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

DYSPNOEA ( 5715 FDA reports)
DRUG INEFFECTIVE ( 4277 FDA reports)
ASTHMA ( 2999 FDA reports)
COUGH ( 2377 FDA reports)
PNEUMONIA ( 2339 FDA reports)
NAUSEA ( 2252 FDA reports)
PAIN ( 2170 FDA reports)
PRODUCT QUALITY ISSUE ( 2074 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2016 FDA reports)
DIZZINESS ( 1837 FDA reports)
FATIGUE ( 1817 FDA reports)
DYSPHONIA ( 1743 FDA reports)
ANXIETY ( 1717 FDA reports)
HEADACHE ( 1707 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1521 FDA reports)
CHEST PAIN ( 1510 FDA reports)
ASTHENIA ( 1376 FDA reports)
VOMITING ( 1350 FDA reports)
DEPRESSION ( 1245 FDA reports)
DIARRHOEA ( 1236 FDA reports)
OEDEMA PERIPHERAL ( 1236 FDA reports)
FALL ( 1205 FDA reports)
INSOMNIA ( 1161 FDA reports)
MALAISE ( 1113 FDA reports)
CHEST DISCOMFORT ( 1089 FDA reports)
ARTHRALGIA ( 1083 FDA reports)
BRONCHITIS ( 1046 FDA reports)
WHEEZING ( 1046 FDA reports)
PAIN IN EXTREMITY ( 1024 FDA reports)
BACK PAIN ( 1023 FDA reports)
WEIGHT DECREASED ( 945 FDA reports)
DEATH ( 936 FDA reports)
WEIGHT INCREASED ( 898 FDA reports)
HYPERTENSION ( 888 FDA reports)
MYOCARDIAL INFARCTION ( 880 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 867 FDA reports)
INJURY ( 867 FDA reports)
RASH ( 864 FDA reports)
TREMOR ( 861 FDA reports)
PYREXIA ( 840 FDA reports)
CONSTIPATION ( 805 FDA reports)
PRURITUS ( 795 FDA reports)
MUSCLE SPASMS ( 777 FDA reports)
ANAEMIA ( 769 FDA reports)
ABDOMINAL PAIN ( 760 FDA reports)
FEELING ABNORMAL ( 746 FDA reports)
CANDIDIASIS ( 740 FDA reports)
VISION BLURRED ( 709 FDA reports)
HYPOTENSION ( 692 FDA reports)
SINUSITIS ( 683 FDA reports)
HYPOAESTHESIA ( 668 FDA reports)
CONDITION AGGRAVATED ( 643 FDA reports)
DRY MOUTH ( 643 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 622 FDA reports)
PULMONARY EMBOLISM ( 618 FDA reports)
PALPITATIONS ( 613 FDA reports)
ATRIAL FIBRILLATION ( 611 FDA reports)
DECREASED APPETITE ( 611 FDA reports)
BLOOD PRESSURE INCREASED ( 608 FDA reports)
HYPERSENSITIVITY ( 597 FDA reports)
HEART RATE INCREASED ( 595 FDA reports)
CATARACT ( 594 FDA reports)
CEREBROVASCULAR ACCIDENT ( 591 FDA reports)
DEHYDRATION ( 589 FDA reports)
GAIT DISTURBANCE ( 577 FDA reports)
MYALGIA ( 564 FDA reports)
DYSGEUSIA ( 550 FDA reports)
URINARY TRACT INFECTION ( 544 FDA reports)
DYSPHAGIA ( 540 FDA reports)
PLEURAL EFFUSION ( 538 FDA reports)
NASOPHARYNGITIS ( 536 FDA reports)
SOMNOLENCE ( 528 FDA reports)
THROAT IRRITATION ( 524 FDA reports)
ABDOMINAL PAIN UPPER ( 523 FDA reports)
EMOTIONAL DISTRESS ( 523 FDA reports)
PARAESTHESIA ( 522 FDA reports)
RESPIRATORY FAILURE ( 513 FDA reports)
OSTEOARTHRITIS ( 508 FDA reports)
LOSS OF CONSCIOUSNESS ( 505 FDA reports)
BLOOD GLUCOSE INCREASED ( 502 FDA reports)
OSTEONECROSIS OF JAW ( 496 FDA reports)
CONFUSIONAL STATE ( 494 FDA reports)
DEEP VEIN THROMBOSIS ( 493 FDA reports)
RENAL FAILURE ( 489 FDA reports)
URTICARIA ( 472 FDA reports)
RENAL FAILURE ACUTE ( 447 FDA reports)
CONTUSION ( 443 FDA reports)
SYNCOPE ( 442 FDA reports)
PRODUCTIVE COUGH ( 441 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 441 FDA reports)
OROPHARYNGEAL PAIN ( 439 FDA reports)
ERYTHEMA ( 429 FDA reports)
ATELECTASIS ( 422 FDA reports)
ILL-DEFINED DISORDER ( 419 FDA reports)
HYPERHIDROSIS ( 417 FDA reports)
OVERDOSE ( 416 FDA reports)
DYSPEPSIA ( 412 FDA reports)
CORONARY ARTERY DISEASE ( 400 FDA reports)
EMPHYSEMA ( 394 FDA reports)
PAIN IN JAW ( 389 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 382 FDA reports)
MUSCULAR WEAKNESS ( 376 FDA reports)
INFECTION ( 374 FDA reports)
NERVOUSNESS ( 371 FDA reports)
CONVULSION ( 369 FDA reports)
OSTEOPOROSIS ( 369 FDA reports)
DIABETES MELLITUS ( 367 FDA reports)
NEUROPATHY PERIPHERAL ( 365 FDA reports)
MUSCULOSKELETAL PAIN ( 363 FDA reports)
ADVERSE EVENT ( 362 FDA reports)
SEPSIS ( 353 FDA reports)
ANHEDONIA ( 350 FDA reports)
CHOLELITHIASIS ( 347 FDA reports)
BONE DISORDER ( 346 FDA reports)
CARDIAC DISORDER ( 346 FDA reports)
CHILLS ( 345 FDA reports)
SWELLING ( 340 FDA reports)
TACHYCARDIA ( 339 FDA reports)
SWELLING FACE ( 338 FDA reports)
DRUG ADMINISTRATION ERROR ( 338 FDA reports)
APHONIA ( 337 FDA reports)
ARTHRITIS ( 334 FDA reports)
CARDIAC ARREST ( 334 FDA reports)
HAEMOGLOBIN DECREASED ( 330 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 326 FDA reports)
OSTEOMYELITIS ( 324 FDA reports)
LUNG DISORDER ( 323 FDA reports)
BALANCE DISORDER ( 314 FDA reports)
STRESS ( 313 FDA reports)
CARDIOMEGALY ( 309 FDA reports)
IMPAIRED HEALING ( 304 FDA reports)
ALOPECIA ( 301 FDA reports)
ANAPHYLACTIC REACTION ( 301 FDA reports)
MEMORY IMPAIRMENT ( 299 FDA reports)
SLEEP APNOEA SYNDROME ( 295 FDA reports)
DRUG INTERACTION ( 294 FDA reports)
DYSPNOEA EXERTIONAL ( 294 FDA reports)
ABDOMINAL DISTENSION ( 291 FDA reports)
SUICIDAL IDEATION ( 291 FDA reports)
MITRAL VALVE INCOMPETENCE ( 289 FDA reports)
RESPIRATORY DISTRESS ( 288 FDA reports)
ABDOMINAL DISCOMFORT ( 287 FDA reports)
ORAL CANDIDIASIS ( 287 FDA reports)
LUNG INFECTION ( 286 FDA reports)
EPISTAXIS ( 274 FDA reports)
CELLULITIS ( 271 FDA reports)
BONE PAIN ( 270 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 270 FDA reports)
JOINT SWELLING ( 269 FDA reports)
FLUSHING ( 267 FDA reports)
SPINAL OSTEOARTHRITIS ( 267 FDA reports)
PULMONARY HYPERTENSION ( 265 FDA reports)
ECONOMIC PROBLEM ( 265 FDA reports)
HYPOXIA ( 265 FDA reports)
MIGRAINE ( 264 FDA reports)
TREATMENT NONCOMPLIANCE ( 263 FDA reports)
VISUAL IMPAIRMENT ( 261 FDA reports)
RESPIRATORY DISORDER ( 259 FDA reports)
NASAL CONGESTION ( 259 FDA reports)
LYMPHADENOPATHY ( 253 FDA reports)
ABNORMAL DREAMS ( 252 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 251 FDA reports)
HIATUS HERNIA ( 250 FDA reports)
AMNESIA ( 247 FDA reports)
HYPERLIPIDAEMIA ( 247 FDA reports)
THROMBOSIS ( 247 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 244 FDA reports)
HAEMOPTYSIS ( 243 FDA reports)
SWOLLEN TONGUE ( 243 FDA reports)
INFLUENZA ( 242 FDA reports)
DYSURIA ( 241 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 241 FDA reports)
LUNG NEOPLASM ( 239 FDA reports)
GALLBLADDER DISORDER ( 238 FDA reports)
DENTAL CARIES ( 237 FDA reports)
NECK PAIN ( 236 FDA reports)
RIB FRACTURE ( 236 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 235 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 233 FDA reports)
HERPES ZOSTER ( 233 FDA reports)
ORAL PAIN ( 232 FDA reports)
HYPOKALAEMIA ( 230 FDA reports)
OXYGEN SATURATION DECREASED ( 229 FDA reports)
SPEECH DISORDER ( 229 FDA reports)
THROAT TIGHTNESS ( 228 FDA reports)
VISUAL ACUITY REDUCED ( 227 FDA reports)
TOOTHACHE ( 225 FDA reports)
RHINORRHOEA ( 224 FDA reports)
TOOTH EXTRACTION ( 224 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 224 FDA reports)
CHOKING ( 224 FDA reports)
DRUG DOSE OMISSION ( 222 FDA reports)
INFLUENZA LIKE ILLNESS ( 222 FDA reports)
DRUG HYPERSENSITIVITY ( 220 FDA reports)
OEDEMA ( 220 FDA reports)
AGITATION ( 219 FDA reports)
OSTEONECROSIS ( 219 FDA reports)
STOMATITIS ( 219 FDA reports)
VERTIGO ( 218 FDA reports)
ABASIA ( 218 FDA reports)
MENTAL DISORDER ( 218 FDA reports)
NEPHROLITHIASIS ( 217 FDA reports)
CARDIO-RESPIRATORY ARREST ( 215 FDA reports)
BURNING SENSATION ( 214 FDA reports)
MENTAL STATUS CHANGES ( 214 FDA reports)
HALLUCINATION ( 213 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 212 FDA reports)
LARYNGITIS ( 212 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 211 FDA reports)
HAEMORRHAGE ( 211 FDA reports)
THROMBOCYTOPENIA ( 211 FDA reports)
MEDICATION ERROR ( 209 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 208 FDA reports)
PULMONARY OEDEMA ( 208 FDA reports)
DISCOMFORT ( 206 FDA reports)
GLOSSODYNIA ( 205 FDA reports)
LUNG NEOPLASM MALIGNANT ( 205 FDA reports)
ARTHROPATHY ( 203 FDA reports)
BLOOD CREATININE INCREASED ( 203 FDA reports)
CHOLECYSTITIS CHRONIC ( 203 FDA reports)
HYPONATRAEMIA ( 203 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 203 FDA reports)
DIVERTICULUM ( 202 FDA reports)
HEART RATE IRREGULAR ( 199 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 199 FDA reports)
PULMONARY CONGESTION ( 199 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 199 FDA reports)
GASTRITIS ( 198 FDA reports)
OSTEOPENIA ( 198 FDA reports)
ANGINA PECTORIS ( 197 FDA reports)
POLLAKIURIA ( 197 FDA reports)
GLAUCOMA ( 196 FDA reports)
HOT FLUSH ( 195 FDA reports)
HYPERGLYCAEMIA ( 194 FDA reports)
RENAL FAILURE CHRONIC ( 194 FDA reports)
SLEEP DISORDER ( 194 FDA reports)
HAEMATURIA ( 192 FDA reports)
LETHARGY ( 191 FDA reports)
PANCREATITIS ( 191 FDA reports)
TOOTH DISORDER ( 190 FDA reports)
TYPE 2 DIABETES MELLITUS ( 189 FDA reports)
VIRAL INFECTION ( 188 FDA reports)
INJECTION SITE PAIN ( 187 FDA reports)
IRRITABILITY ( 187 FDA reports)
STAPHYLOCOCCAL INFECTION ( 185 FDA reports)
ROTATOR CUFF SYNDROME ( 184 FDA reports)
SCAR ( 184 FDA reports)
SINUS TACHYCARDIA ( 184 FDA reports)
BRONCHOSPASM ( 184 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 184 FDA reports)
CARDIAC FAILURE ( 182 FDA reports)
EXOSTOSIS ( 182 FDA reports)
EYE DISORDER ( 181 FDA reports)
EYE PAIN ( 181 FDA reports)
FEELING JITTERY ( 180 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 179 FDA reports)
MOBILITY DECREASED ( 179 FDA reports)
NEUTROPENIA ( 179 FDA reports)
RESPIRATORY ARREST ( 178 FDA reports)
PHARYNGEAL OEDEMA ( 177 FDA reports)
DISTURBANCE IN ATTENTION ( 177 FDA reports)
DRUG EFFECT DECREASED ( 175 FDA reports)
DEFORMITY ( 174 FDA reports)
AGGRESSION ( 173 FDA reports)
BLOOD PRESSURE DECREASED ( 173 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 172 FDA reports)
DECREASED INTEREST ( 171 FDA reports)
FEAR ( 171 FDA reports)
SINUS DISORDER ( 171 FDA reports)
ARRHYTHMIA ( 169 FDA reports)
FLATULENCE ( 169 FDA reports)
PANIC ATTACK ( 168 FDA reports)
HYPOTHYROIDISM ( 167 FDA reports)
RECTAL HAEMORRHAGE ( 167 FDA reports)
INHALATION THERAPY ( 166 FDA reports)
RESPIRATORY TRACT INFECTION ( 165 FDA reports)
HEPATIC ENZYME INCREASED ( 164 FDA reports)
PANCYTOPENIA ( 164 FDA reports)
LEUKOCYTOSIS ( 163 FDA reports)
MOUTH ULCERATION ( 163 FDA reports)
HYPOPHAGIA ( 162 FDA reports)
RHEUMATOID ARTHRITIS ( 162 FDA reports)
SKIN LESION ( 160 FDA reports)
FEELING HOT ( 160 FDA reports)
FLUID RETENTION ( 160 FDA reports)
HAEMORRHOIDS ( 159 FDA reports)
METASTASES TO BONE ( 159 FDA reports)
PULMONARY FIBROSIS ( 159 FDA reports)
DISEASE PROGRESSION ( 157 FDA reports)
HAEMATOCRIT DECREASED ( 157 FDA reports)
PHARYNGITIS ( 156 FDA reports)
NEOPLASM MALIGNANT ( 155 FDA reports)
BRADYCARDIA ( 154 FDA reports)
FUNGAL INFECTION ( 154 FDA reports)
APHASIA ( 153 FDA reports)
AGEUSIA ( 152 FDA reports)
INFLAMMATION ( 152 FDA reports)
URINARY RETENTION ( 151 FDA reports)
LUNG INFILTRATION ( 150 FDA reports)
MULTIPLE INJURIES ( 150 FDA reports)
DIPLOPIA ( 149 FDA reports)
HIP FRACTURE ( 149 FDA reports)
OFF LABEL USE ( 149 FDA reports)
ARTERIOSCLEROSIS ( 148 FDA reports)
DYSARTHRIA ( 148 FDA reports)
FEMUR FRACTURE ( 146 FDA reports)
UNEVALUABLE EVENT ( 146 FDA reports)
ROAD TRAFFIC ACCIDENT ( 145 FDA reports)
URINARY INCONTINENCE ( 145 FDA reports)
ANOREXIA ( 145 FDA reports)
BLOOD POTASSIUM DECREASED ( 145 FDA reports)
COLONIC POLYP ( 145 FDA reports)
RENAL CYST ( 143 FDA reports)
PLATELET COUNT DECREASED ( 142 FDA reports)
SKIN DISCOLOURATION ( 142 FDA reports)
TINNITUS ( 141 FDA reports)
CARDIOMYOPATHY ( 141 FDA reports)
HYPOGLYCAEMIA ( 141 FDA reports)
SURGERY ( 140 FDA reports)
CARDIAC MURMUR ( 139 FDA reports)
ABNORMAL BEHAVIOUR ( 138 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 137 FDA reports)
DISORIENTATION ( 137 FDA reports)
DRY THROAT ( 137 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 137 FDA reports)
ANGER ( 136 FDA reports)
HAEMATOMA ( 136 FDA reports)
RESTLESS LEGS SYNDROME ( 136 FDA reports)
RETCHING ( 135 FDA reports)
HEPATIC STEATOSIS ( 135 FDA reports)
DRY EYE ( 134 FDA reports)
EMOTIONAL DISORDER ( 134 FDA reports)
ACUTE RESPIRATORY FAILURE ( 133 FDA reports)
INTERSTITIAL LUNG DISEASE ( 133 FDA reports)
ADVERSE DRUG REACTION ( 132 FDA reports)
NIGHTMARE ( 132 FDA reports)
FOOT FRACTURE ( 131 FDA reports)
TOOTH FRACTURE ( 131 FDA reports)
GASTROINTESTINAL DISORDER ( 130 FDA reports)
HOARSENESS ( 129 FDA reports)
TOOTH LOSS ( 128 FDA reports)
SCOLIOSIS ( 126 FDA reports)
BLINDNESS ( 126 FDA reports)
EAR PAIN ( 126 FDA reports)
GOUT ( 126 FDA reports)
OESOPHAGITIS ( 126 FDA reports)
COMPRESSION FRACTURE ( 125 FDA reports)
DYSKINESIA ( 125 FDA reports)
LIP SWELLING ( 125 FDA reports)
ORAL DISORDER ( 125 FDA reports)
RESTLESSNESS ( 125 FDA reports)
SUICIDE ATTEMPT ( 124 FDA reports)
BONE LESION ( 124 FDA reports)
INCORRECT DOSE ADMINISTERED ( 124 FDA reports)
PERICARDIAL EFFUSION ( 124 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 123 FDA reports)
EXPIRED DRUG ADMINISTERED ( 122 FDA reports)
HYPERCHOLESTEROLAEMIA ( 120 FDA reports)
TOOTH ABSCESS ( 120 FDA reports)
SPINAL COLUMN STENOSIS ( 119 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 119 FDA reports)
BLOOD GLUCOSE DECREASED ( 118 FDA reports)
DEPRESSED MOOD ( 118 FDA reports)
SPINAL COMPRESSION FRACTURE ( 118 FDA reports)
VISUAL DISTURBANCE ( 118 FDA reports)
MOOD SWINGS ( 117 FDA reports)
OBESITY ( 117 FDA reports)
CRYING ( 116 FDA reports)
GASTRIC DISORDER ( 115 FDA reports)
IRRITABLE BOWEL SYNDROME ( 115 FDA reports)
MACULAR DEGENERATION ( 115 FDA reports)
ORAL DISCOMFORT ( 115 FDA reports)
PRIMARY SEQUESTRUM ( 115 FDA reports)
RASH PRURITIC ( 114 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 114 FDA reports)
MIDDLE INSOMNIA ( 114 FDA reports)
DRY SKIN ( 113 FDA reports)
HEAD INJURY ( 112 FDA reports)
PNEUMOTHORAX ( 112 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 112 FDA reports)
VENTRICULAR TACHYCARDIA ( 111 FDA reports)
JOINT STIFFNESS ( 111 FDA reports)
FIBROMYALGIA ( 110 FDA reports)
NOCTURIA ( 109 FDA reports)
SKIN EXFOLIATION ( 109 FDA reports)
SKIN ULCER ( 109 FDA reports)
HEPATIC FAILURE ( 108 FDA reports)
DEAFNESS ( 107 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 107 FDA reports)
HYPERSOMNIA ( 107 FDA reports)
PRESYNCOPE ( 107 FDA reports)
RENAL IMPAIRMENT ( 107 FDA reports)
RENAL DISORDER ( 106 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 106 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 106 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 105 FDA reports)
CYSTITIS ( 105 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 105 FDA reports)
DIVERTICULITIS ( 105 FDA reports)
INJECTION SITE ERYTHEMA ( 105 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 105 FDA reports)
LACRIMATION INCREASED ( 104 FDA reports)
CYST ( 103 FDA reports)
FEBRILE NEUTROPENIA ( 103 FDA reports)
HYPERKALAEMIA ( 103 FDA reports)
LOBAR PNEUMONIA ( 103 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 103 FDA reports)
AORTIC VALVE INCOMPETENCE ( 102 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 102 FDA reports)
BONE DEBRIDEMENT ( 102 FDA reports)
HYPOAESTHESIA ORAL ( 102 FDA reports)
PHYSICAL DISABILITY ( 102 FDA reports)
SPUTUM DISCOLOURED ( 102 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 101 FDA reports)
TENDERNESS ( 101 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 101 FDA reports)
BLISTER ( 100 FDA reports)
MULTIPLE MYELOMA ( 100 FDA reports)
RHINITIS ALLERGIC ( 100 FDA reports)
TENDON RUPTURE ( 100 FDA reports)
BONE DENSITY DECREASED ( 99 FDA reports)
HAEMATOCHEZIA ( 99 FDA reports)
NIGHT SWEATS ( 99 FDA reports)
CORONARY ARTERY OCCLUSION ( 98 FDA reports)
LIVER DISORDER ( 98 FDA reports)
LOCAL SWELLING ( 98 FDA reports)
BREAST CANCER ( 97 FDA reports)
BURSITIS ( 97 FDA reports)
MULTI-ORGAN FAILURE ( 97 FDA reports)
MYOCARDIAL ISCHAEMIA ( 97 FDA reports)
PRURITUS GENERALISED ( 97 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 96 FDA reports)
EJECTION FRACTION DECREASED ( 96 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 96 FDA reports)
DYSSTASIA ( 95 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 95 FDA reports)
CEREBRAL ATROPHY ( 94 FDA reports)
DISABILITY ( 94 FDA reports)
HEPATIC CYST ( 94 FDA reports)
BLOOD SODIUM DECREASED ( 93 FDA reports)
COLITIS ( 93 FDA reports)
HEART RATE DECREASED ( 93 FDA reports)
RHABDOMYOLYSIS ( 93 FDA reports)
SEPTIC SHOCK ( 92 FDA reports)
COGNITIVE DISORDER ( 92 FDA reports)
FRACTURE ( 92 FDA reports)
INJECTION SITE HAEMATOMA ( 92 FDA reports)
MOVEMENT DISORDER ( 92 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 92 FDA reports)
ANOSMIA ( 91 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 91 FDA reports)
IMPAIRED WORK ABILITY ( 91 FDA reports)
RASH GENERALISED ( 90 FDA reports)
TOOTH INFECTION ( 90 FDA reports)
BRONCHIECTASIS ( 89 FDA reports)
CHOLECYSTITIS ( 89 FDA reports)
CYANOSIS ( 89 FDA reports)
JOINT INJURY ( 89 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 89 FDA reports)
ORAL INFECTION ( 89 FDA reports)
BIPOLAR DISORDER ( 88 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 88 FDA reports)
RHINITIS ( 88 FDA reports)
UNRESPONSIVE TO STIMULI ( 88 FDA reports)
PNEUMONITIS ( 87 FDA reports)
RESPIRATORY TRACT CONGESTION ( 87 FDA reports)
EATING DISORDER ( 87 FDA reports)
BACK DISORDER ( 86 FDA reports)
EXPOSED BONE IN JAW ( 86 FDA reports)
EYE SWELLING ( 86 FDA reports)
FACIAL PAIN ( 86 FDA reports)
GINGIVAL PAIN ( 86 FDA reports)
TONGUE DISORDER ( 86 FDA reports)
RASH ERYTHEMATOUS ( 85 FDA reports)
AORTIC ANEURYSM ( 85 FDA reports)
ATRIAL FLUTTER ( 85 FDA reports)
CIRCULATORY COLLAPSE ( 84 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 84 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 84 FDA reports)
PLEURITIC PAIN ( 83 FDA reports)
SENSATION OF FOREIGN BODY ( 83 FDA reports)
STATUS ASTHMATICUS ( 83 FDA reports)
DYSLIPIDAEMIA ( 83 FDA reports)
INCREASED APPETITE ( 83 FDA reports)
MENISCUS LESION ( 83 FDA reports)
NEURALGIA ( 83 FDA reports)
ACUTE SINUSITIS ( 82 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 82 FDA reports)
DIASTOLIC DYSFUNCTION ( 82 FDA reports)
ERECTILE DYSFUNCTION ( 82 FDA reports)
GINGIVAL BLEEDING ( 82 FDA reports)
HOSPITALISATION ( 82 FDA reports)
SINUS CONGESTION ( 82 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 81 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 81 FDA reports)
CHOLECYSTECTOMY ( 81 FDA reports)
DRUG INTOLERANCE ( 81 FDA reports)
FEELING COLD ( 81 FDA reports)
ORAL FUNGAL INFECTION ( 81 FDA reports)
ENDODONTIC PROCEDURE ( 80 FDA reports)
UPPER LIMB FRACTURE ( 80 FDA reports)
PNEUMONIA ASPIRATION ( 79 FDA reports)
VENTRICULAR FIBRILLATION ( 79 FDA reports)
ANAPHYLACTIC SHOCK ( 79 FDA reports)
BLOOD UREA INCREASED ( 79 FDA reports)
EYE IRRITATION ( 79 FDA reports)
GASTRIC ULCER ( 79 FDA reports)
GASTROENTERITIS ( 79 FDA reports)
INJECTION SITE HAEMORRHAGE ( 79 FDA reports)
LUNG HYPERINFLATION ( 79 FDA reports)
MALNUTRITION ( 79 FDA reports)
OCULAR HYPERAEMIA ( 79 FDA reports)
ORTHOPNOEA ( 79 FDA reports)
ACCIDENTAL OVERDOSE ( 78 FDA reports)
NERVOUS SYSTEM DISORDER ( 78 FDA reports)
SKIN DISORDER ( 78 FDA reports)
SKIN LACERATION ( 78 FDA reports)
BREATH SOUNDS ABNORMAL ( 77 FDA reports)
CHRONIC SINUSITIS ( 77 FDA reports)
COAGULOPATHY ( 77 FDA reports)
DIVERTICULUM INTESTINAL ( 77 FDA reports)
LEFT ATRIAL DILATATION ( 77 FDA reports)
LIMB INJURY ( 77 FDA reports)
BLOOD BILIRUBIN INCREASED ( 76 FDA reports)
BLOOD CALCIUM DECREASED ( 76 FDA reports)
INTESTINAL OBSTRUCTION ( 76 FDA reports)
STOMACH DISCOMFORT ( 76 FDA reports)
SPINAL FRACTURE ( 75 FDA reports)
THYROID DISORDER ( 75 FDA reports)
COMA ( 75 FDA reports)
FLANK PAIN ( 75 FDA reports)
HEMIPARESIS ( 75 FDA reports)
LOCALISED INFECTION ( 75 FDA reports)
ABSCESS ( 74 FDA reports)
ENCEPHALOPATHY ( 74 FDA reports)
GRAND MAL CONVULSION ( 74 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 74 FDA reports)
INTENTIONAL DRUG MISUSE ( 74 FDA reports)
MASTICATION DISORDER ( 74 FDA reports)
PULMONARY MASS ( 74 FDA reports)
SCIATICA ( 74 FDA reports)
STRESS FRACTURE ( 74 FDA reports)
TENDONITIS ( 74 FDA reports)
VENTRICULAR HYPERTROPHY ( 74 FDA reports)
BODY TEMPERATURE INCREASED ( 73 FDA reports)
IRON DEFICIENCY ANAEMIA ( 73 FDA reports)
KYPHOSIS ( 73 FDA reports)
PALLOR ( 73 FDA reports)
HYPERKERATOSIS ( 72 FDA reports)
MENTAL IMPAIRMENT ( 72 FDA reports)
NON-CARDIAC CHEST PAIN ( 72 FDA reports)
PANCREATITIS ACUTE ( 72 FDA reports)
PSYCHOTIC DISORDER ( 72 FDA reports)
SPLENOMEGALY ( 72 FDA reports)
SINUS BRADYCARDIA ( 71 FDA reports)
CARPAL TUNNEL SYNDROME ( 71 FDA reports)
HEPATITIS ( 71 FDA reports)
HEPATOMEGALY ( 71 FDA reports)
ASCITES ( 70 FDA reports)
LEUKOPENIA ( 70 FDA reports)
LUMBAR SPINAL STENOSIS ( 70 FDA reports)
RADICULOPATHY ( 70 FDA reports)
SNEEZING ( 70 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 70 FDA reports)
PLEURISY ( 69 FDA reports)
BILIARY DYSKINESIA ( 69 FDA reports)
BREAST MASS ( 69 FDA reports)
PERIODONTAL DISEASE ( 69 FDA reports)
ABDOMINAL PAIN LOWER ( 68 FDA reports)
FLUID OVERLOAD ( 68 FDA reports)
HYPERCALCAEMIA ( 68 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 68 FDA reports)
MASS ( 68 FDA reports)
ASPIRATION ( 67 FDA reports)
CAROTID ARTERY STENOSIS ( 67 FDA reports)
DILATATION VENTRICULAR ( 67 FDA reports)
GINGIVAL SWELLING ( 67 FDA reports)
METASTASES TO SPINE ( 67 FDA reports)
RESPIRATORY RATE INCREASED ( 67 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 67 FDA reports)
TONGUE DISCOLOURATION ( 67 FDA reports)
VOCAL CORD DISORDER ( 66 FDA reports)
ANGINA UNSTABLE ( 66 FDA reports)
