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

DYSPNOEA ( 1504 FDA reports)
NAUSEA ( 1420 FDA reports)
PAIN ( 1279 FDA reports)
DIZZINESS ( 1113 FDA reports)
ANXIETY ( 1112 FDA reports)
FATIGUE ( 1098 FDA reports)
HEADACHE ( 1017 FDA reports)
DEPRESSION ( 982 FDA reports)
DIARRHOEA ( 884 FDA reports)
CHEST PAIN ( 838 FDA reports)
ARTHRALGIA ( 829 FDA reports)
DRUG INEFFECTIVE ( 828 FDA reports)
HYPERTENSION ( 827 FDA reports)
BACK PAIN ( 819 FDA reports)
FALL ( 816 FDA reports)
VOMITING ( 801 FDA reports)
ASTHENIA ( 766 FDA reports)
PAIN IN EXTREMITY ( 743 FDA reports)
OEDEMA PERIPHERAL ( 734 FDA reports)
RASH ( 710 FDA reports)
PYREXIA ( 661 FDA reports)
COUGH ( 639 FDA reports)
INSOMNIA ( 637 FDA reports)
ANAEMIA ( 630 FDA reports)
ABDOMINAL PAIN ( 625 FDA reports)
MYOCARDIAL INFARCTION ( 600 FDA reports)
PRURITUS ( 588 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 570 FDA reports)
PNEUMONIA ( 554 FDA reports)
HYPOAESTHESIA ( 531 FDA reports)
CEREBROVASCULAR ACCIDENT ( 520 FDA reports)
INJURY ( 509 FDA reports)
MYALGIA ( 506 FDA reports)
CONSTIPATION ( 495 FDA reports)
ABDOMINAL PAIN UPPER ( 492 FDA reports)
WEIGHT INCREASED ( 477 FDA reports)
URINARY TRACT INFECTION ( 467 FDA reports)
WEIGHT DECREASED ( 459 FDA reports)
SINUSITIS ( 454 FDA reports)
PARAESTHESIA ( 453 FDA reports)
DEEP VEIN THROMBOSIS ( 449 FDA reports)
MALAISE ( 449 FDA reports)
ASTHMA ( 441 FDA reports)
DECREASED APPETITE ( 441 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 428 FDA reports)
MUSCLE SPASMS ( 416 FDA reports)
DEHYDRATION ( 414 FDA reports)
HYPOTENSION ( 400 FDA reports)
OSTEOARTHRITIS ( 396 FDA reports)
PULMONARY EMBOLISM ( 395 FDA reports)
PALPITATIONS ( 393 FDA reports)
BLOOD PRESSURE INCREASED ( 386 FDA reports)
BRONCHITIS ( 386 FDA reports)
FEELING ABNORMAL ( 369 FDA reports)
GAIT DISTURBANCE ( 364 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 362 FDA reports)
VISION BLURRED ( 362 FDA reports)
EMOTIONAL DISTRESS ( 354 FDA reports)
CONFUSIONAL STATE ( 352 FDA reports)
HYPERSENSITIVITY ( 349 FDA reports)
URTICARIA ( 349 FDA reports)
TREMOR ( 347 FDA reports)
ERYTHEMA ( 346 FDA reports)
OSTEONECROSIS OF JAW ( 339 FDA reports)
BLOOD GLUCOSE INCREASED ( 338 FDA reports)
CHEST DISCOMFORT ( 333 FDA reports)
CORONARY ARTERY DISEASE ( 332 FDA reports)
SYNCOPE ( 330 FDA reports)
BONE DISORDER ( 326 FDA reports)
DIABETES MELLITUS ( 319 FDA reports)
DYSPEPSIA ( 314 FDA reports)
CONVULSION ( 312 FDA reports)
PLATELET COUNT DECREASED ( 306 FDA reports)
NECK PAIN ( 304 FDA reports)
HYPERHIDROSIS ( 303 FDA reports)
CHOLELITHIASIS ( 299 FDA reports)
SOMNOLENCE ( 297 FDA reports)
LOSS OF CONSCIOUSNESS ( 295 FDA reports)
TACHYCARDIA ( 295 FDA reports)
CONDITION AGGRAVATED ( 276 FDA reports)
CHILLS ( 274 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 274 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 272 FDA reports)
CELLULITIS ( 269 FDA reports)
ATRIAL FIBRILLATION ( 267 FDA reports)
CONTUSION ( 267 FDA reports)
HAEMORRHOIDS ( 266 FDA reports)
IMPAIRED HEALING ( 264 FDA reports)
HYPERLIPIDAEMIA ( 263 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 261 FDA reports)
OSTEOPENIA ( 261 FDA reports)
SPINAL OSTEOARTHRITIS ( 259 FDA reports)
MUSCULAR WEAKNESS ( 258 FDA reports)
PLEURAL EFFUSION ( 255 FDA reports)
PAIN IN JAW ( 253 FDA reports)
OSTEOMYELITIS ( 248 FDA reports)
RENAL FAILURE ACUTE ( 247 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 244 FDA reports)
NEUROPATHY PERIPHERAL ( 238 FDA reports)
FLUSHING ( 237 FDA reports)
GASTRITIS ( 237 FDA reports)
OSTEOPOROSIS ( 234 FDA reports)
CATARACT ( 233 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 232 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 230 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 229 FDA reports)
MIGRAINE ( 226 FDA reports)
DYSPHAGIA ( 225 FDA reports)
JOINT SWELLING ( 223 FDA reports)
OSTEONECROSIS ( 219 FDA reports)
CHOLECYSTITIS CHRONIC ( 215 FDA reports)
ANHEDONIA ( 214 FDA reports)
ARTHRITIS ( 213 FDA reports)
HEART RATE INCREASED ( 213 FDA reports)
JAUNDICE ( 207 FDA reports)
SEPSIS ( 206 FDA reports)
ABDOMINAL DISTENSION ( 205 FDA reports)
SLEEP APNOEA SYNDROME ( 205 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 205 FDA reports)
SWELLING ( 204 FDA reports)
DIVERTICULUM ( 203 FDA reports)
DYSGEUSIA ( 203 FDA reports)
RENAL FAILURE ( 203 FDA reports)
SWELLING FACE ( 203 FDA reports)
CARDIAC DISORDER ( 199 FDA reports)
ATELECTASIS ( 197 FDA reports)
DEATH ( 197 FDA reports)
DRY MOUTH ( 196 FDA reports)
CARDIOMEGALY ( 195 FDA reports)
HYPOKALAEMIA ( 195 FDA reports)
MITRAL VALVE INCOMPETENCE ( 193 FDA reports)
INFECTION ( 191 FDA reports)
MUSCULOSKELETAL PAIN ( 189 FDA reports)
THROMBOCYTOPENIA ( 187 FDA reports)
THROMBOSIS ( 186 FDA reports)
PANCYTOPENIA ( 185 FDA reports)
RHINITIS ALLERGIC ( 185 FDA reports)
AMNESIA ( 183 FDA reports)
WHEEZING ( 183 FDA reports)
ARTHROPATHY ( 182 FDA reports)
TOOTH DISORDER ( 182 FDA reports)
SUICIDAL IDEATION ( 178 FDA reports)
AGITATION ( 175 FDA reports)
GALLBLADDER DISORDER ( 174 FDA reports)
MEMORY IMPAIRMENT ( 173 FDA reports)
MENTAL STATUS CHANGES ( 173 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 172 FDA reports)
ROAD TRAFFIC ACCIDENT ( 172 FDA reports)
DYSURIA ( 170 FDA reports)
OEDEMA ( 169 FDA reports)
HYPERCHOLESTEROLAEMIA ( 168 FDA reports)
LYMPHADENOPATHY ( 168 FDA reports)
HALLUCINATION ( 166 FDA reports)
HIATUS HERNIA ( 164 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 162 FDA reports)
HOT FLUSH ( 162 FDA reports)
TOOTH EXTRACTION ( 161 FDA reports)
HAEMOGLOBIN DECREASED ( 160 FDA reports)
RESPIRATORY FAILURE ( 160 FDA reports)
TOOTHACHE ( 160 FDA reports)
ALOPECIA ( 159 FDA reports)
EPISTAXIS ( 159 FDA reports)
VERTIGO ( 158 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 157 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 157 FDA reports)
EXOSTOSIS ( 156 FDA reports)
SLEEP DISORDER ( 156 FDA reports)
ANAPHYLACTIC REACTION ( 155 FDA reports)
NEPHROLITHIASIS ( 155 FDA reports)
OROPHARYNGEAL PAIN ( 155 FDA reports)
FEMUR FRACTURE ( 154 FDA reports)
ARRHYTHMIA ( 153 FDA reports)
VISUAL IMPAIRMENT ( 153 FDA reports)
BLOOD PRESSURE DECREASED ( 152 FDA reports)
HYPOTHYROIDISM ( 149 FDA reports)
BALANCE DISORDER ( 148 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 148 FDA reports)
ABDOMINAL DISCOMFORT ( 147 FDA reports)
INFLUENZA LIKE ILLNESS ( 145 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 143 FDA reports)
NASAL CONGESTION ( 143 FDA reports)
ROTATOR CUFF SYNDROME ( 143 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 142 FDA reports)
BURSITIS ( 142 FDA reports)
NERVOUSNESS ( 142 FDA reports)
POLLAKIURIA ( 142 FDA reports)
ANGINA PECTORIS ( 140 FDA reports)
BONE PAIN ( 139 FDA reports)
HAEMATURIA ( 139 FDA reports)
SCAR ( 137 FDA reports)
BRADYCARDIA ( 136 FDA reports)
DISTURBANCE IN ATTENTION ( 135 FDA reports)
GASTROINTESTINAL DISORDER ( 135 FDA reports)
TINNITUS ( 134 FDA reports)
DRY SKIN ( 132 FDA reports)
BLOOD CREATININE INCREASED ( 131 FDA reports)
DENTAL CARIES ( 131 FDA reports)
TENDONITIS ( 131 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 130 FDA reports)
LETHARGY ( 129 FDA reports)
OVERDOSE ( 129 FDA reports)
LIVER DISORDER ( 128 FDA reports)
STOMATITIS ( 128 FDA reports)
PANCREATITIS ( 127 FDA reports)
PULMONARY OEDEMA ( 127 FDA reports)
RENAL FAILURE CHRONIC ( 126 FDA reports)
STRESS ( 126 FDA reports)
OBESITY ( 123 FDA reports)
GINGIVAL DISORDER ( 122 FDA reports)
PRODUCT QUALITY ISSUE ( 122 FDA reports)
DRUG INTERACTION ( 121 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 121 FDA reports)
RENAL IMPAIRMENT ( 121 FDA reports)
SINUS DISORDER ( 121 FDA reports)
VISUAL ACUITY REDUCED ( 120 FDA reports)
LUNG NEOPLASM ( 119 FDA reports)
DYSPNOEA EXERTIONAL ( 118 FDA reports)
IRRITABLE BOWEL SYNDROME ( 118 FDA reports)
RHINORRHOEA ( 118 FDA reports)
DYSARTHRIA ( 117 FDA reports)
NASOPHARYNGITIS ( 117 FDA reports)
RENAL DISORDER ( 117 FDA reports)
DYSPHONIA ( 116 FDA reports)
GINGIVITIS ( 116 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 116 FDA reports)
MULTIPLE MYELOMA ( 116 FDA reports)
RASH PRURITIC ( 116 FDA reports)
RIB FRACTURE ( 116 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 116 FDA reports)
CARDIAC MURMUR ( 115 FDA reports)
HAEMORRHAGE ( 115 FDA reports)
HEART RATE IRREGULAR ( 115 FDA reports)
HERPES ZOSTER ( 115 FDA reports)
IRRITABILITY ( 115 FDA reports)
FOOT FRACTURE ( 114 FDA reports)
HEPATIC STEATOSIS ( 114 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 114 FDA reports)
CARPAL TUNNEL SYNDROME ( 113 FDA reports)
ECZEMA ( 112 FDA reports)
PRODUCTIVE COUGH ( 112 FDA reports)
SWOLLEN TONGUE ( 112 FDA reports)
TYPE 2 DIABETES MELLITUS ( 112 FDA reports)
FLATULENCE ( 111 FDA reports)
HYPOGLYCAEMIA ( 111 FDA reports)
STAPHYLOCOCCAL INFECTION ( 111 FDA reports)
COLONIC POLYP ( 110 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 110 FDA reports)
MOUTH ULCERATION ( 110 FDA reports)
NEOPLASM MALIGNANT ( 110 FDA reports)
NEUTROPENIA ( 110 FDA reports)
URINARY INCONTINENCE ( 110 FDA reports)
BLOOD CALCIUM DECREASED ( 109 FDA reports)
CARDIAC ARREST ( 109 FDA reports)
FEAR ( 109 FDA reports)
HYPOXIA ( 109 FDA reports)
OESOPHAGITIS ( 109 FDA reports)
PANIC ATTACK ( 109 FDA reports)
TOOTH ABSCESS ( 109 FDA reports)
CARDIOMYOPATHY ( 108 FDA reports)
VIRAL INFECTION ( 108 FDA reports)
BURNING SENSATION ( 107 FDA reports)
DRUG HYPERSENSITIVITY ( 107 FDA reports)
INFLUENZA ( 107 FDA reports)
INTERSTITIAL LUNG DISEASE ( 107 FDA reports)
JAW DISORDER ( 107 FDA reports)
HIP FRACTURE ( 106 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 105 FDA reports)
INJECTION SITE PAIN ( 105 FDA reports)
SPEECH DISORDER ( 105 FDA reports)
OFF LABEL USE ( 104 FDA reports)
ADVERSE EVENT ( 103 FDA reports)
ORAL PAIN ( 103 FDA reports)
FEELING HOT ( 102 FDA reports)
VENTRICULAR HYPERTROPHY ( 102 FDA reports)
ECONOMIC PROBLEM ( 101 FDA reports)
ARTERIOSCLEROSIS ( 100 FDA reports)
DIVERTICULUM INTESTINAL ( 100 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 100 FDA reports)
RECTAL HAEMORRHAGE ( 100 FDA reports)
ANOREXIA ( 99 FDA reports)
BREAST CANCER ( 99 FDA reports)
HYPONATRAEMIA ( 99 FDA reports)
METASTASES TO BONE ( 99 FDA reports)
RESPIRATORY DISTRESS ( 99 FDA reports)
BLOOD BILIRUBIN INCREASED ( 98 FDA reports)
TREATMENT NONCOMPLIANCE ( 98 FDA reports)
EYE PAIN ( 97 FDA reports)
HEPATIC ENZYME INCREASED ( 97 FDA reports)
GASTRIC ULCER ( 96 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 96 FDA reports)
DISORIENTATION ( 95 FDA reports)
ABNORMAL DREAMS ( 94 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 94 FDA reports)
MENTAL DISORDER ( 94 FDA reports)
URINARY RETENTION ( 94 FDA reports)
FLANK PAIN ( 93 FDA reports)
MASTICATION DISORDER ( 93 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 93 FDA reports)
SCOLIOSIS ( 93 FDA reports)
ACUTE SINUSITIS ( 92 FDA reports)
FISTULA ( 92 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 92 FDA reports)
LEUKOPENIA ( 92 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 92 FDA reports)
LOOSE TOOTH ( 91 FDA reports)
MASS ( 91 FDA reports)
NIGHT SWEATS ( 91 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 90 FDA reports)
NEUTROPHIL COUNT DECREASED ( 90 FDA reports)
GINGIVAL BLEEDING ( 89 FDA reports)
HAEMATOMA ( 89 FDA reports)
INFLAMMATION ( 89 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 89 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 88 FDA reports)
SYNOVIAL CYST ( 88 FDA reports)
CORONARY ARTERY OCCLUSION ( 87 FDA reports)
DECREASED INTEREST ( 87 FDA reports)
GINGIVAL ULCERATION ( 87 FDA reports)
RESPIRATORY DISORDER ( 87 FDA reports)
SINUS TACHYCARDIA ( 87 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 86 FDA reports)
BLOOD POTASSIUM DECREASED ( 86 FDA reports)
GINGIVAL PAIN ( 86 FDA reports)
RESTLESS LEGS SYNDROME ( 86 FDA reports)
CEREBRAL INFARCTION ( 85 FDA reports)
FOOT DEFORMITY ( 85 FDA reports)
RENAL CYST ( 85 FDA reports)
HAEMATOCHEZIA ( 84 FDA reports)
HAEMATOCRIT DECREASED ( 84 FDA reports)
HEPATOMEGALY ( 84 FDA reports)
ABASIA ( 83 FDA reports)
BLOOD GLUCOSE DECREASED ( 83 FDA reports)
CARDIAC FAILURE ( 83 FDA reports)
CHRONIC SINUSITIS ( 83 FDA reports)
DEFORMITY ( 83 FDA reports)
HEPATITIS FULMINANT ( 83 FDA reports)
INFUSION RELATED REACTION ( 83 FDA reports)
MEDICATION ERROR ( 83 FDA reports)
ORTHOSTATIC HYPOTENSION ( 83 FDA reports)
THROAT IRRITATION ( 83 FDA reports)
COORDINATION ABNORMAL ( 82 FDA reports)
DRUG EFFECT DECREASED ( 82 FDA reports)
HYPERGLYCAEMIA ( 82 FDA reports)
MUSCLE TWITCHING ( 82 FDA reports)
RASH GENERALISED ( 82 FDA reports)
CYST ( 81 FDA reports)
DEAFNESS ( 81 FDA reports)
DIVERTICULITIS ( 81 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 81 FDA reports)
ILL-DEFINED DISORDER ( 80 FDA reports)
ACNE ( 79 FDA reports)
CHOLECYSTITIS ( 79 FDA reports)
ENDODONTIC PROCEDURE ( 79 FDA reports)
FLUID RETENTION ( 79 FDA reports)
SKIN LESION ( 79 FDA reports)
UNEVALUABLE EVENT ( 79 FDA reports)
BONE LESION ( 78 FDA reports)
CAROTID ARTERY STENOSIS ( 78 FDA reports)
EMPHYSEMA ( 78 FDA reports)
FACIAL PAIN ( 78 FDA reports)
PHARYNGEAL OEDEMA ( 78 FDA reports)
INJECTION SITE ERYTHEMA ( 77 FDA reports)
PHYSICAL DISABILITY ( 77 FDA reports)
SUICIDE ATTEMPT ( 77 FDA reports)
THROAT TIGHTNESS ( 77 FDA reports)
AGGRESSION ( 76 FDA reports)
ANGINA UNSTABLE ( 76 FDA reports)
FEELING JITTERY ( 76 FDA reports)
ADVERSE DRUG REACTION ( 75 FDA reports)
BONE DEBRIDEMENT ( 75 FDA reports)
EAR PAIN ( 75 FDA reports)
FEBRILE NEUTROPENIA ( 75 FDA reports)
PRESYNCOPE ( 75 FDA reports)
TOOTH LOSS ( 75 FDA reports)
VAGINAL HAEMORRHAGE ( 75 FDA reports)
ABDOMINAL PAIN LOWER ( 74 FDA reports)
ABNORMAL BEHAVIOUR ( 74 FDA reports)
CYSTITIS ( 74 FDA reports)
PRIMARY SEQUESTRUM ( 74 FDA reports)
RASH ERYTHEMATOUS ( 74 FDA reports)
RHINITIS ( 74 FDA reports)
STEVENS-JOHNSON SYNDROME ( 74 FDA reports)
DISABILITY ( 73 FDA reports)
DRUG DOSE OMISSION ( 73 FDA reports)
DRUG ERUPTION ( 73 FDA reports)
DYSKINESIA ( 73 FDA reports)
EYE SWELLING ( 73 FDA reports)
SKIN EXFOLIATION ( 73 FDA reports)
SKIN DISCOLOURATION ( 72 FDA reports)
VENTRICULAR TACHYCARDIA ( 72 FDA reports)
ASCITES ( 71 FDA reports)
BASAL CELL CARCINOMA ( 71 FDA reports)
BLOOD UREA INCREASED ( 71 FDA reports)
DRY EYE ( 71 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 71 FDA reports)
HEPATIC FAILURE ( 71 FDA reports)
HEPATITIS ( 71 FDA reports)
LACERATION ( 71 FDA reports)
LUNG DISORDER ( 71 FDA reports)
PATHOLOGICAL FRACTURE ( 71 FDA reports)
SPINAL COMPRESSION FRACTURE ( 71 FDA reports)
AORTIC VALVE INCOMPETENCE ( 70 FDA reports)
EATING DISORDER ( 70 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 70 FDA reports)
HYPOPHAGIA ( 70 FDA reports)
MYOCARDIAL ISCHAEMIA ( 70 FDA reports)
OXYGEN SATURATION DECREASED ( 70 FDA reports)
PULMONARY CONGESTION ( 70 FDA reports)
TOOTH INFECTION ( 70 FDA reports)
CANDIDIASIS ( 69 FDA reports)
INCORRECT DOSE ADMINISTERED ( 69 FDA reports)
OCULAR HYPERAEMIA ( 69 FDA reports)
CRYING ( 68 FDA reports)
CYANOSIS ( 68 FDA reports)
EMOTIONAL DISORDER ( 68 FDA reports)
GINGIVAL RECESSION ( 68 FDA reports)
LACRIMATION INCREASED ( 68 FDA reports)
LUMBAR SPINAL STENOSIS ( 68 FDA reports)
LYMPHOEDEMA ( 68 FDA reports)
OVARIAN CYST ( 68 FDA reports)
SCIATICA ( 68 FDA reports)
SEASONAL ALLERGY ( 68 FDA reports)
TOOTH FRACTURE ( 68 FDA reports)
AORTIC ANEURYSM ( 67 FDA reports)
COLITIS ( 67 FDA reports)
FIBROMYALGIA ( 67 FDA reports)
HEAD INJURY ( 67 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 67 FDA reports)
MOBILITY DECREASED ( 67 FDA reports)
PHARYNGITIS ( 67 FDA reports)
RESTLESSNESS ( 67 FDA reports)
BLINDNESS ( 66 FDA reports)
DIPLOPIA ( 66 FDA reports)
DISEASE PROGRESSION ( 66 FDA reports)
DRUG DEPENDENCE ( 66 FDA reports)
GASTRIC DISORDER ( 66 FDA reports)
MENISCUS LESION ( 66 FDA reports)
MULTIPLE INJURIES ( 66 FDA reports)
SINUS BRADYCARDIA ( 66 FDA reports)
SPINAL COLUMN STENOSIS ( 66 FDA reports)
VITREOUS FLOATERS ( 66 FDA reports)
CHROMATURIA ( 65 FDA reports)
CROHN'S DISEASE ( 65 FDA reports)
GASTROENTERITIS ( 65 FDA reports)
LUNG INFILTRATION ( 65 FDA reports)
NODULE ( 65 FDA reports)
ULCER ( 65 FDA reports)
ABSCESS ( 64 FDA reports)
GLAUCOMA ( 64 FDA reports)
JOINT INJURY ( 64 FDA reports)
ORAL CANDIDIASIS ( 64 FDA reports)
PALLOR ( 64 FDA reports)
SINUS CONGESTION ( 64 FDA reports)
DISCOMFORT ( 63 FDA reports)
HYDRONEPHROSIS ( 63 FDA reports)
RHABDOMYOLYSIS ( 63 FDA reports)
ANKLE FRACTURE ( 62 FDA reports)
COLITIS ULCERATIVE ( 62 FDA reports)
NIGHTMARE ( 62 FDA reports)
PANCREATITIS ACUTE ( 62 FDA reports)
PERICARDIAL EFFUSION ( 62 FDA reports)
COAGULOPATHY ( 61 FDA reports)
DRUG INTOLERANCE ( 61 FDA reports)
ERECTILE DYSFUNCTION ( 61 FDA reports)
HYPOMAGNESAEMIA ( 61 FDA reports)
INJECTION SITE HAEMORRHAGE ( 61 FDA reports)
JOINT EFFUSION ( 61 FDA reports)
PERIODONTITIS ( 61 FDA reports)
PSORIASIS ( 61 FDA reports)
SPINAL DISORDER ( 61 FDA reports)
SPONDYLOLISTHESIS ( 61 FDA reports)
VITAMIN D DEFICIENCY ( 61 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 60 FDA reports)
APHASIA ( 60 FDA reports)
BLISTER ( 60 FDA reports)
CEREBRAL ISCHAEMIA ( 60 FDA reports)
RADICULOPATHY ( 60 FDA reports)
RETCHING ( 60 FDA reports)
SKIN DISORDER ( 60 FDA reports)
SURGERY ( 60 FDA reports)
COGNITIVE DISORDER ( 59 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 59 FDA reports)
DYSLIPIDAEMIA ( 59 FDA reports)
MULTI-ORGAN FAILURE ( 59 FDA reports)
NERVOUS SYSTEM DISORDER ( 59 FDA reports)
SKIN ULCER ( 59 FDA reports)
TOOTH IMPACTED ( 59 FDA reports)
BACK INJURY ( 58 FDA reports)
BILIARY DYSKINESIA ( 58 FDA reports)
CERVICOBRACHIAL SYNDROME ( 58 FDA reports)
FUNGAL INFECTION ( 58 FDA reports)
ONYCHOMYCOSIS ( 58 FDA reports)
PULMONARY FIBROSIS ( 58 FDA reports)
CARDIO-RESPIRATORY ARREST ( 57 FDA reports)
DEVICE FAILURE ( 57 FDA reports)
FACE OEDEMA ( 57 FDA reports)
METASTASES TO LIVER ( 57 FDA reports)
NEURALGIA ( 57 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 57 FDA reports)
POST PROCEDURAL COMPLICATION ( 57 FDA reports)
ANXIETY DISORDER ( 56 FDA reports)
CORONARY ARTERY STENOSIS ( 56 FDA reports)
HEART RATE DECREASED ( 56 FDA reports)
HEMIPARESIS ( 56 FDA reports)
