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

PAIN ( 2223 FDA reports)
ANXIETY ( 1933 FDA reports)
DYSPNOEA ( 1487 FDA reports)
INJURY ( 1343 FDA reports)
NAUSEA ( 1282 FDA reports)
DIARRHOEA ( 1202 FDA reports)
VOMITING ( 1177 FDA reports)
PYREXIA ( 1126 FDA reports)
FATIGUE ( 1092 FDA reports)
DEPRESSION ( 1084 FDA reports)
ANAEMIA ( 1026 FDA reports)
OSTEONECROSIS OF JAW ( 994 FDA reports)
BACK PAIN ( 980 FDA reports)
HEADACHE ( 958 FDA reports)
ARTHRALGIA ( 902 FDA reports)
DIZZINESS ( 896 FDA reports)
WEIGHT DECREASED ( 867 FDA reports)
ABDOMINAL PAIN ( 862 FDA reports)
CHEST PAIN ( 862 FDA reports)
OEDEMA PERIPHERAL ( 839 FDA reports)
ASTHENIA ( 820 FDA reports)
PNEUMONIA ( 781 FDA reports)
RASH ( 759 FDA reports)
EMOTIONAL DISTRESS ( 756 FDA reports)
FALL ( 756 FDA reports)
HYPERTENSION ( 719 FDA reports)
BONE DISORDER ( 717 FDA reports)
OSTEOARTHRITIS ( 670 FDA reports)
PAIN IN EXTREMITY ( 650 FDA reports)
RENAL FAILURE ACUTE ( 639 FDA reports)
COUGH ( 637 FDA reports)
HYPOAESTHESIA ( 632 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 612 FDA reports)
ANHEDONIA ( 573 FDA reports)
PARAESTHESIA ( 567 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 565 FDA reports)
ABDOMINAL PAIN UPPER ( 564 FDA reports)
URINARY TRACT INFECTION ( 556 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 553 FDA reports)
INFECTION ( 541 FDA reports)
OSTEOMYELITIS ( 535 FDA reports)
MALAISE ( 534 FDA reports)
CHOLELITHIASIS ( 530 FDA reports)
PULMONARY EMBOLISM ( 529 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 526 FDA reports)
DEEP VEIN THROMBOSIS ( 519 FDA reports)
INSOMNIA ( 503 FDA reports)
DRUG INTERACTION ( 502 FDA reports)
SINUSITIS ( 501 FDA reports)
HYPOTENSION ( 493 FDA reports)
PRURITUS ( 490 FDA reports)
DEHYDRATION ( 488 FDA reports)
PLEURAL EFFUSION ( 485 FDA reports)
ERYTHEMA ( 483 FDA reports)
TOOTH EXTRACTION ( 479 FDA reports)
ATRIAL FIBRILLATION ( 471 FDA reports)
DECREASED APPETITE ( 471 FDA reports)
SPINAL OSTEOARTHRITIS ( 453 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 448 FDA reports)
CONSTIPATION ( 444 FDA reports)
OSTEONECROSIS ( 443 FDA reports)
NEUROPATHY PERIPHERAL ( 441 FDA reports)
ATELECTASIS ( 436 FDA reports)
MYOCARDIAL INFARCTION ( 432 FDA reports)
CONFUSIONAL STATE ( 424 FDA reports)
PAIN IN JAW ( 420 FDA reports)
RENAL FAILURE ( 420 FDA reports)
IMPAIRED HEALING ( 418 FDA reports)
DRUG INEFFECTIVE ( 405 FDA reports)
CHOLECYSTITIS CHRONIC ( 396 FDA reports)
METASTASES TO BONE ( 396 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 395 FDA reports)
SWELLING ( 395 FDA reports)
CEREBROVASCULAR ACCIDENT ( 391 FDA reports)
BRONCHITIS ( 376 FDA reports)
DYSPHAGIA ( 374 FDA reports)
URTICARIA ( 370 FDA reports)
MYALGIA ( 367 FDA reports)
VISION BLURRED ( 363 FDA reports)
GAIT DISTURBANCE ( 358 FDA reports)
CONVULSION ( 356 FDA reports)
NECK PAIN ( 354 FDA reports)
THROMBOCYTOPENIA ( 353 FDA reports)
SYNCOPE ( 346 FDA reports)
MUSCULAR WEAKNESS ( 343 FDA reports)
OSTEOPENIA ( 342 FDA reports)
OSTEOPOROSIS ( 340 FDA reports)
CARDIOMEGALY ( 337 FDA reports)
DRUG HYPERSENSITIVITY ( 337 FDA reports)
CELLULITIS ( 333 FDA reports)
HIATUS HERNIA ( 333 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 332 FDA reports)
DYSPEPSIA ( 332 FDA reports)
HYPERSENSITIVITY ( 332 FDA reports)
MUSCLE SPASMS ( 332 FDA reports)
TREMOR ( 332 FDA reports)
SEPSIS ( 328 FDA reports)
RECTAL HAEMORRHAGE ( 324 FDA reports)
LYMPHADENOPATHY ( 323 FDA reports)
DECREASED INTEREST ( 321 FDA reports)
TOOTHACHE ( 316 FDA reports)
NEUTROPENIA ( 310 FDA reports)
GASTRITIS ( 309 FDA reports)
CONDITION AGGRAVATED ( 308 FDA reports)
ECONOMIC PROBLEM ( 302 FDA reports)
HYPERHIDROSIS ( 302 FDA reports)
RESPIRATORY FAILURE ( 301 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 300 FDA reports)
SWELLING FACE ( 299 FDA reports)
DENTAL CARIES ( 295 FDA reports)
BONE LESION ( 291 FDA reports)
SOMNOLENCE ( 288 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 284 FDA reports)
CARDIAC MURMUR ( 284 FDA reports)
PALPITATIONS ( 283 FDA reports)
MITRAL VALVE INCOMPETENCE ( 282 FDA reports)
CORONARY ARTERY DISEASE ( 275 FDA reports)
DEFORMITY ( 275 FDA reports)
TACHYCARDIA ( 275 FDA reports)
BONE PAIN ( 274 FDA reports)
HYPOKALAEMIA ( 274 FDA reports)
MUSCULOSKELETAL PAIN ( 271 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 270 FDA reports)
RENAL FAILURE CHRONIC ( 268 FDA reports)
GALLBLADDER DISORDER ( 266 FDA reports)
CONTUSION ( 265 FDA reports)
NEOPLASM MALIGNANT ( 264 FDA reports)
LOSS OF CONSCIOUSNESS ( 262 FDA reports)
DEATH ( 261 FDA reports)
HAEMORRHOIDS ( 259 FDA reports)
ARTHROPATHY ( 257 FDA reports)
ASTHMA ( 250 FDA reports)
OROPHARYNGEAL PAIN ( 245 FDA reports)
DYSPNOEA EXERTIONAL ( 243 FDA reports)
TOOTH ABSCESS ( 243 FDA reports)
TOOTH DISORDER ( 238 FDA reports)
CHEST DISCOMFORT ( 238 FDA reports)
ARTHRITIS ( 237 FDA reports)
EAR PAIN ( 235 FDA reports)
DISABILITY ( 234 FDA reports)
DIVERTICULUM ( 234 FDA reports)
MIGRAINE ( 234 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 233 FDA reports)
HAEMOGLOBIN DECREASED ( 232 FDA reports)
RIB FRACTURE ( 229 FDA reports)
JOINT SWELLING ( 227 FDA reports)
CHILLS ( 226 FDA reports)
MOUTH ULCERATION ( 225 FDA reports)
FEELING ABNORMAL ( 222 FDA reports)
HYPERLIPIDAEMIA ( 222 FDA reports)
WEIGHT INCREASED ( 219 FDA reports)
HAEMATURIA ( 217 FDA reports)
HERPES ZOSTER ( 216 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 215 FDA reports)
PANCYTOPENIA ( 215 FDA reports)
NEPHROLITHIASIS ( 213 FDA reports)
OEDEMA ( 213 FDA reports)
RHABDOMYOLYSIS ( 212 FDA reports)
VERTIGO ( 212 FDA reports)
ABDOMINAL DISTENSION ( 211 FDA reports)
PRIMARY SEQUESTRUM ( 210 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 209 FDA reports)
JAUNDICE ( 207 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 206 FDA reports)
MUCOSAL INFLAMMATION ( 206 FDA reports)
COMPRESSION FRACTURE ( 205 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 205 FDA reports)
LUNG NEOPLASM ( 205 FDA reports)
CATARACT ( 204 FDA reports)
HYPOGLYCAEMIA ( 201 FDA reports)
ORAL PAIN ( 201 FDA reports)
HYPONATRAEMIA ( 200 FDA reports)
SCAR ( 198 FDA reports)
MENTAL DISORDER ( 196 FDA reports)
MULTIPLE MYELOMA ( 196 FDA reports)
ENDODONTIC PROCEDURE ( 193 FDA reports)
RENAL CYST ( 193 FDA reports)
HYPOPHAGIA ( 192 FDA reports)
CARDIAC ARREST ( 191 FDA reports)
LOOSE TOOTH ( 191 FDA reports)
RASH MACULO-PAPULAR ( 190 FDA reports)
TOOTH LOSS ( 188 FDA reports)
STEVENS-JOHNSON SYNDROME ( 186 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 186 FDA reports)
DIABETES MELLITUS ( 186 FDA reports)
MULTI-ORGAN FAILURE ( 185 FDA reports)
ARRHYTHMIA ( 184 FDA reports)
MULTIPLE INJURIES ( 184 FDA reports)
DEAFNESS ( 182 FDA reports)
HYPERCHOLESTEROLAEMIA ( 182 FDA reports)
VISUAL IMPAIRMENT ( 182 FDA reports)
SCOLIOSIS ( 180 FDA reports)
BLOOD PRESSURE INCREASED ( 180 FDA reports)
BURSITIS ( 179 FDA reports)
RENAL IMPAIRMENT ( 179 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 178 FDA reports)
EPISTAXIS ( 178 FDA reports)
HAEMOPTYSIS ( 178 FDA reports)
OVERDOSE ( 177 FDA reports)
COLITIS ( 176 FDA reports)
GINGIVITIS ( 175 FDA reports)
SLEEP APNOEA SYNDROME ( 175 FDA reports)
ATRIAL SEPTAL DEFECT ( 174 FDA reports)
IRON DEFICIENCY ANAEMIA ( 173 FDA reports)
PERIODONTITIS ( 173 FDA reports)
BLOOD GLUCOSE INCREASED ( 172 FDA reports)
HYPOTHYROIDISM ( 172 FDA reports)
ERECTILE DYSFUNCTION ( 171 FDA reports)
STOMATITIS ( 171 FDA reports)
LUNG DISORDER ( 170 FDA reports)
ORAL DISORDER ( 169 FDA reports)
DYSGEUSIA ( 168 FDA reports)
HAEMATOCHEZIA ( 168 FDA reports)
MEMORY IMPAIRMENT ( 168 FDA reports)
ANAPHYLACTIC REACTION ( 167 FDA reports)
CARDIAC DISORDER ( 166 FDA reports)
GASTROINTESTINAL DISORDER ( 166 FDA reports)
GINGIVAL DISORDER ( 166 FDA reports)
TOOTH FRACTURE ( 166 FDA reports)
LEUKOPENIA ( 165 FDA reports)
PATHOLOGICAL FRACTURE ( 165 FDA reports)
PHARYNGITIS ( 165 FDA reports)
DYSURIA ( 164 FDA reports)
RESPIRATORY DISTRESS ( 164 FDA reports)
TINNITUS ( 164 FDA reports)
DRY MOUTH ( 163 FDA reports)
PULMONARY OEDEMA ( 163 FDA reports)
HEPATIC STEATOSIS ( 162 FDA reports)
HYPOXIA ( 162 FDA reports)
EXOSTOSIS ( 161 FDA reports)
LETHARGY ( 161 FDA reports)
METASTASES TO SPINE ( 161 FDA reports)
RASH ERYTHEMATOUS ( 161 FDA reports)
TOOTH INFECTION ( 161 FDA reports)
SUICIDAL IDEATION ( 160 FDA reports)
BLOOD CREATININE INCREASED ( 160 FDA reports)
RASH GENERALISED ( 159 FDA reports)
UNEVALUABLE EVENT ( 159 FDA reports)
PULMONARY HYPERTENSION ( 158 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 157 FDA reports)
PANCREATITIS ( 157 FDA reports)
DISCOMFORT ( 155 FDA reports)
OSTEOLYSIS ( 155 FDA reports)
RASH PRURITIC ( 155 FDA reports)
HEART RATE INCREASED ( 153 FDA reports)
HYPERKALAEMIA ( 153 FDA reports)
IRRITABLE BOWEL SYNDROME ( 153 FDA reports)
LUNG INFILTRATION ( 153 FDA reports)
ARTERIOSCLEROSIS ( 151 FDA reports)
EMPHYSEMA ( 150 FDA reports)
MENTAL STATUS CHANGES ( 150 FDA reports)
AMNESIA ( 149 FDA reports)
BRADYCARDIA ( 149 FDA reports)
METASTASES TO LIVER ( 149 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 149 FDA reports)
URINARY INCONTINENCE ( 148 FDA reports)
STRESS ( 147 FDA reports)
ANOREXIA ( 147 FDA reports)
CHRONIC SINUSITIS ( 147 FDA reports)
CROHN'S DISEASE ( 147 FDA reports)
HYPERGLYCAEMIA ( 147 FDA reports)
LEUKOCYTOSIS ( 147 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 146 FDA reports)
CARDIOMYOPATHY ( 146 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 146 FDA reports)
SINUS TACHYCARDIA ( 145 FDA reports)
ALOPECIA ( 145 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 144 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 143 FDA reports)
NIGHT SWEATS ( 143 FDA reports)
WHEEZING ( 143 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 141 FDA reports)
BALANCE DISORDER ( 141 FDA reports)
DRUG ERUPTION ( 141 FDA reports)
HEART RATE IRREGULAR ( 141 FDA reports)
ANGINA PECTORIS ( 140 FDA reports)
ANGIOEDEMA ( 140 FDA reports)
HAEMORRHAGE ( 140 FDA reports)
MASTICATION DISORDER ( 140 FDA reports)
SPINAL COLUMN STENOSIS ( 140 FDA reports)
SKIN LESION ( 139 FDA reports)
SPEECH DISORDER ( 139 FDA reports)
AGITATION ( 139 FDA reports)
FEAR ( 139 FDA reports)
IRRITABILITY ( 137 FDA reports)
SUICIDE ATTEMPT ( 137 FDA reports)
LIFE EXPECTANCY SHORTENED ( 136 FDA reports)
BONE DEBRIDEMENT ( 135 FDA reports)
FACE OEDEMA ( 135 FDA reports)
ROAD TRAFFIC ACCIDENT ( 135 FDA reports)
SLEEP DISORDER ( 134 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 134 FDA reports)
PHYSICAL DISABILITY ( 134 FDA reports)
ABSCESS ( 133 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 133 FDA reports)
GINGIVAL BLEEDING ( 133 FDA reports)
CYANOSIS ( 132 FDA reports)
EAR INFECTION ( 132 FDA reports)
POLLAKIURIA ( 132 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 132 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 131 FDA reports)
BLOOD PRESSURE DECREASED ( 131 FDA reports)
COLONIC POLYP ( 131 FDA reports)
MALNUTRITION ( 131 FDA reports)
MEDICATION ERROR ( 131 FDA reports)
NASAL CONGESTION ( 131 FDA reports)
PERIODONTAL DISEASE ( 131 FDA reports)
RENAL DISORDER ( 131 FDA reports)
DISORIENTATION ( 130 FDA reports)
OSTEITIS ( 130 FDA reports)
ROTATOR CUFF SYNDROME ( 130 FDA reports)
DRY EYE ( 129 FDA reports)
EMOTIONAL DISORDER ( 129 FDA reports)
EXPOSED BONE IN JAW ( 129 FDA reports)
MASS ( 129 FDA reports)
PLATELET COUNT DECREASED ( 129 FDA reports)
PRODUCT QUALITY ISSUE ( 129 FDA reports)
CHOLECYSTITIS ( 128 FDA reports)
COAGULOPATHY ( 128 FDA reports)
HEPATITIS ( 128 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 128 FDA reports)
KYPHOSIS ( 128 FDA reports)
INFLAMMATION ( 127 FDA reports)
CONJUNCTIVITIS ( 125 FDA reports)
RHINORRHOEA ( 125 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 125 FDA reports)
STAPHYLOCOCCAL INFECTION ( 124 FDA reports)
DISTURBANCE IN ATTENTION ( 124 FDA reports)
EOSINOPHILIA ( 124 FDA reports)
FEBRILE NEUTROPENIA ( 124 FDA reports)
ABDOMINAL DISCOMFORT ( 123 FDA reports)
COLITIS ULCERATIVE ( 123 FDA reports)
FOOT FRACTURE ( 123 FDA reports)
HOT FLUSH ( 123 FDA reports)
JOINT EFFUSION ( 123 FDA reports)
SINUS DISORDER ( 123 FDA reports)
LUMBAR SPINAL STENOSIS ( 122 FDA reports)
DENTURE WEARER ( 121 FDA reports)
ORAL INFECTION ( 121 FDA reports)
SPINAL COMPRESSION FRACTURE ( 121 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 121 FDA reports)
HALLUCINATION ( 120 FDA reports)
OESOPHAGITIS ( 120 FDA reports)
AGGRESSION ( 119 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 119 FDA reports)
THROMBOSIS ( 119 FDA reports)
FEMUR FRACTURE ( 118 FDA reports)
HYDRONEPHROSIS ( 118 FDA reports)
HEPATIC ENZYME INCREASED ( 117 FDA reports)
ABNORMAL BEHAVIOUR ( 116 FDA reports)
BLOOD BILIRUBIN INCREASED ( 116 FDA reports)
DYSKINESIA ( 116 FDA reports)
ACTINOMYCOSIS ( 115 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 115 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 115 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 115 FDA reports)
SINUS CONGESTION ( 115 FDA reports)
DEBRIDEMENT ( 114 FDA reports)
GINGIVAL INFECTION ( 114 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 114 FDA reports)
BONE DENSITY DECREASED ( 113 FDA reports)
GASTRIC ULCER ( 113 FDA reports)
INTENTIONAL OVERDOSE ( 113 FDA reports)
OSTEOSCLEROSIS ( 113 FDA reports)
ACTINIC KERATOSIS ( 112 FDA reports)
ANAPHYLACTIC SHOCK ( 112 FDA reports)
EJECTION FRACTION DECREASED ( 112 FDA reports)
GINGIVAL PAIN ( 112 FDA reports)
HEPATOMEGALY ( 112 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 112 FDA reports)
LIP SWELLING ( 111 FDA reports)
MELAENA ( 111 FDA reports)
PERICARDIAL EFFUSION ( 111 FDA reports)
PNEUMOTHORAX ( 111 FDA reports)
VIRAL INFECTION ( 110 FDA reports)
TREATMENT NONCOMPLIANCE ( 109 FDA reports)
CARDIAC FAILURE ( 109 FDA reports)
DYSPHONIA ( 109 FDA reports)
PANIC ATTACK ( 109 FDA reports)
ASCITES ( 108 FDA reports)
CHOLESTASIS ( 108 FDA reports)
FISTULA ( 108 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 108 FDA reports)
METABOLIC ACIDOSIS ( 108 FDA reports)
BASAL CELL CARCINOMA ( 107 FDA reports)
BLINDNESS ( 107 FDA reports)
CHOLECYSTECTOMY ( 107 FDA reports)
LIVER DISORDER ( 107 FDA reports)
SURGERY ( 107 FDA reports)
SYNOVIAL CYST ( 107 FDA reports)
DIVERTICULITIS ( 106 FDA reports)
ORAL CAVITY FISTULA ( 106 FDA reports)
INFLUENZA LIKE ILLNESS ( 105 FDA reports)
SEQUESTRECTOMY ( 105 FDA reports)
SWOLLEN TONGUE ( 105 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 104 FDA reports)
HAEMATOCRIT DECREASED ( 104 FDA reports)
BLISTER ( 103 FDA reports)
CARDIO-RESPIRATORY ARREST ( 103 FDA reports)
DISEASE PROGRESSION ( 103 FDA reports)
CARPAL TUNNEL SYNDROME ( 102 FDA reports)
DYSARTHRIA ( 102 FDA reports)
ENCEPHALOPATHY ( 102 FDA reports)
NOCTURIA ( 102 FDA reports)
RESPIRATORY DISORDER ( 102 FDA reports)
SEPTIC SHOCK ( 102 FDA reports)
SPINAL FRACTURE ( 102 FDA reports)
TYPE 2 DIABETES MELLITUS ( 100 FDA reports)
BLOOD UREA INCREASED ( 100 FDA reports)
PNEUMONITIS ( 99 FDA reports)
PRODUCTIVE COUGH ( 99 FDA reports)
GINGIVAL SWELLING ( 98 FDA reports)
HEPATIC FAILURE ( 98 FDA reports)
SENSITIVITY OF TEETH ( 98 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 97 FDA reports)
BONE MARROW FAILURE ( 97 FDA reports)
CANDIDIASIS ( 97 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 97 FDA reports)
ACUTE HEPATIC FAILURE ( 96 FDA reports)
DIPLOPIA ( 96 FDA reports)
HAEMATEMESIS ( 96 FDA reports)
OBESITY ( 96 FDA reports)
SPLENOMEGALY ( 96 FDA reports)
VISUAL ACUITY REDUCED ( 95 FDA reports)
FUNGAL INFECTION ( 95 FDA reports)
GASTROENTERITIS ( 95 FDA reports)
HEPATIC CYST ( 95 FDA reports)
JAW FRACTURE ( 95 FDA reports)
NASOPHARYNGITIS ( 95 FDA reports)
ECZEMA ( 94 FDA reports)
HYPERCALCAEMIA ( 94 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 94 FDA reports)
ORTHOSTATIC HYPOTENSION ( 94 FDA reports)
ERYTHEMA MULTIFORME ( 93 FDA reports)
EYE PAIN ( 93 FDA reports)
MOBILITY DECREASED ( 93 FDA reports)
RADICULOPATHY ( 93 FDA reports)
SKIN EXFOLIATION ( 93 FDA reports)
TRANSAMINASES INCREASED ( 93 FDA reports)
CAESAREAN SECTION ( 92 FDA reports)
CYTOLYTIC HEPATITIS ( 92 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 92 FDA reports)
INTERSTITIAL LUNG DISEASE ( 91 FDA reports)
SPINAL DISORDER ( 91 FDA reports)
SINUS BRADYCARDIA ( 90 FDA reports)
AORTIC VALVE INCOMPETENCE ( 90 FDA reports)
PALLOR ( 90 FDA reports)
BLOOD POTASSIUM DECREASED ( 89 FDA reports)
PULMONARY FIBROSIS ( 89 FDA reports)
BURNING SENSATION ( 88 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 88 FDA reports)
NERVOUSNESS ( 88 FDA reports)
ORAL CANDIDIASIS ( 88 FDA reports)
PROTHROMBIN TIME PROLONGED ( 88 FDA reports)
SKIN DISCOLOURATION ( 88 FDA reports)
TARDIVE DYSKINESIA ( 88 FDA reports)
DRUG TOXICITY ( 86 FDA reports)
PRURITUS GENERALISED ( 86 FDA reports)
PURULENT DISCHARGE ( 86 FDA reports)
RHINITIS ALLERGIC ( 86 FDA reports)
OXYGEN SATURATION DECREASED ( 85 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 84 FDA reports)
GLOSSODYNIA ( 84 FDA reports)
RASH MACULAR ( 84 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 84 FDA reports)
URINARY RETENTION ( 83 FDA reports)
ABSCESS ORAL ( 83 FDA reports)
APHASIA ( 83 FDA reports)
CRYING ( 83 FDA reports)
HEPATIC LESION ( 83 FDA reports)
ILL-DEFINED DISORDER ( 83 FDA reports)
PARAESTHESIA ORAL ( 83 FDA reports)
PREMATURE BABY ( 83 FDA reports)
PROTEINURIA ( 83 FDA reports)
DIVERTICULUM INTESTINAL ( 82 FDA reports)
FLUSHING ( 82 FDA reports)
INFLUENZA ( 82 FDA reports)
METASTASES TO LUNG ( 82 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 82 FDA reports)
SPINAL CORD COMPRESSION ( 82 FDA reports)
TENDERNESS ( 82 FDA reports)
BREATH ODOUR ( 81 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 80 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 80 FDA reports)
SPONDYLOLISTHESIS ( 79 FDA reports)
VENTRICULAR TACHYCARDIA ( 79 FDA reports)
DRUG DEPENDENCE ( 79 FDA reports)
MYOCARDIAL ISCHAEMIA ( 79 FDA reports)
NEURALGIA ( 79 FDA reports)
PRESYNCOPE ( 79 FDA reports)
RESPIRATORY TRACT INFECTION ( 79 FDA reports)
BACK DISORDER ( 78 FDA reports)
HAEMANGIOMA ( 78 FDA reports)
MUSCLE STRAIN ( 78 FDA reports)
PREGNANCY ( 78 FDA reports)
TACHYPNOEA ( 78 FDA reports)
TOXIC SKIN ERUPTION ( 78 FDA reports)
UNRESPONSIVE TO STIMULI ( 78 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 77 FDA reports)
DILATATION VENTRICULAR ( 77 FDA reports)
GINGIVAL RECESSION ( 77 FDA reports)
HEART DISEASE CONGENITAL ( 77 FDA reports)
INGUINAL HERNIA ( 77 FDA reports)
PETECHIAE ( 77 FDA reports)
AGRANULOCYTOSIS ( 76 FDA reports)
DEPRESSED MOOD ( 76 FDA reports)
FEELING HOT ( 76 FDA reports)
RHEUMATOID ARTHRITIS ( 76 FDA reports)
UTERINE LEIOMYOMA ( 76 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 75 FDA reports)
BLOOD CALCIUM DECREASED ( 75 FDA reports)
DEVELOPMENTAL DELAY ( 75 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 75 FDA reports)
DYSLIPIDAEMIA ( 75 FDA reports)
MUSCLE TWITCHING ( 75 FDA reports)
NEOPLASM PROGRESSION ( 75 FDA reports)
OCULAR HYPERAEMIA ( 75 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 74 FDA reports)
BILIARY DYSKINESIA ( 74 FDA reports)
BRONCHOPNEUMONIA ( 74 FDA reports)
DENTAL OPERATION ( 74 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 74 FDA reports)
JOINT INJURY ( 74 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 74 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 73 FDA reports)
COMA ( 73 FDA reports)
FLATULENCE ( 73 FDA reports)
GENERALISED OEDEMA ( 73 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 73 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 73 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 73 FDA reports)
STEM CELL TRANSPLANT ( 73 FDA reports)
BODY TEMPERATURE INCREASED ( 72 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 72 FDA reports)
FLUID RETENTION ( 72 FDA reports)
JAW OPERATION ( 72 FDA reports)
CYSTITIS ( 71 FDA reports)
HEPATIC NECROSIS ( 71 FDA reports)
HYPERKERATOSIS ( 71 FDA reports)
LEFT ATRIAL DILATATION ( 71 FDA reports)
TENDONITIS ( 71 FDA reports)
SCIATICA ( 70 FDA reports)
WALKING AID USER ( 70 FDA reports)
FACIAL PAIN ( 70 FDA reports)
OFF LABEL USE ( 70 FDA reports)
OVARIAN CYST ( 70 FDA reports)
ABDOMINAL PAIN LOWER ( 69 FDA reports)
DERMATITIS EXFOLIATIVE ( 69 FDA reports)
EYE SWELLING ( 69 FDA reports)
OTITIS MEDIA ( 69 FDA reports)
SKIN DISORDER ( 69 FDA reports)
SARCOIDOSIS ( 68 FDA reports)
TRISMUS ( 68 FDA reports)
BARRETT'S OESOPHAGUS ( 68 FDA reports)
FLANK PAIN ( 68 FDA reports)
GRAND MAL CONVULSION ( 68 FDA reports)
INTESTINAL HAEMORRHAGE ( 68 FDA reports)
JAW DISORDER ( 68 FDA reports)
MITRAL VALVE CALCIFICATION ( 68 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 67 FDA reports)
BLOOD POTASSIUM INCREASED ( 67 FDA reports)
COGNITIVE DISORDER ( 67 FDA reports)
DRY SKIN ( 67 FDA reports)
LYMPHOEDEMA ( 67 FDA reports)
PEPTIC ULCER ( 67 FDA reports)
SEBORRHOEIC KERATOSIS ( 67 FDA reports)
SINUS HEADACHE ( 67 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 66 FDA reports)
UROSEPSIS ( 66 FDA reports)
CARDIAC VALVE DISEASE ( 66 FDA reports)
CEREBRAL ISCHAEMIA ( 66 FDA reports)
GOITRE ( 66 FDA reports)
HAEMATOMA ( 66 FDA reports)
HYPOMAGNESAEMIA ( 66 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 66 FDA reports)
PURPURA ( 66 FDA reports)
ABASIA ( 65 FDA reports)
BRAIN OEDEMA ( 65 FDA reports)
CEREBRAL INFARCTION ( 65 FDA reports)
EATING DISORDER ( 65 FDA reports)
LOBAR PNEUMONIA ( 65 FDA reports)
PANCREATITIS ACUTE ( 65 FDA reports)
POST PROCEDURAL COMPLICATION ( 65 FDA reports)
THROAT TIGHTNESS ( 65 FDA reports)
ALVEOLITIS ( 64 FDA reports)