BEDRIDDEN ( 66 FDA reports)
EAR INFECTION ( 66 FDA reports)
LIFE EXPECTANCY SHORTENED ( 66 FDA reports)
MUSCLE TIGHTNESS ( 66 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 65 FDA reports)
COLD SWEAT ( 65 FDA reports)
FISTULA ( 65 FDA reports)
RASH MACULAR ( 65 FDA reports)
SKIN TIGHTNESS ( 65 FDA reports)
PROTHROMBIN TIME PROLONGED ( 64 FDA reports)
GASTROENTERITIS VIRAL ( 64 FDA reports)
LACERATION ( 64 FDA reports)
OSTEOSCLEROSIS ( 64 FDA reports)
PARAESTHESIA ORAL ( 64 FDA reports)
CHOLECYSTITIS ACUTE ( 63 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 63 FDA reports)
DEMENTIA ( 63 FDA reports)
ECCHYMOSIS ( 63 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 63 FDA reports)
INFUSION RELATED REACTION ( 63 FDA reports)
RALES ( 63 FDA reports)
TARDIVE DYSKINESIA ( 63 FDA reports)
THINKING ABNORMAL ( 63 FDA reports)
WRIST FRACTURE ( 63 FDA reports)
POST PROCEDURAL COMPLICATION ( 62 FDA reports)
BLOOD CALCIUM INCREASED ( 62 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 62 FDA reports)
EYE PRURITUS ( 62 FDA reports)
ACNE ( 61 FDA reports)
BLADDER DISORDER ( 61 FDA reports)
ECZEMA ( 61 FDA reports)
METABOLIC ACIDOSIS ( 61 FDA reports)
PATHOLOGICAL FRACTURE ( 61 FDA reports)
SEDATION ( 61 FDA reports)
WOUND ( 61 FDA reports)
POLYNEUROPATHY ( 60 FDA reports)
PROSTATE CANCER ( 60 FDA reports)
SICK SINUS SYNDROME ( 60 FDA reports)
FOOT DEFORMITY ( 60 FDA reports)
KNEE ARTHROPLASTY ( 60 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 59 FDA reports)
CATARACT OPERATION ( 59 FDA reports)
CHEST X-RAY ABNORMAL ( 59 FDA reports)
DIABETIC NEUROPATHY ( 59 FDA reports)
FAMILY STRESS ( 59 FDA reports)
INTERMITTENT CLAUDICATION ( 59 FDA reports)
JAUNDICE ( 59 FDA reports)
JOINT EFFUSION ( 59 FDA reports)
LOOSE TOOTH ( 59 FDA reports)
MYOPATHY ( 59 FDA reports)
SKIN ATROPHY ( 59 FDA reports)
UROSEPSIS ( 59 FDA reports)
POOR QUALITY SLEEP ( 58 FDA reports)
RENAL INJURY ( 58 FDA reports)
SINUS HEADACHE ( 58 FDA reports)
ULCER ( 58 FDA reports)
WALKING AID USER ( 58 FDA reports)
CARDIOVASCULAR DISORDER ( 58 FDA reports)
DEVICE RELATED INFECTION ( 58 FDA reports)
DYSPNOEA EXACERBATED ( 58 FDA reports)
GINGIVAL INFECTION ( 58 FDA reports)
GLOSSITIS ( 58 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 58 FDA reports)
MOOD ALTERED ( 58 FDA reports)
MUSCLE ATROPHY ( 58 FDA reports)
MUSCLE STRAIN ( 58 FDA reports)
MUSCLE TWITCHING ( 58 FDA reports)
NODULE ( 58 FDA reports)
ABDOMINAL TENDERNESS ( 57 FDA reports)
ADRENAL INSUFFICIENCY ( 57 FDA reports)
EYE HAEMORRHAGE ( 57 FDA reports)
HEPATITIS C ( 57 FDA reports)
INCONTINENCE ( 57 FDA reports)
PERIPHERAL COLDNESS ( 57 FDA reports)
ATAXIA ( 56 FDA reports)
BREAST PAIN ( 56 FDA reports)
COORDINATION ABNORMAL ( 56 FDA reports)
HYPOCALCAEMIA ( 56 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 56 FDA reports)
LYMPHOMA ( 56 FDA reports)
PELVIC PAIN ( 56 FDA reports)
PEPTIC ULCER ( 56 FDA reports)
PSORIASIS ( 56 FDA reports)
PHOTOSENSITIVITY REACTION ( 55 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 55 FDA reports)
SENSORY DISTURBANCE ( 55 FDA reports)
SKIN HYPERTROPHY ( 55 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 55 FDA reports)
BACTERIAL INFECTION ( 55 FDA reports)
BLOOD POTASSIUM INCREASED ( 55 FDA reports)
BRONCHITIS CHRONIC ( 55 FDA reports)
DRUG DEPENDENCE ( 55 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 55 FDA reports)
INTENTIONAL OVERDOSE ( 55 FDA reports)
METASTASES TO LIVER ( 55 FDA reports)
BARRETT'S OESOPHAGUS ( 54 FDA reports)
CROHN'S DISEASE ( 54 FDA reports)
MUCOSAL INFLAMMATION ( 54 FDA reports)
PHLEBITIS ( 54 FDA reports)
SECRETION DISCHARGE ( 54 FDA reports)
SKIN INDURATION ( 54 FDA reports)
TIBIA FRACTURE ( 54 FDA reports)
SNORING ( 53 FDA reports)
TACHYPNOEA ( 53 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 53 FDA reports)
ANGIOEDEMA ( 53 FDA reports)
DERMATITIS CONTACT ( 53 FDA reports)
DRUG TOXICITY ( 53 FDA reports)
EXTRASYSTOLES ( 53 FDA reports)
GINGIVAL DISORDER ( 53 FDA reports)
HEPATIC CIRRHOSIS ( 53 FDA reports)
INCREASED TENDENCY TO BRUISE ( 53 FDA reports)
BONE LOSS ( 52 FDA reports)
CARDIAC VALVE DISEASE ( 52 FDA reports)
CEREBROVASCULAR DISORDER ( 52 FDA reports)
DEVICE MALFUNCTION ( 52 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 52 FDA reports)
LOW TURNOVER OSTEOPATHY ( 52 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 52 FDA reports)
MELAENA ( 52 FDA reports)
MOUTH HAEMORRHAGE ( 52 FDA reports)
PURULENT DISCHARGE ( 52 FDA reports)
SARCOIDOSIS ( 52 FDA reports)
THROMBOCYTOSIS ( 51 FDA reports)
BODY HEIGHT DECREASED ( 51 FDA reports)
HYPOMAGNESAEMIA ( 51 FDA reports)
ILEUS ( 51 FDA reports)
JAW DISORDER ( 51 FDA reports)
LIMB DISCOMFORT ( 51 FDA reports)
LYMPHOEDEMA ( 51 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 51 FDA reports)
MEDICATION RESIDUE ( 51 FDA reports)
MUSCLE CRAMP ( 51 FDA reports)
NO THERAPEUTIC RESPONSE ( 51 FDA reports)
OEDEMA MOUTH ( 51 FDA reports)
BACTERAEMIA ( 50 FDA reports)
BLOOD MAGNESIUM DECREASED ( 50 FDA reports)
CEREBRAL ISCHAEMIA ( 50 FDA reports)
CHOKING SENSATION ( 50 FDA reports)
DILATATION ATRIAL ( 50 FDA reports)
DISEASE RECURRENCE ( 50 FDA reports)
FAILURE TO THRIVE ( 50 FDA reports)
FIBROSIS ( 50 FDA reports)
GINGIVITIS ( 50 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 50 FDA reports)
INJECTION SITE SWELLING ( 50 FDA reports)
LIPOMA ( 50 FDA reports)
METASTATIC NEOPLASM ( 50 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 50 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 50 FDA reports)
PREGNANCY ( 49 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 49 FDA reports)
RASH PAPULAR ( 49 FDA reports)
VASCULITIS ( 49 FDA reports)
WITHDRAWAL SYNDROME ( 49 FDA reports)
AORTIC CALCIFICATION ( 49 FDA reports)
EOSINOPHILIA ( 49 FDA reports)
GOITRE ( 49 FDA reports)
HILAR LYMPHADENOPATHY ( 49 FDA reports)
HIP ARTHROPLASTY ( 49 FDA reports)
HYPERCAPNIA ( 49 FDA reports)
JOINT DISLOCATION ( 49 FDA reports)
LIGAMENT SPRAIN ( 49 FDA reports)
ABDOMINAL HERNIA ( 48 FDA reports)
ABORTION SPONTANEOUS ( 48 FDA reports)
ANOXIC ENCEPHALOPATHY ( 48 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 48 FDA reports)
COLLAPSE OF LUNG ( 48 FDA reports)
DERMAL CYST ( 48 FDA reports)
FOREIGN BODY ( 48 FDA reports)
KIDNEY INFECTION ( 48 FDA reports)
NASAL DISCOMFORT ( 48 FDA reports)
SOCIAL PROBLEM ( 48 FDA reports)
SPINAL FUSION SURGERY ( 48 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 48 FDA reports)
VIITH NERVE PARALYSIS ( 48 FDA reports)
RENAL ATROPHY ( 47 FDA reports)
RIGHT ATRIAL DILATATION ( 47 FDA reports)
APHAGIA ( 47 FDA reports)
DECREASED ACTIVITY ( 47 FDA reports)
ELECTROLYTE IMBALANCE ( 47 FDA reports)
EXERCISE TOLERANCE DECREASED ( 47 FDA reports)
EYE DISCHARGE ( 47 FDA reports)
FAECAL INCONTINENCE ( 47 FDA reports)
HYPERMETROPIA ( 47 FDA reports)
LABORATORY TEST ABNORMAL ( 47 FDA reports)
METASTASES TO LUNG ( 47 FDA reports)
MICTURITION URGENCY ( 47 FDA reports)
BLOOD URINE PRESENT ( 46 FDA reports)
CARDIAC FLUTTER ( 46 FDA reports)
CEREBRAL INFARCTION ( 46 FDA reports)
CHROMATURIA ( 46 FDA reports)
FIBULA FRACTURE ( 46 FDA reports)
MYELOMA RECURRENCE ( 46 FDA reports)
ORTHOSTATIC HYPOTENSION ( 46 FDA reports)
PHOTOPHOBIA ( 46 FDA reports)
PLEURAL FIBROSIS ( 46 FDA reports)
RENAL PAIN ( 46 FDA reports)
SYNOVIAL CYST ( 46 FDA reports)
VITAMIN D DEFICIENCY ( 46 FDA reports)
VITREOUS FLOATERS ( 46 FDA reports)
QUALITY OF LIFE DECREASED ( 45 FDA reports)
SENSORY LOSS ( 45 FDA reports)
STENT PLACEMENT ( 45 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 45 FDA reports)
THERMAL BURN ( 45 FDA reports)
BLOOD CHLORIDE DECREASED ( 45 FDA reports)
GENERALISED OEDEMA ( 45 FDA reports)
HAEMATEMESIS ( 45 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 45 FDA reports)
HUNGER ( 45 FDA reports)
HYPOVOLAEMIA ( 45 FDA reports)
ANKLE FRACTURE ( 44 FDA reports)
ASTIGMATISM ( 44 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 44 FDA reports)
CERVICAL SPINAL STENOSIS ( 44 FDA reports)
DECUBITUS ULCER ( 44 FDA reports)
EXCORIATION ( 44 FDA reports)
HAND FRACTURE ( 44 FDA reports)
HERPES VIRUS INFECTION ( 44 FDA reports)
HYDRONEPHROSIS ( 44 FDA reports)
MANIA ( 44 FDA reports)
OROPHARYNGEAL BLISTERING ( 44 FDA reports)
PERONEAL NERVE PALSY ( 44 FDA reports)
RESPIRATION ABNORMAL ( 44 FDA reports)
VAGINAL HAEMORRHAGE ( 44 FDA reports)
SKIN HYPERPIGMENTATION ( 43 FDA reports)
SPONDYLOLISTHESIS ( 43 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 43 FDA reports)
UNDERDOSE ( 43 FDA reports)
VENTRICULAR HYPOKINESIA ( 43 FDA reports)
CARDIAC PACEMAKER INSERTION ( 43 FDA reports)
DEVICE FAILURE ( 43 FDA reports)
DRUG ABUSE ( 43 FDA reports)
HALLUCINATION, VISUAL ( 43 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 43 FDA reports)
LARYNGEAL OEDEMA ( 43 FDA reports)
PERSONALITY CHANGE ( 43 FDA reports)
BLEPHARITIS ( 42 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 42 FDA reports)
EMPYEMA ( 42 FDA reports)
GRANULOMA ( 42 FDA reports)
HERPES SIMPLEX ( 42 FDA reports)
MULTIPLE SCLEROSIS ( 42 FDA reports)
PHARYNGEAL DISORDER ( 42 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 42 FDA reports)
SUFFOCATION FEELING ( 42 FDA reports)
THIRST ( 42 FDA reports)
TOBACCO USER ( 42 FDA reports)
TOOTH DISCOLOURATION ( 42 FDA reports)
SINUS OPERATION ( 41 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 41 FDA reports)
ABNORMAL SENSATION IN EYE ( 41 FDA reports)
BLINDNESS TRANSIENT ( 41 FDA reports)
DEBRIDEMENT ( 41 FDA reports)
DENTAL FISTULA ( 41 FDA reports)
EAR DISCOMFORT ( 41 FDA reports)
HEARING IMPAIRED ( 41 FDA reports)
HEPATIC LESION ( 41 FDA reports)
INTRAOCULAR LENS IMPLANT ( 41 FDA reports)
JOINT CONTRACTURE ( 41 FDA reports)
NERVE INJURY ( 41 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 41 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 41 FDA reports)
BLINDNESS UNILATERAL ( 40 FDA reports)
DELIRIUM ( 40 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 40 FDA reports)
GASTRIC HAEMORRHAGE ( 40 FDA reports)
GROIN PAIN ( 40 FDA reports)
JAW FRACTURE ( 40 FDA reports)
MYOCLONUS ( 40 FDA reports)
OSTEOLYSIS ( 40 FDA reports)
PELVIC FRACTURE ( 40 FDA reports)
PERIODONTITIS ( 40 FDA reports)
PLATELET COUNT INCREASED ( 40 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 40 FDA reports)
POSTNASAL DRIP ( 40 FDA reports)
PULMONARY HAEMORRHAGE ( 40 FDA reports)
TRISMUS ( 40 FDA reports)
VARICOSE VEIN ( 40 FDA reports)
SEASONAL ALLERGY ( 39 FDA reports)
SUBCUTANEOUS ABSCESS ( 39 FDA reports)
TONGUE ULCERATION ( 39 FDA reports)
BASAL CELL CARCINOMA ( 39 FDA reports)
CORONARY ARTERY STENOSIS ( 39 FDA reports)
DRUG SCREEN POSITIVE ( 39 FDA reports)
HYPOACUSIS ( 39 FDA reports)
BLOOD ALBUMIN DECREASED ( 38 FDA reports)
CHAPPED LIPS ( 38 FDA reports)
COLITIS ULCERATIVE ( 38 FDA reports)
FAECES DISCOLOURED ( 38 FDA reports)
IMPAIRED DRIVING ABILITY ( 38 FDA reports)
INJECTION SITE REACTION ( 38 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 38 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 38 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 38 FDA reports)
OESOPHAGEAL DISORDER ( 38 FDA reports)
ORAL SURGERY ( 38 FDA reports)
PARANOIA ( 38 FDA reports)
PAROSMIA ( 38 FDA reports)
PERIPHERAL ISCHAEMIA ( 38 FDA reports)
PROTEINURIA ( 38 FDA reports)
PULMONARY GRANULOMA ( 38 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 38 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 38 FDA reports)
STEVENS-JOHNSON SYNDROME ( 38 FDA reports)
SUDDEN DEATH ( 38 FDA reports)
UTERINE DISORDER ( 38 FDA reports)
PROCEDURAL PAIN ( 37 FDA reports)
RESPIRATORY TRACT IRRITATION ( 37 FDA reports)
TENDON DISORDER ( 37 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 37 FDA reports)
ULCER HAEMORRHAGE ( 37 FDA reports)
URINE FLOW DECREASED ( 37 FDA reports)
VENOUS INSUFFICIENCY ( 37 FDA reports)
ATRIAL TACHYCARDIA ( 37 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 37 FDA reports)
CAROTID BRUIT ( 37 FDA reports)
DIFFICULTY IN WALKING ( 37 FDA reports)
HYPERAESTHESIA ( 37 FDA reports)
HYPOKINESIA ( 37 FDA reports)
IMMUNE SYSTEM DISORDER ( 37 FDA reports)
JOINT SPRAIN ( 37 FDA reports)
MEDICAL DEVICE COMPLICATION ( 37 FDA reports)
NEOPLASM PROGRESSION ( 37 FDA reports)
NO ADVERSE EVENT ( 37 FDA reports)
PARALYSIS ( 37 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 37 FDA reports)
ATRIAL SEPTAL DEFECT ( 36 FDA reports)
BLADDER CANCER ( 36 FDA reports)
BONE OPERATION ( 36 FDA reports)
BRONCHOPNEUMONIA ( 36 FDA reports)
CARDIAC ENZYMES INCREASED ( 36 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 36 FDA reports)
CONJUNCTIVITIS ( 36 FDA reports)
JAW OPERATION ( 36 FDA reports)
LIPASE INCREASED ( 36 FDA reports)
METASTASES TO LYMPH NODES ( 36 FDA reports)
NEUTROPHIL COUNT DECREASED ( 36 FDA reports)
PARKINSON'S DISEASE ( 36 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 36 FDA reports)
PULMONARY THROMBOSIS ( 36 FDA reports)
PULSE ABSENT ( 36 FDA reports)
RENAL MASS ( 36 FDA reports)
RIGHT VENTRICULAR FAILURE ( 36 FDA reports)
STEM CELL TRANSPLANT ( 36 FDA reports)
THROMBOPHLEBITIS ( 36 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 36 FDA reports)
POLYP ( 35 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 35 FDA reports)
PROTEIN URINE PRESENT ( 35 FDA reports)
SKIN BURNING SENSATION ( 35 FDA reports)
SKIN FIBROSIS ( 35 FDA reports)
SQUAMOUS CELL CARCINOMA ( 35 FDA reports)
TROPONIN INCREASED ( 35 FDA reports)
AORTIC STENOSIS ( 35 FDA reports)
BLOOD PRESSURE ABNORMAL ( 35 FDA reports)
CLOSTRIDIAL INFECTION ( 35 FDA reports)
COMPLETED SUICIDE ( 35 FDA reports)
COSTOCHONDRITIS ( 35 FDA reports)
DERMATITIS ( 35 FDA reports)
DYSTONIA ( 35 FDA reports)
FACIAL PALSY ( 35 FDA reports)
FRACTURE NONUNION ( 35 FDA reports)
GINGIVAL EROSION ( 35 FDA reports)
HERNIA ( 35 FDA reports)
HYPERVENTILATION ( 35 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 35 FDA reports)
INGUINAL HERNIA ( 35 FDA reports)
NASAL SEPTUM DEVIATION ( 35 FDA reports)
NERVE COMPRESSION ( 35 FDA reports)
ONYCHOMYCOSIS ( 35 FDA reports)
PANIC REACTION ( 35 FDA reports)
PHARYNGEAL ERYTHEMA ( 35 FDA reports)
CUSHING'S SYNDROME ( 34 FDA reports)
DENTURE WEARER ( 34 FDA reports)
ERUCTATION ( 34 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 34 FDA reports)
FACE OEDEMA ( 34 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 34 FDA reports)
LOWER LIMB FRACTURE ( 34 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 34 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 34 FDA reports)
NONSPECIFIC REACTION ( 34 FDA reports)
RECTAL POLYP ( 34 FDA reports)
REFLUX OESOPHAGITIS ( 34 FDA reports)
SENSATION OF HEAVINESS ( 34 FDA reports)
SKIN NECROSIS ( 34 FDA reports)
WHEELCHAIR USER ( 34 FDA reports)
PSEUDOMONAS INFECTION ( 33 FDA reports)
SEBORRHOEIC KERATOSIS ( 33 FDA reports)
SOFT TISSUE DISORDER ( 33 FDA reports)
THYROID NEOPLASM ( 33 FDA reports)
VITAMIN B12 DEFICIENCY ( 33 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 33 FDA reports)
ANEURYSM ( 33 FDA reports)
HYPERTENSIVE HEART DISEASE ( 33 FDA reports)
ISCHAEMIC STROKE ( 33 FDA reports)
ORAL INTAKE REDUCED ( 33 FDA reports)
OVARIAN CYST ( 33 FDA reports)
ACUTE CORONARY SYNDROME ( 32 FDA reports)
ALVEOLOPLASTY ( 32 FDA reports)
ASPERGILLOSIS ( 32 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 32 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 32 FDA reports)
BREAST CALCIFICATIONS ( 32 FDA reports)
DUODENITIS ( 32 FDA reports)
EYE INFECTION ( 32 FDA reports)
FACIAL BONES FRACTURE ( 32 FDA reports)
FURUNCLE ( 32 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 32 FDA reports)
INCREASED BRONCHIAL SECRETION ( 32 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 32 FDA reports)
MENSTRUATION IRREGULAR ( 32 FDA reports)
MYOSITIS ( 32 FDA reports)
PALATAL OEDEMA ( 32 FDA reports)
PROSTATOMEGALY ( 32 FDA reports)
RHONCHI ( 32 FDA reports)
SPINAL DISORDER ( 32 FDA reports)
TOOTH REPAIR ( 32 FDA reports)
URINE OUTPUT DECREASED ( 32 FDA reports)
WOUND DEHISCENCE ( 32 FDA reports)
PNEUMONIA BACTERIAL ( 31 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 31 FDA reports)
POLYPECTOMY ( 31 FDA reports)
RESORPTION BONE INCREASED ( 31 FDA reports)
RESPIRATORY DEPRESSION ( 31 FDA reports)
THYROID CANCER ( 31 FDA reports)
TONGUE BLISTERING ( 31 FDA reports)
VITAMIN D DECREASED ( 31 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 31 FDA reports)
ABSCESS DRAINAGE ( 31 FDA reports)
ADRENAL MASS ( 31 FDA reports)
BILE DUCT STENOSIS ( 31 FDA reports)
BREATH ODOUR ( 31 FDA reports)
CAESAREAN SECTION ( 31 FDA reports)
CATHETERISATION CARDIAC ( 31 FDA reports)
CHEILITIS ( 31 FDA reports)
COLITIS ISCHAEMIC ( 31 FDA reports)
COLON CANCER ( 31 FDA reports)
DELUSION ( 31 FDA reports)
DEVICE BREAKAGE ( 31 FDA reports)
DRUG DISPENSING ERROR ( 31 FDA reports)
DRUG PRESCRIBING ERROR ( 31 FDA reports)
FORMICATION ( 31 FDA reports)
INITIAL INSOMNIA ( 31 FDA reports)
KERATITIS ( 31 FDA reports)
MAJOR DEPRESSION ( 31 FDA reports)
MOTOR DYSFUNCTION ( 31 FDA reports)
MUSCLE INJURY ( 31 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 31 FDA reports)
ORAL MUCOSAL BLISTERING ( 31 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 30 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 30 FDA reports)
ASPIRATION PLEURAL CAVITY ( 30 FDA reports)
ATRIOVENTRICULAR BLOCK ( 30 FDA reports)
AZOTAEMIA ( 30 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 30 FDA reports)
BLOOD IRON DECREASED ( 30 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 30 FDA reports)
CERUMEN IMPACTION ( 30 FDA reports)
DIABETIC KETOACIDOSIS ( 30 FDA reports)
DRUG ABUSER ( 30 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 30 FDA reports)
GASTRIC POLYPS ( 30 FDA reports)
HERNIA REPAIR ( 30 FDA reports)
HICCUPS ( 30 FDA reports)
HYPERPLASIA ( 30 FDA reports)
INJECTION SITE PRURITUS ( 30 FDA reports)
MITRAL VALVE DISEASE ( 30 FDA reports)
MUSCULOSKELETAL DISORDER ( 30 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 30 FDA reports)
OSTEORADIONECROSIS ( 30 FDA reports)
PULMONARY INFARCTION ( 30 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 30 FDA reports)
PLASMACYTOSIS ( 29 FDA reports)
PRODUCT TASTE ABNORMAL ( 29 FDA reports)
RENAL TUBULAR NECROSIS ( 29 FDA reports)
SPUTUM INCREASED ( 29 FDA reports)
STRESS URINARY INCONTINENCE ( 29 FDA reports)
SYNOVITIS ( 29 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 29 FDA reports)
WEIGHT FLUCTUATION ( 29 FDA reports)
AMMONIA INCREASED ( 29 FDA reports)
ANGIOPATHY ( 29 FDA reports)
APNOEA ( 29 FDA reports)
APPARENT DEATH ( 29 FDA reports)
AUTOIMMUNE DISORDER ( 29 FDA reports)
BIOPSY ( 29 FDA reports)
CERVIX CARCINOMA ( 29 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 29 FDA reports)
EOSINOPHIL COUNT INCREASED ( 29 FDA reports)
EYELID PTOSIS ( 29 FDA reports)
HAEMANGIOMA ( 29 FDA reports)
HEMIPLEGIA ( 29 FDA reports)
HOMICIDAL IDEATION ( 29 FDA reports)
HYPOALBUMINAEMIA ( 29 FDA reports)
INTRACRANIAL ANEURYSM ( 29 FDA reports)
LIGAMENT RUPTURE ( 29 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 29 FDA reports)
MITRAL VALVE PROLAPSE ( 29 FDA reports)
NEUTROPHIL COUNT INCREASED ( 29 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 29 FDA reports)
ACIDOSIS ( 28 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 28 FDA reports)
AMENORRHOEA ( 28 FDA reports)
ANGIONEUROTIC OEDEMA ( 28 FDA reports)
AORTIC VALVE SCLEROSIS ( 28 FDA reports)
BACTERIAL DISEASE CARRIER ( 28 FDA reports)
BREAST CANCER RECURRENT ( 28 FDA reports)
BRUXISM ( 28 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 28 FDA reports)
COR PULMONALE ( 28 FDA reports)
DEAFNESS NEUROSENSORY ( 28 FDA reports)
DEVICE INEFFECTIVE ( 28 FDA reports)
ESSENTIAL HYPERTENSION ( 28 FDA reports)
EYELID OEDEMA ( 28 FDA reports)
FACET JOINT SYNDROME ( 28 FDA reports)
HYPERPHAGIA ( 28 FDA reports)
INCOHERENT ( 28 FDA reports)
LACUNAR INFARCTION ( 28 FDA reports)
LIBIDO DECREASED ( 28 FDA reports)
MELANOCYTIC NAEVUS ( 28 FDA reports)
OESOPHAGEAL STENOSIS ( 28 FDA reports)
PERITONITIS ( 28 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 28 FDA reports)
SMOKER ( 28 FDA reports)
THYROIDECTOMY ( 28 FDA reports)
TONGUE COATED ( 28 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 28 FDA reports)
VISUAL FIELD DEFECT ( 28 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 27 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 27 FDA reports)
TENSION ( 27 FDA reports)
THERAPY NON-RESPONDER ( 27 FDA reports)
VENOUS THROMBOSIS ( 27 FDA reports)
ACCIDENTAL EXPOSURE ( 27 FDA reports)
ACTINOMYCOSIS ( 27 FDA reports)
ACUTE PRERENAL FAILURE ( 27 FDA reports)
BIPOLAR I DISORDER ( 27 FDA reports)
BLOOD TEST ABNORMAL ( 27 FDA reports)
BONE EROSION ( 27 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 27 FDA reports)
CAROTID ARTERY DISEASE ( 27 FDA reports)
CERVICAL DYSPLASIA ( 27 FDA reports)
DRUG ERUPTION ( 27 FDA reports)
FRUSTRATION ( 27 FDA reports)
FUNGAL OESOPHAGITIS ( 27 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 27 FDA reports)
HEART RATE ABNORMAL ( 27 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 27 FDA reports)
ISCHAEMIA ( 27 FDA reports)
MALIGNANT MELANOMA ( 27 FDA reports)
MITRAL VALVE STENOSIS ( 27 FDA reports)
MYDRIASIS ( 27 FDA reports)
OCCULT BLOOD POSITIVE ( 27 FDA reports)
PAINFUL RESPIRATION ( 27 FDA reports)
PANCREATIC DISORDER ( 27 FDA reports)
ABSCESS ORAL ( 26 FDA reports)
BACTERIAL TEST POSITIVE ( 26 FDA reports)
BILIARY DILATATION ( 26 FDA reports)
COELIAC DISEASE ( 26 FDA reports)
