ( 40 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 40 FDA reports)
ERUCTATION ( 40 FDA reports)
HYPOMANIA ( 40 FDA reports)
PHOTOPHOBIA ( 40 FDA reports)
RESPIRATORY DISORDER ( 40 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 40 FDA reports)
ACUTE SINUSITIS ( 39 FDA reports)
BREAST CANCER METASTATIC ( 39 FDA reports)
CATARACT OPERATION ( 39 FDA reports)
CONCUSSION ( 39 FDA reports)
DERMAL CYST ( 39 FDA reports)
DYSAESTHESIA ( 39 FDA reports)
EPILEPSY ( 39 FDA reports)
METABOLIC SYNDROME ( 39 FDA reports)
NO ADVERSE EVENT ( 39 FDA reports)
ORAL INFECTION ( 39 FDA reports)
OVARIAN CYST ( 39 FDA reports)
PROTEINURIA ( 39 FDA reports)
STRESS URINARY INCONTINENCE ( 39 FDA reports)
AZOTAEMIA ( 38 FDA reports)
CAESAREAN SECTION ( 38 FDA reports)
COLITIS ISCHAEMIC ( 38 FDA reports)
DISEASE RECURRENCE ( 38 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 38 FDA reports)
INJECTION SITE SWELLING ( 38 FDA reports)
LIMB DISCOMFORT ( 38 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 38 FDA reports)
MENSTRUAL DISORDER ( 38 FDA reports)
NEOPLASM ( 38 FDA reports)
OXYGEN SATURATION DECREASED ( 38 FDA reports)
SKIN PAPILLOMA ( 38 FDA reports)
ABDOMINAL TENDERNESS ( 37 FDA reports)
ALCOHOL USE ( 37 FDA reports)
BLOOD BILIRUBIN INCREASED ( 37 FDA reports)
CHROMATURIA ( 37 FDA reports)
CORONARY ARTERY STENOSIS ( 37 FDA reports)
EYE DISORDER ( 37 FDA reports)
LIGAMENT SPRAIN ( 37 FDA reports)
LIPOMA ( 37 FDA reports)
MULTI-ORGAN FAILURE ( 37 FDA reports)
NECK INJURY ( 37 FDA reports)
NO THERAPEUTIC RESPONSE ( 37 FDA reports)
NODULE ( 37 FDA reports)
PARKINSONISM ( 37 FDA reports)
RESPIRATORY TRACT INFECTION ( 37 FDA reports)
SINUS HEADACHE ( 37 FDA reports)
SPLENOMEGALY ( 37 FDA reports)
AORTIC VALVE INCOMPETENCE ( 36 FDA reports)
BLOOD PRESSURE ABNORMAL ( 36 FDA reports)
BONE MARROW FAILURE ( 36 FDA reports)
FAILURE TO THRIVE ( 36 FDA reports)
GINGIVAL SWELLING ( 36 FDA reports)
HERNIA ( 36 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 36 FDA reports)
SUICIDAL BEHAVIOUR ( 36 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 36 FDA reports)
VAGINAL DISCHARGE ( 36 FDA reports)
TONGUE DISORDER ( 35 FDA reports)
AORTIC STENOSIS ( 35 FDA reports)
BREAST CANCER FEMALE ( 35 FDA reports)
CARDIOVASCULAR DISORDER ( 35 FDA reports)
DRUG PRESCRIBING ERROR ( 35 FDA reports)
GALLBLADDER INJURY ( 35 FDA reports)
GASTROINTESTINAL PAIN ( 35 FDA reports)
GINGIVITIS ( 35 FDA reports)
HYPERTENSIVE HEART DISEASE ( 35 FDA reports)
METASTASES TO LYMPH NODES ( 35 FDA reports)
PANCREATITIS CHRONIC ( 35 FDA reports)
PARKINSON'S DISEASE ( 35 FDA reports)
PERIPHERAL COLDNESS ( 35 FDA reports)
PLEURAL FIBROSIS ( 35 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 35 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 35 FDA reports)
FRACTURE ( 34 FDA reports)
GINGIVAL EROSION ( 34 FDA reports)
GUN SHOT WOUND ( 34 FDA reports)
HEPATITIS ( 34 FDA reports)
HIP ARTHROPLASTY ( 34 FDA reports)
HYPERPLASIA ( 34 FDA reports)
HYPERTHYROIDISM ( 34 FDA reports)
HYPERVENTILATION ( 34 FDA reports)
INCREASED TENDENCY TO BRUISE ( 34 FDA reports)
MELANOCYTIC NAEVUS ( 34 FDA reports)
PETIT MAL EPILEPSY ( 34 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 34 FDA reports)
RETINOPATHY ( 34 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 34 FDA reports)
TOOTH IMPACTED ( 34 FDA reports)
THERMAL BURN ( 33 FDA reports)
TOOTH INJURY ( 33 FDA reports)
ALCOHOL POISONING ( 33 FDA reports)
APPLICATION SITE ERYTHEMA ( 33 FDA reports)
BREAST PAIN ( 33 FDA reports)
BUNION ( 33 FDA reports)
FLAT AFFECT ( 33 FDA reports)
FORMICATION ( 33 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 33 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 33 FDA reports)
LOSS OF LIBIDO ( 33 FDA reports)
METASTASES TO LIVER ( 33 FDA reports)
PAROSMIA ( 33 FDA reports)
PHOTOSENSITIVITY REACTION ( 33 FDA reports)
PLEURITIC PAIN ( 33 FDA reports)
PREMATURE BABY ( 33 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 33 FDA reports)
BEDRIDDEN ( 32 FDA reports)
BONE FRAGMENTATION ( 32 FDA reports)
CEREBRAL ATROPHY ( 32 FDA reports)
CEREBROVASCULAR DISORDER ( 32 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 32 FDA reports)
FAECES DISCOLOURED ( 32 FDA reports)
FOOD CRAVING ( 32 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 32 FDA reports)
GENERALISED OEDEMA ( 32 FDA reports)
HERPES SIMPLEX ( 32 FDA reports)
HYPERCALCAEMIA ( 32 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 32 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 32 FDA reports)
LOWER LIMB FRACTURE ( 32 FDA reports)
LUNG INFECTION ( 32 FDA reports)
MUSCLE ATROPHY ( 32 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 32 FDA reports)
ORAL HERPES ( 32 FDA reports)
PEPTIC ULCER ( 32 FDA reports)
POLYNEUROPATHY ( 32 FDA reports)
RENAL INJURY ( 32 FDA reports)
SHOULDER PAIN ( 32 FDA reports)
THERAPY NON-RESPONDER ( 32 FDA reports)
UTERINE HAEMORRHAGE ( 32 FDA reports)
APPENDICECTOMY ( 31 FDA reports)
BILIARY COLIC ( 31 FDA reports)
BLOOD URINE PRESENT ( 31 FDA reports)
BREAST CYST ( 31 FDA reports)
CHRONIC FATIGUE SYNDROME ( 31 FDA reports)
DECUBITUS ULCER ( 31 FDA reports)
EYE DISCHARGE ( 31 FDA reports)
FACE OEDEMA ( 31 FDA reports)
FURUNCLE ( 31 FDA reports)
GLYCOSURIA ( 31 FDA reports)
HAEMANGIOMA ( 31 FDA reports)
JOINT STIFFNESS ( 31 FDA reports)
LOBAR PNEUMONIA ( 31 FDA reports)
METABOLIC ACIDOSIS ( 31 FDA reports)
MUSCLE SPASTICITY ( 31 FDA reports)
NERVE COMPRESSION ( 31 FDA reports)
PLANTAR FASCIITIS ( 31 FDA reports)
PULMONARY MASS ( 31 FDA reports)
SINUS POLYP ( 31 FDA reports)
SKIN BURNING SENSATION ( 31 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 31 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 30 FDA reports)
AGEUSIA ( 30 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 30 FDA reports)
ASCITES ( 30 FDA reports)
CEREBRAL HAEMORRHAGE ( 30 FDA reports)
DILATATION VENTRICULAR ( 30 FDA reports)
HYPERAESTHESIA ( 30 FDA reports)
INJECTION SITE BRUISING ( 30 FDA reports)
MASTECTOMY ( 30 FDA reports)
MUSCLE DISORDER ( 30 FDA reports)
NEUROPATHY ( 30 FDA reports)
PHARYNGITIS ( 30 FDA reports)
RASH PAPULAR ( 30 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 30 FDA reports)
SMOKER ( 30 FDA reports)
STATUS EPILEPTICUS ( 30 FDA reports)
STRESS FRACTURE ( 30 FDA reports)
TIC ( 30 FDA reports)
TOOTH DEPOSIT ( 30 FDA reports)
WRIST FRACTURE ( 30 FDA reports)
THIRST ( 29 FDA reports)
ANORGASMIA ( 29 FDA reports)
ASBESTOSIS ( 29 FDA reports)
BILE DUCT STONE ( 29 FDA reports)
BLOOD ALBUMIN DECREASED ( 29 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 29 FDA reports)
CAROTID ARTERY OCCLUSION ( 29 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 29 FDA reports)
CHOKING ( 29 FDA reports)
DENTAL PLAQUE ( 29 FDA reports)
DENTAL PROSTHESIS USER ( 29 FDA reports)
EAR INFECTION ( 29 FDA reports)
ELECTROLYTE IMBALANCE ( 29 FDA reports)
FOLLICULITIS ( 29 FDA reports)
FRUSTRATION ( 29 FDA reports)
HEPATIC LESION ( 29 FDA reports)
HYPOAESTHESIA FACIAL ( 29 FDA reports)
JOINT DISLOCATION ( 29 FDA reports)
LOW TURNOVER OSTEOPATHY ( 29 FDA reports)
MENOPAUSE ( 29 FDA reports)
MUSCLE RIGIDITY ( 29 FDA reports)
NEUROMA ( 29 FDA reports)
PAIN OF SKIN ( 29 FDA reports)
PRURITUS GENERALISED ( 29 FDA reports)
SEQUESTRECTOMY ( 29 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 29 FDA reports)
BACTERIAL DISEASE CARRIER ( 28 FDA reports)
BREAST CANCER IN SITU ( 28 FDA reports)
COCCYDYNIA ( 28 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 28 FDA reports)
DEPRESSION SUICIDAL ( 28 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 28 FDA reports)
DUODENITIS ( 28 FDA reports)
GLAUCOMA ( 28 FDA reports)
LIPASE INCREASED ( 28 FDA reports)
LUMBAR RADICULOPATHY ( 28 FDA reports)
MEDICATION RESIDUE ( 28 FDA reports)
MIGRAINE WITH AURA ( 28 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 28 FDA reports)
ORGAN FAILURE ( 28 FDA reports)
PLATELET COUNT INCREASED ( 28 FDA reports)
PLEURISY ( 28 FDA reports)
SEPTIC SHOCK ( 28 FDA reports)
SHOCK ( 28 FDA reports)
SKIN HYPERPIGMENTATION ( 28 FDA reports)
SLEEP WALKING ( 28 FDA reports)
TINEA PEDIS ( 28 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 28 FDA reports)
URINE OUTPUT DECREASED ( 28 FDA reports)
VENTRICULAR HYPOKINESIA ( 28 FDA reports)
TOBACCO USER ( 27 FDA reports)
UNDERDOSE ( 27 FDA reports)
ALVEOLOPLASTY ( 27 FDA reports)
ANAPHYLACTIC SHOCK ( 27 FDA reports)
ANIMAL BITE ( 27 FDA reports)
ASPIRATION ( 27 FDA reports)
BLOOD MAGNESIUM DECREASED ( 27 FDA reports)
BODY HEIGHT DECREASED ( 27 FDA reports)
BONE SCAN ABNORMAL ( 27 FDA reports)
BREAST CANCER RECURRENT ( 27 FDA reports)
DENTAL OPERATION ( 27 FDA reports)
FACE INJURY ( 27 FDA reports)
FEELINGS OF WORTHLESSNESS ( 27 FDA reports)
FIBULA FRACTURE ( 27 FDA reports)
KIDNEY INFECTION ( 27 FDA reports)
LOSS OF EMPLOYMENT ( 27 FDA reports)
MELAENA ( 27 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 27 FDA reports)
MUSCLE INJURY ( 27 FDA reports)
SCHIZOPHRENIA ( 27 FDA reports)
SKIN IRRITATION ( 27 FDA reports)
SYNOVIAL CYST ( 27 FDA reports)
AGORAPHOBIA ( 26 FDA reports)
APPENDICITIS ( 26 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 26 FDA reports)
BLINDNESS UNILATERAL ( 26 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 26 FDA reports)
CONVERSION DISORDER ( 26 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 26 FDA reports)
CYSTOCELE ( 26 FDA reports)
DIASTOLIC DYSFUNCTION ( 26 FDA reports)
DILATATION ATRIAL ( 26 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 26 FDA reports)
EXPIRED DRUG ADMINISTERED ( 26 FDA reports)
FAMILY STRESS ( 26 FDA reports)
FEBRILE NEUTROPENIA ( 26 FDA reports)
GINGIVAL ULCERATION ( 26 FDA reports)
GOITRE ( 26 FDA reports)
HEMIPLEGIA ( 26 FDA reports)
INCOHERENT ( 26 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 26 FDA reports)
KETOACIDOSIS ( 26 FDA reports)
LIBIDO INCREASED ( 26 FDA reports)
LIGAMENT RUPTURE ( 26 FDA reports)
NEOPLASM RECURRENCE ( 26 FDA reports)
NEUROGENIC BLADDER ( 26 FDA reports)
OCULAR HYPERAEMIA ( 26 FDA reports)
PERFORMANCE STATUS DECREASED ( 26 FDA reports)
QRS AXIS ABNORMAL ( 26 FDA reports)
QUALITY OF LIFE DECREASED ( 26 FDA reports)
REFLUX OESOPHAGITIS ( 26 FDA reports)
SALIVARY HYPERSECRETION ( 26 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 26 FDA reports)
SKIN NEOPLASM EXCISION ( 26 FDA reports)
STREPTOCOCCAL INFECTION ( 26 FDA reports)
SUDDEN DEATH ( 26 FDA reports)
SYNCOPE VASOVAGAL ( 26 FDA reports)
WEIGHT FLUCTUATION ( 26 FDA reports)
TRISMUS ( 25 FDA reports)
UPPER LIMB FRACTURE ( 25 FDA reports)
URINARY HESITATION ( 25 FDA reports)
ANGIOEDEMA ( 25 FDA reports)
ATHEROSCLEROSIS ( 25 FDA reports)
BIFASCICULAR BLOCK ( 25 FDA reports)
BLADDER MASS ( 25 FDA reports)
BLADDER NEOPLASM ( 25 FDA reports)
BRONCHOSPASM ( 25 FDA reports)
CAROTID ARTERY DISEASE ( 25 FDA reports)
CERVICOBRACHIAL SYNDROME ( 25 FDA reports)
CLAUSTROPHOBIA ( 25 FDA reports)
DEMYELINATION ( 25 FDA reports)
DRUG DISPENSING ERROR ( 25 FDA reports)
EYELID PTOSIS ( 25 FDA reports)
INJECTION SITE RASH ( 25 FDA reports)
INJECTION SITE URTICARIA ( 25 FDA reports)
INTESTINAL HAEMORRHAGE ( 25 FDA reports)
LABYRINTHITIS ( 25 FDA reports)
LACTOSE INTOLERANCE ( 25 FDA reports)
NERVE INJURY ( 25 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 25 FDA reports)
POSTICTAL STATE ( 25 FDA reports)
POSTURE ABNORMAL ( 25 FDA reports)
PROCTALGIA ( 25 FDA reports)
PSYCHIATRIC SYMPTOM ( 25 FDA reports)
SPINAL DISORDER ( 25 FDA reports)
SUBSTANCE ABUSE ( 25 FDA reports)
ANEURYSM ( 24 FDA reports)
BLADDER CANCER ( 24 FDA reports)
BLADDER PROLAPSE ( 24 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 24 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 24 FDA reports)
CATHETERISATION CARDIAC ( 24 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 24 FDA reports)
DYSPHORIA ( 24 FDA reports)
EDENTULOUS ( 24 FDA reports)
FACIAL PALSY ( 24 FDA reports)
FEELING GUILTY ( 24 FDA reports)
FIBROUS HISTIOCYTOMA ( 24 FDA reports)
GASTRIC POLYPS ( 24 FDA reports)
GINGIVAL OEDEMA ( 24 FDA reports)
GYNAECOMASTIA ( 24 FDA reports)
HAEMORRHAGIC STROKE ( 24 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 24 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 24 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 24 FDA reports)
INTENTIONAL MISUSE ( 24 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 24 FDA reports)
LIVER INJURY ( 24 FDA reports)
MACULOPATHY ( 24 FDA reports)
MICROCYTIC ANAEMIA ( 24 FDA reports)
MYDRIASIS ( 24 FDA reports)
MYOSITIS ( 24 FDA reports)
OPTIC NEURITIS ( 24 FDA reports)
ORAL INTAKE REDUCED ( 24 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 24 FDA reports)
PERICARDITIS ( 24 FDA reports)
PERIPHERAL ISCHAEMIA ( 24 FDA reports)
PRESBYOPIA ( 24 FDA reports)
PRODUCT ADHESION ISSUE ( 24 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 24 FDA reports)
SENSATION OF HEAVINESS ( 24 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 24 FDA reports)
TRAUMATIC BRAIN INJURY ( 24 FDA reports)
TONGUE INJURY ( 23 FDA reports)
VENOUS INSUFFICIENCY ( 23 FDA reports)
WOUND HAEMORRHAGE ( 23 FDA reports)
ACIDOSIS ( 23 FDA reports)
ADRENAL DISORDER ( 23 FDA reports)
ANGIONEUROTIC OEDEMA ( 23 FDA reports)
APPLICATION SITE PRURITUS ( 23 FDA reports)
APPLICATION SITE RASH ( 23 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 23 FDA reports)
BRAIN NEOPLASM ( 23 FDA reports)
CIRCULATORY COLLAPSE ( 23 FDA reports)
DIABETIC FOOT ( 23 FDA reports)
DRUG EFFECT INCREASED ( 23 FDA reports)
ECZEMA ASTEATOTIC ( 23 FDA reports)
EMPYEMA ( 23 FDA reports)
ESSENTIAL HYPERTENSION ( 23 FDA reports)
EYE HAEMORRHAGE ( 23 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 23 FDA reports)
FOOT DEFORMITY ( 23 FDA reports)
GALLBLADDER OPERATION ( 23 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 23 FDA reports)
HALLUCINATIONS, MIXED ( 23 FDA reports)
ICHTHYOSIS ( 23 FDA reports)
IMPULSIVE BEHAVIOUR ( 23 FDA reports)
ISCHAEMIA ( 23 FDA reports)
ISCHAEMIC STROKE ( 23 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 23 FDA reports)
MEDICAL DEVICE REMOVAL ( 23 FDA reports)
MOUTH HAEMORRHAGE ( 23 FDA reports)
OESOPHAGEAL SPASM ( 23 FDA reports)
ORAL DISCHARGE ( 23 FDA reports)
ORAL MUCOSA ATROPHY ( 23 FDA reports)
OSTEITIS DEFORMANS ( 23 FDA reports)
POST CONCUSSION SYNDROME ( 23 FDA reports)
STOOL ANALYSIS ABNORMAL ( 23 FDA reports)
ABSCESS DRAINAGE ( 22 FDA reports)
ACUTE CORONARY SYNDROME ( 22 FDA reports)
ADENOCARCINOMA ( 22 FDA reports)
APNOEA ( 22 FDA reports)
ATROPHIC VULVOVAGINITIS ( 22 FDA reports)
AUTOIMMUNE DISORDER ( 22 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 22 FDA reports)
BRAIN CONTUSION ( 22 FDA reports)
CLOSTRIDIAL INFECTION ( 22 FDA reports)
CONGENITAL ANOMALY ( 22 FDA reports)
DRUG ERUPTION ( 22 FDA reports)
EYE MOVEMENT DISORDER ( 22 FDA reports)
FIBROSIS ( 22 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 22 FDA reports)
HEPATIC FAILURE ( 22 FDA reports)
HYPOGONADISM ( 22 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 22 FDA reports)
LOSS OF CONTROL OF LEGS ( 22 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 22 FDA reports)
MULTIPLE ALLERGIES ( 22 FDA reports)
MUSCLE CRAMP ( 22 FDA reports)
MYOPIA ( 22 FDA reports)
NEURODERMATITIS ( 22 FDA reports)
ODYNOPHAGIA ( 22 FDA reports)
PHLEBITIS ( 22 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 22 FDA reports)
PULSE ABSENT ( 22 FDA reports)
RADIATION INJURY ( 22 FDA reports)
RADIUS FRACTURE ( 22 FDA reports)
RESPIRATORY RATE INCREASED ( 22 FDA reports)
STARING ( 22 FDA reports)
TACHYARRHYTHMIA ( 22 FDA reports)
TENSION HEADACHE ( 22 FDA reports)
THYROID NEOPLASM ( 22 FDA reports)
UTERINE DISORDER ( 22 FDA reports)
VARICOSE VEIN ( 22 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 22 FDA reports)
TERMINAL INSOMNIA ( 21 FDA reports)
THORACOTOMY ( 21 FDA reports)
TONGUE COATED ( 21 FDA reports)
VAGINAL INFECTION ( 21 FDA reports)
ANOGENITAL WARTS ( 21 FDA reports)
APHAGIA ( 21 FDA reports)
APHONIA ( 21 FDA reports)
ATRIAL FLUTTER ( 21 FDA reports)
AUTOIMMUNE HEPATITIS ( 21 FDA reports)
BUTTOCK PAIN ( 21 FDA reports)
CARDIAC VALVE DISEASE ( 21 FDA reports)
COLLAPSE OF LUNG ( 21 FDA reports)
COMPRESSION FRACTURE ( 21 FDA reports)
DEAFNESS UNILATERAL ( 21 FDA reports)
EPIDIDYMITIS ( 21 FDA reports)
FEMORAL NECK FRACTURE ( 21 FDA reports)