BRUXISM ( 64 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 64 FDA reports)
LACERATION ( 64 FDA reports)
METASTASES TO LYMPH NODES ( 64 FDA reports)
COMPLETED SUICIDE ( 63 FDA reports)
NIGHTMARE ( 63 FDA reports)
ONYCHOMYCOSIS ( 63 FDA reports)
PREMATURE LABOUR ( 63 FDA reports)
PULMONARY CONGESTION ( 63 FDA reports)
PURULENCE ( 63 FDA reports)
RESTLESS LEGS SYNDROME ( 63 FDA reports)
SUBDURAL HAEMATOMA ( 63 FDA reports)
AORTIC STENOSIS ( 62 FDA reports)
BREAST CANCER METASTATIC ( 62 FDA reports)
EXCORIATION ( 62 FDA reports)
FLUID OVERLOAD ( 62 FDA reports)
ORTHOPNOEA ( 62 FDA reports)
PULMONARY MASS ( 62 FDA reports)
CAROTID ARTERY STENOSIS ( 61 FDA reports)
DILATATION ATRIAL ( 61 FDA reports)
DUODENITIS ( 61 FDA reports)
HELICOBACTER INFECTION ( 61 FDA reports)
HEPATITIS CHOLESTATIC ( 61 FDA reports)
HIP FRACTURE ( 61 FDA reports)
HYPOVOLAEMIA ( 61 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 61 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 61 FDA reports)
VENTRICULAR FIBRILLATION ( 61 FDA reports)
VENTRICULAR HYPERTROPHY ( 60 FDA reports)
BLOOD GLUCOSE DECREASED ( 60 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 60 FDA reports)
DYSSTASIA ( 60 FDA reports)
FOOT DEFORMITY ( 60 FDA reports)
HEAD INJURY ( 60 FDA reports)
MOOD SWINGS ( 60 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 60 FDA reports)
PLEURAL FIBROSIS ( 60 FDA reports)
RENAL TUBULAR NECROSIS ( 60 FDA reports)
DELIRIUM ( 59 FDA reports)
FAECAL INCONTINENCE ( 59 FDA reports)
GASTRIC DISORDER ( 59 FDA reports)
NEUTROPHIL COUNT DECREASED ( 59 FDA reports)
ABDOMINAL TENDERNESS ( 58 FDA reports)
ABSCESS DRAINAGE ( 58 FDA reports)
CHOLECYSTITIS ACUTE ( 58 FDA reports)
HERPES SIMPLEX ( 58 FDA reports)
INCORRECT DOSE ADMINISTERED ( 58 FDA reports)
MITRAL VALVE DISEASE ( 58 FDA reports)
NERVOUS SYSTEM DISORDER ( 58 FDA reports)
PERONEAL NERVE PALSY ( 58 FDA reports)
PSYCHOTIC DISORDER ( 58 FDA reports)
BRONCHOSPASM ( 57 FDA reports)
CARDIOVASCULAR DISORDER ( 57 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 57 FDA reports)
DIALYSIS ( 57 FDA reports)
FAILURE TO THRIVE ( 57 FDA reports)
HYPOCALCAEMIA ( 57 FDA reports)
LIP DRY ( 57 FDA reports)
NECK MASS ( 57 FDA reports)
RADIOTHERAPY ( 57 FDA reports)
SHOCK ( 57 FDA reports)
SKIN ULCER ( 57 FDA reports)
SQUAMOUS CELL CARCINOMA ( 57 FDA reports)
VITREOUS FLOATERS ( 57 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 56 FDA reports)
ATAXIA ( 56 FDA reports)
BACTERIAL INFECTION ( 56 FDA reports)
BONE SCAN ABNORMAL ( 56 FDA reports)
ECCHYMOSIS ( 56 FDA reports)
HEARING IMPAIRED ( 56 FDA reports)
HIP ARTHROPLASTY ( 56 FDA reports)
HYPERSOMNIA ( 56 FDA reports)
INTESTINAL OBSTRUCTION ( 56 FDA reports)
MELANOCYTIC NAEVUS ( 56 FDA reports)
RASH PUSTULAR ( 56 FDA reports)
CERVICAL SPINAL STENOSIS ( 55 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 55 FDA reports)
HAEMOLYTIC ANAEMIA ( 55 FDA reports)
JOINT SPRAIN ( 55 FDA reports)
LIVER INJURY ( 55 FDA reports)
LUMBAR RADICULOPATHY ( 55 FDA reports)
MOOD ALTERED ( 55 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 55 FDA reports)
ANGINA UNSTABLE ( 54 FDA reports)
CYST ( 54 FDA reports)
GOUT ( 54 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 54 FDA reports)
LACTIC ACIDOSIS ( 54 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 54 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 54 FDA reports)
SICK SINUS SYNDROME ( 53 FDA reports)
VASCULITIS ( 53 FDA reports)
ABDOMINAL HERNIA ( 53 FDA reports)
ABORTION SPONTANEOUS ( 53 FDA reports)
ABSCESS JAW ( 53 FDA reports)
ANEURYSM ( 53 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 53 FDA reports)
DEMENTIA ( 53 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 53 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 52 FDA reports)
DRUG DOSE OMISSION ( 52 FDA reports)
GENERALISED ERYTHEMA ( 52 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 52 FDA reports)
ODYNOPHAGIA ( 52 FDA reports)
PULMONARY VALVE STENOSIS ( 52 FDA reports)
RHINITIS ( 52 FDA reports)
SKIN PAPILLOMA ( 52 FDA reports)
BLEPHARITIS ( 51 FDA reports)
BLOOD SODIUM DECREASED ( 51 FDA reports)
DRUG LEVEL INCREASED ( 51 FDA reports)
DYSTONIA ( 51 FDA reports)
EDENTULOUS ( 51 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 51 FDA reports)
HEPATITIS ACUTE ( 51 FDA reports)
JAUNDICE CHOLESTATIC ( 51 FDA reports)
JOINT STIFFNESS ( 51 FDA reports)
LACRIMATION INCREASED ( 51 FDA reports)
NODULE ( 51 FDA reports)
OSTEOMYELITIS CHRONIC ( 51 FDA reports)
OTITIS EXTERNA ( 51 FDA reports)
RENAL INJURY ( 51 FDA reports)
ADVERSE DRUG REACTION ( 50 FDA reports)
ADVERSE EVENT ( 50 FDA reports)
APLASTIC ANAEMIA ( 50 FDA reports)
CEREBRAL ATROPHY ( 50 FDA reports)
CONGENITAL ANOMALY ( 50 FDA reports)
DENTAL FISTULA ( 50 FDA reports)
ILEUS ( 50 FDA reports)
MITRAL VALVE PROLAPSE ( 50 FDA reports)
ORAL SURGERY ( 50 FDA reports)
OSTEOTOMY ( 50 FDA reports)
PHARYNGEAL OEDEMA ( 50 FDA reports)
PLASMACYTOMA ( 50 FDA reports)
PNEUMONIA ASPIRATION ( 50 FDA reports)
SPINAL DEFORMITY ( 50 FDA reports)
SUDDEN DEATH ( 50 FDA reports)
WOUND CLOSURE ( 50 FDA reports)
VIITH NERVE PARALYSIS ( 49 FDA reports)
BLOOD ALBUMIN DECREASED ( 49 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 49 FDA reports)
CHROMATURIA ( 49 FDA reports)
DERMATOMYOSITIS ( 49 FDA reports)
HEART RATE DECREASED ( 49 FDA reports)
HYPOALBUMINAEMIA ( 49 FDA reports)
LIPOMA ( 49 FDA reports)
AZOTAEMIA ( 48 FDA reports)
BILIARY COLIC ( 48 FDA reports)
CACHEXIA ( 48 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 48 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 48 FDA reports)
LUNG NEOPLASM MALIGNANT ( 48 FDA reports)
ACCIDENTAL OVERDOSE ( 47 FDA reports)
EYELID OEDEMA ( 47 FDA reports)
GINGIVAL ULCERATION ( 47 FDA reports)
IMPAIRED WORK ABILITY ( 47 FDA reports)
LOCAL SWELLING ( 47 FDA reports)
MOVEMENT DISORDER ( 47 FDA reports)
MYOPIA ( 47 FDA reports)
ORAL DISCOMFORT ( 47 FDA reports)
PERIORBITAL OEDEMA ( 47 FDA reports)
PLATELET COUNT INCREASED ( 47 FDA reports)
PSEUDOMONAS INFECTION ( 47 FDA reports)
PYURIA ( 47 FDA reports)
STRESS FRACTURE ( 47 FDA reports)
THYROID DISORDER ( 46 FDA reports)
ACUTE SINUSITIS ( 46 FDA reports)
AFFECTIVE DISORDER ( 46 FDA reports)
APNOEA ( 46 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 46 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 46 FDA reports)
DUODENAL ULCER ( 46 FDA reports)
FACET JOINT SYNDROME ( 46 FDA reports)
MENISCUS LESION ( 46 FDA reports)
MICTURITION URGENCY ( 46 FDA reports)
OESOPHAGEAL ULCER ( 46 FDA reports)
OPEN WOUND ( 46 FDA reports)
PLEURITIC PAIN ( 46 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 45 FDA reports)
ADRENAL INSUFFICIENCY ( 45 FDA reports)
CEREBRAL HAEMORRHAGE ( 45 FDA reports)
CIRCULATORY COLLAPSE ( 45 FDA reports)
DEVICE RELATED INFECTION ( 45 FDA reports)
HYPERCOAGULATION ( 45 FDA reports)
MENINGITIS ASEPTIC ( 45 FDA reports)
MULTIPLE SCLEROSIS ( 45 FDA reports)
POLYP ( 45 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 45 FDA reports)
SPINAL LAMINECTOMY ( 45 FDA reports)
ULCER ( 45 FDA reports)
VAGINAL INFECTION ( 45 FDA reports)
ANGER ( 44 FDA reports)
ANKLE FRACTURE ( 44 FDA reports)
CERVICOBRACHIAL SYNDROME ( 44 FDA reports)
DEVICE FAILURE ( 44 FDA reports)
EPILEPSY ( 44 FDA reports)
HYPOACUSIS ( 44 FDA reports)
LUNG HYPERINFLATION ( 44 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 44 FDA reports)
RESPIRATORY ARREST ( 44 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 43 FDA reports)
DRUG DISPENSING ERROR ( 43 FDA reports)
DRUG EFFECT DECREASED ( 43 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 43 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 43 FDA reports)
FIBROSIS ( 43 FDA reports)
HEPATIC CIRRHOSIS ( 43 FDA reports)
HEPATITIS C ( 43 FDA reports)
INTERMITTENT CLAUDICATION ( 43 FDA reports)
LARYNGITIS ( 43 FDA reports)
LYMPH NODE PAIN ( 43 FDA reports)
MYOSITIS ( 43 FDA reports)
NEURODERMATITIS ( 43 FDA reports)
TALIPES ( 43 FDA reports)
TONGUE DISCOLOURATION ( 43 FDA reports)
VISUAL FIELD DEFECT ( 43 FDA reports)
SEXUAL DYSFUNCTION ( 42 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 42 FDA reports)
VAGINAL HAEMORRHAGE ( 42 FDA reports)
ACIDOSIS ( 42 FDA reports)
ALCOHOL USE ( 42 FDA reports)
BONE MARROW TRANSPLANT ( 42 FDA reports)
DECUBITUS ULCER ( 42 FDA reports)
ENCEPHALITIS ( 42 FDA reports)
FAECES DISCOLOURED ( 42 FDA reports)
HODGKIN'S DISEASE ( 42 FDA reports)
LIMB DISCOMFORT ( 42 FDA reports)
LIMB INJURY ( 42 FDA reports)
PELVIC PAIN ( 42 FDA reports)
PHOTOPHOBIA ( 42 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 41 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 41 FDA reports)
BREAST CANCER ( 41 FDA reports)
DRUG ABUSE ( 41 FDA reports)
FIBROMYALGIA ( 41 FDA reports)
GINGIVAL ERYTHEMA ( 41 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 41 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 41 FDA reports)
RESPIRATORY RATE INCREASED ( 41 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 41 FDA reports)
TENOSYNOVITIS ( 41 FDA reports)
TONGUE ULCERATION ( 41 FDA reports)
VARICOSE VEIN ( 41 FDA reports)
VITAMIN D DEFICIENCY ( 41 FDA reports)
SKIN HYPERPIGMENTATION ( 40 FDA reports)
SOFT TISSUE INFECTION ( 40 FDA reports)
STREPTOCOCCAL INFECTION ( 40 FDA reports)
TONGUE DISORDER ( 40 FDA reports)
VITAMIN B12 DEFICIENCY ( 40 FDA reports)
ATRIOVENTRICULAR BLOCK ( 40 FDA reports)
BONE LOSS ( 40 FDA reports)
COLON ADENOMA ( 40 FDA reports)
DERMATITIS ( 40 FDA reports)
DIABETIC KETOACIDOSIS ( 40 FDA reports)
FEELING COLD ( 40 FDA reports)
GYNAECOMASTIA ( 40 FDA reports)
HYPOKINESIA ( 40 FDA reports)
OCCULT BLOOD POSITIVE ( 40 FDA reports)
PERITONITIS ( 40 FDA reports)
PHLEBITIS ( 40 FDA reports)
PLANTAR FASCIITIS ( 40 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 40 FDA reports)
PROSTATE CANCER ( 40 FDA reports)
ATRIAL FLUTTER ( 39 FDA reports)
CORONARY ARTERY OCCLUSION ( 39 FDA reports)
DEAFNESS NEUROSENSORY ( 39 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 39 FDA reports)
GLAUCOMA ( 39 FDA reports)
HYDROCEPHALUS ( 39 FDA reports)
LYMPHADENITIS ( 39 FDA reports)
MENSTRUATION IRREGULAR ( 39 FDA reports)
MENTAL IMPAIRMENT ( 39 FDA reports)
ORAL HERPES ( 39 FDA reports)
PATHOLOGICAL GAMBLING ( 39 FDA reports)
POOR PERSONAL HYGIENE ( 39 FDA reports)
PROSTATOMEGALY ( 39 FDA reports)
RALES ( 39 FDA reports)
TENDON DISORDER ( 39 FDA reports)
SEDATION ( 38 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 38 FDA reports)
THROAT IRRITATION ( 38 FDA reports)
THYROID NEOPLASM ( 38 FDA reports)
TONSILLITIS ( 38 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 38 FDA reports)
ACUTE RESPIRATORY FAILURE ( 38 FDA reports)
ASPIRATION ( 38 FDA reports)
BLOOD DISORDER ( 38 FDA reports)
HEPATOTOXICITY ( 38 FDA reports)
HYPERTONIC BLADDER ( 38 FDA reports)
LIGAMENT SPRAIN ( 38 FDA reports)
MOUTH HAEMORRHAGE ( 38 FDA reports)
AMENORRHOEA ( 37 FDA reports)
AORTIC ANEURYSM ( 37 FDA reports)
COLD SWEAT ( 37 FDA reports)
COLON CANCER ( 37 FDA reports)
DISEASE RECURRENCE ( 37 FDA reports)
DRUG ADMINISTRATION ERROR ( 37 FDA reports)
ENTEROCOCCAL INFECTION ( 37 FDA reports)
EOSINOPHIL COUNT DECREASED ( 37 FDA reports)
EYE DISORDER ( 37 FDA reports)
HEMIPARESIS ( 37 FDA reports)
METRORRHAGIA ( 37 FDA reports)
THINKING ABNORMAL ( 37 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 37 FDA reports)
URINE OUTPUT DECREASED ( 37 FDA reports)
WOUND DEHISCENCE ( 37 FDA reports)
SPONDYLITIS ( 36 FDA reports)
VERTEBROPLASTY ( 36 FDA reports)
WOUND SECRETION ( 36 FDA reports)
ABDOMINAL ABSCESS ( 36 FDA reports)
ALVEOLOPLASTY ( 36 FDA reports)
ANGIONEUROTIC OEDEMA ( 36 FDA reports)
ANOSMIA ( 36 FDA reports)
AORTIC DILATATION ( 36 FDA reports)
COLITIS ISCHAEMIC ( 36 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 36 FDA reports)
CORONARY ARTERY STENOSIS ( 36 FDA reports)
DENTAL PROSTHESIS USER ( 36 FDA reports)
DERMATITIS CONTACT ( 36 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 36 FDA reports)
EYE IRRITATION ( 36 FDA reports)
HERNIA ( 36 FDA reports)
HYPERPLASIA ( 36 FDA reports)
HYPERTHYROIDISM ( 36 FDA reports)
HYPOAESTHESIA ORAL ( 36 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 36 FDA reports)
ISCHAEMIC STROKE ( 36 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 36 FDA reports)
OSTEORADIONECROSIS ( 36 FDA reports)
PULMONARY HAEMORRHAGE ( 36 FDA reports)
RASH PAPULAR ( 36 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 36 FDA reports)
RETCHING ( 36 FDA reports)
BONE EROSION ( 35 FDA reports)
CARDIOGENIC SHOCK ( 35 FDA reports)
CLOSTRIDIAL INFECTION ( 35 FDA reports)
DRUG INTOLERANCE ( 35 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 35 FDA reports)
HYPOTONIA ( 35 FDA reports)
JOINT DISLOCATION ( 35 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 35 FDA reports)
MYELOPATHY ( 35 FDA reports)
NECROSIS ( 35 FDA reports)
PERIPHERAL COLDNESS ( 35 FDA reports)
PROCEDURAL PAIN ( 35 FDA reports)
PULPITIS DENTAL ( 35 FDA reports)
PYELONEPHRITIS ( 35 FDA reports)
SECONDARY SEQUESTRUM ( 35 FDA reports)
TIBIA FRACTURE ( 35 FDA reports)
VENTRICULAR DYSFUNCTION ( 35 FDA reports)
VENTRICULAR HYPOKINESIA ( 35 FDA reports)
WOUND INFECTION ( 35 FDA reports)
SKIN LACERATION ( 34 FDA reports)
STRIDOR ( 34 FDA reports)
ANGIOPATHY ( 34 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 34 FDA reports)
AORTIC VALVE DISEASE ( 34 FDA reports)
BIOPSY BONE MARROW ( 34 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 34 FDA reports)
BONE GRAFT ( 34 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 34 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 34 FDA reports)
DIASTOLIC DYSFUNCTION ( 34 FDA reports)
ESSENTIAL HYPERTENSION ( 34 FDA reports)
EXPIRED DRUG ADMINISTERED ( 34 FDA reports)
MANIA ( 34 FDA reports)
METAPLASIA ( 34 FDA reports)
OLIGURIA ( 34 FDA reports)
PARANOIA ( 34 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 34 FDA reports)
APHTHOUS STOMATITIS ( 33 FDA reports)
BLADDER CANCER ( 33 FDA reports)
BREATH SOUNDS ABNORMAL ( 33 FDA reports)
CALCULUS URETERIC ( 33 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 33 FDA reports)
CHOKING ( 33 FDA reports)
COORDINATION ABNORMAL ( 33 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 33 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 33 FDA reports)
DERMATITIS ALLERGIC ( 33 FDA reports)
DIABETIC NEUROPATHY ( 33 FDA reports)
FOETAL DISTRESS SYNDROME ( 33 FDA reports)
GASTRITIS EROSIVE ( 33 FDA reports)
HAEMODIALYSIS ( 33 FDA reports)
HALLUCINATION, AUDITORY ( 33 FDA reports)
HEART VALVE INCOMPETENCE ( 33 FDA reports)
HEPATIC ENCEPHALOPATHY ( 33 FDA reports)
HYPOPHOSPHATAEMIA ( 33 FDA reports)
ILEUS PARALYTIC ( 33 FDA reports)
LOCALISED INFECTION ( 33 FDA reports)
MAJOR DEPRESSION ( 33 FDA reports)
MULTIPLE DRUG OVERDOSE ( 33 FDA reports)
NEUTROPHIL COUNT INCREASED ( 33 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 33 FDA reports)
OEDEMA MOUTH ( 33 FDA reports)
ORAL DISCHARGE ( 33 FDA reports)
PARALYSIS ( 33 FDA reports)
PRESBYOPIA ( 33 FDA reports)
TEMPERATURE INTOLERANCE ( 33 FDA reports)
TOOTH IMPACTED ( 33 FDA reports)
URINE ODOUR ABNORMAL ( 33 FDA reports)
SNORING ( 32 FDA reports)
THROMBOPHLEBITIS ( 32 FDA reports)
TOOTH REPAIR ( 32 FDA reports)
VASCULAR CALCIFICATION ( 32 FDA reports)
VISUAL DISTURBANCE ( 32 FDA reports)
ADENOCARCINOMA ( 32 FDA reports)
BACTERAEMIA ( 32 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 32 FDA reports)
DERMAL CYST ( 32 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 32 FDA reports)
GALLBLADDER INJURY ( 32 FDA reports)
GROIN PAIN ( 32 FDA reports)
HILAR LYMPHADENOPATHY ( 32 FDA reports)
LIVE BIRTH ( 32 FDA reports)
NEURITIS ( 32 FDA reports)
PELVIC FRACTURE ( 32 FDA reports)
PULMONARY THROMBOSIS ( 32 FDA reports)
CHEST X-RAY ABNORMAL ( 31 FDA reports)
CHOLESTASIS OF PREGNANCY ( 31 FDA reports)
CLOSTRIDIUM COLITIS ( 31 FDA reports)
ELECTROLYTE IMBALANCE ( 31 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 31 FDA reports)
GASTROINTESTINAL PAIN ( 31 FDA reports)
HALLUCINATION, VISUAL ( 31 FDA reports)
HYPERVENTILATION ( 31 FDA reports)
JAUNDICE NEONATAL ( 31 FDA reports)
KLEBSIELLA INFECTION ( 31 FDA reports)
LIBIDO DECREASED ( 31 FDA reports)
LICHEN PLANUS ( 31 FDA reports)
MUSCLE TIGHTNESS ( 31 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 31 FDA reports)
NASAL SEPTUM DEVIATION ( 31 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 31 FDA reports)
PERICARDITIS ( 31 FDA reports)
PULMONARY INFARCTION ( 31 FDA reports)
RESTLESSNESS ( 31 FDA reports)
WEIGHT GAIN POOR ( 31 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 30 FDA reports)
SENSORY LOSS ( 30 FDA reports)
WRONG DRUG ADMINISTERED ( 30 FDA reports)
ANURIA ( 30 FDA reports)
FEMORAL NECK FRACTURE ( 30 FDA reports)
HEPATITIS B ( 30 FDA reports)
HYPOAESTHESIA FACIAL ( 30 FDA reports)
LYMPHOPENIA ( 30 FDA reports)
METASTASES TO SKIN ( 30 FDA reports)
NEPHRITIS INTERSTITIAL ( 30 FDA reports)
POLYNEUROPATHY ( 30 FDA reports)
ACUTE PSYCHOSIS ( 29 FDA reports)
AGEUSIA ( 29 FDA reports)
ANAL FISTULA ( 29 FDA reports)
AORTIC VALVE SCLEROSIS ( 29 FDA reports)
BIPOLAR DISORDER ( 29 FDA reports)
BLOOD PRESSURE ABNORMAL ( 29 FDA reports)
DENTAL CARE ( 29 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 29 FDA reports)
ENDOTRACHEAL INTUBATION ( 29 FDA reports)
FAMILY STRESS ( 29 FDA reports)
GINGIVAL OEDEMA ( 29 FDA reports)
INGROWING NAIL ( 29 FDA reports)
LABORATORY TEST ABNORMAL ( 29 FDA reports)
MACULAR DEGENERATION ( 29 FDA reports)
MULTI-ORGAN DISORDER ( 29 FDA reports)
MYELOMA RECURRENCE ( 29 FDA reports)
NO THERAPEUTIC RESPONSE ( 29 FDA reports)
OEDEMA MUCOSAL ( 29 FDA reports)
PIERRE ROBIN SYNDROME ( 29 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 29 FDA reports)
SYNOVITIS ( 29 FDA reports)
TENDON RUPTURE ( 29 FDA reports)
ULNA FRACTURE ( 29 FDA reports)
SENSORY DISTURBANCE ( 28 FDA reports)
THIRST ( 28 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 28 FDA reports)
ABORTION INDUCED ( 28 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 28 FDA reports)
BREAST PAIN ( 28 FDA reports)
BRONCHIECTASIS ( 28 FDA reports)
BULLOUS LUNG DISEASE ( 28 FDA reports)
DELUSION ( 28 FDA reports)
DENTAL IMPLANTATION ( 28 FDA reports)
GRANULOMA ( 28 FDA reports)
HEPATIC CONGESTION ( 28 FDA reports)
HYPERPARATHYROIDISM ( 28 FDA reports)
ILEITIS ( 28 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 28 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 28 FDA reports)
KIDNEY INFECTION ( 28 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 28 FDA reports)
MENINGIOMA ( 28 FDA reports)
MYOCLONUS ( 28 FDA reports)
NERVE INJURY ( 28 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 28 FDA reports)
OROANTRAL FISTULA ( 28 FDA reports)
PSORIASIS ( 28 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 28 FDA reports)
RASH MORBILLIFORM ( 28 FDA reports)
REFLUX OESOPHAGITIS ( 28 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 27 FDA reports)
AXILLARY MASS ( 27 FDA reports)
BEDRIDDEN ( 27 FDA reports)
BLINDNESS TRANSIENT ( 27 FDA reports)
BLOOD URINE PRESENT ( 27 FDA reports)
BONE FORMATION INCREASED ( 27 FDA reports)
BONE MARROW OEDEMA ( 27 FDA reports)
BREAST ENLARGEMENT ( 27 FDA reports)
CERVICITIS ( 27 FDA reports)
GINGIVAL EROSION ( 27 FDA reports)
HICCUPS ( 27 FDA reports)
INCONTINENCE ( 27 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 27 FDA reports)
LOW TURNOVER OSTEOPATHY ( 27 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 27 FDA reports)
MAXILLOFACIAL OPERATION ( 27 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 27 FDA reports)
PERIPHERAL ISCHAEMIA ( 27 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 27 FDA reports)
RADIATION SKIN INJURY ( 27 FDA reports)
RADIUS FRACTURE ( 27 FDA reports)
SPINAL FUSION SURGERY ( 27 FDA reports)
TACHYCARDIA FOETAL ( 27 FDA reports)
WOUND ( 27 FDA reports)
SCRATCH ( 26 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 26 FDA reports)
STOMACH DISCOMFORT ( 26 FDA reports)
STRESS URINARY INCONTINENCE ( 26 FDA reports)
THERAPY NON-RESPONDER ( 26 FDA reports)
THYROID CYST ( 26 FDA reports)
TINEA PEDIS ( 26 FDA reports)
TOBACCO ABUSE ( 26 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 26 FDA reports)
ACOUSTIC NEUROMA ( 26 FDA reports)
ANAL ABSCESS ( 26 FDA reports)
BLOOD CHLORIDE DECREASED ( 26 FDA reports)
BONE NEOPLASM MALIGNANT ( 26 FDA reports)
BREAST MASS ( 26 FDA reports)
BUNION ( 26 FDA reports)
CARDIAC PACEMAKER INSERTION ( 26 FDA reports)
FRACTURE NONUNION ( 26 FDA reports)
FURUNCLE ( 26 FDA reports)
HAIR GROWTH ABNORMAL ( 26 FDA reports)
HYPERBILIRUBINAEMIA ( 26 FDA reports)
IMMUNE SYSTEM DISORDER ( 26 FDA reports)
LUNG INFECTION ( 26 FDA reports)
LYMPHOMA ( 26 FDA reports)
MENORRHAGIA ( 26 FDA reports)
NECROTISING FASCIITIS ( 26 FDA reports)
NON-CARDIAC CHEST PAIN ( 26 FDA reports)
ORAL FIBROMA ( 26 FDA reports)
PANCREATIC CYST ( 26 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 26 FDA reports)
PSEUDOPOLYP ( 26 FDA reports)
QUALITY OF LIFE DECREASED ( 26 FDA reports)
RESPIRATORY TRACT CONGESTION ( 26 FDA reports)
ADNEXA UTERI MASS ( 25 FDA reports)
AMMONIA INCREASED ( 25 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 25 FDA reports)
BLINDNESS UNILATERAL ( 25 FDA reports)
BRAIN HERNIATION ( 25 FDA reports)
CATHETER PLACEMENT ( 25 FDA reports)
DEPRESSIVE SYMPTOM ( 25 FDA reports)
DRUG SCREEN POSITIVE ( 25 FDA reports)
ERYTHEMA NODOSUM ( 25 FDA reports)
FIBROMA ( 25 FDA reports)
GASTRIC POLYPS ( 25 FDA reports)
HEPATOCELLULAR INJURY ( 25 FDA reports)
HYSTERECTOMY ( 25 FDA reports)
INTRA-UTERINE DEATH ( 25 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 25 FDA reports)
LIPASE INCREASED ( 25 FDA reports)