DENTAL OPERATION ( 26 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 26 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 26 FDA reports)
EXOPHTHALMOS ( 26 FDA reports)
GINGIVAL RECESSION ( 26 FDA reports)
HORDEOLUM ( 26 FDA reports)
HYPERTHYROIDISM ( 26 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 26 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 26 FDA reports)
HYPOVENTILATION ( 26 FDA reports)
MAMMOPLASTY ( 26 FDA reports)
OROPHARYNGITIS FUNGAL ( 26 FDA reports)
OTORRHOEA ( 26 FDA reports)
PARAPLEGIA ( 26 FDA reports)
PROCEDURAL COMPLICATION ( 26 FDA reports)
RETINAL HAEMORRHAGE ( 26 FDA reports)
SHOULDER ARTHROPLASTY ( 26 FDA reports)
SINUS ARRHYTHMIA ( 26 FDA reports)
SKIN CANCER ( 26 FDA reports)
TYPE 1 DIABETES MELLITUS ( 26 FDA reports)
VULVOVAGINAL DRYNESS ( 26 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 25 FDA reports)
SENSITIVITY OF TEETH ( 25 FDA reports)
SKIN PAPILLOMA ( 25 FDA reports)
SUBDURAL HAEMATOMA ( 25 FDA reports)
TEMPERATURE INTOLERANCE ( 25 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 25 FDA reports)
ARTHROPOD BITE ( 25 FDA reports)
BACK INJURY ( 25 FDA reports)
BLOOD AMYLASE INCREASED ( 25 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 25 FDA reports)
BONE SCAN ABNORMAL ( 25 FDA reports)
BREAST CANCER METASTATIC ( 25 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 25 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 25 FDA reports)
EUPHORIC MOOD ( 25 FDA reports)
GINGIVAL ULCERATION ( 25 FDA reports)
HALLUCINATION, AUDITORY ( 25 FDA reports)
HEAD DISCOMFORT ( 25 FDA reports)
HEART INJURY ( 25 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 25 FDA reports)
INTRACARDIAC THROMBUS ( 25 FDA reports)
IRITIS ( 25 FDA reports)
MENOPAUSE ( 25 FDA reports)
METASTASIS ( 25 FDA reports)
MUCOUS MEMBRANE DISORDER ( 25 FDA reports)
NASAL ULCER ( 25 FDA reports)
NEOPLASM ( 25 FDA reports)
OTITIS MEDIA ( 25 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 24 FDA reports)
ANXIETY DISORDER ( 24 FDA reports)
BILIARY COLIC ( 24 FDA reports)
BRAIN NEOPLASM ( 24 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 24 FDA reports)
BRONCHIOLITIS ( 24 FDA reports)
CEREBRAL HAEMORRHAGE ( 24 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 24 FDA reports)
CRANIOTOMY ( 24 FDA reports)
CYSTOCELE ( 24 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 24 FDA reports)
HAEMODIALYSIS ( 24 FDA reports)
HUMERUS FRACTURE ( 24 FDA reports)
HYPERTONIC BLADDER ( 24 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 24 FDA reports)
INJECTION SITE BRUISING ( 24 FDA reports)
INJECTION SITE MASS ( 24 FDA reports)
LEUKOPLAKIA ORAL ( 24 FDA reports)
LIP DRY ( 24 FDA reports)
MULTIPLE ALLERGIES ( 24 FDA reports)
MYOPIA ( 24 FDA reports)
NAIL DISORDER ( 24 FDA reports)
OCULAR ICTERUS ( 24 FDA reports)
ORAL HERPES ( 24 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 24 FDA reports)
ORAL PRURITUS ( 24 FDA reports)
OXYGEN SUPPLEMENTATION ( 24 FDA reports)
PLANTAR FASCIITIS ( 24 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 24 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 24 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 24 FDA reports)
SHOCK ( 24 FDA reports)
SLUGGISHNESS ( 24 FDA reports)
THORACOTOMY ( 24 FDA reports)
TOOTH EROSION ( 24 FDA reports)
TRIGEMINAL NEURALGIA ( 24 FDA reports)
UMBILICAL HERNIA ( 24 FDA reports)
UTERINE LEIOMYOMA ( 24 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 23 FDA reports)
PRESCRIBED OVERDOSE ( 23 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 23 FDA reports)
RETINAL DETACHMENT ( 23 FDA reports)
SKIN HAEMORRHAGE ( 23 FDA reports)
SKIN IRRITATION ( 23 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 23 FDA reports)
APATHY ( 23 FDA reports)
ATRIAL THROMBOSIS ( 23 FDA reports)
BLOOD CREATININE DECREASED ( 23 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 23 FDA reports)
BODY TEMPERATURE DECREASED ( 23 FDA reports)
BREAST CANCER FEMALE ( 23 FDA reports)
CARBON DIOXIDE INCREASED ( 23 FDA reports)
CARDIAC OPERATION ( 23 FDA reports)
DROOLING ( 23 FDA reports)
ENURESIS ( 23 FDA reports)
EPIGASTRIC DISCOMFORT ( 23 FDA reports)
FACE INJURY ( 23 FDA reports)
HEPATITIS B ( 23 FDA reports)
HYPERCOAGULATION ( 23 FDA reports)
HYPOAESTHESIA FACIAL ( 23 FDA reports)
LICHEN PLANUS ( 23 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 23 FDA reports)
NASAL OEDEMA ( 23 FDA reports)
PANCREATITIS CHRONIC ( 23 FDA reports)
PERICARDITIS ( 23 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 22 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 22 FDA reports)
APPLICATION SITE PRURITUS ( 22 FDA reports)
APPLICATION SITE RASH ( 22 FDA reports)
ASTHENOPIA ( 22 FDA reports)
BONE FRAGMENTATION ( 22 FDA reports)
CARDIOGENIC SHOCK ( 22 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 22 FDA reports)
CEREBELLAR INFARCTION ( 22 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 22 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 22 FDA reports)
CREPITATIONS ( 22 FDA reports)
CYSTITIS INTERSTITIAL ( 22 FDA reports)
DEVELOPMENTAL DELAY ( 22 FDA reports)
DIZZINESS POSTURAL ( 22 FDA reports)
DYSTHYMIC DISORDER ( 22 FDA reports)
FOREIGN BODY ASPIRATION ( 22 FDA reports)
HYDROPNEUMOTHORAX ( 22 FDA reports)
IMPLANT SITE INFECTION ( 22 FDA reports)
KLEBSIELLA INFECTION ( 22 FDA reports)
LUNG OPERATION ( 22 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 22 FDA reports)
METASTATIC PAIN ( 22 FDA reports)
MITRAL VALVE CALCIFICATION ( 22 FDA reports)
NEUROPATHY ( 22 FDA reports)
NICOTINE DEPENDENCE ( 22 FDA reports)
OESOPHAGEAL PAIN ( 22 FDA reports)
OPTIC NERVE CUPPING ( 22 FDA reports)
PALATAL DISORDER ( 22 FDA reports)
PATHOLOGICAL GAMBLING ( 22 FDA reports)
PERSONALITY DISORDER ( 22 FDA reports)
PETECHIAE ( 22 FDA reports)
PRESBYOPIA ( 22 FDA reports)
PROCTALGIA ( 22 FDA reports)
PULPITIS DENTAL ( 22 FDA reports)
RECTAL PROLAPSE ( 22 FDA reports)
RECTOCELE ( 22 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 22 FDA reports)
SCAB ( 22 FDA reports)
SPINAL DEFORMITY ( 22 FDA reports)
TOOTH INJURY ( 22 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 22 FDA reports)
ROTATOR CUFF REPAIR ( 21 FDA reports)
SEPSIS SYNDROME ( 21 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 21 FDA reports)
STREPTOCOCCAL INFECTION ( 21 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 21 FDA reports)
TENDON PAIN ( 21 FDA reports)
URINE ABNORMALITY ( 21 FDA reports)
VASCULAR CALCIFICATION ( 21 FDA reports)
WOUND DRAINAGE ( 21 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 21 FDA reports)
APPLICATION SITE ERYTHEMA ( 21 FDA reports)
BONE SWELLING ( 21 FDA reports)
BOWEN'S DISEASE ( 21 FDA reports)
ENTEROCOCCAL INFECTION ( 21 FDA reports)
FEELING DRUNK ( 21 FDA reports)
FISTULA DISCHARGE ( 21 FDA reports)
GALLBLADDER OPERATION ( 21 FDA reports)
HELICOBACTER INFECTION ( 21 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 21 FDA reports)
HYDROCEPHALUS ( 21 FDA reports)
INTESTINAL PERFORATION ( 21 FDA reports)
LIP DISCOLOURATION ( 21 FDA reports)
LUNG CONSOLIDATION ( 21 FDA reports)
MUSCLE DISORDER ( 21 FDA reports)
NEURITIS ( 21 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 21 FDA reports)
OPEN REDUCTION OF FRACTURE ( 21 FDA reports)
OPEN WOUND ( 21 FDA reports)
ABNORMAL FAECES ( 20 FDA reports)
ACUTE STRESS DISORDER ( 20 FDA reports)
ADRENAL DISORDER ( 20 FDA reports)
APPENDICITIS ( 20 FDA reports)
BLOOD BLISTER ( 20 FDA reports)
BLOOD CORTISOL DECREASED ( 20 FDA reports)
BREAST LUMP REMOVAL ( 20 FDA reports)
BRONCHOPLEURAL FISTULA ( 20 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 20 FDA reports)
CUSHINGOID ( 20 FDA reports)
DIALYSIS ( 20 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 20 FDA reports)
EYE NAEVUS ( 20 FDA reports)
FAECALOMA ( 20 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 20 FDA reports)
GALLBLADDER INJURY ( 20 FDA reports)
GRIP STRENGTH DECREASED ( 20 FDA reports)
GUILLAIN-BARRE SYNDROME ( 20 FDA reports)
HEPATIC CONGESTION ( 20 FDA reports)
LYMPHOPENIA ( 20 FDA reports)
MENORRHAGIA ( 20 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 20 FDA reports)
METABOLIC ENCEPHALOPATHY ( 20 FDA reports)
NECK MASS ( 20 FDA reports)
NOCTURNAL DYSPNOEA ( 20 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 20 FDA reports)
OROPHARYNGEAL SWELLING ( 20 FDA reports)
OSTEOMYELITIS CHRONIC ( 20 FDA reports)
PAPILLOEDEMA ( 20 FDA reports)
PLASMACYTOMA ( 20 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 20 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 20 FDA reports)
RADIATION ASSOCIATED PAIN ( 20 FDA reports)
SCREAMING ( 20 FDA reports)
SELF-INJURIOUS IDEATION ( 20 FDA reports)
SEXUAL DYSFUNCTION ( 20 FDA reports)
SKELETAL INJURY ( 20 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 20 FDA reports)
TIC ( 20 FDA reports)
TOOTH IMPACTED ( 20 FDA reports)
TRANSAMINASES INCREASED ( 20 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 20 FDA reports)
VESICAL FISTULA ( 20 FDA reports)
POLYDIPSIA ( 19 FDA reports)
PRE-ECLAMPSIA ( 19 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 19 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 19 FDA reports)
RENAL CANCER ( 19 FDA reports)
TENOSYNOVITIS ( 19 FDA reports)
TONSILLAR DISORDER ( 19 FDA reports)
URINARY HESITATION ( 19 FDA reports)
VITREOUS DETACHMENT ( 19 FDA reports)
ADVERSE REACTION ( 19 FDA reports)
AFFECTIVE DISORDER ( 19 FDA reports)
ANAEMIA POSTOPERATIVE ( 19 FDA reports)
ARTHRITIS BACTERIAL ( 19 FDA reports)
BLADDER NEOPLASM ( 19 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 19 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 19 FDA reports)
CALCINOSIS ( 19 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 19 FDA reports)
CHANGE OF BOWEL HABIT ( 19 FDA reports)
CLUMSINESS ( 19 FDA reports)
CONCUSSION ( 19 FDA reports)
CONDUCTION DISORDER ( 19 FDA reports)
DIABETIC COMA ( 19 FDA reports)
EAR DISORDER ( 19 FDA reports)
FACIAL PARESIS ( 19 FDA reports)
GASTRITIS EROSIVE ( 19 FDA reports)
HAEMORRHAGIC ANAEMIA ( 19 FDA reports)
HEPATITIS ACUTE ( 19 FDA reports)
HORMONE LEVEL ABNORMAL ( 19 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 19 FDA reports)
IMMUNOSUPPRESSION ( 19 FDA reports)
INFARCTION ( 19 FDA reports)
LEG AMPUTATION ( 19 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 19 FDA reports)
LIPIDS INCREASED ( 19 FDA reports)
METABOLIC SYNDROME ( 19 FDA reports)
MICROCYTIC ANAEMIA ( 19 FDA reports)
MYELODYSPLASTIC SYNDROME ( 19 FDA reports)
NON-SMALL CELL LUNG CANCER ( 19 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 19 FDA reports)
ODYNOPHAGIA ( 19 FDA reports)
OPTIC NERVE DISORDER ( 19 FDA reports)
OSTEITIS DEFORMANS ( 19 FDA reports)
PERIORBITAL OEDEMA ( 19 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 18 FDA reports)
APHTHOUS STOMATITIS ( 18 FDA reports)
APLASIA PURE RED CELL ( 18 FDA reports)
ASPIRATION JOINT ( 18 FDA reports)
ASTERIXIS ( 18 FDA reports)
ATROPHY ( 18 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 18 FDA reports)
BLOOD PH DECREASED ( 18 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 18 FDA reports)
BONE MARROW FAILURE ( 18 FDA reports)
BREAKTHROUGH PAIN ( 18 FDA reports)
CHOLECYSTITIS INFECTIVE ( 18 FDA reports)
CORONARY ARTERY BYPASS ( 18 FDA reports)
DENTAL CARE ( 18 FDA reports)
DUODENAL ULCER ( 18 FDA reports)
DYSPLASIA ( 18 FDA reports)
EARLY SATIETY ( 18 FDA reports)
ESCHERICHIA INFECTION ( 18 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 18 FDA reports)
GENERALISED ANXIETY DISORDER ( 18 FDA reports)
HEPATOSPLENOMEGALY ( 18 FDA reports)
HEPATOTOXICITY ( 18 FDA reports)
HYPOTONIA ( 18 FDA reports)
INADEQUATE ANALGESIA ( 18 FDA reports)
INJECTION SITE RASH ( 18 FDA reports)
INJECTION SITE WARMTH ( 18 FDA reports)
LOSS OF EMPLOYMENT ( 18 FDA reports)
MACULOPATHY ( 18 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 18 FDA reports)
NASAL DRYNESS ( 18 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 18 FDA reports)
PROTEIN TOTAL INCREASED ( 18 FDA reports)
PURULENCE ( 18 FDA reports)
RASH MACULO-PAPULAR ( 18 FDA reports)
RESPIRATORY RATE DECREASED ( 18 FDA reports)
SPONDYLOLYSIS ( 18 FDA reports)
SPUTUM PURULENT ( 18 FDA reports)
TOE AMPUTATION ( 18 FDA reports)
TOOTH DEPOSIT ( 18 FDA reports)
UVEITIS ( 18 FDA reports)
VENTRICULAR DYSFUNCTION ( 18 FDA reports)
WOUND INFECTION ( 18 FDA reports)
PHYSICAL ASSAULT ( 17 FDA reports)
RADICULITIS LUMBOSACRAL ( 17 FDA reports)
SENSATION OF PRESSURE ( 17 FDA reports)
SKIN INFECTION ( 17 FDA reports)
STOMATITIS NECROTISING ( 17 FDA reports)
SYNCOPE VASOVAGAL ( 17 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 17 FDA reports)
URINARY TRACT OBSTRUCTION ( 17 FDA reports)
VEIN DISORDER ( 17 FDA reports)
VENTRICULAR ARRHYTHMIA ( 17 FDA reports)
ADENOMA BENIGN ( 17 FDA reports)
AORTIC VALVE CALCIFICATION ( 17 FDA reports)
ASTROCYTOMA ( 17 FDA reports)
AUTOIMMUNE HEPATITIS ( 17 FDA reports)
BLADDER PROLAPSE ( 17 FDA reports)
BLOOD DISORDER ( 17 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 17 FDA reports)
BRADYARRHYTHMIA ( 17 FDA reports)
BREAST ENLARGEMENT ( 17 FDA reports)
BREAST TENDERNESS ( 17 FDA reports)
CAPILLARY LEAK SYNDROME ( 17 FDA reports)
CAROTID ARTERY OCCLUSION ( 17 FDA reports)
COLON POLYPECTOMY ( 17 FDA reports)
DISORDER OF ORBIT ( 17 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 17 FDA reports)
DISSOCIATION ( 17 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 17 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 17 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 17 FDA reports)
FIBRIN D DIMER INCREASED ( 17 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 17 FDA reports)
GASTRIC PERFORATION ( 17 FDA reports)
GENERALISED ERYTHEMA ( 17 FDA reports)
GLIOSIS ( 17 FDA reports)
GROWTH RETARDATION ( 17 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 17 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 17 FDA reports)
HYPOPNOEA ( 17 FDA reports)
INCORRECT STORAGE OF DRUG ( 17 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 17 FDA reports)
INJECTION SITE IRRITATION ( 17 FDA reports)
INJECTION SITE URTICARIA ( 17 FDA reports)
INTENTIONAL SELF-INJURY ( 17 FDA reports)
JUGULAR VEIN DISTENSION ( 17 FDA reports)
LABYRINTHITIS ( 17 FDA reports)
LARYNGOSPASM ( 17 FDA reports)
LIP BLISTER ( 17 FDA reports)
LUMBAR RADICULOPATHY ( 17 FDA reports)
NASAL POLYPS ( 17 FDA reports)
OESOPHAGEAL RUPTURE ( 17 FDA reports)
ORGAN FAILURE ( 17 FDA reports)
OSTEITIS ( 17 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 16 FDA reports)
ABSCESS JAW ( 16 FDA reports)
ABSCESS NECK ( 16 FDA reports)
ACCIDENT ( 16 FDA reports)
ANGIOPLASTY ( 16 FDA reports)
APPLICATION SITE PAIN ( 16 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 16 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 16 FDA reports)
BASEDOW'S DISEASE ( 16 FDA reports)
BLOOD CREATINE INCREASED ( 16 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 16 FDA reports)
BREAST OEDEMA ( 16 FDA reports)
BRONCHIAL OBSTRUCTION ( 16 FDA reports)
BUNION ( 16 FDA reports)
CHONDROMALACIA ( 16 FDA reports)
CONVERSION DISORDER ( 16 FDA reports)
CORNEAL DYSTROPHY ( 16 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 16 FDA reports)
DRUG EFFECT INCREASED ( 16 FDA reports)
ENDOTRACHEAL INTUBATION ( 16 FDA reports)
EYE INJURY ( 16 FDA reports)
FOLLICULITIS ( 16 FDA reports)
HOSTILITY ( 16 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 16 FDA reports)
INJURY CORNEAL ( 16 FDA reports)
LIVEDO RETICULARIS ( 16 FDA reports)
MASTOCYTOSIS ( 16 FDA reports)
MEDICAL DEVICE REMOVAL ( 16 FDA reports)
MULTIPLE FRACTURES ( 16 FDA reports)
OCCULT BLOOD ( 16 FDA reports)
OLIGURIA ( 16 FDA reports)
ORAL CAVITY FISTULA ( 16 FDA reports)
PAIN OF SKIN ( 16 FDA reports)
PATHOGEN RESISTANCE ( 16 FDA reports)
PHOTOPSIA ( 16 FDA reports)
PLEURAL CALCIFICATION ( 16 FDA reports)
POLYURIA ( 16 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 16 FDA reports)
PREMATURE LABOUR ( 16 FDA reports)
PROSTATIC DISORDER ( 16 FDA reports)
PSYCHIATRIC SYMPTOM ( 16 FDA reports)
PSYCHOLOGICAL TRAUMA ( 16 FDA reports)
PULMONARY AIR LEAKAGE ( 16 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 16 FDA reports)
RESPIRATORY ACIDOSIS ( 16 FDA reports)
RESUSCITATION ( 16 FDA reports)
SCOTOMA ( 16 FDA reports)
SEBORRHOEIC DERMATITIS ( 16 FDA reports)
SELF-MEDICATION ( 16 FDA reports)
SEQUESTRECTOMY ( 16 FDA reports)
SHOULDER PAIN ( 16 FDA reports)
SINUS ANTROSTOMY ( 16 FDA reports)
TALIPES ( 16 FDA reports)
TRAUMATIC LUNG INJURY ( 16 FDA reports)
VASCULAR PSEUDOANEURYSM ( 16 FDA reports)
WEIGHT LOSS POOR ( 16 FDA reports)
PITTING OEDEMA ( 15 FDA reports)
POST PROCEDURAL INFECTION ( 15 FDA reports)
POSTOPERATIVE INFECTION ( 15 FDA reports)
PYELONEPHRITIS ( 15 FDA reports)
REGURGITATION ( 15 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 15 FDA reports)
RHEUMATIC HEART DISEASE ( 15 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 15 FDA reports)
SPINAL CORD COMPRESSION ( 15 FDA reports)
THROMBOSIS IN DEVICE ( 15 FDA reports)
TOBACCO ABUSE ( 15 FDA reports)
URINE ANALYSIS ABNORMAL ( 15 FDA reports)
VERTIGO POSITIONAL ( 15 FDA reports)
ADENOCARCINOMA ( 15 FDA reports)
ALCOHOL USE ( 15 FDA reports)
ANURIA ( 15 FDA reports)
ARTHRITIS INFECTIVE ( 15 FDA reports)
BILE DUCT STONE ( 15 FDA reports)
BLOOD CHLORIDE INCREASED ( 15 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 15 FDA reports)
BONE ABSCESS ( 15 FDA reports)
BREAST CYST ( 15 FDA reports)
CHEMOTHERAPY ( 15 FDA reports)
CHRONIC HEPATITIS ( 15 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 15 FDA reports)
CORRECTIVE LENS USER ( 15 FDA reports)
CUTIS LAXA ( 15 FDA reports)
DERMATITIS ALLERGIC ( 15 FDA reports)
DEVICE OCCLUSION ( 15 FDA reports)
DIABETIC FOOT ( 15 FDA reports)
DRUG LEVEL INCREASED ( 15 FDA reports)
DYSMENORRHOEA ( 15 FDA reports)
EJECTION FRACTION ABNORMAL ( 15 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 15 FDA reports)
ENCEPHALOMALACIA ( 15 FDA reports)
ENERGY INCREASED ( 15 FDA reports)
EROSIVE OESOPHAGITIS ( 15 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 15 FDA reports)
FOREIGN BODY TRAUMA ( 15 FDA reports)
FUSOBACTERIUM INFECTION ( 15 FDA reports)
HAEMOLYTIC ANAEMIA ( 15 FDA reports)
HAEMOTHORAX ( 15 FDA reports)
HEPATIC ENCEPHALOPATHY ( 15 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 15 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 15 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 15 FDA reports)
INCISION SITE COMPLICATION ( 15 FDA reports)
INJECTION SITE NODULE ( 15 FDA reports)
INTESTINAL ISCHAEMIA ( 15 FDA reports)
LUNG LOBECTOMY ( 15 FDA reports)
MACULAR HOLE ( 15 FDA reports)
MENOMETRORRHAGIA ( 15 FDA reports)
MUSCLE RIGIDITY ( 15 FDA reports)
NIGHT BLINDNESS ( 15 FDA reports)
PANCREATIC CARCINOMA ( 15 FDA reports)
PARTNER STRESS ( 15 FDA reports)
ADDISON'S DISEASE ( 14 FDA reports)
ADRENAL SUPPRESSION ( 14 FDA reports)
AKATHISIA ( 14 FDA reports)
AORTIC VALVE STENOSIS ( 14 FDA reports)
APPENDIX DISORDER ( 14 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 14 FDA reports)
BLADDER DYSFUNCTION ( 14 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 14 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 14 FDA reports)
BREAST NECROSIS ( 14 FDA reports)
BRONCHITIS ACUTE ( 14 FDA reports)
BRONCHITIS VIRAL ( 14 FDA reports)
CALCULUS URETERIC ( 14 FDA reports)
CARDIAC TAMPONADE ( 14 FDA reports)
CATARACT NUCLEAR ( 14 FDA reports)
DEMYELINATION ( 14 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 14 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 14 FDA reports)
ENAMEL ANOMALY ( 14 FDA reports)
FEELING GUILTY ( 14 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 14 FDA reports)
FEMORAL NECK FRACTURE ( 14 FDA reports)
GANGRENE ( 14 FDA reports)
GYNAECOMASTIA ( 14 FDA reports)
HAEMOLYSIS ( 14 FDA reports)
HAEMORRHOID OPERATION ( 14 FDA reports)
HEPATIC MASS ( 14 FDA reports)
HEPATOCELLULAR DAMAGE ( 14 FDA reports)
HYPERNATRAEMIA ( 14 FDA reports)
HYSTERECTOMY ( 14 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 14 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 14 FDA reports)
INJECTION SITE INDURATION ( 14 FDA reports)
INTESTINAL POLYP ( 14 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 14 FDA reports)
ISCHAEMIC HEPATITIS ( 14 FDA reports)
LIP PAIN ( 14 FDA reports)
MONOCYTE COUNT DECREASED ( 14 FDA reports)
MONOPLEGIA ( 14 FDA reports)
MYASTHENIA GRAVIS ( 14 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 14 FDA reports)
NASAL MUCOSAL DISORDER ( 14 FDA reports)
NECK INJURY ( 14 FDA reports)
NEOPLASM SKIN ( 14 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 14 FDA reports)
OESOPHAGEAL ULCER ( 14 FDA reports)
PERIARTHRITIS ( 14 FDA reports)
PERIORBITAL HAEMATOMA ( 14 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 14 FDA reports)
PSEUDOMONAL SEPSIS ( 14 FDA reports)
PYURIA ( 14 FDA reports)
ROSACEA ( 14 FDA reports)
SKIN HYPOPIGMENTATION ( 14 FDA reports)
SKIN NODULE ( 14 FDA reports)
SKIN WARM ( 14 FDA reports)
SKIN WRINKLING ( 14 FDA reports)
SPIROMETRY ( 14 FDA reports)
SUDDEN CARDIAC DEATH ( 14 FDA reports)
SUICIDAL BEHAVIOUR ( 14 FDA reports)
THROAT LESION ( 14 FDA reports)
TRIGGER FINGER ( 14 FDA reports)
VAGINAL INFECTION ( 14 FDA reports)
VERTEBROPLASTY ( 14 FDA reports)
VOCAL CORD INFLAMMATION ( 14 FDA reports)
PNEUMONIA VIRAL ( 13 FDA reports)
POST PROCEDURAL HAEMATOMA ( 13 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 13 FDA reports)
PRODUCT ADHESION ISSUE ( 13 FDA reports)