HEPATIC CIRRHOSIS ( 21 FDA reports)
HODGKIN'S DISEASE ( 21 FDA reports)
HYPOTHERMIA ( 21 FDA reports)
INGROWING NAIL ( 21 FDA reports)
INTRACRANIAL ANEURYSM ( 21 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 21 FDA reports)
KLEBSIELLA INFECTION ( 21 FDA reports)
LYMPHADENITIS ( 21 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 21 FDA reports)
MYELOPATHY ( 21 FDA reports)
OESOPHAGEAL DISORDER ( 21 FDA reports)
OPEN WOUND ( 21 FDA reports)
ORTHODONTIC APPLIANCE USER ( 21 FDA reports)
PROCEDURAL COMPLICATION ( 21 FDA reports)
PROSTATE CANCER ( 21 FDA reports)
SCRATCH ( 21 FDA reports)
SENSORY LOSS ( 21 FDA reports)
SINUS OPERATION ( 21 FDA reports)
SOFT TISSUE DISORDER ( 21 FDA reports)
SOFT TISSUE INFLAMMATION ( 21 FDA reports)
SUBDURAL HAEMATOMA ( 21 FDA reports)
ABDOMINAL ADHESIONS ( 20 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 20 FDA reports)
ALCOHOL ABUSE ( 20 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 20 FDA reports)
ARTHROPOD BITE ( 20 FDA reports)
BIOPSY BONE ( 20 FDA reports)
BONE MARROW OEDEMA ( 20 FDA reports)
BREAST FIBROSIS ( 20 FDA reports)
BREAST LUMP REMOVAL ( 20 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 20 FDA reports)
DECREASED ACTIVITY ( 20 FDA reports)
DEVICE MALFUNCTION ( 20 FDA reports)
DROWNING ( 20 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 20 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 20 FDA reports)
EAR CONGESTION ( 20 FDA reports)
EPIGASTRIC DISCOMFORT ( 20 FDA reports)
ESCHERICHIA INFECTION ( 20 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 20 FDA reports)
INJECTION SITE WARMTH ( 20 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 20 FDA reports)
LACUNAR INFARCTION ( 20 FDA reports)
LIP DISCOLOURATION ( 20 FDA reports)
LYMPHADENECTOMY ( 20 FDA reports)
MALIGNANT MELANOMA ( 20 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 20 FDA reports)
MENINGITIS ( 20 FDA reports)
METABOLIC ENCEPHALOPATHY ( 20 FDA reports)
OROANTRAL FISTULA ( 20 FDA reports)
PERONEAL NERVE PALSY ( 20 FDA reports)
PLASMACYTOMA ( 20 FDA reports)
POLYMENORRHOEA ( 20 FDA reports)
PROSTATITIS ( 20 FDA reports)
PYELONEPHRITIS ( 20 FDA reports)
RECTOCELE ( 20 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 20 FDA reports)
RESORPTION BONE INCREASED ( 20 FDA reports)
RESPIRATORY TRACT CONGESTION ( 20 FDA reports)
SKELETAL INJURY ( 20 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 20 FDA reports)
TONGUE DISCOLOURATION ( 20 FDA reports)
URETERAL DISORDER ( 20 FDA reports)
VENTRICULAR DYSFUNCTION ( 20 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 20 FDA reports)
WOUND DRAINAGE ( 20 FDA reports)
TONGUE ULCERATION ( 19 FDA reports)
VEIN DISORDER ( 19 FDA reports)
VIITH NERVE PARALYSIS ( 19 FDA reports)
ACCIDENTAL EXPOSURE ( 19 FDA reports)
ACCOMMODATION DISORDER ( 19 FDA reports)
ACROCHORDON ( 19 FDA reports)
APHTHOUS STOMATITIS ( 19 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 19 FDA reports)
BONE GRAFT ( 19 FDA reports)
CALCULUS URETERIC ( 19 FDA reports)
CERVICAL DYSPLASIA ( 19 FDA reports)
EOSINOPHIL COUNT INCREASED ( 19 FDA reports)
EPICONDYLITIS ( 19 FDA reports)
EYE INJURY ( 19 FDA reports)
EYE PRURITUS ( 19 FDA reports)
HYDROCELE ( 19 FDA reports)
HYPERCAPNIA ( 19 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 19 FDA reports)
INJECTION SITE INDURATION ( 19 FDA reports)
INJECTION SITE INFECTION ( 19 FDA reports)
IUCD COMPLICATION ( 19 FDA reports)
JOINT CONTRACTURE ( 19 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 19 FDA reports)
LABORATORY TEST ABNORMAL ( 19 FDA reports)
LOGORRHOEA ( 19 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 19 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 19 FDA reports)
MAMMOGRAM ABNORMAL ( 19 FDA reports)
MECHANICAL VENTILATION ( 19 FDA reports)
MITRAL VALVE DISEASE ( 19 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 19 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 19 FDA reports)
ORTHOPNOEA ( 19 FDA reports)
OSTEOMYELITIS CHRONIC ( 19 FDA reports)
PENIS DISORDER ( 19 FDA reports)
PERSONALITY DISORDER ( 19 FDA reports)
POOR PERIPHERAL CIRCULATION ( 19 FDA reports)
PUPIL FIXED ( 19 FDA reports)
RECTAL DISCHARGE ( 19 FDA reports)
RENAL ISCHAEMIA ( 19 FDA reports)
RENAL TUBULAR NECROSIS ( 19 FDA reports)
SELF MUTILATION ( 19 FDA reports)
SEROMA ( 19 FDA reports)
SPINAL CORD COMPRESSION ( 19 FDA reports)
SPUTUM DISCOLOURED ( 19 FDA reports)
STRESS SYMPTOMS ( 19 FDA reports)
TACHYPHRENIA ( 19 FDA reports)
ACCIDENT ( 18 FDA reports)
ARTERIOSPASM CORONARY ( 18 FDA reports)
AURA ( 18 FDA reports)
BLOOD POTASSIUM INCREASED ( 18 FDA reports)
BREAST CALCIFICATIONS ( 18 FDA reports)
BRONCHOPLEURAL FISTULA ( 18 FDA reports)
CARDIAC VALVE ABSCESS ( 18 FDA reports)
CHEILITIS ( 18 FDA reports)
COMPULSIONS ( 18 FDA reports)
DEVICE BREAKAGE ( 18 FDA reports)
DIZZINESS POSTURAL ( 18 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 18 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 18 FDA reports)
FRACTURE NONUNION ( 18 FDA reports)
HAND FRACTURE ( 18 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 18 FDA reports)
HYDROPNEUMOTHORAX ( 18 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 18 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 18 FDA reports)
LIP DISORDER ( 18 FDA reports)
OSTEORADIONECROSIS ( 18 FDA reports)
PERIPHERAL EMBOLISM ( 18 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 18 FDA reports)
POST THROMBOTIC SYNDROME ( 18 FDA reports)
PROTEIN TOTAL INCREASED ( 18 FDA reports)
PULMONARY INFARCTION ( 18 FDA reports)
PYELOCALIECTASIS ( 18 FDA reports)
RECTAL POLYP ( 18 FDA reports)
SELF ESTEEM DECREASED ( 18 FDA reports)
SKIN HYPERTROPHY ( 18 FDA reports)
SKIN INDURATION ( 18 FDA reports)
SKIN WARM ( 18 FDA reports)
SKULL FRACTURE ( 18 FDA reports)
SLUGGISHNESS ( 18 FDA reports)
SNORING ( 18 FDA reports)
STRESS INCONTINENCE ( 18 FDA reports)
TEMPERATURE INTOLERANCE ( 18 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 18 FDA reports)
UROSEPSIS ( 18 FDA reports)
VASCULITIS ( 18 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 18 FDA reports)
THROMBOCYTOSIS ( 17 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 17 FDA reports)
TREATMENT FAILURE ( 17 FDA reports)
UTERINE RUPTURE ( 17 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 17 FDA reports)
VULVOVAGINAL PRURITUS ( 17 FDA reports)
WEIGHT LOSS POOR ( 17 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 17 FDA reports)
ADENOMYOSIS ( 17 FDA reports)
ADJUSTMENT DISORDER ( 17 FDA reports)
ADRENAL INSUFFICIENCY ( 17 FDA reports)
AORTIC ANEURYSM ( 17 FDA reports)
ASTIGMATISM ( 17 FDA reports)
AUTOIMMUNE THYROIDITIS ( 17 FDA reports)
BLOOD IRON DECREASED ( 17 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 17 FDA reports)
BONE GIANT CELL TUMOUR ( 17 FDA reports)
BONE OPERATION ( 17 FDA reports)
BREAST ENLARGEMENT ( 17 FDA reports)
BREAST RECONSTRUCTION ( 17 FDA reports)
CAROTID BRUIT ( 17 FDA reports)
CORNEAL ABRASION ( 17 FDA reports)
CORONARY ARTERY RESTENOSIS ( 17 FDA reports)
DRUG LEVEL INCREASED ( 17 FDA reports)
DYSMENORRHOEA ( 17 FDA reports)
EARLY MORNING AWAKENING ( 17 FDA reports)
ENTERITIS ( 17 FDA reports)
ESSENTIAL TREMOR ( 17 FDA reports)
EXOPHTHALMOS ( 17 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 17 FDA reports)
HAIR GROWTH ABNORMAL ( 17 FDA reports)
HANGOVER ( 17 FDA reports)
HYPOTRICHOSIS ( 17 FDA reports)
ILEUS PARALYTIC ( 17 FDA reports)
INGUINAL HERNIA ( 17 FDA reports)
IUD MIGRATION ( 17 FDA reports)
MIOSIS ( 17 FDA reports)
MORBID THOUGHTS ( 17 FDA reports)
MUCOSAL ULCERATION ( 17 FDA reports)
NASAL ULCER ( 17 FDA reports)
OESOPHAGEAL STENOSIS ( 17 FDA reports)
ORCHITIS ( 17 FDA reports)
OVERWEIGHT ( 17 FDA reports)
PETECHIAE ( 17 FDA reports)
PLASMACYTOSIS ( 17 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 17 FDA reports)
PSORIATIC ARTHROPATHY ( 17 FDA reports)
RALES ( 17 FDA reports)
RASH MACULO-PAPULAR ( 17 FDA reports)
RETINAL HAEMORRHAGE ( 17 FDA reports)
SKIN NECROSIS ( 17 FDA reports)
SMEAR CERVIX ABNORMAL ( 17 FDA reports)
SUBCUTANEOUS ABSCESS ( 17 FDA reports)
SYNOVITIS ( 17 FDA reports)
ANAEMIA POSTOPERATIVE ( 16 FDA reports)
ANDROGENS DECREASED ( 16 FDA reports)
ARTERIAL THROMBOSIS ( 16 FDA reports)
BLADDER PAIN ( 16 FDA reports)
BLOOD TEST ABNORMAL ( 16 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 16 FDA reports)
BRAIN OEDEMA ( 16 FDA reports)
BREAKTHROUGH PAIN ( 16 FDA reports)
BREAST DISORDER ( 16 FDA reports)
CLAVICLE FRACTURE ( 16 FDA reports)
COLON CANCER ( 16 FDA reports)
COMPARTMENT SYNDROME ( 16 FDA reports)
ERYTHEMA MULTIFORME ( 16 FDA reports)
EXERCISE TOLERANCE DECREASED ( 16 FDA reports)
EYE ROLLING ( 16 FDA reports)
EYELID OEDEMA ( 16 FDA reports)
FACIAL BONES FRACTURE ( 16 FDA reports)
FACIAL PARESIS ( 16 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 16 FDA reports)
GESTATIONAL DIABETES ( 16 FDA reports)
HYPERREFLEXIA ( 16 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 16 FDA reports)
IMPATIENCE ( 16 FDA reports)
INJURY CORNEAL ( 16 FDA reports)
INTENTION TREMOR ( 16 FDA reports)
LIP PAIN ( 16 FDA reports)
METASTASIS ( 16 FDA reports)
OBSESSIVE THOUGHTS ( 16 FDA reports)
OCCULT BLOOD POSITIVE ( 16 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 16 FDA reports)
OOPHORECTOMY ( 16 FDA reports)
ORAL FIBROMA ( 16 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 16 FDA reports)
PERIODONTAL DESTRUCTION ( 16 FDA reports)
POLYSUBSTANCE ABUSE ( 16 FDA reports)
RADIATION SKIN INJURY ( 16 FDA reports)
RESPIRATORY DEPRESSION ( 16 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 16 FDA reports)
SECRETION DISCHARGE ( 16 FDA reports)
SELF-MEDICATION ( 16 FDA reports)
SERUM SICKNESS ( 16 FDA reports)
SINUS ARRHYTHMIA ( 16 FDA reports)
SKIN HAEMORRHAGE ( 16 FDA reports)
SLEEP TALKING ( 16 FDA reports)
SPINAL DECOMPRESSION ( 16 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 16 FDA reports)
STENT OCCLUSION ( 16 FDA reports)
TESTICULAR SWELLING ( 16 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 16 FDA reports)
TOOTH REPAIR ( 15 FDA reports)
TUMOUR EXCISION ( 15 FDA reports)
UTERINE DILATION AND CURETTAGE ( 15 FDA reports)
VERTIGO POSITIONAL ( 15 FDA reports)
WOUND INFECTION ( 15 FDA reports)
ABDOMINAL HERNIA ( 15 FDA reports)
ABSCESS NECK ( 15 FDA reports)
ANOXIC ENCEPHALOPATHY ( 15 FDA reports)
APPETITE DISORDER ( 15 FDA reports)
ATRIAL TACHYCARDIA ( 15 FDA reports)
ATRIAL THROMBOSIS ( 15 FDA reports)
BIOPSY BLADDER ABNORMAL ( 15 FDA reports)
BIOPSY BREAST ABNORMAL ( 15 FDA reports)
BIOPSY SKIN ABNORMAL ( 15 FDA reports)
BIPOLAR II DISORDER ( 15 FDA reports)
BLINDNESS TRANSIENT ( 15 FDA reports)
BLOOD CHLORIDE DECREASED ( 15 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 15 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 15 FDA reports)
BONE CYST ( 15 FDA reports)
BRONCHIECTASIS ( 15 FDA reports)
CHEMICAL POISONING ( 15 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 15 FDA reports)
DENTAL CARE ( 15 FDA reports)
DYSGRAPHIA ( 15 FDA reports)
DYSPAREUNIA ( 15 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 15 FDA reports)
FEAR OF DEATH ( 15 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 15 FDA reports)
GANGRENE ( 15 FDA reports)
HEART INJURY ( 15 FDA reports)
HEPATITIS ACUTE ( 15 FDA reports)
HEPATITIS B ( 15 FDA reports)
HEPATOTOXICITY ( 15 FDA reports)
HYPERSEXUALITY ( 15 FDA reports)
HYPERURICAEMIA ( 15 FDA reports)
HYPOALBUMINAEMIA ( 15 FDA reports)
HYPOMENORRHOEA ( 15 FDA reports)
HYPOTONIA ( 15 FDA reports)
IMPAIRED SELF-CARE ( 15 FDA reports)
INJECTION SITE DISCOLOURATION ( 15 FDA reports)
INJECTION SITE NODULE ( 15 FDA reports)
INTESTINAL POLYP ( 15 FDA reports)
JUDGEMENT IMPAIRED ( 15 FDA reports)
LIGAMENT INJURY ( 15 FDA reports)
MICTURITION DISORDER ( 15 FDA reports)
MULTIPLE FRACTURES ( 15 FDA reports)
NEURECTOMY ( 15 FDA reports)
OBSTRUCTION ( 15 FDA reports)
OXYGEN SUPPLEMENTATION ( 15 FDA reports)
PERITONITIS ( 15 FDA reports)
PRE-ECLAMPSIA ( 15 FDA reports)
PURPURA ( 15 FDA reports)
SNEEZING ( 15 FDA reports)
SPINAL FUSION SURGERY ( 15 FDA reports)
ABNORMAL SENSATION IN EYE ( 14 FDA reports)
ABORTION INDUCED ( 14 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 14 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 14 FDA reports)
APPLICATION SITE IRRITATION ( 14 FDA reports)
ATRIOVENTRICULAR BLOCK ( 14 FDA reports)
BILE DUCT OBSTRUCTION ( 14 FDA reports)
BLOOD DISORDER ( 14 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 14 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 14 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 14 FDA reports)
BONE MARROW TRANSPLANT ( 14 FDA reports)
BREAST DISCHARGE ( 14 FDA reports)
BREATH SOUNDS ABNORMAL ( 14 FDA reports)
BRONCHITIS CHRONIC ( 14 FDA reports)
CARDIAC FLUTTER ( 14 FDA reports)
CERVICAL CYST ( 14 FDA reports)
CERVICAL SPINE FLATTENING ( 14 FDA reports)
CHEST X-RAY ABNORMAL ( 14 FDA reports)
CHONDROMALACIA ( 14 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 14 FDA reports)
DEPRESSIVE SYMPTOM ( 14 FDA reports)
DEVICE LEAKAGE ( 14 FDA reports)
DIALYSIS ( 14 FDA reports)
DIURETIC THERAPY ( 14 FDA reports)
EJACULATION DISORDER ( 14 FDA reports)
ENDOMETRIOSIS ( 14 FDA reports)
ERYTHEMA OF EYELID ( 14 FDA reports)
EXTRADURAL ABSCESS ( 14 FDA reports)
FLIGHT OF IDEAS ( 14 FDA reports)
FLUID REPLACEMENT ( 14 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 14 FDA reports)
GASTROINTESTINAL NECROSIS ( 14 FDA reports)
HORDEOLUM ( 14 FDA reports)
HYPERMETROPIA ( 14 FDA reports)
HYPERTONIC BLADDER ( 14 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 14 FDA reports)
INAPPROPRIATE AFFECT ( 14 FDA reports)
LIGAMENT DISORDER ( 14 FDA reports)
LIVE BIRTH ( 14 FDA reports)
LYMPHOMA ( 14 FDA reports)
LYMPHOPENIA ( 14 FDA reports)
MACROCYTOSIS ( 14 FDA reports)
MASS EXCISION ( 14 FDA reports)
MITRAL VALVE CALCIFICATION ( 14 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 14 FDA reports)
NASAL DISCOMFORT ( 14 FDA reports)
NEURITIS ( 14 FDA reports)
NONSPECIFIC REACTION ( 14 FDA reports)
OPEN REDUCTION OF FRACTURE ( 14 FDA reports)
ORGASM ABNORMAL ( 14 FDA reports)
OVARIAN DISORDER ( 14 FDA reports)
PALATAL DISORDER ( 14 FDA reports)
PATELLA FRACTURE ( 14 FDA reports)
PELVIC VENOUS THROMBOSIS ( 14 FDA reports)
PHYSIOTHERAPY ( 14 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 14 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 14 FDA reports)
PSEUDOMONAS INFECTION ( 14 FDA reports)
PULMONARY AIR LEAKAGE ( 14 FDA reports)
PULMONARY THROMBOSIS ( 14 FDA reports)
RADIOTHERAPY TO BRAIN ( 14 FDA reports)
RASH PUSTULAR ( 14 FDA reports)
SCAB ( 14 FDA reports)
SENSATION OF FOREIGN BODY ( 14 FDA reports)
SHOULDER ARTHROPLASTY ( 14 FDA reports)
SICK SINUS SYNDROME ( 14 FDA reports)
SKIN ODOUR ABNORMAL ( 14 FDA reports)
SKIN REACTION ( 14 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 14 FDA reports)
SUPERINFECTION ( 14 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 14 FDA reports)
TRANSAMINASES INCREASED ( 14 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 14 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 14 FDA reports)
URINE ODOUR ABNORMAL ( 14 FDA reports)
VITAMIN D DEFICIENCY ( 14 FDA reports)
WEIGHT BEARING DIFFICULTY ( 14 FDA reports)
WOUND DEBRIDEMENT ( 14 FDA reports)
TENDON INJURY ( 13 FDA reports)
TOE DEFORMITY ( 13 FDA reports)
TORTICOLLIS ( 13 FDA reports)
TRIGEMINAL NEURALGIA ( 13 FDA reports)
URINE ANALYSIS ABNORMAL ( 13 FDA reports)
VESTIBULAR DISORDER ( 13 FDA reports)
ACCIDENT AT WORK ( 13 FDA reports)
ANAL FISSURE ( 13 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 13 FDA reports)
AORTIC CALCIFICATION ( 13 FDA reports)
APPLICATION SITE REACTION ( 13 FDA reports)
BIOPSY BREAST ( 13 FDA reports)
BLEPHAROSPASM ( 13 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 13 FDA reports)
BLOOD PROLACTIN INCREASED ( 13 FDA reports)
BODY TEMPERATURE DECREASED ( 13 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 13 FDA reports)
BREAST NECROSIS ( 13 FDA reports)
BULIMIA NERVOSA ( 13 FDA reports)
BUNION OPERATION ( 13 FDA reports)
CONNECTIVE TISSUE DISORDER ( 13 FDA reports)
CORONARY ARTERY BYPASS ( 13 FDA reports)
COSTOCHONDRITIS ( 13 FDA reports)
DERMATITIS EXFOLIATIVE ( 13 FDA reports)
DISSOCIATIVE DISORDER ( 13 FDA reports)