LIGAMENT SPRAIN ( 56 FDA reports)
ORAL INFECTION ( 56 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 56 FDA reports)
BREAST PAIN ( 55 FDA reports)
FIBULA FRACTURE ( 55 FDA reports)
MENOPAUSE ( 55 FDA reports)
OTITIS MEDIA ( 55 FDA reports)
REFLUX OESOPHAGITIS ( 55 FDA reports)
TIBIA FRACTURE ( 55 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 54 FDA reports)
DEPRESSED MOOD ( 54 FDA reports)
ERUCTATION ( 54 FDA reports)
EXCORIATION ( 54 FDA reports)
METRORRHAGIA ( 54 FDA reports)
MUSCLE STRAIN ( 54 FDA reports)
SPLENOMEGALY ( 54 FDA reports)
WOUND DEHISCENCE ( 54 FDA reports)
BARRETT'S OESOPHAGUS ( 53 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 53 FDA reports)
BONE LOSS ( 53 FDA reports)
DRUG TOXICITY ( 53 FDA reports)
GOUT ( 53 FDA reports)
HYPERKALAEMIA ( 53 FDA reports)
IRON DEFICIENCY ANAEMIA ( 53 FDA reports)
ORAL SURGERY ( 53 FDA reports)
SEPTIC SHOCK ( 53 FDA reports)
UMBILICAL HERNIA ( 53 FDA reports)
UTERINE LEIOMYOMA ( 53 FDA reports)
VISUAL DISTURBANCE ( 53 FDA reports)
BREAST CANCER FEMALE ( 52 FDA reports)
ERYTHEMA MULTIFORME ( 52 FDA reports)
FACIAL PALSY ( 52 FDA reports)
GENERALISED ANXIETY DISORDER ( 52 FDA reports)
GROIN PAIN ( 52 FDA reports)
MOOD SWINGS ( 52 FDA reports)
MORTON'S NEUROMA ( 52 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 52 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 52 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 52 FDA reports)
PNEUMOTHORAX ( 52 FDA reports)
RHEUMATOID ARTHRITIS ( 52 FDA reports)
SKIN PAPILLOMA ( 52 FDA reports)
STOMACH DISCOMFORT ( 52 FDA reports)
THINKING ABNORMAL ( 52 FDA reports)
THYROID NEOPLASM ( 52 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 52 FDA reports)
BACK DISORDER ( 51 FDA reports)
CARDIOVASCULAR DISORDER ( 51 FDA reports)
DELIRIUM ( 51 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 51 FDA reports)
GOITRE ( 51 FDA reports)
HEPATIC CIRRHOSIS ( 51 FDA reports)
LEUKOCYTOSIS ( 51 FDA reports)
MYOCLONUS ( 51 FDA reports)
OSTEITIS ( 51 FDA reports)
PELVIC PAIN ( 51 FDA reports)
PULMONARY HYPERTENSION ( 51 FDA reports)
PYELONEPHRITIS ( 51 FDA reports)
ANGER ( 50 FDA reports)
COMPRESSION FRACTURE ( 50 FDA reports)
DERMAL CYST ( 50 FDA reports)
EYE DISORDER ( 50 FDA reports)
HAEMOPTYSIS ( 50 FDA reports)
HYPOACUSIS ( 50 FDA reports)
LUNG NEOPLASM MALIGNANT ( 50 FDA reports)
PROTEINURIA ( 50 FDA reports)
STRESS FRACTURE ( 50 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 50 FDA reports)
BODY TEMPERATURE INCREASED ( 49 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 49 FDA reports)
EXPOSED BONE IN JAW ( 49 FDA reports)
GINGIVAL SWELLING ( 49 FDA reports)
ISCHAEMIA ( 49 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 49 FDA reports)
LUMBAR RADICULOPATHY ( 49 FDA reports)
NOCTURIA ( 49 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 49 FDA reports)
BREAST CYST ( 48 FDA reports)
DIABETIC NEUROPATHY ( 48 FDA reports)
PLEURITIC PAIN ( 48 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 48 FDA reports)
WITHDRAWAL SYNDROME ( 48 FDA reports)
BACTERIAL INFECTION ( 47 FDA reports)
BLOOD URINE PRESENT ( 47 FDA reports)
BONE DENSITY DECREASED ( 47 FDA reports)
BREAST MASS ( 47 FDA reports)
CAROTID ARTERY DISEASE ( 47 FDA reports)
DIFFICULTY IN WALKING ( 47 FDA reports)
EJECTION FRACTION DECREASED ( 47 FDA reports)
ENCEPHALOPATHY ( 47 FDA reports)
EYE IRRITATION ( 47 FDA reports)
HERPES SIMPLEX ( 47 FDA reports)
HYPERCALCAEMIA ( 47 FDA reports)
LIP SWELLING ( 47 FDA reports)
OSTEOLYSIS ( 47 FDA reports)
PATHOLOGICAL GAMBLING ( 47 FDA reports)
UPPER LIMB FRACTURE ( 47 FDA reports)
CARDIAC PACEMAKER INSERTION ( 46 FDA reports)
LOBAR PNEUMONIA ( 46 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 46 FDA reports)
POLYP ( 46 FDA reports)
PRURITUS GENERALISED ( 46 FDA reports)
BLEPHARITIS ( 45 FDA reports)
CERVICAL SPINAL STENOSIS ( 45 FDA reports)
CIRCULATORY COLLAPSE ( 45 FDA reports)
COLD SWEAT ( 45 FDA reports)
DERMATITIS ( 45 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 45 FDA reports)
JAW FRACTURE ( 45 FDA reports)
LIMB INJURY ( 45 FDA reports)
ORAL DISORDER ( 45 FDA reports)
PERIODONTAL DISEASE ( 45 FDA reports)
PROTEIN URINE PRESENT ( 45 FDA reports)
BLADDER CANCER ( 44 FDA reports)
CHANGE OF BOWEL HABIT ( 44 FDA reports)
EAR INFECTION ( 44 FDA reports)
FAECAL INCONTINENCE ( 44 FDA reports)
HYPERSOMNIA ( 44 FDA reports)
JOINT SPRAIN ( 44 FDA reports)
METABOLIC ACIDOSIS ( 44 FDA reports)
OEDEMA MOUTH ( 44 FDA reports)
PERONEAL NERVE PALSY ( 44 FDA reports)
ANGIOEDEMA ( 43 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 43 FDA reports)
CHOLECYSTECTOMY ( 43 FDA reports)
COMA ( 43 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 43 FDA reports)
INJECTION SITE HAEMATOMA ( 43 FDA reports)
LIPASE INCREASED ( 43 FDA reports)
OPEN WOUND ( 43 FDA reports)
PHOTOSENSITIVITY REACTION ( 43 FDA reports)
PLATELET COUNT INCREASED ( 43 FDA reports)
THIRST ( 43 FDA reports)
THYROID DISORDER ( 43 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 42 FDA reports)
FEELING COLD ( 42 FDA reports)
FRACTURE NONUNION ( 42 FDA reports)
GASTROENTERITIS VIRAL ( 42 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 42 FDA reports)
ISCHAEMIC STROKE ( 42 FDA reports)
JOINT STIFFNESS ( 42 FDA reports)
LUNG INFECTION ( 42 FDA reports)
PANIC DISORDER ( 42 FDA reports)
RECTAL POLYP ( 42 FDA reports)
VENOUS INSUFFICIENCY ( 42 FDA reports)
ATRIAL TACHYCARDIA ( 41 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 41 FDA reports)
HAEMATEMESIS ( 41 FDA reports)
MITRAL VALVE PROLAPSE ( 41 FDA reports)
PHOTOPSIA ( 41 FDA reports)
PLANTAR FASCIITIS ( 41 FDA reports)
PROTHROMBIN TIME PROLONGED ( 41 FDA reports)
SQUAMOUS CELL CARCINOMA ( 41 FDA reports)
UROSEPSIS ( 41 FDA reports)
WRIST FRACTURE ( 41 FDA reports)
WOUND DRAINAGE ( 40 FDA reports)
BILIARY COLIC ( 40 FDA reports)
DRUG ABUSE ( 40 FDA reports)
INTENTIONAL DRUG MISUSE ( 40 FDA reports)
LOW TURNOVER OSTEOPATHY ( 40 FDA reports)
MUSCLE TIGHTNESS ( 40 FDA reports)
MYOSITIS ( 40 FDA reports)
ORTHOPNOEA ( 40 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 40 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 40 FDA reports)
ABORTION SPONTANEOUS ( 39 FDA reports)
BRONCHOSPASM ( 39 FDA reports)
DEAFNESS NEUROSENSORY ( 39 FDA reports)
FIBROSIS ( 39 FDA reports)
FLUID OVERLOAD ( 39 FDA reports)
HYPERTONIC BLADDER ( 39 FDA reports)
HYPOCALCAEMIA ( 39 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 39 FDA reports)
INCREASED TENDENCY TO BRUISE ( 39 FDA reports)
LOCALISED INFECTION ( 39 FDA reports)
MALNUTRITION ( 39 FDA reports)
ORAL HERPES ( 39 FDA reports)
RESPIRATORY TRACT INFECTION ( 39 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 39 FDA reports)
UNRESPONSIVE TO STIMULI ( 39 FDA reports)
CALCULUS URETERIC ( 38 FDA reports)
DYSPAREUNIA ( 38 FDA reports)
ESCHERICHIA INFECTION ( 38 FDA reports)
INCONTINENCE ( 38 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 38 FDA reports)
LOCAL SWELLING ( 38 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 38 FDA reports)
MELANOCYTIC NAEVUS ( 38 FDA reports)
MULTIPLE SCLEROSIS ( 38 FDA reports)
PETECHIAE ( 38 FDA reports)
SHOCK ( 38 FDA reports)
COLON CANCER ( 37 FDA reports)
DEVICE MALFUNCTION ( 37 FDA reports)
DISEASE RECURRENCE ( 37 FDA reports)
GLOSSODYNIA ( 37 FDA reports)
HAEMORRHAGIC ANAEMIA ( 37 FDA reports)
HEARING IMPAIRED ( 37 FDA reports)
INJECTION SITE REACTION ( 37 FDA reports)
JAW OPERATION ( 37 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 37 FDA reports)
LOWER LIMB FRACTURE ( 37 FDA reports)
MENORRHAGIA ( 37 FDA reports)
MICTURITION URGENCY ( 37 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 37 FDA reports)
MUSCLE ATROPHY ( 37 FDA reports)
NAIL DISORDER ( 37 FDA reports)
PELVIC FRACTURE ( 37 FDA reports)
PLASMACYTOSIS ( 37 FDA reports)
POLYURIA ( 37 FDA reports)
SJOGREN'S SYNDROME ( 37 FDA reports)
SKIN INFECTION ( 37 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 37 FDA reports)
TARDIVE DYSKINESIA ( 37 FDA reports)
TONGUE DISORDER ( 37 FDA reports)
WOUND ( 37 FDA reports)
ATAXIA ( 36 FDA reports)
CHOLECYSTITIS ACUTE ( 36 FDA reports)
COLON ADENOMA ( 36 FDA reports)
DECUBITUS ULCER ( 36 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 36 FDA reports)
DYSSTASIA ( 36 FDA reports)
EYELID PTOSIS ( 36 FDA reports)
FRACTURE ( 36 FDA reports)
HERNIA ( 36 FDA reports)
INTESTINAL OBSTRUCTION ( 36 FDA reports)
PNEUMONIA ASPIRATION ( 36 FDA reports)
SEBORRHOEIC KERATOSIS ( 36 FDA reports)
VARICOSE VEIN ( 36 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 35 FDA reports)
CEREBRAL ATROPHY ( 35 FDA reports)
CERVICAL DYSPLASIA ( 35 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 35 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 35 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 35 FDA reports)
GENERALISED ERYTHEMA ( 35 FDA reports)
GINGIVAL OEDEMA ( 35 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 35 FDA reports)
HEPATITIS C ( 35 FDA reports)
HYPERKERATOSIS ( 35 FDA reports)
HYPOALBUMINAEMIA ( 35 FDA reports)
LIFE EXPECTANCY SHORTENED ( 35 FDA reports)
PREGNANCY ( 35 FDA reports)
PROCTALGIA ( 35 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 35 FDA reports)
RASH PAPULAR ( 35 FDA reports)
SICK SINUS SYNDROME ( 35 FDA reports)
SKIN CANCER ( 35 FDA reports)
SNEEZING ( 35 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 35 FDA reports)
TONGUE ULCERATION ( 35 FDA reports)
ABNORMAL SENSATION IN EYE ( 34 FDA reports)
ACCIDENTAL OVERDOSE ( 34 FDA reports)
ANGIOPATHY ( 34 FDA reports)
AORTIC STENOSIS ( 34 FDA reports)
CEREBRAL HAEMORRHAGE ( 34 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 34 FDA reports)
EMPYEMA ( 34 FDA reports)
HEPATIC CYST ( 34 FDA reports)
HYPERTHYROIDISM ( 34 FDA reports)
HYPOAESTHESIA ORAL ( 34 FDA reports)
INTRAOCULAR LENS IMPLANT ( 34 FDA reports)
LIBIDO DECREASED ( 34 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 34 FDA reports)
MIDDLE INSOMNIA ( 34 FDA reports)
MOUTH HAEMORRHAGE ( 34 FDA reports)
PARANOIA ( 34 FDA reports)
RESPIRATORY ARREST ( 34 FDA reports)
SPINAL FUSION SURGERY ( 34 FDA reports)
TENDERNESS ( 34 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 34 FDA reports)
VENTRICULAR FIBRILLATION ( 34 FDA reports)
ANEURYSM ( 33 FDA reports)
BLADDER DISORDER ( 33 FDA reports)
CONJUNCTIVITIS ( 33 FDA reports)
DERMATITIS ACNEIFORM ( 33 FDA reports)
ECCHYMOSIS ( 33 FDA reports)
EYE PRURITUS ( 33 FDA reports)
GRAND MAL CONVULSION ( 33 FDA reports)
HEPATIC ENCEPHALOPATHY ( 33 FDA reports)
IMPAIRED DRIVING ABILITY ( 33 FDA reports)
LABYRINTHITIS ( 33 FDA reports)
LARYNGEAL OEDEMA ( 33 FDA reports)
MAMMOGRAM ABNORMAL ( 33 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 33 FDA reports)
SKIN BURNING SENSATION ( 33 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 33 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 33 FDA reports)
X-RAY ABNORMAL ( 33 FDA reports)
ACTINIC KERATOSIS ( 32 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 32 FDA reports)
APHTHOUS STOMATITIS ( 32 FDA reports)
AREFLEXIA ( 32 FDA reports)
ATRIAL SEPTAL DEFECT ( 32 FDA reports)
BONE FRAGMENTATION ( 32 FDA reports)
CARDIAC VALVE DISEASE ( 32 FDA reports)
CARDIOGENIC SHOCK ( 32 FDA reports)
CHONDROMALACIA ( 32 FDA reports)
COMPLETED SUICIDE ( 32 FDA reports)
EPICONDYLITIS ( 32 FDA reports)
FACIAL BONES FRACTURE ( 32 FDA reports)
HYPERAESTHESIA ( 32 FDA reports)
IMPAIRED WORK ABILITY ( 32 FDA reports)
JOINT DISLOCATION ( 32 FDA reports)
MACROCYTOSIS ( 32 FDA reports)
MELAENA ( 32 FDA reports)
MOVEMENT DISORDER ( 32 FDA reports)
NECK INJURY ( 32 FDA reports)
NEURITIS ( 32 FDA reports)
PARAPLEGIA ( 32 FDA reports)
PROCTITIS ( 32 FDA reports)
PURULENT DISCHARGE ( 32 FDA reports)
RASH MACULAR ( 32 FDA reports)
SEBORRHOEIC DERMATITIS ( 32 FDA reports)
ABSCESS JAW ( 31 FDA reports)
BRUXISM ( 31 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 31 FDA reports)
CONCUSSION ( 31 FDA reports)
DRY THROAT ( 31 FDA reports)
ESSENTIAL HYPERTENSION ( 31 FDA reports)
EYE NAEVUS ( 31 FDA reports)
HYPERNATRAEMIA ( 31 FDA reports)
INJECTION SITE PRURITUS ( 31 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 31 FDA reports)
LYMPHOMA ( 31 FDA reports)
ORAL DISCOMFORT ( 31 FDA reports)
PHOTOPHOBIA ( 31 FDA reports)
POOR QUALITY SLEEP ( 31 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 31 FDA reports)
PRESCRIBED OVERDOSE ( 31 FDA reports)
RHONCHI ( 31 FDA reports)
SOFT TISSUE INFLAMMATION ( 31 FDA reports)
SPINAL CORD COMPRESSION ( 31 FDA reports)
TENDON RUPTURE ( 31 FDA reports)
THERMAL BURN ( 31 FDA reports)
UTERINE HAEMORRHAGE ( 31 FDA reports)
VIITH NERVE PARALYSIS ( 31 FDA reports)
VITAMIN B12 DEFICIENCY ( 31 FDA reports)
ANAPHYLACTIC SHOCK ( 30 FDA reports)
ANOGENITAL WARTS ( 30 FDA reports)
CEREBROVASCULAR DISORDER ( 30 FDA reports)
CHOKING ( 30 FDA reports)
DENTAL CARE ( 30 FDA reports)
DIABETIC KETOACIDOSIS ( 30 FDA reports)
EYE DISCHARGE ( 30 FDA reports)
FACET JOINT SYNDROME ( 30 FDA reports)
GENITAL RASH ( 30 FDA reports)
KNEE ARTHROPLASTY ( 30 FDA reports)
LIMB DISCOMFORT ( 30 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 30 FDA reports)
MAJOR DEPRESSION ( 30 FDA reports)
MENSTRUATION IRREGULAR ( 30 FDA reports)
PERSONALITY CHANGE ( 30 FDA reports)
PSYCHIATRIC SYMPTOM ( 30 FDA reports)
PSYCHOTIC DISORDER ( 30 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 30 FDA reports)
SEXUAL DYSFUNCTION ( 30 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 30 FDA reports)
THYROID ADENOMA ( 30 FDA reports)
TYPE 1 DIABETES MELLITUS ( 30 FDA reports)
ANGIONEUROTIC OEDEMA ( 29 FDA reports)
BIPOLAR DISORDER ( 29 FDA reports)
BRAIN OEDEMA ( 29 FDA reports)
DEMENTIA ( 29 FDA reports)
FRACTURE DELAYED UNION ( 29 FDA reports)
GENERALISED OEDEMA ( 29 FDA reports)
HAND FRACTURE ( 29 FDA reports)
HEPATIC LESION ( 29 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 29 FDA reports)
INJECTION SITE SWELLING ( 29 FDA reports)
MALIGNANT MELANOMA ( 29 FDA reports)
NEUROPATHY ( 29 FDA reports)
POSTNASAL DRIP ( 29 FDA reports)
RASH MACULO-PAPULAR ( 29 FDA reports)
RENAL INJURY ( 29 FDA reports)
RETINOPATHY ( 29 FDA reports)
TENOSYNOVITIS ( 29 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 29 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 28 FDA reports)
AXILLARY PAIN ( 28 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 28 FDA reports)
BOWEN'S DISEASE ( 28 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 28 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 28 FDA reports)
EOSINOPHILIA ( 28 FDA reports)
HALLUCINATION, AUDITORY ( 28 FDA reports)
HEART DISEASE CONGENITAL ( 28 FDA reports)
HEPATITIS B ( 28 FDA reports)
MACULAR HOLE ( 28 FDA reports)
METASTASES TO LYMPH NODES ( 28 FDA reports)
MITRAL VALVE CALCIFICATION ( 28 FDA reports)
MOOD ALTERED ( 28 FDA reports)
MULTIPLE ALLERGIES ( 28 FDA reports)
MYELOMA RECURRENCE ( 28 FDA reports)
ORAL TORUS ( 28 FDA reports)
OSTEORADIONECROSIS ( 28 FDA reports)
OSTEOSCLEROSIS ( 28 FDA reports)
PEPTIC ULCER ( 28 FDA reports)
RENAL CELL CARCINOMA ( 28 FDA reports)
SARCOIDOSIS ( 28 FDA reports)
SENSORY DISTURBANCE ( 28 FDA reports)
SINUS POLYP ( 28 FDA reports)
STEM CELL TRANSPLANT ( 28 FDA reports)
VASCULITIS ( 28 FDA reports)
VENTRICULAR HYPOKINESIA ( 28 FDA reports)
ADRENAL MASS ( 27 FDA reports)
ANOSMIA ( 27 FDA reports)
ATHEROSCLEROSIS ( 27 FDA reports)
CATARACT OPERATION ( 27 FDA reports)
COCCYDYNIA ( 27 FDA reports)
DENTAL FISTULA ( 27 FDA reports)
DEVICE RELATED INFECTION ( 27 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 27 FDA reports)
FAILURE TO THRIVE ( 27 FDA reports)
FOLLICULITIS ( 27 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 27 FDA reports)
INCREASED APPETITE ( 27 FDA reports)
INTESTINAL HAEMORRHAGE ( 27 FDA reports)
IRON DEFICIENCY ( 27 FDA reports)
LIPIDS INCREASED ( 27 FDA reports)
MICROCYTIC ANAEMIA ( 27 FDA reports)
NEOPLASM PROGRESSION ( 27 FDA reports)
PNEUMONITIS ( 27 FDA reports)
PULMONARY GRANULOMA ( 27 FDA reports)
RALES ( 27 FDA reports)
RAYNAUD'S PHENOMENON ( 27 FDA reports)
SINUS HEADACHE ( 27 FDA reports)
SKIN TIGHTNESS ( 27 FDA reports)
SNORING ( 27 FDA reports)
TACHYPNOEA ( 27 FDA reports)
TRIGGER FINGER ( 27 FDA reports)
VENOUS THROMBOSIS ( 27 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 27 FDA reports)
VITAMIN D DECREASED ( 27 FDA reports)
WALKING AID USER ( 27 FDA reports)
ANKLE OPERATION ( 26 FDA reports)
APPLICATION SITE REACTION ( 26 FDA reports)
ASTIGMATISM ( 26 FDA reports)
BLOOD SODIUM DECREASED ( 26 FDA reports)
BLOOD URIC ACID INCREASED ( 26 FDA reports)
DERMATITIS ALLERGIC ( 26 FDA reports)
HYPERMETROPIA ( 26 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 26 FDA reports)
INJECTION SITE URTICARIA ( 26 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 26 FDA reports)
JOINT INSTABILITY ( 26 FDA reports)
KIDNEY INFECTION ( 26 FDA reports)
LARYNGITIS ( 26 FDA reports)
MACULAR DEGENERATION ( 26 FDA reports)
MECHANICAL URTICARIA ( 26 FDA reports)
MONONEUROPATHY ( 26 FDA reports)
MUCOSAL INFLAMMATION ( 26 FDA reports)
MULTI-ORGAN DISORDER ( 26 FDA reports)
NASAL DISCOMFORT ( 26 FDA reports)
NON-CARDIAC CHEST PAIN ( 26 FDA reports)
OESOPHAGEAL DISORDER ( 26 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 26 FDA reports)
PROCEDURAL PAIN ( 26 FDA reports)
SEDATION ( 26 FDA reports)
SENSITIVITY OF TEETH ( 26 FDA reports)
SINUS OPERATION ( 26 FDA reports)
SPONDYLOARTHROPATHY ( 26 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 26 FDA reports)
ACUTE CORONARY SYNDROME ( 25 FDA reports)
ATRIAL FLUTTER ( 25 FDA reports)
DIASTOLIC DYSFUNCTION ( 25 FDA reports)
DRUG ABUSER ( 25 FDA reports)
DRUG ADMINISTRATION ERROR ( 25 FDA reports)
GALLBLADDER INJURY ( 25 FDA reports)
GASTRITIS EROSIVE ( 25 FDA reports)
GINGIVAL INFECTION ( 25 FDA reports)
HUNGER ( 25 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 25 FDA reports)
MUSCLE CRAMP ( 25 FDA reports)
OPTIC NERVE CUPPING ( 25 FDA reports)
OROPHARYNGEAL PLAQUE ( 25 FDA reports)
PARAESTHESIA ORAL ( 25 FDA reports)
PNEUMONIA BACTERIAL ( 25 FDA reports)
RESPIRATORY TRACT CONGESTION ( 25 FDA reports)
SCREAMING ( 25 FDA reports)
TENOSYNOVITIS STENOSANS ( 25 FDA reports)
VESICAL FISTULA ( 25 FDA reports)
APPENDICITIS ( 24 FDA reports)