PROTEIN TOTAL DECREASED ( 13 FDA reports)
PSEUDOMONAS BRONCHITIS ( 13 FDA reports)
PULMONARY CALCIFICATION ( 13 FDA reports)
RADICULAR PAIN ( 13 FDA reports)
RESPIRATORY MONILIASIS ( 13 FDA reports)
SCHIZOPHRENIA ( 13 FDA reports)
SERUM FERRITIN INCREASED ( 13 FDA reports)
SOFT TISSUE INFLAMMATION ( 13 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 13 FDA reports)
SPLEEN DISORDER ( 13 FDA reports)
SPONDYLITIS ( 13 FDA reports)
SPUTUM ABNORMAL ( 13 FDA reports)
SPUTUM RETENTION ( 13 FDA reports)
STASIS DERMATITIS ( 13 FDA reports)
STATUS EPILEPTICUS ( 13 FDA reports)
TONSILLITIS ( 13 FDA reports)
VOCAL CORD THICKENING ( 13 FDA reports)
YELLOW SKIN ( 13 FDA reports)
ACUTE PULMONARY OEDEMA ( 13 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 13 FDA reports)
ANGIOMYOLIPOMA ( 13 FDA reports)
AORTIC DILATATION ( 13 FDA reports)
APICAL GRANULOMA ( 13 FDA reports)
APPLICATION SITE BURN ( 13 FDA reports)
ARRESTED LABOUR ( 13 FDA reports)
ARTERIOSPASM CORONARY ( 13 FDA reports)
BLADDER OBSTRUCTION ( 13 FDA reports)
BLOOD GASES ABNORMAL ( 13 FDA reports)
BLOOD URIC ACID INCREASED ( 13 FDA reports)
BONE MARROW TRANSPLANT ( 13 FDA reports)
BREAST SWELLING ( 13 FDA reports)
BRONCHOSPASM PARADOXICAL ( 13 FDA reports)
CARDIAC ABLATION ( 13 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 13 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 13 FDA reports)
CHOLESTEROSIS ( 13 FDA reports)
CHOREA ( 13 FDA reports)
COMPULSIVE SHOPPING ( 13 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 13 FDA reports)
CRANIAL NERVE DISORDER ( 13 FDA reports)
DENTAL PLAQUE ( 13 FDA reports)
DIVERTICULAR PERFORATION ( 13 FDA reports)
DYSAESTHESIA ( 13 FDA reports)
DYSGRAPHIA ( 13 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 13 FDA reports)
EMBOLISM ( 13 FDA reports)
ENCEPHALITIS ( 13 FDA reports)
EPILEPSY ( 13 FDA reports)
ERB'S PALSY ( 13 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 13 FDA reports)
GALLBLADDER POLYP ( 13 FDA reports)
GASTRINOMA ( 13 FDA reports)
GASTROINTESTINAL NECROSIS ( 13 FDA reports)
GINGIVAL ERYTHEMA ( 13 FDA reports)
HAIR GROWTH ABNORMAL ( 13 FDA reports)
HALO VISION ( 13 FDA reports)
HEPATIC NEOPLASM ( 13 FDA reports)
HYPERACUSIS ( 13 FDA reports)
HYPERCHLORHYDRIA ( 13 FDA reports)
IMPULSIVE BEHAVIOUR ( 13 FDA reports)
INTESTINAL HAEMORRHAGE ( 13 FDA reports)
KERATOACANTHOMA ( 13 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 13 FDA reports)
LAZINESS ( 13 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 13 FDA reports)
LUNG ABSCESS ( 13 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 13 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 13 FDA reports)
MICTURITION DISORDER ( 13 FDA reports)
MONOCLONAL GAMMOPATHY ( 13 FDA reports)
NEPHROPATHY ( 13 FDA reports)
NEPHROSCLEROSIS ( 13 FDA reports)
NEUROGENIC BLADDER ( 13 FDA reports)
OBSTRUCTION ( 13 FDA reports)
OESOPHAGEAL SPASM ( 13 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 13 FDA reports)
PERFORMANCE STATUS DECREASED ( 13 FDA reports)
PERIODONTAL OPERATION ( 13 FDA reports)
ABSCESS LIMB ( 12 FDA reports)
ACTINIC KERATOSIS ( 12 FDA reports)
ADNEXA UTERI CYST ( 12 FDA reports)
APPETITE DISORDER ( 12 FDA reports)
AXILLARY PAIN ( 12 FDA reports)
BALANITIS ( 12 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 12 FDA reports)
BIOPSY BONE ( 12 FDA reports)
BLOOD COUNT ABNORMAL ( 12 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 12 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 12 FDA reports)
BONE CYST ( 12 FDA reports)
BREAST OPERATION ( 12 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 12 FDA reports)
BRONCHIAL DISORDER ( 12 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 12 FDA reports)
CERVICOBRACHIAL SYNDROME ( 12 FDA reports)
CLAUSTROPHOBIA ( 12 FDA reports)
COLON ADENOMA ( 12 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 12 FDA reports)
CORNEAL OEDEMA ( 12 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 12 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 12 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 12 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 12 FDA reports)
DYSPHEMIA ( 12 FDA reports)
ENDOCARDIAL FIBROSIS ( 12 FDA reports)
ENDOMETRIOSIS ( 12 FDA reports)
EXFOLIATIVE RASH ( 12 FDA reports)
EXTREMITY NECROSIS ( 12 FDA reports)
EYE MOVEMENT DISORDER ( 12 FDA reports)
FISTULA REPAIR ( 12 FDA reports)
FOOD ALLERGY ( 12 FDA reports)
FOOD INTOLERANCE ( 12 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 12 FDA reports)
GASTROINTESTINAL PAIN ( 12 FDA reports)
GINGIVAL OEDEMA ( 12 FDA reports)
GRANULOCYTOPENIA ( 12 FDA reports)
HEPATOJUGULAR REFLUX ( 12 FDA reports)
HIP SURGERY ( 12 FDA reports)
HODGKIN'S DISEASE ( 12 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 12 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 12 FDA reports)
JOINT ARTHROPLASTY ( 12 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 12 FDA reports)
LARGE INTESTINE PERFORATION ( 12 FDA reports)
LIVER INJURY ( 12 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 12 FDA reports)
LYMPHADENECTOMY ( 12 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 12 FDA reports)
NODAL RHYTHM ( 12 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 12 FDA reports)
OROPHARYNGEAL PLAQUE ( 12 FDA reports)
OVERWEIGHT ( 12 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 12 FDA reports)
PANCREATIC CYST ( 12 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 12 FDA reports)
POST THROMBOTIC SYNDROME ( 12 FDA reports)
PROSTATITIS ( 12 FDA reports)
PULMONARY VASCULAR DISORDER ( 12 FDA reports)
RECTAL PROLAPSE REPAIR ( 12 FDA reports)
RENAL CELL CARCINOMA ( 12 FDA reports)
RETINOPATHY ( 12 FDA reports)
RHEUMATIC FEVER ( 12 FDA reports)
SALIVARY HYPERSECRETION ( 12 FDA reports)
SEBACEOUS GLAND DISORDER ( 12 FDA reports)
SENSATION OF BLOOD FLOW ( 12 FDA reports)
SHOCK HAEMORRHAGIC ( 12 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 12 FDA reports)
SKIN ODOUR ABNORMAL ( 12 FDA reports)
SKIN REACTION ( 12 FDA reports)
SOFT TISSUE INJURY ( 12 FDA reports)
SPINAL CORD DISORDER ( 12 FDA reports)
SPLENIC INFARCTION ( 12 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 12 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 12 FDA reports)
THYROIDITIS ( 12 FDA reports)
TONGUE BITING ( 12 FDA reports)
URGE INCONTINENCE ( 12 FDA reports)
URINE ODOUR ABNORMAL ( 12 FDA reports)
VAGINAL DISCHARGE ( 12 FDA reports)
VITREOUS HAEMORRHAGE ( 12 FDA reports)
WRONG DRUG ADMINISTERED ( 12 FDA reports)
PILONIDAL CYST ( 11 FDA reports)
PNEUMOCOCCAL INFECTION ( 11 FDA reports)
PNEUMONIA KLEBSIELLA ( 11 FDA reports)
PO2 DECREASED ( 11 FDA reports)
POOR PERSONAL HYGIENE ( 11 FDA reports)
PROSTATIC OBSTRUCTION ( 11 FDA reports)
PUBIS FRACTURE ( 11 FDA reports)
PULMONARY ARTERY ATRESIA ( 11 FDA reports)
RADIOTHERAPY ( 11 FDA reports)
RENAL ARTERY STENOSIS ( 11 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 11 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 11 FDA reports)
SCAN ABNORMAL ( 11 FDA reports)
SCRATCH ( 11 FDA reports)
SKIN OEDEMA ( 11 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 11 FDA reports)
SPINAL LAMINECTOMY ( 11 FDA reports)
SPUTUM CULTURE POSITIVE ( 11 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 11 FDA reports)
SUDDEN ONSET OF SLEEP ( 11 FDA reports)
TACHYARRHYTHMIA ( 11 FDA reports)
TEARFULNESS ( 11 FDA reports)
THROAT CANCER ( 11 FDA reports)
TINEA INFECTION ( 11 FDA reports)
TONGUE DRY ( 11 FDA reports)
TONGUE PARALYSIS ( 11 FDA reports)
TOOTH RESORPTION ( 11 FDA reports)
ULCERATIVE KERATITIS ( 11 FDA reports)
UTERINE CANCER ( 11 FDA reports)
VASODILATATION ( 11 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 11 FDA reports)
ABDOMINAL MASS ( 11 FDA reports)
ACUTE HEPATIC FAILURE ( 11 FDA reports)
ALCOHOL POISONING ( 11 FDA reports)
ALLERGY TO CHEMICALS ( 11 FDA reports)
ANAPHYLACTOID REACTION ( 11 FDA reports)
APPLICATION SITE IRRITATION ( 11 FDA reports)
APPLICATION SITE REACTION ( 11 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 11 FDA reports)
ATROPHIC VULVOVAGINITIS ( 11 FDA reports)
AXILLARY MASS ( 11 FDA reports)
BLEPHAROSPASM ( 11 FDA reports)
BRAIN OEDEMA ( 11 FDA reports)
BRONCHIAL SECRETION RETENTION ( 11 FDA reports)
BRONCHOSTENOSIS ( 11 FDA reports)
BURNING MOUTH SYNDROME ( 11 FDA reports)
CARBON DIOXIDE DECREASED ( 11 FDA reports)
CARDIOVERSION ( 11 FDA reports)
CARTILAGE INJURY ( 11 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 11 FDA reports)
DEVICE LEAKAGE ( 11 FDA reports)
DIABETIC RETINOPATHY ( 11 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 11 FDA reports)
EOSINOPHIL COUNT DECREASED ( 11 FDA reports)
EPICONDYLITIS ( 11 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 11 FDA reports)
FALLOT'S TETRALOGY ( 11 FDA reports)
FEAR OF DEATH ( 11 FDA reports)
FULL BLOOD COUNT DECREASED ( 11 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 11 FDA reports)
HISTOPLASMOSIS ( 11 FDA reports)
HYPERPARATHYROIDISM ( 11 FDA reports)
IMMOBILE ( 11 FDA reports)
INJECTION SITE EXTRAVASATION ( 11 FDA reports)
IRON DEFICIENCY ( 11 FDA reports)
JOINT CREPITATION ( 11 FDA reports)
JUDGEMENT IMPAIRED ( 11 FDA reports)
LASER THERAPY ( 11 FDA reports)
LEFT VENTRICULAR FAILURE ( 11 FDA reports)
LIMB CRUSHING INJURY ( 11 FDA reports)
LITHOTRIPSY ( 11 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 11 FDA reports)
MACROGLOSSIA ( 11 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 11 FDA reports)
MECHANICAL VENTILATION ( 11 FDA reports)
METASTASES TO SPLEEN ( 11 FDA reports)
METRORRHAGIA ( 11 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 11 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 11 FDA reports)
NARCOLEPSY ( 11 FDA reports)
NASAL OBSTRUCTION ( 11 FDA reports)
NEURODERMATITIS ( 11 FDA reports)
OEDEMA MUCOSAL ( 11 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 11 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 11 FDA reports)
PANCREATIC DUCT STENOSIS ( 11 FDA reports)
PANIC DISORDER ( 11 FDA reports)
PARTIAL SEIZURES ( 11 FDA reports)
PERICARDIAL HAEMORRHAGE ( 11 FDA reports)
PERITONITIS BACTERIAL ( 11 FDA reports)
PERNICIOUS ANAEMIA ( 11 FDA reports)
ADJUSTMENT DISORDER ( 10 FDA reports)
ADNEXA UTERI MASS ( 10 FDA reports)
ALVEOLITIS ( 10 FDA reports)
ANAL FISSURE ( 10 FDA reports)
ANAL STENOSIS ( 10 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 10 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 10 FDA reports)
APPENDICITIS PERFORATED ( 10 FDA reports)
APPLICATION SITE VESICLES ( 10 FDA reports)
ASEPTIC NECROSIS BONE ( 10 FDA reports)
ASTEATOSIS ( 10 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 10 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 10 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 10 FDA reports)
BLOOD IRON INCREASED ( 10 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 10 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 10 FDA reports)
CACHEXIA ( 10 FDA reports)
CAECUM OPERATION ( 10 FDA reports)
CALCULUS URINARY ( 10 FDA reports)
CANCER PAIN ( 10 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 10 FDA reports)
CARCINOID TUMOUR ( 10 FDA reports)
CARDIOPULMONARY FAILURE ( 10 FDA reports)
CATHETER PLACEMENT ( 10 FDA reports)
CHEST WALL PAIN ( 10 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 10 FDA reports)
DEPENDENCE ( 10 FDA reports)
DIABETIC NEPHROPATHY ( 10 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 10 FDA reports)
ECHOCARDIOGRAM ( 10 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 10 FDA reports)
EMBOLIC STROKE ( 10 FDA reports)
EOSINOPHILIC PNEUMONIA ( 10 FDA reports)
EXCESSIVE EYE BLINKING ( 10 FDA reports)
EXTREMITY CONTRACTURE ( 10 FDA reports)
FEELING HOT AND COLD ( 10 FDA reports)
FLUID INTAKE REDUCED ( 10 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 10 FDA reports)
GASTRIC CANCER ( 10 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 10 FDA reports)
HEPATIC FIBROSIS ( 10 FDA reports)
HYPERPHOSPHATAEMIA ( 10 FDA reports)
HYPERURICAEMIA ( 10 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 10 FDA reports)
HYPOREFLEXIA ( 10 FDA reports)
ILEUS PARALYTIC ( 10 FDA reports)
IMMUNODEFICIENCY ( 10 FDA reports)
INCISIONAL DRAINAGE ( 10 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 10 FDA reports)
INFUSION SITE REACTION ( 10 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 10 FDA reports)
INTESTINAL RESECTION ( 10 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 10 FDA reports)
LEUKAEMIA ( 10 FDA reports)
LIP DISORDER ( 10 FDA reports)
LIP EXFOLIATION ( 10 FDA reports)
LUNG ADENOCARCINOMA ( 10 FDA reports)
MACULAR OEDEMA ( 10 FDA reports)
MARROW HYPERPLASIA ( 10 FDA reports)
MENINGIOMA ( 10 FDA reports)
MENINGITIS ( 10 FDA reports)
MONOCYTE COUNT INCREASED ( 10 FDA reports)
MOUTH INJURY ( 10 FDA reports)
MUCOSAL EROSION ( 10 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 10 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 10 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 10 FDA reports)
ONYCHALGIA ( 10 FDA reports)
OPEN ANGLE GLAUCOMA ( 10 FDA reports)
OPTIC NERVE INJURY ( 10 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 10 FDA reports)
ORAL MUCOSAL HYPERTROPHY ( 10 FDA reports)
ORAL TORUS ( 10 FDA reports)
PAINFUL DEFAECATION ( 10 FDA reports)
PAROTITIS ( 10 FDA reports)
PHARYNGEAL ULCERATION ( 10 FDA reports)
POSTOPERATIVE ABSCESS ( 10 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 10 FDA reports)
PURPURA ( 10 FDA reports)
RADICAL HYSTERECTOMY ( 10 FDA reports)
RADIUS FRACTURE ( 10 FDA reports)
RASH VESICULAR ( 10 FDA reports)
READING DISORDER ( 10 FDA reports)
REFLUX GASTRITIS ( 10 FDA reports)
RETINAL DISORDER ( 10 FDA reports)
RETINAL VEIN OCCLUSION ( 10 FDA reports)
RETINITIS ( 10 FDA reports)
SACROILIITIS ( 10 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 10 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 10 FDA reports)
SKIN PLAQUE ( 10 FDA reports)
SOMNAMBULISM ( 10 FDA reports)
STERNAL FRACTURE ( 10 FDA reports)
STERNOTOMY ( 10 FDA reports)
STRIDOR ( 10 FDA reports)
TEMPORAL ARTERITIS ( 10 FDA reports)
TERMINAL STATE ( 10 FDA reports)
TINEA PEDIS ( 10 FDA reports)
TREATMENT FAILURE ( 10 FDA reports)
TUBERCULOSIS ( 10 FDA reports)
ULNA FRACTURE ( 10 FDA reports)
URINARY TRACT DISORDER ( 10 FDA reports)
URINE OUTPUT INCREASED ( 10 FDA reports)
UTERINE POLYP ( 10 FDA reports)
VENOUS OCCLUSION ( 10 FDA reports)
VOCAL CORD CYST ( 10 FDA reports)
VULVOVAGINAL PRURITUS ( 10 FDA reports)
WRIST SURGERY ( 10 FDA reports)
PLEURECTOMY ( 9 FDA reports)
PORTAL HYPERTENSION ( 9 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 9 FDA reports)
PROCEDURAL HYPOTENSION ( 9 FDA reports)
PRODUCT ODOUR ABNORMAL ( 9 FDA reports)
PROLONGED EXPIRATION ( 9 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 9 FDA reports)
PROSTHESIS IMPLANTATION ( 9 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 9 FDA reports)
PYELOCALIECTASIS ( 9 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 9 FDA reports)
RHEUMATOID LUNG ( 9 FDA reports)
SEROMA ( 9 FDA reports)
SEROTONIN SYNDROME ( 9 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 9 FDA reports)
SPLENIC LESION ( 9 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 9 FDA reports)
TELANGIECTASIA ( 9 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 9 FDA reports)
TONGUE HAEMORRHAGE ( 9 FDA reports)
TONGUE OEDEMA ( 9 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 9 FDA reports)
TRANSFUSION ( 9 FDA reports)
TRICUSPID VALVE DISEASE ( 9 FDA reports)
VASCULAR OPERATION ( 9 FDA reports)
VENA CAVA FILTER INSERTION ( 9 FDA reports)
VENA CAVA THROMBOSIS ( 9 FDA reports)
VESTIBULAR DISORDER ( 9 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
WEIGHT BEARING DIFFICULTY ( 9 FDA reports)
WOUND SECRETION ( 9 FDA reports)
ADHESION ( 9 FDA reports)
AFFECT LABILITY ( 9 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 9 FDA reports)
ALCOHOL ABUSE ( 9 FDA reports)
ALLERGIC SINUSITIS ( 9 FDA reports)
ALVEOLAR OSTEITIS ( 9 FDA reports)
ANAEMIA MACROCYTIC ( 9 FDA reports)
ANAL INFLAMMATION ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 9 FDA reports)
ANTISOCIAL BEHAVIOUR ( 9 FDA reports)
APPLICATION SITE ULCER ( 9 FDA reports)
AREFLEXIA ( 9 FDA reports)
ARTERIOVENOUS MALFORMATION ( 9 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 9 FDA reports)
BLOOD CULTURE POSITIVE ( 9 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 9 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 9 FDA reports)
BONE TRIMMING ( 9 FDA reports)
BREAST CANCER IN SITU ( 9 FDA reports)
CARCINOID TUMOUR PULMONARY ( 9 FDA reports)
CARDIAC ANEURYSM ( 9 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 9 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 9 FDA reports)
CATHETER SITE HAEMORRHAGE ( 9 FDA reports)
CHEST TUBE INSERTION ( 9 FDA reports)
CHOROIDAL DETACHMENT ( 9 FDA reports)
CIRCUMORAL OEDEMA ( 9 FDA reports)
COLONOSCOPY ABNORMAL ( 9 FDA reports)
COMPLEX PARTIAL SEIZURES ( 9 FDA reports)
CORONARY ARTERY EMBOLISM ( 9 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 9 FDA reports)
DERMATITIS EXFOLIATIVE ( 9 FDA reports)
DEVICE DISLOCATION ( 9 FDA reports)
DEVICE MISUSE ( 9 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 9 FDA reports)
DUODENAL ULCER PERFORATION ( 9 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 9 FDA reports)
ENANTHEMA ( 9 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 9 FDA reports)
ENTERITIS ( 9 FDA reports)
EPIDURAL LIPOMATOSIS ( 9 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 9 FDA reports)
EXPOSURE TO TOXIC AGENT ( 9 FDA reports)
FEAR OF FALLING ( 9 FDA reports)
FIBROMA ( 9 FDA reports)
FULGURATION ( 9 FDA reports)
FUNGAL SKIN INFECTION ( 9 FDA reports)
GAMBLING ( 9 FDA reports)
GLOBULINS INCREASED ( 9 FDA reports)
GOUTY ARTHRITIS ( 9 FDA reports)
HAIR TEXTURE ABNORMAL ( 9 FDA reports)
HALLUCINATIONS, MIXED ( 9 FDA reports)
HANGOVER ( 9 FDA reports)
HEART VALVE INCOMPETENCE ( 9 FDA reports)
HEPATIC ADENOMA ( 9 FDA reports)
HIRSUTISM ( 9 FDA reports)
HYPERBILIRUBINAEMIA ( 9 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 9 FDA reports)
INGUINAL HERNIA REPAIR ( 9 FDA reports)
INJECTION SITE DISCOLOURATION ( 9 FDA reports)
INJECTION SITE DISCOMFORT ( 9 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 9 FDA reports)
IUCD COMPLICATION ( 9 FDA reports)
JOINT LOCK ( 9 FDA reports)
KIDNEY ENLARGEMENT ( 9 FDA reports)
KIDNEY FIBROSIS ( 9 FDA reports)
LEUKODYSTROPHY ( 9 FDA reports)
LIBIDO INCREASED ( 9 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 9 FDA reports)
MAMMOGRAM ( 9 FDA reports)
MENINGITIS ASEPTIC ( 9 FDA reports)
MITRAL VALVE SCLEROSIS ( 9 FDA reports)
MYELOPATHY ( 9 FDA reports)
MYOMECTOMY ( 9 FDA reports)
NEGATIVE THOUGHTS ( 9 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 9 FDA reports)
NO ADVERSE EFFECT ( 9 FDA reports)
ONYCHOMADESIS ( 9 FDA reports)
ORAL MUCOSAL ERUPTION ( 9 FDA reports)
OROANTRAL FISTULA ( 9 FDA reports)
ORTHOPEDIC PROCEDURE ( 9 FDA reports)
OSTEOCHONDROMA ( 9 FDA reports)
OSTEOMYELITIS ACUTE ( 9 FDA reports)
PAPILLOMA ( 9 FDA reports)
PARANASAL SINUS DISCOMFORT ( 9 FDA reports)
PARONYCHIA ( 9 FDA reports)
PHARYNGEAL INFLAMMATION ( 9 FDA reports)
ABDOMINAL SYMPTOM ( 8 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 8 FDA reports)
AORTIC VALVE REPLACEMENT ( 8 FDA reports)
APPLICATION SITE EXFOLIATION ( 8 FDA reports)
APTYALISM ( 8 FDA reports)
ARTERIAL DISORDER ( 8 FDA reports)
BENIGN LUNG NEOPLASM ( 8 FDA reports)
BENIGN NEOPLASM ( 8 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 8 FDA reports)
BLADDER DISCOMFORT ( 8 FDA reports)
BLOOD ALBUMIN INCREASED ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 8 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 8 FDA reports)
BONE NEOPLASM ( 8 FDA reports)
BORDERLINE GLAUCOMA ( 8 FDA reports)
BREAST DISORDER ( 8 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 8 FDA reports)
BRONCHIAL HYPERACTIVITY ( 8 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 8 FDA reports)
CARDIAC HYPERTROPHY ( 8 FDA reports)
CATHETER RELATED COMPLICATION ( 8 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 8 FDA reports)
CEREBELLAR ATROPHY ( 8 FDA reports)
CHROMATOPSIA ( 8 FDA reports)
CLAVICLE FRACTURE ( 8 FDA reports)
CLOSTRIDIUM COLITIS ( 8 FDA reports)
CLUSTER HEADACHE ( 8 FDA reports)
CONNECTIVE TISSUE DISORDER ( 8 FDA reports)
CONVULSION NEONATAL ( 8 FDA reports)
CULTURE URINE POSITIVE ( 8 FDA reports)
DERMATITIS BULLOUS ( 8 FDA reports)
DEVICE RELATED SEPSIS ( 8 FDA reports)
DIABETIC GASTROPARESIS ( 8 FDA reports)
DROP ATTACKS ( 8 FDA reports)
DRUG TOLERANCE ( 8 FDA reports)
DYSPNOEA AT REST ( 8 FDA reports)
EAR CONGESTION ( 8 FDA reports)
EAR HAEMORRHAGE ( 8 FDA reports)
ECTROPION ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 8 FDA reports)
ENCEPHALITIS HERPES ( 8 FDA reports)
ENLARGED CLITORIS ( 8 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 8 FDA reports)
FIBROUS HISTIOCYTOMA ( 8 FDA reports)
FINGER DEFORMITY ( 8 FDA reports)
GENITAL RASH ( 8 FDA reports)
H1N1 INFLUENZA ( 8 FDA reports)
HAEMOPHILUS INFECTION ( 8 FDA reports)
HEPATIC NECROSIS ( 8 FDA reports)
HERPES OESOPHAGITIS ( 8 FDA reports)
HYPERSEXUALITY ( 8 FDA reports)
HYPOTONY OF EYE ( 8 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 8 FDA reports)
IMPAIRED FASTING GLUCOSE ( 8 FDA reports)
IMPATIENCE ( 8 FDA reports)
INFUSION SITE ERYTHEMA ( 8 FDA reports)
INFUSION SITE SWELLING ( 8 FDA reports)