ENDOMETRIAL DISORDER ( 13 FDA reports)
EYE ALLERGY ( 13 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 13 FDA reports)
FULL BLOOD COUNT DECREASED ( 13 FDA reports)
GASTRIC BYPASS ( 13 FDA reports)
GASTRIC HAEMORRHAGE ( 13 FDA reports)
GASTRITIS EROSIVE ( 13 FDA reports)
GINGIVAL GRAFT ( 13 FDA reports)
HAEMODIALYSIS ( 13 FDA reports)
HYDROCEPHALUS ( 13 FDA reports)
IMPULSE-CONTROL DISORDER ( 13 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 13 FDA reports)
LUNG CONSOLIDATION ( 13 FDA reports)
MALABSORPTION ( 13 FDA reports)
MAMMOPLASTY ( 13 FDA reports)
MARITAL PROBLEM ( 13 FDA reports)
MENINGITIS VIRAL ( 13 FDA reports)
NASAL SEPTUM DEVIATION ( 13 FDA reports)
NERVE ROOT LESION ( 13 FDA reports)
NEUTROPHIL COUNT DECREASED ( 13 FDA reports)
OESOPHAGEAL RUPTURE ( 13 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 13 FDA reports)
PARTNER STRESS ( 13 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 13 FDA reports)
PHOTOPSIA ( 13 FDA reports)
PINGUECULA ( 13 FDA reports)
POSTMENOPAUSE ( 13 FDA reports)
PULMONARY HILUM MASS ( 13 FDA reports)
SACROILIITIS ( 13 FDA reports)
SEBORRHOEIC KERATOSIS ( 13 FDA reports)
SENSATION OF PRESSURE ( 13 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 13 FDA reports)
ABNORMAL FAECES ( 12 FDA reports)
ACTINIC KERATOSIS ( 12 FDA reports)
ANKYLOSING SPONDYLITIS ( 12 FDA reports)
BLOOD ALCOHOL INCREASED ( 12 FDA reports)
BLOOD AMYLASE INCREASED ( 12 FDA reports)
BLOOD CREATININE DECREASED ( 12 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 12 FDA reports)
BRONCHOPNEUMONIA ( 12 FDA reports)
CARDIAC OPERATION ( 12 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 12 FDA reports)
CHAPPED LIPS ( 12 FDA reports)
CHOLESTEROSIS ( 12 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 12 FDA reports)
CORONARY ARTERY THROMBOSIS ( 12 FDA reports)
DEPERSONALISATION ( 12 FDA reports)
DEVELOPMENTAL DELAY ( 12 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 12 FDA reports)
DUODENOGASTRIC REFLUX ( 12 FDA reports)
DYSHIDROSIS ( 12 FDA reports)
ERECTION INCREASED ( 12 FDA reports)
FACET JOINT SYNDROME ( 12 FDA reports)
FIBRIN D DIMER INCREASED ( 12 FDA reports)
GENITAL HAEMORRHAGE ( 12 FDA reports)
H1N1 INFLUENZA ( 12 FDA reports)
HEPATIC ENCEPHALOPATHY ( 12 FDA reports)
HEPATITIS VIRAL ( 12 FDA reports)
HEPATOCELLULAR DAMAGE ( 12 FDA reports)
HILAR LYMPHADENOPATHY ( 12 FDA reports)
HYPERMETABOLISM ( 12 FDA reports)
HYPOGLYCAEMIC COMA ( 12 FDA reports)
IMMUNE SYSTEM DISORDER ( 12 FDA reports)
JOINT ARTHROPLASTY ( 12 FDA reports)
JUGULAR VEIN THROMBOSIS ( 12 FDA reports)
LIP DRY ( 12 FDA reports)
LIPIDS INCREASED ( 12 FDA reports)
LIVEDO RETICULARIS ( 12 FDA reports)
LOCALISED OEDEMA ( 12 FDA reports)
MALIGNANT TUMOUR EXCISION ( 12 FDA reports)
METASTASES TO PELVIS ( 12 FDA reports)
MUCOSAL HAEMORRHAGE ( 12 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 12 FDA reports)
NEONATAL DISORDER ( 12 FDA reports)
NEPHROPATHY ( 12 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 12 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 12 FDA reports)
OVARIAN CANCER ( 12 FDA reports)
PENILE PAIN ( 12 FDA reports)
PHYSICAL ASSAULT ( 12 FDA reports)
PNEUMONIA BACTERIAL ( 12 FDA reports)
POLYCYTHAEMIA ( 12 FDA reports)
POOR DENTAL CONDITION ( 12 FDA reports)
POSTOPERATIVE INFECTION ( 12 FDA reports)
PREMATURE LABOUR ( 12 FDA reports)
PRESBYOESOPHAGUS ( 12 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 12 FDA reports)
PROSTATIC DISORDER ( 12 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 12 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 12 FDA reports)
PULPITIS DENTAL ( 12 FDA reports)
REGURGITATION ( 12 FDA reports)
RETINAL DETACHMENT ( 12 FDA reports)
SARCOIDOSIS ( 12 FDA reports)
SINUSITIS FUNGAL ( 12 FDA reports)
SKIN FIBROSIS ( 12 FDA reports)
SPONDYLITIS ( 12 FDA reports)
TENOSYNOVITIS STENOSANS ( 12 FDA reports)
TOBACCO ABUSE ( 12 FDA reports)
UNINTENDED PREGNANCY ( 12 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 12 FDA reports)
UTERINE POLYP ( 12 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 12 FDA reports)
VOCAL CORD PARALYSIS ( 12 FDA reports)
VOCAL CORD THICKENING ( 12 FDA reports)
YAWNING ( 12 FDA reports)
YELLOW SKIN ( 12 FDA reports)
TENOSYNOVITIS ( 11 FDA reports)
TONIC CLONIC MOVEMENTS ( 11 FDA reports)
TRIGGER FINGER ( 11 FDA reports)
TUMOUR MARKER INCREASED ( 11 FDA reports)
UVEITIS ( 11 FDA reports)
VULVAL DISORDER ( 11 FDA reports)
ABSCESS JAW ( 11 FDA reports)
ACUTE PULMONARY OEDEMA ( 11 FDA reports)
ADHESION ( 11 FDA reports)
ANAL HAEMORRHAGE ( 11 FDA reports)
ANGIOPLASTY ( 11 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 11 FDA reports)
ARTERIAL DISORDER ( 11 FDA reports)
BELLIGERENCE ( 11 FDA reports)
BINGE EATING ( 11 FDA reports)
BLOOD CHLORIDE INCREASED ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 11 FDA reports)
BRAIN DAMAGE ( 11 FDA reports)
BRAIN DEATH ( 11 FDA reports)
CANCER PAIN ( 11 FDA reports)
CAPILLARY DISORDER ( 11 FDA reports)
CARDIAC FAILURE CHRONIC ( 11 FDA reports)
CHOLANGITIS ( 11 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 11 FDA reports)
CLUMSINESS ( 11 FDA reports)
CLUSTER HEADACHE ( 11 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 11 FDA reports)
DEVICE DISLOCATION ( 11 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 11 FDA reports)
ENCEPHALOMALACIA ( 11 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 11 FDA reports)
FOAMING AT MOUTH ( 11 FDA reports)
FOETAL GROWTH RETARDATION ( 11 FDA reports)
FOOD INTOLERANCE ( 11 FDA reports)
FRACTURE DELAYED UNION ( 11 FDA reports)
GINGIVAL OPERATION ( 11 FDA reports)
HAEMOTHORAX ( 11 FDA reports)
HEART DISEASE CONGENITAL ( 11 FDA reports)
HEMIANOPIA HOMONYMOUS ( 11 FDA reports)
HEPATITIS CHOLESTATIC ( 11 FDA reports)
HYPERACUSIS ( 11 FDA reports)
HYPOPHOSPHATAEMIA ( 11 FDA reports)
IMPAIRED FASTING GLUCOSE ( 11 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 11 FDA reports)
INTRAOCULAR LENS IMPLANT ( 11 FDA reports)
KNEE OPERATION ( 11 FDA reports)
LACK OF SATIETY ( 11 FDA reports)
LENTIGO ( 11 FDA reports)
LISTLESS ( 11 FDA reports)
MACULAR DEGENERATION ( 11 FDA reports)
METAMORPHOPSIA ( 11 FDA reports)
MOTION SICKNESS ( 11 FDA reports)
NASAL DRYNESS ( 11 FDA reports)
NEGATIVE THOUGHTS ( 11 FDA reports)
OCULAR ICTERUS ( 11 FDA reports)
ORAL DISCOMFORT ( 11 FDA reports)
PLAGIOCEPHALY ( 11 FDA reports)
POLYP ( 11 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 11 FDA reports)
RAYNAUD'S PHENOMENON ( 11 FDA reports)
RESPIRATORY ACIDOSIS ( 11 FDA reports)
RESPIRATORY RATE DECREASED ( 11 FDA reports)
ROTATOR CUFF REPAIR ( 11 FDA reports)
SEPSIS SYNDROME ( 11 FDA reports)
SKIN SWELLING ( 11 FDA reports)
SOCIAL PROBLEM ( 11 FDA reports)
SPINAL LAMINECTOMY ( 11 FDA reports)
TALIPES ( 11 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 10 FDA reports)
ACUTE STRESS DISORDER ( 10 FDA reports)
ADVERSE REACTION ( 10 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 10 FDA reports)
ALCOHOLIC LIVER DISEASE ( 10 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 10 FDA reports)
ARTERIAL STENOSIS ( 10 FDA reports)
ASPIRATION PLEURAL CAVITY ( 10 FDA reports)
ATROPHY ( 10 FDA reports)
AUTISM ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 10 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 10 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 10 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 10 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 10 FDA reports)
BRADYPHRENIA ( 10 FDA reports)
CARDIORENAL SYNDROME ( 10 FDA reports)
CEREBRAL DISORDER ( 10 FDA reports)
CRANIOSYNOSTOSIS ( 10 FDA reports)
DEREALISATION ( 10 FDA reports)
DERMATITIS ACNEIFORM ( 10 FDA reports)
DIABETIC EYE DISEASE ( 10 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 10 FDA reports)
EARLY SATIETY ( 10 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 10 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 10 FDA reports)
ELECTROLYTE DEPLETION ( 10 FDA reports)
EMBOLISM ( 10 FDA reports)
ENCOPRESIS ( 10 FDA reports)
FIBROADENOMA OF BREAST ( 10 FDA reports)
FOOD AVERSION ( 10 FDA reports)
GALACTORRHOEA ( 10 FDA reports)
GALLBLADDER PAIN ( 10 FDA reports)
GAMBLING ( 10 FDA reports)
GENERALISED ERYTHEMA ( 10 FDA reports)
HAIR TEXTURE ABNORMAL ( 10 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 10 FDA reports)
HERPES VIRUS INFECTION ( 10 FDA reports)
HICCUPS ( 10 FDA reports)
HYPERCOAGULATION ( 10 FDA reports)
ILEITIS ( 10 FDA reports)
IMPETIGO ( 10 FDA reports)
INCISION SITE COMPLICATION ( 10 FDA reports)
INCISION SITE PAIN ( 10 FDA reports)
INJECTION SITE IRRITATION ( 10 FDA reports)
INJECTION SITE MASS ( 10 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 10 FDA reports)
INTESTINAL PERFORATION ( 10 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 10 FDA reports)
LAZINESS ( 10 FDA reports)
LEG AMPUTATION ( 10 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 10 FDA reports)
MASTOIDITIS ( 10 FDA reports)
MEIBOMIANITIS ( 10 FDA reports)
MENSTRUATION DELAYED ( 10 FDA reports)
METASTATIC NEOPLASM ( 10 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 10 FDA reports)
MONOCYTE COUNT INCREASED ( 10 FDA reports)
MORTON'S NEUROMA ( 10 FDA reports)
MUCOUS STOOLS ( 10 FDA reports)
NIPPLE PAIN ( 10 FDA reports)
OEDEMA MOUTH ( 10 FDA reports)
OESOPHAGEAL ULCER ( 10 FDA reports)
OLIGOMENORRHOEA ( 10 FDA reports)
OPEN ANGLE GLAUCOMA ( 10 FDA reports)
PHARYNGEAL DISORDER ( 10 FDA reports)
POLYP COLORECTAL ( 10 FDA reports)
POST LAMINECTOMY SYNDROME ( 10 FDA reports)
PRIAPISM ( 10 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 10 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 10 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 10 FDA reports)
PULMONARY VASCULAR DISORDER ( 10 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 10 FDA reports)
SKIN INFECTION ( 10 FDA reports)
SKIN TIGHTNESS ( 10 FDA reports)
SKULL FRACTURED BASE ( 10 FDA reports)
SMALL INTESTINAL PERFORATION ( 10 FDA reports)
SOCIAL PHOBIA ( 10 FDA reports)
SURGICAL PROCEDURE REPEATED ( 10 FDA reports)
THROMBOPHLEBITIS ( 10 FDA reports)
TRACHEOBRONCHITIS ( 10 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 10 FDA reports)
TROPONIN INCREASED ( 10 FDA reports)
TUBERCULOSIS ( 10 FDA reports)
TUMOUR INVASION ( 10 FDA reports)
URINARY TRACT DISORDER ( 10 FDA reports)
URINE COLOUR ABNORMAL ( 10 FDA reports)
VAGINITIS BACTERIAL ( 10 FDA reports)
VASCULAR OCCLUSION ( 10 FDA reports)
VERTEBRAL WEDGING ( 10 FDA reports)
WRONG DRUG ADMINISTERED ( 10 FDA reports)
TORSADE DE POINTES ( 9 FDA reports)
VENOUS OCCLUSION ( 9 FDA reports)
VENOUS THROMBOSIS ( 9 FDA reports)
VITAMIN D DECREASED ( 9 FDA reports)
ABDOMINAL SEPSIS ( 9 FDA reports)
ACUTE PSYCHOSIS ( 9 FDA reports)
AGRANULOCYTOSIS ( 9 FDA reports)
ALLODYNIA ( 9 FDA reports)
AMBLYOPIA ( 9 FDA reports)
AMPHETAMINES POSITIVE ( 9 FDA reports)
ANOSMIA ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 9 FDA reports)
ANTICHOLINERGIC SYNDROME ( 9 FDA reports)
APPENDIX DISORDER ( 9 FDA reports)
APPLICATION SITE BURN ( 9 FDA reports)
APPLICATION SITE PAIN ( 9 FDA reports)
APPLICATION SITE VESICLES ( 9 FDA reports)
BACTERIAL SEPSIS ( 9 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 9 FDA reports)
BLADDER DYSFUNCTION ( 9 FDA reports)
BLEPHARITIS ( 9 FDA reports)
BLOOD CALCIUM INCREASED ( 9 FDA reports)
BLOOD CULTURE POSITIVE ( 9 FDA reports)
BLOOD OESTROGEN DECREASED ( 9 FDA reports)
BLOOD PH DECREASED ( 9 FDA reports)
BLOOD UREA DECREASED ( 9 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 9 FDA reports)
BREECH PRESENTATION ( 9 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 9 FDA reports)
CARBON DIOXIDE DECREASED ( 9 FDA reports)
CARDIAC ANEURYSM ( 9 FDA reports)
CARDIAC PACEMAKER INSERTION ( 9 FDA reports)
CARTILAGE ATROPHY ( 9 FDA reports)
CATATONIA ( 9 FDA reports)
CATHETER RELATED INFECTION ( 9 FDA reports)
CATHETER SEPSIS ( 9 FDA reports)
CAUDA EQUINA SYNDROME ( 9 FDA reports)
CELLULITIS ORBITAL ( 9 FDA reports)
CHANGE OF BOWEL HABIT ( 9 FDA reports)
CHEMOTHERAPY ( 9 FDA reports)
CHEST TUBE INSERTION ( 9 FDA reports)
CHEST WALL PAIN ( 9 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 9 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 9 FDA reports)
COMMUNICATION DISORDER ( 9 FDA reports)
COMPLEX PARTIAL SEIZURES ( 9 FDA reports)
CONDUCTION DISORDER ( 9 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 9 FDA reports)
CONJUNCTIVITIS VIRAL ( 9 FDA reports)
CORNEAL OEDEMA ( 9 FDA reports)
CRYPTORCHISM ( 9 FDA reports)
CUTIS LAXA ( 9 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 9 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 9 FDA reports)
DENTAL TREATMENT ( 9 FDA reports)
DEVICE RELATED SEPSIS ( 9 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 9 FDA reports)
DIAPHRAGMATIC HERNIA ( 9 FDA reports)
DROOLING ( 9 FDA reports)
DRUG CLEARANCE DECREASED ( 9 FDA reports)
DRY THROAT ( 9 FDA reports)
ELECTRIC SHOCK ( 9 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 9 FDA reports)
ENCEPHALITIS ( 9 FDA reports)
ENCEPHALITIS VIRAL ( 9 FDA reports)
ENDOCARDITIS ( 9 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 9 FDA reports)
EXTRASKELETAL OSSIFICATION ( 9 FDA reports)
EXTRASYSTOLES ( 9 FDA reports)
FACIAL NERVE DISORDER ( 9 FDA reports)
FAT NECROSIS ( 9 FDA reports)
FEELING HOT AND COLD ( 9 FDA reports)
GASTROINTESTINAL INFECTION ( 9 FDA reports)
GENITAL HERPES ( 9 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 9 FDA reports)
HIRSUTISM ( 9 FDA reports)
HOMELESS ( 9 FDA reports)
HOMICIDE ( 9 FDA reports)
HYPERTENSIVE CRISIS ( 9 FDA reports)
HYPERTHERMIA MALIGNANT ( 9 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 9 FDA reports)
IMMOBILE ( 9 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 9 FDA reports)
INGROWN HAIR ( 9 FDA reports)
INJECTION SITE CELLULITIS ( 9 FDA reports)
INJECTION SITE INFLAMMATION ( 9 FDA reports)
INSULIN RESISTANCE ( 9 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 9 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 9 FDA reports)
MASTOCYTOSIS ( 9 FDA reports)
MENOMETRORRHAGIA ( 9 FDA reports)
METATARSUS PRIMUS VARUS ( 9 FDA reports)
MONONEURITIS ( 9 FDA reports)
MUSCLE CONTRACTURE ( 9 FDA reports)
MYELOMA RECURRENCE ( 9 FDA reports)
NEPHRITIS INTERSTITIAL ( 9 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 9 FDA reports)
NO ADVERSE EFFECT ( 9 FDA reports)
NODULE ON EXTREMITY ( 9 FDA reports)
OPTIC NEUROPATHY ( 9 FDA reports)
OROPHARYNGEAL SWELLING ( 9 FDA reports)
PAIN EXACERBATED ( 9 FDA reports)
PARONYCHIA ( 9 FDA reports)
PARTIAL SEIZURES ( 9 FDA reports)
PERIORBITAL HAEMATOMA ( 9 FDA reports)
PIGMENTATION DISORDER ( 9 FDA reports)
PITTING OEDEMA ( 9 FDA reports)
POISONING ( 9 FDA reports)
POLYARTHRITIS ( 9 FDA reports)
POST PROCEDURAL OEDEMA ( 9 FDA reports)
POSTNASAL DRIP ( 9 FDA reports)
POSTOPERATIVE ADHESION ( 9 FDA reports)
PREMENSTRUAL SYNDROME ( 9 FDA reports)
PSYCHOMOTOR RETARDATION ( 9 FDA reports)
PUBIS FRACTURE ( 9 FDA reports)
PULSE ABNORMAL ( 9 FDA reports)
REFLUX GASTRITIS ( 9 FDA reports)
RENAL CELL CARCINOMA ( 9 FDA reports)
SHOULDER OPERATION ( 9 FDA reports)
SKIN ATROPHY ( 9 FDA reports)
SKIN INJURY ( 9 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
AKINESIA ( 8 FDA reports)
AMMONIA INCREASED ( 8 FDA reports)
ANAPHYLACTOID REACTION ( 8 FDA reports)
AORTIC VALVE SCLEROSIS ( 8 FDA reports)
APGAR SCORE LOW ( 8 FDA reports)
APPARENT DEATH ( 8 FDA reports)
APPENDICITIS PERFORATED ( 8 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 8 FDA reports)
ARTERIAL INSUFFICIENCY ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 8 FDA reports)
BENIGN GASTRIC NEOPLASM ( 8 FDA reports)
BILIARY DILATATION ( 8 FDA reports)
BIOPSY ENDOMETRIUM ( 8 FDA reports)
BLADDER DISCOMFORT ( 8 FDA reports)
BLOOD BICARBONATE DECREASED ( 8 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 8 FDA reports)
BLOOD SODIUM INCREASED ( 8 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 8 FDA reports)
BLOOD URIC ACID INCREASED ( 8 FDA reports)
BRAIN COMPRESSION ( 8 FDA reports)
BRAIN MIDLINE SHIFT ( 8 FDA reports)
BREAST OPERATION ( 8 FDA reports)
BREAST SWELLING ( 8 FDA reports)
BRONCHITIS ACUTE ( 8 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 8 FDA reports)
BUNDLE BRANCH BLOCK ( 8 FDA reports)