AUTOIMMUNE INNER EAR DISEASE ( 24 FDA reports)
BLOOD POTASSIUM INCREASED ( 24 FDA reports)
BREAST LUMP REMOVAL ( 24 FDA reports)
CAROTID ARTERY OCCLUSION ( 24 FDA reports)
CATHETERISATION CARDIAC ( 24 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 24 FDA reports)
DRUG TOLERANCE ( 24 FDA reports)
DYSTONIA ( 24 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 24 FDA reports)
FIBROMA ( 24 FDA reports)
GINGIVAL HYPERPLASIA ( 24 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 24 FDA reports)
HYPOPHOSPHATAEMIA ( 24 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 24 FDA reports)
LIGAMENT DISORDER ( 24 FDA reports)
MENTAL IMPAIRMENT ( 24 FDA reports)
METABOLIC ENCEPHALOPATHY ( 24 FDA reports)
METASTASES TO SPINE ( 24 FDA reports)
MUCOSAL DRYNESS ( 24 FDA reports)
OESOPHAGEAL ULCER ( 24 FDA reports)
ORAL CAVITY FISTULA ( 24 FDA reports)
PELVIC DEFORMITY ( 24 FDA reports)
RENAL TUBULAR NECROSIS ( 24 FDA reports)
SHOULDER PAIN ( 24 FDA reports)
SKIN HYPERPIGMENTATION ( 24 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 24 FDA reports)
TELANGIECTASIA ( 24 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 24 FDA reports)
AGEUSIA ( 23 FDA reports)
ANAEMIA POSTOPERATIVE ( 23 FDA reports)
BACTERIAL DISEASE CARRIER ( 23 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 23 FDA reports)
BODY HEIGHT DECREASED ( 23 FDA reports)
DEBRIDEMENT ( 23 FDA reports)
DENTAL PLAQUE ( 23 FDA reports)
DERMATITIS CONTACT ( 23 FDA reports)
DYSPHEMIA ( 23 FDA reports)
FRACTURED SACRUM ( 23 FDA reports)
HOMICIDAL IDEATION ( 23 FDA reports)
HYPOTHERMIA ( 23 FDA reports)
HYPOVOLAEMIA ( 23 FDA reports)
OCCULT BLOOD POSITIVE ( 23 FDA reports)
PERIORBITAL OEDEMA ( 23 FDA reports)
PLEURISY ( 23 FDA reports)
SPINAL FRACTURE ( 23 FDA reports)
VAGINAL INFECTION ( 23 FDA reports)
WOUND INFECTION ( 23 FDA reports)
AFFECTIVE DISORDER ( 22 FDA reports)
AMMONIA INCREASED ( 22 FDA reports)
ASPIRATION ( 22 FDA reports)
BACTERAEMIA ( 22 FDA reports)
BLOOD AMYLASE INCREASED ( 22 FDA reports)
BREAST CANCER METASTATIC ( 22 FDA reports)
DENTAL IMPLANTATION ( 22 FDA reports)
EAR DISCOMFORT ( 22 FDA reports)
EYELID OEDEMA ( 22 FDA reports)
FAECES DISCOLOURED ( 22 FDA reports)
GRANULOMA ( 22 FDA reports)
HAEMANGIOMA OF LIVER ( 22 FDA reports)
HERPES VIRUS INFECTION ( 22 FDA reports)
LIP DRY ( 22 FDA reports)
MAMMOPLASTY ( 22 FDA reports)
METASTATIC NEOPLASM ( 22 FDA reports)
MUSCLE DISORDER ( 22 FDA reports)
MYCOSIS FUNGOIDES ( 22 FDA reports)
PARONYCHIA ( 22 FDA reports)
ROTATOR CUFF REPAIR ( 22 FDA reports)
SKIN LACERATION ( 22 FDA reports)
SYNOVITIS ( 22 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 22 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 21 FDA reports)
AKATHISIA ( 21 FDA reports)
APATHY ( 21 FDA reports)
APLASIA PURE RED CELL ( 21 FDA reports)
BLINDNESS UNILATERAL ( 21 FDA reports)
BLOOD DISORDER ( 21 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 21 FDA reports)
CHEST X-RAY ABNORMAL ( 21 FDA reports)
DELUSION ( 21 FDA reports)
DUODENITIS ( 21 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 21 FDA reports)
EOSINOPHIL COUNT INCREASED ( 21 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 21 FDA reports)
FURUNCLE ( 21 FDA reports)
HAEMATOCRIT ABNORMAL ( 21 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 21 FDA reports)
HIP ARTHROPLASTY ( 21 FDA reports)
LABORATORY TEST ABNORMAL ( 21 FDA reports)
MYELOPATHY ( 21 FDA reports)
PANCREATITIS CHRONIC ( 21 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 21 FDA reports)
PULMONARY THROMBOSIS ( 21 FDA reports)
RADIOTHERAPY ( 21 FDA reports)
SKIN FIBROSIS ( 21 FDA reports)
SKIN FISSURES ( 21 FDA reports)
SKIN IRRITATION ( 21 FDA reports)
VISUAL FIELD DEFECT ( 21 FDA reports)
WOUND SECRETION ( 21 FDA reports)
ABDOMINAL TENDERNESS ( 20 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 20 FDA reports)
ANOXIC ENCEPHALOPATHY ( 20 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 20 FDA reports)
AORTIC VALVE SCLEROSIS ( 20 FDA reports)
ATRIOVENTRICULAR BLOCK ( 20 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 20 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 20 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 20 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 20 FDA reports)
BRAIN DEATH ( 20 FDA reports)
BREAST CALCIFICATIONS ( 20 FDA reports)
BRONCHIECTASIS ( 20 FDA reports)
CARDIAC FAILURE ACUTE ( 20 FDA reports)
CHRONIC FATIGUE SYNDROME ( 20 FDA reports)
COLITIS ISCHAEMIC ( 20 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 20 FDA reports)
CORONARY ARTERY RESTENOSIS ( 20 FDA reports)
COSTOCHONDRITIS ( 20 FDA reports)
EPILEPSY ( 20 FDA reports)
EXTRASYSTOLES ( 20 FDA reports)
EYE LASER SURGERY ( 20 FDA reports)
GASTRIC POLYPS ( 20 FDA reports)
HEPATITIS ACUTE ( 20 FDA reports)
HYPERTENSIVE HEART DISEASE ( 20 FDA reports)
HYPOAESTHESIA FACIAL ( 20 FDA reports)
ILEUS ( 20 FDA reports)
INGUINAL HERNIA ( 20 FDA reports)
KLEBSIELLA INFECTION ( 20 FDA reports)
LACUNAR INFARCTION ( 20 FDA reports)
LUNG CONSOLIDATION ( 20 FDA reports)
MEDICAL DEVICE COMPLICATION ( 20 FDA reports)
METASTASES TO LUNG ( 20 FDA reports)
MOTOR DYSFUNCTION ( 20 FDA reports)
MYOPATHY ( 20 FDA reports)
NASAL SEPTUM DEVIATION ( 20 FDA reports)
NEOPLASM ( 20 FDA reports)
NEPHROTIC SYNDROME ( 20 FDA reports)
OLIGURIA ( 20 FDA reports)
ORTHOPEDIC PROCEDURE ( 20 FDA reports)
OVERWEIGHT ( 20 FDA reports)
PAROSMIA ( 20 FDA reports)
PERIPHERAL COLDNESS ( 20 FDA reports)
POLYNEUROPATHY ( 20 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 20 FDA reports)
RESPIRATORY ACIDOSIS ( 20 FDA reports)
RETINAL DETACHMENT ( 20 FDA reports)
SCLERODERMA ( 20 FDA reports)
SELF-INJURIOUS IDEATION ( 20 FDA reports)
SHUNT INFECTION ( 20 FDA reports)
SUDDEN DEATH ( 20 FDA reports)
TRACHEITIS ( 20 FDA reports)
TRISMUS ( 20 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 20 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 20 FDA reports)
UVEITIS ( 20 FDA reports)
ACUTE RESPIRATORY FAILURE ( 19 FDA reports)
AGRANULOCYTOSIS ( 19 FDA reports)
ANORECTAL DISCOMFORT ( 19 FDA reports)
AORTIC CALCIFICATION ( 19 FDA reports)
APHONIA ( 19 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 19 FDA reports)
BILIARY DILATATION ( 19 FDA reports)
BLOOD CALCIUM INCREASED ( 19 FDA reports)
BRAIN HERNIATION ( 19 FDA reports)
BRONCHITIS ACUTE ( 19 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 19 FDA reports)
CERUMEN IMPACTION ( 19 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 19 FDA reports)
CLUSTER HEADACHE ( 19 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 19 FDA reports)
DILATATION VENTRICULAR ( 19 FDA reports)
DIZZINESS POSTURAL ( 19 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 19 FDA reports)
EMBOLIC STROKE ( 19 FDA reports)
ENTEROCOCCAL INFECTION ( 19 FDA reports)
EUPHORIC MOOD ( 19 FDA reports)
EXERCISE TOLERANCE DECREASED ( 19 FDA reports)
HYPERBILIRUBINAEMIA ( 19 FDA reports)
INCISIONAL DRAINAGE ( 19 FDA reports)
INITIAL INSOMNIA ( 19 FDA reports)
IRITIS ( 19 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 19 FDA reports)
OCULAR ICTERUS ( 19 FDA reports)
ORAL INTAKE REDUCED ( 19 FDA reports)
OTITIS EXTERNA ( 19 FDA reports)
PARALYSIS ( 19 FDA reports)
PROCEDURAL COMPLICATION ( 19 FDA reports)
RADICULAR PAIN ( 19 FDA reports)
RETINAL VEIN OCCLUSION ( 19 FDA reports)
SKIN INDURATION ( 19 FDA reports)
TOE AMPUTATION ( 19 FDA reports)
VERTIGO POSITIONAL ( 19 FDA reports)
ACCOMMODATION DISORDER ( 18 FDA reports)
AZOTAEMIA ( 18 FDA reports)
BREATH ODOUR ( 18 FDA reports)
BRONCHOPLEURAL FISTULA ( 18 FDA reports)
CAESAREAN SECTION ( 18 FDA reports)
CATATONIA ( 18 FDA reports)
CERVICAL MYELOPATHY ( 18 FDA reports)
CHEILITIS ( 18 FDA reports)
DENTURE WEARER ( 18 FDA reports)
DERMATITIS EXFOLIATIVE ( 18 FDA reports)
ENCEPHALOMALACIA ( 18 FDA reports)
GINGIVAL ERYTHEMA ( 18 FDA reports)
HIP SURGERY ( 18 FDA reports)
HYDROPNEUMOTHORAX ( 18 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 18 FDA reports)
HYPERPHAGIA ( 18 FDA reports)
IMMUNOSUPPRESSION ( 18 FDA reports)
INCOHERENT ( 18 FDA reports)
INDURATION ( 18 FDA reports)
INJECTION SITE RASH ( 18 FDA reports)
INNER EAR DISORDER ( 18 FDA reports)
INTENTIONAL OVERDOSE ( 18 FDA reports)
INTRACRANIAL ANEURYSM ( 18 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 18 FDA reports)
MEDICAL DEVICE REMOVAL ( 18 FDA reports)
NEURODERMATITIS ( 18 FDA reports)
NEUROMA ( 18 FDA reports)
NO ADVERSE EVENT ( 18 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 18 FDA reports)
ODYNOPHAGIA ( 18 FDA reports)
OESOPHAGEAL SPASM ( 18 FDA reports)
OSTEOCHONDROSIS ( 18 FDA reports)
OSTEOMYELITIS CHRONIC ( 18 FDA reports)
OTITIS MEDIA ACUTE ( 18 FDA reports)
OVARIAN DISORDER ( 18 FDA reports)
PARKINSONISM ( 18 FDA reports)
PERITONITIS ( 18 FDA reports)
PHOTOPHERESIS ( 18 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 18 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 18 FDA reports)
PULMONARY RADIATION INJURY ( 18 FDA reports)
RADICAL MASTECTOMY ( 18 FDA reports)
SPUTUM DISCOLOURED ( 18 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 18 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 18 FDA reports)
THERAPY NON-RESPONDER ( 18 FDA reports)
THORACIC OUTLET SYNDROME ( 18 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 18 FDA reports)
TINEA PEDIS ( 18 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 18 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 18 FDA reports)
ADENOMYOSIS ( 17 FDA reports)
ANAL FISSURE ( 17 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 17 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 17 FDA reports)
BONE MARROW FAILURE ( 17 FDA reports)
BONE METABOLISM DISORDER ( 17 FDA reports)
CATHETER REMOVAL ( 17 FDA reports)
CORNEAL ABRASION ( 17 FDA reports)
EAR HAEMORRHAGE ( 17 FDA reports)
HAEMANGIOMA ( 17 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 17 FDA reports)
HEARING AID USER ( 17 FDA reports)
INGROWING NAIL ( 17 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 17 FDA reports)
LIP DISCOLOURATION ( 17 FDA reports)
LYMPHADENECTOMY ( 17 FDA reports)
MANIA ( 17 FDA reports)
MASTOIDITIS ( 17 FDA reports)
NERVE INJURY ( 17 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 17 FDA reports)
PHLEBITIS ( 17 FDA reports)
PHYSICAL ASSAULT ( 17 FDA reports)
PITTING OEDEMA ( 17 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 17 FDA reports)
PULMONARY INFARCTION ( 17 FDA reports)
RADICULITIS LUMBOSACRAL ( 17 FDA reports)
RESPIRATORY RATE INCREASED ( 17 FDA reports)
ROSACEA ( 17 FDA reports)
SEQUESTRECTOMY ( 17 FDA reports)
SICCA SYNDROME ( 17 FDA reports)
SKELETAL INJURY ( 17 FDA reports)
SPUTUM PURULENT ( 17 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 17 FDA reports)
TOXIC SKIN ERUPTION ( 17 FDA reports)
URETERAL DISORDER ( 17 FDA reports)
VENTRICULAR HYPOPLASIA ( 17 FDA reports)
VITREOUS HAEMORRHAGE ( 17 FDA reports)
WOUND HAEMORRHAGE ( 17 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 16 FDA reports)
ADRENAL ADENOMA ( 16 FDA reports)
AFFECT LABILITY ( 16 FDA reports)
AMAUROSIS FUGAX ( 16 FDA reports)
AMENORRHOEA ( 16 FDA reports)
BREAST INDURATION ( 16 FDA reports)
BREATH SOUNDS ABNORMAL ( 16 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 16 FDA reports)
CARDIAC FLUTTER ( 16 FDA reports)
CHARLES BONNET SYNDROME ( 16 FDA reports)
CHOROIDAL DETACHMENT ( 16 FDA reports)
DILATATION ATRIAL ( 16 FDA reports)
DROP ATTACKS ( 16 FDA reports)
DRUG LEVEL INCREASED ( 16 FDA reports)
EAR NEOPLASM ( 16 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 16 FDA reports)
FAECES PALE ( 16 FDA reports)
GASTROINTESTINAL PAIN ( 16 FDA reports)
GENITAL HERPES ( 16 FDA reports)
GLOSSITIS ( 16 FDA reports)
HAIR GROWTH ABNORMAL ( 16 FDA reports)
HALLUCINATION, VISUAL ( 16 FDA reports)
HEPATOSPLENOMEGALY ( 16 FDA reports)
HILAR LYMPHADENOPATHY ( 16 FDA reports)
HODGKIN'S DISEASE ( 16 FDA reports)
HYPERURICAEMIA ( 16 FDA reports)
HYPOKINESIA ( 16 FDA reports)
IMPULSIVE BEHAVIOUR ( 16 FDA reports)
INJECTION SITE BRUISING ( 16 FDA reports)
INJURY CORNEAL ( 16 FDA reports)
LIMB OPERATION ( 16 FDA reports)
MACROGLOSSIA ( 16 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 16 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 16 FDA reports)
MEDICATION RESIDUE ( 16 FDA reports)
MENIERE'S DISEASE ( 16 FDA reports)
MONOCYTE COUNT INCREASED ( 16 FDA reports)
NERVE COMPRESSION ( 16 FDA reports)
OPEN REDUCTION OF FRACTURE ( 16 FDA reports)
ORGAN FAILURE ( 16 FDA reports)
PANCREATIC MASS ( 16 FDA reports)
PARKINSON'S DISEASE ( 16 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 16 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 16 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 16 FDA reports)
PSEUDOMONAS INFECTION ( 16 FDA reports)
RETINAL HAEMORRHAGE ( 16 FDA reports)
SACROILIITIS ( 16 FDA reports)
SEPSIS SYNDROME ( 16 FDA reports)
STRESS SYMPTOMS ( 16 FDA reports)
TENDON DISORDER ( 16 FDA reports)
THYROID CANCER ( 16 FDA reports)
TONGUE INJURY ( 16 FDA reports)
UMBILICAL HERNIA REPAIR ( 16 FDA reports)
UNIVENTRICULAR HEART ( 16 FDA reports)
UTERINE DISORDER ( 16 FDA reports)
VAGINAL DISCHARGE ( 16 FDA reports)
VASCULAR CALCIFICATION ( 16 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 16 FDA reports)
VENTRICULAR DYSFUNCTION ( 16 FDA reports)
ABDOMINAL HERNIA ( 15 FDA reports)
ACTINIC ELASTOSIS ( 15 FDA reports)
ADRENAL INSUFFICIENCY ( 15 FDA reports)
BEDRIDDEN ( 15 FDA reports)
BENIGN NEOPLASM ( 15 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 15 FDA reports)
BLOOD ALBUMIN DECREASED ( 15 FDA reports)
BLOOD CULTURE POSITIVE ( 15 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 15 FDA reports)
CATHETER PLACEMENT ( 15 FDA reports)
CHOLANGITIS ( 15 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 15 FDA reports)
COLECTOMY ( 15 FDA reports)
COLLAPSE OF LUNG ( 15 FDA reports)
CORONARY ARTERY BYPASS ( 15 FDA reports)
CYSTOCELE ( 15 FDA reports)
DEPENDENCE ( 15 FDA reports)
DEVICE OCCLUSION ( 15 FDA reports)
EAR DISORDER ( 15 FDA reports)
ELECTROLYTE IMBALANCE ( 15 FDA reports)
ENDOMETRIOSIS ( 15 FDA reports)
FLAT AFFECT ( 15 FDA reports)
FOOD INTOLERANCE ( 15 FDA reports)
HAEMODIALYSIS ( 15 FDA reports)
HAEMOLYTIC ANAEMIA ( 15 FDA reports)
HEPATOCELLULAR DAMAGE ( 15 FDA reports)
HERNIA REPAIR ( 15 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 15 FDA reports)
IMPETIGO ( 15 FDA reports)
LIGAMENT INJURY ( 15 FDA reports)
LUNG HYPERINFLATION ( 15 FDA reports)
NAIL AVULSION ( 15 FDA reports)
NARCOLEPSY ( 15 FDA reports)
PURULENCE ( 15 FDA reports)
QRS AXIS ABNORMAL ( 15 FDA reports)
RASH VESICULAR ( 15 FDA reports)
SALIVARY HYPERSECRETION ( 15 FDA reports)
SENSORY LOSS ( 15 FDA reports)
SKIN HYPERTROPHY ( 15 FDA reports)
SOMNAMBULISM ( 15 FDA reports)
SUDDEN CARDIAC DEATH ( 15 FDA reports)
TENDON INJURY ( 15 FDA reports)
TENSION ( 15 FDA reports)
TOBACCO ABUSE ( 15 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 15 FDA reports)
YELLOW SKIN ( 14 FDA reports)
ABORTION INDUCED ( 14 FDA reports)
ABSCESS DRAINAGE ( 14 FDA reports)
ACCIDENT ( 14 FDA reports)
ACROCHORDON ( 14 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 14 FDA reports)
ASTEATOSIS ( 14 FDA reports)
AXILLARY MASS ( 14 FDA reports)
BLOOD PRESSURE ABNORMAL ( 14 FDA reports)
BODY TEMPERATURE DECREASED ( 14 FDA reports)
BODY TINEA ( 14 FDA reports)
BONE MARROW TRANSPLANT ( 14 FDA reports)
BONE SWELLING ( 14 FDA reports)
BREAST CANCER IN SITU ( 14 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 14 FDA reports)
CATHETER SITE INFECTION ( 14 FDA reports)
CHEMICAL POISONING ( 14 FDA reports)
CHOLESTASIS ( 14 FDA reports)
CLOSTRIDIAL INFECTION ( 14 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 14 FDA reports)
CORONARY ARTERY THROMBOSIS ( 14 FDA reports)
DEVELOPMENTAL DELAY ( 14 FDA reports)
DRUG PRESCRIBING ERROR ( 14 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 14 FDA reports)
EROSIVE OESOPHAGITIS ( 14 FDA reports)
EXPIRED DRUG ADMINISTERED ( 14 FDA reports)
FEELING DRUNK ( 14 FDA reports)
FEMORAL NECK FRACTURE ( 14 FDA reports)
HEMIPLEGIA ( 14 FDA reports)
HORDEOLUM ( 14 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 14 FDA reports)
HUMERUS FRACTURE ( 14 FDA reports)
HYPERCHLORAEMIA ( 14 FDA reports)
ILEITIS ( 14 FDA reports)
INADEQUATE ANALGESIA ( 14 FDA reports)
INFANTILE SPASMS ( 14 FDA reports)
LARGE INTESTINAL ULCER ( 14 FDA reports)
LOGORRHOEA ( 14 FDA reports)
LYMPHOCYTIC INFILTRATION ( 14 FDA reports)
MALABSORPTION ( 14 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 14 FDA reports)
MENINGITIS ASEPTIC ( 14 FDA reports)
METASTATIC PAIN ( 14 FDA reports)
MITRAL VALVE STENOSIS ( 14 FDA reports)
MUSCULOSKELETAL DISORDER ( 14 FDA reports)
NO THERAPEUTIC RESPONSE ( 14 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 14 FDA reports)
PLEURAL FIBROSIS ( 14 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 14 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 14 FDA reports)
POUCHITIS ( 14 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 14 FDA reports)
PULMONARY AIR LEAKAGE ( 14 FDA reports)
RADIUS FRACTURE ( 14 FDA reports)
RENAL MASS ( 14 FDA reports)
RESORPTION BONE INCREASED ( 14 FDA reports)
SKIN CHAPPED ( 14 FDA reports)
SKIN ODOUR ABNORMAL ( 14 FDA reports)
SLUGGISHNESS ( 14 FDA reports)
SMOKER ( 14 FDA reports)
SPINAL CORD DISORDER ( 14 FDA reports)
STENT PLACEMENT ( 14 FDA reports)
STRIDOR ( 14 FDA reports)
SUBILEUS ( 14 FDA reports)
TEMPERATURE INTOLERANCE ( 14 FDA reports)
TONGUE DISCOLOURATION ( 14 FDA reports)
TRACHEOBRONCHITIS ( 14 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 14 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 14 FDA reports)
URETERIC OBSTRUCTION ( 14 FDA reports)
URINARY TRACT DISORDER ( 14 FDA reports)
VAGINITIS BACTERIAL ( 14 FDA reports)
ANAL HAEMORRHAGE ( 13 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 13 FDA reports)
APNOEA ( 13 FDA reports)
ASTERIXIS ( 13 FDA reports)
ATROPHY ( 13 FDA reports)
BIOPSY BONE ABNORMAL ( 13 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 13 FDA reports)
BONE LESION EXCISION ( 13 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 13 FDA reports)
BRONCHOPNEUMONIA ( 13 FDA reports)