INJECTION SITE COLDNESS ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 8 FDA reports)
INTRAVENOUS CATHETER MANAGEMENT ( 8 FDA reports)
KNEE OPERATION ( 8 FDA reports)
LABILE BLOOD PRESSURE ( 8 FDA reports)
LACTIC ACIDOSIS ( 8 FDA reports)
LACTOSE INTOLERANCE ( 8 FDA reports)
LEARNING DISABILITY ( 8 FDA reports)
LIFE SUPPORT ( 8 FDA reports)
LIPID METABOLISM DISORDER ( 8 FDA reports)
LIPOMA EXCISION ( 8 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 8 FDA reports)
LOWER EXTREMITY MASS ( 8 FDA reports)
LUNG INJURY ( 8 FDA reports)
LUPUS-LIKE SYNDROME ( 8 FDA reports)
LYMPH NODE PAIN ( 8 FDA reports)
LYMPH NODE PALPABLE ( 8 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 8 FDA reports)
MENIERE'S DISEASE ( 8 FDA reports)
MENSTRUATION DELAYED ( 8 FDA reports)
METAPLASIA ( 8 FDA reports)
METASTASES TO ADRENALS ( 8 FDA reports)
METASTASES TO BONE MARROW ( 8 FDA reports)
MIDDLE EAR EFFUSION ( 8 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 8 FDA reports)
MUSCLE CONTRACTURE ( 8 FDA reports)
MUSCLE RUPTURE ( 8 FDA reports)
MUSCLE SPASTICITY ( 8 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 8 FDA reports)
MYOCARDIAL FIBROSIS ( 8 FDA reports)
NASOPHARYNGEAL DISORDER ( 8 FDA reports)
NECROSIS ( 8 FDA reports)
NEUROLOGICAL SYMPTOM ( 8 FDA reports)
NEUTROPENIC SEPSIS ( 8 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 8 FDA reports)
NEUTROPHILIA ( 8 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 8 FDA reports)
NORMAL NEWBORN ( 8 FDA reports)
OCULAR DISCOMFORT ( 8 FDA reports)
ONYCHOCLASIS ( 8 FDA reports)
OPTIC NEURITIS ( 8 FDA reports)
ORAL SOFT TISSUE DISORDER ( 8 FDA reports)
ORGANISING PNEUMONIA ( 8 FDA reports)
OTITIS EXTERNA ( 8 FDA reports)
PANCREATIC ENZYMES INCREASED ( 8 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 8 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 8 FDA reports)
PCO2 INCREASED ( 8 FDA reports)
PHARYNX DISCOMFORT ( 8 FDA reports)
PIGMENTATION DISORDER ( 8 FDA reports)
PNEUMOCONIOSIS ( 8 FDA reports)
POISONING ( 8 FDA reports)
POLYARTHRITIS ( 8 FDA reports)
POLYP COLORECTAL ( 8 FDA reports)
POSTERIOR CAPSULOTOMY ( 8 FDA reports)
POSTICTAL STATE ( 8 FDA reports)
POSTOPERATIVE ILEUS ( 8 FDA reports)
PSORIATIC ARTHROPATHY ( 8 FDA reports)
PULMONARY HILUM MASS ( 8 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 8 FDA reports)
RENAL NEOPLASM ( 8 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 8 FDA reports)
SJOGREN'S SYNDROME ( 8 FDA reports)
SKIN CHAPPED ( 8 FDA reports)
SOFT TISSUE INFECTION ( 8 FDA reports)
SPIDER VEIN ( 8 FDA reports)
STARING ( 8 FDA reports)
SUNBURN ( 8 FDA reports)
TENSION HEADACHE ( 8 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 8 FDA reports)
TRACHEOSTOMY ( 8 FDA reports)
TUMOUR INVASION ( 8 FDA reports)
URETERAL STENT INSERTION ( 8 FDA reports)
VASCULAR INSUFFICIENCY ( 8 FDA reports)
VENOOCCLUSIVE DISEASE ( 8 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 7 FDA reports)
PINGUECULA ( 7 FDA reports)
PLACENTA PRAEVIA ( 7 FDA reports)
POOR PERIPHERAL CIRCULATION ( 7 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 7 FDA reports)
PROSTATE CANCER METASTATIC ( 7 FDA reports)
PSEUDOCYST ( 7 FDA reports)
PUPIL FIXED ( 7 FDA reports)
QRS AXIS ABNORMAL ( 7 FDA reports)
RADIATION PNEUMONITIS ( 7 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 7 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 7 FDA reports)
RESIDUAL URINE VOLUME ( 7 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 7 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 7 FDA reports)
RETINAL TEAR ( 7 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 7 FDA reports)
SALIVA ALTERED ( 7 FDA reports)
SERUM SICKNESS ( 7 FDA reports)
SEXUAL ABUSE ( 7 FDA reports)
SHOULDER OPERATION ( 7 FDA reports)
SINUS POLYP ( 7 FDA reports)
SKIN CYST EXCISION ( 7 FDA reports)
SKIN FISSURES ( 7 FDA reports)
SLEEP TALKING ( 7 FDA reports)
SLEEP TERROR ( 7 FDA reports)
SPINAL CORD INJURY ( 7 FDA reports)
SUBCUTANEOUS NODULE ( 7 FDA reports)
SUBSTANCE ABUSE ( 7 FDA reports)
SURGICAL PROCEDURE REPEATED ( 7 FDA reports)
SYSTEMIC CANDIDA ( 7 FDA reports)
TEETH BRITTLE ( 7 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 7 FDA reports)
THERAPY REGIMEN CHANGED ( 7 FDA reports)
THYMOMA ( 7 FDA reports)
TINEA VERSICOLOUR ( 7 FDA reports)
TONIC CLONIC MOVEMENTS ( 7 FDA reports)
TOOTH HYPOPLASIA ( 7 FDA reports)
TORSADE DE POINTES ( 7 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 7 FDA reports)
TRAUMATIC BRAIN INJURY ( 7 FDA reports)
TUMOUR LYSIS SYNDROME ( 7 FDA reports)
UNDERWEIGHT ( 7 FDA reports)
UNINTENDED PREGNANCY ( 7 FDA reports)
UTERINE HAEMORRHAGE ( 7 FDA reports)
VARICES OESOPHAGEAL ( 7 FDA reports)
VASCULAR GRAFT ( 7 FDA reports)
VASCULAR INJURY ( 7 FDA reports)
VASCULAR RUPTURE ( 7 FDA reports)
VENOUS THROMBOSIS LIMB ( 7 FDA reports)
VITILIGO ( 7 FDA reports)
VOCAL CORD PARALYSIS ( 7 FDA reports)
VOMITING PROJECTILE ( 7 FDA reports)
VULVOVAGINAL DISCOMFORT ( 7 FDA reports)
X-RAY ABNORMAL ( 7 FDA reports)
ABDOMINAL ABSCESS ( 7 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 7 FDA reports)
ADENOMYOSIS ( 7 FDA reports)
ADRENAL ADENOMA ( 7 FDA reports)
AGRANULOCYTOSIS ( 7 FDA reports)
AMYLOIDOSIS ( 7 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 7 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 7 FDA reports)
AORTIC VALVE DISEASE ( 7 FDA reports)
APPENDICECTOMY ( 7 FDA reports)
ASPHYXIA ( 7 FDA reports)
ASTHMA EXERCISE INDUCED ( 7 FDA reports)
B-CELL LYMPHOMA ( 7 FDA reports)
BACTERIAL SEPSIS ( 7 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 7 FDA reports)
BLOOD BICARBONATE DECREASED ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 7 FDA reports)
BLOOD UREA DECREASED ( 7 FDA reports)
BONE MARROW GRANULOMA ( 7 FDA reports)
BONE NEOPLASM MALIGNANT ( 7 FDA reports)
BONE SARCOMA ( 7 FDA reports)
BRADYPHRENIA ( 7 FDA reports)
BRAIN DEATH ( 7 FDA reports)
BRAIN INJURY ( 7 FDA reports)
BREAST RECONSTRUCTION ( 7 FDA reports)
BULIMIA NERVOSA ( 7 FDA reports)
BUNDLE BRANCH BLOCK ( 7 FDA reports)
CALCULUS URETHRAL ( 7 FDA reports)
CATHETER RELATED INFECTION ( 7 FDA reports)
CATHETER REMOVAL ( 7 FDA reports)
CEREBELLAR SYNDROME ( 7 FDA reports)
CEREBRAL CALCIFICATION ( 7 FDA reports)
CEREBRAL CYST ( 7 FDA reports)
CEREBRAL DISORDER ( 7 FDA reports)
COARCTATION OF THE AORTA ( 7 FDA reports)
COMMINUTED FRACTURE ( 7 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 7 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 7 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 7 FDA reports)
ECLAMPSIA ( 7 FDA reports)
EDENTULOUS ( 7 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 7 FDA reports)
ENDOCARDITIS ( 7 FDA reports)
ENDOCARDITIS BACTERIAL ( 7 FDA reports)
ENZYME ABNORMALITY ( 7 FDA reports)
ESCHERICHIA BACTERAEMIA ( 7 FDA reports)
FEELING OF DESPAIR ( 7 FDA reports)
FLAT AFFECT ( 7 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 7 FDA reports)
FOETAL HEART RATE ABNORMAL ( 7 FDA reports)
FOOD CRAVING ( 7 FDA reports)
FOOT OPERATION ( 7 FDA reports)
FRACTURE DELAYED UNION ( 7 FDA reports)
GASTRIC BYPASS ( 7 FDA reports)
GASTRIC INFECTION ( 7 FDA reports)
GASTRODUODENAL ULCER ( 7 FDA reports)
GASTROINTESTINAL INFECTION ( 7 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 7 FDA reports)
GASTROINTESTINAL INJURY ( 7 FDA reports)
GINGIVAL DISCOLOURATION ( 7 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 7 FDA reports)
GLYCOSURIA ( 7 FDA reports)
GROIN INFECTION ( 7 FDA reports)
HAIR COLOUR CHANGES ( 7 FDA reports)
HEART DISEASE CONGENITAL ( 7 FDA reports)
HEART SOUNDS ABNORMAL ( 7 FDA reports)
HERNIA HIATUS REPAIR ( 7 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 7 FDA reports)
HYPERTENSIVE CRISIS ( 7 FDA reports)
HYPOTRICHOSIS ( 7 FDA reports)
INJECTION SITE SCAR ( 7 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 7 FDA reports)
INTESTINAL PROLAPSE ( 7 FDA reports)
KNEE DEFORMITY ( 7 FDA reports)
LENTIGO ( 7 FDA reports)
LIPIDS ABNORMAL ( 7 FDA reports)
LOCALISED OEDEMA ( 7 FDA reports)
LOSS OF LIBIDO ( 7 FDA reports)
LYMPHADENITIS ( 7 FDA reports)
MALIGNANT TUMOUR EXCISION ( 7 FDA reports)
MALLORY-WEISS SYNDROME ( 7 FDA reports)
MEIBOMIANITIS ( 7 FDA reports)
METABOLIC DISORDER ( 7 FDA reports)
MUSCLE FATIGUE ( 7 FDA reports)
NAIL DISCOLOURATION ( 7 FDA reports)
NASAL OPERATION ( 7 FDA reports)
NOSOCOMIAL INFECTION ( 7 FDA reports)
NYSTAGMUS ( 7 FDA reports)
OSTEOCHONDROSIS ( 7 FDA reports)
OSTEOMALACIA ( 7 FDA reports)
OSTEOPETROSIS ( 7 FDA reports)
OVARIAN DISORDER ( 7 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 7 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 7 FDA reports)
PARKINSONISM ( 7 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 7 FDA reports)
PERIPHERAL EMBOLISM ( 7 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 7 FDA reports)
PERIVASCULAR DERMATITIS ( 7 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 7 FDA reports)
ACANTHOSIS ( 6 FDA reports)
ACARODERMATITIS ( 6 FDA reports)
ACCIDENTAL DEATH ( 6 FDA reports)
ACROCHORDON ( 6 FDA reports)
ACTH STIMULATION TEST ABNORMAL ( 6 FDA reports)
ADRENAL NEOPLASM ( 6 FDA reports)
ALLODYNIA ( 6 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 6 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 6 FDA reports)
AORTIC ATHEROSCLEROSIS ( 6 FDA reports)
APPLICATION SITE SCAR ( 6 FDA reports)
ASBESTOSIS ( 6 FDA reports)
AURA ( 6 FDA reports)
BILE DUCT CANCER ( 6 FDA reports)
BLADDER PAIN ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 6 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 6 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 6 FDA reports)
BRONCHITIS BACTERIAL ( 6 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 6 FDA reports)
CARDIAC FIBRILLATION ( 6 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 6 FDA reports)
CATHETER SEPSIS ( 6 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 6 FDA reports)
CHONDROSARCOMA ( 6 FDA reports)
CHRONIC FATIGUE SYNDROME ( 6 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 6 FDA reports)
COMPLICATION OF DELIVERY ( 6 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 6 FDA reports)
CONGENITAL HAIR DISORDER ( 6 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 6 FDA reports)
CORNEAL ABRASION ( 6 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 6 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 6 FDA reports)
DEFORMITY THORAX ( 6 FDA reports)
DEPRESSIVE SYMPTOM ( 6 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 6 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 6 FDA reports)
DISEASE COMPLICATION ( 6 FDA reports)
DISINHIBITION ( 6 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 6 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 6 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 6 FDA reports)
DRUG LEVEL DECREASED ( 6 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 6 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 6 FDA reports)
DYSPHASIA ( 6 FDA reports)
DYSPHORIA ( 6 FDA reports)
EAR DEFORMITY ACQUIRED ( 6 FDA reports)
EFFUSION ( 6 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 6 FDA reports)
ERYTHEMA OF EYELID ( 6 FDA reports)
EXECUTIVE DYSFUNCTION ( 6 FDA reports)
EYE OPERATION ( 6 FDA reports)
EYELID MARGIN CRUSTING ( 6 FDA reports)
FACTOR VIII DEFICIENCY ( 6 FDA reports)
FAECES HARD ( 6 FDA reports)
FAT NECROSIS ( 6 FDA reports)
FEMORAL ARTERY OCCLUSION ( 6 FDA reports)
GALLBLADDER CANCER ( 6 FDA reports)
GAMMOPATHY ( 6 FDA reports)
GASTRIC DILATATION ( 6 FDA reports)
GASTRIC PH DECREASED ( 6 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 6 FDA reports)
GESTATIONAL DIABETES ( 6 FDA reports)
GINGIVAL ABSCESS ( 6 FDA reports)
GUN SHOT WOUND ( 6 FDA reports)
HAEMODYNAMIC INSTABILITY ( 6 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 6 FDA reports)
HAEMORRHAGIC DIATHESIS ( 6 FDA reports)
HAEMORRHAGIC DISORDER ( 6 FDA reports)
HAIR DISORDER ( 6 FDA reports)
HEPATIC PAIN ( 6 FDA reports)
HYDROCELE ( 6 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 6 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 6 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 6 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 6 FDA reports)
HYPOVOLAEMIC SHOCK ( 6 FDA reports)
IMPLANT SITE THROMBOSIS ( 6 FDA reports)
INCISIONAL HERNIA ( 6 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 6 FDA reports)
INFUSION SITE PAIN ( 6 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 6 FDA reports)
INTERCOSTAL NEURALGIA ( 6 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 6 FDA reports)
INTRA-UTERINE DEATH ( 6 FDA reports)
JAUNDICE NEONATAL ( 6 FDA reports)
LARYNGEAL DISORDER ( 6 FDA reports)
LEUKOPLAKIA ( 6 FDA reports)
LIP OEDEMA ( 6 FDA reports)
LIPOHYPERTROPHY ( 6 FDA reports)
LISTLESS ( 6 FDA reports)
LIVE BIRTH ( 6 FDA reports)
LOOSE STOOLS ( 6 FDA reports)
MASTOIDITIS ( 6 FDA reports)
MENINGISM ( 6 FDA reports)
METABOLIC ALKALOSIS ( 6 FDA reports)
METAMORPHOPSIA ( 6 FDA reports)
METASTASES TO PLEURA ( 6 FDA reports)
MORPHOEA ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE ( 6 FDA reports)
MUSCLE FLAP OPERATION ( 6 FDA reports)
MYOPATHY TOXIC ( 6 FDA reports)
NEOPLASM PROSTATE ( 6 FDA reports)
NEURILEMMOMA ( 6 FDA reports)
NEUROFIBROMA ( 6 FDA reports)
NIPPLE DISORDER ( 6 FDA reports)
NIPPLE PAIN ( 6 FDA reports)
NODAL ARRHYTHMIA ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 6 FDA reports)
OBSESSIVE THOUGHTS ( 6 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 6 FDA reports)
OPTIC ATROPHY ( 6 FDA reports)
ORAL MUCOSAL DISORDER ( 6 FDA reports)
ORCHITIS ( 6 FDA reports)
OSTECTOMY ( 6 FDA reports)
OXYGEN SATURATION ( 6 FDA reports)
PANCREATITIS RELAPSING ( 6 FDA reports)
PARAPARESIS ( 6 FDA reports)
PATELLA FRACTURE ( 6 FDA reports)
PENIS DISORDER ( 6 FDA reports)
PERTUSSIS ( 6 FDA reports)
PNEUMONIA FUNGAL ( 6 FDA reports)
POLYTRAUMATISM ( 6 FDA reports)
PORTAL VEIN THROMBOSIS ( 6 FDA reports)
POST HERPETIC NEURALGIA ( 6 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 6 FDA reports)
POSTPARTUM HAEMORRHAGE ( 6 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 6 FDA reports)
PSYCHOMOTOR RETARDATION ( 6 FDA reports)
PTERYGIUM COLLI ( 6 FDA reports)
PULMONARY MYCOSIS ( 6 FDA reports)
PULMONARY VALVE STENOSIS ( 6 FDA reports)
RADIATION OESOPHAGITIS ( 6 FDA reports)
RATHKE'S CLEFT CYST ( 6 FDA reports)
RAYNAUD'S PHENOMENON ( 6 FDA reports)
RECURRENT CANCER ( 6 FDA reports)
RENAL HAEMATOMA ( 6 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 6 FDA reports)
RETINAL ARTERY THROMBOSIS ( 6 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 6 FDA reports)
SIALOADENITIS ( 6 FDA reports)
SINOBRONCHITIS ( 6 FDA reports)
SKIN NEOPLASM EXCISION ( 6 FDA reports)
SKIN STRIAE ( 6 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 6 FDA reports)
SOFT TISSUE MASS ( 6 FDA reports)
SPONDYLOARTHROPATHY ( 6 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 6 FDA reports)
TACHYPHRENIA ( 6 FDA reports)
TEMPERATURE REGULATION DISORDER ( 6 FDA reports)
TENDON GRAFT ( 6 FDA reports)
TENDON INJURY ( 6 FDA reports)
TONGUE BLACK HAIRY ( 6 FDA reports)
TOXIC ENCEPHALOPATHY ( 6 FDA reports)
TRAUMATIC SHOCK ( 6 FDA reports)
TUMOUR EXCISION ( 6 FDA reports)
TUMOUR FLARE ( 6 FDA reports)
TURNER'S SYNDROME ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
URETERIC OBSTRUCTION ( 6 FDA reports)
URETHRAL OBSTRUCTION ( 6 FDA reports)
URETHRAL STENOSIS ( 6 FDA reports)
URINE COLOUR ABNORMAL ( 6 FDA reports)
VAGINAL SWELLING ( 6 FDA reports)
VASCULAR DEMENTIA ( 6 FDA reports)
VASCULAR HEADACHE ( 6 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 6 FDA reports)
VIRAL LABYRINTHITIS ( 6 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 5 FDA reports)
POIKILOCYTOSIS ( 5 FDA reports)
POLYCYTHAEMIA ( 5 FDA reports)
POLYMYOSITIS ( 5 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 5 FDA reports)
POST PROCEDURAL NAUSEA ( 5 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 5 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 5 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 5 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 5 FDA reports)
PULMONARY SARCOIDOSIS ( 5 FDA reports)
PYLORIC STENOSIS ( 5 FDA reports)
RADICAL MASTECTOMY ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
RECTAL DISCHARGE ( 5 FDA reports)
RENAL COLIC ( 5 FDA reports)
RHEUMATOID NODULE ( 5 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 5 FDA reports)
SCLERODERMA ( 5 FDA reports)
SCROTAL PAIN ( 5 FDA reports)
SHIFT TO THE LEFT ( 5 FDA reports)
SKIN FRAGILITY ( 5 FDA reports)
SKULL FRACTURE ( 5 FDA reports)
SLEEP WALKING ( 5 FDA reports)
SPONTANEOUS PENILE ERECTION ( 5 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 5 FDA reports)
STARVATION ( 5 FDA reports)
STENOTROPHOMONAS INFECTION ( 5 FDA reports)
STRABISMUS ( 5 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 5 FDA reports)
SUBRETINAL FIBROSIS ( 5 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 5 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 5 FDA reports)
THERAPY CESSATION ( 5 FDA reports)
THROMBOCYTHAEMIA ( 5 FDA reports)
THYROIDITIS CHRONIC ( 5 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 5 FDA reports)
TONGUE GEOGRAPHIC ( 5 FDA reports)
TOTAL LUNG CAPACITY INCREASED ( 5 FDA reports)
TRACHEAL DISORDER ( 5 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 5 FDA reports)
TRANSPLANT FAILURE ( 5 FDA reports)
TRICHOMONIASIS ( 5 FDA reports)
TUMOUR MARKER INCREASED ( 5 FDA reports)
TUNNEL VISION ( 5 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 5 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 5 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 5 FDA reports)
UPPER LIMB DEFORMITY ( 5 FDA reports)
URETERAL DISORDER ( 5 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
URINE KETONE BODY PRESENT ( 5 FDA reports)
UTERINE PERFORATION ( 5 FDA reports)
VAGINAL BURNING SENSATION ( 5 FDA reports)
VAGINAL MYCOSIS ( 5 FDA reports)
VAGINAL PAIN ( 5 FDA reports)
VAGINITIS BACTERIAL ( 5 FDA reports)
VASCULAR OCCLUSION ( 5 FDA reports)
VERTEBRAL WEDGING ( 5 FDA reports)
VITREOUS DEGENERATION ( 5 FDA reports)
VOMITING IN PREGNANCY ( 5 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 5 FDA reports)
WEANING FAILURE ( 5 FDA reports)
YAWNING ( 5 FDA reports)
ABDOMINAL ADHESIONS ( 5 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 5 FDA reports)
ABORTION INDUCED ( 5 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 5 FDA reports)
ANION GAP INCREASED ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
AORTIC ANEURYSM RUPTURE ( 5 FDA reports)
APPARENT LIFE THREATENING EVENT ( 5 FDA reports)
APPLICATION SITE INFECTION ( 5 FDA reports)
APPLICATION SITE SCAB ( 5 FDA reports)
APRAXIA ( 5 FDA reports)
ARTERIAL STENOSIS ( 5 FDA reports)
ARTHROSCOPIC SURGERY ( 5 FDA reports)
BILE DUCT OBSTRUCTION ( 5 FDA reports)
BILIARY TRACT DISORDER ( 5 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 5 FDA reports)
BLADDER SPASM ( 5 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 5 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 5 FDA reports)
BLOOD SODIUM INCREASED ( 5 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 5 FDA reports)
BONE METABOLISM DISORDER ( 5 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 5 FDA reports)
BRAIN DAMAGE ( 5 FDA reports)
BRONCHIAL IRRITATION ( 5 FDA reports)
BRONCHOSCOPY ( 5 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 5 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 5 FDA reports)
CHEST INJURY ( 5 FDA reports)
CHOLANGITIS ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 5 FDA reports)
COCCIDIOIDOMYCOSIS ( 5 FDA reports)
COMMUNICATION DISORDER ( 5 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 5 FDA reports)
CONGENITAL TRACHEOMALACIA ( 5 FDA reports)
CONJUNCTIVAL ABRASION ( 5 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 5 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 5 FDA reports)
CORNEAL DISORDER ( 5 FDA reports)
CORONARY ARTERY THROMBOSIS ( 5 FDA reports)
COUGH DECREASED ( 5 FDA reports)
DENTAL DISCOMFORT ( 5 FDA reports)
DEPRESSION SUICIDAL ( 5 FDA reports)
DERMATITIS ATOPIC ( 5 FDA reports)
DERMATOMYOSITIS ( 5 FDA reports)
DEXTROCARDIA ( 5 FDA reports)
DIABETES INSIPIDUS ( 5 FDA reports)
DIABETIC ULCER ( 5 FDA reports)
DIAPHRAGMATIC DISORDER ( 5 FDA reports)
DISTRACTIBILITY ( 5 FDA reports)
DRUG CLEARANCE DECREASED ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
EAR PRURITUS ( 5 FDA reports)
EDUCATIONAL PROBLEM ( 5 FDA reports)
ELDERLY ( 5 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 5 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 5 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 5 FDA reports)
EXTRASKELETAL OSSIFICATION ( 5 FDA reports)
EYE OEDEMA ( 5 FDA reports)
EYELID DISORDER ( 5 FDA reports)
EYELID PAIN ( 5 FDA reports)
FAT INTOLERANCE ( 5 FDA reports)
FOOD POISONING ( 5 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 5 FDA reports)
FRACTURED COCCYX ( 5 FDA reports)
GALLBLADDER ENLARGEMENT ( 5 FDA reports)
GRAVITATIONAL OEDEMA ( 5 FDA reports)
HAEMOBILIA ( 5 FDA reports)
HAEMORRHAGIC STROKE ( 5 FDA reports)
HAND DEFORMITY ( 5 FDA reports)
HEMICEPHALALGIA ( 5 FDA reports)
HEPATIC CANCER METASTATIC ( 5 FDA reports)
HEPATITIS CHOLESTATIC ( 5 FDA reports)
HOSPICE CARE ( 5 FDA reports)
HYPERPROTEINAEMIA ( 5 FDA reports)
HYPERTROPHY ( 5 FDA reports)
HYPERTROPHY BREAST ( 5 FDA reports)
HYPOCHROMASIA ( 5 FDA reports)
HYPOGEUSIA ( 5 FDA reports)