MACROGLOSSIA ( 25 FDA reports)
MASTECTOMY ( 25 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 25 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 25 FDA reports)
PULMONARY GRANULOMA ( 25 FDA reports)
SCAB ( 25 FDA reports)
SEROMA ( 25 FDA reports)
SKIN TEST POSITIVE ( 25 FDA reports)
STRABISMUS ( 25 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 25 FDA reports)
ULCER HAEMORRHAGE ( 25 FDA reports)
SINUS OPERATION ( 24 FDA reports)
SKIN EROSION ( 24 FDA reports)
SNEEZING ( 24 FDA reports)
TENDON INJURY ( 24 FDA reports)
ULCERATIVE KERATITIS ( 24 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 24 FDA reports)
ADRENAL NEOPLASM ( 24 FDA reports)
ASTIGMATISM ( 24 FDA reports)
BONE NEOPLASM ( 24 FDA reports)
BREAST CYST ( 24 FDA reports)
EPIGASTRIC DISCOMFORT ( 24 FDA reports)
FAECES PALE ( 24 FDA reports)
GRANULOCYTOPENIA ( 24 FDA reports)
HAEMODYNAMIC INSTABILITY ( 24 FDA reports)
KNEE ARTHROPLASTY ( 24 FDA reports)
LARYNGEAL OEDEMA ( 24 FDA reports)
METASTASES TO PELVIS ( 24 FDA reports)
MONOCYTE COUNT DECREASED ( 24 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 24 FDA reports)
MUSCULOSKELETAL DISORDER ( 24 FDA reports)
NEOPLASM ( 24 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 24 FDA reports)
ORTHOSIS USER ( 24 FDA reports)
PAPILLOEDEMA ( 24 FDA reports)
PHOTOPSIA ( 24 FDA reports)
PROTEIN TOTAL INCREASED ( 24 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 24 FDA reports)
ACNE ( 23 FDA reports)
ACUTE CORONARY SYNDROME ( 23 FDA reports)
AKATHISIA ( 23 FDA reports)
ANAEMIA POSTOPERATIVE ( 23 FDA reports)
ARTERIAL STENOSIS ( 23 FDA reports)
ATROPHY ( 23 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 23 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 23 FDA reports)
BONE FRAGMENTATION ( 23 FDA reports)
CATARACT OPERATION ( 23 FDA reports)
CERUMEN IMPACTION ( 23 FDA reports)
CLEFT PALATE ( 23 FDA reports)
CREPITATIONS ( 23 FDA reports)
DEVICE MALFUNCTION ( 23 FDA reports)
DIABETIC NEPHROPATHY ( 23 FDA reports)
DYSAESTHESIA ( 23 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 23 FDA reports)
EXTRASYSTOLES ( 23 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 23 FDA reports)
HYPOTHERMIA ( 23 FDA reports)
IMMUNODEFICIENCY ( 23 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 23 FDA reports)
LACUNAR INFARCTION ( 23 FDA reports)
LOWER LIMB FRACTURE ( 23 FDA reports)
METASTATIC NEOPLASM ( 23 FDA reports)
NASAL DRYNESS ( 23 FDA reports)
NASAL MUCOSAL DISORDER ( 23 FDA reports)
NO ADVERSE EVENT ( 23 FDA reports)
ORAL TORUS ( 23 FDA reports)
POLYPECTOMY ( 23 FDA reports)
PROCEDURAL COMPLICATION ( 23 FDA reports)
PROCTITIS ( 23 FDA reports)
PULMONARY ARTERY DILATATION ( 23 FDA reports)
RIGHT ATRIAL DILATATION ( 23 FDA reports)
SEASONAL ALLERGY ( 23 FDA reports)
SOCIAL PROBLEM ( 23 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 23 FDA reports)
TOOTH DISCOLOURATION ( 23 FDA reports)
URINE COLOUR ABNORMAL ( 23 FDA reports)
VENOUS INSUFFICIENCY ( 23 FDA reports)
RIGHT VENTRICULAR FAILURE ( 22 FDA reports)
SCREAMING ( 22 FDA reports)
SMEAR CERVIX ABNORMAL ( 22 FDA reports)
SOFT TISSUE DISORDER ( 22 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 22 FDA reports)
TRIGEMINAL NEURALGIA ( 22 FDA reports)
TUBERCULOSIS ( 22 FDA reports)
VENTRICULAR HYPOPLASIA ( 22 FDA reports)
VERTEBRAL WEDGING ( 22 FDA reports)
ABDOMINAL ADHESIONS ( 22 FDA reports)
APHAGIA ( 22 FDA reports)
APPENDICITIS ( 22 FDA reports)
CERVICAL DYSPLASIA ( 22 FDA reports)
CHAPPED LIPS ( 22 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 22 FDA reports)
DENTAL PLAQUE ( 22 FDA reports)
EAR CONGESTION ( 22 FDA reports)
FACIAL PALSY ( 22 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 22 FDA reports)
FRACTURE ( 22 FDA reports)
GRAFT VERSUS HOST DISEASE ( 22 FDA reports)
HAEMANGIOMA OF LIVER ( 22 FDA reports)
HAND FRACTURE ( 22 FDA reports)
HEPATIC MASS ( 22 FDA reports)
HEPATIC NEOPLASM ( 22 FDA reports)
ILIAC ARTERY THROMBOSIS ( 22 FDA reports)
INCREASED TENDENCY TO BRUISE ( 22 FDA reports)
INJECTION SITE REACTION ( 22 FDA reports)
INTENTIONAL DRUG MISUSE ( 22 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 22 FDA reports)
MECHANICAL VENTILATION ( 22 FDA reports)
MONARTHRITIS ( 22 FDA reports)
MOTOR DYSFUNCTION ( 22 FDA reports)
MYOPATHY ( 22 FDA reports)
NASAL ULCER ( 22 FDA reports)
OVARIAN MASS ( 22 FDA reports)
PERSONALITY CHANGE ( 22 FDA reports)
POLYDIPSIA ( 22 FDA reports)
POLYURIA ( 22 FDA reports)
POOR QUALITY SLEEP ( 22 FDA reports)
RENAL MASS ( 22 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 21 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 21 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 21 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 21 FDA reports)
BREAST CALCIFICATIONS ( 21 FDA reports)
CARDIAC ANEURYSM ( 21 FDA reports)
CEREBRAL THROMBOSIS ( 21 FDA reports)
COARCTATION OF THE AORTA ( 21 FDA reports)
COMPULSIONS ( 21 FDA reports)
DERMATITIS BULLOUS ( 21 FDA reports)
DEVICE BREAKAGE ( 21 FDA reports)
EAR DISCOMFORT ( 21 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 21 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 21 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 21 FDA reports)
HEPATOCELLULAR DAMAGE ( 21 FDA reports)
HYPOVENTILATION ( 21 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 21 FDA reports)
INTRACRANIAL ANEURYSM ( 21 FDA reports)
IRITIS ( 21 FDA reports)
ISCHAEMIA ( 21 FDA reports)
KELOID SCAR ( 21 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 21 FDA reports)
MALIGNANT MELANOMA ( 21 FDA reports)
MENINGITIS ( 21 FDA reports)
MUCOSAL ULCERATION ( 21 FDA reports)
MUCOUS STOOLS ( 21 FDA reports)
NYSTAGMUS ( 21 FDA reports)
OPTIC NEURITIS ( 21 FDA reports)
OSTEOCHONDROSIS ( 21 FDA reports)
PLEURAL DISORDER ( 21 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 21 FDA reports)
POST THROMBOTIC SYNDROME ( 21 FDA reports)
PROTEIN URINE PRESENT ( 21 FDA reports)
PSYCHIATRIC SYMPTOM ( 21 FDA reports)
SINUS ARRHYTHMIA ( 21 FDA reports)
SPLENIC GRANULOMA ( 21 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 21 FDA reports)
VOCAL CORD PARALYSIS ( 21 FDA reports)
WHITE BLOOD CELL COUNT ( 21 FDA reports)
WOUND DRAINAGE ( 21 FDA reports)
SELF ESTEEM DECREASED ( 20 FDA reports)
SKIN IRRITATION ( 20 FDA reports)
SMALL INTESTINE OPERATION ( 20 FDA reports)
SPINAL OPERATION ( 20 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 20 FDA reports)
TEMPORAL ARTERITIS ( 20 FDA reports)
TONGUE OEDEMA ( 20 FDA reports)
UMBILICAL HERNIA ( 20 FDA reports)
URINE ANALYSIS ( 20 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 20 FDA reports)
APPENDICECTOMY ( 20 FDA reports)
BACTERIAL TEST NEGATIVE ( 20 FDA reports)
BIOPSY BONE ( 20 FDA reports)
BLOOD CULTURE POSITIVE ( 20 FDA reports)
BONE SARCOMA ( 20 FDA reports)
CEREBROVASCULAR DISORDER ( 20 FDA reports)
COLONIC STENOSIS ( 20 FDA reports)
CRANIAL NERVE DISORDER ( 20 FDA reports)
DECREASED ACTIVITY ( 20 FDA reports)
ESCHERICHIA INFECTION ( 20 FDA reports)
EYE PRURITUS ( 20 FDA reports)
GASTROENTERITIS RADIATION ( 20 FDA reports)
HEPATOSPLENOMEGALY ( 20 FDA reports)
INTRAOCULAR LENS IMPLANT ( 20 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 20 FDA reports)
LABILE BLOOD PRESSURE ( 20 FDA reports)
LIP OEDEMA ( 20 FDA reports)
LOSS OF EMPLOYMENT ( 20 FDA reports)
LUNG CONSOLIDATION ( 20 FDA reports)
MYASTHENIA GRAVIS ( 20 FDA reports)
NASAL DISORDER ( 20 FDA reports)
NEUROGENIC BLADDER ( 20 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 20 FDA reports)
OCCIPITAL NEURALGIA ( 20 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 20 FDA reports)
PANCOAST'S TUMOUR ( 20 FDA reports)
PAPILLOMA ( 20 FDA reports)
PARKINSONISM ( 20 FDA reports)
PAROSMIA ( 20 FDA reports)
QRS AXIS ABNORMAL ( 20 FDA reports)
RED BLOOD CELLS URINE ( 20 FDA reports)
ABNORMAL DREAMS ( 19 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 19 FDA reports)
ADRENAL ADENOMA ( 19 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 19 FDA reports)
ATRIAL TACHYCARDIA ( 19 FDA reports)
BARTHOLIN'S CYST ( 19 FDA reports)
BONE GIANT CELL TUMOUR ( 19 FDA reports)
BRAIN INJURY ( 19 FDA reports)
CAROTID ARTERY DISEASE ( 19 FDA reports)
CLUSTER HEADACHE ( 19 FDA reports)
DEVICE RELATED SEPSIS ( 19 FDA reports)
ENURESIS ( 19 FDA reports)
EXFOLIATIVE RASH ( 19 FDA reports)
FACE INJURY ( 19 FDA reports)
FAT NECROSIS ( 19 FDA reports)
FRACTURE DISPLACEMENT ( 19 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 19 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 19 FDA reports)
HEART VALVE CALCIFICATION ( 19 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 19 FDA reports)
HYPERTHERMIA ( 19 FDA reports)
INFERTILITY ( 19 FDA reports)
LARGE INTESTINE PERFORATION ( 19 FDA reports)
LEFT VENTRICULAR FAILURE ( 19 FDA reports)
LOCALISED OEDEMA ( 19 FDA reports)
MACROCYTOSIS ( 19 FDA reports)
MYCOSIS FUNGOIDES ( 19 FDA reports)
MYELODYSPLASTIC SYNDROME ( 19 FDA reports)
NEONATAL DISORDER ( 19 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 19 FDA reports)
NEOPLASM SKIN ( 19 FDA reports)
NEPHROSCLEROSIS ( 19 FDA reports)
OESOPHAGEAL SPASM ( 19 FDA reports)
ORAL PUSTULE ( 19 FDA reports)
OSTEOMALACIA ( 19 FDA reports)
PULSE ABSENT ( 19 FDA reports)
RAYNAUD'S PHENOMENON ( 19 FDA reports)
RECTAL POLYP ( 19 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 19 FDA reports)
SKIN CANCER ( 19 FDA reports)
SYNOVIAL RUPTURE ( 19 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 19 FDA reports)
TONGUE BITING ( 19 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 19 FDA reports)
TOXIC SHOCK SYNDROME ( 19 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 19 FDA reports)
URGE INCONTINENCE ( 19 FDA reports)
URINARY HESITATION ( 19 FDA reports)
URINE ABNORMALITY ( 19 FDA reports)
UTERINE HAEMORRHAGE ( 19 FDA reports)
VULVOVAGINAL DRYNESS ( 19 FDA reports)
SEBORRHOEIC DERMATITIS ( 18 FDA reports)
SENSATION OF HEAVINESS ( 18 FDA reports)
SERUM FERRITIN INCREASED ( 18 FDA reports)
SIALOADENITIS ( 18 FDA reports)
SKIN INFECTION ( 18 FDA reports)
THYROIDECTOMY ( 18 FDA reports)
VESICOURETERIC REFLUX ( 18 FDA reports)
ADENOMA BENIGN ( 18 FDA reports)
BILE DUCT STONE ( 18 FDA reports)
CARDIOPULMONARY FAILURE ( 18 FDA reports)
CATARACT NUCLEAR ( 18 FDA reports)
CONTRAST MEDIA REACTION ( 18 FDA reports)
COSTOCHONDRITIS ( 18 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 18 FDA reports)
DIZZINESS POSTURAL ( 18 FDA reports)
DYSMENORRHOEA ( 18 FDA reports)
DYSMORPHISM ( 18 FDA reports)
ENDOCARDITIS ( 18 FDA reports)
ENDOMETRIOSIS ( 18 FDA reports)
ENTEROBACTER INFECTION ( 18 FDA reports)
EOSINOPHIL COUNT INCREASED ( 18 FDA reports)
EXERCISE TOLERANCE DECREASED ( 18 FDA reports)
EYELID PTOSIS ( 18 FDA reports)
FEMORAL ARTERY EMBOLISM ( 18 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 18 FDA reports)
HAEMOTHORAX ( 18 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 18 FDA reports)
HYDROURETER ( 18 FDA reports)
INTRACARDIAC THROMBUS ( 18 FDA reports)
LIVER TRANSPLANT ( 18 FDA reports)
MUSCLE ATROPHY ( 18 FDA reports)
MUSCLE HAEMORRHAGE ( 18 FDA reports)
MYELITIS TRANSVERSE ( 18 FDA reports)
NASAL DISCOMFORT ( 18 FDA reports)
NEPHROTIC SYNDROME ( 18 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 18 FDA reports)
ORAL INTAKE REDUCED ( 18 FDA reports)
ORGANISING PNEUMONIA ( 18 FDA reports)
PALATAL OEDEMA ( 18 FDA reports)
PANIC REACTION ( 18 FDA reports)
PINEAL GLAND CYST ( 18 FDA reports)
PROSTATIC OBSTRUCTION ( 18 FDA reports)
PYOGENIC GRANULOMA ( 18 FDA reports)
RENAL TUBULAR ACIDOSIS ( 18 FDA reports)
RETINOPATHY ( 18 FDA reports)
ABNORMAL FAECES ( 17 FDA reports)
ACCIDENT ( 17 FDA reports)
APICECTOMY ( 17 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 17 FDA reports)
CHOLECYSTITIS INFECTIVE ( 17 FDA reports)
CHOLESTEROSIS ( 17 FDA reports)
CHONDROMALACIA ( 17 FDA reports)
CONGENITAL AORTIC ATRESIA ( 17 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 17 FDA reports)
DENTAL DISCOMFORT ( 17 FDA reports)
DIABETIC RETINOPATHY ( 17 FDA reports)
DYSPHEMIA ( 17 FDA reports)
EAR MALFORMATION ( 17 FDA reports)
ENGRAFTMENT SYNDROME ( 17 FDA reports)
ENTERITIS ( 17 FDA reports)
ERUCTATION ( 17 FDA reports)
FACIAL BONES FRACTURE ( 17 FDA reports)
FALLOT'S TETRALOGY ( 17 FDA reports)
FEBRILE BONE MARROW APLASIA ( 17 FDA reports)
GASTROENTERITIS VIRAL ( 17 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 17 FDA reports)
GINGIVAL ABSCESS ( 17 FDA reports)
GLOBULINS INCREASED ( 17 FDA reports)
HEPATITIS TOXIC ( 17 FDA reports)
HYPERTROPHY ( 17 FDA reports)
HYPOGLYCAEMIC COMA ( 17 FDA reports)
HYPOREFLEXIA ( 17 FDA reports)
INFUSION RELATED REACTION ( 17 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 17 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 17 FDA reports)
JUGULAR VEIN DISTENSION ( 17 FDA reports)
KYPHOSCOLIOSIS ( 17 FDA reports)
LENTIGO ( 17 FDA reports)
LOSS OF LIBIDO ( 17 FDA reports)
MALOCCLUSION ( 17 FDA reports)
MEDIASTINAL DISORDER ( 17 FDA reports)
METABOLIC SYNDROME ( 17 FDA reports)
MICROCYTIC ANAEMIA ( 17 FDA reports)
MUSCLE RIGIDITY ( 17 FDA reports)
NEUTROPENIC SEPSIS ( 17 FDA reports)
OSTEOGENESIS IMPERFECTA ( 17 FDA reports)
PALATAL DISORDER ( 17 FDA reports)
PEMPHIGUS ( 17 FDA reports)
PROSTATISM ( 17 FDA reports)
RADICULITIS CERVICAL ( 17 FDA reports)
RENAL PAIN ( 17 FDA reports)
RETINAL HAEMORRHAGE ( 17 FDA reports)
RETINAL TEAR ( 17 FDA reports)
RHONCHI ( 17 FDA reports)
SPUTUM DISCOLOURED ( 17 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 17 FDA reports)
SUBCUTANEOUS ABSCESS ( 17 FDA reports)
TOOTH DECALCIFICATION ( 17 FDA reports)
VAGINAL DISCHARGE ( 17 FDA reports)
VITAMIN A DEFICIENCY ( 17 FDA reports)
SELF-MEDICATION ( 16 FDA reports)
SERUM SICKNESS ( 16 FDA reports)
SKIN BURNING SENSATION ( 16 FDA reports)
SKIN OEDEMA ( 16 FDA reports)
SLEEP TERROR ( 16 FDA reports)
SOMNAMBULISM ( 16 FDA reports)
SPINAL CORD OEDEMA ( 16 FDA reports)
SUBDURAL HAEMORRHAGE ( 16 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 16 FDA reports)
TUMOUR INVASION ( 16 FDA reports)
UPPER LIMB FRACTURE ( 16 FDA reports)
VASCULAR INJURY ( 16 FDA reports)
ABSCESS NECK ( 16 FDA reports)
ALCOHOLISM ( 16 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 16 FDA reports)
AMYLOIDOSIS ( 16 FDA reports)
ANOREXIA NERVOSA ( 16 FDA reports)
AORTIC DISSECTION ( 16 FDA reports)
APPENDICITIS PERFORATED ( 16 FDA reports)
ARTERIAL DISORDER ( 16 FDA reports)
BACK INJURY ( 16 FDA reports)
BLADDER MASS ( 16 FDA reports)
BODY TEMPERATURE DECREASED ( 16 FDA reports)
BONE CYST ( 16 FDA reports)
BONE OPERATION ( 16 FDA reports)
CARDIAC TAMPONADE ( 16 FDA reports)
CHARLES BONNET SYNDROME ( 16 FDA reports)
CHEILITIS ( 16 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 16 FDA reports)
CLAVICLE FRACTURE ( 16 FDA reports)
COLECTOMY ( 16 FDA reports)
CONGENITAL AORTIC STENOSIS ( 16 FDA reports)
CORONARY ARTERY BYPASS ( 16 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 16 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 16 FDA reports)
EAR NEOPLASM ( 16 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 16 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 16 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 16 FDA reports)
EROSIVE OESOPHAGITIS ( 16 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 16 FDA reports)
EYE MOVEMENT DISORDER ( 16 FDA reports)
FAT TISSUE INCREASED ( 16 FDA reports)
FEELING GUILTY ( 16 FDA reports)
FEELING JITTERY ( 16 FDA reports)
FOETAL GROWTH RETARDATION ( 16 FDA reports)
GAMMOPATHY ( 16 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 16 FDA reports)
HAEMOLYSIS ( 16 FDA reports)
HEART RATE ABNORMAL ( 16 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 16 FDA reports)
INJECTION SITE ERYTHEMA ( 16 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 16 FDA reports)
INTESTINAL ISCHAEMIA ( 16 FDA reports)
JUGULAR VEIN THROMBOSIS ( 16 FDA reports)
LYMPHADENECTOMY ( 16 FDA reports)
MITRAL VALVE STENOSIS ( 16 FDA reports)
MONOCLONAL GAMMOPATHY ( 16 FDA reports)
MUCOUS MEMBRANE DISORDER ( 16 FDA reports)
NIGHT BLINDNESS ( 16 FDA reports)
PARAPLEGIA ( 16 FDA reports)
PARKINSON'S DISEASE ( 16 FDA reports)
PERIARTHRITIS ( 16 FDA reports)
PHARYNGEAL ERYTHEMA ( 16 FDA reports)
POISONING ( 16 FDA reports)
POLYP COLORECTAL ( 16 FDA reports)
PROTEIN TOTAL DECREASED ( 16 FDA reports)
RESORPTION BONE INCREASED ( 16 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 16 FDA reports)
ANOGENITAL WARTS ( 15 FDA reports)
AORTIC VALVE REPLACEMENT ( 15 FDA reports)
ARTHRITIS BACTERIAL ( 15 FDA reports)
ASPIRATION PLEURAL CAVITY ( 15 FDA reports)
ASTHENOPIA ( 15 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 15 FDA reports)
BLADDER OPERATION ( 15 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 15 FDA reports)
BLOOD PH DECREASED ( 15 FDA reports)
BREAST DISORDER ( 15 FDA reports)
CARBON DIOXIDE INCREASED ( 15 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 15 FDA reports)
CATHETERISATION CARDIAC ( 15 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 15 FDA reports)
CHANGE OF BOWEL HABIT ( 15 FDA reports)
CHEST INJURY ( 15 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 15 FDA reports)
CONDUCTION DISORDER ( 15 FDA reports)
CONJUNCTIVAL ABRASION ( 15 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 15 FDA reports)
CSF PROTEIN INCREASED ( 15 FDA reports)
CULTURE URINE POSITIVE ( 15 FDA reports)
CYSTOCELE ( 15 FDA reports)
DEAFNESS UNILATERAL ( 15 FDA reports)
DEPRESSION SUICIDAL ( 15 FDA reports)
DEXTROCARDIA ( 15 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 15 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 15 FDA reports)
ENDOCRINE DISORDER ( 15 FDA reports)
FAECALOMA ( 15 FDA reports)
FASCIITIS ( 15 FDA reports)
FEBRILE CONVULSION ( 15 FDA reports)
FIBRIN D DIMER INCREASED ( 15 FDA reports)
FOOD POISONING ( 15 FDA reports)
FOREARM FRACTURE ( 15 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 15 FDA reports)
GLOSSITIS ( 15 FDA reports)
HYPERAEMIA ( 15 FDA reports)
HYPERALDOSTERONISM ( 15 FDA reports)
HYPERTENSIVE HEART DISEASE ( 15 FDA reports)
HYPERURICAEMIA ( 15 FDA reports)
HYPOMETABOLISM ( 15 FDA reports)
HYPOSPADIAS ( 15 FDA reports)
INADEQUATE ANALGESIA ( 15 FDA reports)
INCISION SITE INFECTION ( 15 FDA reports)
INJECTION SITE PAIN ( 15 FDA reports)
LARYNGOSPASM ( 15 FDA reports)
LERICHE SYNDROME ( 15 FDA reports)
LEUKODYSTROPHY ( 15 FDA reports)
LIP PAIN ( 15 FDA reports)
LISTLESS ( 15 FDA reports)
MONOCYTOSIS ( 15 FDA reports)
MUSCLE DISORDER ( 15 FDA reports)
NAIL DISORDER ( 15 FDA reports)
NEPHROPATHY ( 15 FDA reports)
NEUROENDOCRINE CARCINOMA ( 15 FDA reports)
NEUTROPHILIA ( 15 FDA reports)
OESOPHAGEAL STENOSIS ( 15 FDA reports)
PARAPROTEINAEMIA ( 15 FDA reports)
PNEUMONIA FUNGAL ( 15 FDA reports)
POLYHYDRAMNIOS ( 15 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 15 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 15 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 15 FDA reports)
PROCEDURAL HYPERTENSION ( 15 FDA reports)
PYELOCALIECTASIS ( 15 FDA reports)
PYODERMA GANGRENOSUM ( 15 FDA reports)
RESUSCITATION ( 15 FDA reports)
ROSACEA ( 15 FDA reports)
SACROILIITIS ( 15 FDA reports)
SELF-INJURIOUS IDEATION ( 15 FDA reports)
SHOULDER PAIN ( 15 FDA reports)
SICCA SYNDROME ( 15 FDA reports)
SPINA BIFIDA ( 15 FDA reports)
SUPERINFECTION ( 15 FDA reports)
THORACOTOMY ( 15 FDA reports)
TORSADE DE POINTES ( 15 FDA reports)
TROPONIN INCREASED ( 15 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 15 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 15 FDA reports)
URTICARIA GENERALISED ( 15 FDA reports)
VASCULAR PSEUDOANEURYSM ( 15 FDA reports)
VENOUS THROMBOSIS ( 15 FDA reports)
VITAMIN C DEFICIENCY ( 15 FDA reports)
SIGMOIDITIS ( 14 FDA reports)
SKIN ATROPHY ( 14 FDA reports)
STREPTOCOCCAL SEPSIS ( 14 FDA reports)
TENSION HEADACHE ( 14 FDA reports)
TESTICULAR PAIN ( 14 FDA reports)
THERMAL BURN ( 14 FDA reports)
TINEA CRURIS ( 14 FDA reports)
TONGUE INJURY ( 14 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 14 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 14 FDA reports)
VENTRICULAR DYSKINESIA ( 14 FDA reports)
WHEELCHAIR USER ( 14 FDA reports)
ACUTE LEUKAEMIA ( 14 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 14 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 14 FDA reports)
ALKALOSIS ( 14 FDA reports)
AORTIC VALVE STENOSIS ( 14 FDA reports)
AUTOIMMUNE HEPATITIS ( 14 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 14 FDA reports)
BLADDER SPASM ( 14 FDA reports)
BODY DYSMORPHIC DISORDER ( 14 FDA reports)
BONE ATROPHY ( 14 FDA reports)
BONE MARROW DISORDER ( 14 FDA reports)
BREAST RECONSTRUCTION ( 14 FDA reports)
BREAST TENDERNESS ( 14 FDA reports)
BREECH PRESENTATION ( 14 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 14 FDA reports)
BRONCHIOLITIS ( 14 FDA reports)
BUNDLE BRANCH BLOCK ( 14 FDA reports)
CARDIORENAL SYNDROME ( 14 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 14 FDA reports)
CONCUSSION ( 14 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 14 FDA reports)
CORNEAL ABRASION ( 14 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 14 FDA reports)
ENTEROCOLITIS ( 14 FDA reports)
EXCESSIVE EYE BLINKING ( 14 FDA reports)
FEELING OF DESPAIR ( 14 FDA reports)
FOREIGN BODY ( 14 FDA reports)
GASTRIC HAEMORRHAGE ( 14 FDA reports)
HYPERCAPNIA ( 14 FDA reports)
HYPERPHAGIA ( 14 FDA reports)
IMPAIRED DRIVING ABILITY ( 14 FDA reports)
INCISIONAL HERNIA ( 14 FDA reports)
KERATITIS ( 14 FDA reports)
KOUNIS SYNDROME ( 14 FDA reports)
LEUKOPLAKIA ORAL ( 14 FDA reports)
MEDICAL DEVICE COMPLICATION ( 14 FDA reports)
METABOLIC DISORDER ( 14 FDA reports)