CARDIOGENIC SHOCK ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 8 FDA reports)
CERVICAL MYELOPATHY ( 8 FDA reports)
CHEST WALL MASS ( 8 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 8 FDA reports)
CHONDROPATHY ( 8 FDA reports)
CHOREA ( 8 FDA reports)
CLOSTRIDIUM COLITIS ( 8 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 8 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 8 FDA reports)
CRANIOCEREBRAL INJURY ( 8 FDA reports)
DIABETIC GASTROPARESIS ( 8 FDA reports)
DRUG TOLERANCE INCREASED ( 8 FDA reports)
DYSPHASIA ( 8 FDA reports)
EAR DISORDER ( 8 FDA reports)
EJACULATION DELAYED ( 8 FDA reports)
EMBOLIC STROKE ( 8 FDA reports)
EMBOLISM ARTERIAL ( 8 FDA reports)
ENTEROCOCCAL INFECTION ( 8 FDA reports)
ENURESIS ( 8 FDA reports)
EXTREMITY NECROSIS ( 8 FDA reports)
EYES SUNKEN ( 8 FDA reports)
FAILURE OF IMPLANT ( 8 FDA reports)
FLASHBACK ( 8 FDA reports)
FLUID INTAKE REDUCED ( 8 FDA reports)
FUNGAL SKIN INFECTION ( 8 FDA reports)
GRANULOCYTE COUNT DECREASED ( 8 FDA reports)
GRANULOCYTOPENIA ( 8 FDA reports)
GRIP STRENGTH DECREASED ( 8 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 8 FDA reports)
HEPATIC FIBROSIS ( 8 FDA reports)
HEPATIC NECROSIS ( 8 FDA reports)
HERNIA REPAIR ( 8 FDA reports)
HORNER'S SYNDROME ( 8 FDA reports)
HYPERCHLORHYDRIA ( 8 FDA reports)
HYPERNATRAEMIA ( 8 FDA reports)
HYPERTHERMIA ( 8 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 8 FDA reports)
HYPOVENTILATION ( 8 FDA reports)
HYPOVOLAEMIC SHOCK ( 8 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 8 FDA reports)
IMMUNOSUPPRESSION ( 8 FDA reports)
INCISIONAL HERNIA ( 8 FDA reports)
INFANTILE APNOEIC ATTACK ( 8 FDA reports)
INTESTINAL RESECTION ( 8 FDA reports)
INTESTINAL ULCER ( 8 FDA reports)
IRITIS ( 8 FDA reports)
JAUNDICE NEONATAL ( 8 FDA reports)
JOINT CREPITATION ( 8 FDA reports)
JOINT LOCK ( 8 FDA reports)
KETONURIA ( 8 FDA reports)
LIPOGRANULOMA ( 8 FDA reports)
LUPUS-LIKE SYNDROME ( 8 FDA reports)
LYME DISEASE ( 8 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 8 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 8 FDA reports)
MULTI-ORGAN DISORDER ( 8 FDA reports)
MURDER ( 8 FDA reports)
NAIL BED TENDERNESS ( 8 FDA reports)
NASAL POLYPS ( 8 FDA reports)
NEUROLOGICAL SYMPTOM ( 8 FDA reports)
OPTIC ATROPHY ( 8 FDA reports)
ORAL NEOPLASM ( 8 FDA reports)
OTITIS EXTERNA ( 8 FDA reports)
PANCREATIC CYST ( 8 FDA reports)
PANCREATIC DISORDER ( 8 FDA reports)
PANCREATITIS RELAPSING ( 8 FDA reports)
PARADOXICAL DRUG REACTION ( 8 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 8 FDA reports)
PCO2 DECREASED ( 8 FDA reports)
PELVIC FRACTURE ( 8 FDA reports)
PERIORBITAL CELLULITIS ( 8 FDA reports)
PEYRONIE'S DISEASE ( 8 FDA reports)
PHLEBOLITH ( 8 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 8 FDA reports)
POLYMYALGIA RHEUMATICA ( 8 FDA reports)
POST PROCEDURAL PAIN ( 8 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 8 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 8 FDA reports)
PROSTATOMEGALY ( 8 FDA reports)
PURULENCE ( 8 FDA reports)
READING DISORDER ( 8 FDA reports)
REGURGITATION OF FOOD ( 8 FDA reports)
ROSACEA ( 8 FDA reports)
SCHAMBERG'S DISEASE ( 8 FDA reports)
SCLERAL DISORDER ( 8 FDA reports)
SEBORRHOEIC DERMATITIS ( 8 FDA reports)
SERUM FERRITIN INCREASED ( 8 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 8 FDA reports)
SKIN CANCER ( 8 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 8 FDA reports)
SPINAL COLUMN INJURY ( 8 FDA reports)
STENT PLACEMENT ( 8 FDA reports)
STRIDOR ( 8 FDA reports)
SUBCUTANEOUS NODULE ( 8 FDA reports)
SUDDEN CARDIAC DEATH ( 8 FDA reports)
SUNBURN ( 8 FDA reports)
TACHYPNOEA ( 8 FDA reports)
TARSAL TUNNEL SYNDROME ( 8 FDA reports)
TENDON SHEATH LESION EXCISION ( 8 FDA reports)
TINEA CRURIS ( 8 FDA reports)
UMBILICAL CORD ABNORMALITY ( 8 FDA reports)
UMBILICAL HERNIA ( 8 FDA reports)
VAGINAL MYCOSIS ( 8 FDA reports)
VASCULAR CALCIFICATION ( 8 FDA reports)
VASOCONSTRICTION ( 8 FDA reports)
VENOUS THROMBOSIS LIMB ( 8 FDA reports)
VENTRICULAR ARRHYTHMIA ( 8 FDA reports)
VIRAL LABYRINTHITIS ( 8 FDA reports)
VULVOVAGINAL PAIN ( 8 FDA reports)
TESTICULAR DISORDER ( 7 FDA reports)
TRICUSPID VALVE DISEASE ( 7 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
URGE INCONTINENCE ( 7 FDA reports)
URINARY TRACT OBSTRUCTION ( 7 FDA reports)
URINE AMPHETAMINE POSITIVE ( 7 FDA reports)
UTERINE PERFORATION ( 7 FDA reports)
VARICES OESOPHAGEAL ( 7 FDA reports)
VASCULAR DEMENTIA ( 7 FDA reports)
VASODILATATION ( 7 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 7 FDA reports)
VENTRICULAR HYPOPLASIA ( 7 FDA reports)
VULVAR DYSPLASIA ( 7 FDA reports)
VULVOVAGINAL DISCOMFORT ( 7 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 7 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 7 FDA reports)
ADNEXA UTERI MASS ( 7 FDA reports)
ADNEXA UTERI PAIN ( 7 FDA reports)
ADRENAL ADENOMA ( 7 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 7 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 7 FDA reports)
ANORECTAL DISCOMFORT ( 7 FDA reports)
ANTIBODY TEST POSITIVE ( 7 FDA reports)
ANTISOCIAL BEHAVIOUR ( 7 FDA reports)
AORTIC VALVE STENOSIS ( 7 FDA reports)
APALLIC SYNDROME ( 7 FDA reports)
ASPHYXIA ( 7 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 7 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 7 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 7 FDA reports)
BITE ( 7 FDA reports)
BLADDER SPASM ( 7 FDA reports)
BLOOD AMYLASE DECREASED ( 7 FDA reports)
BLOOD CREATINE INCREASED ( 7 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 7 FDA reports)
BLOOD IRON INCREASED ( 7 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 7 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 7 FDA reports)
BONE SWELLING ( 7 FDA reports)
BRADYKINESIA ( 7 FDA reports)
BREAST CELLULITIS ( 7 FDA reports)
BREAST HYPERPLASIA ( 7 FDA reports)
CALCINOSIS ( 7 FDA reports)
CARDIAC ENZYMES INCREASED ( 7 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 7 FDA reports)
CEPHALHAEMATOMA ( 7 FDA reports)
CEREBELLAR INFARCTION ( 7 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 7 FDA reports)
CHOKING SENSATION ( 7 FDA reports)
COLECTOMY PARTIAL ( 7 FDA reports)
COMPULSIVE SHOPPING ( 7 FDA reports)
CREPITATIONS ( 7 FDA reports)
CULTURE URINE POSITIVE ( 7 FDA reports)
CUSHING'S SYNDROME ( 7 FDA reports)
CYSTITIS INTERSTITIAL ( 7 FDA reports)
DEAFNESS NEUROSENSORY ( 7 FDA reports)
DEFAECATION URGENCY ( 7 FDA reports)
DELIRIUM TREMENS ( 7 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 7 FDA reports)
DERMATITIS ALLERGIC ( 7 FDA reports)
DIPLEGIA ( 7 FDA reports)
DRUG LEVEL DECREASED ( 7 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 7 FDA reports)
EAR PRURITUS ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 7 FDA reports)
ERYTHEMA NODOSUM ( 7 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 7 FDA reports)
FOOD ALLERGY ( 7 FDA reports)
GASTRITIS BACTERIAL ( 7 FDA reports)
GENITAL RASH ( 7 FDA reports)
GINGIVAL ERYTHEMA ( 7 FDA reports)
GLUCOSE URINE PRESENT ( 7 FDA reports)
GRANULOMA ANNULARE ( 7 FDA reports)
HAEMODYNAMIC INSTABILITY ( 7 FDA reports)
HAEMOLYSIS ( 7 FDA reports)
HAEMOLYTIC ANAEMIA ( 7 FDA reports)
HALLUCINATION, OLFACTORY ( 7 FDA reports)
HEART RATE ABNORMAL ( 7 FDA reports)
HELICOBACTER INFECTION ( 7 FDA reports)
HEPATIC PAIN ( 7 FDA reports)
HEPATITIS ALCOHOLIC ( 7 FDA reports)
HEREDITARY ANGIOEDEMA ( 7 FDA reports)
HIDRADENITIS ( 7 FDA reports)
HORMONE LEVEL ABNORMAL ( 7 FDA reports)
HYPERBILIRUBINAEMIA ( 7 FDA reports)
HYPERMAGNESAEMIA ( 7 FDA reports)
HYPOCHLORAEMIA ( 7 FDA reports)
IMPAIRED REASONING ( 7 FDA reports)
IMPRISONMENT ( 7 FDA reports)
INADEQUATE DIET ( 7 FDA reports)
INJECTION SITE NECROSIS ( 7 FDA reports)
INJECTION SITE PAPULE ( 7 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 7 FDA reports)
INTRACARDIAC THROMBUS ( 7 FDA reports)
LARGE INTESTINE PERFORATION ( 7 FDA reports)
LIVER ABSCESS ( 7 FDA reports)
LYMPH NODE PAIN ( 7 FDA reports)
MEDICAL DEVICE COMPLICATION ( 7 FDA reports)
MENINGITIS ASEPTIC ( 7 FDA reports)
MENTAL DISABILITY ( 7 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 7 FDA reports)
MITRAL VALVE STENOSIS ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 7 FDA reports)
MUSCLE FATIGUE ( 7 FDA reports)
MUSCLE RUPTURE ( 7 FDA reports)
NAIL DISORDER ( 7 FDA reports)
NARCOTIC INTOXICATION ( 7 FDA reports)
NEPHROSCLEROSIS ( 7 FDA reports)
NEUTROPHIL COUNT INCREASED ( 7 FDA reports)
OEDEMA MUCOSAL ( 7 FDA reports)
OLIGOHYDRAMNIOS ( 7 FDA reports)
ORAL SURGERY ( 7 FDA reports)
ORBITAL OEDEMA ( 7 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 7 FDA reports)
OSTEOCHONDROSIS ( 7 FDA reports)
OVARIAN CYST RUPTURED ( 7 FDA reports)
PARAPROTEINAEMIA ( 7 FDA reports)
PAROTID GLAND ENLARGEMENT ( 7 FDA reports)
PELVIC ABSCESS ( 7 FDA reports)
PELVIC FLUID COLLECTION ( 7 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 7 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 7 FDA reports)
PERINEAL ABSCESS ( 7 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 7 FDA reports)
PH BODY FLUID ABNORMAL ( 7 FDA reports)
PITUITARY TUMOUR ( 7 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 7 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 7 FDA reports)
POSTOPERATIVE ILEUS ( 7 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 7 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 7 FDA reports)
PSYCHOLOGICAL TRAUMA ( 7 FDA reports)
RADIATION NECROSIS ( 7 FDA reports)
RASH VESICULAR ( 7 FDA reports)
RECTAL EXAMINATION ABNORMAL ( 7 FDA reports)
RENAL ARTERY STENOSIS ( 7 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 7 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 7 FDA reports)
RETINAL DISORDER ( 7 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 7 FDA reports)
RHINITIS SEASONAL ( 7 FDA reports)
SCLERODERMA ( 7 FDA reports)
SCOTOMA ( 7 FDA reports)
SOMATOFORM DISORDER ( 7 FDA reports)
SPLINT APPLICATION ( 7 FDA reports)
SQUAMOUS CELL CARCINOMA ( 7 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 7 FDA reports)
SUBDURAL HAEMORRHAGE ( 7 FDA reports)
SURGICAL FAILURE ( 7 FDA reports)
SWEAT GLAND TUMOUR ( 7 FDA reports)
ACETONAEMIA ( 6 FDA reports)
ALCOHOL PROBLEM ( 6 FDA reports)
ALCOHOLIC PANCREATITIS ( 6 FDA reports)
ANAL INFLAMMATION ( 6 FDA reports)
ANION GAP INCREASED ( 6 FDA reports)
ANISOMETROPIA ( 6 FDA reports)
ANORECTAL DISORDER ( 6 FDA reports)
ANURIA ( 6 FDA reports)
AORTIC DILATATION ( 6 FDA reports)
APPLICATION SITE URTICARIA ( 6 FDA reports)
AREFLEXIA ( 6 FDA reports)
ASPIRATION BREAST ( 6 FDA reports)
BENIGN BREAST NEOPLASM ( 6 FDA reports)
BICUSPID AORTIC VALVE ( 6 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 6 FDA reports)
BILIARY TRACT DISORDER ( 6 FDA reports)
BIOPSY ( 6 FDA reports)
BIOPSY COLON ABNORMAL ( 6 FDA reports)
BRAIN NEOPLASM BENIGN ( 6 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 6 FDA reports)
BRAIN SCAN ABNORMAL ( 6 FDA reports)
BREAST DISORDER FEMALE ( 6 FDA reports)
BREAST HAEMATOMA ( 6 FDA reports)
BRONCHOPULMONARY DISEASE ( 6 FDA reports)
BURSA DISORDER ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CARBON MONOXIDE POISONING ( 6 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 6 FDA reports)
CARDIOVERSION ( 6 FDA reports)
CARTILAGE INJURY ( 6 FDA reports)
CATARACT NUCLEAR ( 6 FDA reports)
CATHETER RELATED COMPLICATION ( 6 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 6 FDA reports)
CHOLECYSTITIS INFECTIVE ( 6 FDA reports)
CHRONIC HEPATIC FAILURE ( 6 FDA reports)
COELIAC DISEASE ( 6 FDA reports)
COLON CANCER STAGE III ( 6 FDA reports)
COLONOSCOPY ABNORMAL ( 6 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 6 FDA reports)
CONTRAST MEDIA REACTION ( 6 FDA reports)
COR PULMONALE ( 6 FDA reports)
CORNEAL EROSION ( 6 FDA reports)
CORONARY ARTERY ANEURYSM ( 6 FDA reports)
CRANIAL NERVE DISORDER ( 6 FDA reports)
DARK CIRCLES UNDER EYES ( 6 FDA reports)
DEAFNESS BILATERAL ( 6 FDA reports)
DISINHIBITION ( 6 FDA reports)
DUODENAL SCARRING ( 6 FDA reports)
EATING DISORDER SYMPTOM ( 6 FDA reports)
ECTOPIC KIDNEY ( 6 FDA reports)
EJACULATION FAILURE ( 6 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 6 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 6 FDA reports)
ENDOCERVICAL CURETTAGE ( 6 FDA reports)
ESCHAR ( 6 FDA reports)
EXCESSIVE MASTURBATION ( 6 FDA reports)
EXCITABILITY ( 6 FDA reports)
EYE NAEVUS ( 6 FDA reports)
EYE OEDEMA ( 6 FDA reports)
FAT TISSUE INCREASED ( 6 FDA reports)
FEAR OF DISEASE ( 6 FDA reports)
FOOT OPERATION ( 6 FDA reports)
FOREIGN BODY TRAUMA ( 6 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 6 FDA reports)
GASTRIC VOLVULUS ( 6 FDA reports)
GASTROINTESTINAL OEDEMA ( 6 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 6 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 6 FDA reports)
GASTROSTOMY TUBE INSERTION ( 6 FDA reports)
GENETIC COUNSELLING ( 6 FDA reports)
GRANDIOSITY ( 6 FDA reports)
GROIN ABSCESS ( 6 FDA reports)
GRUNTING ( 6 FDA reports)
HEAD DISCOMFORT ( 6 FDA reports)
HEART SOUNDS ABNORMAL ( 6 FDA reports)
HEPATIC TRAUMA ( 6 FDA reports)
HEPATOSPLENOMEGALY ( 6 FDA reports)
HYDROCHOLECYSTIS ( 6 FDA reports)
HYDROMETRA ( 6 FDA reports)
HYDROPS FOETALIS ( 6 FDA reports)
HYPERAMMONAEMIA ( 6 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 6 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 6 FDA reports)
HYSTEROSCOPY ( 6 FDA reports)
IATROGENIC INJURY ( 6 FDA reports)
ILEAL STENOSIS ( 6 FDA reports)
ILIAC ARTERY STENOSIS ( 6 FDA reports)
INCISIONAL DRAINAGE ( 6 FDA reports)
INJECTION SITE SCAB ( 6 FDA reports)
INTERCOSTAL NEURALGIA ( 6 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 6 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 6 FDA reports)
KELOID SCAR ( 6 FDA reports)
LARYNGEAL WEB ( 6 FDA reports)
LEGAL PROBLEM ( 6 FDA reports)
LIVER TRANSPLANT REJECTION ( 6 FDA reports)
LOWER EXTREMITY MASS ( 6 FDA reports)
LUNG OPERATION ( 6 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 6 FDA reports)
MACULAR OEDEMA ( 6 FDA reports)
MALE ORGASMIC DISORDER ( 6 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 6 FDA reports)
MARROW HYPERPLASIA ( 6 FDA reports)
MENIERE'S DISEASE ( 6 FDA reports)
METASTASES TO MENINGES ( 6 FDA reports)
MICROCEPHALY ( 6 FDA reports)
MIGRAINE WITHOUT AURA ( 6 FDA reports)
MONARTHRITIS ( 6 FDA reports)
MONOPLEGIA ( 6 FDA reports)
MOUTH INJURY ( 6 FDA reports)
MUMPS ( 6 FDA reports)
MUSCLE FLAP OPERATION ( 6 FDA reports)
MYASTHENIA GRAVIS ( 6 FDA reports)
NASAL OBSTRUCTION ( 6 FDA reports)
NASAL OEDEMA ( 6 FDA reports)
NASAL VESTIBULITIS ( 6 FDA reports)
NECK MASS ( 6 FDA reports)
NEOPLASM OF APPENDIX ( 6 FDA reports)
NOSOCOMIAL INFECTION ( 6 FDA reports)
OESOPHAGEAL PAIN ( 6 FDA reports)
OESOPHAGITIS ULCERATIVE ( 6 FDA reports)
OESTRADIOL DECREASED ( 6 FDA reports)
ORAL MUCOSAL BLISTERING ( 6 FDA reports)
PAINFUL ERECTION ( 6 FDA reports)
PAINFUL RESPIRATION ( 6 FDA reports)
PANCREATIC ENZYMES INCREASED ( 6 FDA reports)
PARANASAL SINUS DISCOMFORT ( 6 FDA reports)
PARANOID PERSONALITY DISORDER ( 6 FDA reports)
PARAPARESIS ( 6 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 6 FDA reports)
PELVIC PROLAPSE ( 6 FDA reports)
PERNICIOUS ANAEMIA ( 6 FDA reports)
PICKWICKIAN SYNDROME ( 6 FDA reports)
PLEURAL DISORDER ( 6 FDA reports)
POLYTRAUMATISM ( 6 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 6 FDA reports)
PROCTITIS ( 6 FDA reports)
PROCTOCOLITIS ( 6 FDA reports)
PROTEIN URINE PRESENT ( 6 FDA reports)
PROTRUSION TONGUE ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
PULMONARY HYPOPLASIA ( 6 FDA reports)
PULMONARY VALVE STENOSIS ( 6 FDA reports)
PYODERMA GANGRENOSUM ( 6 FDA reports)
PYURIA ( 6 FDA reports)
RADICULAR PAIN ( 6 FDA reports)
RENAL HAEMORRHAGE ( 6 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 6 FDA reports)
RESPIRATION ABNORMAL ( 6 FDA reports)
SEBORRHOEA ( 6 FDA reports)
SKIN PLAQUE ( 6 FDA reports)
SLEEP TERROR ( 6 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 6 FDA reports)
SMALL FOR DATES BABY ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
STILLBIRTH ( 6 FDA reports)
STUPOR ( 6 FDA reports)
TENDON GRAFT ( 6 FDA reports)
TESTICULAR ATROPHY ( 6 FDA reports)
THEFT ( 6 FDA reports)
THERAPY REGIMEN CHANGED ( 6 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 6 FDA reports)