HYPOPITUITARISM ( 5 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 5 FDA reports)
ILIAC ARTERY STENOSIS ( 5 FDA reports)
INFERIOR VENA CAVA DILATATION ( 5 FDA reports)
INJECTION SITE SCAB ( 5 FDA reports)
INTESTINAL STENOSIS ( 5 FDA reports)
JUGULAR VEIN THROMBOSIS ( 5 FDA reports)
KERATITIS INTERSTITIAL ( 5 FDA reports)
KERATOSIS PILARIS ( 5 FDA reports)
LARYNGEAL NEOPLASM ( 5 FDA reports)
LATEX ALLERGY ( 5 FDA reports)
LEARNING DISORDER ( 5 FDA reports)
LIGAMENT INJURY ( 5 FDA reports)
LIP ULCERATION ( 5 FDA reports)
LOSS OF CONTROL OF LEGS ( 5 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
LYME DISEASE ( 5 FDA reports)
LYMPHANGITIS ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
MACULAR SCAR ( 5 FDA reports)
MADAROSIS ( 5 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 5 FDA reports)
MALIGNANT HYPERTENSION ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 5 FDA reports)
MEDIASTINOSCOPY ( 5 FDA reports)
MENINGITIS VIRAL ( 5 FDA reports)
METASTASES TO HEART ( 5 FDA reports)
METASTASES TO MOUTH ( 5 FDA reports)
MILIA ( 5 FDA reports)
MONOCYTOSIS ( 5 FDA reports)
MONOPARESIS ( 5 FDA reports)
MOUTH PLAQUE ( 5 FDA reports)
MUCOSAL ULCERATION ( 5 FDA reports)
MUCOUS STOOLS ( 5 FDA reports)
MUSCLE HAEMORRHAGE ( 5 FDA reports)
MYCOBACTERIAL INFECTION ( 5 FDA reports)
MYELITIS TRANSVERSE ( 5 FDA reports)
MYOCARDITIS ( 5 FDA reports)
MYOPERICARDITIS ( 5 FDA reports)
NEPHROPATHY TOXIC ( 5 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 5 FDA reports)
OESOPHAGITIS ULCERATIVE ( 5 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 5 FDA reports)
OSTEOPOROTIC FRACTURE ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
OVARIAN MASS ( 5 FDA reports)
OXYGEN SATURATION ABNORMAL ( 5 FDA reports)
PANCREATIC NEOPLASM ( 5 FDA reports)
PARATHYROID DISORDER ( 5 FDA reports)
PERIODONTAL DESTRUCTION ( 5 FDA reports)
PERITONEAL HAEMORRHAGE ( 5 FDA reports)
PERITONEAL INFECTION ( 5 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 5 FDA reports)
PETIT MAL EPILEPSY ( 5 FDA reports)
ABDOMINAL SEPSIS ( 4 FDA reports)
ABSCESS INTESTINAL ( 4 FDA reports)
ACCIDENT AT WORK ( 4 FDA reports)
ACOUSTIC NEUROMA ( 4 FDA reports)
AGONAL DEATH STRUGGLE ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
ALVEOLITIS ALLERGIC ( 4 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 4 FDA reports)
ANIMAL BITE ( 4 FDA reports)
ANORECTAL DISCOMFORT ( 4 FDA reports)
ANOXIA ( 4 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
AORTIC BRUIT ( 4 FDA reports)
AORTIC BYPASS ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
APPLICATION SITE DISCOLOURATION ( 4 FDA reports)
APPLICATION SITE SWELLING ( 4 FDA reports)
ARTERIAL BYPASS OPERATION ( 4 FDA reports)
ARTERIAL INSUFFICIENCY ( 4 FDA reports)
ARTERIAL THROMBOSIS ( 4 FDA reports)
ASTHMATIC CRISIS ( 4 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 4 FDA reports)
BACTERIURIA ( 4 FDA reports)
BALANITIS CANDIDA ( 4 FDA reports)
BIOPSY BONE ABNORMAL ( 4 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 4 FDA reports)
BLADDER CATHETERISATION ( 4 FDA reports)
BODY DYSMORPHIC DISORDER ( 4 FDA reports)
BODY MASS INDEX INCREASED ( 4 FDA reports)
BONE DENSITY ABNORMAL ( 4 FDA reports)
BONE MARROW TOXICITY ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 4 FDA reports)
BREAST CANCER STAGE II ( 4 FDA reports)
BREAST DISCHARGE ( 4 FDA reports)
BREAST FIBROSIS ( 4 FDA reports)
BREAST HYPERPLASIA ( 4 FDA reports)
BREAST MICROCALCIFICATION ( 4 FDA reports)
BREATH SOUNDS DECREASED ( 4 FDA reports)
BUNION OPERATION ( 4 FDA reports)
CALCIFICATION METASTATIC ( 4 FDA reports)
CARDIAC FAILURE CHRONIC ( 4 FDA reports)
CAROTID ARTERY STENT INSERTION ( 4 FDA reports)
CATHETER SITE INFECTION ( 4 FDA reports)
CAUSTIC INJURY ( 4 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM MASS ( 4 FDA reports)
CEREBRAL THROMBOSIS ( 4 FDA reports)
CERVICAL INCOMPETENCE ( 4 FDA reports)
CHORIORETINOPATHY ( 4 FDA reports)
CLEFT PALATE ( 4 FDA reports)
COLONIC STENOSIS ( 4 FDA reports)
COLORECTAL CANCER ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 4 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 4 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 4 FDA reports)
CONGENITAL ANOMALY ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
CULTURE WOUND POSITIVE ( 4 FDA reports)
DEAFNESS TRANSITORY ( 4 FDA reports)
DEAFNESS UNILATERAL ( 4 FDA reports)
DELUSIONAL PERCEPTION ( 4 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 4 FDA reports)
DIABETIC COMPLICATION ( 4 FDA reports)
DIVORCED ( 4 FDA reports)
DUPUYTREN'S CONTRACTURE ( 4 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 4 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 4 FDA reports)
ENTEROBACTER INFECTION ( 4 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 4 FDA reports)
ENTHESOPATHY ( 4 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
ETHMOID SINUS SURGERY ( 4 FDA reports)
EXCESSIVE MASTURBATION ( 4 FDA reports)
EXTRAVASATION BLOOD ( 4 FDA reports)
EYE ROLLING ( 4 FDA reports)
EYELIDS PRURITUS ( 4 FDA reports)
FAECES PALE ( 4 FDA reports)
FASCIITIS ( 4 FDA reports)
FAT TISSUE INCREASED ( 4 FDA reports)
FEAR OF DISEASE ( 4 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
FOLATE DEFICIENCY ( 4 FDA reports)
FOOD AVERSION ( 4 FDA reports)
FRACTURED SACRUM ( 4 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 4 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 4 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 4 FDA reports)
GINGIVAL ATROPHY ( 4 FDA reports)
GLARE ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
GRIMACING ( 4 FDA reports)
GROIN ABSCESS ( 4 FDA reports)
GRUNTING ( 4 FDA reports)
HAEMOCONCENTRATION ( 4 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 4 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 4 FDA reports)
HEPATITIS TOXIC ( 4 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 4 FDA reports)
HEREDITARY ANGIOEDEMA ( 4 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 4 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 4 FDA reports)
HYPERAEMIA ( 4 FDA reports)
HYPERALBUMINAEMIA ( 4 FDA reports)
HYPERCHLORAEMIA ( 4 FDA reports)
HYPERREFLEXIA ( 4 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 4 FDA reports)
HYPOGONADISM ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
HYPOSPADIAS ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
HYPOVITAMINOSIS ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
INJECTION SITE BURNING ( 4 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 4 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 4 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 4 FDA reports)
INTUSSUSCEPTION ( 4 FDA reports)
IRON OVERLOAD ( 4 FDA reports)
JAUNDICE CHOLESTATIC ( 4 FDA reports)
JOINT WARMTH ( 4 FDA reports)
LARYNGEAL INFLAMMATION ( 4 FDA reports)
LARYNGEAL ULCERATION ( 4 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 4 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 4 FDA reports)
LIMB ASYMMETRY ( 4 FDA reports)
LIMB OPERATION ( 4 FDA reports)
LIP HAEMORRHAGE ( 4 FDA reports)
LONG QT SYNDROME ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
LUNG CANCER METASTATIC ( 4 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 4 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 4 FDA reports)
MARITAL PROBLEM ( 4 FDA reports)
MASTECTOMY ( 4 FDA reports)
MAY-THURNER SYNDROME ( 4 FDA reports)
MEAN CELL VOLUME INCREASED ( 4 FDA reports)
MEDICAL DIET ( 4 FDA reports)
MENINGOMYELOCELE ( 4 FDA reports)
METASTATIC CARCINOID TUMOUR ( 4 FDA reports)
MICROANGIOPATHY ( 4 FDA reports)
MICROCYTOSIS ( 4 FDA reports)
MILK ALLERGY ( 4 FDA reports)
MINERAL METABOLISM DISORDER ( 4 FDA reports)
MIXED HYPERLIPIDAEMIA ( 4 FDA reports)
MIXED OLIGO-ASTROCYTOMA ( 4 FDA reports)
MUCOSAL DISCOLOURATION ( 4 FDA reports)
MUCOSAL DRYNESS ( 4 FDA reports)
MYASTHENIC SYNDROME ( 4 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 4 FDA reports)
NASAL DISORDER ( 4 FDA reports)
NASAL SEPTUM PERFORATION ( 4 FDA reports)
NEPHROCALCINOSIS ( 4 FDA reports)
NEURAL TUBE DEFECT ( 4 FDA reports)
OBSTRUCTION GASTRIC ( 4 FDA reports)
OESOPHAGEAL ACHALASIA ( 4 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 4 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 4 FDA reports)
ORBITAL OEDEMA ( 4 FDA reports)
OROMANDIBULAR DYSTONIA ( 4 FDA reports)
OROPHARYNGEAL SPASM ( 4 FDA reports)
OSTEODYSTROPHY ( 4 FDA reports)
OSTEOGENESIS IMPERFECTA ( 4 FDA reports)
OXYGEN CONSUMPTION ( 4 FDA reports)
OXYGEN SATURATION INCREASED ( 4 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 4 FDA reports)
PANCREATITIS NECROTISING ( 4 FDA reports)
PAPULE ( 4 FDA reports)
PARANASAL BIOPSY ABNORMAL ( 4 FDA reports)
PARANEOPLASTIC SYNDROME ( 4 FDA reports)
PARAPROTEINAEMIA ( 4 FDA reports)
PCO2 DECREASED ( 4 FDA reports)
PECTUS EXCAVATUM ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PERFUME SENSITIVITY ( 4 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 4 FDA reports)
PICA ( 4 FDA reports)
PICKWICKIAN SYNDROME ( 4 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 4 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
POLYCHROMASIA ( 4 FDA reports)
POLYCYSTIC OVARIES ( 4 FDA reports)
POLYMEDICATION ( 4 FDA reports)
POSITIVE ROMBERGISM ( 4 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 4 FDA reports)
POST PROCEDURAL FISTULA ( 4 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 4 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 4 FDA reports)
POSTURE ABNORMAL ( 4 FDA reports)
PREMATURE BABY ( 4 FDA reports)
PRODUCT FORMULATION ISSUE ( 4 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 4 FDA reports)
PROTEIN URINE ( 4 FDA reports)
PULMONARY EOSINOPHILIA ( 4 FDA reports)
REBOUND EFFECT ( 4 FDA reports)
RED BLOOD CELL ABNORMALITY ( 4 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 4 FDA reports)
RENAL CYST HAEMORRHAGE ( 4 FDA reports)
RENAL SURGERY ( 4 FDA reports)
RENAL VESSEL DISORDER ( 4 FDA reports)
RESIDUAL URINE ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
RESPIRATORY RATE ( 4 FDA reports)
RESPIRATORY THERAPY ( 4 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 4 FDA reports)
RETINAL DEGENERATION ( 4 FDA reports)
RETROPERITONEAL CANCER ( 4 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 4 FDA reports)
RHINALGIA ( 4 FDA reports)
RHYTHM IDIOVENTRICULAR ( 4 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 4 FDA reports)
SALIVARY GLAND DISORDER ( 4 FDA reports)
SCLERAL DISORDER ( 4 FDA reports)
SCLERITIS ( 4 FDA reports)
SEBORRHOEA ( 4 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 4 FDA reports)
SHOPLIFTING ( 4 FDA reports)
SITUS INVERSUS ( 4 FDA reports)
SKIN BACTERIAL INFECTION ( 4 FDA reports)
SPINA BIFIDA ( 4 FDA reports)
SPINAL COLUMN INJURY ( 4 FDA reports)
SPINAL PAIN ( 4 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 4 FDA reports)
STENT OCCLUSION ( 4 FDA reports)
STILL'S DISEASE ADULT ONSET ( 4 FDA reports)
STILLBIRTH ( 4 FDA reports)
STOMACH MASS ( 4 FDA reports)
SYRINGOMYELIA ( 4 FDA reports)
TERMINAL INSOMNIA ( 4 FDA reports)
TESTICULAR ATROPHY ( 4 FDA reports)
THYROID CANCER METASTATIC ( 4 FDA reports)
TINEA CRURIS ( 4 FDA reports)
TONGUE ERUPTION ( 4 FDA reports)
TONSIL CANCER ( 4 FDA reports)
TONSILLECTOMY ( 4 FDA reports)
TRACHEOBRONCHITIS ( 4 FDA reports)
TRANSPLANT REJECTION ( 4 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 4 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 4 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 4 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 4 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 4 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 4 FDA reports)
VACCINATION FAILURE ( 4 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 4 FDA reports)
VAGINAL PROLAPSE ( 4 FDA reports)
VARICELLA ( 4 FDA reports)
VASCULAR GRAFT OCCLUSION ( 4 FDA reports)
VEIN DISCOLOURATION ( 4 FDA reports)
VENOUS STASIS ( 4 FDA reports)
VERTIGO CNS ORIGIN ( 4 FDA reports)
VIRILISM ( 4 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 4 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 4 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 4 FDA reports)
VITAMIN B12 DECREASED ( 4 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 4 FDA reports)
WEIGHT ABNORMAL ( 4 FDA reports)
WEIGHT GAIN POOR ( 4 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
WOUND HAEMORRHAGE ( 4 FDA reports)
PHLEBITIS SUPERFICIAL ( 3 FDA reports)
PLASMA VISCOSITY DECREASED ( 3 FDA reports)
PLATELET AGGREGATION INCREASED ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
PLEURODESIS ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PNEUMONIA MYCOPLASMAL ( 3 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 3 FDA reports)
PNEUMONITIS CHEMICAL ( 3 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 3 FDA reports)
POOR DENTAL CONDITION ( 3 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 3 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 3 FDA reports)
POST PROCEDURAL DRAINAGE ( 3 FDA reports)
POSTOPERATIVE ADHESION ( 3 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 3 FDA reports)
POSTURING ( 3 FDA reports)
POTENTIATING DRUG INTERACTION ( 3 FDA reports)
POUCHITIS ( 3 FDA reports)
PRECANCEROUS CELLS PRESENT ( 3 FDA reports)
PREGNANCY OF PARTNER ( 3 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 3 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 3 FDA reports)
PRIAPISM ( 3 FDA reports)
PROCEDURAL SITE REACTION ( 3 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 3 FDA reports)
PROSTATIC ABSCESS ( 3 FDA reports)
PROTEIN TOTAL ABNORMAL ( 3 FDA reports)
PROTRUSION TONGUE ( 3 FDA reports)
PSYCHOSOMATIC DISEASE ( 3 FDA reports)
PULMONARY FUNCTION CHALLENGE TEST ABNORMAL ( 3 FDA reports)
PULMONARY TOXICITY ( 3 FDA reports)
PULSE ABNORMAL ( 3 FDA reports)
RADIATION FIBROSIS ( 3 FDA reports)
RADIATION INJURY ( 3 FDA reports)
RECALL PHENOMENON ( 3 FDA reports)
REGURGITATION OF FOOD ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 3 FDA reports)
RETICULOCYTE COUNT INCREASED ( 3 FDA reports)
RETICULOCYTOSIS ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RETINOPATHY HYPERTENSIVE ( 3 FDA reports)
RETROPERITONEAL HAEMATOMA ( 3 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 3 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 3 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 3 FDA reports)
SALIVA DISCOLOURATION ( 3 FDA reports)
SALMONELLA BACTERAEMIA ( 3 FDA reports)
SALMONELLOSIS ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 3 FDA reports)
SCIATIC NERVE NEUROPATHY ( 3 FDA reports)
SEBACEOUS HYPERPLASIA ( 3 FDA reports)
SEMEN VOLUME DECREASED ( 3 FDA reports)
SEPSIS NEONATAL ( 3 FDA reports)
SERUM FERRITIN DECREASED ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SINUSITIS FUNGAL ( 3 FDA reports)
SKIN CANDIDA ( 3 FDA reports)
SKIN DESQUAMATION ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
SMALL CELL CARCINOMA ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
SOMATOFORM DISORDER ( 3 FDA reports)
SPERMATOZOA ABNORMAL ( 3 FDA reports)
SPINAL HAEMANGIOMA ( 3 FDA reports)
SPIROMETRY ABNORMAL ( 3 FDA reports)
SPLEEN CONGESTION ( 3 FDA reports)
SPLENIC RUPTURE ( 3 FDA reports)
STEATORRHOEA ( 3 FDA reports)
STREPTOCOCCAL SEPSIS ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
STRESS INCONTINENCE ( 3 FDA reports)
STRESS SYMPTOMS ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 3 FDA reports)
SUBDURAL HAEMORRHAGE ( 3 FDA reports)
SYMPHYSIOLYSIS ( 3 FDA reports)
SYRINGE ISSUE ( 3 FDA reports)
TARSAL TUNNEL SYNDROME ( 3 FDA reports)
TENOSYNOVITIS STENOSANS ( 3 FDA reports)
TESTICULAR PAIN ( 3 FDA reports)
THOUGHT BLOCKING ( 3 FDA reports)
THREATENED LABOUR ( 3 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
THYROID MASS ( 3 FDA reports)
THYROID OPERATION ( 3 FDA reports)
TORTICOLLIS ( 3 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 3 FDA reports)
TRACHEAL INJURY ( 3 FDA reports)
TRACHEAL STENOSIS ( 3 FDA reports)
TRACHEITIS ( 3 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 3 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 3 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 3 FDA reports)
URINE AMPHETAMINE POSITIVE ( 3 FDA reports)
URINE ARSENIC INCREASED ( 3 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
UTERINE ATROPHY ( 3 FDA reports)
UTERINE CYST ( 3 FDA reports)
VASCULAR ACCESS COMPLICATION ( 3 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 3 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 3 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 3 FDA reports)
VENTRICULAR FAILURE ( 3 FDA reports)
VERBAL ABUSE ( 3 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 3 FDA reports)
VESSEL PERFORATION ( 3 FDA reports)
VESTIBULAR NEURONITIS ( 3 FDA reports)
VIRAL PHARYNGITIS ( 3 FDA reports)
VISCERAL CONGESTION ( 3 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 3 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 3 FDA reports)
ABDOMINAL WALL NEOPLASM ( 3 FDA reports)
ABNORMAL WEIGHT GAIN ( 3 FDA reports)
ADENOCARCINOMA PANCREAS ( 3 FDA reports)
ADRENAL HAEMORRHAGE ( 3 FDA reports)
AGONAL RHYTHM ( 3 FDA reports)
AGORAPHOBIA ( 3 FDA reports)
ALBUMIN URINE PRESENT ( 3 FDA reports)
ALLERGY TO VACCINE ( 3 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 3 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAESTHETIC COMPLICATION ( 3 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 3 FDA reports)
ANIMAL SCRATCH ( 3 FDA reports)
ANISOCYTOSIS ( 3 FDA reports)
ANOGENITAL WARTS ( 3 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 3 FDA reports)
ANTICOAGULANT THERAPY ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
AORTIC DISORDER ( 3 FDA reports)
APALLIC SYNDROME ( 3 FDA reports)
APPLICATION SITE URTICARIA ( 3 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 3 FDA reports)
ASPLENIA ( 3 FDA reports)
ATHEROSCLEROSIS ( 3 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 3 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 3 FDA reports)
AUTONOMIC NEUROPATHY ( 3 FDA reports)
BACILLUS INFECTION ( 3 FDA reports)
BARTHOLIN'S CYST ( 3 FDA reports)
BED REST ( 3 FDA reports)
BEHCET'S SYNDROME ( 3 FDA reports)
BELLIGERENCE ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 3 FDA reports)
BIOPSY BREAST ABNORMAL ( 3 FDA reports)
BIOPSY COLON ( 3 FDA reports)
BIOPSY LIVER ABNORMAL ( 3 FDA reports)
BLADDER CANCER RECURRENT ( 3 FDA reports)
BLINDNESS CORTICAL ( 3 FDA reports)
BLOOD ALCOHOL INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ( 3 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 3 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM INCREASED ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD OSMOLARITY INCREASED ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 3 FDA reports)
BLUNTED AFFECT ( 3 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 3 FDA reports)
BONE DENSITY INCREASED ( 3 FDA reports)
BRAIN MASS ( 3 FDA reports)
BREAST CANCER STAGE I ( 3 FDA reports)
BREAST INFECTION ( 3 FDA reports)
BREAST NEOPLASM ( 3 FDA reports)
BRONCHOSCOPY ABNORMAL ( 3 FDA reports)
BUTTOCK PAIN ( 3 FDA reports)
CALCIUM DEFICIENCY ( 3 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 3 FDA reports)
CARCINOMA IN SITU ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIAC OUTPUT DECREASED ( 3 FDA reports)
CARDIAC VALVE VEGETATION ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CATAPLEXY ( 3 FDA reports)
CATATONIA ( 3 FDA reports)
CATHETER SITE RELATED REACTION ( 3 FDA reports)
CELLULITIS ORBITAL ( 3 FDA reports)
CENTRAL OBESITY ( 3 FDA reports)
CEREBRAL MICROANGIOPATHY ( 3 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 3 FDA reports)
CHEMICAL POISONING ( 3 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 3 FDA reports)
COLON CANCER STAGE III ( 3 FDA reports)
COLON GANGRENE ( 3 FDA reports)
COLONOSCOPY ( 3 FDA reports)
COLOUR BLINDNESS ( 3 FDA reports)
COMPLICATED MIGRAINE ( 3 FDA reports)
COMPUTERISED TOMOGRAM ( 3 FDA reports)
CONTRALATERAL BREAST CANCER ( 3 FDA reports)
COR PULMONALE CHRONIC ( 3 FDA reports)
CORNEAL EROSION ( 3 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 3 FDA reports)
CORONARY ARTERY SURGERY ( 3 FDA reports)
CORYNEBACTERIUM INFECTION ( 3 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 3 FDA reports)
CSF TEST ABNORMAL ( 3 FDA reports)
CULTURE POSITIVE ( 3 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 3 FDA reports)
DAYDREAMING ( 3 FDA reports)
DEATH OF RELATIVE ( 3 FDA reports)
DEATH OF SPOUSE ( 3 FDA reports)
DELAYED SLEEP PHASE ( 3 FDA reports)
DENTAL DISORDER PROPHYLAXIS ( 3 FDA reports)
DENTAL PROSTHESIS USER ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DERMATITIS HERPETIFORMIS ( 3 FDA reports)
DERMATITIS PSORIASIFORM ( 3 FDA reports)
DETOXIFICATION ( 3 FDA reports)
DEVICE INTERACTION ( 3 FDA reports)
DIAGNOSTIC PROCEDURE ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE III ( 3 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 3 FDA reports)
DISACCHARIDE METABOLISM DISORDER ( 3 FDA reports)
DREAMY STATE ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DYSKINESIA OESOPHAGEAL ( 3 FDA reports)
DYSTROPHIC CALCIFICATION ( 3 FDA reports)
ECZEMA HERPETICUM ( 3 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 3 FDA reports)
ENDOMETRIAL CANCER ( 3 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 3 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EROSIVE DUODENITIS ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