MIDDLE INSOMNIA ( 14 FDA reports)
MONOCYTE COUNT INCREASED ( 14 FDA reports)
MUCOSAL EROSION ( 14 FDA reports)
MYOCARDITIS ( 14 FDA reports)
MYOFASCITIS ( 14 FDA reports)
OROPHARYNGEAL BLISTERING ( 14 FDA reports)
OSTEOMYELITIS ACUTE ( 14 FDA reports)
PANCREATIC DISORDER ( 14 FDA reports)
PERIODONTAL OPERATION ( 14 FDA reports)
PERIORBITAL HAEMATOMA ( 14 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 14 FDA reports)
PNEUMOCONIOSIS ( 14 FDA reports)
POST LAMINECTOMY SYNDROME ( 14 FDA reports)
PRURIGO ( 14 FDA reports)
PULMONARY ARTERIOVENOUS FISTULA ( 14 FDA reports)
RENAL COLIC ( 14 FDA reports)
RHINITIS SEASONAL ( 14 FDA reports)
ABDOMINAL NEOPLASM ( 13 FDA reports)
ABNORMAL PALMAR/PLANTAR CREASES ( 13 FDA reports)
ADJUSTMENT DISORDER ( 13 FDA reports)
ANAL SPHINCTER ATONY ( 13 FDA reports)
ANIMAL BITE ( 13 FDA reports)
ANXIETY DISORDER ( 13 FDA reports)
APGAR SCORE LOW ( 13 FDA reports)
APHONIA ( 13 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 13 FDA reports)
ASBESTOSIS ( 13 FDA reports)
ATHEROSCLEROSIS ( 13 FDA reports)
BLADDER NEOPLASM ( 13 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 13 FDA reports)
BRAIN DAMAGE ( 13 FDA reports)
BRAIN MASS ( 13 FDA reports)
BRONCHITIS CHRONIC ( 13 FDA reports)
CARDIAC OPERATION ( 13 FDA reports)
CATHETER SITE INFECTION ( 13 FDA reports)
CELL DEATH ( 13 FDA reports)
CHRONIC TONSILLITIS ( 13 FDA reports)
CONVERSION DISORDER ( 13 FDA reports)
CRANIOSYNOSTOSIS ( 13 FDA reports)
DRUG PRESCRIBING ERROR ( 13 FDA reports)
ENCEPHALITIS HERPES ( 13 FDA reports)
ESCHERICHIA SEPSIS ( 13 FDA reports)
FEEDING DISORDER NEONATAL ( 13 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 13 FDA reports)
GALLBLADDER POLYP ( 13 FDA reports)
GANGRENE ( 13 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 13 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 13 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 13 FDA reports)
GRIMACING ( 13 FDA reports)
HEAD DEFORMITY ( 13 FDA reports)
HELICOBACTER GASTRITIS ( 13 FDA reports)
HELICOBACTER TEST POSITIVE ( 13 FDA reports)
HEMIPLEGIA ( 13 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 13 FDA reports)
HERPES VIRUS INFECTION ( 13 FDA reports)
HYPERCORTICOIDISM ( 13 FDA reports)
HYPERNATRAEMIA ( 13 FDA reports)
HYPERREFLEXIA ( 13 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 13 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 13 FDA reports)
KIDNEY MALROTATION ( 13 FDA reports)
LABYRINTHITIS ( 13 FDA reports)
LEG AMPUTATION ( 13 FDA reports)
LOWER EXTREMITY MASS ( 13 FDA reports)
LYMPHOCELE ( 13 FDA reports)
LYMPHOCYTOSIS ( 13 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 13 FDA reports)
MELANOSIS COLI ( 13 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 13 FDA reports)
MUSCLE INJURY ( 13 FDA reports)
NECK INJURY ( 13 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 13 FDA reports)
NERVE ROOT COMPRESSION ( 13 FDA reports)
OESOPHAGEAL DISORDER ( 13 FDA reports)
OSTEITIS DEFORMANS ( 13 FDA reports)
OVERWEIGHT ( 13 FDA reports)
OXYGEN SATURATION ABNORMAL ( 13 FDA reports)
PELVIC ADHESIONS ( 13 FDA reports)
PHYSIOTHERAPY ( 13 FDA reports)
PNEUMOPERITONEUM ( 13 FDA reports)
POOR DENTAL CONDITION ( 13 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 13 FDA reports)
POUCHITIS ( 13 FDA reports)
PROSTATE CANCER METASTATIC ( 13 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 13 FDA reports)
PYODERMA ( 13 FDA reports)
RADIOTHERAPY TO BRAIN ( 13 FDA reports)
RASH VESICULAR ( 13 FDA reports)
RENAL ARTERY STENOSIS ( 13 FDA reports)
RESPIRATORY ALKALOSIS ( 13 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 13 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 13 FDA reports)
SECRETION DISCHARGE ( 13 FDA reports)
SJOGREN'S SYNDROME ( 13 FDA reports)
SKELETAL SURVEY ABNORMAL ( 13 FDA reports)
SKIN NECROSIS ( 13 FDA reports)
SKIN TIGHTNESS ( 13 FDA reports)
SKULL MALFORMATION ( 13 FDA reports)
SPINAL MYELOGRAM ( 13 FDA reports)
TENSION ( 13 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 13 FDA reports)
TOOTH EROSION ( 13 FDA reports)
TORTICOLLIS ( 13 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 13 FDA reports)
URINARY TRACT DISORDER ( 13 FDA reports)
URINE ANALYSIS ABNORMAL ( 13 FDA reports)
VULVAL DISORDER ( 13 FDA reports)
WOUND COMPLICATION ( 13 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 12 FDA reports)
SALPINGITIS ( 12 FDA reports)
SHOCK HAEMORRHAGIC ( 12 FDA reports)
SKIN REACTION ( 12 FDA reports)
THROMBOCYTOSIS ( 12 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 12 FDA reports)
VASOCONSTRICTION ( 12 FDA reports)
VEIN DISORDER ( 12 FDA reports)
VENA CAVA FILTER INSERTION ( 12 FDA reports)
VITREOUS DETACHMENT ( 12 FDA reports)
WISDOM TEETH REMOVAL ( 12 FDA reports)
WRIST FRACTURE ( 12 FDA reports)
X-RAY ABNORMAL ( 12 FDA reports)
ABDOMINAL MASS ( 12 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 12 FDA reports)
ADNEXA UTERI CYST ( 12 FDA reports)
ADRENAL MASS ( 12 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 12 FDA reports)
ANOXIC ENCEPHALOPATHY ( 12 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 12 FDA reports)
ARTERIOSPASM CORONARY ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 12 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 12 FDA reports)
BLINDNESS CORTICAL ( 12 FDA reports)
BLOOD LACTIC ACID INCREASED ( 12 FDA reports)
BLOODY DISCHARGE ( 12 FDA reports)
BONE INFARCTION ( 12 FDA reports)
BONE METABOLISM DISORDER ( 12 FDA reports)
BREAST CANCER RECURRENT ( 12 FDA reports)
CARTILAGE INJURY ( 12 FDA reports)
CERVICAL SPINE FLATTENING ( 12 FDA reports)
CHEST WALL MASS ( 12 FDA reports)
CHEST WALL PAIN ( 12 FDA reports)
CLAUSTROPHOBIA ( 12 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 12 FDA reports)
CONGENITAL MITRAL VALVE STENOSIS ( 12 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 12 FDA reports)
DEMYELINATION ( 12 FDA reports)
DIFFICULTY IN WALKING ( 12 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 12 FDA reports)
DRUG ABUSER ( 12 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 12 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 12 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 12 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 12 FDA reports)
HAEMORRHAGIC ANAEMIA ( 12 FDA reports)
HOSPITALISATION ( 12 FDA reports)
HUMERUS FRACTURE ( 12 FDA reports)
HYPERAMMONAEMIA ( 12 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 12 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 12 FDA reports)
IMMUNOSUPPRESSION ( 12 FDA reports)
INTERCOSTAL NEURALGIA ( 12 FDA reports)
JOINT CREPITATION ( 12 FDA reports)
LINEAR IGA DISEASE ( 12 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 12 FDA reports)
MANDIBULOFACIAL DYSOSTOSIS ( 12 FDA reports)
MARROW HYPERPLASIA ( 12 FDA reports)
MASTOIDITIS ( 12 FDA reports)
MEAN CELL VOLUME INCREASED ( 12 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 12 FDA reports)
MYDRIASIS ( 12 FDA reports)
NEOPLASM RECURRENCE ( 12 FDA reports)
NEUROLOGICAL SYMPTOM ( 12 FDA reports)
NEUTROPENIC COLITIS ( 12 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 12 FDA reports)
OCULOAURICULOVERTEBRAL DYSPLASIA ( 12 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 12 FDA reports)
OTORRHOEA ( 12 FDA reports)
PAINFUL RESPIRATION ( 12 FDA reports)
PARANASAL SINUS BENIGN NEOPLASM ( 12 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 12 FDA reports)
PERFORMANCE STATUS DECREASED ( 12 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 12 FDA reports)
PERIRECTAL ABSCESS ( 12 FDA reports)
PILONIDAL CYST ( 12 FDA reports)
PIRIFORMIS SYNDROME ( 12 FDA reports)
PITTING OEDEMA ( 12 FDA reports)
PNEUMOCEPHALUS ( 12 FDA reports)
POSTURE ABNORMAL ( 12 FDA reports)
PRODUCT COUNTERFEIT ( 12 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 12 FDA reports)
PRURITUS GENITAL ( 12 FDA reports)
PUBIS FRACTURE ( 12 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 12 FDA reports)
PULMONARY HYPOPLASIA ( 12 FDA reports)
RADIATION OESOPHAGITIS ( 12 FDA reports)
RESPIRATION ABNORMAL ( 12 FDA reports)
RESPIRATORY ACIDOSIS ( 12 FDA reports)
RETICULOCYTE COUNT INCREASED ( 12 FDA reports)
RETINAL MELANOMA ( 12 FDA reports)
ALCOHOL ABUSE ( 11 FDA reports)
ANAL FISSURE ( 11 FDA reports)
AORTIC CALCIFICATION ( 11 FDA reports)
AORTIC DISORDER ( 11 FDA reports)
APALLIC SYNDROME ( 11 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 11 FDA reports)
ATROPHIC VULVOVAGINITIS ( 11 FDA reports)
BLOOD BICARBONATE INCREASED ( 11 FDA reports)
BLOOD CHLORIDE INCREASED ( 11 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 11 FDA reports)
BLOOD CREATININE DECREASED ( 11 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 11 FDA reports)
BLOOD PROLACTIN INCREASED ( 11 FDA reports)
BONE FISTULA ( 11 FDA reports)
BRADYKINESIA ( 11 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 11 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 11 FDA reports)
CEREBRAL ARTERY STENOSIS ( 11 FDA reports)
CHOLANGITIS ( 11 FDA reports)
COCCYDYNIA ( 11 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 11 FDA reports)
CUSHINGOID ( 11 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 11 FDA reports)
DEPENDENCE ( 11 FDA reports)
DIABETIC MICROANGIOPATHY ( 11 FDA reports)
DYSGRAPHIA ( 11 FDA reports)
DYSPAREUNIA ( 11 FDA reports)
EAR HAEMORRHAGE ( 11 FDA reports)
EFFUSION ( 11 FDA reports)
ENANTHEMA ( 11 FDA reports)
ENDOSCOPY ( 11 FDA reports)
ESCHERICHIA BACTERAEMIA ( 11 FDA reports)
FACIAL OPERATION ( 11 FDA reports)
FISTULA REPAIR ( 11 FDA reports)
FOLLICULITIS ( 11 FDA reports)
FORAMEN MAGNUM STENOSIS ( 11 FDA reports)
FRACTURE DELAYED UNION ( 11 FDA reports)
HEAD BANGING ( 11 FDA reports)
HEART SOUNDS ABNORMAL ( 11 FDA reports)
HERNIA REPAIR ( 11 FDA reports)
HOSTILITY ( 11 FDA reports)
HYPERKINESIA ( 11 FDA reports)
ILEAL PERFORATION ( 11 FDA reports)
IMPETIGO ( 11 FDA reports)
INJECTION SITE HAEMATOMA ( 11 FDA reports)
INTENTIONAL SELF-INJURY ( 11 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 11 FDA reports)
LIP ULCERATION ( 11 FDA reports)
LIVEDO RETICULARIS ( 11 FDA reports)
LYMPH NODE PALPABLE ( 11 FDA reports)
MALIGNANT TUMOUR EXCISION ( 11 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 11 FDA reports)
MEDIASTINAL MASS ( 11 FDA reports)
MENSTRUAL DISORDER ( 11 FDA reports)
MONONEURITIS ( 11 FDA reports)
MUSCLE NECROSIS ( 11 FDA reports)
NASAL OBSTRUCTION ( 11 FDA reports)
NEPHRITIC SYNDROME ( 11 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 11 FDA reports)
OBSTRUCTION GASTRIC ( 11 FDA reports)
OEDEMA GENITAL ( 11 FDA reports)
OESOPHAGITIS ULCERATIVE ( 11 FDA reports)
OLIGOHYDRAMNIOS ( 11 FDA reports)
OSTEOSARCOMA METASTATIC ( 11 FDA reports)
PERITONEAL ADHESIONS ( 11 FDA reports)
PHONOPHOBIA ( 11 FDA reports)
PILONIDAL CYST CONGENITAL ( 11 FDA reports)
PNEUMONIA BACTERIAL ( 11 FDA reports)
POSTNASAL DRIP ( 11 FDA reports)
PROCEDURAL NAUSEA ( 11 FDA reports)
PROCEDURAL VOMITING ( 11 FDA reports)
PROTHROMBIN TIME SHORTENED ( 11 FDA reports)
PROTRUSION TONGUE ( 11 FDA reports)
PULMONARY VASCULAR DISORDER ( 11 FDA reports)
RECTAL FISSURE ( 11 FDA reports)
RENAL TUBULAR DISORDER ( 11 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 11 FDA reports)
SEPSIS SYNDROME ( 11 FDA reports)
SINOATRIAL BLOCK ( 11 FDA reports)
SKIN CANDIDA ( 11 FDA reports)
SMALL FOR DATES BABY ( 11 FDA reports)
SPINAL DECOMPRESSION ( 11 FDA reports)
STENOTROPHOMONAS INFECTION ( 11 FDA reports)
STERNAL FRACTURE ( 11 FDA reports)
TELANGIECTASIA ( 11 FDA reports)
TEMPORAL LOBE EPILEPSY ( 11 FDA reports)
THROMBOSIS IN DEVICE ( 11 FDA reports)
TINEL'S SIGN ( 11 FDA reports)
TOBACCO USER ( 11 FDA reports)
TYPE 1 DIABETES MELLITUS ( 11 FDA reports)
TYPE I HYPERSENSITIVITY ( 11 FDA reports)
UTERINE CANCER ( 11 FDA reports)
VITH NERVE PARALYSIS ( 11 FDA reports)
VULVOVAGINAL PRURITUS ( 11 FDA reports)
WEIGHT BEARING DIFFICULTY ( 11 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 10 FDA reports)
SCOTOMA ( 10 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 10 FDA reports)
SPUTUM CULTURE POSITIVE ( 10 FDA reports)
STENT PLACEMENT ( 10 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 10 FDA reports)
SUDDEN CARDIAC DEATH ( 10 FDA reports)
SUICIDAL BEHAVIOUR ( 10 FDA reports)
SUNBURN ( 10 FDA reports)
SUTURE RELATED COMPLICATION ( 10 FDA reports)
TENOSYNOVITIS STENOSANS ( 10 FDA reports)
THROMBOCYTOPENIC PURPURA ( 10 FDA reports)
TONSILLAR HYPERTROPHY ( 10 FDA reports)
TREATMENT FAILURE ( 10 FDA reports)
URETERAL STENT INSERTION ( 10 FDA reports)
URINARY TRACT OBSTRUCTION ( 10 FDA reports)
UTERINE SPASM ( 10 FDA reports)
UVEITIS ( 10 FDA reports)
VARICELLA ( 10 FDA reports)
VARICES OESOPHAGEAL ( 10 FDA reports)
VENOUS STENOSIS ( 10 FDA reports)
VENOUS THROMBOSIS LIMB ( 10 FDA reports)
VENTRICULAR ARRHYTHMIA ( 10 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 10 FDA reports)
WITHDRAWAL SYNDROME ( 10 FDA reports)
ABDOMINAL INJURY ( 10 FDA reports)
ACETABULUM FRACTURE ( 10 FDA reports)
ADRENAL SUPPRESSION ( 10 FDA reports)
ALCOHOLIC LIVER DISEASE ( 10 FDA reports)
AORTIC VALVE CALCIFICATION ( 10 FDA reports)
APLASIA PURE RED CELL ( 10 FDA reports)
APNOEIC ATTACK ( 10 FDA reports)
APPLICATION SITE ERYTHEMA ( 10 FDA reports)
AREFLEXIA ( 10 FDA reports)
ARTHROPOD BITE ( 10 FDA reports)
ASPERGILLOSIS ( 10 FDA reports)
ATELECTASIS NEONATAL ( 10 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 10 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 10 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 10 FDA reports)
BACTERIAL DIARRHOEA ( 10 FDA reports)
BACTERIAL DISEASE CARRIER ( 10 FDA reports)
BACTERIAL SEPSIS ( 10 FDA reports)
BALANITIS ( 10 FDA reports)
BASAL GANGLIA INFARCTION ( 10 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 10 FDA reports)
BILIARY TRACT DISORDER ( 10 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 10 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 10 FDA reports)
BRADYCARDIA FOETAL ( 10 FDA reports)
BREAST DISCOMFORT ( 10 FDA reports)
BRONCHITIS ACUTE ( 10 FDA reports)
BURNS THIRD DEGREE ( 10 FDA reports)
CAROTID BRUIT ( 10 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 10 FDA reports)
CHRONIC FATIGUE SYNDROME ( 10 FDA reports)
COLONOSCOPY ( 10 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 10 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 10 FDA reports)
DENTAL CLEANING ( 10 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 10 FDA reports)
DIABETIC COMPLICATION ( 10 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 10 FDA reports)
DRUG LEVEL DECREASED ( 10 FDA reports)
EARLY SATIETY ( 10 FDA reports)
ENDOMETRIAL ATROPHY ( 10 FDA reports)
ENDOMETRIAL CANCER ( 10 FDA reports)
ERYSIPELAS ( 10 FDA reports)
EXPLORATORY OPERATION ( 10 FDA reports)
EYE HAEMORRHAGE ( 10 FDA reports)
FOETAL DAMAGE ( 10 FDA reports)
FOETAL HYPOKINESIA ( 10 FDA reports)
FOETAL MACROSOMIA ( 10 FDA reports)
GASTRITIS ATROPHIC ( 10 FDA reports)
GENITAL EROSION ( 10 FDA reports)
HAEMORRHOID OPERATION ( 10 FDA reports)
HEAD TITUBATION ( 10 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 10 FDA reports)
HORNER'S SYNDROME ( 10 FDA reports)
HUNGER ( 10 FDA reports)
HYDROPS FOETALIS ( 10 FDA reports)
IMPAIRED SELF-CARE ( 10 FDA reports)
INFECTIVE TENOSYNOVITIS ( 10 FDA reports)
INGROWN HAIR ( 10 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 10 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 10 FDA reports)
MEDIASTINUM NEOPLASM ( 10 FDA reports)
METATARSUS PRIMUS VARUS ( 10 FDA reports)
MORGANELLA INFECTION ( 10 FDA reports)
MUSCLE RUPTURE ( 10 FDA reports)
NERVE BLOCK ( 10 FDA reports)
NERVE ROOT LESION ( 10 FDA reports)
NODAL RHYTHM ( 10 FDA reports)
NODULE ON EXTREMITY ( 10 FDA reports)
OPTIC NERVE DISORDER ( 10 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 10 FDA reports)
OROPHARYNGEAL PLAQUE ( 10 FDA reports)
OTITIS MEDIA CHRONIC ( 10 FDA reports)
PENILE PAIN ( 10 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 10 FDA reports)
PERITONITIS BACTERIAL ( 10 FDA reports)
PERSONALITY DISORDER ( 10 FDA reports)
PHIMOSIS ( 10 FDA reports)
PHOTOSENSITIVITY REACTION ( 10 FDA reports)
POLYCYSTIC OVARIES ( 10 FDA reports)
PORTAL VEIN THROMBOSIS ( 10 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 10 FDA reports)
PROSTATE CANCER RECURRENT ( 10 FDA reports)
PROSTATITIS ( 10 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 10 FDA reports)
PUPIL FIXED ( 10 FDA reports)
RECURRENT CANCER ( 10 FDA reports)
RED BLOOD CELL ABNORMALITY ( 10 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 10 FDA reports)
RENAL CANCER ( 10 FDA reports)
RENAL CANCER METASTATIC ( 10 FDA reports)
RENAL LIPOMATOSIS ( 10 FDA reports)
RETROPERITONEAL HAEMATOMA ( 10 FDA reports)
ACCIDENTAL EXPOSURE ( 9 FDA reports)
ACUTE PRERENAL FAILURE ( 9 FDA reports)
ADHESION ( 9 FDA reports)
AKINESIA ( 9 FDA reports)
ALLODYNIA ( 9 FDA reports)
ALVEOLAR OSTEITIS ( 9 FDA reports)
ANDROGENS ABNORMAL ( 9 FDA reports)
ANEURYSM REPAIR ( 9 FDA reports)
APPETITE DISORDER ( 9 FDA reports)
ARTERIAL THROMBOSIS ( 9 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 9 FDA reports)
ASTERIXIS ( 9 FDA reports)
AUTONOMIC NEUROPATHY ( 9 FDA reports)
BILIARY DILATATION ( 9 FDA reports)
BIPOLAR I DISORDER ( 9 FDA reports)
BLADDER CATHETERISATION ( 9 FDA reports)
BLADDER PROLAPSE ( 9 FDA reports)
BLEPHAROSPASM ( 9 FDA reports)
BLOOD BICARBONATE DECREASED ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 9 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 9 FDA reports)
BLOOD MAGNESIUM DECREASED ( 9 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 9 FDA reports)
BODY HEIGHT DECREASED ( 9 FDA reports)
BODY TINEA ( 9 FDA reports)
BREAST SWELLING ( 9 FDA reports)
CARDIAC FIBRILLATION ( 9 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 9 FDA reports)
CARTILAGE ATROPHY ( 9 FDA reports)
CAUDA EQUINA SYNDROME ( 9 FDA reports)
CEREBELLAR SYNDROME ( 9 FDA reports)
CERUMEN REMOVAL ( 9 FDA reports)
CLEFT LIP ( 9 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 9 FDA reports)
CORNEAL DYSTROPHY ( 9 FDA reports)
CRYPTORCHISM ( 9 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 9 FDA reports)
DERMATITIS HERPETIFORMIS ( 9 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 9 FDA reports)
DISEASE COMPLICATION ( 9 FDA reports)
DUODENAL POLYP ( 9 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 9 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 9 FDA reports)
EOSINOPHILIC PNEUMONIA ( 9 FDA reports)
EPICONDYLITIS ( 9 FDA reports)
FACET JOINT BLOCK ( 9 FDA reports)
FACIAL ASYMMETRY ( 9 FDA reports)
FEAR OF DEATH ( 9 FDA reports)
FIBROADENOMA OF BREAST ( 9 FDA reports)
FORMICATION ( 9 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 9 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 9 FDA reports)
GINGIVECTOMY ( 9 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 9 FDA reports)
GROWTH RETARDATION ( 9 FDA reports)
GUN SHOT WOUND ( 9 FDA reports)
HEPATIC ENZYME ABNORMAL ( 9 FDA reports)
HEPATIC FIBROSIS ( 9 FDA reports)
HEPATIC TRAUMA ( 9 FDA reports)
HEPATITIS FULMINANT ( 9 FDA reports)
HEPATOJUGULAR REFLUX ( 9 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 9 FDA reports)
HOMICIDAL IDEATION ( 9 FDA reports)
HOSPICE CARE ( 9 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 9 FDA reports)
ILEAL STENOSIS ( 9 FDA reports)
INCOHERENT ( 9 FDA reports)
INTESTINAL ULCER ( 9 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 9 FDA reports)
JOINT SURGERY ( 9 FDA reports)
KNEE DEFORMITY ( 9 FDA reports)
LARYNGOSCOPY ( 9 FDA reports)
LEARNING DISORDER ( 9 FDA reports)
LEIOMYOMA ( 9 FDA reports)
LIMB DEFORMITY ( 9 FDA reports)
LIP EROSION ( 9 FDA reports)
LIPOGRANULOMA ( 9 FDA reports)
MAGNESIUM DEFICIENCY ( 9 FDA reports)
MALLORY-WEISS SYNDROME ( 9 FDA reports)
MENOPAUSE ( 9 FDA reports)
MUCOSAL DISCOLOURATION ( 9 FDA reports)
MULTIPLE FRACTURES ( 9 FDA reports)
MUSCLE SPASTICITY ( 9 FDA reports)
NASAL FLARING ( 9 FDA reports)
NEPHROPATHY TOXIC ( 9 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 9 FDA reports)
NEUROPATHY ( 9 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 9 FDA reports)
OBSESSIVE THOUGHTS ( 9 FDA reports)
OESOPHAGEAL MASS ( 9 FDA reports)
OESOPHAGEAL PAIN ( 9 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 9 FDA reports)
OVARIAN CANCER ( 9 FDA reports)
PARAPARESIS ( 9 FDA reports)
PARTNER STRESS ( 9 FDA reports)
PCO2 DECREASED ( 9 FDA reports)
PERICARDIAL CYST ( 9 FDA reports)
PERIVASCULAR DERMATITIS ( 9 FDA reports)
PLEURISY ( 9 FDA reports)
PORTAL HYPERTENSION ( 9 FDA reports)
POSTPARTUM DEPRESSION ( 9 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 9 FDA reports)
PRODUCT TASTE ABNORMAL ( 9 FDA reports)
RADICULITIS ( 9 FDA reports)
RED MAN SYNDROME ( 9 FDA reports)
RHABDOMYOSARCOMA ( 9 FDA reports)
SCROTAL CYST ( 9 FDA reports)
SCROTAL IRRITATION ( 9 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 9 FDA reports)
SENSATION OF PRESSURE ( 9 FDA reports)
SEROTONIN SYNDROME ( 9 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 9 FDA reports)
SINUS POLYP ( 9 FDA reports)
SKIN FISSURES ( 9 FDA reports)
SKIN INDURATION ( 9 FDA reports)
SKIN LESION EXCISION ( 9 FDA reports)
SOCIAL FEAR ( 9 FDA reports)
STARING ( 9 FDA reports)
STATUS EPILEPTICUS ( 9 FDA reports)
STILLBIRTH ( 9 FDA reports)
SYSTEMIC SCLEROSIS ( 9 FDA reports)
THYROID ADENOMA ( 9 FDA reports)
TOOTH DEPOSIT ( 9 FDA reports)
TOXIC ENCEPHALOPATHY ( 9 FDA reports)
TRAUMATIC LUNG INJURY ( 9 FDA reports)
TUMOUR EXCISION ( 9 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 9 FDA reports)
VOCAL CORD DISORDER ( 9 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 9 FDA reports)