CATHETER RELATED INFECTION ( 13 FDA reports)
CHOLESTATIC LIVER INJURY ( 13 FDA reports)
CONDUCTION DISORDER ( 13 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 13 FDA reports)
DERMATITIS ATOPIC ( 13 FDA reports)
DEVICE DISLOCATION ( 13 FDA reports)
DIABETIC NEPHROPATHY ( 13 FDA reports)
DUODENAL ULCER ( 13 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 13 FDA reports)
EPIGASTRIC DISCOMFORT ( 13 FDA reports)
EYE HAEMORRHAGE ( 13 FDA reports)
EYE INFECTION ( 13 FDA reports)
FIBROUS HISTIOCYTOMA ( 13 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 13 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 13 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 13 FDA reports)
HYDROCEPHALUS ( 13 FDA reports)
HYSTERECTOMY ( 13 FDA reports)
IMMUNE SYSTEM DISORDER ( 13 FDA reports)
INFUSION SITE PAIN ( 13 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 13 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 13 FDA reports)
LIPOMA ( 13 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 13 FDA reports)
MENSTRUAL DISORDER ( 13 FDA reports)
MUSCLE INJURY ( 13 FDA reports)
MUSCLE RIGIDITY ( 13 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 13 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 13 FDA reports)
PAIN OF SKIN ( 13 FDA reports)
PANIC REACTION ( 13 FDA reports)
POLYTRAUMATISM ( 13 FDA reports)
PROCEDURAL HYPERTENSION ( 13 FDA reports)
QUALITY OF LIFE DECREASED ( 13 FDA reports)
TOOTH EROSION ( 13 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 13 FDA reports)
UTERINE CANCER ( 13 FDA reports)
VESTIBULAR DISORDER ( 13 FDA reports)
WEIGHT BEARING DIFFICULTY ( 13 FDA reports)
ACCIDENTAL EXPOSURE ( 12 FDA reports)
ACETABULUM FRACTURE ( 12 FDA reports)
ALCOHOL USE ( 12 FDA reports)
ANAPHYLACTOID REACTION ( 12 FDA reports)
APPENDICECTOMY ( 12 FDA reports)
APPLICATION SITE ERYTHEMA ( 12 FDA reports)
ARTERIAL DISORDER ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 12 FDA reports)
ATROPHIC VULVOVAGINITIS ( 12 FDA reports)
BASEDOW'S DISEASE ( 12 FDA reports)
BLINDNESS TRANSIENT ( 12 FDA reports)
BLOOD CHLORIDE DECREASED ( 12 FDA reports)
BLOOD TEST ABNORMAL ( 12 FDA reports)
BREAST ENLARGEMENT ( 12 FDA reports)
BURNS SECOND DEGREE ( 12 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 12 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 12 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 12 FDA reports)
DYSAESTHESIA ( 12 FDA reports)
DYSTHYMIC DISORDER ( 12 FDA reports)
EFFUSION ( 12 FDA reports)
ENDOMETRIAL CANCER ( 12 FDA reports)
FEELING OF DESPAIR ( 12 FDA reports)
FUNGAL SKIN INFECTION ( 12 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 12 FDA reports)
HYPERMETABOLISM ( 12 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 12 FDA reports)
INTERMITTENT CLAUDICATION ( 12 FDA reports)
INTESTINAL DILATATION ( 12 FDA reports)
INTESTINAL PERFORATION ( 12 FDA reports)
INTRACARDIAC THROMBUS ( 12 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 12 FDA reports)
JOINT CONTRACTURE ( 12 FDA reports)
LEFT ATRIAL DILATATION ( 12 FDA reports)
LIVER TRANSPLANT REJECTION ( 12 FDA reports)
LUPUS-LIKE SYNDROME ( 12 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 12 FDA reports)
MADAROSIS ( 12 FDA reports)
MIGRAINE WITH AURA ( 12 FDA reports)
MITRAL VALVE DISEASE ( 12 FDA reports)
MONOCYTE COUNT DECREASED ( 12 FDA reports)
MUSCLE SPASTICITY ( 12 FDA reports)
MYELODYSPLASTIC SYNDROME ( 12 FDA reports)
NEUROGENIC BLADDER ( 12 FDA reports)
NYSTAGMUS ( 12 FDA reports)
PERIARTHRITIS ( 12 FDA reports)
PHARYNGEAL ERYTHEMA ( 12 FDA reports)
POOR PERSONAL HYGIENE ( 12 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 12 FDA reports)
POSTOPERATIVE INFECTION ( 12 FDA reports)
PROSTATITIS ( 12 FDA reports)
SCAB ( 12 FDA reports)
SCHAMBERG'S DISEASE ( 12 FDA reports)
SCLERAL OPERATION ( 12 FDA reports)
SEBACEOUS GLAND DISORDER ( 12 FDA reports)
SENSATION OF HEAVINESS ( 12 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 12 FDA reports)
STREPTOCOCCAL INFECTION ( 12 FDA reports)
SUBDURAL HAEMORRHAGE ( 12 FDA reports)
THERAPEUTIC PROCEDURE ( 12 FDA reports)
TOXIC ENCEPHALOPATHY ( 12 FDA reports)
TUBERCULIN TEST POSITIVE ( 12 FDA reports)
UNDERDOSE ( 12 FDA reports)
URINARY HESITATION ( 12 FDA reports)
ACUTE HEPATIC FAILURE ( 11 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 11 FDA reports)
ALOPECIA AREATA ( 11 FDA reports)
APPENDIX DISORDER ( 11 FDA reports)
APPLICATION SITE RASH ( 11 FDA reports)
ARRESTED LABOUR ( 11 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 11 FDA reports)
BREAST DISORDER ( 11 FDA reports)
CAECITIS ( 11 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 11 FDA reports)
CAROTID ARTERY ANEURYSM ( 11 FDA reports)
CAROTID BRUIT ( 11 FDA reports)
CATHETER RELATED COMPLICATION ( 11 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 11 FDA reports)
CHOLESTEROSIS ( 11 FDA reports)
CUSHING'S SYNDROME ( 11 FDA reports)
CYSTOPEXY ( 11 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 11 FDA reports)
DYSPHORIA ( 11 FDA reports)
DYSPLASTIC NAEVUS ( 11 FDA reports)
ECZEMA INFECTED ( 11 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 11 FDA reports)
EYE INJURY ( 11 FDA reports)
FIBRIN D DIMER INCREASED ( 11 FDA reports)
FISTULA REPAIR ( 11 FDA reports)
FOOD POISONING ( 11 FDA reports)
FORMICATION ( 11 FDA reports)
FULGURATION ( 11 FDA reports)
GASTRIC CANCER ( 11 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 11 FDA reports)
GAZE PALSY ( 11 FDA reports)
HAEMORRHAGIC DIATHESIS ( 11 FDA reports)
HEART INJURY ( 11 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 11 FDA reports)
HEPATIC MASS ( 11 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 11 FDA reports)
HYPERCOAGULATION ( 11 FDA reports)
INCISIONAL HERNIA ( 11 FDA reports)
LACTIC ACIDOSIS ( 11 FDA reports)
LIMB DEFORMITY ( 11 FDA reports)
LISTLESS ( 11 FDA reports)
LORDOSIS ( 11 FDA reports)
LOSS OF EMPLOYMENT ( 11 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 11 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 11 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 11 FDA reports)
MENINGIOMA ( 11 FDA reports)
MENOPAUSAL SYMPTOMS ( 11 FDA reports)
METATARSALGIA ( 11 FDA reports)
MUMPS ( 11 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 11 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 11 FDA reports)
OSTEOMALACIA ( 11 FDA reports)
OVARIAN CANCER ( 11 FDA reports)
OVARIAN FAILURE ( 11 FDA reports)
PAINFUL RESPIRATION ( 11 FDA reports)
PANCREATIC CYST ( 11 FDA reports)
PARTIAL SEIZURES ( 11 FDA reports)
PATELLA FRACTURE ( 11 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 11 FDA reports)
POST THROMBOTIC SYNDROME ( 11 FDA reports)
PRESBYOPIA ( 11 FDA reports)
PROCEDURAL VOMITING ( 11 FDA reports)
PROTEIN TOTAL DECREASED ( 11 FDA reports)
PROTEIN URINE ( 11 FDA reports)
PULMONARY MASS ( 11 FDA reports)
PURPURA ( 11 FDA reports)
RUBELLA ( 11 FDA reports)
SCARLET FEVER ( 11 FDA reports)
SECONDARY SEQUESTRUM ( 11 FDA reports)
SUBGALEAL HAEMATOMA ( 11 FDA reports)
SYNCOPE VASOVAGAL ( 11 FDA reports)
TACHYARRHYTHMIA ( 11 FDA reports)
TINEA CRURIS ( 11 FDA reports)
URINE ODOUR ABNORMAL ( 11 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 11 FDA reports)
VENA CAVA FILTER INSERTION ( 11 FDA reports)
VULVAL DISORDER ( 11 FDA reports)
WHIPLASH INJURY ( 11 FDA reports)
WOUND DEBRIDEMENT ( 10 FDA reports)
ABSCESS NECK ( 10 FDA reports)
ANASTOMOTIC STENOSIS ( 10 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 10 FDA reports)
APHAGIA ( 10 FDA reports)
APPLICATION SITE PRURITUS ( 10 FDA reports)
BIOPSY BREAST ABNORMAL ( 10 FDA reports)
BLOOD MAGNESIUM DECREASED ( 10 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 10 FDA reports)
BUNION ( 10 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 10 FDA reports)
CAUSTIC INJURY ( 10 FDA reports)
CHOLESTEATOMA ( 10 FDA reports)
COLONOSCOPY ( 10 FDA reports)
CREPITATIONS ( 10 FDA reports)
CULTURE URINE POSITIVE ( 10 FDA reports)
DYSMENORRHOEA ( 10 FDA reports)
EARLY MORNING AWAKENING ( 10 FDA reports)
EJACULATION DISORDER ( 10 FDA reports)
EJECTION FRACTION ABNORMAL ( 10 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 10 FDA reports)
EMBOLISM ( 10 FDA reports)
ENDOTRACHEAL INTUBATION ( 10 FDA reports)
FAMILY STRESS ( 10 FDA reports)
FAT NECROSIS ( 10 FDA reports)
FOREIGN BODY IN EYE ( 10 FDA reports)
GALLBLADDER OPERATION ( 10 FDA reports)
GASTRIC HAEMORRHAGE ( 10 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 10 FDA reports)
GINGIVAL ABSCESS ( 10 FDA reports)
HAEMODYNAMIC INSTABILITY ( 10 FDA reports)
HAIR COLOUR CHANGES ( 10 FDA reports)
HEPATIC NECROSIS ( 10 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 10 FDA reports)
HYPERACUSIS ( 10 FDA reports)
HYPERCHLORHYDRIA ( 10 FDA reports)
IMPAIRED SELF-CARE ( 10 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 10 FDA reports)
INTRA-UTERINE DEATH ( 10 FDA reports)
KYPHOSIS ( 10 FDA reports)
LARGE INTESTINE PERFORATION ( 10 FDA reports)
LEUKAEMIA ( 10 FDA reports)
LIMB ASYMMETRY ( 10 FDA reports)
LOOSE STOOLS ( 10 FDA reports)
MECHANICAL VENTILATION ( 10 FDA reports)
NASAL DISORDER ( 10 FDA reports)
NASAL DRYNESS ( 10 FDA reports)
NEPHRITIS INTERSTITIAL ( 10 FDA reports)
NEUTROPENIC COLITIS ( 10 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 10 FDA reports)
OBSTRUCTIVE UROPATHY ( 10 FDA reports)
OESOPHAGEAL PAIN ( 10 FDA reports)
ORAL FUNGAL INFECTION ( 10 FDA reports)
OROPHARYNGEAL BLISTERING ( 10 FDA reports)
OTITIS MEDIA CHRONIC ( 10 FDA reports)
PAPILLOMA VIRAL INFECTION ( 10 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 10 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 10 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 10 FDA reports)
POLYPECTOMY ( 10 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 10 FDA reports)
PULMONARY HAEMORRHAGE ( 10 FDA reports)
PULPITIS DENTAL ( 10 FDA reports)
PULSE ABSENT ( 10 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 10 FDA reports)
RETINITIS ( 10 FDA reports)
RHINITIS SEASONAL ( 10 FDA reports)
SEROMA ( 10 FDA reports)
SPONDYLITIS ( 10 FDA reports)
SURGICAL PROCEDURE REPEATED ( 10 FDA reports)
TEARFULNESS ( 10 FDA reports)
TONGUE COATED ( 10 FDA reports)
TOOTH RESORPTION ( 10 FDA reports)
TRAUMATIC BRAIN INJURY ( 10 FDA reports)
TRIGONITIS ( 10 FDA reports)
TRYPTASE INCREASED ( 10 FDA reports)
VESICOURETERIC REFLUX ( 10 FDA reports)
VIRAL LABYRINTHITIS ( 10 FDA reports)
VOCAL CORD POLYP ( 10 FDA reports)
ABDOMINAL MASS ( 9 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 9 FDA reports)
ACIDOSIS ( 9 FDA reports)
ACTINOMYCOSIS ( 9 FDA reports)
ACUTE STRESS DISORDER ( 9 FDA reports)
ADRENALECTOMY ( 9 FDA reports)
ALCOHOL ABUSE ( 9 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 9 FDA reports)
ANGIOMYOLIPOMA ( 9 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 9 FDA reports)
ANIMAL BITE ( 9 FDA reports)
ANORECTAL DISORDER ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 9 FDA reports)
AORTIC DISORDER ( 9 FDA reports)
ATYPICAL MYCOBACTERIAL LYMPHADENITIS ( 9 FDA reports)
AUTOIMMUNE HEPATITIS ( 9 FDA reports)
BIOPSY LYMPH GLAND ( 9 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 9 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 9 FDA reports)
BONE MARROW OEDEMA ( 9 FDA reports)
BONE OPERATION ( 9 FDA reports)
BRAIN NEOPLASM ( 9 FDA reports)
BREAST CANCER RECURRENT ( 9 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 9 FDA reports)
CALCINOSIS ( 9 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 9 FDA reports)
CEREBELLAR HAEMORRHAGE ( 9 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 9 FDA reports)
COLITIS COLLAGENOUS ( 9 FDA reports)
CONGENITAL ANOMALY ( 9 FDA reports)
COR PULMONALE ( 9 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 9 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 9 FDA reports)
DENTAL OPERATION ( 9 FDA reports)
DENTAL TREATMENT ( 9 FDA reports)
DEPERSONALISATION ( 9 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 9 FDA reports)
DIABETIC RETINOPATHY ( 9 FDA reports)
DIAPHRAGMATIC HERNIA ( 9 FDA reports)
DROOLING ( 9 FDA reports)
DYSPNOEA EXACERBATED ( 9 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 9 FDA reports)
EDENTULOUS ( 9 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 9 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 9 FDA reports)
ENTEROVESICAL FISTULA ( 9 FDA reports)
ENTHESOPATHY ( 9 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 9 FDA reports)
EXFOLIATIVE RASH ( 9 FDA reports)
FEMALE STERILISATION ( 9 FDA reports)
GALLBLADDER POLYP ( 9 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 9 FDA reports)
GASTRIC VARICES ( 9 FDA reports)
GASTRITIS HAEMORRHAGIC ( 9 FDA reports)
GRIP STRENGTH DECREASED ( 9 FDA reports)
HAIR TEXTURE ABNORMAL ( 9 FDA reports)
HEART RATE ABNORMAL ( 9 FDA reports)
HEPATOTOXICITY ( 9 FDA reports)
HORMONE LEVEL ABNORMAL ( 9 FDA reports)
HOSPITALISATION ( 9 FDA reports)
HYPERPHOSPHATAEMIA ( 9 FDA reports)
HYPERSEXUALITY ( 9 FDA reports)
HYPOPROTEINAEMIA ( 9 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 9 FDA reports)
INJECTION SITE INFLAMMATION ( 9 FDA reports)
INJECTION SITE WARMTH ( 9 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 9 FDA reports)
LIVER CARCINOMA RUPTURED ( 9 FDA reports)
LIVER INJURY ( 9 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 9 FDA reports)
LYMPH NODE TUBERCULOSIS ( 9 FDA reports)
MACULAR OEDEMA ( 9 FDA reports)
MASTECTOMY ( 9 FDA reports)
MEGAKARYOCYTES DECREASED ( 9 FDA reports)
MENINGITIS ( 9 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 9 FDA reports)
NASAL SINUS DRAINAGE ( 9 FDA reports)
NIGHT BLINDNESS ( 9 FDA reports)
OESOPHAGEAL STENOSIS ( 9 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 9 FDA reports)
ORAL PRURITUS ( 9 FDA reports)
OROANTRAL FISTULA ( 9 FDA reports)
OROPHARYNGEAL SWELLING ( 9 FDA reports)
OSTEOMYELITIS DRAINAGE ( 9 FDA reports)
OVARIAN CANCER RECURRENT ( 9 FDA reports)
PHARYNGEAL DISORDER ( 9 FDA reports)
PLAGUE ( 9 FDA reports)
PREMATURE LABOUR ( 9 FDA reports)
PROSTATE CANCER ( 9 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 9 FDA reports)
PULMONARY TOXICITY ( 9 FDA reports)
RECTOCELE ( 9 FDA reports)
REHABILITATION THERAPY ( 9 FDA reports)
RENAL ABSCESS ( 9 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 9 FDA reports)
SALIVARY GLAND CANCER ( 9 FDA reports)
SENSATION OF FOREIGN BODY ( 9 FDA reports)
SERUM FERRITIN INCREASED ( 9 FDA reports)
SERUM SICKNESS ( 9 FDA reports)
SKIN CANDIDA ( 9 FDA reports)
SPINAL LAMINECTOMY ( 9 FDA reports)
SPLENIC VEIN THROMBOSIS ( 9 FDA reports)
STARING ( 9 FDA reports)
STATUS ASTHMATICUS ( 9 FDA reports)
TEMPORAL ARTERITIS ( 9 FDA reports)
THORACOTOMY ( 9 FDA reports)
TONSILLITIS ( 9 FDA reports)
TRANSFUSION ( 9 FDA reports)
ULCER HAEMORRHAGE ( 9 FDA reports)
URINE OUTPUT DECREASED ( 9 FDA reports)
URTICARIA GENERALISED ( 9 FDA reports)
VAGINAL BURNING SENSATION ( 9 FDA reports)
VOCAL CORD DISORDER ( 9 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 8 FDA reports)
ACRODERMATITIS ( 8 FDA reports)
ADENOCARCINOMA ( 8 FDA reports)
ADJUSTMENT DISORDER ( 8 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 8 FDA reports)
ALLERGIC SINUSITIS ( 8 FDA reports)
ANAEMIA MACROCYTIC ( 8 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 8 FDA reports)
ANAL FISTULA ( 8 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 8 FDA reports)
B-CELL LYMPHOMA ( 8 FDA reports)
BETA GLOBULIN INCREASED ( 8 FDA reports)
BIOPSY GINGIVAL ( 8 FDA reports)
BLADDER CANCER RECURRENT ( 8 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 8 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 8 FDA reports)
BRADYPHRENIA ( 8 FDA reports)
BREAST SWELLING ( 8 FDA reports)
BREAST TENDERNESS ( 8 FDA reports)
CACHEXIA ( 8 FDA reports)
CARCINOID SYNDROME ( 8 FDA reports)
CEREBELLAR INFARCTION ( 8 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 8 FDA reports)
CHEMOTHERAPY ( 8 FDA reports)
CHEST TUBE INSERTION ( 8 FDA reports)
CHOKING SENSATION ( 8 FDA reports)
CLEFT LIP AND PALATE ( 8 FDA reports)
CLOSED FRACTURE MANIPULATION ( 8 FDA reports)
COELIAC DISEASE ( 8 FDA reports)
CONVERSION DISORDER ( 8 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 8 FDA reports)
DENTAL PULP DISORDER ( 8 FDA reports)
DIABETIC GASTROPARESIS ( 8 FDA reports)
DIALYSIS ( 8 FDA reports)
DISSOCIATION ( 8 FDA reports)
DROWNING ( 8 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 8 FDA reports)
DUPUYTREN'S CONTRACTURE ( 8 FDA reports)
EARLY SATIETY ( 8 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 8 FDA reports)
ENTEROCUTANEOUS FISTULA ( 8 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 8 FDA reports)
ESCHERICHIA BACTERAEMIA ( 8 FDA reports)
EXPOSURE TO TOXIC AGENT ( 8 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 8 FDA reports)
FAECES HARD ( 8 FDA reports)
FIBROADENOMA OF BREAST ( 8 FDA reports)
FOOT OPERATION ( 8 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 8 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 8 FDA reports)
GASTROINTESTINAL TOXICITY ( 8 FDA reports)
GENITAL PRURITUS FEMALE ( 8 FDA reports)
GUN SHOT WOUND ( 8 FDA reports)
HAEMOGLOBIN ABNORMAL ( 8 FDA reports)
HAEMORRHAGIC STROKE ( 8 FDA reports)
HELICOBACTER INFECTION ( 8 FDA reports)
HEPATIC FIBROSIS ( 8 FDA reports)
HERPES ZOSTER DISSEMINATED ( 8 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 8 FDA reports)
HYPERCAPNIA ( 8 FDA reports)
HYPOVENTILATION ( 8 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 8 FDA reports)
IMPULSE-CONTROL DISORDER ( 8 FDA reports)
INCISION SITE INFECTION ( 8 FDA reports)
INJECTION SITE INDURATION ( 8 FDA reports)
INTENTIONAL SELF-INJURY ( 8 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 8 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 8 FDA reports)
LACRIMAL DISORDER ( 8 FDA reports)
LEUKOENCEPHALOPATHY ( 8 FDA reports)
LIP ULCERATION ( 8 FDA reports)
MASS EXCISION ( 8 FDA reports)
METABOLIC DISORDER ( 8 FDA reports)
METABOLIC SYNDROME ( 8 FDA reports)
METASTASES TO BONE MARROW ( 8 FDA reports)
METASTASES TO THORAX ( 8 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 8 FDA reports)
MYDRIASIS ( 8 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 8 FDA reports)