ESSENTIAL TREMOR ( 3 FDA reports)
EXCITABILITY ( 3 FDA reports)
EXPOSURE TO ALLERGEN ( 3 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 3 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 3 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 3 FDA reports)
EXTRAVASATION ( 3 FDA reports)
EYELID FUNCTION DISORDER ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
FAECAL VOLUME INCREASED ( 3 FDA reports)
FAILURE OF IMPLANT ( 3 FDA reports)
FAMILIAL TREMOR ( 3 FDA reports)
FEMORAL NERVE INJURY ( 3 FDA reports)
FIBROADENOMA OF BREAST ( 3 FDA reports)
FINGER AMPUTATION ( 3 FDA reports)
FLOPPY IRIS SYNDROME ( 3 FDA reports)
FOETAL GROWTH RETARDATION ( 3 FDA reports)
FOOD INTERACTION ( 3 FDA reports)
FORCED EXPIRATORY VOLUME ABNORMAL ( 3 FDA reports)
FOREIGN BODY IN EYE ( 3 FDA reports)
FRACTURE TREATMENT ( 3 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 3 FDA reports)
GALACTORRHOEA ( 3 FDA reports)
GASTRECTOMY ( 3 FDA reports)
GASTRIC VARICES ( 3 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 3 FDA reports)
GASTROENTERITIS SALMONELLA ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GENE MUTATION ( 3 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 3 FDA reports)
GIARDIASIS ( 3 FDA reports)
GLOMERULONEPHRITIS ( 3 FDA reports)
GRIEF REACTION ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HAEMOGLOBIN ABNORMAL ( 3 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 3 FDA reports)
HEART VALVE STENOSIS ( 3 FDA reports)
HEAT STROKE ( 3 FDA reports)
HEPATIC ENZYME ABNORMAL ( 3 FDA reports)
HEPATIC TRAUMA ( 3 FDA reports)
HERNIA PAIN ( 3 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
HIGH RISK PREGNANCY ( 3 FDA reports)
HOMICIDE ( 3 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 3 FDA reports)
HYPEREMESIS GRAVIDARUM ( 3 FDA reports)
HYPOCHLORAEMIA ( 3 FDA reports)
HYPOPERFUSION ( 3 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 3 FDA reports)
ILIAC ARTERY OCCLUSION ( 3 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 3 FDA reports)
IMPULSE-CONTROL DISORDER ( 3 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 3 FDA reports)
INCISION SITE HAEMORRHAGE ( 3 FDA reports)
INCISION SITE INFECTION ( 3 FDA reports)
INCISION SITE PAIN ( 3 FDA reports)
INFECTED SKIN ULCER ( 3 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
INFUSION SITE EXTRAVASATION ( 3 FDA reports)
INJECTION SITE CELLULITIS ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
INTESTINAL MASS ( 3 FDA reports)
INTESTINAL OPERATION ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
INTUBATION ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 3 FDA reports)
KELOID SCAR ( 3 FDA reports)
KYPHOSCOLIOSIS ( 3 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LARYNGEAL CANCER STAGE 0 ( 3 FDA reports)
LARYNGEAL ERYTHEMA ( 3 FDA reports)
LARYNGEAL INJURY ( 3 FDA reports)
LATENT TUBERCULOSIS ( 3 FDA reports)
LEIOMYOSARCOMA ( 3 FDA reports)
LIP NEOPLASM ( 3 FDA reports)
LIVER TRANSPLANT ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 3 FDA reports)
LUNG TRANSPLANT ( 3 FDA reports)
LUNG WEDGE RESECTION ( 3 FDA reports)
LYMPHOCYTIC INFILTRATION ( 3 FDA reports)
MACROCYTOSIS ( 3 FDA reports)
MALABSORPTION ( 3 FDA reports)
MAMMOGRAM ABNORMAL ( 3 FDA reports)
MEAN CELL VOLUME DECREASED ( 3 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 3 FDA reports)
MEDIASTINAL SHIFT ( 3 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 3 FDA reports)
MEGACOLON ( 3 FDA reports)
MEGAKARYOCYTES INCREASED ( 3 FDA reports)
MENOPAUSAL SYMPTOMS ( 3 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 3 FDA reports)
METASTASES TO BLADDER ( 3 FDA reports)
METASTASES TO KIDNEY ( 3 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 3 FDA reports)
MIGRAINE WITHOUT AURA ( 3 FDA reports)
MITRAL VALVE REPLACEMENT ( 3 FDA reports)
MONONEURITIS ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MUSCLE ENZYME INCREASED ( 3 FDA reports)
MUSCLE HYPERTROPHY ( 3 FDA reports)
MYCOTIC ALLERGY ( 3 FDA reports)
MYELOFIBROSIS ( 3 FDA reports)
MYELOMALACIA ( 3 FDA reports)
MYOCARDIAL STRAIN ( 3 FDA reports)
NAIL INFECTION ( 3 FDA reports)
NASAL SEPTAL OPERATION ( 3 FDA reports)
NASAL SEPTUM DISORDER ( 3 FDA reports)
NEAR DROWNING ( 3 FDA reports)
NEPHRITIS ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUROMA ( 3 FDA reports)
NEUROPATHIC ARTHROPATHY ( 3 FDA reports)
NOCARDIOSIS ( 3 FDA reports)
NODULE ON EXTREMITY ( 3 FDA reports)
NOSE DEFORMITY ( 3 FDA reports)
NUCHAL RIGIDITY ( 3 FDA reports)
OCULAR HYPERTENSION ( 3 FDA reports)
OCULAR MYASTHENIA ( 3 FDA reports)
OEDEMA GENITAL ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
OESOPHAGEAL INJURY ( 3 FDA reports)
OESOPHAGEAL OEDEMA ( 3 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 3 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 3 FDA reports)
ORAL DISCHARGE ( 3 FDA reports)
OSTEOARTHROPATHY ( 3 FDA reports)
PANCREATIC INSUFFICIENCY ( 3 FDA reports)
PELVIC ABSCESS ( 3 FDA reports)
PELVIC ADHESIONS ( 3 FDA reports)
PELVIC DISCOMFORT ( 3 FDA reports)
PELVIC HAEMATOMA ( 3 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 3 FDA reports)
PERFORATION BILE DUCT ( 3 FDA reports)
PERIDIVERTICULAR ABSCESS ( 3 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 3 FDA reports)
PERIRECTAL ABSCESS ( 3 FDA reports)
PERITONEAL DIALYSIS ( 3 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 3 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABDOMINAL OPERATION ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABDOMINAL WALL DISORDER ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACUTE ENDOCARDITIS ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE PHASE REACTION ( 2 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 2 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE III ( 2 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 2 FDA reports)
ADMINISTRATION SITE REACTION ( 2 FDA reports)
ADRENALITIS ( 2 FDA reports)
ADRENOMEGALY ( 2 FDA reports)
AGITATED DEPRESSION ( 2 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 2 FDA reports)
ALCOHOLIC LIVER DISEASE ( 2 FDA reports)
ALLERGY TO ANIMAL ( 2 FDA reports)
ALLERGY TO PLANTS ( 2 FDA reports)
AMBLYOPIA ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAL CANDIDIASIS ( 2 FDA reports)
ANAL SPHINCTER ATONY ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
ANEURYSM REPAIR ( 2 FDA reports)
ANGIOGRAM ( 2 FDA reports)
ANGIOGRAM ABNORMAL ( 2 FDA reports)
ANGIOSARCOMA ( 2 FDA reports)
ANION GAP DECREASED ( 2 FDA reports)
ANKLE OPERATION ( 2 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
AORTIC ELONGATION ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
APPLICATION SITE BLEEDING ( 2 FDA reports)
APPLICATION SITE DISCOMFORT ( 2 FDA reports)
APPLICATION SITE HAEMATOMA ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ARTERIOGRAM CORONARY ( 2 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 2 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 2 FDA reports)
ARTHROFIBROSIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ASPERGILLOMA ( 2 FDA reports)
ATELECTASIS NEONATAL ( 2 FDA reports)
ATONIC URINARY BLADDER ( 2 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
AVULSION FRACTURE ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
BASE EXCESS ( 2 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 2 FDA reports)
BETA-2 GLYCOPROTEIN ANTIBODY POSITIVE ( 2 FDA reports)
BIFASCICULAR BLOCK ( 2 FDA reports)
BILE DUCT STENT INSERTION ( 2 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BILIARY FIBROSIS ( 2 FDA reports)
BILIARY FISTULA ( 2 FDA reports)
BINGE EATING ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BIOPSY HEART ABNORMAL ( 2 FDA reports)
BIOPSY LUNG ( 2 FDA reports)
BIOPSY VOCAL CORD ( 2 FDA reports)
BLADDER DIVERTICULUM ( 2 FDA reports)
BLADDER NEOPLASM SURGERY ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN ( 2 FDA reports)
BLOOD CORTISOL ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD HOMOCYSTEINE DECREASED ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BLOOD SODIUM ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BLOOD UREA ABNORMAL ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
BLUE TOE SYNDROME ( 2 FDA reports)
BODY MASS INDEX DECREASED ( 2 FDA reports)
BODY TINEA ( 2 FDA reports)
BONE DENSITOMETRY ( 2 FDA reports)
BONE FORMATION INCREASED ( 2 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 2 FDA reports)
BRACHIAL PLEXUS INJURY ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN LOBECTOMY ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 2 FDA reports)
BRAIN OPERATION ( 2 FDA reports)
BRAIN SCAN ABNORMAL ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREAST CANCER STAGE III ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BREATH SOUNDS ( 2 FDA reports)
BRONCHIAL OEDEMA ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 2 FDA reports)
BUCCAL POLYP ( 2 FDA reports)
BURN OESOPHAGEAL ( 2 FDA reports)
BURNING SENSATION MUCOSAL ( 2 FDA reports)
BURNS FIRST DEGREE ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
BURNS THIRD DEGREE ( 2 FDA reports)
CAPILLARY FRAGILITY ( 2 FDA reports)
CARBON DIOXIDE ABNORMAL ( 2 FDA reports)
CARBON MONOXIDE POISONING ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIAC PSEUDOANEURYSM ( 2 FDA reports)
CARDIAC SEPTAL DEFECT ( 2 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 2 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 2 FDA reports)
CARDIORENAL SYNDROME ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CEREBROSPINAL FLUID DRAINAGE ( 2 FDA reports)
CERVICAL CYST ( 2 FDA reports)
CHALAZION ( 2 FDA reports)
CHEMICAL INJURY ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHORIOAMNIONITIS ( 2 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
CHRONIC LEFT VENTRICULAR FAILURE ( 2 FDA reports)
CHRONIC LEUKAEMIA ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COCCYDYNIA ( 2 FDA reports)
COITAL BLEEDING ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 2 FDA reports)
COLON CANCER STAGE IV ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COLONIC FISTULA ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
COMPLICATION OF PREGNANCY ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
CONGENITAL EYE DISORDER ( 2 FDA reports)
CONGENITAL EYE NAEVUS ( 2 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 2 FDA reports)
CONGENITAL OESOPHAGEAL ANOMALY ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONJUNCTIVAL PALLOR ( 2 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
CORNEAL DEGENERATION ( 2 FDA reports)
CORNEAL OPERATION ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CORONARY ARTERY DISSECTION ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CORTISOL FREE URINE INCREASED ( 2 FDA reports)
CROUP INFECTIOUS ( 2 FDA reports)
CRYPTOCOCCOSIS ( 2 FDA reports)
CUBITAL TUNNEL SYNDROME ( 2 FDA reports)
CYANOPSIA ( 2 FDA reports)
CYSTIC FIBROSIS ( 2 FDA reports)
CYSTIC FIBROSIS LUNG ( 2 FDA reports)
CYSTITIS GLANDULARIS ( 2 FDA reports)
CYSTOPEXY ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 2 FDA reports)
DENTAL NECROSIS ( 2 FDA reports)
DENTAL PULP DISORDER ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DESQUAMATION MOUTH ( 2 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 2 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DISLOCATION OF VERTEBRA ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DISTAL INTESTINAL OBSTRUCTION SYNDROME ( 2 FDA reports)
DIZZINESS EXERTIONAL ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DUODENAL OBSTRUCTION ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
EARLY MORNING AWAKENING ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
ELECTRIC SHOCK ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
EMERGENCY CARE ( 2 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
ENDOVENOUS ABLATION ( 2 FDA reports)
ENTEROCELE ( 2 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
EPIGLOTTIC OEDEMA ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 2 FDA reports)
EX-TOBACCO USER ( 2 FDA reports)
EXERCISE LACK OF ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EYE ALLERGY ( 2 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
EYE INFECTION VIRAL ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE LASER SURGERY ( 2 FDA reports)
EYE OPERATION COMPLICATION ( 2 FDA reports)
EYE PENETRATION ( 2 FDA reports)
EYELID CYST ( 2 FDA reports)
FACIAL NERVE DISORDER ( 2 FDA reports)
FACIAL WASTING ( 2 FDA reports)
FACTOR VII DEFICIENCY ( 2 FDA reports)
FAILED INDUCTION OF LABOUR ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FEAR OF NEEDLES ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FEEDING TUBE COMPLICATION ( 2 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 2 FDA reports)
FIBRINOLYSIS INCREASED ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FOLLICLE CENTRE LYMPHOMA DIFFUSE SMALL CELL LYMPHOMA ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FUNGAL CYSTITIS ( 2 FDA reports)
FUNGAL TEST POSITIVE ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GASTRIC OPERATION ( 2 FDA reports)
GASTRITIS ATROPHIC ( 2 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 2 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ( 2 FDA reports)
GENERAL SYMPTOM ( 2 FDA reports)
GENITAL BURNING SENSATION ( 2 FDA reports)
GENITAL HERPES ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GESTATIONAL HYPERTENSION ( 2 FDA reports)
GINGIVAL HYPOPLASIA ( 2 FDA reports)
GLIOBLASTOMA ( 2 FDA reports)
GLOBAL AMNESIA ( 2 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 2 FDA reports)
GLOMUS TUMOUR ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 2 FDA reports)
GRANULOCYTES ABNORMAL ( 2 FDA reports)
GROWING PAINS ( 2 FDA reports)
HAEMANGIOMA OF SKIN ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HALITOSIS ( 2 FDA reports)
HAND AMPUTATION ( 2 FDA reports)
HEAD AND NECK CANCER ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEPATIC INFECTION ( 2 FDA reports)
HEPATIC VEIN THROMBOSIS ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS C POSITIVE ( 2 FDA reports)
HEPATITIS VIRAL ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HIP SWELLING ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 2 FDA reports)
HYDROXYCORTICOSTEROIDS INCREASED ( 2 FDA reports)
HYPERCORTICOIDISM ( 2 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 2 FDA reports)
HYPERMETABOLISM ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
HYPERVOLAEMIA ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOMETABOLISM ( 2 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
IGA NEPHROPATHY ( 2 FDA reports)
ILEAL GANGRENE ( 2 FDA reports)
ILLITERACY ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INCORRECT PRODUCT STORAGE ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFERTILITY ( 2 FDA reports)
INFLAMMATION OF WOUND ( 2 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 2 FDA reports)
INFUSION SITE PRURITUS ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INFUSION SITE URTICARIA ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INJECTION SITE ANAESTHESIA ( 2 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 2 FDA reports)
INJECTION SITE MOVEMENT IMPAIRMENT ( 2 FDA reports)
INJECTION SITE STREAKING ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTENSIVE CARE ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTERMEDIATE DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTESTINAL MUCOSAL ATROPHY ( 2 FDA reports)
INTESTINAL STOMA COMPLICATION ( 2 FDA reports)
INTESTINAL STRANGULATION ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
IRREGULAR SLEEP PHASE ( 2 FDA reports)
JAW CYST ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LACRIMAL DISORDER ( 2 FDA reports)
LAPAROSCOPIC SURGERY ( 2 FDA reports)
LARGE FOR DATES BABY ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LARYNGEAL MASS ( 2 FDA reports)
LARYNGEAL STENOSIS ( 2 FDA reports)
LARYNGOMALACIA ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LICHEN SCLEROSUS ( 2 FDA reports)
LIGAMENT CALCIFICATION ( 2 FDA reports)
LIVER OPERATION ( 2 FDA reports)
LOCAL REACTION ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE II ( 2 FDA reports)
LUNG HERNIA ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPHOCYTE COUNT ( 2 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 2 FDA reports)
LYMPHORRHOEA ( 2 FDA reports)
MACULE ( 2 FDA reports)
MALIGNANT MELANOMA IN SITU ( 2 FDA reports)
MARFAN'S SYNDROME ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
MENTAL RETARDATION ( 2 FDA reports)
MESENTERIC ARTERY STENOSIS ( 2 FDA reports)
METANEPHRINE URINE INCREASED ( 2 FDA reports)
METASTASES TO SMALL INTESTINE ( 2 FDA reports)
METASTATIC LYMPHOMA ( 2 FDA reports)
METASTATIC UTERINE CANCER ( 2 FDA reports)
MICTURITION FREQUENCY DECREASED ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MILLER FISHER SYNDROME ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MOANING ( 2 FDA reports)
MOLE EXCISION ( 2 FDA reports)
MUCOSAL INFECTION ( 2 FDA reports)
MULTIMORBIDITY ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MUSCLE FIBROSIS ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 2 FDA reports)
MYELOID LEUKAEMIA ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
NAIL HYPERTROPHY ( 2 FDA reports)
NASAL INFLAMMATION ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NEURILEMMOMA BENIGN ( 2 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 2 FDA reports)
NITRITE URINE ABSENT ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NOREPINEPHRINE INCREASED ( 2 FDA reports)
NORMAL DELIVERY ( 2 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 2 FDA reports)
OESOPHAGEAL DILATATION ( 2 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL INFECTION ( 2 FDA reports)
OESOPHAGEAL POLYP ( 2 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 2 FDA reports)
ON AND OFF PHENOMENON ( 2 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
OPTIC DISC DRUSEN ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL LICHEN PLANUS ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORTHOSIS USER ( 2 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 2 FDA reports)
PALLIATIVE CARE ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PANCREATIC CALCIFICATION ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANCREATOBILIARY SPHINCTEROTOMY ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE INCREASED ( 2 FDA reports)
PEDAL PULSE ABNORMAL ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PELVIC MASS ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PENILE OEDEMA ( 2 FDA reports)
PERIOSTITIS ( 2 FDA reports)
PERIPHERAL NERVE OPERATION ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PHARMACOPHOBIA ( 2 FDA reports)
PHARYNGEAL NEOPLASM ( 2 FDA reports)
PHLEBOTHROMBOSIS ( 2 FDA reports)
PHOTODERMATOSIS ( 2 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PHYSICAL EXAMINATION NORMAL ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PLAGUE ( 2 FDA reports)
PLATELET TRANSFUSION ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PLEURAL RUB ( 2 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONIA INFLUENZAL ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 2 FDA reports)
POLYPOIDAL CHOROIDAL VASCULOPATHY ( 2 FDA reports)
PORTAL VEIN PHLEBITIS ( 2 FDA reports)
POST LAMINECTOMY SYNDROME ( 2 FDA reports)
POST PROCEDURAL CELLULITIS ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 2 FDA reports)
POST PROCEDURAL PNEUMONIA ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
POSTICTAL HEADACHE ( 2 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PROCEDURAL HYPERTENSION ( 2 FDA reports)
PRODUCT COLOUR ISSUE ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 2 FDA reports)
PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
PROSTATE INFECTION ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 2 FDA reports)
PROTEIN C DECREASED ( 2 FDA reports)
PROTEIN C DEFICIENCY ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PRURITUS ANI ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 2 FDA reports)
PULMONARY BULLA ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY FUNCTION TEST INCREASED ( 2 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 2 FDA reports)
PULMONARY OEDEMA NEONATAL ( 2 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PURPURA SENILE ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RADIATION NEUROPATHY ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RECTAL FISSURE ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
REFRACTION DISORDER ( 2 FDA reports)
RENAL ANEURYSM ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RENAL STONE REMOVAL ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RETINITIS PIGMENTOSA ( 2 FDA reports)
RETROPERITONEAL EFFUSION ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
SALIVARY GLAND MASS ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SARCOMA ( 2 FDA reports)
SCARLET FEVER ( 2 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 2 FDA reports)
SCLERODACTYLIA ( 2 FDA reports)
SECONDARY HYPOTHYROIDISM ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SEMEN DISCOLOURATION ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SEPTAL PANNICULITIS ( 2 FDA reports)
SEROSITIS ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SKIN TEST POSITIVE ( 2 FDA reports)
SKIN ULCER HAEMORRHAGE ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