YELLOW SKIN ( 9 FDA reports)
SALIVARY GLAND MASS ( 8 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 8 FDA reports)
SCLERAL HAEMORRHAGE ( 8 FDA reports)
SHONE COMPLEX ( 8 FDA reports)
SKIN HYPOPIGMENTATION ( 8 FDA reports)
SKIN NODULE ( 8 FDA reports)
SPLEEN DISORDER ( 8 FDA reports)
SPONDYLITIC MYELOPATHY ( 8 FDA reports)
STOMATITIS NECROTISING ( 8 FDA reports)
STRESS ULCER ( 8 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 8 FDA reports)
SUTURE INSERTION ( 8 FDA reports)
TACHYARRHYTHMIA ( 8 FDA reports)
THYROIDITIS ( 8 FDA reports)
TRACHEAL INJURY ( 8 FDA reports)
TRACHEOMALACIA ( 8 FDA reports)
TRICUSPID VALVE DISEASE ( 8 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 8 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 8 FDA reports)
UNINTENDED PREGNANCY ( 8 FDA reports)
VARICOCELE ( 8 FDA reports)
VOLVULUS ( 8 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 8 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 8 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 8 FDA reports)
ABSCESS LIMB ( 8 FDA reports)
ACANTHOSIS NIGRICANS ( 8 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 8 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 8 FDA reports)
AFFECT LABILITY ( 8 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 8 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 8 FDA reports)
ANAL SKIN TAGS ( 8 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 8 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 8 FDA reports)
AORTA HYPOPLASIA ( 8 FDA reports)
APATHY ( 8 FDA reports)
ARACHNOID CYST ( 8 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 8 FDA reports)
ARTERIOVENOUS GRAFT ANEURYSM ( 8 FDA reports)
AUTOIMMUNE DISORDER ( 8 FDA reports)
B-CELL LYMPHOMA ( 8 FDA reports)
BACTERIAL TEST POSITIVE ( 8 FDA reports)
BACTERIURIA ( 8 FDA reports)
BEREAVEMENT ( 8 FDA reports)
BEREAVEMENT REACTION ( 8 FDA reports)
BLADDER DISORDER ( 8 FDA reports)
BLOOD ALBUMIN INCREASED ( 8 FDA reports)
BLOOD BLISTER ( 8 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 8 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 8 FDA reports)
BLOOD URIC ACID INCREASED ( 8 FDA reports)
BRAIN DEATH ( 8 FDA reports)
BREAST CANCER FEMALE ( 8 FDA reports)
CALCIFICATION METASTATIC ( 8 FDA reports)
CALCULUS URETHRAL ( 8 FDA reports)
CARBON DIOXIDE DECREASED ( 8 FDA reports)
CARDIAC FAILURE CHRONIC ( 8 FDA reports)
CARDIOVERSION ( 8 FDA reports)
CEREBRAL DISORDER ( 8 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 8 FDA reports)
CHOKING SENSATION ( 8 FDA reports)
CHOREA ( 8 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 8 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 8 FDA reports)
CONJUNCTIVITIS VIRAL ( 8 FDA reports)
CORONARY ARTERY THROMBOSIS ( 8 FDA reports)
CYST REMOVAL ( 8 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 8 FDA reports)
DENTAL NECROSIS ( 8 FDA reports)
DERMOID CYST ( 8 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 8 FDA reports)
DUPUYTREN'S CONTRACTURE ( 8 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 8 FDA reports)
ENTHESOPATHY ( 8 FDA reports)
EYE INFECTION ( 8 FDA reports)
FAT INTOLERANCE ( 8 FDA reports)
FEELING DRUNK ( 8 FDA reports)
FIBULA FRACTURE ( 8 FDA reports)
FISTULA DISCHARGE ( 8 FDA reports)
FLIGHT OF IDEAS ( 8 FDA reports)
FOOD INTOLERANCE ( 8 FDA reports)
GASTRECTOMY ( 8 FDA reports)
GASTRIC CANCER RECURRENT ( 8 FDA reports)
GESTATIONAL DIABETES ( 8 FDA reports)
HAEMARTHROSIS ( 8 FDA reports)
HAEMOGLOBIN INCREASED ( 8 FDA reports)
HAEMOPHILUS INFECTION ( 8 FDA reports)
HEART INJURY ( 8 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 8 FDA reports)
HEMIANOPIA ( 8 FDA reports)
HEPATIC ATROPHY ( 8 FDA reports)
HIDRADENITIS ( 8 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 8 FDA reports)
INDUCED LABOUR ( 8 FDA reports)
INFUSION SITE SWELLING ( 8 FDA reports)
INHIBITORY DRUG INTERACTION ( 8 FDA reports)
INTERCOSTAL RETRACTION ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 8 FDA reports)
INTESTINAL DILATATION ( 8 FDA reports)
INTESTINAL POLYP ( 8 FDA reports)
KLEBSIELLA BACTERAEMIA ( 8 FDA reports)
LARYNGITIS ALLERGIC ( 8 FDA reports)
LIP DISCOLOURATION ( 8 FDA reports)
LITHOTRIPSY ( 8 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 8 FDA reports)
LUNG CANCER METASTATIC ( 8 FDA reports)
LYMPH GLAND INFECTION ( 8 FDA reports)
MAMMOGRAM ABNORMAL ( 8 FDA reports)
MASKED FACIES ( 8 FDA reports)
MEDICAL DEVICE REMOVAL ( 8 FDA reports)
MENIERE'S DISEASE ( 8 FDA reports)
MENINGITIS VIRAL ( 8 FDA reports)
METASTASES TO MENINGES ( 8 FDA reports)
MIDDLE EAR EFFUSION ( 8 FDA reports)
MUSCLE ABSCESS ( 8 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 8 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 8 FDA reports)
NECROTISING RETINITIS ( 8 FDA reports)
NEUTROPENIC INFECTION ( 8 FDA reports)
NOCTURNAL DYSPNOEA ( 8 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 8 FDA reports)
OOPHORECTOMY ( 8 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 8 FDA reports)
PATHOGEN RESISTANCE ( 8 FDA reports)
PEAU D'ORANGE ( 8 FDA reports)
PERIPHERAL NERVE INJURY ( 8 FDA reports)
PHARYNGEAL DISORDER ( 8 FDA reports)
POST HERPETIC NEURALGIA ( 8 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 8 FDA reports)
POSTPARTUM HAEMORRHAGE ( 8 FDA reports)
PRESCRIBED OVERDOSE ( 8 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 8 FDA reports)
PSEUDOMONAL SEPSIS ( 8 FDA reports)
PSYCHOLOGICAL TRAUMA ( 8 FDA reports)
PYELECTASIA ( 8 FDA reports)
RECTAL TENESMUS ( 8 FDA reports)
RENAL HAEMORRHAGE ( 8 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 8 FDA reports)
RHINALGIA ( 8 FDA reports)
RIB DEFORMITY ( 8 FDA reports)
ABDOMINAL BRUIT ( 7 FDA reports)
ABDOMINAL RIGIDITY ( 7 FDA reports)
ACCIDENT AT WORK ( 7 FDA reports)
ACUTE PULMONARY OEDEMA ( 7 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 7 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 7 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 7 FDA reports)
ANION GAP INCREASED ( 7 FDA reports)
ANISOCYTOSIS ( 7 FDA reports)
ANORECTAL DISCOMFORT ( 7 FDA reports)
ANORECTAL DISORDER ( 7 FDA reports)
APICAL GRANULOMA ( 7 FDA reports)
APPLICATION SITE PRURITUS ( 7 FDA reports)
ARTERIAL INJURY ( 7 FDA reports)
ASPLENIA ( 7 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 7 FDA reports)
AURICULAR SWELLING ( 7 FDA reports)
AUTOIMMUNE THYROIDITIS ( 7 FDA reports)
BACTERIAL TRACHEITIS ( 7 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 7 FDA reports)
BLOOD IRON DECREASED ( 7 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 7 FDA reports)
BLOOD SODIUM INCREASED ( 7 FDA reports)
BLOOD UREA DECREASED ( 7 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 7 FDA reports)
BONE SWELLING ( 7 FDA reports)
BRONCHIAL CARCINOMA ( 7 FDA reports)
BRONCHIAL OBSTRUCTION ( 7 FDA reports)
BUTTOCK PAIN ( 7 FDA reports)
CARDIAC FLUTTER ( 7 FDA reports)
CARDIAC OUTPUT DECREASED ( 7 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 7 FDA reports)
CARDIAC VALVE VEGETATION ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 7 FDA reports)
CATATONIA ( 7 FDA reports)
CATHETER RELATED COMPLICATION ( 7 FDA reports)
CATHETER RELATED INFECTION ( 7 FDA reports)
CEREBRAL CYST ( 7 FDA reports)
CHEST TUBE INSERTION ( 7 FDA reports)
CHYLOTHORAX ( 7 FDA reports)
CLEFT LIP AND PALATE ( 7 FDA reports)
COELIAC DISEASE ( 7 FDA reports)
COLON CANCER METASTATIC ( 7 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 7 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 7 FDA reports)
CONVULSION NEONATAL ( 7 FDA reports)
CYSTITIS HAEMORRHAGIC ( 7 FDA reports)
CYTOGENETIC ABNORMALITY ( 7 FDA reports)
DEATH NEONATAL ( 7 FDA reports)
DEFAECATION URGENCY ( 7 FDA reports)
DERMATITIS ACNEIFORM ( 7 FDA reports)
DEVICE DISLOCATION ( 7 FDA reports)
DIAPHRAGMATIC INJURY ( 7 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 7 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 7 FDA reports)
DUODENAL ULCER PERFORATION ( 7 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 7 FDA reports)
ENCEPHALOMALACIA ( 7 FDA reports)
ENDOCARDITIS BACTERIAL ( 7 FDA reports)
EXTREMITY CONTRACTURE ( 7 FDA reports)
EYELID CYST ( 7 FDA reports)
FOLATE DEFICIENCY ( 7 FDA reports)
FOOT OPERATION ( 7 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 7 FDA reports)
FUNGAL SKIN INFECTION ( 7 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 7 FDA reports)
GASTRIC CANCER ( 7 FDA reports)
GASTROINTESTINAL ULCER ( 7 FDA reports)
GASTROSCHISIS ( 7 FDA reports)
GLIOSIS ( 7 FDA reports)
GLYCOSURIA ( 7 FDA reports)
GRANULOMA ANNULARE ( 7 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 7 FDA reports)
HAEMORRHAGIC DIATHESIS ( 7 FDA reports)
HIGH-PITCHED CRYING ( 7 FDA reports)
HIP SURGERY ( 7 FDA reports)
HYPERAESTHESIA ( 7 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 7 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 7 FDA reports)
HYPERMAGNESAEMIA ( 7 FDA reports)
HYPERPHOSPHATAEMIA ( 7 FDA reports)
HYPOTONIA NEONATAL ( 7 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 7 FDA reports)
INCISION SITE ABSCESS ( 7 FDA reports)
INITIAL INSOMNIA ( 7 FDA reports)
IRON DEFICIENCY ( 7 FDA reports)
KIDNEY MALFORMATION ( 7 FDA reports)
LARGE INTESTINAL ULCER ( 7 FDA reports)
LARYNGEAL REPAIR ( 7 FDA reports)
LOCKED-IN SYNDROME ( 7 FDA reports)
LOGORRHOEA ( 7 FDA reports)
LYME DISEASE ( 7 FDA reports)
LYMPHOCYTIC INFILTRATION ( 7 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 7 FDA reports)
MACULOPATHY ( 7 FDA reports)
MALABSORPTION ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 7 FDA reports)
MEDIASTINITIS ( 7 FDA reports)
METABOLIC ENCEPHALOPATHY ( 7 FDA reports)
MICROANGIOPATHY ( 7 FDA reports)
MICROGNATHIA ( 7 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 7 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 7 FDA reports)
MULTIPLE ALLERGIES ( 7 FDA reports)
MYOPATHY TOXIC ( 7 FDA reports)
NASAL SEPTAL OPERATION ( 7 FDA reports)
NEPHRITIS ( 7 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 7 FDA reports)
NIKOLSKY'S SIGN ( 7 FDA reports)
NORMAL NEWBORN ( 7 FDA reports)
NUCHAL RIGIDITY ( 7 FDA reports)
OCCUPATIONAL EXPOSURE TO DRUG ( 7 FDA reports)
OCULAR ICTERUS ( 7 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 7 FDA reports)
OLIGOMENORRHOEA ( 7 FDA reports)
ORAL NEOPLASM ( 7 FDA reports)
ORGAN FAILURE ( 7 FDA reports)
PANCREATIC ENZYMES INCREASED ( 7 FDA reports)
PANIC DISORDER ( 7 FDA reports)
PAPILLOMA VIRAL INFECTION ( 7 FDA reports)
PARONYCHIA ( 7 FDA reports)
PARTIAL SEIZURES ( 7 FDA reports)
PERCUSSION TEST ABNORMAL ( 7 FDA reports)
PERITONSILLAR ABSCESS ( 7 FDA reports)
PLASMACYTOSIS ( 7 FDA reports)
PNEUMONECTOMY ( 7 FDA reports)
PNEUMONIA LEGIONELLA ( 7 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 7 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 7 FDA reports)
PRE-ECLAMPSIA ( 7 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE II ( 7 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 7 FDA reports)
PROSTATIC DISORDER ( 7 FDA reports)
PTERYGIUM ( 7 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 7 FDA reports)
RENAL ATROPHY ( 7 FDA reports)
RETINITIS ( 7 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 7 FDA reports)
SENSATION OF FOREIGN BODY ( 7 FDA reports)
SHOULDER DEFORMITY ( 7 FDA reports)
SINUS RHYTHM ( 7 FDA reports)
SKELETAL INJURY ( 7 FDA reports)
SKIN HAEMORRHAGE ( 7 FDA reports)
SKIN NEOPLASM EXCISION ( 7 FDA reports)
SKIN PLAQUE ( 7 FDA reports)
SOFT TISSUE INFLAMMATION ( 7 FDA reports)
SPINAL CORD INJURY ( 7 FDA reports)
SPINAL PAIN ( 7 FDA reports)
SPLENIC RUPTURE ( 7 FDA reports)
SPONDYLOLYSIS ( 7 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 7 FDA reports)
SUBCUTANEOUS NODULE ( 7 FDA reports)
SUBSTANCE ABUSE ( 7 FDA reports)
SWEAT GLAND TUMOUR ( 7 FDA reports)
TETANY ( 7 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 7 FDA reports)
TOOTH HYPOPLASIA ( 7 FDA reports)
TUBERCULIN TEST POSITIVE ( 7 FDA reports)
UTERINE POLYP ( 7 FDA reports)
VAGINAL SWELLING ( 7 FDA reports)
VAGOTOMY ( 7 FDA reports)
VENA CAVA THROMBOSIS ( 7 FDA reports)
VIRAL RASH ( 7 FDA reports)
WOUND TREATMENT ( 7 FDA reports)
RIGHT AORTIC ARCH ( 6 FDA reports)
SEBORRHOEA ( 6 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 6 FDA reports)
SKIN GRAFT ( 6 FDA reports)
SKIN MASS ( 6 FDA reports)
SKIN WARM ( 6 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 6 FDA reports)
STUPOR ( 6 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 6 FDA reports)
SUBRETINAL FIBROSIS ( 6 FDA reports)
SYNCOPE VASOVAGAL ( 6 FDA reports)
T-CELL LYMPHOMA ( 6 FDA reports)
TEARFULNESS ( 6 FDA reports)
TERATOMA ( 6 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 6 FDA reports)
THYROID CANCER ( 6 FDA reports)
TOE AMPUTATION ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
TRACHEAL DEVIATION ( 6 FDA reports)
TUMOUR LYSIS SYNDROME ( 6 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 6 FDA reports)
UMBILICAL CORD ABNORMALITY ( 6 FDA reports)
URETHRAL STENOSIS ( 6 FDA reports)
URINARY BLADDER POLYP ( 6 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 6 FDA reports)
URTICARIA PAPULAR ( 6 FDA reports)
VASODILATATION ( 6 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 6 FDA reports)
VENOUS INJURY ( 6 FDA reports)
VENTRICULAR FAILURE ( 6 FDA reports)
VERTIGO POSITIONAL ( 6 FDA reports)
VESTIBULAR DISORDER ( 6 FDA reports)
VITREOUS DEGENERATION ( 6 FDA reports)
WALKING DISABILITY ( 6 FDA reports)
WEIGHT FLUCTUATION ( 6 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 6 FDA reports)
WOUND DECOMPOSITION ( 6 FDA reports)
X-RAY ( 6 FDA reports)
ADENOIDECTOMY ( 6 FDA reports)
ADENOTONSILLECTOMY ( 6 FDA reports)
ADENOVIRUS INFECTION ( 6 FDA reports)
AGORAPHOBIA ( 6 FDA reports)
AMAUROSIS FUGAX ( 6 FDA reports)
ANAEMIA MACROCYTIC ( 6 FDA reports)
ANAL ATRESIA ( 6 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 6 FDA reports)
APHAKIA ( 6 FDA reports)
APPENDIX DISORDER ( 6 FDA reports)
ARTERIOVENOUS MALFORMATION ( 6 FDA reports)
AUTISM ( 6 FDA reports)
AXILLARY PAIN ( 6 FDA reports)
BACTERIA STOOL IDENTIFIED ( 6 FDA reports)
BARTHOLIN'S ABSCESS ( 6 FDA reports)
BENIGN GASTRIC NEOPLASM ( 6 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 6 FDA reports)
BLOOD CREATINE INCREASED ( 6 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 6 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 6 FDA reports)
BRACHIAL PLEXOPATHY ( 6 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 6 FDA reports)
CELL MARKER INCREASED ( 6 FDA reports)
CENTRAL OBESITY ( 6 FDA reports)
CERVICAL NEURITIS ( 6 FDA reports)
CHOLANGIECTASIS ACQUIRED ( 6 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 6 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 6 FDA reports)
COAGULATION TEST ABNORMAL ( 6 FDA reports)
COGWHEEL RIGIDITY ( 6 FDA reports)
CONGENITAL FOOT MALFORMATION ( 6 FDA reports)
CORNEAL REFLEX DECREASED ( 6 FDA reports)
CORONARY ANGIOPLASTY ( 6 FDA reports)
CUTIS LAXA ( 6 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 6 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 6 FDA reports)
DERMATOPHYTOSIS ( 6 FDA reports)
DISBACTERIOSIS ( 6 FDA reports)
DISSEMINATED TUBERCULOSIS ( 6 FDA reports)
DIVERTICULAR HERNIA ( 6 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 6 FDA reports)
DYSHIDROSIS ( 6 FDA reports)
DYSPHASIA ( 6 FDA reports)
DYSTROPHIC CALCIFICATION ( 6 FDA reports)
EMBOLISM VENOUS ( 6 FDA reports)
ENCEPHALITIS VIRAL ( 6 FDA reports)
ENDOCARDIAL FIBROSIS ( 6 FDA reports)
EXOPHTHALMOS ( 6 FDA reports)
EYE INJURY ( 6 FDA reports)
EYE NAEVUS ( 6 FDA reports)
FANCONI SYNDROME ( 6 FDA reports)
FIBRINOLYSIS ( 6 FDA reports)
FLAT AFFECT ( 6 FDA reports)
GALLBLADDER CANCER ( 6 FDA reports)
GALLBLADDER PAIN ( 6 FDA reports)
GALLOP RHYTHM PRESENT ( 6 FDA reports)
GASTROENTERITIS SALMONELLA ( 6 FDA reports)
GASTROINTESTINAL CARCINOMA ( 6 FDA reports)
GASTROINTESTINAL INFECTION ( 6 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 6 FDA reports)
GASTROINTESTINAL INJURY ( 6 FDA reports)
GASTROINTESTINAL NECROSIS ( 6 FDA reports)
GLUCOSE URINE PRESENT ( 6 FDA reports)
HAEMATOCRIT INCREASED ( 6 FDA reports)
HAEMOCHROMATOSIS ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 6 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 6 FDA reports)
HEART TRANSPLANT ( 6 FDA reports)
HEPATORENAL SYNDROME ( 6 FDA reports)
HIP DYSPLASIA ( 6 FDA reports)
HISTOPLASMOSIS ( 6 FDA reports)
HOMICIDE ( 6 FDA reports)
HOMOCYSTINAEMIA ( 6 FDA reports)
HORDEOLUM ( 6 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 6 FDA reports)
HYDROCELE ( 6 FDA reports)
ICHTHYOSIS ( 6 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
INFUSION SITE ERYTHEMA ( 6 FDA reports)
INGUINAL HERNIA REPAIR ( 6 FDA reports)
INJECTION SITE HAEMORRHAGE ( 6 FDA reports)
INJECTION SITE RASH ( 6 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 6 FDA reports)
KERATOSIS OBTURANS ( 6 FDA reports)
KETOACIDOSIS ( 6 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 6 FDA reports)
LEUKAEMIA ( 6 FDA reports)
LEUKOCYTURIA ( 6 FDA reports)
LIMB ASYMMETRY ( 6 FDA reports)
LIP INJURY ( 6 FDA reports)
LISTERIOSIS ( 6 FDA reports)
LOOSE STOOLS ( 6 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 6 FDA reports)
MACULAR SCAR ( 6 FDA reports)
MALARIA ( 6 FDA reports)
MALIGNANT MELANOMA STAGE I ( 6 FDA reports)
MARITAL PROBLEM ( 6 FDA reports)
MEDIASTINAL BIOPSY ( 6 FDA reports)
MEGACOLON ( 6 FDA reports)
MENINGOMYELOCELE ( 6 FDA reports)
MENOPAUSAL SYMPTOMS ( 6 FDA reports)
METABOLIC ALKALOSIS ( 6 FDA reports)
METASTASES TO EYE ( 6 FDA reports)
METASTATIC PAIN ( 6 FDA reports)
MICTURITION DISORDER ( 6 FDA reports)
MIXED HYPERLIPIDAEMIA ( 6 FDA reports)
NASAL TURBINATE ABNORMALITY ( 6 FDA reports)
NEOPLASM PROSTATE ( 6 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 6 FDA reports)
NEUROENDOCRINE TUMOUR ( 6 FDA reports)
NEUROTOXICITY ( 6 FDA reports)
OESOPHAGEAL DILATATION ( 6 FDA reports)
OESOPHAGEAL RUPTURE ( 6 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 6 FDA reports)
ONYCHOGRYPHOSIS ( 6 FDA reports)
ORAL MUCOSA EROSION ( 6 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 6 FDA reports)
OSTEOPOROTIC FRACTURE ( 6 FDA reports)
OVARIAN ENLARGEMENT ( 6 FDA reports)
OVARIAN FAILURE ( 6 FDA reports)
OVERLAP SYNDROME ( 6 FDA reports)
PANCREATIC CARCINOMA ( 6 FDA reports)
PANCREATITIS CHRONIC ( 6 FDA reports)
PAROTITIS ( 6 FDA reports)
PCO2 INCREASED ( 6 FDA reports)
PERIORBITAL HAEMORRHAGE ( 6 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 6 FDA reports)
PITYRIASIS RUBRA PILARIS ( 6 FDA reports)
PLEURAL ADHESION ( 6 FDA reports)
PO2 DECREASED ( 6 FDA reports)
POLYARTHRITIS ( 6 FDA reports)
POLYMYALGIA RHEUMATICA ( 6 FDA reports)
POLYTRAUMATISM ( 6 FDA reports)
POOR SUCKING REFLEX ( 6 FDA reports)
PROSTATECTOMY ( 6 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 6 FDA reports)
PSEUDOHYPERKALAEMIA ( 6 FDA reports)
PSYCHOMOTOR RETARDATION ( 6 FDA reports)
PUSTULAR PSORIASIS ( 6 FDA reports)
RADIATION INJURY ( 6 FDA reports)
RECTAL PROLAPSE ( 6 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 6 FDA reports)
REHABILITATION THERAPY ( 6 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 6 FDA reports)
RENAL INFARCT ( 6 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 6 FDA reports)
RETINAL DETACHMENT ( 6 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 5 FDA reports)
ABNORMAL SENSATION IN EYE ( 5 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 5 FDA reports)
ACHLORHYDRIA ( 5 FDA reports)
AGRAPHIA ( 5 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 5 FDA reports)
ALVEOLITIS FIBROSING ( 5 FDA reports)
AMNIOTIC BAND SYNDROME ( 5 FDA reports)
AMYLASE INCREASED ( 5 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 5 FDA reports)
ANAPHYLACTOID REACTION ( 5 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 5 FDA reports)
ANEURYSM RUPTURED ( 5 FDA reports)
ANGIOMYOLIPOMA ( 5 FDA reports)
ANGIOPLASTY ( 5 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 5 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 5 FDA reports)
ANTISOCIAL BEHAVIOUR ( 5 FDA reports)
APPLICATION SITE IRRITATION ( 5 FDA reports)
ARTHRITIS INFECTIVE ( 5 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 5 FDA reports)
BIFASCICULAR BLOCK ( 5 FDA reports)
BIOPSY ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 5 FDA reports)
BONE MARROW DEPRESSION ( 5 FDA reports)
BONE MARROW NECROSIS ( 5 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 5 FDA reports)
BRADYPHRENIA ( 5 FDA reports)
BREAST DISCHARGE ( 5 FDA reports)
BRONCHIAL HYPERACTIVITY ( 5 FDA reports)
BRONCHOSCOPY ( 5 FDA reports)
CARDIAC ABLATION ( 5 FDA reports)
CARDIAC ENZYMES INCREASED ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
CAROTID ARTERY DISSECTION ( 5 FDA reports)
CAROTID ARTERY OCCLUSION ( 5 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 5 FDA reports)
CHLAMYDIAL INFECTION ( 5 FDA reports)
CHORIOAMNIONITIS ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 5 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 5 FDA reports)
CLUBBING ( 5 FDA reports)
COMPULSIVE SHOPPING ( 5 FDA reports)
CORNEAL OPACITY ( 5 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 5 FDA reports)
CRANIOTOMY ( 5 FDA reports)
CUTANEOUS SARCOIDOSIS ( 5 FDA reports)
DARK CIRCLES UNDER EYES ( 5 FDA reports)
DERMATITIS ATOPIC ( 5 FDA reports)
DIZZINESS EXERTIONAL ( 5 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
DRY THROAT ( 5 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 5 FDA reports)
EAR DISORDER ( 5 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 5 FDA reports)