NEPHROGENIC ANAEMIA ( 8 FDA reports)
NEUROENDOCRINE TUMOUR ( 8 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 8 FDA reports)
ORTHOSIS USER ( 8 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR METASTATIC ( 8 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 8 FDA reports)
PERICARDITIS ( 8 FDA reports)
PERIPHERAL ISCHAEMIA ( 8 FDA reports)
PERIRECTAL ABSCESS ( 8 FDA reports)
PHARYNGEAL POLYP ( 8 FDA reports)
PHONOPHOBIA ( 8 FDA reports)
PIGMENTARY GLAUCOMA ( 8 FDA reports)
POISONING ( 8 FDA reports)
POLYCYSTIC OVARIES ( 8 FDA reports)
POLYMYOSITIS ( 8 FDA reports)
POLYP COLORECTAL ( 8 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 8 FDA reports)
POST PROCEDURAL HAEMATOMA ( 8 FDA reports)
POSTURE ABNORMAL ( 8 FDA reports)
PROCEDURAL NAUSEA ( 8 FDA reports)
PULMONARY HILUM MASS ( 8 FDA reports)
PULMONARY SARCOIDOSIS ( 8 FDA reports)
PUPIL FIXED ( 8 FDA reports)
RADICULITIS CERVICAL ( 8 FDA reports)
RECTAL ULCER ( 8 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 8 FDA reports)
RESPIRATORY DEPRESSION ( 8 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 8 FDA reports)
SCLERAL DISORDER ( 8 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 8 FDA reports)
SKIN ATROPHY ( 8 FDA reports)
SKIN NODULE ( 8 FDA reports)
SKIN REACTION ( 8 FDA reports)
SKIN STRIAE ( 8 FDA reports)
STATUS EPILEPTICUS ( 8 FDA reports)
STRESS URINARY INCONTINENCE ( 8 FDA reports)
SUBCUTANEOUS ABSCESS ( 8 FDA reports)
SUTURE RELATED COMPLICATION ( 8 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 8 FDA reports)
SYSTEMIC SCLEROSIS ( 8 FDA reports)
THROAT LESION ( 8 FDA reports)
THROMBOCYTHAEMIA ( 8 FDA reports)
TOE DEFORMITY ( 8 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 8 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 8 FDA reports)
URETHRAL OBSTRUCTION ( 8 FDA reports)
UTERINE DILATION AND CURETTAGE ( 8 FDA reports)
UTERINE POLYP ( 8 FDA reports)
VENOUS OCCLUSION ( 8 FDA reports)
VENTRICULAR ARRHYTHMIA ( 8 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 8 FDA reports)
VIRAL MYOCARDITIS ( 8 FDA reports)
VULVOVAGINAL DRYNESS ( 8 FDA reports)
WEIGHT FLUCTUATION ( 8 FDA reports)
WRONG DRUG ADMINISTERED ( 8 FDA reports)
WRIST SURGERY ( 8 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 7 FDA reports)
ABDOMINAL PANNICULECTOMY ( 7 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 7 FDA reports)
ABDOMINAL SYMPTOM ( 7 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 7 FDA reports)
ACCELERATED HYPERTENSION ( 7 FDA reports)
ACUTE PRERENAL FAILURE ( 7 FDA reports)
ADENOMA BENIGN ( 7 FDA reports)
ADRENAL NEOPLASM ( 7 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 7 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 7 FDA reports)
AORTIC VALVE DISEASE ( 7 FDA reports)
APPLICATION SITE IRRITATION ( 7 FDA reports)
APRAXIA ( 7 FDA reports)
ARTERIOSPASM CORONARY ( 7 FDA reports)
ARTHRITIS INFECTIVE ( 7 FDA reports)
ARTHROPOD BITE ( 7 FDA reports)
AUTOIMMUNE DISORDER ( 7 FDA reports)
BILIARY ANASTOMOSIS ( 7 FDA reports)
BLOOD CHOLESTEROL ( 7 FDA reports)
BLOOD CREATINE INCREASED ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 7 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 7 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 7 FDA reports)
BLOOD SODIUM INCREASED ( 7 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 7 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 7 FDA reports)
BONE GRAFT ( 7 FDA reports)
BRACHIAL PLEXOPATHY ( 7 FDA reports)
BREAST CANCER STAGE I ( 7 FDA reports)
BREAST HYPERPLASIA ( 7 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 7 FDA reports)
BURNING MOUTH SYNDROME ( 7 FDA reports)
CALCIUM DEFICIENCY ( 7 FDA reports)
CARDIAC ANEURYSM ( 7 FDA reports)
CAROTID ARTERY THROMBOSIS ( 7 FDA reports)
CATHETER SEPSIS ( 7 FDA reports)
CATHETER SITE HAEMORRHAGE ( 7 FDA reports)
CERVICAL NEURITIS ( 7 FDA reports)
CHAPPED LIPS ( 7 FDA reports)
CHEST WALL PAIN ( 7 FDA reports)
CHOLECYSTITIS INFECTIVE ( 7 FDA reports)
CHOREA ( 7 FDA reports)
CORNEAL OPACITY ( 7 FDA reports)
DENTAL CLEANING ( 7 FDA reports)
DEPRESSIVE SYMPTOM ( 7 FDA reports)
DERMATOPHYTOSIS ( 7 FDA reports)
DYSGRAPHIA ( 7 FDA reports)
DYSPHASIA ( 7 FDA reports)
ECTOPIC PREGNANCY ( 7 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 7 FDA reports)
EMBOLISM VENOUS ( 7 FDA reports)
ENDOMETRIAL DISORDER ( 7 FDA reports)
ENTERITIS ( 7 FDA reports)
ENTEROCOLITIS ( 7 FDA reports)
ENTEROCOLITIS BACTERIAL ( 7 FDA reports)
EPIDERMAL NAEVUS ( 7 FDA reports)
EYE OPERATION ( 7 FDA reports)
EYE ROLLING ( 7 FDA reports)
FISTULA DISCHARGE ( 7 FDA reports)
FOOD ALLERGY ( 7 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 7 FDA reports)
GALACTORRHOEA ( 7 FDA reports)
GANGLION ( 7 FDA reports)
GASTROINTESTINAL INFECTION ( 7 FDA reports)
HAEMOCHROMATOSIS ( 7 FDA reports)
HEAT RASH ( 7 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 7 FDA reports)
HYPERPARATHYROIDISM ( 7 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 7 FDA reports)
HYPOMENORRHOEA ( 7 FDA reports)
HYPOTRICHOSIS ( 7 FDA reports)
IATROGENIC INJURY ( 7 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 7 FDA reports)
INFARCTION ( 7 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 7 FDA reports)
INFERTILITY ( 7 FDA reports)
INFUSION SITE ERYTHEMA ( 7 FDA reports)
INJECTION SITE IRRITATION ( 7 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 7 FDA reports)
INTERTRIGO ( 7 FDA reports)
INTESTINAL RESECTION ( 7 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 7 FDA reports)
JOINT CREPITATION ( 7 FDA reports)
JOINT LOCK ( 7 FDA reports)
KNEE OPERATION ( 7 FDA reports)
LIVER TRANSPLANT ( 7 FDA reports)
LOCALISED OEDEMA ( 7 FDA reports)
LUNG OPERATION ( 7 FDA reports)
LYMPHOPENIA ( 7 FDA reports)
MACULOPATHY ( 7 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 7 FDA reports)
METASTASES TO ADRENALS ( 7 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 7 FDA reports)
MUCOUS MEMBRANE DISORDER ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ( 7 FDA reports)
MULTIPLE FRACTURES ( 7 FDA reports)
MUSCLE CONTRACTURE ( 7 FDA reports)
MYASTHENIA GRAVIS ( 7 FDA reports)
MYOFASCIAL SPASM ( 7 FDA reports)
NASAL OBSTRUCTION ( 7 FDA reports)
NECROSIS ( 7 FDA reports)
NEUTROPHIL COUNT INCREASED ( 7 FDA reports)
OBSTRUCTION ( 7 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 7 FDA reports)
OPTIC NERVE DISORDER ( 7 FDA reports)
PARALYSIS FLACCID ( 7 FDA reports)
PCO2 DECREASED ( 7 FDA reports)
PELVIC MASS ( 7 FDA reports)
PEMPHIGUS ( 7 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 7 FDA reports)
PERITONITIS BACTERIAL ( 7 FDA reports)
PHIMOSIS ( 7 FDA reports)
PIGMENTATION DISORDER ( 7 FDA reports)
PLEURAL DISORDER ( 7 FDA reports)
POLYDIPSIA ( 7 FDA reports)
POLYMYALGIA RHEUMATICA ( 7 FDA reports)
PORTAL HYPERTENSION ( 7 FDA reports)
POST CONCUSSION SYNDROME ( 7 FDA reports)
POSTICTAL STATE ( 7 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 7 FDA reports)
PRODUCT TASTE ABNORMAL ( 7 FDA reports)
PROSTATOMEGALY ( 7 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 7 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 7 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 7 FDA reports)
PULSE PRESSURE DECREASED ( 7 FDA reports)
RADIATION INJURY ( 7 FDA reports)
RENAL CANCER ( 7 FDA reports)
RENAL PAIN ( 7 FDA reports)
SALPINGITIS ( 7 FDA reports)
SCRATCH ( 7 FDA reports)
SLEEP TALKING ( 7 FDA reports)
SLEEP WALKING ( 7 FDA reports)
SOFT TISSUE DISORDER ( 7 FDA reports)
SOFT TISSUE MASS ( 7 FDA reports)
SPINAL CORD INJURY ( 7 FDA reports)
SPLENIC INFARCTION ( 7 FDA reports)
SPLINTER ( 7 FDA reports)
SPONTANEOUS PENILE ERECTION ( 7 FDA reports)
SUBDURAL HAEMATOMA ( 7 FDA reports)
TENDON SHEATH LESION EXCISION ( 7 FDA reports)
TENSION HEADACHE ( 7 FDA reports)
TRAUMATIC HAEMATOMA ( 7 FDA reports)
TROPONIN INCREASED ( 7 FDA reports)
TUBERCULOSIS ( 7 FDA reports)
TUNNEL VISION ( 7 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 7 FDA reports)
URINARY TRACT PAIN ( 7 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 7 FDA reports)
VERTEBROPLASTY ( 7 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
ABDOMINAL INFECTION ( 6 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 6 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 6 FDA reports)
ALLODYNIA ( 6 FDA reports)
ANAL ATRESIA ( 6 FDA reports)
APPLICATION SITE PAIN ( 6 FDA reports)
ARTHROSCOPIC SURGERY ( 6 FDA reports)
ARTHROSCOPY ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 6 FDA reports)
AUTOIMMUNE THYROIDITIS ( 6 FDA reports)
BILE DUCT STENOSIS ( 6 FDA reports)
BILE DUCT STONE ( 6 FDA reports)
BIOPSY ( 6 FDA reports)
BLEPHAROSPASM ( 6 FDA reports)
BLIGHTED OVUM ( 6 FDA reports)
BLOOD CREATININE DECREASED ( 6 FDA reports)
BLOOD IRON DECREASED ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 6 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 6 FDA reports)
BONE EROSION ( 6 FDA reports)
BRAIN CONTUSION ( 6 FDA reports)
BRAIN INJURY ( 6 FDA reports)
BRAIN SCAN ABNORMAL ( 6 FDA reports)
BRAIN STEM INFARCTION ( 6 FDA reports)
BREAST MICROCALCIFICATION ( 6 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 6 FDA reports)
BRONCHIAL OBSTRUCTION ( 6 FDA reports)
CANCER PAIN ( 6 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 6 FDA reports)
CARDIOPULMONARY FAILURE ( 6 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 6 FDA reports)
CARTILAGE INJURY ( 6 FDA reports)
CAUDA EQUINA SYNDROME ( 6 FDA reports)
CEREBELLAR SYNDROME ( 6 FDA reports)
CEREBRAL DISORDER ( 6 FDA reports)
CEREBRAL THROMBOSIS ( 6 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 6 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 6 FDA reports)
CLOSTRIDIUM COLITIS ( 6 FDA reports)
COITAL BLEEDING ( 6 FDA reports)
COLON CANCER STAGE III ( 6 FDA reports)
COLON OPERATION ( 6 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 6 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 6 FDA reports)
CUSHINGOID ( 6 FDA reports)
CYST REMOVAL ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DEMYELINATION ( 6 FDA reports)
DERMATOMYOSITIS ( 6 FDA reports)
DRUG DISPENSING ERROR ( 6 FDA reports)
DYSLALIA ( 6 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
ECZEMA NUMMULAR ( 6 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 6 FDA reports)
ENDOCARDITIS ( 6 FDA reports)
ENDOCERVICAL CURETTAGE ( 6 FDA reports)
ENDOMETRIAL ATROPHY ( 6 FDA reports)
EXCESSIVE EYE BLINKING ( 6 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 6 FDA reports)
EYE BURNS ( 6 FDA reports)
EYE MOVEMENT DISORDER ( 6 FDA reports)
EYE OEDEMA ( 6 FDA reports)
FACE INJURY ( 6 FDA reports)
FRACTURE DISPLACEMENT ( 6 FDA reports)
GASTROSCHISIS ( 6 FDA reports)
GENETIC COUNSELLING ( 6 FDA reports)
GLUCOSE URINE PRESENT ( 6 FDA reports)
GROWTH RETARDATION ( 6 FDA reports)
HAEMOCONCENTRATION ( 6 FDA reports)
HAIR DISORDER ( 6 FDA reports)
HEART TRANSPLANT ( 6 FDA reports)
HEPATIC ENZYME ABNORMAL ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 6 FDA reports)
HEPATIC PAIN ( 6 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 6 FDA reports)
HEPATOJUGULAR REFLUX ( 6 FDA reports)
HEREDITARY ANGIOEDEMA ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 6 FDA reports)
HYPERAMMONAEMIA ( 6 FDA reports)
HYPERTENSIVE CRISIS ( 6 FDA reports)
HYPERVENTILATION ( 6 FDA reports)
HYPOREFLEXIA ( 6 FDA reports)
HYSTEROSCOPY ( 6 FDA reports)
ICHTHYOSIS ( 6 FDA reports)
ILLUSION ( 6 FDA reports)
IMMOBILE ( 6 FDA reports)
INCISION SITE COMPLICATION ( 6 FDA reports)
INJECTION SITE ABSCESS ( 6 FDA reports)
INTERCOSTAL NEURALGIA ( 6 FDA reports)
INTESTINAL PROLAPSE ( 6 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 6 FDA reports)
ISCHAEMIC HEPATITIS ( 6 FDA reports)
KERATITIS ( 6 FDA reports)
LIBIDO INCREASED ( 6 FDA reports)
LICHEN PLANUS ( 6 FDA reports)
LIGAMENT RUPTURE ( 6 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 6 FDA reports)
LUNG CANCER METASTATIC ( 6 FDA reports)
LYMPH NODE PAIN ( 6 FDA reports)
LYMPHADENITIS ( 6 FDA reports)
LYMPHATIC OBSTRUCTION ( 6 FDA reports)
MEDIASTINITIS ( 6 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 6 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 6 FDA reports)
METATARSUS PRIMUS VARUS ( 6 FDA reports)
MIXED HYPERLIPIDAEMIA ( 6 FDA reports)
MUSCLE FATIGUE ( 6 FDA reports)
MUSCLE FLAP OPERATION ( 6 FDA reports)
MUSCLE GRAFT ( 6 FDA reports)
NASAL ULCER ( 6 FDA reports)
NEPHROPATHY ( 6 FDA reports)
NEPHROPATHY TOXIC ( 6 FDA reports)
NEUROTOXICITY ( 6 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 6 FDA reports)
NODAL OSTEOARTHRITIS ( 6 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 6 FDA reports)
OCCULT BLOOD ( 6 FDA reports)
OPTIC ATROPHY ( 6 FDA reports)
OPTIC NEURITIS ( 6 FDA reports)
ORAL NEOPLASM ( 6 FDA reports)
ORGANISING PNEUMONIA ( 6 FDA reports)
OTORRHOEA ( 6 FDA reports)
OVARIAN ADHESION ( 6 FDA reports)
PALATAL DISORDER ( 6 FDA reports)
PALMAR ERYTHEMA ( 6 FDA reports)
PANCREATIC CARCINOMA ( 6 FDA reports)
PANCREATIC ENZYMES INCREASED ( 6 FDA reports)
PAPILLOEDEMA ( 6 FDA reports)
PARACENTESIS ( 6 FDA reports)
PARATHYROID TUMOUR BENIGN ( 6 FDA reports)
PELVIC ADHESIONS ( 6 FDA reports)
PHLEBOLITH ( 6 FDA reports)
PNEUMONIA KLEBSIELLA ( 6 FDA reports)
POLYARTHRITIS ( 6 FDA reports)
POLYMENORRHOEA ( 6 FDA reports)
POLYSUBSTANCE ABUSE ( 6 FDA reports)
PORTAL VEIN THROMBOSIS ( 6 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 6 FDA reports)
PRODUCT ADHESION ISSUE ( 6 FDA reports)
PROSTATE CANCER METASTATIC ( 6 FDA reports)
PROTEIN TOTAL INCREASED ( 6 FDA reports)
PROTEUS INFECTION ( 6 FDA reports)
PSYCHOLOGICAL TRAUMA ( 6 FDA reports)
PUBIS FRACTURE ( 6 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 6 FDA reports)
PYURIA ( 6 FDA reports)
RADIATION PNEUMONITIS ( 6 FDA reports)
REGURGITATION ( 6 FDA reports)
RENAL ARTERY STENOSIS ( 6 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 6 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 6 FDA reports)
RETINAL TEAR ( 6 FDA reports)
RIGHT ATRIAL DILATATION ( 6 FDA reports)
RIGHT VENTRICULAR FAILURE ( 6 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 6 FDA reports)
SCOTOMA ( 6 FDA reports)
SHOULDER OPERATION ( 6 FDA reports)
SINUS ARREST ( 6 FDA reports)
SINUS ARRHYTHMIA ( 6 FDA reports)
SMALL INTESTINAL PERFORATION ( 6 FDA reports)
SUBCUTANEOUS NODULE ( 6 FDA reports)
SUFFOCATION FEELING ( 6 FDA reports)
SUICIDAL BEHAVIOUR ( 6 FDA reports)
SUNBURN ( 6 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 6 FDA reports)
TERATOMA ( 6 FDA reports)
TONSILLAR DISORDER ( 6 FDA reports)
TORTICOLLIS ( 6 FDA reports)
TRANSFERRIN DECREASED ( 6 FDA reports)
TREATMENT FAILURE ( 6 FDA reports)
ULCERATIVE KERATITIS ( 6 FDA reports)
URINE ABNORMALITY ( 6 FDA reports)
VENOUS THROMBOSIS LIMB ( 6 FDA reports)
VERTEBRAL WEDGING ( 6 FDA reports)
VITREOUS DETACHMENT ( 6 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 6 FDA reports)
VULVOVAGINAL DISCOMFORT ( 5 FDA reports)
WOUND SEPSIS ( 5 FDA reports)
ABDOMINAL ADHESIONS ( 5 FDA reports)
ABNORMAL FAECES ( 5 FDA reports)
ABSCESS INTESTINAL ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 5 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 5 FDA reports)
AGORAPHOBIA ( 5 FDA reports)
ALCOHOL POISONING ( 5 FDA reports)
ALCOHOLISM ( 5 FDA reports)
ALLERGY TO ANIMAL ( 5 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
ALVEOLITIS ALLERGIC ( 5 FDA reports)
AMYLASE INCREASED ( 5 FDA reports)
AMYLOIDOSIS ( 5 FDA reports)
ANAL ABSCESS ( 5 FDA reports)
ANDROGENETIC ALOPECIA ( 5 FDA reports)
ANION GAP DECREASED ( 5 FDA reports)
ANTISOCIAL BEHAVIOUR ( 5 FDA reports)
AORTIC DISSECTION ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
APPLICATION SITE BURN ( 5 FDA reports)
APPLICATION SITE VESICLES ( 5 FDA reports)
ARTERIAL STENOSIS ( 5 FDA reports)
ARTERIOVENOUS FISTULA ( 5 FDA reports)
ASEPTIC NECROSIS BONE ( 5 FDA reports)
ASPIRATION PLEURAL CAVITY ( 5 FDA reports)
AXILLARY VEIN THROMBOSIS ( 5 FDA reports)
BENIGN BREAST NEOPLASM ( 5 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
BINGE EATING ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 5 FDA reports)
BLOOD CORTISOL DECREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 5 FDA reports)
BLOOD PH DECREASED ( 5 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 5 FDA reports)
BLOOD PROLACTIN INCREASED ( 5 FDA reports)
BONE MARROW NECROSIS ( 5 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 5 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 5 FDA reports)
BREAST ADENOMA ( 5 FDA reports)
BREAST DISCHARGE ( 5 FDA reports)
BRONCHITIS CHRONIC ( 5 FDA reports)
BRUGADA SYNDROME ( 5 FDA reports)
CALCIUM METABOLISM DISORDER ( 5 FDA reports)
CARBON DIOXIDE DECREASED ( 5 FDA reports)
CARDIAC ENZYMES INCREASED ( 5 FDA reports)
CARDIAC FAILURE CHRONIC ( 5 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 5 FDA reports)
CAROTID ARTERY ATHEROMA ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 5 FDA reports)
CERVICAL SPINE FLATTENING ( 5 FDA reports)
CHEST INJURY ( 5 FDA reports)
CLAUSTROPHOBIA ( 5 FDA reports)
COCCIDIOIDOMYCOSIS ( 5 FDA reports)
COLORECTAL CANCER ( 5 FDA reports)
COMMUNICATION DISORDER ( 5 FDA reports)
COMPARTMENT SYNDROME ( 5 FDA reports)
COMPLEX PARTIAL SEIZURES ( 5 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 5 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 5 FDA reports)
DEVICE RELATED SEPSIS ( 5 FDA reports)
DIABETIC FOOT INFECTION ( 5 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 5 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 5 FDA reports)
DRUG TOLERANCE DECREASED ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 5 FDA reports)
DYSPONESIS ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 5 FDA reports)
ENERGY INCREASED ( 5 FDA reports)
EOSINOPHILIC PNEUMONIA ( 5 FDA reports)
EXERCISE TEST ABNORMAL ( 5 FDA reports)
EXOPHTHALMOS ( 5 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 5 FDA reports)
FEELINGS OF WORTHLESSNESS ( 5 FDA reports)
GANGRENE ( 5 FDA reports)
GASTRODUODENITIS ( 5 FDA reports)
GASTROINTESTINAL INJURY ( 5 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 5 FDA reports)
GYNAECOMASTIA ( 5 FDA reports)
HAEMORRHAGIC DISORDER ( 5 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 5 FDA reports)