SPERM COUNT DECREASED ( 2 FDA reports)
SPINAL HAEMATOMA ( 2 FDA reports)
SPLINTER HAEMORRHAGES ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SURGICAL FAILURE ( 2 FDA reports)
SUTURE INSERTION ( 2 FDA reports)
SYNOVIAL DISORDER ( 2 FDA reports)
T-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
TACHYPHYLAXIS ( 2 FDA reports)
TENDON CALCIFICATION ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
TESTICULAR TORSION ( 2 FDA reports)
TETANY ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THALAMUS HAEMORRHAGE ( 2 FDA reports)
THEFT ( 2 FDA reports)
THORACIC OUTLET SYNDROME ( 2 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX ABNORMAL ( 2 FDA reports)
THYROID CYST ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
THYROXINE INCREASED ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TONSILLITIS BACTERIAL ( 2 FDA reports)
TOOTH MALFORMATION ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 2 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 2 FDA reports)
TRANCE ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
TRICHOTILLOMANIA ( 2 FDA reports)
TRIGONITIS ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
TUMOUR NECROSIS ( 2 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 2 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 2 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY BLADDER POLYP ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 2 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 2 FDA reports)
URINE CALCIUM ( 2 FDA reports)
URTICARIA THERMAL ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
UTERINE ENLARGEMENT ( 2 FDA reports)
VAGINAL CANCER ( 2 FDA reports)
VAGINAL CANDIDIASIS ( 2 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VASCULAR STENT INSERTION ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VENOUS RECANALISATION ( 2 FDA reports)
VENOUS VALVE RUPTURED ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VERTEBRAL INJURY ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VIRAL PERICARDITIS ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VITAL CAPACITY DECREASED ( 2 FDA reports)
VITAMIN A DEFICIENCY ( 2 FDA reports)
VITAMIN D ABNORMAL ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VOCAL CORD POLYP ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
VULVOVAGINAL ERYTHEMA ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WATER POLLUTION ( 2 FDA reports)
WEGENER'S GRANULOMATOSIS ( 2 FDA reports)
WEIGHT ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 2 FDA reports)
WOUND DEBRIDEMENT ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
PHENYLKETONURIA ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PINEAL NEOPLASM ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PITUITARY TUMOUR RECURRENT ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLATELET PRODUCTION DECREASED ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONECTOMY ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA LIPOID ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORCELAIN GALLBLADDER ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POSTPARTUM DEPRESSION ( 1 FDA reports)
POSTPARTUM DISORDER ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 1 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL HEADACHE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATE TENDERNESS ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC MASS ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROTEIN C INCREASED ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSEUDOPAPILLOEDEMA ( 1 FDA reports)
PSEUDOPOLYPOSIS ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY COCCIDIOIDES ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUNCTURE SITE PAIN ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PURPURA FULMINANS ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYELONEPHRITIS CHRONIC ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
PYOGENIC GRANULOMA ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
RADIATION FIBROSIS - LUNG ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RADIOALLERGOSORBENT TEST POSITIVE ( 1 FDA reports)
RASH PAPULOSQUAMOUS ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO DRUG EXCIPIENT ( 1 FDA reports)
RECTAL ADENOMA ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFLEX TEST ABNORMAL ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RESPIROVIRUS TEST POSITIVE ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL CYST ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RIB DEFORMITY ( 1 FDA reports)
RIB EXCISION ( 1 FDA reports)
RICHTER'S SYNDROME ( 1 FDA reports)
RIFT VALLEY FEVER ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SCAN ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN BONE MARROW ABNORMAL ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SEMEN ABNORMAL ( 1 FDA reports)
SEMEN LIQUEFACTION ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 1 FDA reports)
SEXUAL INHIBITION ( 1 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 1 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHONE COMPLEX ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SKELETAL MUSCLE ENZYMES ( 1 FDA reports)
SKELETON DYSPLASIA ( 1 FDA reports)
SKIN CANCER METASTATIC ( 1 FDA reports)
SKIN DEGENERATIVE DISORDER ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SMOKE SENSITIVITY ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SOLAR ELASTOSIS ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 1 FDA reports)
SPINAL CORD INFARCTION ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC VEIN OCCLUSION ( 1 FDA reports)
SPLENITIS ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
SPUTUM DECREASED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 1 FDA reports)
STERNAL WIRING ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STRUCK BY LIGHTNING ( 1 FDA reports)
STUBBORNNESS ( 1 FDA reports)
SUBCLAVIAN ARTERY OCCLUSION ( 1 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 1 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUPRANUCLEAR PALSY ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
SYPHILIS TEST POSITIVE ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TANDEM GAIT TEST ( 1 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TERMINAL DRIBBLING ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
THANATOPHOBIA ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYMOMA MALIGNANT ( 1 FDA reports)
THYMUS HYPERTROPHY ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TINEA CAPITIS ( 1 FDA reports)
TOCOLYSIS ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE CYST ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR ATROPHY ( 1 FDA reports)
TONSILLAR CYST ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH CROWDING ( 1 FDA reports)
TOOTH DECALCIFICATION ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TOTAL LUNG CAPACITY ABNORMAL ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBAL LIGATION ( 1 FDA reports)
TUMOUR THROMBOSIS ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
TYPHUS RICKETTSIA TEST POSITIVE ( 1 FDA reports)
ULTRASOUND ABDOMEN ( 1 FDA reports)
ULTRASOUND SCAN ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URETHRAL DILATION PROCEDURE ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHRAL STRICTURE ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URETHRITIS NONINFECTIVE ( 1 FDA reports)
URINARY CYSTECTOMY ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT INFLAMMATION ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE POTASSIUM INCREASED ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CERVIX ATROPHY ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE RUPTURE ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL DYSPLASIA ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL PH INCREASED ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VANILLYL MANDELIC ACID URINE INCREASED ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR FRAGILITY ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASCULAR SKIN DISORDER ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENOUS ANEURYSM ( 1 FDA reports)
VENOUS HAEMORRHAGE ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS PRESSURE JUGULAR ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENTILATION PERFUSION MISMATCH ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VERTEBRAL ARTERY DISSECTION ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VIOLENT IDEATION ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VITAL CAPACITY ABNORMAL ( 1 FDA reports)
VITAMIN E DECREASED ( 1 FDA reports)
VITAMIN K DECREASED ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
VULVOVAGINITIS TRICHOMONAL ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WISDOM TEETH REMOVAL ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
X-RAY LIMB ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
XEROSIS ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL OBESITY ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABDOMINOPLASTY ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACCESSORY MUSCLE ( 1 FDA reports)
ACCESSORY SALIVARY GLAND ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACQUIRED PHIMOSIS ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOLIPOMA ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
ALCOHOLIC ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLEN'S TEST ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANKLE DEFORMITY ( 1 FDA reports)
ANOGENITAL DYSPLASIA ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHRODISIAC THERAPY ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE ECZEMA ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE PERSPIRATION ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOGRAM ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMORRHAGE ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ARTIFICIAL MENOPAUSE ( 1 FDA reports)
ARTIFICIAL URINARY SPHINCTER IMPLANT ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION JOINT ABNORMAL ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
ASSISTED FERTILISATION ( 1 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL FOOD POISONING ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BASAL GANGLION DEGENERATION ( 1 FDA reports)
BASILAR ARTERY STENOSIS ( 1 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BED BUG INFESTATION ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN LARYNGEAL NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF PINEAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BENIGN UTERINE NEOPLASM ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILE OUTPUT INCREASED ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BIOPSY ABDOMINAL WALL ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ABNORMAL ( 1 FDA reports)
BIOPSY PHARYNX ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER ABLATION ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER SPHINCTER ATONY ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALDOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CARBON MONOXIDE ( 1 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CREATINE ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD OESTROGEN DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE DECALCIFICATION ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOGENIC CYST ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
BURNING FEET SYNDROME ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
BURSA CALCIFICATION ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CARBOHYDRATE TOLERANCE INCREASED ( 1 FDA reports)
CARCINOID TUMOUR OF THE PROSTATE ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC MALPOSITION ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC SARCOIDOSIS ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 1 FDA reports)
CARDIOPLEGIA ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATARACT DIABETIC ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATECHOLAMINES URINE INCREASED ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE PHLEBITIS ( 1 FDA reports)
CATHETER SITE PRURITUS ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBELLAR TUMOUR ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL PARENCHYMAL CALCIFICATION ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVICOGENIC HEADACHE ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST X-RAY ( 1 FDA reports)
CHILDHOOD PSYCHOSIS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 1 FDA reports)
CHOLESTEATOMA ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 1 FDA reports)
COAGULATION FACTOR V LEVEL ABNORMAL ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON INJURY ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CONGENITAL ACROCHORDON ( 1 FDA reports)
CONGENITAL ADRENAL GLAND HYPOPLASIA ( 1 FDA reports)
CONGENITAL AORTIC STENOSIS ( 1 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
CONGENITAL APLASTIC ANAEMIA ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL JAW MALFORMATION ( 1 FDA reports)
CONJUNCTIVAL CYST ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTACT LENS INTOLERANCE ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CORNEAL THINNING ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
COW'S MILK INTOLERANCE ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CRANIOPHARYNGIOMA ( 1 FDA reports)
CRANIOSYNOSTOSIS ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CRYSTAL ARTHROPATHY ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYSTOSTOMY ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
DACRYOCANALICULITIS ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DERMOID CYST ( 1 FDA reports)
DEVICE ALARM ISSUE ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE INFUSION ISSUE ( 1 FDA reports)
DEVICE INTOLERANCE ( 1 FDA reports)
DEVICE THERAPY ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAPEDESIS ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIAPHRAGMATIC RUPTURE ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSLOGIA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPLASTIC NAEVUS ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECTOPIC KIDNEY ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ECTOPIC PREGNANCY WITH INTRAUTERINE DEVICE ( 1 FDA reports)
ECTROPION OF CERVIX ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM NORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE BIPHASIC ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROLYTE SUBSTITUTION THERAPY ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
EMERGENCY CARE EXAMINATION ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
EPIGLOTTIC CARCINOMA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EVANS SYNDROME ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE MUSCLE OPERATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID OPERATION ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 1 FDA reports)
FALSE NEGATIVE LABORATORY RESULT ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FEMORAL HERNIA ( 1 FDA reports)
FEMORAL HERNIA REPAIR ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOETAL DEATH ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FORCED EXPIRATORY VOLUME INCREASED ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FOREIGN TRAVEL ( 1 FDA reports)
FRACTURE REDUCTION ( 1 FDA reports)
FROSTBITE ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
GALACTOCELE ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GASTRIC HYPERTONIA ( 1 FDA reports)
GASTRIC HYPOMOTILITY ( 1 FDA reports)
GASTRIC ILEUS ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL PRURITUS ( 1 FDA reports)
GINGIVITIS ULCERATIVE ( 1 FDA reports)
GLAUCOMATOUS OPTIC DISC ATROPHY ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GOODPASTURE'S SYNDROME ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOGLOBIN S INCREASED ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HEART BLOCK CONGENITAL ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC ENZYME DECREASED ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HETEROTAXIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 1 FDA reports)
HISTONE ANTIBODY POSITIVE ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE IV ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HUMAN ANTI-HUMAN ANTIBODY TEST ( 1 FDA reports)
HUMAN HERPESVIRUS 7 INFECTION ( 1 FDA reports)
HYDROCELE OPERATION ( 1 FDA reports)
HYDROPS FOETALIS ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPEREXPLEXIA ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERMAGNESAEMIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE RASH ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REMOVAL ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCREASED INSULIN REQUIREMENT ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE THROMBOSIS ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE CYST ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INSULIN RESISTANT DIABETES ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRIS HYPERPIGMENTATION ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT STABILISATION ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LABOUR ONSET DELAYED ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LANGERHANS' CELL HISTIOCYTOSIS ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL DYSPLASIA ( 1 FDA reports)
LARYNGEAL HAEMORRHAGE ( 1 FDA reports)
LARYNGOSCOPY ( 1 FDA reports)
LARYNGOSCOPY ABNORMAL ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LESION EXCISION ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LICE INFESTATION ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGAMENT PAIN ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIPECTOMY ( 1 FDA reports)
LIPOSUCTION ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOOSE BODY IN JOINT ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG ADENOCARCINOMA RECURRENT ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE IV ( 1 FDA reports)
LUPUS MYOCARDITIS ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
LYMPHOID TISSUE OPERATION ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACULAR OPACITY ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 1 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 1 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MECHANICAL URTICARIA ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDIASTINAL FIBROSIS ( 1 FDA reports)
MEDIASTINAL INFECTION ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEDICAL DEVICE CHANGE ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEDICAL INDUCTION OF COMA ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENTAL DISABILITY ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO LARGE INTESTINE ( 1 FDA reports)
METASTASES TO OVARY ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MICROCOCCUS INFECTION ( 1 FDA reports)
MICROSPORUM INFECTION ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 1 FDA reports)
MULTIPLE PREGNANCY ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYCETOMA MYCOTIC ( 1 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOCARDIAL OEDEMA ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
N-TELOPEPTIDE URINE DECREASED ( 1 FDA reports)
NAIL AVULSION ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NAIL PICKING ( 1 FDA reports)
NAIL PIGMENTATION ( 1 FDA reports)
NAIL PSORIASIS ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NARROW ANTERIOR CHAMBER ANGLE ( 1 FDA reports)
NASAL CANDIDIASIS ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 1 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEONATAL TACHYPNOEA ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROMUSCULAR BLOCKADE ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NIPPLE SWELLING ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
ODDI'S SPHINCTER CONSTRICTION ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL LESION EXCISION ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OESOPHAGOENTEROSTOMY ( 1 FDA reports)
OFFICE VISIT ( 1 FDA reports)
OLFACTORY NERVE DISORDER ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORAL BACTERIAL INFECTION ( 1 FDA reports)
ORAL HAIRY LEUKOPLAKIA ( 1 FDA reports)
ORAL NEOPLASM ( 1 FDA reports)
ORAL NEOPLASM BENIGN ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
ORGASMIC SENSATION DECREASED ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OVARIAN OPERATION ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OVERSENSING ( 1 FDA reports)
OVULATION PAIN ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PALATAL DYSPLASIA ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREAS DIVISUM ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PAPILLARY SEROUS ENDOMETRIAL CARCINOMA ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PARTIAL LIPODYSTROPHY ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE ABNORMAL ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDIOTOMY ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERIDIVERTICULITIS ( 1 FDA reports)
PERIPHERAL ARTERY DISSECTION ( 1 FDA reports)
PERIPHERAL NERVE PARESIS ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERIPROSTHETIC FRACTURE ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL LESION ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PH BODY FLUID ABNORMAL ( 1 FDA reports)
PHARYNGEAL CANDIDIASIS ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)

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