EMBOLIC STROKE ( 5 FDA reports)
EMPYEMA ( 5 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 5 FDA reports)
EROSIVE DUODENITIS ( 5 FDA reports)
ERYTHEMA OF EYELID ( 5 FDA reports)
ESCHAR ( 5 FDA reports)
EXPOSURE TO TOXIC AGENT ( 5 FDA reports)
EYE INFLAMMATION ( 5 FDA reports)
EYELID DISORDER ( 5 FDA reports)
FALLOPIAN TUBE OPERATION ( 5 FDA reports)
FEMORAL ARTERY OCCLUSION ( 5 FDA reports)
FIBROUS HISTIOCYTOMA ( 5 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 5 FDA reports)
FRUSTRATION ( 5 FDA reports)
FULL BLOOD COUNT DECREASED ( 5 FDA reports)
FUNGAEMIA ( 5 FDA reports)
GALLBLADDER OPERATION ( 5 FDA reports)
GASTROINTESTINAL MALFORMATION ( 5 FDA reports)
GENE MUTATION ( 5 FDA reports)
GENERALISED ANXIETY DISORDER ( 5 FDA reports)
GENITAL HERPES ( 5 FDA reports)
GLOMERULONEPHRITIS ( 5 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 5 FDA reports)
GOUTY ARTHRITIS ( 5 FDA reports)
GUILLAIN-BARRE SYNDROME ( 5 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 5 FDA reports)
HAEMORRHAGIC STROKE ( 5 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 5 FDA reports)
HEPATIC PAIN ( 5 FDA reports)
HEPATIC VEIN THROMBOSIS ( 5 FDA reports)
HIV INFECTION ( 5 FDA reports)
HYDROMYELIA ( 5 FDA reports)
HYPERTONIA ( 5 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 5 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 5 FDA reports)
IMMOBILE ( 5 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
INDURATION ( 5 FDA reports)
INFLAMMATION OF WOUND ( 5 FDA reports)
INFUSION SITE HAEMORRHAGE ( 5 FDA reports)
INFUSION SITE PAIN ( 5 FDA reports)
INJECTION SITE INFECTION ( 5 FDA reports)
INJECTION SITE IRRITATION ( 5 FDA reports)
INTENTIONAL MISUSE ( 5 FDA reports)
JOINT CONTRACTURE ( 5 FDA reports)
LASER THERAPY ( 5 FDA reports)
LIGAMENT DISORDER ( 5 FDA reports)
LIGAMENT LAXITY ( 5 FDA reports)
LIMB MALFORMATION ( 5 FDA reports)
LIPOATROPHY ( 5 FDA reports)
LIPOMA EXCISION ( 5 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
LUNG NEOPLASM SURGERY ( 5 FDA reports)
LUPUS NEPHRITIS ( 5 FDA reports)
LYMPHANGITIS ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
MACROCEPHALY ( 5 FDA reports)
MALIGNANT ASCITES ( 5 FDA reports)
MEDICATION RESIDUE ( 5 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 5 FDA reports)
METASTASES TO STOMACH ( 5 FDA reports)
METASTASES TO THE MEDIASTINUM ( 5 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 5 FDA reports)
MORAXELLA INFECTION ( 5 FDA reports)
MOUTH INJURY ( 5 FDA reports)
MUTISM ( 5 FDA reports)
NEPHROGENIC ANAEMIA ( 5 FDA reports)
NERVE ROOT INJURY LUMBAR ( 5 FDA reports)
NEURILEMMOMA ( 5 FDA reports)
NEUROFIBROMA ( 5 FDA reports)
NEUROPATHIC PAIN ( 5 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 5 FDA reports)
NODAL ARRHYTHMIA ( 5 FDA reports)
OCULOGYRIC CRISIS ( 5 FDA reports)
OPTIC NERVE CUPPING ( 5 FDA reports)
ORAL FUNGAL INFECTION ( 5 FDA reports)
ORAL MUCOSAL BLISTERING ( 5 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 5 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 5 FDA reports)
ORTHOSTATIC INTOLERANCE ( 5 FDA reports)
OVARIAN ADHESION ( 5 FDA reports)
PACEMAKER COMPLICATION ( 5 FDA reports)
PAIN OF SKIN ( 5 FDA reports)
PALMAR ERYTHEMA ( 5 FDA reports)
PANCREATITIS RELAPSING ( 5 FDA reports)
PANNICULITIS ( 5 FDA reports)
PERICARDIAL HAEMORRHAGE ( 5 FDA reports)
PERIHEPATIC ABSCESS ( 5 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
PHARYNGEAL INFLAMMATION ( 5 FDA reports)
PHARYNGEAL ULCERATION ( 5 FDA reports)
PLASMA CELLS INCREASED ( 5 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 5 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 5 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 5 FDA reports)
POOR VENOUS ACCESS ( 5 FDA reports)
POST CONCUSSION SYNDROME ( 5 FDA reports)
POSTERIOR CAPSULOTOMY ( 5 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 5 FDA reports)
PREMATURE DELIVERY ( 5 FDA reports)
PRODUCT CONTAMINATION ( 5 FDA reports)
PULMONARY MALFORMATION ( 5 FDA reports)
PULSE ABNORMAL ( 5 FDA reports)
PUPILLARY DISORDER ( 5 FDA reports)
RADICULITIS BRACHIAL ( 5 FDA reports)
RECTAL ULCER ( 5 FDA reports)
REFLUX GASTRITIS ( 5 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 5 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 5 FDA reports)
RETROGNATHIA ( 5 FDA reports)
RHEUMATIC FEVER ( 5 FDA reports)
SALIVARY HYPERSECRETION ( 5 FDA reports)
SCAPULA FRACTURE ( 5 FDA reports)
SENSE OF OPPRESSION ( 5 FDA reports)
SINUS TARSI SYNDROME ( 5 FDA reports)
SINUSITIS FUNGAL ( 5 FDA reports)
SKIN ODOUR ABNORMAL ( 5 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 5 FDA reports)
SLEEP PARALYSIS ( 5 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 5 FDA reports)
SPINAL X-RAY ABNORMAL ( 5 FDA reports)
SPONDYLOARTHROPATHY ( 5 FDA reports)
SPUTUM ABNORMAL ( 5 FDA reports)
SPUTUM PURULENT ( 5 FDA reports)
SPUTUM RETENTION ( 5 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 5 FDA reports)
STEROID THERAPY ( 5 FDA reports)
SUBMANDIBULAR MASS ( 5 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 5 FDA reports)
TENDON PAIN ( 5 FDA reports)
TONGUE BLACK HAIRY ( 5 FDA reports)
TONGUE PARALYSIS ( 5 FDA reports)
TRANSPLANT FAILURE ( 5 FDA reports)
TRAUMATIC SHOCK ( 5 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 5 FDA reports)
TROPONIN I INCREASED ( 5 FDA reports)
TUMOUR MARKER INCREASED ( 5 FDA reports)
URETERIC STENOSIS ( 5 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 5 FDA reports)
UTERINE DISORDER ( 5 FDA reports)
VAGINAL CANCER ( 5 FDA reports)
VAGINAL MYCOSIS ( 5 FDA reports)
VASCULAR PURPURA ( 5 FDA reports)
VELOPHARYNGEAL INCOMPETENCE ( 5 FDA reports)
VENA CAVA INJURY ( 5 FDA reports)
VENOUS BRUIT ( 5 FDA reports)
VENOUS OCCLUSION ( 5 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 5 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 5 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 4 FDA reports)
SALPINGO-OOPHORECTOMY ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 4 FDA reports)
SEPSIS NEONATAL ( 4 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 4 FDA reports)
SEROSITIS ( 4 FDA reports)
SKIN WRINKLING ( 4 FDA reports)
SLOW RESPONSE TO STIMULI ( 4 FDA reports)
SPASTIC PARAPLEGIA ( 4 FDA reports)
SPINAL CORPECTOMY ( 4 FDA reports)
SPLINTER HAEMORRHAGES ( 4 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 4 FDA reports)
STRESS SYMPTOMS ( 4 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 4 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 4 FDA reports)
TEMPERATURE REGULATION DISORDER ( 4 FDA reports)
TESTICULAR RETRACTION ( 4 FDA reports)
TETANUS ( 4 FDA reports)
THORACIC OPERATION ( 4 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 4 FDA reports)
THYROXINE FREE INCREASED ( 4 FDA reports)
TOE OPERATION ( 4 FDA reports)
TONGUE BLISTERING ( 4 FDA reports)
TONGUE DRY ( 4 FDA reports)
TOOTH AVULSION ( 4 FDA reports)
TOOTH INJURY ( 4 FDA reports)
TOXOPLASMOSIS ( 4 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 4 FDA reports)
TUMOUR NECROSIS ( 4 FDA reports)
TURNER'S SYNDROME ( 4 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 4 FDA reports)
UNEMPLOYMENT ( 4 FDA reports)
UNSTABLE FOETAL LIE ( 4 FDA reports)
URETERAL DISORDER ( 4 FDA reports)
URETHRAL CARUNCLE ( 4 FDA reports)
URETHRAL MEATUS STENOSIS ( 4 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
UTERINE MASS ( 4 FDA reports)
VAGINAL ABSCESS ( 4 FDA reports)
VAGINAL DYSPLASIA ( 4 FDA reports)
VAGINITIS BACTERIAL ( 4 FDA reports)
VASCULAR INSUFFICIENCY ( 4 FDA reports)
VASCULAR OPERATION ( 4 FDA reports)
VASOMOTOR RHINITIS ( 4 FDA reports)
VERBAL ABUSE ( 4 FDA reports)
VERTEBRAL COLUMN MASS ( 4 FDA reports)
VITAMIN D DECREASED ( 4 FDA reports)
VITREOUS HAEMORRHAGE ( 4 FDA reports)
VOMITING PROJECTILE ( 4 FDA reports)
VULVAL OEDEMA ( 4 FDA reports)
VULVOVAGINAL DISCOMFORT ( 4 FDA reports)
WOUND ABSCESS ( 4 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 4 FDA reports)
ABORTION THREATENED ( 4 FDA reports)
ABSCESS INTESTINAL ( 4 FDA reports)
ABSCESS MANAGEMENT ( 4 FDA reports)
ABSCESS RUPTURE ( 4 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 4 FDA reports)
ACUTE POLYNEUROPATHY ( 4 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 4 FDA reports)
ADNEXA UTERI PAIN ( 4 FDA reports)
ALCOHOL POISONING ( 4 FDA reports)
AMINO ACID LEVEL INCREASED ( 4 FDA reports)
ANIMAL SCRATCH ( 4 FDA reports)
ANOXIA ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
AORTIC ATHEROSCLEROSIS ( 4 FDA reports)
APPARENT DEATH ( 4 FDA reports)
APRAXIA ( 4 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 4 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 4 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 4 FDA reports)
ASEPTIC NECROSIS BONE ( 4 FDA reports)
ASTHMATIC CRISIS ( 4 FDA reports)
AVULSION FRACTURE ( 4 FDA reports)
BEHCET'S SYNDROME ( 4 FDA reports)
BICUSPID AORTIC VALVE ( 4 FDA reports)
BIOPSY SKIN ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 4 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 4 FDA reports)
BLOOD IRON INCREASED ( 4 FDA reports)
BONE DEFORMITY ( 4 FDA reports)
BONE DENSITY INCREASED ( 4 FDA reports)
BONE TRIMMING ( 4 FDA reports)
BRADYARRHYTHMIA ( 4 FDA reports)
BRAIN MIDLINE SHIFT ( 4 FDA reports)
BRAIN NEOPLASM ( 4 FDA reports)
BREAST DISORDER FEMALE ( 4 FDA reports)
BRONCHITIS BACTERIAL ( 4 FDA reports)
BUNION OPERATION ( 4 FDA reports)
CALCINOSIS ( 4 FDA reports)
CANDIDA SEPSIS ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CATHETER SITE PAIN ( 4 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 4 FDA reports)
CERVIX CARCINOMA RECURRENT ( 4 FDA reports)
CHEMICAL POISONING ( 4 FDA reports)
CHEST WALL ABSCESS ( 4 FDA reports)
CHOLURIA ( 4 FDA reports)
CHONDROCALCINOSIS ( 4 FDA reports)
CHORIOMENINGITIS LYMPHOCYTIC ( 4 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 4 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 4 FDA reports)
COLON CANCER STAGE I ( 4 FDA reports)
COMMINUTED FRACTURE ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 4 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 4 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 4 FDA reports)
CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 4 FDA reports)
CRYPTOCOCCOSIS ( 4 FDA reports)
CRYSTALLURIA ( 4 FDA reports)
CYSTITIS NONINFECTIVE ( 4 FDA reports)
DEATH OF RELATIVE ( 4 FDA reports)
DELAYED SLEEP PHASE ( 4 FDA reports)
DELUSION OF GRANDEUR ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DENTAL TREATMENT ( 4 FDA reports)
DEREALISATION ( 4 FDA reports)
DERMATITIS PSORIASIFORM ( 4 FDA reports)
DEVICE OCCLUSION ( 4 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 4 FDA reports)
DIABETIC GASTROPARESIS ( 4 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 4 FDA reports)
DROOLING ( 4 FDA reports)
DRUG EFFECT INCREASED ( 4 FDA reports)
DRUG INTERACTION POTENTIATION ( 4 FDA reports)
DRUG TOLERANCE ( 4 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 4 FDA reports)
DYSPNOEA AT REST ( 4 FDA reports)
EAGLE BARRETT SYNDROME ( 4 FDA reports)
EJACULATION DISORDER ( 4 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 4 FDA reports)
EMBOLISM ( 4 FDA reports)
ENERGY INCREASED ( 4 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
EXOMPHALOS ( 4 FDA reports)
EYE OPERATION ( 4 FDA reports)
FACE LIFT ( 4 FDA reports)
FACIAL NERVE DISORDER ( 4 FDA reports)
FACIAL PARESIS ( 4 FDA reports)
FACTOR V LEIDEN MUTATION ( 4 FDA reports)
FEEDING DISORDER ( 4 FDA reports)
FEEDING TUBE COMPLICATION ( 4 FDA reports)
FLUID INTAKE REDUCED ( 4 FDA reports)
FOETAL CARDIAC DISORDER ( 4 FDA reports)
FOETAL HEART RATE DECELERATION ( 4 FDA reports)
FOREIGN BODY ASPIRATION ( 4 FDA reports)
GASTRIC BYPASS ( 4 FDA reports)
GASTROINTESTINAL EROSION ( 4 FDA reports)
GASTROINTESTINAL TOXICITY ( 4 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
GENITAL PRURITUS FEMALE ( 4 FDA reports)
GINGIVAL ATROPHY ( 4 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 4 FDA reports)
GRANULOMA SKIN ( 4 FDA reports)
GRIEF REACTION ( 4 FDA reports)
GRUNTING ( 4 FDA reports)
HAEMANGIOMA OF SKIN ( 4 FDA reports)
HAIR DISORDER ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HALLUCINATIONS, MIXED ( 4 FDA reports)
HAND AMPUTATION ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 4 FDA reports)
HERNIA OBSTRUCTIVE ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 4 FDA reports)
HYDROPNEUMOTHORAX ( 4 FDA reports)
HYPERSEXUALITY ( 4 FDA reports)
HYPERVISCOSITY SYNDROME ( 4 FDA reports)
HYPOCOAGULABLE STATE ( 4 FDA reports)
HYPOPERFUSION ( 4 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 4 FDA reports)
INAPPROPRIATE AFFECT ( 4 FDA reports)
INCISION SITE PAIN ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
INFUSION SITE HAEMATOMA ( 4 FDA reports)
INJECTION SITE DISCOLOURATION ( 4 FDA reports)
INJECTION SITE INDURATION ( 4 FDA reports)
INJECTION SITE WARMTH ( 4 FDA reports)
INTENTION TREMOR ( 4 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 4 FDA reports)
INTESTINAL PERFORATION ( 4 FDA reports)
INTESTINAL STENOSIS ( 4 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 4 FDA reports)
INTUBATION ( 4 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 4 FDA reports)
JC VIRUS INFECTION ( 4 FDA reports)
JUDGEMENT IMPAIRED ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
LARYNGOMALACIA ( 4 FDA reports)
LESION EXCISION ( 4 FDA reports)
LHERMITTE'S SIGN ( 4 FDA reports)
LICE INFESTATION ( 4 FDA reports)
LICHENOID KERATOSIS ( 4 FDA reports)
LIGAMENT INJURY ( 4 FDA reports)
LIMB REDUCTION DEFECT ( 4 FDA reports)
LIPOMATOSIS ( 4 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 4 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
LUPUS-LIKE SYNDROME ( 4 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 4 FDA reports)
MACULAR OEDEMA ( 4 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 4 FDA reports)
MALIGNANT MELANOMA IN SITU ( 4 FDA reports)
MASTOID DISORDER ( 4 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 4 FDA reports)
MEDICAL DIET ( 4 FDA reports)
MENINGIOMA BENIGN ( 4 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 4 FDA reports)
MENISCUS REMOVAL ( 4 FDA reports)
MENSTRUATION DELAYED ( 4 FDA reports)
METASTASES TO PLEURA ( 4 FDA reports)
METASTASIS ( 4 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 4 FDA reports)
MIOSIS ( 4 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 4 FDA reports)
MONONEUROPATHY MULTIPLEX ( 4 FDA reports)
MUSCLE CONTRACTURE ( 4 FDA reports)
MUSCLE FLAP OPERATION ( 4 FDA reports)
MYCOBACTERIAL INFECTION ( 4 FDA reports)
MYOCARDIAL FIBROSIS ( 4 FDA reports)
MYOCARDITIS POST INFECTION ( 4 FDA reports)
NAIL DYSTROPHY ( 4 FDA reports)
NAIL INFECTION ( 4 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 4 FDA reports)
NARCOLEPSY ( 4 FDA reports)
NASAL POLYPS ( 4 FDA reports)
NASOGASTRIC OUTPUT HIGH ( 4 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 4 FDA reports)
NEUROMA ( 4 FDA reports)
NIPPLE DISORDER ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 4 FDA reports)
OESTROGEN DEFICIENCY ( 4 FDA reports)
OOPHORECTOMY BILATERAL ( 4 FDA reports)
OPISTHOTONUS ( 4 FDA reports)
OPTIC NERVE INJURY ( 4 FDA reports)
OPTIC NEUROPATHY ( 4 FDA reports)
ORAL SOFT TISSUE DISORDER ( 4 FDA reports)
OROPHARYNGEAL SPASM ( 4 FDA reports)
OROPHARYNGEAL SWELLING ( 4 FDA reports)
OTITIS MEDIA ACUTE ( 4 FDA reports)
OVARIAN ATROPHY ( 4 FDA reports)
PANCREATITIS NECROTISING ( 4 FDA reports)
PARAESTHESIA OF GENITAL MALE ( 4 FDA reports)
PARAKERATOSIS ( 4 FDA reports)
PARANASAL CYST ( 4 FDA reports)
PATELLA FRACTURE ( 4 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 4 FDA reports)
PECTUS EXCAVATUM ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PEMPHIGOID ( 4 FDA reports)
PHARYNGEAL ABSCESS ( 4 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 4 FDA reports)
PIGMENTATION DISORDER ( 4 FDA reports)
PLATELET DISORDER ( 4 FDA reports)
PNEUMOCOCCAL SEPSIS ( 4 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 4 FDA reports)
PNEUMONIA KLEBSIELLA ( 4 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 4 FDA reports)
PNEUMONIA VIRAL ( 4 FDA reports)
POLYDACTYLY ( 4 FDA reports)
PORPHYRIA ACUTE ( 4 FDA reports)
POST PROCEDURAL INFECTION ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
PROCTALGIA ( 4 FDA reports)
PROCTOCOLITIS ( 4 FDA reports)
PROTEUS INFECTION ( 4 FDA reports)
PULMONARY CALCIFICATION ( 4 FDA reports)
PULMONARY CAVITATION ( 4 FDA reports)
PULMONARY SEQUESTRATION ( 4 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
RADICULAR PAIN ( 4 FDA reports)
READING DISORDER ( 4 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 4 FDA reports)
RENAL ABSCESS ( 4 FDA reports)
RENAL OSTEODYSTROPHY ( 4 FDA reports)
RESPIRATORY RATE DECREASED ( 4 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 4 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 4 FDA reports)
ABORTION SPONTANEOUS COMPLETE ( 3 FDA reports)
ABSCESS SOFT TISSUE ( 3 FDA reports)
ACANTHOSIS ( 3 FDA reports)
ACNE PUSTULAR ( 3 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 3 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 3 FDA reports)
ACUTE STRESS DISORDER ( 3 FDA reports)
ACUTE TONSILLITIS ( 3 FDA reports)
AIR EMBOLISM ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ALLERGIC MYOCARDITIS ( 3 FDA reports)
ALLERGIC PHARYNGITIS ( 3 FDA reports)
ALLERGY TEST POSITIVE ( 3 FDA reports)
ALOPECIA AREATA ( 3 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES STAGE II ( 3 FDA reports)
ANASTOMOTIC COMPLICATION ( 3 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 3 FDA reports)
ANION GAP DECREASED ( 3 FDA reports)
ANKYLOSING SPONDYLITIS ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 3 FDA reports)
APPLICATION SITE PAIN ( 3 FDA reports)
APPLICATION SITE RASH ( 3 FDA reports)
ARTERIAL BYPASS OPERATION ( 3 FDA reports)
ARTERIOGRAM CORONARY ( 3 FDA reports)
ARTHROFIBROSIS ( 3 FDA reports)
ASPERGILLUS TEST POSITIVE ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 3 FDA reports)
BACILLUS INFECTION ( 3 FDA reports)
BENIGN BONE NEOPLASM ( 3 FDA reports)
BENIGN NEOPLASM ( 3 FDA reports)
BICYTOPENIA ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 3 FDA reports)
BIOPSY STOMACH ( 3 FDA reports)
BK VIRUS INFECTION ( 3 FDA reports)
BLEEDING TIME PROLONGED ( 3 FDA reports)
BLOOD BILIRUBIN DECREASED ( 3 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BLOOD CREATINE DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 3 FDA reports)
BLOOD OESTROGEN DECREASED ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BONE CALLUS EXCESSIVE ( 3 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 3 FDA reports)
BRADYCARDIA NEONATAL ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BRAIN MALFORMATION ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BREAST CELLULITIS ( 3 FDA reports)
BREAST HAEMATOMA ( 3 FDA reports)
BRONCHIAL DISORDER ( 3 FDA reports)
BRONCHITIS CHEMICAL ( 3 FDA reports)
BRONCHITIS VIRAL ( 3 FDA reports)
BUDD-CHIARI SYNDROME ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 3 FDA reports)
CARDIAC STRESS TEST ( 3 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 3 FDA reports)
CAROTID ARTERY THROMBOSIS ( 3 FDA reports)
CATHETER SEPSIS ( 3 FDA reports)
CATHETER SITE HAEMORRHAGE ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CEREBRAL MICROANGIOPATHY ( 3 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 3 FDA reports)
CERULOPLASMIN DECREASED ( 3 FDA reports)
CERVIX CARCINOMA ( 3 FDA reports)
CHEMOTHERAPY ( 3 FDA reports)
CHILD ABUSE ( 3 FDA reports)
CHOLESTEATOMA ( 3 FDA reports)
CHROMOSOME ABNORMALITY ( 3 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 3 FDA reports)
CLUMSINESS ( 3 FDA reports)
COITAL BLEEDING ( 3 FDA reports)
COLORECTAL CANCER ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 3 FDA reports)
CONDUCT DISORDER ( 3 FDA reports)
CONGENITAL ACROCHORDON ( 3 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 3 FDA reports)
CONGENITAL GREAT VESSEL ANOMALY ( 3 FDA reports)
CONGENITAL HEARING DISORDER ( 3 FDA reports)
CONGENITAL HIP DEFORMITY ( 3 FDA reports)
CONGENITAL HYDROCEPHALUS ( 3 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 3 FDA reports)
CONJUNCTIVAL PALLOR ( 3 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 3 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 3 FDA reports)
COR TRIATRIATUM ( 3 FDA reports)
CORNEAL EROSION ( 3 FDA reports)
CORNEAL NEOVASCULARISATION ( 3 FDA reports)
CORNEAL SCAR ( 3 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 3 FDA reports)
CROSS SENSITIVITY REACTION ( 3 FDA reports)
CULTURE POSITIVE ( 3 FDA reports)
CULTURE STOOL POSITIVE ( 3 FDA reports)
CYSTIC LYMPHANGIOMA ( 3 FDA reports)
CYSTITIS RADIATION ( 3 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 3 FDA reports)
DAYDREAMING ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DELIRIUM TREMENS ( 3 FDA reports)
DEPENDENCE ON RESPIRATOR ( 3 FDA reports)
DEPERSONALISATION ( 3 FDA reports)
DERMATITIS DIAPER ( 3 FDA reports)
DERMATITIS PAPILLARIS CAPILLITII ( 3 FDA reports)
DIABETIC EYE DISEASE ( 3 FDA reports)
DIABETIC FOOT ( 3 FDA reports)
DIAPHRAGMATIC HERNIA ( 3 FDA reports)
DIARRHOEA INFECTIOUS ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 3 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 3 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
DYSPLASIA ( 3 FDA reports)
DYSPNOEA EXACERBATED ( 3 FDA reports)
DYSTHYMIC DISORDER ( 3 FDA reports)
ECTOPIC PREGNANCY ( 3 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 3 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 3 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 3 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 3 FDA reports)