TOXIC ENCEPHALOPATHY ( 6 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 6 FDA reports)
TRANSFUSION ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
URETHRAL STRICTURE ( 6 FDA reports)
URINE ABNORMALITY ( 6 FDA reports)
URINE OUTPUT INCREASED ( 6 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 6 FDA reports)
VAGINAL ODOUR ( 6 FDA reports)
VASCULAR PSEUDOANEURYSM ( 6 FDA reports)
VICTIM OF SEXUAL ABUSE ( 6 FDA reports)
VIRAL LOAD INCREASED ( 6 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
VOCAL CORD DISORDER ( 6 FDA reports)
VULVAL CANCER ( 6 FDA reports)
VULVAL OEDEMA ( 6 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 5 FDA reports)
TRAUMATIC FRACTURE ( 5 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 5 FDA reports)
ULCER HAEMORRHAGE ( 5 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 5 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 5 FDA reports)
URINE FLOW DECREASED ( 5 FDA reports)
VASCULAR BYPASS GRAFT ( 5 FDA reports)
VASCULAR INJURY ( 5 FDA reports)
VASOSPASM ( 5 FDA reports)
VENTRICULAR FAILURE ( 5 FDA reports)
VESTIBULOPLASTY ( 5 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 5 FDA reports)
VITRECTOMY ( 5 FDA reports)
VOCAL CORD POLYP ( 5 FDA reports)
VOMITING PROJECTILE ( 5 FDA reports)
VULVAL ULCERATION ( 5 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 5 FDA reports)
WALKING AID USER ( 5 FDA reports)
WHIPLASH INJURY ( 5 FDA reports)
WOUND SECRETION ( 5 FDA reports)
ABDOMINAL MASS ( 5 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
AMAUROSIS FUGAX ( 5 FDA reports)
AMNIOTIC BAND SYNDROME ( 5 FDA reports)
ANAL FISTULA ( 5 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 5 FDA reports)
AORTIC BYPASS ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
APPLICATION SITE DERMATITIS ( 5 FDA reports)
ARTHRITIS INFECTIVE ( 5 FDA reports)
ARTHROSCOPIC SURGERY ( 5 FDA reports)
ASTHENOPIA ( 5 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 5 FDA reports)
AXILLARY VEIN THROMBOSIS ( 5 FDA reports)
BASEDOW'S DISEASE ( 5 FDA reports)
BLEEDING TIME PROLONGED ( 5 FDA reports)
BLOOD URINE ( 5 FDA reports)
BLOODY DISCHARGE ( 5 FDA reports)
BONE FORMATION INCREASED ( 5 FDA reports)
BONE MARROW NECROSIS ( 5 FDA reports)
BONE NEOPLASM ( 5 FDA reports)
BONE TRIMMING ( 5 FDA reports)
BRAIN STEM INFARCTION ( 5 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 5 FDA reports)
CACHEXIA ( 5 FDA reports)
CARCINOMA IN SITU OF EYE ( 5 FDA reports)
CARDIAC HYPERTROPHY ( 5 FDA reports)
CARDIAC OUTPUT DECREASED ( 5 FDA reports)
CATHETER SITE HAEMORRHAGE ( 5 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
COLONOSCOPY ( 5 FDA reports)
COLOSTOMY ( 5 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 5 FDA reports)
CORONARY ARTERY SURGERY ( 5 FDA reports)
CYSTITIS HAEMORRHAGIC ( 5 FDA reports)
DENTOFACIAL ANOMALY ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 5 FDA reports)
DIABETIC ULCER ( 5 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 5 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
DUODENAL ULCER ( 5 FDA reports)
DYSPLASIA ( 5 FDA reports)
EAR HAEMORRHAGE ( 5 FDA reports)
EAR MALFORMATION ( 5 FDA reports)
EFFUSION ( 5 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 5 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENTEROBACTER INFECTION ( 5 FDA reports)
EOSINOPHILIA ( 5 FDA reports)
FACTITIOUS DISORDER ( 5 FDA reports)
FACTOR V LEIDEN MUTATION ( 5 FDA reports)
FANCONI SYNDROME ACQUIRED ( 5 FDA reports)
FEELING OF RELAXATION ( 5 FDA reports)
FEMALE ORGASMIC DISORDER ( 5 FDA reports)
FLAT FEET ( 5 FDA reports)
FOOD POISONING ( 5 FDA reports)
FRACTURE MALUNION ( 5 FDA reports)
FRACTURED COCCYX ( 5 FDA reports)
GASTRIC OPERATION ( 5 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 5 FDA reports)
HAEMANGIOMA OF LIVER ( 5 FDA reports)
HAEMATOCRIT INCREASED ( 5 FDA reports)
HAIR COLOUR CHANGES ( 5 FDA reports)
HAIR METAL TEST ABNORMAL ( 5 FDA reports)
HALLUCINATION, TACTILE ( 5 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 5 FDA reports)
HEPATIC MASS ( 5 FDA reports)
HEPATIC NEOPLASM ( 5 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 5 FDA reports)
HOARSENESS ( 5 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 5 FDA reports)
HYPERINSULINISM ( 5 FDA reports)
HYPERPHOSPHATAEMIA ( 5 FDA reports)
HYPOREFLEXIA ( 5 FDA reports)
ILLUSION ( 5 FDA reports)
IMMUNODEFICIENCY ( 5 FDA reports)
INCISION SITE HAEMORRHAGE ( 5 FDA reports)
INDURATION ( 5 FDA reports)
INJECTION SITE EXTRAVASATION ( 5 FDA reports)
INTRA-UTERINE DEATH ( 5 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 5 FDA reports)
IODINE ALLERGY ( 5 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 5 FDA reports)
ITCHING SCAR ( 5 FDA reports)
LARGE INTESTINAL ULCER ( 5 FDA reports)
LARYNGEAL OEDEMA ( 5 FDA reports)
LEARNING DISORDER ( 5 FDA reports)
LIP ULCERATION ( 5 FDA reports)
LUNG ADENOCARCINOMA ( 5 FDA reports)
LUNG TRANSPLANT ( 5 FDA reports)
LYMPH NODE FIBROSIS ( 5 FDA reports)
MACULAR HOLE ( 5 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 5 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 5 FDA reports)
MEGAKARYOCYTES INCREASED ( 5 FDA reports)
MENINGEAL NEOPLASM ( 5 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 5 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 5 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 5 FDA reports)
NAIL DYSTROPHY ( 5 FDA reports)
NEPHROCALCINOSIS ( 5 FDA reports)
NEUTROPENIC COLITIS ( 5 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 5 FDA reports)
NORMAL NEWBORN ( 5 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 5 FDA reports)
NYSTAGMUS ( 5 FDA reports)
OBSTRUCTIVE UROPATHY ( 5 FDA reports)
OLIGURIA ( 5 FDA reports)
ONYCHALGIA ( 5 FDA reports)
OPTIC DISC DRUSEN ( 5 FDA reports)
OPTIC NERVE DISORDER ( 5 FDA reports)
ORAL SOFT TISSUE DISORDER ( 5 FDA reports)
OVARIAN NEOPLASM ( 5 FDA reports)
PANCREATIC CARCINOMA ( 5 FDA reports)
PANCREATIC PSEUDOCYST ( 5 FDA reports)
PARANEOPLASTIC SYNDROME ( 5 FDA reports)
PELVIC HAEMATOMA ( 5 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 5 FDA reports)
PERIDIVERTICULAR ABSCESS ( 5 FDA reports)
PHARYNGEAL ERYTHEMA ( 5 FDA reports)
PHYSICAL ABUSE ( 5 FDA reports)
PLACENTAL DISORDER ( 5 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 5 FDA reports)
POLYCYSTIC OVARIES ( 5 FDA reports)
POLYPECTOMY ( 5 FDA reports)
POST PROCEDURAL HAEMATOMA ( 5 FDA reports)
POST PROCEDURAL INFECTION ( 5 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 5 FDA reports)
PROCEDURAL SITE REACTION ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
PSYCHOTIC BEHAVIOUR ( 5 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 5 FDA reports)
PULMONARY GRANULOMA ( 5 FDA reports)
PULMONARY MYCOSIS ( 5 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 5 FDA reports)
PUPILS UNEQUAL ( 5 FDA reports)
PUSTULAR PSORIASIS ( 5 FDA reports)
QUADRIPARESIS ( 5 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 5 FDA reports)
RETICULOCYTOSIS ( 5 FDA reports)
RETINAL EXUDATES ( 5 FDA reports)
RETINAL VEIN OCCLUSION ( 5 FDA reports)
RHONCHI ( 5 FDA reports)
SALIVA ALTERED ( 5 FDA reports)
SCAPHOCEPHALY ( 5 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 5 FDA reports)
SERUM FERRITIN DECREASED ( 5 FDA reports)
SHIFT TO THE LEFT ( 5 FDA reports)
SHORTENED CERVIX ( 5 FDA reports)
SIMPLE PARTIAL SEIZURES ( 5 FDA reports)
SKIN CANCER METASTATIC ( 5 FDA reports)
SKIN TURGOR DECREASED ( 5 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 5 FDA reports)
SPUTUM PURULENT ( 5 FDA reports)
STENOTROPHOMONAS INFECTION ( 5 FDA reports)
SYSTEMIC CANDIDA ( 5 FDA reports)
ABDOMINAL ABSCESS ( 4 FDA reports)
ABSCESS INTESTINAL ( 4 FDA reports)
ACCIDENTAL DEATH ( 4 FDA reports)
ACNE CYSTIC ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 4 FDA reports)
ACUTE LEUKAEMIA ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 4 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 4 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 4 FDA reports)
AMYLOIDOSIS ( 4 FDA reports)
ANENCEPHALY ( 4 FDA reports)
ANISOCYTOSIS ( 4 FDA reports)
ANKLE OPERATION ( 4 FDA reports)
ANKLE RECONSTRUCTION ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
APNOEIC ATTACK ( 4 FDA reports)
APRAXIA ( 4 FDA reports)
ARRESTED LABOUR ( 4 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
ARTHRODESIS ( 4 FDA reports)
ARTHROSCOPY ( 4 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 4 FDA reports)
AUTONOMIC NEUROPATHY ( 4 FDA reports)
BALANITIS ( 4 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD CORTISOL DECREASED ( 4 FDA reports)
BLOOD GLUCOSE ( 4 FDA reports)
BLOOD LACTIC ACID INCREASED ( 4 FDA reports)
BLUNTED AFFECT ( 4 FDA reports)
BODY DYSMORPHIC DISORDER ( 4 FDA reports)
BONE CANCER METASTATIC ( 4 FDA reports)
BORDERLINE GLAUCOMA ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BRACHIAL PLEXOPATHY ( 4 FDA reports)
BREAST MICROCALCIFICATION ( 4 FDA reports)
CARCINOID TUMOUR PULMONARY ( 4 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 4 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 4 FDA reports)
CATHETER REMOVAL ( 4 FDA reports)
CATHETER SITE INFECTION ( 4 FDA reports)
CATHETER SITE RELATED REACTION ( 4 FDA reports)
CEREBELLAR ATAXIA ( 4 FDA reports)
CEREBELLAR SYNDROME ( 4 FDA reports)
CEREBRAL ARTERY STENOSIS ( 4 FDA reports)
CEREBRAL THROMBOSIS ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 4 FDA reports)
CHEYNE-STOKES RESPIRATION ( 4 FDA reports)
CHONDROPLASTY ( 4 FDA reports)
CHOREOATHETOSIS ( 4 FDA reports)
CHRONIC HEPATITIS ( 4 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 4 FDA reports)
CLONUS ( 4 FDA reports)
COITAL BLEEDING ( 4 FDA reports)
COLONIC FISTULA ( 4 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 4 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 4 FDA reports)
CONVULSION NEONATAL ( 4 FDA reports)
CSF PROTEIN INCREASED ( 4 FDA reports)
CULDOPLASTY ( 4 FDA reports)
DENTAL DISCOMFORT ( 4 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 4 FDA reports)
DERMATITIS ATOPIC ( 4 FDA reports)
DISSOCIATIVE FUGUE ( 4 FDA reports)
DISTRACTIBILITY ( 4 FDA reports)
DIVERTICULAR PERFORATION ( 4 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
DRUG SCREEN NEGATIVE ( 4 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 4 FDA reports)
DUODENAL ULCER PERFORATION ( 4 FDA reports)
DURAL FISTULA ( 4 FDA reports)
DYSMORPHISM ( 4 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 4 FDA reports)
EDUCATIONAL PROBLEM ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 4 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 4 FDA reports)
ELEVATED MOOD ( 4 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 4 FDA reports)
EPILEPTIC AURA ( 4 FDA reports)
EROSIVE OESOPHAGITIS ( 4 FDA reports)
EXPOSURE TO TOXIC AGENT ( 4 FDA reports)
EYE INFECTION ( 4 FDA reports)
FAECALOMA ( 4 FDA reports)
FEAR OF WEIGHT GAIN ( 4 FDA reports)
FEEDING DISORDER NEONATAL ( 4 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 4 FDA reports)
FROSTBITE ( 4 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 4 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 4 FDA reports)
GENERAL SYMPTOM ( 4 FDA reports)
GINGIVAL ABSCESS ( 4 FDA reports)
GLOSSITIS ( 4 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 4 FDA reports)
GRANULOMA ( 4 FDA reports)
GRIMACING ( 4 FDA reports)
HALITOSIS ( 4 FDA reports)
HEAT RASH ( 4 FDA reports)
HELICOBACTER GASTRITIS ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HIP DYSPLASIA ( 4 FDA reports)
HIP SURGERY ( 4 FDA reports)
HIV INFECTION ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 4 FDA reports)
HYPERTROPHIC SCAR ( 4 FDA reports)
HYPERVIGILANCE ( 4 FDA reports)
HYPOTELORISM OF ORBIT ( 4 FDA reports)
HYPOVITAMINOSIS ( 4 FDA reports)
ILEOSTOMY ( 4 FDA reports)
IMPLANT SITE REACTION ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
INCISION SITE ERYTHEMA ( 4 FDA reports)
INCISION SITE INFECTION ( 4 FDA reports)
INDIFFERENCE ( 4 FDA reports)
INFERTILITY ( 4 FDA reports)
INFERTILITY FEMALE ( 4 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
INFUSION SITE ERYTHEMA ( 4 FDA reports)
INFUSION SITE SWELLING ( 4 FDA reports)
INJECTION SITE ABSCESS ( 4 FDA reports)
INJECTION SITE DISCOMFORT ( 4 FDA reports)
INJECTION SITE VESICLES ( 4 FDA reports)
INJURY ASPHYXIATION ( 4 FDA reports)
INNER EAR DISORDER ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 4 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 4 FDA reports)
INTESTINAL STENOSIS ( 4 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
JOB DISSATISFACTION ( 4 FDA reports)
KERATITIS ( 4 FDA reports)
KIDNEY ENLARGEMENT ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 4 FDA reports)
LIBIDO DISORDER ( 4 FDA reports)
LIMB OPERATION ( 4 FDA reports)
LIP OEDEMA ( 4 FDA reports)
LIVER OPERATION ( 4 FDA reports)
LOSS OF PROPRIOCEPTION ( 4 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 4 FDA reports)
LUNG INJURY ( 4 FDA reports)
LYMPH NODE CANCER METASTATIC ( 4 FDA reports)
MADAROSIS ( 4 FDA reports)
MANDIBULECTOMY ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
MENINGITIS BACTERIAL ( 4 FDA reports)
MENOPAUSAL DEPRESSION ( 4 FDA reports)
MIDDLE EAR EFFUSION ( 4 FDA reports)
MUCOUS MEMBRANE DISORDER ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
MYELOMALACIA ( 4 FDA reports)
MYOCARDITIS ( 4 FDA reports)
NAIL DISCOLOURATION ( 4 FDA reports)
NASAL CYST ( 4 FDA reports)
NASAL DISORDER ( 4 FDA reports)
NASAL MUCOSAL DISORDER ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
NECROTISING FASCIITIS ( 4 FDA reports)
NEONATAL ASPIRATION ( 4 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 4 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 4 FDA reports)
NIGHT BLINDNESS ( 4 FDA reports)
NO ADVERSE DRUG EFFECT ( 4 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 4 FDA reports)
OLIGODENDROGLIOMA ( 4 FDA reports)
ONYCHOMADESIS ( 4 FDA reports)
OPISTHOTONUS ( 4 FDA reports)
OROPHARYNGEAL BLISTERING ( 4 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 4 FDA reports)
OSTEOMYELITIS FUNGAL ( 4 FDA reports)
PAINFUL DEFAECATION ( 4 FDA reports)
PANCREATIC INJURY ( 4 FDA reports)
PANCREATITIS NECROTISING ( 4 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 4 FDA reports)
PEAU D'ORANGE ( 4 FDA reports)
PECTUS CARINATUM ( 4 FDA reports)
PENILE DISCHARGE ( 4 FDA reports)
PERIPHERAL PULSE DECREASED ( 4 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 4 FDA reports)
PERIRECTAL ABSCESS ( 4 FDA reports)
PHIMOSIS ( 4 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 4 FDA reports)
PITUITARY TUMOUR BENIGN ( 4 FDA reports)
PLACENTAL INSUFFICIENCY ( 4 FDA reports)
PLEURAL NEOPLASM ( 4 FDA reports)
PNEUMONIA HAEMOPHILUS ( 4 FDA reports)
PNEUMOPERITONEUM ( 4 FDA reports)
PO2 DECREASED ( 4 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 4 FDA reports)
PORPHYRIA NON-ACUTE ( 4 FDA reports)
POST HERPETIC NEURALGIA ( 4 FDA reports)
POSTICTAL HEADACHE ( 4 FDA reports)
POSTPARTUM DISORDER ( 4 FDA reports)
PRODUCT COUNTERFEIT ( 4 FDA reports)
PRODUCT TASTE ABNORMAL ( 4 FDA reports)
PROSTATE INFECTION ( 4 FDA reports)
PSEUDODEMENTIA ( 4 FDA reports)
PYLORIC STENOSIS ( 4 FDA reports)
RECTOCELE REPAIR ( 4 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 4 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 4 FDA reports)
REFLEXES ABNORMAL ( 4 FDA reports)
RENAL INFARCT ( 4 FDA reports)
RENAL MASS ( 4 FDA reports)
RENAL NEOPLASM ( 4 FDA reports)
RENAL PAIN ( 4 FDA reports)
RENAL TUBULAR DISORDER ( 4 FDA reports)
REPETITIVE SPEECH ( 4 FDA reports)
RETICULOCYTE COUNT INCREASED ( 4 FDA reports)
RETINAL VEIN THROMBOSIS ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 4 FDA reports)
SALPINGO-OOPHORECTOMY ( 4 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 4 FDA reports)
SENILE DEMENTIA ( 4 FDA reports)
SEXUAL ABUSE ( 4 FDA reports)
SKIN CHAPPED ( 4 FDA reports)
SKIN CYST EXCISION ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN HYPOPIGMENTATION ( 4 FDA reports)
SKIN OEDEMA ( 4 FDA reports)
SKIN STRIAE ( 4 FDA reports)
SKIN WRINKLING ( 4 FDA reports)
SOFT TISSUE INFECTION ( 4 FDA reports)
SPINAL OPERATION ( 4 FDA reports)
SPONDYLOARTHROPATHY ( 4 FDA reports)
SPONDYLOSIS ( 4 FDA reports)
SPONTANEOUS PENILE ERECTION ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