HEPATIC CONGESTION ( 5 FDA reports)
HEPATIC TRAUMA ( 5 FDA reports)
HEPATORENAL SYNDROME ( 5 FDA reports)
HIRSUTISM ( 5 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 5 FDA reports)
HYPERADRENOCORTICISM ( 5 FDA reports)
HYPERAEMIA ( 5 FDA reports)
HYPERPHOSPHATASAEMIA ( 5 FDA reports)
HYPOCOAGULABLE STATE ( 5 FDA reports)
HYPOGEUSIA ( 5 FDA reports)
HYPOGONADISM ( 5 FDA reports)
HYPOSPADIAS ( 5 FDA reports)
ILEUS PARALYTIC ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 5 FDA reports)
INCISION SITE HAEMORRHAGE ( 5 FDA reports)
INCORRECT STORAGE OF DRUG ( 5 FDA reports)
INFECTED SKIN ULCER ( 5 FDA reports)
INFUSION SITE SWELLING ( 5 FDA reports)
INGROWN HAIR ( 5 FDA reports)
INJECTION SITE OEDEMA ( 5 FDA reports)
INJECTION SITE VESICLES ( 5 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 5 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 5 FDA reports)
INTRINSIC FACTOR ANTIBODY NEGATIVE ( 5 FDA reports)
IRIS ADHESIONS ( 5 FDA reports)
IUCD COMPLICATION ( 5 FDA reports)
JUGULAR VEIN DISTENSION ( 5 FDA reports)
KERATOACANTHOMA ( 5 FDA reports)
LATEX ALLERGY ( 5 FDA reports)
LEFT VENTRICULAR FAILURE ( 5 FDA reports)
LEG AMPUTATION ( 5 FDA reports)
LICHEN SCLEROSUS ( 5 FDA reports)
LIP PAIN ( 5 FDA reports)
LIVER TENDERNESS ( 5 FDA reports)
LOCKED-IN SYNDROME ( 5 FDA reports)
LUNG ABSCESS ( 5 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 5 FDA reports)
MEASLES ( 5 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 5 FDA reports)
METABOLIC ALKALOSIS ( 5 FDA reports)
METAPLASIA ( 5 FDA reports)
MICROANGIOPATHY ( 5 FDA reports)
MIDDLE EAR EFFUSION ( 5 FDA reports)
MILIA ( 5 FDA reports)
MIXED INCONTINENCE ( 5 FDA reports)
MIXED LIVER INJURY ( 5 FDA reports)
MYRINGITIS ( 5 FDA reports)
NASAL SINUS CANCER ( 5 FDA reports)
NECK MASS ( 5 FDA reports)
OBSESSIVE THOUGHTS ( 5 FDA reports)
OCULAR VASCULAR DISORDER ( 5 FDA reports)
OLIGOMENORRHOEA ( 5 FDA reports)
OPPORTUNISTIC INFECTION ( 5 FDA reports)
ORAL LEUKOEDEMA ( 5 FDA reports)
ORAL MUCOSAL BLISTERING ( 5 FDA reports)
ORAL MUCOSAL DISORDER ( 5 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 5 FDA reports)
PAIN EXACERBATED ( 5 FDA reports)
PARTNER STRESS ( 5 FDA reports)
PEDAL PULSE DECREASED ( 5 FDA reports)
PELVIC VENOUS THROMBOSIS ( 5 FDA reports)
PERIORBITAL HAEMATOMA ( 5 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
PLEURODESIS ( 5 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 5 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 5 FDA reports)
POST PROCEDURAL INFECTION ( 5 FDA reports)
PRECOCIOUS PUBERTY ( 5 FDA reports)
PRINZMETAL ANGINA ( 5 FDA reports)
PROCEDURAL HYPOTENSION ( 5 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 5 FDA reports)
PROTEIN S INCREASED ( 5 FDA reports)
PROTHROMBIN TIME SHORTENED ( 5 FDA reports)
PULMONARY CALCIFICATION ( 5 FDA reports)
PYELONEPHRITIS ACUTE ( 5 FDA reports)
RADICULITIS ( 5 FDA reports)
READING DISORDER ( 5 FDA reports)
RECTAL CANCER ( 5 FDA reports)
RECURRING SKIN BOILS ( 5 FDA reports)
RESPIRATORY ALKALOSIS ( 5 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 5 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 5 FDA reports)
SEBORRHOEA ( 5 FDA reports)
SELF MUTILATION ( 5 FDA reports)
SELF-MEDICATION ( 5 FDA reports)
SHOULDER ARTHROPLASTY ( 5 FDA reports)
SKIN DISCOMFORT ( 5 FDA reports)
SKIN HAEMORRHAGE ( 5 FDA reports)
SKIN MASS ( 5 FDA reports)
SKIN WARM ( 5 FDA reports)
SOCIAL PROBLEM ( 5 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 5 FDA reports)
SPLEEN DISORDER ( 5 FDA reports)
SPUTUM RETENTION ( 5 FDA reports)
STRABISMUS ( 5 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 5 FDA reports)
TENDON PAIN ( 5 FDA reports)
TESTICULAR PAIN ( 5 FDA reports)
THALAMIC INFARCTION ( 5 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 5 FDA reports)
THYROID CYST ( 5 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 5 FDA reports)
TINEA INFECTION ( 5 FDA reports)
TOBACCO USER ( 5 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 5 FDA reports)
TOOTH DISCOLOURATION ( 5 FDA reports)
TORSADE DE POINTES ( 5 FDA reports)
TUMOUR EXCISION ( 5 FDA reports)
ULNA FRACTURE ( 5 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 5 FDA reports)
UMBILICAL CORD ABNORMALITY ( 5 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 5 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 5 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 5 FDA reports)
URINE ANALYSIS ABNORMAL ( 5 FDA reports)
UTERINE PROLAPSE ( 5 FDA reports)
VASCULAR DEMENTIA ( 5 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 5 FDA reports)
VULVAL ABSCESS ( 5 FDA reports)
ABDOMINAL ABSCESS ( 4 FDA reports)
ABORTION ( 4 FDA reports)
ABSCESS ORAL ( 4 FDA reports)
ACCIDENTAL DEATH ( 4 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
ADVERSE REACTION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 4 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 4 FDA reports)
ALOPECIA UNIVERSALIS ( 4 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 4 FDA reports)
ANAL SPHINCTER ATONY ( 4 FDA reports)
ANASTOMOTIC ULCER ( 4 FDA reports)
ANTICHOLINERGIC SYNDROME ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
ANURIA ( 4 FDA reports)
AORTIC BRUIT ( 4 FDA reports)
AORTIC DILATATION ( 4 FDA reports)
AORTIC VALVE CALCIFICATION ( 4 FDA reports)
AORTIC VALVE STENOSIS ( 4 FDA reports)
APPARENT DEATH ( 4 FDA reports)
APPETITE DISORDER ( 4 FDA reports)
ARTHROFIBROSIS ( 4 FDA reports)
ASPERGILLOSIS ( 4 FDA reports)
BACTERIAL SEPSIS ( 4 FDA reports)
BEHCET'S SYNDROME ( 4 FDA reports)
BENIGN BREAST LUMP REMOVAL ( 4 FDA reports)
BILE DUCT OBSTRUCTION ( 4 FDA reports)
BILIARY TRACT DISORDER ( 4 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 4 FDA reports)
BIOPSY LIVER ABNORMAL ( 4 FDA reports)
BLADDER DISCOMFORT ( 4 FDA reports)
BLADDER NEOPLASM ( 4 FDA reports)
BLADDER OPERATION ( 4 FDA reports)
BLADDER SPASM ( 4 FDA reports)
BLISTER INFECTED ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD COUNT ABNORMAL ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 4 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 4 FDA reports)
BLOOD UREA DECREASED ( 4 FDA reports)
BLOOD VISCOSITY INCREASED ( 4 FDA reports)
BONE DENSITY INCREASED ( 4 FDA reports)
BOTULISM ( 4 FDA reports)
BRAIN ABSCESS ( 4 FDA reports)
BREAST CANCER STAGE II ( 4 FDA reports)
BREAST OEDEMA ( 4 FDA reports)
BREAST RECONSTRUCTION ( 4 FDA reports)
BREATH SOUNDS DECREASED ( 4 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 4 FDA reports)
BURNOUT SYNDROME ( 4 FDA reports)
CARDIAC OPERATION ( 4 FDA reports)
CATARACT SUBCAPSULAR ( 4 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 4 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 4 FDA reports)
CERVIX CARCINOMA ( 4 FDA reports)
CHEST EXPANSION DECREASED ( 4 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 4 FDA reports)
CLAVICLE FRACTURE ( 4 FDA reports)
CLOSED HEAD INJURY ( 4 FDA reports)
COAGULATION TIME PROLONGED ( 4 FDA reports)
COLITIS MICROSCOPIC ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 4 FDA reports)
COMPULSIVE SHOPPING ( 4 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 4 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 4 FDA reports)
CONJUNCTIVAL PRIMARY ACQUIRED MELANOSIS ( 4 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 4 FDA reports)
CONTRAST MEDIA REACTION ( 4 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 4 FDA reports)
CRANIECTOMY ( 4 FDA reports)
CULDOPLASTY ( 4 FDA reports)
CULTURE POSITIVE ( 4 FDA reports)
DEAFNESS UNILATERAL ( 4 FDA reports)
DEPRESSION SUICIDAL ( 4 FDA reports)
DIABETIC COMA ( 4 FDA reports)
DIABETIC FOOT ( 4 FDA reports)
DIAPHRAGMATIC DISORDER ( 4 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
DYSPLASIA ( 4 FDA reports)
EAR CONGESTION ( 4 FDA reports)
EDUCATIONAL PROBLEM ( 4 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 4 FDA reports)
ENANTHEMA ( 4 FDA reports)
ENZYME ABNORMALITY ( 4 FDA reports)
EPIDERMAL NECROSIS ( 4 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 4 FDA reports)
EROSIVE DUODENITIS ( 4 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 4 FDA reports)
EXTRADURAL HAEMATOMA ( 4 FDA reports)
EYE INFLAMMATION ( 4 FDA reports)
EYELID DISORDER ( 4 FDA reports)
FACE LIFT ( 4 FDA reports)
FACIAL SPASM ( 4 FDA reports)
FACTOR VIII DEFICIENCY ( 4 FDA reports)
FAILED INDUCTION OF LABOUR ( 4 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
FOETAL HEART RATE ABNORMAL ( 4 FDA reports)
FOLATE DEFICIENCY ( 4 FDA reports)
FOREIGN BODY ASPIRATION ( 4 FDA reports)
FOREIGN BODY TRAUMA ( 4 FDA reports)
FRACTURE MALUNION ( 4 FDA reports)
FRUSTRATION ( 4 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 4 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 4 FDA reports)
GALLBLADDER ENLARGEMENT ( 4 FDA reports)
GALLBLADDER PAIN ( 4 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 4 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 4 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 4 FDA reports)
GINGIVAL OPERATION ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
GLOMERULONEPHRITIS ( 4 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 4 FDA reports)
GLYCOSURIA ( 4 FDA reports)
GRANULOCYTE COUNT INCREASED ( 4 FDA reports)
GROIN INFECTION ( 4 FDA reports)
HAEMATOMETRA ( 4 FDA reports)
HAEMOGLOBIN INCREASED ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HAEMOPHILUS INFECTION ( 4 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 4 FDA reports)
HALLUCINATION, TACTILE ( 4 FDA reports)
HALLUCINATIONS, MIXED ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HEPATITIS C VIRUS ( 4 FDA reports)
HOARSENESS ( 4 FDA reports)
HOSTILITY ( 4 FDA reports)
HYPERKINESIA ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
HYPOGLYCAEMIC COMA ( 4 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 4 FDA reports)
HYPOSMIA ( 4 FDA reports)
HYPOTONIA ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 4 FDA reports)
IMPATIENCE ( 4 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 4 FDA reports)
INFUSION SITE CELLULITIS ( 4 FDA reports)
INFUSION SITE WARMTH ( 4 FDA reports)
INJECTION SITE CELLULITIS ( 4 FDA reports)
INJECTION SITE DISCOLOURATION ( 4 FDA reports)
INJECTION SITE DISCOMFORT ( 4 FDA reports)
INJECTION SITE MASS ( 4 FDA reports)
INJECTION SITE NODULE ( 4 FDA reports)
INJECTION SITE PAPULE ( 4 FDA reports)
INSTILLATION SITE IRRITATION ( 4 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 4 FDA reports)
INTRACRANIAL HYPOTENSION ( 4 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 4 FDA reports)
JUGULAR VEIN THROMBOSIS ( 4 FDA reports)
KIDNEY SMALL ( 4 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 4 FDA reports)
LIMB CRUSHING INJURY ( 4 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 4 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 4 FDA reports)
MASTOCYTOSIS ( 4 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 4 FDA reports)
MENOMETRORRHAGIA ( 4 FDA reports)
MICROALBUMINURIA ( 4 FDA reports)
MONOPARESIS ( 4 FDA reports)
MORBID THOUGHTS ( 4 FDA reports)
MUCOSAL ATROPHY ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
MYCOTIC ALLERGY ( 4 FDA reports)
MYOCARDITIS ( 4 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 4 FDA reports)
MYOPIA ( 4 FDA reports)
NEONATAL ASPHYXIA ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NEUROMYOPATHY ( 4 FDA reports)
NEUTROPENIC SEPSIS ( 4 FDA reports)
NODAL RHYTHM ( 4 FDA reports)
OCCIPITAL NEURALGIA ( 4 FDA reports)
OCULAR DISCOMFORT ( 4 FDA reports)
OEDEMA GENITAL ( 4 FDA reports)
OPTIC NEUROPATHY ( 4 FDA reports)
ORAL SOFT TISSUE DISORDER ( 4 FDA reports)
ORCHITIS ( 4 FDA reports)
OSTEOMYELITIS FUNGAL ( 4 FDA reports)
OVARIAN CYST RUPTURED ( 4 FDA reports)
OVARIAN MASS ( 4 FDA reports)
OXYGEN SUPPLEMENTATION ( 4 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 4 FDA reports)
PANCREATIC INSUFFICIENCY ( 4 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 4 FDA reports)
PELVIC CONGESTION ( 4 FDA reports)
PERFORMANCE STATUS DECREASED ( 4 FDA reports)
PERNICIOUS ANAEMIA ( 4 FDA reports)
PERSONALITY DISORDER ( 4 FDA reports)
PHAGOPHOBIA ( 4 FDA reports)
PHLEBITIS SUPERFICIAL ( 4 FDA reports)
PLATYBASIA ( 4 FDA reports)
PNEUMOCEPHALUS ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
PNEUMONIA VIRAL ( 4 FDA reports)
POOR PERIPHERAL CIRCULATION ( 4 FDA reports)
POST COITAL BLEEDING ( 4 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
POSTOPERATIVE ILEUS ( 4 FDA reports)
PRESBYOESOPHAGUS ( 4 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 4 FDA reports)
PRODUCT ODOUR ABNORMAL ( 4 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 4 FDA reports)
PSORIATIC ARTHROPATHY ( 4 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 4 FDA reports)
PULMONARY TUBERCULOSIS ( 4 FDA reports)
PULMONARY VASCULAR DISORDER ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RECTAL TENESMUS ( 4 FDA reports)
RECTOCELE REPAIR ( 4 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 4 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 4 FDA reports)
RENAL INFARCT ( 4 FDA reports)
RESPIRATORY TRACT IRRITATION ( 4 FDA reports)
RESUSCITATION ( 4 FDA reports)
RETINAL ARTERY OCCLUSION ( 4 FDA reports)
RHEUMATIC HEART DISEASE ( 4 FDA reports)
RHEUMATOID LUNG ( 4 FDA reports)
RHINALGIA ( 4 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 4 FDA reports)
SCHIZOPHRENIA ( 4 FDA reports)
SCLERITIS ( 4 FDA reports)
SCROTAL PAIN ( 4 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 4 FDA reports)
SHIGELLA INFECTION ( 4 FDA reports)
SHOCK HAEMORRHAGIC ( 4 FDA reports)
SINUS PAIN ( 4 FDA reports)
SKIN GRAFT ( 4 FDA reports)
SKIN OEDEMA ( 4 FDA reports)
SKIN TEST POSITIVE ( 4 FDA reports)
SLOW RESPONSE TO STIMULI ( 4 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 4 FDA reports)
SOMATIC DELUSION ( 4 FDA reports)
SPLINT APPLICATION ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
STENT OCCLUSION ( 4 FDA reports)
STUPOR ( 4 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 4 FDA reports)
THROMBOSIS IN DEVICE ( 4 FDA reports)
TOE OPERATION ( 4 FDA reports)
TONGUE HAEMORRHAGE ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TONSILLAR HYPERTROPHY ( 4 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 4 FDA reports)
TRIGEMINAL NEURALGIA ( 4 FDA reports)
UPPER EXTREMITY MASS ( 4 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
URETHRAL STENOSIS ( 4 FDA reports)
URINARY TRACT OBSTRUCTION ( 4 FDA reports)
URINE FLOW DECREASED ( 4 FDA reports)
UROBILINOGEN URINE INCREASED ( 4 FDA reports)
URTICARIA CHRONIC ( 4 FDA reports)
UTERINE MASS ( 4 FDA reports)
UTERINE PERFORATION ( 4 FDA reports)
VAGINAL MYCOSIS ( 4 FDA reports)
VASCULAR GRAFT ( 4 FDA reports)
VASCULAR GRAFT OCCLUSION ( 4 FDA reports)
VASCULAR PSEUDOANEURYSM ( 4 FDA reports)
VENA CAVA THROMBOSIS ( 4 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 4 FDA reports)
VITH NERVE PARALYSIS ( 4 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
WEST NILE VIRAL INFECTION ( 4 FDA reports)
XEROSIS ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 3 FDA reports)
ABDOMINAL WALL DISORDER ( 3 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 3 FDA reports)
ACCIDENTAL NEEDLE STICK ( 3 FDA reports)
ACINETOBACTER INFECTION ( 3 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 3 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ADHESION ( 3 FDA reports)
ADNEXA UTERI PAIN ( 3 FDA reports)
ADRENAL HAEMORRHAGE ( 3 FDA reports)
ALCOHOLIC LIVER DISEASE ( 3 FDA reports)
ALDOLASE INCREASED ( 3 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 3 FDA reports)
ANGIODYSPLASIA ( 3 FDA reports)
ANGIOSARCOMA ( 3 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 3 FDA reports)
ANORGASMIA ( 3 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 3 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
APNOEIC ATTACK ( 3 FDA reports)
APPLICATION SITE SCAB ( 3 FDA reports)
ARACHNOIDITIS ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 3 FDA reports)
BEREAVEMENT REACTION ( 3 FDA reports)
BILIARY CIRRHOSIS ( 3 FDA reports)
BIOPSY BREAST ( 3 FDA reports)
BITE ( 3 FDA reports)
BLADDER NECK SUSPENSION ( 3 FDA reports)
BLADDER PAIN ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 3 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 3 FDA reports)
BONE ABSCESS ( 3 FDA reports)
BONE SCAN ABNORMAL ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 3 FDA reports)
BREAST CANCER STAGE III ( 3 FDA reports)
BREAST DISORDER FEMALE ( 3 FDA reports)
BREAST NECROSIS ( 3 FDA reports)
BRONCHIAL SECRETION RETENTION ( 3 FDA reports)
BRUCELLOSIS ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
BURSA CALCIFICATION ( 3 FDA reports)
BUTTOCK PAIN ( 3 FDA reports)
CANDIDURIA ( 3 FDA reports)
CAROTID ARTERY DISSECTION ( 3 FDA reports)
CATHETER SITE ERYTHEMA ( 3 FDA reports)
CATHETER SITE PAIN ( 3 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CERVICAL INCOMPETENCE ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CERVIX DISORDER ( 3 FDA reports)
CHEST WALL MASS ( 3 FDA reports)
CHORIOAMNIONITIS ( 3 FDA reports)
CHRONIC HEPATIC FAILURE ( 3 FDA reports)
COLON CANCER METASTATIC ( 3 FDA reports)
COLONIC OBSTRUCTION ( 3 FDA reports)
COLOSTOMY ( 3 FDA reports)
COMPLICATED MIGRAINE ( 3 FDA reports)
CONDUCT DISORDER ( 3 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 3 FDA reports)
CONGENITAL SCOLIOSIS ( 3 FDA reports)
CONGENITAL TORTICOLLIS ( 3 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 3 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 3 FDA reports)
CORONARY ARTERY PERFORATION ( 3 FDA reports)
CORONARY OSTIAL STENOSIS ( 3 FDA reports)
COW'S MILK INTOLERANCE ( 3 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
CYANOPSIA ( 3 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 3 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 3 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 3 FDA reports)
DENTAL NECROSIS ( 3 FDA reports)
DEPENDENCE ON RESPIRATOR ( 3 FDA reports)
DEREALISATION ( 3 FDA reports)
DERMOGRAPHISM ( 3 FDA reports)
DERMOID CYST ( 3 FDA reports)
DEVICE BREAKAGE ( 3 FDA reports)