ENTEROCOCCAL SEPSIS ( 3 FDA reports)
ENZYME ABNORMALITY ( 3 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 3 FDA reports)
EPILEPTIC AURA ( 3 FDA reports)
ERYTHEMA INFECTIOSUM ( 3 FDA reports)
EUSTACHIAN TUBE PATULOUS ( 3 FDA reports)
EXCITABILITY ( 3 FDA reports)
EXTERNAL EAR DISORDER ( 3 FDA reports)
EXTERNAL EAR INFLAMMATION ( 3 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 3 FDA reports)
EXTRAVASATION BLOOD ( 3 FDA reports)
EYE REDNESS ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FACIAL DYSMORPHISM ( 3 FDA reports)
FAECAL VOLUME INCREASED ( 3 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
GASTRIC NEOPLASM ( 3 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 3 FDA reports)
GASTRIC ULCER HELICOBACTER ( 3 FDA reports)
GASTRODUODENAL ULCER ( 3 FDA reports)
GASTRODUODENITIS ( 3 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 3 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 3 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 3 FDA reports)
GASTROSTOMY TUBE INSERTION ( 3 FDA reports)
GENERAL SYMPTOM ( 3 FDA reports)
GINGIVAL HYPERPLASIA ( 3 FDA reports)
GRAM STAIN POSITIVE ( 3 FDA reports)
H1N1 INFLUENZA ( 3 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 3 FDA reports)
HEART VALVE STENOSIS ( 3 FDA reports)
HEPATIC VEIN OCCLUSION ( 3 FDA reports)
HEPATITIS A ( 3 FDA reports)
HIGH FREQUENCY ABLATION ( 3 FDA reports)
HIP DEFORMITY ( 3 FDA reports)
HISTOLOGY ABNORMAL ( 3 FDA reports)
HYPERACUSIS ( 3 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 3 FDA reports)
HYPERPROLACTINAEMIA ( 3 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 3 FDA reports)
HYPERTRANSAMINASAEMIA ( 3 FDA reports)
HYPERVIGILANCE ( 3 FDA reports)
HYPOGONADISM ( 3 FDA reports)
HYPOMANIA ( 3 FDA reports)
HYPOMENORRHOEA ( 3 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 3 FDA reports)
IATROGENIC INJURY ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
IMPULSE-CONTROL DISORDER ( 3 FDA reports)
INADEQUATE DIET ( 3 FDA reports)
INCISION SITE HAEMORRHAGE ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 3 FDA reports)
INFANTILE APNOEIC ATTACK ( 3 FDA reports)
INFECTED CYST ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
INFUSION SITE EXTRAVASATION ( 3 FDA reports)
INFUSION SITE PRURITUS ( 3 FDA reports)
INFUSION SITE WARMTH ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INTESTINAL INFARCTION ( 3 FDA reports)
IVTH NERVE PARALYSIS ( 3 FDA reports)
JOINT ARTHROPLASTY ( 3 FDA reports)
KAPOSI'S SARCOMA ( 3 FDA reports)
KERATOACANTHOMA ( 3 FDA reports)
KETONURIA ( 3 FDA reports)
KIDNEY ENLARGEMENT ( 3 FDA reports)
KIDNEY FIBROSIS ( 3 FDA reports)
LARGE FOR DATES BABY ( 3 FDA reports)
LARYNGEAL DISORDER ( 3 FDA reports)
LDL/HDL RATIO INCREASED ( 3 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 3 FDA reports)
LEUKAEMIC INFILTRATION RENAL ( 3 FDA reports)
LIBIDO INCREASED ( 3 FDA reports)
LICHENIFICATION ( 3 FDA reports)
LIP HAEMORRHAGE ( 3 FDA reports)
LIPIDS INCREASED ( 3 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 3 FDA reports)
LONG QT SYNDROME ( 3 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
LYMPHANGIOMA ( 3 FDA reports)
MACULAR FIBROSIS ( 3 FDA reports)
MADAROSIS ( 3 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 3 FDA reports)
MENINGISM ( 3 FDA reports)
MENINGITIS NEONATAL ( 3 FDA reports)
METAMORPHOPSIA ( 3 FDA reports)
METASTASES TO MOUTH ( 3 FDA reports)
METASTASES TO SPLEEN ( 3 FDA reports)
METASTATIC GASTRIC CANCER ( 3 FDA reports)
MICROCEPHALY ( 3 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 3 FDA reports)
MIGRAINE WITH AURA ( 3 FDA reports)
MITRAL VALVE REPAIR ( 3 FDA reports)
MITRAL VALVE SCLEROSIS ( 3 FDA reports)
MOANING ( 3 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MUCOSAL DRYNESS ( 3 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 3 FDA reports)
MUSCLE FATIGUE ( 3 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 3 FDA reports)
MYELITIS ( 3 FDA reports)
MYELOCYTOSIS ( 3 FDA reports)
MYELOMALACIA ( 3 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 3 FDA reports)
MYOCARDITIS BACTERIAL ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
MYRINGOTOMY ( 3 FDA reports)
NAEVUS FLAMMEUS ( 3 FDA reports)
NAIL AVULSION ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NASAL NEOPLASM ( 3 FDA reports)
NASOPHARYNGEAL CANCER ( 3 FDA reports)
NASOPHARYNGEAL DISORDER ( 3 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 3 FDA reports)
NEONATAL RESPIRATORY ARREST ( 3 FDA reports)
NEPHRECTOMY ( 3 FDA reports)
NERVE COMPRESSION ( 3 FDA reports)
NEUROGENIC BOWEL ( 3 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 3 FDA reports)
NICOTINE DEPENDENCE ( 3 FDA reports)
OBSTRUCTIVE UROPATHY ( 3 FDA reports)
OCULAR VASCULAR DISORDER ( 3 FDA reports)
OESOPHAGEAL NEOPLASM ( 3 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 3 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
OLIGODIPSIA ( 3 FDA reports)
ONYCHOLYSIS ( 3 FDA reports)
ORAL PAPILLOMA ( 3 FDA reports)
ORBITAL OEDEMA ( 3 FDA reports)
OSTEOCHONDRITIS ( 3 FDA reports)
OSTEOPETROSIS ( 3 FDA reports)
PANNICULITIS LOBULAR ( 3 FDA reports)
PAPULE ( 3 FDA reports)
PELVIC PROLAPSE ( 3 FDA reports)
PELVIC VENOUS THROMBOSIS ( 3 FDA reports)
PENILE DISCHARGE ( 3 FDA reports)
PENIS DEVIATION ( 3 FDA reports)
PERFORATED ULCER ( 3 FDA reports)
PERIODONTAL INFECTION ( 3 FDA reports)
PERIPHERAL NERVE LESION ( 3 FDA reports)
PERIRENAL HAEMATOMA ( 3 FDA reports)
PERITONEAL DISORDER ( 3 FDA reports)
PERITONEAL EFFUSION ( 3 FDA reports)
PNEUMOCOCCAL INFECTION ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
POLYMENORRHOEA ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
PORPHYRIA ( 3 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 3 FDA reports)
POST PROCEDURAL BILE LEAK ( 3 FDA reports)
POST PROCEDURAL DIARRHOEA ( 3 FDA reports)
POST PROCEDURAL DRAINAGE ( 3 FDA reports)
POSTMENOPAUSE ( 3 FDA reports)
POSTOPERATIVE ILEUS ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
PREGNANCY TEST POSITIVE ( 3 FDA reports)
PRESBYACUSIS ( 3 FDA reports)
PROCALCITONIN INCREASED ( 3 FDA reports)
PRODUCT ODOUR ABNORMAL ( 3 FDA reports)
PROSTATE INFECTION ( 3 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 3 FDA reports)
PSYCHOTIC BEHAVIOUR ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULMONARY OEDEMA NEONATAL ( 3 FDA reports)
PULMONARY TOXICITY ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PULSE PRESSURE INCREASED ( 3 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 3 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
PYLORIC STENOSIS ( 3 FDA reports)
PYROGLUTAMATE INCREASED ( 3 FDA reports)
RADIATION FIBROSIS - LUNG ( 3 FDA reports)
RADIATION NEUROPATHY ( 3 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 3 FDA reports)
RASH SCALY ( 3 FDA reports)
RECTAL CANCER ( 3 FDA reports)
RENAL DYSPLASIA ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RENAL TUBULAR ATROPHY ( 3 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 3 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 3 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 3 FDA reports)
RETINAL DISORDER ( 3 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 3 FDA reports)
RHABDOMYOMA ( 3 FDA reports)
RIB HYPOPLASIA ( 3 FDA reports)
SALIVARY GLAND CALCULUS ( 3 FDA reports)
SCHIZOPHRENIA ( 3 FDA reports)
SCLEREMA ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SCROTAL SWELLING ( 3 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SITUS INVERSUS ( 3 FDA reports)
SKIN CHAPPED ( 3 FDA reports)
SKIN HYPERTROPHY ( 3 FDA reports)
SKIN INFLAMMATION ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
SKIN TOXICITY ( 3 FDA reports)
SKULL X-RAY ABNORMAL ( 3 FDA reports)
SLEEP INERTIA ( 3 FDA reports)
SOMATIC DELUSION ( 3 FDA reports)
SOMATOFORM DISORDER ( 3 FDA reports)
SPERMATOGENESIS ABNORMAL ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
SPLEEN CONGESTION ( 3 FDA reports)
SPLENECTOMY ( 3 FDA reports)
SPLENIC VARICES ( 3 FDA reports)
SPLENIC VEIN THROMBOSIS ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STASIS DERMATITIS ( 3 FDA reports)
STEREOTYPY ( 3 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 3 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 3 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
SURGICAL FAILURE ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
SYSTEMIC CANDIDA ( 3 FDA reports)
TACHYPHRENIA ( 3 FDA reports)
TENDON CALCIFICATION ( 3 FDA reports)
TERMINAL STATE ( 3 FDA reports)
TESTICULAR DISORDER ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
THYMECTOMY ( 3 FDA reports)
THYROID MASS ( 3 FDA reports)
THYROXINE FREE DECREASED ( 3 FDA reports)
THYROXINE INCREASED ( 3 FDA reports)
TIC ( 3 FDA reports)
TINEA VERSICOLOUR ( 3 FDA reports)
TONGUE COATED ( 3 FDA reports)
TONGUE EXFOLIATION ( 3 FDA reports)
TONSILLECTOMY ( 3 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 3 FDA reports)
TRACHEITIS ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
TRANSFUSION REACTION ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TRIGGER FINGER ( 3 FDA reports)
TRISOMY 21 ( 3 FDA reports)
TRYPTASE INCREASED ( 3 FDA reports)
TUBEROUS SCLEROSIS ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
URETERIC OBSTRUCTION ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
VAGINAL DISORDER ( 3 FDA reports)
VAGINAL INFLAMMATION ( 3 FDA reports)
VAGINAL PROLAPSE ( 3 FDA reports)
VASCULAR GRAFT ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VASCULAR RUPTURE ( 3 FDA reports)
VASOSPASM ( 3 FDA reports)
VIRAL PHARYNGITIS ( 3 FDA reports)
VIRAL SKIN INFECTION ( 3 FDA reports)
VIRAL TEST POSITIVE ( 3 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 3 FDA reports)
VOCAL CORD ATROPHY ( 3 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
ROSEOLOVIRUS TEST POSITIVE ( 2 FDA reports)
SALIVARY GLAND RESECTION ( 2 FDA reports)
SALPINGECTOMY ( 2 FDA reports)
SALPINGOSTOMY ( 2 FDA reports)
SCAN LYMPH NODES ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 2 FDA reports)
SCARLET FEVER ( 2 FDA reports)
SEMEN VOLUME DECREASED ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SENSORY GANGLIONITIS ( 2 FDA reports)
SINGLE UMBILICAL ARTERY ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN FIBROSIS ( 2 FDA reports)
SKIN TEST ( 2 FDA reports)
SKIN TEST NEGATIVE ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SMOKER ( 2 FDA reports)
SOCIAL PHOBIA ( 2 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 2 FDA reports)
SOFT TISSUE INJURY ( 2 FDA reports)
SOFT TISSUE MASS ( 2 FDA reports)
SOFT TISSUE NEOPLASM ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SPASTIC DIPLEGIA ( 2 FDA reports)
SPIROMETRY ABNORMAL ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SPLENIC NECROSIS ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 2 FDA reports)
STOOLS WATERY ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
SUBSTANCE ABUSER ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUPERINFECTION BACTERIAL ( 2 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
SYMBLEPHARON ( 2 FDA reports)
SYNOVIAL DISORDER ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
TESTICULAR CYST ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THORACIC SPINE FLATTENING ( 2 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
THYMUS DISORDER ( 2 FDA reports)
TOE DEFORMITY ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TONSILLAR DISORDER ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TRACHEAL DISORDER ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TRIGONITIS ( 2 FDA reports)
ULNAR NEURITIS ( 2 FDA reports)
ULTRAFILTRATION FAILURE ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
UMBILICAL CORD SHORT ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
UPPER EXTREMITY MASS ( 2 FDA reports)
URETERITIS ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URETHRAL PAIN ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
URINE BILIRUBIN INCREASED ( 2 FDA reports)
URINE CYTOMEGALOVIRUS POSITIVE ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
URINE KETONE BODY ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
UROGENITAL DISORDER ( 2 FDA reports)
URTICARIA PRESSURE ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
UTERINE ENLARGEMENT ( 2 FDA reports)
UTERINE INFECTION ( 2 FDA reports)
UTERINE RUPTURE ( 2 FDA reports)
VAGINAL EROSION ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VANISHING BILE DUCT SYNDROME ( 2 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VIBRATORY SENSE INCREASED ( 2 FDA reports)
VICTIM OF CRIME ( 2 FDA reports)
VICTIM OF ELDER ABUSE ( 2 FDA reports)
VICTIM OF HOMICIDE ( 2 FDA reports)
VISCERAL CONGESTION ( 2 FDA reports)
VITAL CAPACITY DECREASED ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VOMITING IN PREGNANCY ( 2 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
VULVOVAGINITIS STREPTOCOCCAL ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
WEGENER'S GRANULOMATOSIS ( 2 FDA reports)
WEIGHT LOSS POOR ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
WOUND DEBRIDEMENT ( 2 FDA reports)
X-RAY LIMB ABNORMAL ( 2 FDA reports)
ZYGOMYCOSIS ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ABORTION INCOMPLETE ( 2 FDA reports)
ACALCULIA ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 2 FDA reports)
ACINETOBACTER BACTERAEMIA ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE CHEST SYNDROME ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ADAMS-STOKES SYNDROME ( 2 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
AMIMIA ( 2 FDA reports)
AMNESTIC DISORDER ( 2 FDA reports)
AMNIORRHOEA ( 2 FDA reports)
ANAEMIA OF PREGNANCY ( 2 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ANAL CANCER STAGE III ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANAL INFLAMMATION ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES REFRACTORY ( 2 FDA reports)
ANDROGEN DEFICIENCY ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
AORTIC ANEURYSM REPAIR ( 2 FDA reports)
AORTIC EMBOLUS ( 2 FDA reports)
AORTIC VALVE REPAIR ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
APPLICATION SITE BURN ( 2 FDA reports)
APPLICATION SITE HAEMATOMA ( 2 FDA reports)
ASPIRATION BONE MARROW ( 2 FDA reports)
ASTHMA EXERCISE INDUCED ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 2 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BENIGN CARDIAC NEOPLASM ( 2 FDA reports)
BENIGN OVARIAN TUMOUR ( 2 FDA reports)
BILIARY CYST ( 2 FDA reports)
BILIARY NEOPLASM ( 2 FDA reports)
BINGE EATING ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLADDER DIVERTICULUM ( 2 FDA reports)
BLADDER NEOPLASM SURGERY ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLEEDING PERIPARTUM ( 2 FDA reports)
BLOOD ALCOHOL ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD HIV RNA DECREASED ( 2 FDA reports)
BLOOD KETONE BODY ( 2 FDA reports)
BLOOD KETONE BODY INCREASED ( 2 FDA reports)
BLOOD OSMOLARITY INCREASED ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BODY MASS INDEX INCREASED ( 2 FDA reports)
BONE FISSURE ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRACHYCEPHALY ( 2 FDA reports)
BRAIN COMPRESSION ( 2 FDA reports)
BRAIN OPERATION ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BREAKTHROUGH PAIN ( 2 FDA reports)
BREAST CANCER IN SITU ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BREATH SOUNDS ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CAPILLARY DISORDER ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIAC MALPOSITION ( 2 FDA reports)
CARDIAC SEPTAL DEFECT ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 2 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 2 FDA reports)
CATARACT SUBCAPSULAR ( 2 FDA reports)
CATHETER SITE CELLULITIS ( 2 FDA reports)
CATHETER SITE ERYTHEMA ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBELLAR HYPOPLASIA ( 2 FDA reports)
CEREBELLAR ISCHAEMIA ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL CALCIFICATION ( 2 FDA reports)
CEREBRAL MICROHAEMORRHAGE ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CEREBRAL REVASCULARISATION SYNANGIOSIS ( 2 FDA reports)
CERVICAL CYST ( 2 FDA reports)
CHEST EXPANSION DECREASED ( 2 FDA reports)
CHILD MALTREATMENT SYNDROME ( 2 FDA reports)
CHOLANGITIS SCLEROSING ( 2 FDA reports)
CHORIORETINAL ATROPHY ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
CNS VENTRICULITIS ( 2 FDA reports)
COCCIDIOIDOMYCOSIS ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLOBOMA ( 2 FDA reports)
COLONOSCOPY ABNORMAL ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
COMPLICATED MIGRAINE ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 2 FDA reports)
CONGENITAL GASTRIC ANOMALY ( 2 FDA reports)
CONGENITAL PHARYNGEAL ANOMALY ( 2 FDA reports)
CONGENITAL TRACHEOMALACIA ( 2 FDA reports)
CONGENITAL TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
CRANIOCEREBRAL INJURY ( 2 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CYANOSIS NEONATAL ( 2 FDA reports)
CYSTITIS INTERSTITIAL ( 2 FDA reports)
CYSTITIS KLEBSIELLA ( 2 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DELUSIONAL PERCEPTION ( 2 FDA reports)
DERMATOSIS ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DIABETIC ULCER ( 2 FDA reports)
DIASTOLIC HYPOTENSION ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 2 FDA reports)
DIVORCED ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DROP ATTACKS ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DYSCALCULIA ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
EGOBRONCHOPHONY ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 2 FDA reports)
ENAMEL ANOMALY ( 2 FDA reports)
ENDARTERECTOMY ( 2 FDA reports)
ENDOMETRITIS ( 2 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
ENDOTOXIC SHOCK ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
ENLARGED CLITORIS ( 2 FDA reports)
ENTEROBACTER PNEUMONIA ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 2 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 2 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EPIDIDYMAL INFECTION ( 2 FDA reports)
EPISCLERITIS ( 2 FDA reports)
ERYTHRODERMIC PSORIASIS ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
ESCHERICHIA VAGINITIS ( 2 FDA reports)
EX-TOBACCO USER ( 2 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
EYELID MARGIN CRUSTING ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FACTOR VIII INHIBITION ( 2 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FIXED ERUPTION ( 2 FDA reports)
FOETAL MALFORMATION ( 2 FDA reports)
FONTANELLE BULGING ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FRACTURE MALUNION ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
GALACTOSTASIS ( 2 FDA reports)
GAMBLING ( 2 FDA reports)
GASTRIC HYPOMOTILITY ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 2 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTRIC POLYPECTOMY ( 2 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA IN SITU ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL ULCERATION ( 2 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 2 FDA reports)
GLOSSOPTOSIS ( 2 FDA reports)
GRAFT DYSFUNCTION ( 2 FDA reports)
GRAFT INFECTION ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HAND DEFORMITY ( 2 FDA reports)
HEART AND LUNG TRANSPLANT ( 2 FDA reports)
HEART TRANSPLANT REJECTION ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HELLP SYNDROME ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 2 FDA reports)
HEPATIC CALCIFICATION ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 2 FDA reports)
HERPES ZOSTER OTICUS ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HOIGNE'S SYNDROME ( 2 FDA reports)
HUMAN HERPESVIRUS 7 INFECTION ( 2 FDA reports)
HUNTINGTON'S DISEASE ( 2 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 2 FDA reports)
HYPERINSULINAEMIA ( 2 FDA reports)
HYPERLACTACIDAEMIA ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPERVOLAEMIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOCHROMASIA ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOKALAEMIC SYNDROME ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOTHERMIA NEONATAL ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INCISION SITE ERYTHEMA ( 2 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INFUSION SITE URTICARIA ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INSULIN RESISTANCE SYNDROME ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL ADHESION LYSIS ( 2 FDA reports)
INTESTINAL OPERATION ( 2 FDA reports)
INTRACRANIAL HYPOTENSION ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
IRIS TRANSILLUMINATION DEFECT ( 2 FDA reports)
IRON METABOLISM DISORDER ( 2 FDA reports)
IUCD COMPLICATION ( 2 FDA reports)
JARISCH-HERXHEIMER REACTION ( 2 FDA reports)
JEJUNAL ULCER ( 2 FDA reports)
JOINT INJECTION ( 2 FDA reports)
JUVENILE ARTHRITIS ( 2 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 2 FDA reports)
KERATITIS INTERSTITIAL ( 2 FDA reports)
KETOSIS ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
KLEPTOMANIA ( 2 FDA reports)
KLINEFELTER'S SYNDROME ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LABOUR COMPLICATION ( 2 FDA reports)
LACTATION DISORDER ( 2 FDA reports)
LARYNGITIS FUNGAL ( 2 FDA reports)
LEARNING DISABILITY ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LISTERIA SEPSIS ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVER TENDERNESS ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LONG THORACIC NERVE PALSY ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
LYMPHOCYTE TRANSFORMATION TEST POSITIVE ( 2 FDA reports)