STRABISMUS ( 4 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 4 FDA reports)
SUPRAPUBIC PAIN ( 4 FDA reports)
SYMPTOM MASKED ( 4 FDA reports)
THERAPEUTIC PROCEDURE ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
THROMBOSIS IN DEVICE ( 4 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
THYROID GLAND CANCER ( 4 FDA reports)
THYROID OPERATION ( 4 FDA reports)
TINEA INFECTION ( 4 FDA reports)
TOE OPERATION ( 4 FDA reports)
TONGUE BLISTERING ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TONSILLITIS ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
TRACHEAL STENOSIS ( 4 FDA reports)
TRISOMY 21 ( 4 FDA reports)
ULNA FRACTURE ( 4 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 4 FDA reports)
URTICARIA GENERALISED ( 4 FDA reports)
UTERINE INFECTION ( 4 FDA reports)
UTERINE PROLAPSE ( 4 FDA reports)
VAGINITIS ATROPHIC ( 4 FDA reports)
VARICOSE VEIN OPERATION ( 4 FDA reports)
VASCULAR GRAFT ( 4 FDA reports)
VENA CAVA THROMBOSIS ( 4 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 4 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
WOUND NECROSIS ( 4 FDA reports)
TERMINAL STATE ( 3 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 3 FDA reports)
THYROID MASS ( 3 FDA reports)
TONGUE DRY ( 3 FDA reports)
TONSILLECTOMY ( 3 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 3 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 3 FDA reports)
TRANSPLANT ( 3 FDA reports)
TRAUMATIC ARTHROPATHY ( 3 FDA reports)
TRAUMATIC LUNG INJURY ( 3 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 3 FDA reports)
TRICHORRHEXIS ( 3 FDA reports)
TRIGEMINAL NERVE DISORDER ( 3 FDA reports)
TROPONIN I INCREASED ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
UHTHOFF'S PHENOMENON ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UMBILICAL CORD PROLAPSE ( 3 FDA reports)
UNEMPLOYMENT ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
URETHRAL DISORDER ( 3 FDA reports)
URETHRAL MEATUS STENOSIS ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
URTICARIA CHRONIC ( 3 FDA reports)
UTERINE MASS ( 3 FDA reports)
UTERINE SPASM ( 3 FDA reports)
VAGINAL BURNING SENSATION ( 3 FDA reports)
VAGINAL SWELLING ( 3 FDA reports)
VARICELLA ( 3 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 3 FDA reports)
VASCULAR RUPTURE ( 3 FDA reports)
VELOPHARYNGEAL INCOMPETENCE ( 3 FDA reports)
VENOUS INJURY ( 3 FDA reports)
VESSEL PERFORATION ( 3 FDA reports)
VIRILISM ( 3 FDA reports)
VITAMIN B12 INCREASED ( 3 FDA reports)
VITREOUS DISORDER ( 3 FDA reports)
VOCAL CORD NEOPLASM ( 3 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 3 FDA reports)
ABDOMINOPLASTY ( 3 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 3 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ABSCESS ORAL ( 3 FDA reports)
ACCIDENTAL POISONING ( 3 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 3 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
ALCOHOL INTOLERANCE ( 3 FDA reports)
ALLERGY TEST POSITIVE ( 3 FDA reports)
ALLERGY TO ANIMAL ( 3 FDA reports)
ALLERGY TO CHEMICALS ( 3 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 3 FDA reports)
ALVEOLAR PROTEINOSIS ( 3 FDA reports)
ALVEOLITIS ALLERGIC ( 3 FDA reports)
AMNIOCENTESIS ABNORMAL ( 3 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 3 FDA reports)
ANAEMIA OF PREGNANCY ( 3 FDA reports)
ANAESTHETIC COMPLICATION ( 3 FDA reports)
ANAL PRURITUS ( 3 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANDROGEN DEFICIENCY ( 3 FDA reports)
ANGIOMYOLIPOMA ( 3 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 3 FDA reports)
ANTIDEPRESSANT DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC OCCLUSION ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
AORTIC VALVE DISEASE ( 3 FDA reports)
APPLICATION SITE BLEEDING ( 3 FDA reports)
APPLICATION SITE EROSION ( 3 FDA reports)
APPLICATION SITE SWELLING ( 3 FDA reports)
ARACHNOID CYST ( 3 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ASTERIXIS ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 3 FDA reports)
BACTERIAL TEST POSITIVE ( 3 FDA reports)
BILIARY NEOPLASM ( 3 FDA reports)
BLAST CELL COUNT DECREASED ( 3 FDA reports)
BLEEDING PERIPARTUM ( 3 FDA reports)
BLOOD BICARBONATE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN DECREASED ( 3 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 3 FDA reports)
BLOOD OSMOLARITY INCREASED ( 3 FDA reports)
BLOOD PH INCREASED ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BRADYCARDIA NEONATAL ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BREAST DYSPLASIA ( 3 FDA reports)
BREAST ENGORGEMENT ( 3 FDA reports)
BREAST INFECTION ( 3 FDA reports)
BREAST OEDEMA ( 3 FDA reports)
BREATH ODOUR ( 3 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 3 FDA reports)
BURNS SECOND DEGREE ( 3 FDA reports)
BURNS THIRD DEGREE ( 3 FDA reports)
CALCULUS URETHRAL ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 3 FDA reports)
CARDIAC PERFORATION ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CATHETER PLACEMENT ( 3 FDA reports)
CATHETERISATION VENOUS ( 3 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CERVICITIS ( 3 FDA reports)
CHEMICAL PERITONITIS ( 3 FDA reports)
CHEST INJURY ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 3 FDA reports)
CLONIC CONVULSION ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
COLORECTAL CANCER METASTATIC ( 3 FDA reports)
COMPLICATED MIGRAINE ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 3 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 3 FDA reports)
CONGENITAL TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 3 FDA reports)
CONSTRICTED AFFECT ( 3 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 3 FDA reports)
CORONARY ARTERY EMBOLISM ( 3 FDA reports)
CRUSH INJURY ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
CYANOSIS NEONATAL ( 3 FDA reports)
DEATH NEONATAL ( 3 FDA reports)
DEATH OF RELATIVE ( 3 FDA reports)
DELAYED FONTANELLE CLOSURE ( 3 FDA reports)
DELIVERY ( 3 FDA reports)
DEVICE OCCLUSION ( 3 FDA reports)
DIET REFUSAL ( 3 FDA reports)
DRUG ADDICT ( 3 FDA reports)
DRUG DIVERSION ( 3 FDA reports)
DRUG TOLERANCE DECREASED ( 3 FDA reports)
DYSPNOEA EXACERBATED ( 3 FDA reports)
DYSSOMNIA ( 3 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 3 FDA reports)
EROSIVE DUODENITIS ( 3 FDA reports)
ERYTHEMA INFECTIOSUM ( 3 FDA reports)
EXCESSIVE EYE BLINKING ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
EYELID FUNCTION DISORDER ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
FAECES HARD ( 3 FDA reports)
FALLOT'S TETRALOGY ( 3 FDA reports)
FASCIITIS ( 3 FDA reports)
FEEDING DISORDER ( 3 FDA reports)
FINGER DEFORMITY ( 3 FDA reports)
FOETAL HEART RATE INCREASED ( 3 FDA reports)
FOOD INTERACTION ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 3 FDA reports)
GALLBLADDER POLYP ( 3 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 3 FDA reports)
GOUTY ARTHRITIS ( 3 FDA reports)
GRIEF REACTION ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 3 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 3 FDA reports)
HEAD BANGING ( 3 FDA reports)
HEAD TITUBATION ( 3 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
HEMIVERTEBRA ( 3 FDA reports)
HEPATIC HAEMORRHAGE ( 3 FDA reports)
HEPATIC INFARCTION ( 3 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
HOUSE DUST ALLERGY ( 3 FDA reports)
HUMERUS FRACTURE ( 3 FDA reports)
HYDROTHORAX ( 3 FDA reports)
HYDROURETER ( 3 FDA reports)
HYPERPROLACTINAEMIA ( 3 FDA reports)
HYPERTELORISM OF ORBIT ( 3 FDA reports)
HYPOPERFUSION ( 3 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 3 FDA reports)
ILIAC VEIN OCCLUSION ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 3 FDA reports)
INADEQUATE LUBRICATION ( 3 FDA reports)
INCISION SITE OEDEMA ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 3 FDA reports)
INDUCED LABOUR ( 3 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 3 FDA reports)
INJECTION SITE ATROPHY ( 3 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 3 FDA reports)
INJECTION SITE SCAR ( 3 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
INTRACRANIAL HYPOTENSION ( 3 FDA reports)
JUVENILE ARTHRITIS ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LARYNGOSPASM ( 3 FDA reports)
LATEX ALLERGY ( 3 FDA reports)
LIMB MALFORMATION ( 3 FDA reports)
LIMB REDUCTION DEFECT ( 3 FDA reports)
LIPIDS ABNORMAL ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
LUNG LOBECTOMY ( 3 FDA reports)
LYMPHOCYTOSIS ( 3 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 3 FDA reports)
MALE SEXUAL DYSFUNCTION ( 3 FDA reports)
MALIGNANT HYPERTENSION ( 3 FDA reports)
MEAN CELL VOLUME DECREASED ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 3 FDA reports)
MEDIASTINOSCOPY ( 3 FDA reports)
MENINGIOMA BENIGN ( 3 FDA reports)
MENISCUS REMOVAL ( 3 FDA reports)
MENOPAUSAL SYMPTOMS ( 3 FDA reports)
MENTAL RETARDATION ( 3 FDA reports)
METAL POISONING ( 3 FDA reports)
METASTASES TO PERITONEUM ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
MICROPENIS ( 3 FDA reports)
MILIA ( 3 FDA reports)
MILK ALLERGY ( 3 FDA reports)
MOANING ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MUCOSAL DRYNESS ( 3 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 3 FDA reports)
MUSCULAR DYSTROPHY ( 3 FDA reports)
NAIL GROWTH ABNORMAL ( 3 FDA reports)
NAIL INFECTION ( 3 FDA reports)
NARCOLEPSY ( 3 FDA reports)
NERVE BLOCK ( 3 FDA reports)
NEUROGENIC BOWEL ( 3 FDA reports)
NEUROMYOPATHY ( 3 FDA reports)
NEUTROPHILIA ( 3 FDA reports)
NOCTURNAL DYSPNOEA ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE II ( 3 FDA reports)
NUCHAL RIGIDITY ( 3 FDA reports)
OBSTRUCTION GASTRIC ( 3 FDA reports)
OCULOGYRIC CRISIS ( 3 FDA reports)
OEDEMA GENITAL ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 3 FDA reports)
OPEN FRACTURE ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
OPHTHALMOPLEGIA ( 3 FDA reports)
OPIATES POSITIVE ( 3 FDA reports)
ORAL FUNGAL INFECTION ( 3 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
ORTHOSTATIC HYPERTENSION ( 3 FDA reports)
OSTEOGENESIS IMPERFECTA ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
OVARIAN MASS ( 3 FDA reports)
PALATAL OEDEMA ( 3 FDA reports)
PANCREATIC NEOPLASM ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PARATHYROID DISORDER ( 3 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERICARDIAL HAEMORRHAGE ( 3 FDA reports)
PERITONEAL ADHESIONS ( 3 FDA reports)
PERITONITIS BACTERIAL ( 3 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 3 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 3 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 3 FDA reports)
PILOERECTION ( 3 FDA reports)
PILONIDAL CYST ( 3 FDA reports)
PLAGUE ( 3 FDA reports)
PLATELET COUNT ABNORMAL ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
PLICA SYNDROME ( 3 FDA reports)
PNEUMONIA KLEBSIELLA ( 3 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
POOR PERSONAL HYGIENE ( 3 FDA reports)
POOR VENOUS ACCESS ( 3 FDA reports)
PORPHYRIA ( 3 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 3 FDA reports)
POST PROCEDURAL DRAINAGE ( 3 FDA reports)
POST PROCEDURAL NAUSEA ( 3 FDA reports)
POST PROCEDURAL PNEUMONIA ( 3 FDA reports)
POSTERIOR CAPSULOTOMY ( 3 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 3 FDA reports)
POSTURING ( 3 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 3 FDA reports)
PREMATURE DELIVERY ( 3 FDA reports)
PREMATURE EJACULATION ( 3 FDA reports)
PRESSURE OF SPEECH ( 3 FDA reports)
PROCEDURAL VOMITING ( 3 FDA reports)
PRODUCT PHYSICAL ISSUE ( 3 FDA reports)
PROTEIN S INCREASED ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
PULMONARY SARCOIDOSIS ( 3 FDA reports)
PUS IN STOOL ( 3 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 3 FDA reports)
RASH MORBILLIFORM ( 3 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 3 FDA reports)
REGRESSIVE BEHAVIOUR ( 3 FDA reports)
RELATIONSHIP BREAKDOWN ( 3 FDA reports)
RENAL TUBULAR ACIDOSIS ( 3 FDA reports)
RESPIRATORY THERAPY ( 3 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RETINAL TEAR ( 3 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 3 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 3 FDA reports)
RHEUMATOID NODULE ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SCROTAL PAIN ( 3 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 3 FDA reports)
SEXUAL ASSAULT VICTIM ( 3 FDA reports)
SHOCK HYPOGLYCAEMIC ( 3 FDA reports)
SINOATRIAL BLOCK ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN LESION EXCISION ( 3 FDA reports)
SKIN MASS ( 3 FDA reports)
SKIN ULCER HAEMORRHAGE ( 3 FDA reports)
SLEEP PARALYSIS ( 3 FDA reports)
SOCIAL FEAR ( 3 FDA reports)
SOFT TISSUE MASS ( 3 FDA reports)
SPLENECTOMY ( 3 FDA reports)
SPLENIC CYST ( 3 FDA reports)
SPLENIC INFARCTION ( 3 FDA reports)
STERNAL FRACTURE ( 3 FDA reports)
STRESS AT WORK ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
STUBBORNNESS ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
SUPPRESSED LACTATION ( 3 FDA reports)
SUSPICIOUSNESS ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 3 FDA reports)
TEMPERATURE REGULATION DISORDER ( 3 FDA reports)
5-HYDROXYINDOLACETIC ACID IN URINE INCREASED ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACCIDENT AT HOME ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACROCHORDON EXCISION ( 2 FDA reports)
ADHESIOLYSIS ( 2 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 2 FDA reports)
AGNOSIA ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAESTHESIA ( 2 FDA reports)
ANAL SPHINCTER ATONY ( 2 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 2 FDA reports)
ANOVULATORY CYCLE ( 2 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
APPLICATION SITE BURNING ( 2 FDA reports)
APPLICATION SITE DISCOMFORT ( 2 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 2 FDA reports)
APPLICATION SITE ULCER ( 2 FDA reports)
APTYALISM ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIOGRAM CORONARY ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTHROFIBROSIS ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ASPERMIA ( 2 FDA reports)
ASTHMA EXERCISE INDUCED ( 2 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
AUTISM SPECTRUM DISORDER ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
AVULSION FRACTURE ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BACK CRUSHING ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BALLISMUS ( 2 FDA reports)
BEHCET'S SYNDROME ( 2 FDA reports)
BIOPSY LIVER ( 2 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 2 FDA reports)
BLADDER DILATATION ( 2 FDA reports)
BLISTER INFECTED ( 2 FDA reports)
BLOOD CALCITONIN INCREASED ( 2 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 2 FDA reports)
BLOOD KETONE BODY ( 2 FDA reports)
BLOOD PRESSURE NORMAL ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLOOD THROMBIN ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BLUE TOE SYNDROME ( 2 FDA reports)
BODY HEIGHT BELOW NORMAL ( 2 FDA reports)
BONE INFARCTION ( 2 FDA reports)
BONE INFECTION ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN OPERATION ( 2 FDA reports)
BRAIN STEM ISCHAEMIA ( 2 FDA reports)
BREAST ABSCESS ( 2 FDA reports)
BREAST CANCER STAGE I ( 2 FDA reports)
BREAST CANCER STAGE II ( 2 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 2 FDA reports)
BREECH DELIVERY ( 2 FDA reports)
BURNOUT SYNDROME ( 2 FDA reports)
BURSA INJURY ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CAFFEINE CONSUMPTION ( 2 FDA reports)
CALCULUS PROSTATIC ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CAPILLARY FRAGILITY ( 2 FDA reports)
CARCINOID SYNDROME ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CAROTID ARTERY ATHEROMA ( 2 FDA reports)
CAT SCRATCH DISEASE ( 2 FDA reports)
CATARACT CORTICAL ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CATHETER SITE ERYTHEMA ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 2 FDA reports)
CEREBRAL ARTERITIS ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CERVIX CARCINOMA ( 2 FDA reports)
CHEST CRUSHING ( 2 FDA reports)
CHILLBLAINS ( 2 FDA reports)
CHLOASMA ( 2 FDA reports)
CHONDROMATOSIS ( 2 FDA reports)
CHORIOAMNIONITIS ( 2 FDA reports)
CHOROIDAL EFFUSION ( 2 FDA reports)
CHROMOSOME ABNORMALITY ( 2 FDA reports)
CIRCUMORAL OEDEMA ( 2 FDA reports)