DEVICE LEAKAGE ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DIPLEGIA ( 3 FDA reports)
DIVERTICULAR PERFORATION ( 3 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
EAR PRURITUS ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 3 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
ERYTHEMA OF EYELID ( 3 FDA reports)
ESCHERICHIA TEST POSITIVE ( 3 FDA reports)
ESSENTIAL TREMOR ( 3 FDA reports)
EXTREMITY CONTRACTURE ( 3 FDA reports)
EYELIDS PRURITUS ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
FACIAL WASTING ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
FAT TISSUE INCREASED ( 3 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 3 FDA reports)
FINGER DEFORMITY ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FOETAL MOVEMENTS DECREASED ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
GAIT SPASTIC ( 3 FDA reports)
GAMBLING ( 3 FDA reports)
GASTRIC BYPASS ( 3 FDA reports)
GASTROENTERITIS BACTERIAL ( 3 FDA reports)
GASTROINTESTINAL NECROSIS ( 3 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
GYNAECOLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
HAEMARTHROSIS ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
HEMIANOPIA ( 3 FDA reports)
HEPATIC HAEMATOMA ( 3 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 3 FDA reports)
HERPES DERMATITIS ( 3 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 3 FDA reports)
HISTOPLASMOSIS ( 3 FDA reports)
HORNER'S SYNDROME ( 3 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 3 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 3 FDA reports)
HYPOPERFUSION ( 3 FDA reports)
HYPOTONIA NEONATAL ( 3 FDA reports)
HYPOVITAMINOSIS ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
INAPPROPRIATE AFFECT ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INDUCED LABOUR ( 3 FDA reports)
INFECTED SEBACEOUS CYST ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
INFERTILITY FEMALE ( 3 FDA reports)
INFUSION SITE REACTION ( 3 FDA reports)
INFUSION SITE URTICARIA ( 3 FDA reports)
INJECTION SITE EXTRAVASATION ( 3 FDA reports)
INJECTION SITE ULCER ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
JUDGEMENT IMPAIRED ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
KYPHOSCOLIOSIS ( 3 FDA reports)
LARYNGEAL DISORDER ( 3 FDA reports)
LIP EROSION ( 3 FDA reports)
LIPOSARCOMA ( 3 FDA reports)
LOSS OF CONTROL OF LEGS ( 3 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 3 FDA reports)
LOWER EXTREMITY MASS ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MALIGNANT HYPERTENSION ( 3 FDA reports)
MANDIBULECTOMY ( 3 FDA reports)
MARROW HYPERPLASIA ( 3 FDA reports)
MASTITIS ( 3 FDA reports)
MAXILLOFACIAL OPERATION ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 3 FDA reports)
MEAN CELL VOLUME DECREASED ( 3 FDA reports)
MENINGITIS VIRAL ( 3 FDA reports)
MENOPAUSE DELAYED ( 3 FDA reports)
MENSTRUATION DELAYED ( 3 FDA reports)
MERALGIA PARAESTHETICA ( 3 FDA reports)
MESENTERIC OCCLUSION ( 3 FDA reports)
METASTASES TO MENINGES ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MINERAL METABOLISM DISORDER ( 3 FDA reports)
MOANING ( 3 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MUCORMYCOSIS ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MUSCLE SWELLING ( 3 FDA reports)
MYOFASCITIS ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NAIL INJURY ( 3 FDA reports)
NASAL CYST ( 3 FDA reports)
NEGATIVISM ( 3 FDA reports)
NEOPLASM SKIN ( 3 FDA reports)
NERVE ROOT COMPRESSION ( 3 FDA reports)
NEUROSIS ( 3 FDA reports)
NICOTINE DEPENDENCE ( 3 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
OEDEMA MUCOSAL ( 3 FDA reports)
OESOPHAGEAL INFECTION ( 3 FDA reports)
OESOPHAGEAL OEDEMA ( 3 FDA reports)
ONYCHOLYSIS ( 3 FDA reports)
OPTIC NERVE INFARCTION ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
ORAL MUCOSAL ERUPTION ( 3 FDA reports)
ORBITAL INFECTION ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
OVARIAN CANCER METASTATIC ( 3 FDA reports)
PALATAL OEDEMA ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PARADOXICAL DRUG REACTION ( 3 FDA reports)
PARANASAL CYST ( 3 FDA reports)
PAROPHTHALMIA ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 3 FDA reports)
PARVOVIRUS INFECTION ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PENIS DISORDER ( 3 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 3 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 3 FDA reports)
PERITONSILLAR ABSCESS ( 3 FDA reports)
PHARYNGEAL MASS ( 3 FDA reports)
PILONIDAL CYST ( 3 FDA reports)
PLASTIC SURGERY TO THE FACE ( 3 FDA reports)
PNEUMONITIS CHEMICAL ( 3 FDA reports)
POLYARTERITIS NODOSA ( 3 FDA reports)
POOR VENOUS ACCESS ( 3 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 3 FDA reports)
POST HERPETIC NEURALGIA ( 3 FDA reports)
POSTOPERATIVE THROMBOSIS ( 3 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 3 FDA reports)
PRECANCEROUS CELLS PRESENT ( 3 FDA reports)
PRECANCEROUS SKIN LESION ( 3 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 3 FDA reports)
PRIAPISM ( 3 FDA reports)
PROCEDURAL SITE REACTION ( 3 FDA reports)
PROCTITIS HERPES ( 3 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 3 FDA reports)
PRODUCT LABEL ON WRONG PRODUCT ( 3 FDA reports)
PROTEIN C DEFICIENCY ( 3 FDA reports)
PULMONARY EOSINOPHILIA ( 3 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
RASH PAPULOSQUAMOUS ( 3 FDA reports)
RASH SCALY ( 3 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 3 FDA reports)
REBOUND EFFECT ( 3 FDA reports)
RECTAL FISSURE ( 3 FDA reports)
RECTAL PROLAPSE ( 3 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 3 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 3 FDA reports)
REFLUX GASTRITIS ( 3 FDA reports)
RENAL ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL TUMOUR EXCISION ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RESIDUAL URINE ( 3 FDA reports)
RESPIRATION ABNORMAL ( 3 FDA reports)
RESPIRATORY RATE DECREASED ( 3 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 3 FDA reports)
RETINAL DISORDER ( 3 FDA reports)
RETINAL OEDEMA ( 3 FDA reports)
RHEUMATOID FACTOR INCREASED ( 3 FDA reports)
RIGHT AORTIC ARCH ( 3 FDA reports)
SEBACEOUS CARCINOMA ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SENILE OSTEOPOROSIS ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SERUM SEROTONIN DECREASED ( 3 FDA reports)
SHORT-BOWEL SYNDROME ( 3 FDA reports)
SKIN FRAGILITY ( 3 FDA reports)
SKIN INFLAMMATION ( 3 FDA reports)
SKIN NEOPLASM EXCISION ( 3 FDA reports)
SKULL FRACTURED BASE ( 3 FDA reports)
SMALL INTESTINE CARCINOMA ( 3 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 3 FDA reports)
SOFT TISSUE INFECTION ( 3 FDA reports)
SPLEEN CONGESTION ( 3 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STARVATION ( 3 FDA reports)
STRESS AT WORK ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
SUDDEN ONSET OF SLEEP ( 3 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
SWEAT GLAND INFECTION ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 3 FDA reports)
TACHYCARDIA FOETAL ( 3 FDA reports)
TALIPES ( 3 FDA reports)
TANGENTIALITY ( 3 FDA reports)
TEMPERATURE REGULATION DISORDER ( 3 FDA reports)
THERAPY CESSATION ( 3 FDA reports)
THROMBOCYTOSIS ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
THYROID GLAND CANCER ( 3 FDA reports)
THYROIDECTOMY ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 3 FDA reports)
TRAUMATIC LUNG INJURY ( 3 FDA reports)
TRICHORRHEXIS ( 3 FDA reports)
TUMOUR PAIN ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 3 FDA reports)
URETHRITIS ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 3 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
URINE SODIUM ABNORMAL ( 3 FDA reports)
VAGINAL CANDIDIASIS ( 3 FDA reports)
VAGINAL DISORDER ( 3 FDA reports)
VARICES OESOPHAGEAL ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
VENOUS INJURY ( 3 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
VITREOUS DISORDER ( 3 FDA reports)
VOMITING PROJECTILE ( 3 FDA reports)
VULVA CYST ( 3 FDA reports)
VULVAL OEDEMA ( 3 FDA reports)
ABDOMINAL SEPSIS ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ABNORMAL CLOTTING FACTOR ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ABSCESS RUPTURE ( 2 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACNE CYSTIC ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 2 FDA reports)
ADENOTONSILLECTOMY ( 2 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 2 FDA reports)
AGITATED DEPRESSION ( 2 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 2 FDA reports)
ALLERGY TO CHEMICALS ( 2 FDA reports)
AMPHETAMINES POSITIVE ( 2 FDA reports)
AMPULLA OF VATER STENOSIS ( 2 FDA reports)
ANGIOFIBROMA ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTICONVULSANT TOXICITY ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
APPLICATION SITE EXFOLIATION ( 2 FDA reports)
APPLICATION SITE ODOUR ( 2 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 2 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ATOPY ( 2 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AURA ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
AUTOMATIC BLADDER ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BASOPHIL PERCENTAGE DECREASED ( 2 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BASOSQUAMOUS CARCINOMA ( 2 FDA reports)
BENIGN COLONIC NEOPLASM ( 2 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 2 FDA reports)
BETA-2 GLYCOPROTEIN ANTIBODY POSITIVE ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIARY NEOPLASM ( 2 FDA reports)
BIOPSY BONE MARROW ( 2 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 2 FDA reports)
BIOPSY LIP ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLADDER MASS ( 2 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 2 FDA reports)
BLOOD CORTISOL ABNORMAL ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD OESTROGEN DECREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLOOD TRIGLYCERIDES ( 2 FDA reports)
BLOOD UREA ABNORMAL ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BODY HEIGHT INCREASED ( 2 FDA reports)
BONE FORMATION INCREASED ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE NEOPLASM ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN STEM THROMBOSIS ( 2 FDA reports)
BREAKTHROUGH PAIN ( 2 FDA reports)
BREAST COSMETIC SURGERY ( 2 FDA reports)
BREAST CYST EXCISION ( 2 FDA reports)
BREAST FIBROMA ( 2 FDA reports)
BREAST FIBROSIS ( 2 FDA reports)
BREAST INFLAMMATION ( 2 FDA reports)
BREAST MALFORMATION ( 2 FDA reports)
BREATH SOUNDS ( 2 FDA reports)
BRONCHITIS BACTERIAL ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
BUDD-CHIARI SYNDROME ( 2 FDA reports)
BURKITT'S LYMPHOMA ( 2 FDA reports)
BURNS THIRD DEGREE ( 2 FDA reports)
CAFE AU LAIT SPOTS ( 2 FDA reports)
CAPILLARY DISORDER ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL CYST ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 2 FDA reports)
CERULOPLASMIN DECREASED ( 2 FDA reports)
CERVICAL CYST ( 2 FDA reports)
CERVICITIS ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHOLESTASIS OF PREGNANCY ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CHOREOATHETOSIS ( 2 FDA reports)
CHORIORETINOPATHY ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
CHROMOSOME ABNORMALITY ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COCHLEA IMPLANT ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLD AGGLUTININS POSITIVE ( 2 FDA reports)
COLECTOMY TOTAL ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
COLON POLYPECTOMY ( 2 FDA reports)
COLONIC FISTULA ( 2 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
COMPLICATION OF DELIVERY ( 2 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 2 FDA reports)
COMPULSIVE LIP BITING ( 2 FDA reports)
CONGENITAL AORTIC ATRESIA ( 2 FDA reports)
CONGENITAL AORTIC STENOSIS ( 2 FDA reports)
CONGENITAL PNEUMONIA ( 2 FDA reports)
CONJUNCTIVAL IRRITATION ( 2 FDA reports)
CONNECTIVE TISSUE DISORDER ( 2 FDA reports)
CONTRAST MEDIA ALLERGY ( 2 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 2 FDA reports)
CORNEAL DEGENERATION ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORTISOL FREE URINE INCREASED ( 2 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 2 FDA reports)
CRYOGLOBULINAEMIA ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
CYSTITIS BACTERIAL ( 2 FDA reports)
CYSTITIS INTERSTITIAL ( 2 FDA reports)
CYSTITIS RADIATION ( 2 FDA reports)
CYSTOSCOPY ( 2 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEFICIENCY ANAEMIA ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 2 FDA reports)
DENTAL PROSTHESIS USER ( 2 FDA reports)
DERMATILLOMANIA ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 2 FDA reports)
DIABETIC EYE DISEASE ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIABETIC ULCER ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DISTRACTIBILITY ( 2 FDA reports)
DIVERTICULITIS MECKEL'S ( 2 FDA reports)
DIVERTICULUM DUODENAL ( 2 FDA reports)
DREAMY STATE ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DRUG TOLERANCE INCREASED ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DUODENITIS HAEMORRHAGIC ( 2 FDA reports)
DYSACUSIS ( 2 FDA reports)
DYSCALCULIA ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ECZEMA EYELIDS ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
ELECTRIC SHOCK ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENDOCARDITIS BACTERIAL ( 2 FDA reports)
ENDOCARDITIS VIRAL ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 2 FDA reports)
ENDOMETRITIS ( 2 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 2 FDA reports)
EPIDERMOLYSIS ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
EYE PENETRATION ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
FACTOR V DEFICIENCY ( 2 FDA reports)
FAILURE OF IMPLANT ( 2 FDA reports)
FAT INTOLERANCE ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FEEDING TUBE COMPLICATION ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FOETAL GROWTH RESTRICTION ( 2 FDA reports)
FOETAL HEART RATE DECREASED ( 2 FDA reports)
FOOD INTERACTION ( 2 FDA reports)
FORAMINOTOMY ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GALLBLADDER OBSTRUCTION ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 2 FDA reports)
GASTRIC HYPOMOTILITY ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTRIC ULCER SURGERY ( 2 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GENERAL SYMPTOM ( 2 FDA reports)
GENERALISED NON-CONVULSIVE EPILEPSY ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GLOBAL AMNESIA ( 2 FDA reports)
GRAFT INFECTION ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GRANULOMA ANNULARE ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAEMOGLOBIN ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEARING DISABILITY ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HEAT ILLNESS ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HERNIA PAIN ( 2 FDA reports)
HIV ANTIGEN POSITIVE ( 2 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE III ( 2 FDA reports)
HOUSE DUST ALLERGY ( 2 FDA reports)
HUNGRY BONE SYNDROME ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERCORTICOIDISM ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPERTROPHY ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOCHONDRIASIS ( 2 FDA reports)
HYPOHIDROSIS ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOPARATHYROIDISM ( 2 FDA reports)
HYPOPITUITARISM ( 2 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 2 FDA reports)
ILEAL STENOSIS ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
IMMINENT ABORTION ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
INDIFFERENCE ( 2 FDA reports)
INFECTIVE SPONDYLITIS ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE PHLEBITIS ( 2 FDA reports)
INHALATION THERAPY ( 2 FDA reports)
INJECTION SITE BURNING ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INSTILLATION SITE PAIN ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTESTINAL MALROTATION ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
INTRANASAL PARAESTHESIA ( 2 FDA reports)
INTRASPINAL ABSCESS ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
IUD MIGRATION ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
JOINT ARTHROPLASTY ( 2 FDA reports)
JUVENILE ARTHRITIS ( 2 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 2 FDA reports)
KERATITIS HERPETIC ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KETOSIS ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LACTATION DISORDER ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIP PRURITUS ( 2 FDA reports)
LIPOPROTEIN (A) ABNORMAL ( 2 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
LISTERIA SEPSIS ( 2 FDA reports)
LOCALISED OSTEOARTHRITIS ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LUPUS NEPHRITIS ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 2 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 2 FDA reports)
MEDICAL DEVICE PAIN ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MUCOSAL ULCERATION ( 2 FDA reports)
MUIR-TORRE SYNDROME ( 2 FDA reports)
MURPHY'S SIGN POSITIVE ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOGLOBIN URINE PRESENT ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NASAL OPERATION ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NASAL SEPTAL OPERATION ( 2 FDA reports)
NEOPLASM PROSTATE ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NERVE ROOT INJURY ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NEUTROPHIL COUNT ( 2 FDA reports)
NO ADVERSE REACTION ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
OEDEMATOUS PANCREATITIS ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL DILATATION ( 2 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
OPTIC DISC DRUSEN ( 2 FDA reports)
OPTIC NERVE INJURY ( 2 FDA reports)
ORGASM ABNORMAL ( 2 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 2 FDA reports)
OROPHARYNGEAL NEOPLASM ( 2 FDA reports)
OSCILLOPSIA ( 2 FDA reports)
OVARIAN NEOPLASM ( 2 FDA reports)
OVARIAN RUPTURE ( 2 FDA reports)
OVERGROWTH BACTERIAL ( 2 FDA reports)
OVULATION DISORDER ( 2 FDA reports)
PAEDOPHILIA ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PANCREATIC ABSCESS ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PAPILLOMA ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARANASAL SINUS DISCOMFORT ( 2 FDA reports)