MACROSOMIA ( 2 FDA reports)
MACROSTOMIA ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MAMMOGRAM ( 2 FDA reports)
MAMMOPLASTY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MEAN CELL VOLUME DECREASED ( 2 FDA reports)
MEASLES ( 2 FDA reports)
MECHANICAL URTICARIA ( 2 FDA reports)
MEDIASTINOSCOPY ( 2 FDA reports)
MEIBOMIANITIS ( 2 FDA reports)
MENINGEAL DISORDER ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MENINGITIS LISTERIA ( 2 FDA reports)
MENISCUS OPERATION ( 2 FDA reports)
MENOMETRORRHAGIA ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
METASTASES TO CHEST WALL ( 2 FDA reports)
METASTASES TO KIDNEY ( 2 FDA reports)
METASTASES TO RETROPERITONEUM ( 2 FDA reports)
MICROSCOPIC POLYANGIITIS ( 2 FDA reports)
MILIA ( 2 FDA reports)
MITOCHONDRIAL TOXICITY ( 2 FDA reports)
MITRAL VALVE HYPOPLASIA ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MONONUCLEOSIS HETEROPHILE TEST POSITIVE ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MOUTH CYST ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MUSCLE HYPERTROPHY ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
MYCOPLASMA TEST POSITIVE ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NECK DEFORMITY ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEGATIVE THOUGHTS ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
NEONATAL HYPOXIA ( 2 FDA reports)
NEONATAL TACHYCARDIA ( 2 FDA reports)
NEPHRITIS ALLERGIC ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEUTROPENIA NEONATAL ( 2 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NITRITE URINE ABSENT ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 2 FDA reports)
OBLIQUE PRESENTATION ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
ODONTOGENIC CYST ( 2 FDA reports)
OESOPHAGEAL PAPILLOMA ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
ONYCHALGIA ( 2 FDA reports)
ONYCHOMADESIS ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OSTEOMA ( 2 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 2 FDA reports)
OVARIAN ABSCESS ( 2 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 2 FDA reports)
OVERGROWTH BACTERIAL ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PAPILLARY MUSCLE RUPTURE ( 2 FDA reports)
PARACENTESIS ( 2 FDA reports)
PARATHYROID TUMOUR ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PASSIVE SMOKING ( 2 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 2 FDA reports)
PERICARDITIS CONSTRICTIVE ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PERNICIOUS ANAEMIA ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 2 FDA reports)
PHARYNGEAL MASS ( 2 FDA reports)
PHLEBITIS SUPERFICIAL ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PILOERECTION ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLASMAPHERESIS ( 2 FDA reports)
PLASTIC SURGERY ( 2 FDA reports)
PLASTIC SURGERY TO THE FACE ( 2 FDA reports)
PLATELET AGGREGATION INCREASED ( 2 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 2 FDA reports)
PLEURODESIS ( 2 FDA reports)
PLEUROPERICARDITIS ( 2 FDA reports)
PLEUROTHOTONUS ( 2 FDA reports)
PNEUMATOSIS ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
POIKILOCYTOSIS ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 2 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 2 FDA reports)
POSTPARTUM DISORDER ( 2 FDA reports)
PRECOCIOUS PUBERTY ( 2 FDA reports)
PREMATURE EJACULATION ( 2 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 2 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PROLONGED LABOUR ( 2 FDA reports)
PROTEIN C DECREASED ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PULMONARY PERCUSSION TEST ABNORMALITY ( 2 FDA reports)
PULMONARY VALVE DISEASE ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PYLORUS DILATATION ( 2 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
RASH SCARLATINIFORM ( 2 FDA reports)
REACTION TO AZO-DYES ( 2 FDA reports)
RECURRING SKIN BOILS ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
REFRACTORY ANAEMIA ( 2 FDA reports)
REMOVAL OF FOREIGN BODY ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL CYST HAEMORRHAGE ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RHINOVIRUS INFECTION ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABORTION COMPLETE ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACQUIRED GENE MUTATION ( 1 FDA reports)
ACQUIRED NIGHT BLINDNESS ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOIDITIS ( 1 FDA reports)
ADENOSINE DEAMINASE DEFICIENCY ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENAL GLAND TUBERCULOSIS ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOLIC ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALOPECIA UNIVERSALIS ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA GLOBULIN INCREASED ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMINO ACID LEVEL DECREASED ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL NEOPLASM ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANOTIA ( 1 FDA reports)
ANTI FACTOR V ANTIBODY POSITIVE ( 1 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC IGM ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
ANTIVIRAL DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME ( 1 FDA reports)
AUTOSOMAL CHROMOSOME ANOMALY ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BANDAEMIA ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BASILAR ARTERY THROMBOSIS ( 1 FDA reports)
BED REST ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILE OUTPUT ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLADDER IRRITATION ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER SPHINCTER ATONY ( 1 FDA reports)
BLADDER STENOSIS ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CYANIDE INCREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 1 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BREAST PROSTHESIS USER ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHOGENIC CYST ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BULLOUS IMPETIGO ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
BURNING MOUTH SYNDROME ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDA NAPPY RASH ( 1 FDA reports)
CAPSULE ISSUE ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARCINOID TUMOUR OF THE PROSTATE ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ANEURYSM REPAIR ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CAROTID PULSE INCREASED ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CELLULITIS GANGRENOUS ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ARTERITIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CERVIX HAEMATOMA UTERINE ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHLAMYDIA SEROLOGY POSITIVE ( 1 FDA reports)
CHOLECYSTOSTOMY ( 1 FDA reports)
CHONDROLYSIS ( 1 FDA reports)
CHORIORETINITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRCULATING ANTICOAGULANT POSITIVE ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
COAGULATION FACTOR V LEVEL INCREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COCHLEA IMPLANT ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPULSIVE LIP BITING ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL BRAIN DAMAGE ( 1 FDA reports)
CONGENITAL CYST ( 1 FDA reports)
CONGENITAL MEGACOLON ( 1 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
CONGENITAL PNEUMONIA ( 1 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 1 FDA reports)
CONGENITAL RENAL CYST ( 1 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVAL ULCER ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONA VIRUS INFECTION ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF BACTERIA IDENTIFIED ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CSF GLUCOSE ABNORMAL ( 1 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYLINDRURIA ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 1 FDA reports)
DANDY-WALKER SYNDROME ( 1 FDA reports)
DEAFNESS CONGENITAL ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DEPILATION ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DERMOGRAPHISM ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE INTOLERANCE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DEVICE TOXICITY ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC CARDIOMYOPATHY ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIAPHRAGMALGIA ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG CHEMICAL INCOMPATIBILITY ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DUCTUS ARTERIOSUS PREMATURE CLOSURE ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DYSMORPHOPHOBIA ( 1 FDA reports)
DYSPHONIA PSYCHOGENIC ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
ENZYME INHIBITION ( 1 FDA reports)
EOSINOPHIL COUNT ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIDURAL ANAESTHESIA ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERYTHROPHAGOCYTOSIS ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EYE COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FALSE LABOUR ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FASCIOTOMY ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOETAL HEART RATE DISORDER ( 1 FDA reports)
FOETAL MONITORING ( 1 FDA reports)
FONTANELLE DEPRESSED ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FORCED EXPIRATORY VOLUME ABNORMAL ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FREE FATTY ACIDS ABNORMAL ( 1 FDA reports)
FUCHS' SYNDROME ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNGATING WOUND ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTRIC ADENOMA ( 1 FDA reports)
GASTRIC CANCER STAGE III ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRINOMA ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GAUCHER'S DISEASE ( 1 FDA reports)
GENDER IDENTITY DISORDER ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION NORMAL ( 1 FDA reports)
GENETIC COUNSELLING ( 1 FDA reports)
GENITAL ABSCESS ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL LABIAL ADHESIONS ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHROPATHY ( 1 FDA reports)
GLUCAGONOMA ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
HAEMATINURIA ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMOLYSIS NEONATAL ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 1 FDA reports)
HEPATECTOMY ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC ENZYME DECREASED ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS C ANTIBODY ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERPES PHARYNGITIS ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HETEROTAXIA ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE IV ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HYDROCELE OPERATION ( 1 FDA reports)
HYDROMETRA ( 1 FDA reports)
HYGROMA COLLI ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERGASTRINAEMIA ( 1 FDA reports)
HYPERGLOBULINAEMIA ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTENSION NEONATAL ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPERTROPHIC ANAL PAPILLA ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOKINESIA NEONATAL ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 1 FDA reports)
IDIOPATHIC CAPILLARITIS ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
IIIRD NERVE INJURY ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILEUS SPASTIC ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILIAC VEIN OCCLUSION ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMPACTED FRACTURE ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPINGEMENT SYNDROME ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE HAEMATOMA ( 1 FDA reports)
IMPLANT SITE INFLAMMATION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INDIRECT INFECTION TRANSMISSION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFECTION TRANSMISSION VIA PERSONAL CONTACT ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
INFUSION SITE MASS ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INNER EAR INFLAMMATION ( 1 FDA reports)
INTERCEPTED DRUG ADMINISTRATION ERROR ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL STOMA COMPLICATION ( 1 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRIS HYPOPIGMENTATION ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ISOIMMUNE HAEMOLYTIC DISEASE ( 1 FDA reports)
JAW CYST ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT STABILISATION ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KORSAKOFF'S PSYCHOSIS ALCOHOLIC ( 1 FDA reports)
LABIA ENLARGED ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LACTATE PYRUVATE RATIO INCREASED ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARYNGEAL MASS ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 1 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP NEOPLASM ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
LOCAL ANAESTHESIA ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOCALISED SKIN REACTION ( 1 FDA reports)
LONG QT SYNDROME CONGENITAL ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG CYST BENIGN ( 1 FDA reports)
LUNG HERNIA ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOMATOID PAPULOSIS ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MACULE ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MASTOIDECTOMY ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MECONIUM ABNORMAL ( 1 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MEGAKARYOCYTES DECREASED ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENTAL DISABILITY ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTASES TO SALIVARY GLAND ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICROSPORUM INFECTION ( 1 FDA reports)
MICROVASCULAR ANGINA ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MUCOCUTANEOUS FLAP OPERATION ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS VI ( 1 FDA reports)
MUCOSAL ATROPHY ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOBACTERIUM ULCERANS INFECTION ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOKYMIA ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEPHROPTOSIS ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROFIBROMATOSIS ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUTROPHIL PERCENTAGE ABNORMAL ( 1 FDA reports)
NIEMANN-PICK DISEASE ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NITRITURIA ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING THORACIC ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCCUPATIONAL ASTHMA ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OFFICE VISIT ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL NEOPLASM ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
OSCILLOPSIA ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OTITIS EXTERNA BACTERIAL ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PAROTID GLAND INFLAMMATION ( 1 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS REPAIR ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE INCREASED ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PENILE EXFOLIATION ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PENILE PROSTHESIS INSERTION ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL DRAINAGE TEST ABNORMAL ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERINEPHRIC ABSCESS ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPORTAL OEDEMA ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PHAGOPHOBIA ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHARYNGOTONSILLITIS ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PITYRIASIS ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLACENTA PRAEVIA HAEMORRHAGE ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLATELET AGGREGATION DECREASED ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POPLITEAL STENOSIS ( 1 FDA reports)
POROKERATOSIS ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST PROCEDURAL URINE LEAK ( 1 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 1 FDA reports)
POSTICTAL HEADACHE ( 1 FDA reports)
POSTMATURE BABY ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
POSTURING ( 1 FDA reports)
POVERTY ( 1 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 1 FDA reports)
PREGNANCY WITH INJECTABLE CONTRACEPTIVE ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCTITIS ULCERATIVE ( 1 FDA reports)
PRODUCT CONTAINER ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION CHEMICAL ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT TAMPERING ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATE TENDERNESS ( 1 FDA reports)
PROSTATIC CALCIFICATION ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROTEIN ALBUMIN RATIO DECREASED ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PRURITUS ALLERGIC ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOSIS POSTOPERATIVE ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY ATRESIA ( 1 FDA reports)
PULMONARY ARTERY STENOSIS ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY PNEUMATOCELE ( 1 FDA reports)
PULMONARY VALVE CALCIFICATION ( 1 FDA reports)
PULMONARY VASCULITIS ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PURPURA FULMINANS ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADIATION EXPOSURE ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
RASH PAPULOSQUAMOUS ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RED BLOOD CELL ACANTHOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL STONE REMOVAL ( 1 FDA reports)
RENAL VEIN OCCLUSION ( 1 FDA reports)
REPERFUSION ARRHYTHMIA ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DEPTH DECREASED ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RETAINED PRODUCTS OF CONCEPTION ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINOL BINDING PROTEIN INCREASED ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
REYE'S SYNDROME ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
RIGHT VENTRICULAR HEAVE ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 1 FDA reports)
SCHOOL REFUSAL ( 1 FDA reports)
SCINTIGRAPHY ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSITISATION ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SEROLOGY POSITIVE ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SEXUAL ASSAULT VICTIM ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN CANCER METASTATIC ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPLEEN PALPABLE ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL IMPETIGO ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STERNAL INJURY ( 1 FDA reports)
STERNAL WIRING ( 1 FDA reports)
STICKY SKIN ( 1 FDA reports)
STRAWBERRY TONGUE ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRESS ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
SUBCLAVIAN ARTERY OCCLUSION ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 1 FDA reports)
SUPPRESSED LACTATION ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SYMBOLIC DYSFUNCTION ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SURGERY ( 1 FDA reports)
TENODESIS ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TESTICULAR MASS ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THOUGHT INSERTION ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYROIDITIS FIBROUS CHRONIC ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TONGUE ATROPHY ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONGUE PRURITUS ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR INFLAMMATION ( 1 FDA reports)
TOOTH MALFORMATION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOTAL LUNG CAPACITY INCREASED ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEAL ULCER ( 1 FDA reports)
TRANSFERRIN ABNORMAL ( 1 FDA reports)
TRANSFERRIN DECREASED ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC LIVER INJURY ( 1 FDA reports)
TRAUMATIC OCCLUSION ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TRUNCUS COELIACUS THROMBOSIS ( 1 FDA reports)
TUBERCULOSIS OF INTRATHORACIC LYMPH NODES ( 1 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 1 FDA reports)
TUMOUR FLARE ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
ULTRASOUND ABDOMEN ( 1 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 1 FDA reports)
ULTRASOUND CHEST ( 1 FDA reports)
UNEQUAL LIMB LENGTH ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
URETHRAL DILATATION ( 1 FDA reports)
URETHRAL DILATION PROCEDURE ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URETHRAL STRICTURE ( 1 FDA reports)
URETHRAL VALVES ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY SEDIMENT ABNORMAL ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE POTASSIUM INCREASED ( 1 FDA reports)
URINE PROTEIN, QUANTITATIVE ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO ABNORMAL ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
UTERINE STENOSIS ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VACCINE EXPOSURE DURING PREGNANCY ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGINAL RELAXATION ( 1 FDA reports)
VAGINITIS GARDNERELLA ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VENOUS RECANALISATION ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 1 FDA reports)
VERTIGO LABYRINTHINE ( 1 FDA reports)
VESTIBULAR ATAXIA ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL DNA TEST POSITIVE ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VIRAL OESOPHAGITIS ( 1 FDA reports)
VISCERAL LEISHMANIASIS ( 1 FDA reports)
VITAMIN B1 DEFICIENCY ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITAMIN B6 DECREASED ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 1 FDA reports)
VULVOVAGINAL SWELLING ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEIGHT CONTROL ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)
XEROSIS ( 1 FDA reports)

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