COGNITIVE DETERIORATION ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 2 FDA reports)
COMPUTERISED TOMOGRAM ( 2 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 2 FDA reports)
CONGENITAL SCOLIOSIS ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONJUNCTIVAL IRRITATION ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORNEAL REFLEX DECREASED ( 2 FDA reports)
CORONARY ARTERY REOCCLUSION ( 2 FDA reports)
CORRECTIVE LENS USER ( 2 FDA reports)
CUBITAL TUNNEL SYNDROME ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CULTURE THROAT POSITIVE ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
CYST REMOVAL ( 2 FDA reports)
CYSTOPEXY ( 2 FDA reports)
CYSTOSCOPY ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
DEAFNESS TRANSITORY ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DEJA VU ( 2 FDA reports)
DELUSION OF GRANDEUR ( 2 FDA reports)
DELUSIONAL DISORDER, EROTOMANIC TYPE ( 2 FDA reports)
DELUSIONS, MIXED ( 2 FDA reports)
DENTAL IMPLANTATION ( 2 FDA reports)
DEVICE ADHESION ISSUE ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 2 FDA reports)
DIABETIC CARDIOMYOPATHY ( 2 FDA reports)
DIABETIC GASTROPATHY ( 2 FDA reports)
DIABETIC MONONEUROPATHY ( 2 FDA reports)
DIAPHRAGMALGIA ( 2 FDA reports)
DIARRHOEA INFECTIOUS ( 2 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 2 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 2 FDA reports)
DRUG LEVEL ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 2 FDA reports)
DYSLEXIA ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ECTOPIC PREGNANCY WITH INTRAUTERINE DEVICE ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 2 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 2 FDA reports)
ENDOCRINE DISORDER ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
ENLARGED CLITORIS ( 2 FDA reports)
ENTERAL NUTRITION ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ERYTHEMA ELEVATUM DIUTINUM ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EX-SMOKER ( 2 FDA reports)
EX-TOBACCO USER ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EXTERNAL EAR CELLULITIS ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
EYE OPERATION COMPLICATION ( 2 FDA reports)
EYELID BLEEDING ( 2 FDA reports)
EYELID OPERATION ( 2 FDA reports)
FABRY'S DISEASE ( 2 FDA reports)
FACTOR V INHIBITION ( 2 FDA reports)
FEAR OF FALLING ( 2 FDA reports)
FEAR OF NEEDLES ( 2 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 2 FDA reports)
FEMALE STERILISATION ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FINE MOTOR DELAY ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FOETAL GROWTH RESTRICTION ( 2 FDA reports)
FOETAL HEART RATE DECREASED ( 2 FDA reports)
FOETAL MOVEMENTS DECREASED ( 2 FDA reports)
FREEZING PHENOMENON ( 2 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GALLBLADDER ENLARGEMENT ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 2 FDA reports)
GLARE ( 2 FDA reports)
GRAVITATIONAL OEDEMA ( 2 FDA reports)
GROIN INFECTION ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMOGLOBINURIA ( 2 FDA reports)
HAEMORRHAGE URINARY TRACT ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HALO VISION ( 2 FDA reports)
HEAD AND NECK CANCER ( 2 FDA reports)
HEAD AND NECK CANCER STAGE III ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HEART VALVE STENOSIS ( 2 FDA reports)
HEAT EXHAUSTION ( 2 FDA reports)
HELICOBACTER TEST POSITIVE ( 2 FDA reports)
HEMISENSORY NEGLECT ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HIGH ARCHED PALATE ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERCORTICOIDISM ( 2 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERTONIA NEONATAL ( 2 FDA reports)
HYPERTROPHY ( 2 FDA reports)
HYPERTROPHY BREAST ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPOSPADIAS ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INABILITY TO CRAWL ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INHALATION THERAPY ( 2 FDA reports)
INJECTION SITE ANAESTHESIA ( 2 FDA reports)
INJECTION SITE MACULE ( 2 FDA reports)
INJECTION SITE THROMBOSIS ( 2 FDA reports)
INSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
INTESTINAL SPASM ( 2 FDA reports)
INTESTINAL STRANGULATION ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE INSERTION ( 2 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 2 FDA reports)
INVESTIGATION ( 2 FDA reports)
IRON BINDING CAPACITY UNSATURATED DECREASED ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
ISCHAEMIC ULCER ( 2 FDA reports)
JEALOUS DELUSION ( 2 FDA reports)
JOINT LIGAMENT RUPTURE ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LAPAROTOMY ( 2 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LENS DISORDER ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIGAMENT PAIN ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIP EXFOLIATION ( 2 FDA reports)
LIP NEOPLASM ( 2 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LUMBAR PUNCTURE ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LYMPH NODE CALCIFICATION ( 2 FDA reports)
LYMPHATIC DISORDER ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MALIGNANT OMENTUM NEOPLASM ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 2 FDA reports)
MEDICAL DEVICE PAIN ( 2 FDA reports)
MEDICATION TAMPERING ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENINGEAL DISORDER ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MERALGIA PARAESTHETICA ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METANEPHRINE URINE INCREASED ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
METASTASES TO BONE MARROW ( 2 FDA reports)
METASTASES TO NASAL SINUSES ( 2 FDA reports)
METASTASES TO OVARY ( 2 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MIDDLE EAR DISORDER ( 2 FDA reports)
MIXED RECEPTIVE-EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MULTIPLE EPIPHYSEAL DYSPLASIA ( 2 FDA reports)
MURPHY'S SIGN POSITIVE ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
NAIL TINEA ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NASAL SINUS DRAINAGE ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NEEDLE ISSUE ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEONATAL TACHYPNOEA ( 2 FDA reports)
NEPHRITIC SYNDROME ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NERVE ROOT COMPRESSION ( 2 FDA reports)
NERVE ROOT INJURY CERVICAL ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NEUROSIS ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NOREPINEPHRINE INCREASED ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL DILATATION ( 2 FDA reports)
OESOPHAGEAL DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL PERFORATION ( 2 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA METASTATIC ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
OPTIC DISC DISORDER ( 2 FDA reports)
ORAL TORUS ( 2 FDA reports)
ORGAN TRANSPLANT ( 2 FDA reports)
ORGASMIC SENSATION DECREASED ( 2 FDA reports)
OSCILLOPSIA ( 2 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 2 FDA reports)
OTITIS MEDIA CHRONIC ( 2 FDA reports)
OVARIAN CANCER METASTATIC ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PAPILLOMA VIRAL INFECTION ( 2 FDA reports)
PARAESTHESIA MUCOSAL ( 2 FDA reports)
PARASOMNIA ( 2 FDA reports)
PARATHYROID TUMOUR BENIGN ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARKINSONIAN REST TREMOR ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PECTUS EXCAVATUM ( 2 FDA reports)
PENILE PROSTHESIS USER ( 2 FDA reports)
PENILE ULCERATION ( 2 FDA reports)
PEPTIC ULCER PERFORATION, OBSTRUCTIVE ( 2 FDA reports)
PERIANAL ERYTHEMA ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 2 FDA reports)
PERITONEAL ABSCESS ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 2 FDA reports)
PLEURODESIS ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 2 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
POSTOPERATIVE THROMBOSIS ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PRECANCEROUS CELLS PRESENT ( 2 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 2 FDA reports)
PREGNANCY WITH CONTRACEPTIVE PATCH ( 2 FDA reports)
PREMATURE MENOPAUSE ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PROCEDURAL HYPERTENSION ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PROGESTERONE DECREASED ( 2 FDA reports)
PROLACTINOMA ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTHROMBIN CONSUMPTION TIME PROLONGED ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PSEUDO LYMPHOMA ( 2 FDA reports)
PSEUDOCYST ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 2 FDA reports)
PTERYGIUM ( 2 FDA reports)
PULMONARY ARTERY ATRESIA ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
RECTAL FISSURE ( 2 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 2 FDA reports)
REFUSAL OF EXAMINATION ( 2 FDA reports)
REITER'S SYNDROME ( 2 FDA reports)
RENAL ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RENAL CORTICAL NECROSIS ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RESTING TREMOR ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETICULOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
RETINAL DYSTROPHY ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RETINITIS ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
SALPINGITIS ( 2 FDA reports)
SCAN ABDOMEN ABNORMAL ( 2 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 2 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 2 FDA reports)
SCIATIC NERVE INJURY ( 2 FDA reports)
SCLERAL OEDEMA ( 2 FDA reports)
SELF ESTEEM INFLATED ( 2 FDA reports)
SEMEN VOLUME DECREASED ( 2 FDA reports)
SENSATION OF PRESSURE IN EAR ( 2 FDA reports)
SENSE OF OPPRESSION ( 2 FDA reports)
SERRATIA SEPSIS ( 2 FDA reports)
SERUM SEROTONIN INCREASED ( 2 FDA reports)
SEX CHROMOSOME ABNORMALITY ( 2 FDA reports)
SHIGELLA INFECTION ( 2 FDA reports)
SHOPLIFTING ( 2 FDA reports)
SIGMOIDECTOMY ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SINUS RHYTHM ( 2 FDA reports)
SINUSITIS BACTERIAL ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SOFT TISSUE NECROSIS ( 2 FDA reports)
SPERM COUNT DECREASED ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SPINAL CORD INFARCTION ( 2 FDA reports)
SPINAL CORD INFECTION ( 2 FDA reports)
SPINAL CORD INJURY THORACIC ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPLENIC INJURY ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STITCH ABSCESS ( 2 FDA reports)
STOOLS WATERY ( 2 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
SYSTOLIC HYPERTENSION ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THORACIC OUTLET SYNDROME ( 2 FDA reports)
THROAT LESION ( 2 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
THYROID CANCER METASTATIC ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
TINEL'S SIGN ( 2 FDA reports)
TONGUE SPASM ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TRIGONITIS ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
UTERINE CYST ( 2 FDA reports)
UTERINE ENLARGEMENT ( 2 FDA reports)
UTERINE NEOPLASM ( 2 FDA reports)
VAGINAL PH DECREASED ( 2 FDA reports)
VAGINAL PROLAPSE ( 2 FDA reports)
VASCULAR GRAFT COMPLICATION ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VENOUS VALVE RUPTURED ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VERBIGERATION ( 2 FDA reports)
VERTEBRAL COLUMN MASS ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
VIBRATORY SENSE INCREASED ( 2 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
VITAMIN D ABNORMAL ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VOLVULUS OF BOWEL ( 2 FDA reports)
VOMITING IN PREGNANCY ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WATER INTOXICATION ( 2 FDA reports)
WOUND ABSCESS ( 2 FDA reports)
WOUND CLOSURE ( 2 FDA reports)
WOUND EVISCERATION ( 2 FDA reports)
WOUND INFECTION BACTERIAL ( 2 FDA reports)
TENDINOUS CONTRACTURE ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
TESTIS DISCOMFORT ( 1 FDA reports)
TETANY ( 1 FDA reports)
THALASSAEMIA ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPEUTIC RESPONSE PROLONGED ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THREAT OF REDUNDANCY ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYROGLOBULIN INCREASED ( 1 FDA reports)
THYROID CYST ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLAR ULCER ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOURETTE'S DISORDER ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
TRAUMATIC DELIVERY ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC LIVER INJURY ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
TRICHOTILLOMANIA ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TRISOMY 13 ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNEQUAL LIMB LENGTH ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETERAL STENT REMOVAL ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URETERIC CANCER METASTATIC ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URETEROSCOPY ( 1 FDA reports)
URETHRAL DILATION PROCEDURE ( 1 FDA reports)
URETHRAL DISCHARGE ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL MEATOTOMY ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY CALCULUS REMOVAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE ALCOHOL TEST NEGATIVE ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE OPERATION ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VAGAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
VAGINAL CANCER ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL EROSION ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGINITIS ( 1 FDA reports)
VAGINITIS GARDNERELLA ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULAR FRAGILITY ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VENOUS LAKE ( 1 FDA reports)
VENOUS RECANALISATION ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VIOLENT IDEATION ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL LOAD ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIROLOGIC FAILURE ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN A DECREASED ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVAL OPERATION ( 1 FDA reports)
VULVOVAGINITIS STREPTOCOCCAL ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WAXY FLEXIBILITY ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS INCREASED ( 1 FDA reports)
WITHDRAWAL BLEEDING IRREGULAR ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
XANTHOCHROMIA ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)
XEROSIS ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABDOMINAL WALL ANOMALY ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABSCESS OF EXTERNAL AUDITORY MEATUS ( 1 FDA reports)
ABSCESS SWEAT GLAND ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 1 FDA reports)
ACQUIRED NIGHT BLINDNESS ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE MEGAKARYOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOVIRAL CONJUNCTIVITIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AGITATION NEONATAL ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
AIR-BORNE TRANSMISSION ( 1 FDA reports)
ALBUMIN URINE ABSENT ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOL DETOXIFICATION ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 1 FDA reports)
ALLERGY TO METALS ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN ABNORMAL ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMNIOTIC FLUID VOLUME INCREASED ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAL CANDIDIASIS ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL SPASM ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANDROGENS ABNORMAL ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME DECREASED ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANOREXIA NERVOSA ( 1 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOGRAM CORONARY NORMAL ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
ASPERGER'S DISORDER ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ASTHMA PROPHYLAXIS ( 1 FDA reports)
ATONIC SEIZURES ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 1 FDA reports)
AUTOPSY ( 1 FDA reports)
AVOIDANT PERSONALITY DISORDER ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIAL TOXAEMIA ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BALANOPOSTHITIS ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN LARYNGEAL NEOPLASM ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN MESOTHELIOMA ( 1 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 1 FDA reports)
BIOPSY ABDOMINAL WALL ABNORMAL ( 1 FDA reports)
BIOPSY BRAIN ABNORMAL ( 1 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 1 FDA reports)
BIOPSY VAGINA ( 1 FDA reports)
BIOPSY VOCAL CORD ( 1 FDA reports)
BLADDER CANCER STAGE IV ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER TUMOUR RESECTION ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD CAFFEINE INCREASED ( 1 FDA reports)
BLOOD CANNABINOIDS ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD KETONE BODY DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD OESTROGEN ABNORMAL ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD UREA ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE DENSITOMETRY ( 1 FDA reports)
BONE DENSITY INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRACHIAL PLEXUS LESION ( 1 FDA reports)
BRADYCARDIA FOETAL ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST FEEDING ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREAST PROSTHESIS USER ( 1 FDA reports)
BREATH HOLDING ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRIEF PSYCHOTIC DISORDER, WITH POSTPARTUM ONSET ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHITIS CHEMICAL ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
BURNING FEET SYNDROME ( 1 FDA reports)
BURNING MOUTH SYNDROME ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC REHABILITATION THERAPY ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOLIPIN ANTIBODY ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAST APPLICATION ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL AMYLOID ANGIOPATHY ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ARTERIOVENOUS MALFORMATION HAEMORRHAGIC ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CERVIX CARCINOMA STAGE IV ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHLAMYDIA TEST POSITIVE ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOLEDOCHAL CYST ( 1 FDA reports)
CHOLESTASIS OF PREGNANCY ( 1 FDA reports)
CHOLINERGIC SYNDROME ( 1 FDA reports)
CHOROID MELANOMA ( 1 FDA reports)
CHOROID NEOPLASM ( 1 FDA reports)
CHOROIDAL DETACHMENT ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CILIARY BODY DISORDER ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CIRCUMCISION ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLOBOMA ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOSTOMY INFECTION ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL ECTODERMAL DYSPLASIA ( 1 FDA reports)
CONGENITAL EYE DISORDER ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 1 FDA reports)
CONGENITAL SYPHILIS ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTACT LENS INTOLERANCE ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COPROLALIA ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL GRAFT REJECTION ( 1 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
COW'S MILK INTOLERANCE ( 1 FDA reports)
CRANIAL NERVE INFECTION ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CRIME ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CRYPTOPHTHALMOS ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYST ASPIRATION ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTOURETHROCELE ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DAWN PHENOMENON ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DEATH OF SIBLING ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEEP BRAIN STIMULATION ( 1 FDA reports)
DEFORMITY THORAX ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DEMENTIA OF THE ALZHEIMER'S TYPE, WITH DELIRIUM ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DENTAL PULP DISORDER ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DERMATILLOMANIA ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DERMOID CYST OF OVARY ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE ISSUE ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DEVICE SIGNAL DETECTION ISSUE ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC NEUROPATHIC ULCER ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIAPHRAGMATIC INJURY ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE I ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG LEVEL THERAPEUTIC ( 1 FDA reports)
DUODENAL OPERATION ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPLASTIC NAEVUS ( 1 FDA reports)
EAR CANAL STENOSIS ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ECTOPIC PREGNANCY TERMINATION ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCONVULSIVE THERAPY ( 1 FDA reports)
ELECTROCUTION ( 1 FDA reports)
EMOTIONAL POVERTY ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCELE ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EXCESSIVE SEXUAL FANTASIES ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE ABSCESS ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID BOIL ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR II MUTATION ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FACTOR X DEFICIENCY ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FALLOPIAN TUBE ABSCESS ( 1 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAMILIAL RISK FACTOR ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FEAR OF EATING ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEMALE GENITAL OPERATION ( 1 FDA reports)
FEMALE REPRODUCTIVE NEOPLASM ( 1 FDA reports)
FEMALE SEXUAL AROUSAL DISORDER ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FIGHT IN SCHOOL ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL CHROMOSOME ABNORMALITY ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOLLICULAR THYROID CANCER ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FREE FATTY ACIDS DECREASED ( 1 FDA reports)
FREE THYROXINE INDEX DECREASED ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
GALACTOSE URINE ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GALLSTONE ILEUS ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GARDNERELLA TEST POSITIVE ( 1 FDA reports)
GAS POISONING ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROENTERITIS PARACOLON BACILLUS ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL DYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITAL HYPOAESTHESIA ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL PAIN MALE ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GENITAL TRACT INFLAMMATION ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL HYPOPLASIA ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 1 FDA reports)
HAIR PLUCKING ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIANOPIA HETERONYMOUS ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ARTERY EMBOLISM ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HERNIA CONGENITAL ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HIGH RISK SEXUAL BEHAVIOUR ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HISTONE ANTIBODY POSITIVE ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HOMANS' SIGN ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HUMAN ANTICHIMERIC ANTIBODY POSITIVE ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPEREMESIS GRAVIDARUM ( 1 FDA reports)
HYPERGONADISM ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPNAGOGIC HALLUCINATION ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOTONIC URINARY BLADDER ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISION SITE BLISTER ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTIOUS DISEASE CARRIER ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE SCAR ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE EROSION ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE FIBROSIS ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PALLOR ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INSULIN RESISTANT DIABETES ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 1 FDA reports)
INTERNAL FIXATION OF SPINE ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRIS HYPERPIGMENTATION ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 1 FDA reports)
IRREGULAR SLEEP PHASE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
JOINT INJECTION ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACTASE DEFICIENCY ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARGE INTESTINAL STRICTURE ( 1 FDA reports)
LARYNGEAL INFLAMMATION ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LARYNGOMALACIA ( 1 FDA reports)
LARYNX IRRITATION ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LDL/HDL RATIO INCREASED ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LIGAMENT OPERATION ( 1 FDA reports)
LIGAMENT REPAIR ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIPIDOSIS ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LIPOSUCTION ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOCHIA MALODOUROUS ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
LUMBOSACRAL PLEXUS INJURY ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 1 FDA reports)
LUNG CYST BENIGN ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPH GLAND INFECTION ( 1 FDA reports)
LYMPHADENITIS BACTERIAL ( 1 FDA reports)
LYMPHADENITIS FUNGAL ( 1 FDA reports)
LYMPHANGIECTASIA ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOPLASIA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACROGNATHIA ( 1 FDA reports)
MACULAR CYST ( 1 FDA reports)
MACULE ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALIGNANT HISTIOCYTOSIS ( 1 FDA reports)
MALIGNANT MELANOMA STAGE III ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEGACOLON ACQUIRED ( 1 FDA reports)
MELANOMA RECURRENT ( 1 FDA reports)
MELKERSSON-ROSENTHAL SYNDROME ( 1 FDA reports)
MENINGITIS FUNGAL ( 1 FDA reports)
MENINGOCELE ( 1 FDA reports)
MENSTRUAL DISCOMFORT ( 1 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 1 FDA reports)
MENTALLY LATE DEVELOPER ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO PROSTATE ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METASTATIC PAIN ( 1 FDA reports)
METATARSAL EXCISION ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICROGNATHIA ( 1 FDA reports)
MICROTIA ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYELOCYTE COUNT INCREASED ( 1 FDA reports)
MYOFASCIAL SPASM ( 1 FDA reports)
NAIL PSORIASIS ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NASAL SEPTAL OPERATION ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NECK EXPLORATION ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NIPPLE EXUDATE BLOODY ( 1 FDA reports)
NIPPLE INFECTION ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NORMAL DELIVERY ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING SPINAL CORD ABNORMAL ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGOENTEROSTOMY ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OMENTECTOMY ( 1 FDA reports)
OMPHALITIS ( 1 FDA reports)
ONCOCYTOMA ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OPTIC NERVE HYPOPLASIA ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL PAPILLOMA ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
OSTECTOMY ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OTOSCLEROSIS ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN FAILURE ( 1 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 1 FDA reports)
OVARIAN LOW MALIGNANT POTENTIAL TUMOUR ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC ENZYMES NORMAL ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PAPILLARY THYROID CANCER ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARADOXICAL EMBOLISM ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARAPHILIA ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARATHYROID HORMONE-RELATED PROTEIN ABNORMAL ( 1 FDA reports)
PARATHYROID TUMOUR MALIGNANT ( 1 FDA reports)
PARENT-CHILD PROBLEM ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PATIENT RESTRAINT ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PELVIC MUSCLES INADEQUATE ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PENILE OPERATION ( 1 FDA reports)
PENILE SIZE REDUCED ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERINEURIAL CYST ( 1 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 1 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERIPROSTHETIC FRACTURE ( 1 FDA reports)
PERITONEAL FIBROSIS ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHONOLOGICAL DISORDER ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHOTOKERATITIS ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PILONIDAL CYST CONGENITAL ( 1 FDA reports)
PITUITARY ENLARGEMENT ( 1 FDA reports)
PITUITARY HAEMORRHAGE ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 1 FDA reports)
PORPHYROMONAS INFECTION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL CONSTIPATION ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POVERTY OF THOUGHT CONTENT ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 1 FDA reports)
PRECOCIOUS PUBERTY ( 1 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 1 FDA reports)
PREHYPERTENSION ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROLONGED LABOUR ( 1 FDA reports)
PROMYELOCYTE COUNT INCREASED ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHOPATHIC PERSONALITY ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PTOSIS REPAIR ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY STENOSIS ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY COCCIDIOIDES ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURGING ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYOGENIC GRANULOMA ( 1 FDA reports)
PYROMANIA ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIAL PULSE ( 1 FDA reports)
RADIATION OESOPHAGITIS ( 1 FDA reports)
RADICAL NECK DISSECTION ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
RAPID CORRECTION OF HYPONATRAEMIA ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL CANCER STAGE III ( 1 FDA reports)
RECTAL FISTULA REPAIR ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RECTAL SPASM ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFLUX LARYNGITIS ( 1 FDA reports)
REMOVAL OF FOREIGN BODY FROM GASTROINTESTINAL TRACT ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY SIGHS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL ARTERY STENOSIS ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
RETINAL FIBROSIS ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL LASER COAGULATION ( 1 FDA reports)
RETINAL OPERATION ( 1 FDA reports)
RETINAL SCAR ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RETROPERITONEAL CANCER ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALIVARY GLAND DISORDER ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCAN BONE MARROW ABNORMAL ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SCAR EXCISION ( 1 FDA reports)
SCHISTOSOMA TEST POSITIVE ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCROTAL CYST ( 1 FDA reports)
SCROTAL INFECTION ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEIZURE LIKE PHENOMENA ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SENSITISATION ( 1 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 1 FDA reports)
SENSORY LEVEL ABNORMAL ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SERUM SEROTONIN DECREASED ( 1 FDA reports)
SHARED PSYCHOTIC DISORDER ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINGLE UMBILICAL ARTERY ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SINUSITIS NONINFECTIVE ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN GRAFT FAILURE ( 1 FDA reports)
SKIN GRAFT INFECTION ( 1 FDA reports)
SKIN NEOPLASM BLEEDING ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOLAR ELASTOSIS ( 1 FDA reports)
SOMOGYI PHENOMENON ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPERM CONCENTRATION DECREASED ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORPECTOMY ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLEEN MALFORMATION ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPONDYLOLYSIS ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STREPTOBACILLUS INFECTION ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPERINFECTION ORAL ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SWOLLEN TEAR DUCT ( 1 FDA reports)
SYNOVIAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
SYSTEMIC LEAKAGE ( 1 FDA reports)
T-CELL PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TEETHING ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)