PARANEOPLASTIC SYNDROME ( 2 FDA reports)
PARANOID PERSONALITY DISORDER ( 2 FDA reports)
PARKINSONIAN GAIT ( 2 FDA reports)
PECTUS EXCAVATUM ( 2 FDA reports)
PELVIC ABSCESS ( 2 FDA reports)
PENILE ADHESION ( 2 FDA reports)
PENIS DEVIATION ( 2 FDA reports)
PERICARDIAL DISEASE ( 2 FDA reports)
PERINEPHRIC ABSCESS ( 2 FDA reports)
PERIODONTAL INFECTION ( 2 FDA reports)
PERIORBITAL CELLULITIS ( 2 FDA reports)
PERIOSTITIS ( 2 FDA reports)
PERIPHERAL NERVE OPERATION ( 2 FDA reports)
PERIPHERAL NERVE TRANSPOSITION ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHOBIA OF DRIVING ( 2 FDA reports)
PITYRIASIS ROSEA ( 2 FDA reports)
PLAGIOCEPHALY ( 2 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 2 FDA reports)
POST PROCEDURAL PNEUMONIA ( 2 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 2 FDA reports)
POSTPARTUM DISORDER ( 2 FDA reports)
POSTRENAL FAILURE ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PROCTITIS ULCERATIVE ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROTEIN S DEFICIENCY ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PSEUDOALDOSTERONISM ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY COCCIDIOIDES ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RADIAL PULSE ABNORMAL ( 2 FDA reports)
RADIATION NECROSIS ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RASH SCARLATINIFORM ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
REMOVAL OF FOREIGN BODY ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RENAL VEIN THROMBOSIS ( 2 FDA reports)
REPERFUSION ARRHYTHMIA ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
RETINAL EXUDATES ( 2 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 2 FDA reports)
RHINITIS PERENNIAL ( 2 FDA reports)
RHYTHM IDIOVENTRICULAR ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 2 FDA reports)
SALMONELLA SEPSIS ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SCIATIC NERVE INJURY ( 2 FDA reports)
SCLEROTHERAPY ( 2 FDA reports)
SEBACEOUS ADENOMA ( 2 FDA reports)
SEBACEOUS CYST EXCISION ( 2 FDA reports)
SENSATION OF BLOOD FLOW ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SERUM FERRITIN DECREASED ( 2 FDA reports)
SERUM SEROTONIN INCREASED ( 2 FDA reports)
SIALOADENITIS ( 2 FDA reports)
SICKLE CELL ANAEMIA ( 2 FDA reports)
SIGMOIDECTOMY ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
SINOBRONCHITIS ( 2 FDA reports)
SINUS RHYTHM ( 2 FDA reports)
SINUSITIS BACTERIAL ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN DEGENERATIVE DISORDER ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN HYPOPIGMENTATION ( 2 FDA reports)
SKIN TURGOR DECREASED ( 2 FDA reports)
SKIN WRINKLING ( 2 FDA reports)
SKULL FRACTURE ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SLEEP TERROR ( 2 FDA reports)
SMALL INTESTINAL STENOSIS ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SOFT TISSUE NECROSIS ( 2 FDA reports)
SPERM COUNT ZERO ( 2 FDA reports)
SPERMATOZOA ABNORMAL ( 2 FDA reports)
SPINAL CORD NEOPLASM ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
SUBSTANCE ABUSER ( 2 FDA reports)
SUPERFICIAL INJURY OF EYE ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
TENDON CALCIFICATION ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
TESTICULAR TORSION ( 2 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
THYROIDITIS ( 2 FDA reports)
THYROIDITIS ACUTE ( 2 FDA reports)
THYROXINE INCREASED ( 2 FDA reports)
TIC ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TRACHEAL INFLAMMATION ( 2 FDA reports)
TRACHEAL STENOSIS ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 2 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
TUMOUR INVASION ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
UMBILICAL CORD AROUND NECK ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URETHRAL INJURY ( 2 FDA reports)
URINARY BLADDER POLYP ( 2 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
UROGENITAL DISORDER ( 2 FDA reports)
UROGRAM ( 2 FDA reports)
UTERINE SPASM ( 2 FDA reports)
UTERINE STENOSIS ( 2 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 2 FDA reports)
VAGINAL LESION ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
VAGINAL SWELLING ( 2 FDA reports)
VAGINISMUS ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASOMOTOR RHINITIS ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
VICTIM OF HOMICIDE ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VITAMIN K DEFICIENCY ( 2 FDA reports)
VOLVULUS OF BOWEL ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
XANTHELASMA ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
WOUND EVISCERATION ( 1 FDA reports)
WOUND HAEMATOMA ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND INFECTION FUNGAL ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WEIGHT CONTROL ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
XANTHOGRANULOMA ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
YAWNING ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABDOMINOPLASTY ( 1 FDA reports)
ABSCESS OF EXTERNAL AUDITORY MEATUS ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACETONAEMIA ( 1 FDA reports)
ACHLORHYDRIA ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACNE PUSTULAR ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DISTURBANCE OF CONDUCT ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AIDS ENCEPHALOPATHY ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANDROGEN INSENSITIVITY SYNDROME ( 1 FDA reports)
ANENCEPHALY ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANGIOSARCOMA METASTATIC ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANKLE ARTHROPLASTY ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE ECZEMA ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASTHENOSPERMIA ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATYPICAL FEMUR FRACTURE ( 1 FDA reports)
AUTISM ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARIUM SWALLOW ABNORMAL ( 1 FDA reports)
BARTHOLIN'S CYST ( 1 FDA reports)
BASOPHIL PERCENTAGE ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN CARDIAC NEOPLASM ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILE OUTPUT ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIARY FIBROSIS ( 1 FDA reports)
BILOMA ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER IRRITATION ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLEEDING PERIPARTUM ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLEPHAROPLASTY ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CALCITONIN INCREASED ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CYANIDE INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GASTRIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC INCREASED ( 1 FDA reports)
BLOOD THROMBIN DECREASED ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BLOODY AIRWAY DISCHARGE ( 1 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BODY HEIGHT BELOW NORMAL ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE DECALCIFICATION ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST OPERATION ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOGENIC CYST ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURKITT'S LYMPHOMA STAGE II ( 1 FDA reports)
BURN DRESSING ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
BURSA REMOVAL ( 1 FDA reports)
BURSAL OPERATION ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CAPILLARY NAIL REFILL TEST ABNORMAL ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARCINOID TUMOUR OF THE PROSTATE ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC SARCOIDOSIS ( 1 FDA reports)
CARDIAC STRESS TEST NORMAL ( 1 FDA reports)
CARDIAC TELEMETRY ABNORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOPLEGIA ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CEPHALHAEMATOMA ( 1 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 1 FDA reports)
CEREBELLAR ARTERY THROMBOSIS ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERULOPLASMIN INCREASED ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CERVIX CERCLAGE PROCEDURE ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOLANGIOLITIS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLECYSTOSTOMY ( 1 FDA reports)
CHOLELITHOTOMY ( 1 FDA reports)
CHORDEE ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CILIARY BODY DISORDER ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR V LEVEL ABNORMAL ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COLD-STIMULUS HEADACHE ( 1 FDA reports)
COLECTOMY PARTIAL ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPULSIVE HOARDING ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONGENITAL PANCREATIC ANOMALY ( 1 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 1 FDA reports)
CONTACT LENS INTOLERANCE ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL EPITHELIUM DISORDER ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CYSTIC FIBROSIS ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTOURETHROCELE ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOKINE STORM ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DEPRESSION POSTOPERATIVE ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DEXTROCARDIA ( 1 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIFFUSE LAMELLAR KERATITIS ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DOLICHOCOLON ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 1 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EOSINOPHIL PERCENTAGE ABNORMAL ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 1 FDA reports)
ERYTHROMELALGIA ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EUSTACHIAN TUBE PATULOUS ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCESSIVE SKIN ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTERNAL EAR DISORDER ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID EROSION ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FACTOR III DEFICIENCY ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FALLOPIAN TUBE DISORDER ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEEDING TUBE INSERTION ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEMALE GENITAL OPERATION ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLUCTUANCE ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
GAIT DEVIATION ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
GASTRIC HYPERMOTILITY ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTRITIS VIRAL ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL LABIAL ADHESIONS ( 1 FDA reports)
GENITAL PROLAPSE ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOGLOBIN URINE ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOPNEUMOTHORAX ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAIR METAL TEST ( 1 FDA reports)
HAIRY CELL LEUKAEMIA ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEART ALTERNATION ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATITIS B ANTIBODY ABNORMAL ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B DNA ASSAY POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HIP DEFORMITY ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE IV ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HUMAN ANTI-HUMAN ANTIBODY TEST ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERDYNAMIC PRECORDIUM ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERKINETIC HEART SYNDROME ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 1 FDA reports)
HYPERTROPHIC ANAL PAPILLA ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOZINCAEMIA ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
IDIOSYNCRATIC ALCOHOL INTOXICATION ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILEOSTOMY CLOSURE ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFERTILITY MALE ( 1 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE OEDEMA ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE JOINT SWELLING ( 1 FDA reports)
INJECTION SITE LACERATION ( 1 FDA reports)
INJECTION SITE PALLOR ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN TOLERANCE TEST ABNORMAL ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERTRIGO CANDIDA ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL STRANGULATION ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTESTINAL VILLI ATROPHY ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 1 FDA reports)
INTRANASAL NUMBNESS ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LABOUR ONSET DELAYED ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LAPAROSCOPIC SURGERY ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 1 FDA reports)
LARYNGEAL INJURY ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LESION EXCISION ( 1 FDA reports)
LEUKAEMIA MONOCYTIC ( 1 FDA reports)
LEUKODYSTROPHY ( 1 FDA reports)
LICE INFESTATION ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT PAIN ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPECTOMY ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIPOMA EXCISION ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER SARCOIDOSIS ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 1 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 1 FDA reports)
LOSS OF DREAMING ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 1 FDA reports)
LUNG CYST BENIGN ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUPUS VASCULITIS ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPH NODE PALPABLE ( 1 FDA reports)
LYMPHADENITIS BACTERIAL ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
MACROPHAGE ACTIVATION ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALE PATTERN BALDNESS ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT MELANOMA STAGE III ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASTOPTOSIS ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MAY-THURNER SYNDROME ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
MEDIASTINOSCOPY ( 1 FDA reports)
MEDICAL DEVICE CHANGE ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEIBOMIANITIS ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MELANODERMIA ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
METAPNEUMOVIRUS INFECTION ( 1 FDA reports)
METASTASES TO PERIPHERAL VASCULAR SYSTEM ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
METASTATIC CARCINOID TUMOUR ( 1 FDA reports)
METHYLENETETRAHYDROFOLATE REDUCTASE POLYMORPHISM ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOMECTOMY ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
N-TELOPEPTIDE URINE DECREASED ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NAIL PIGMENTATION ( 1 FDA reports)
NAIL RIDGING ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEOVASCULARISATION ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHRITIS AUTOIMMUNE ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROMUSCULAR BLOCKADE ( 1 FDA reports)
NEUROPATHIC ULCER ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODULAR FASCIITIS ( 1 FDA reports)
NON-HIGH-DENSITY LIPOPROTEIN CHOLESTEROL DECREASED ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE I ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA UNSPECIFIED HISTOLOGY INDOLENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL OPERATION ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
ORTHOPEDIC EXAMINATION ABNORMAL ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOGENESIS IMPERFECTA ( 1 FDA reports)
OVARIAN CYSTECTOMY ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC HAEMORRHAGE ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE INCREASED ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PELVIC DISCOMFORT ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PENIS INJURY ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PEPTIC ULCER REACTIVATED ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDITIS MALIGNANT ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPROCTITIS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERITONEAL MEMBRANE FAILURE ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARYNGEAL GONOCOCCAL INFECTION ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PIGMENTATION LIP ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR RECURRENT ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET DESTRUCTION INCREASED ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
PORPHYRIA ACUTE ( 1 FDA reports)
PORTOPULMONARY HYPERTENSION ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST LAMINECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)
POSTICTAL HEADACHE ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTPARTUM DEPRESSION ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL HEADACHE ( 1 FDA reports)
PRODUCT COATING ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCT TAMPERING ( 1 FDA reports)
PROLACTINOMA ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROLONGED LABOUR ( 1 FDA reports)
PROLONGED PREGNANCY ( 1 FDA reports)
PROPIONIBACTERIUM INFECTION ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATIC ABSCESS ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PTOSIS REPAIR ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY SEQUESTRATION ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
RADIATION FIBROSIS - LUNG ( 1 FDA reports)
RADIATION OESOPHAGITIS ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
RENAL CORTICAL NECROSIS ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL OSTEODYSTROPHY ( 1 FDA reports)
RENAL STONE REMOVAL ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RHEUMATOID FACTOR DECREASED ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
RIB DEFORMITY ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 1 FDA reports)
SALMONELLA BACTERAEMIA ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN BONE MARROW ABNORMAL ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCHISTOSOMA TEST POSITIVE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER DEPRESSIVE TYPE ( 1 FDA reports)
SCHOOL REFUSAL ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEPTIC PHLEBITIS ( 1 FDA reports)
SEPTOPLASTY ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SICKLE CELL TRAIT ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SLIPPED FEMORAL EPIPHYSIS ( 1 FDA reports)
SMALL INTESTINAL BACTERIAL OVERGROWTH ( 1 FDA reports)
SOCIAL FEAR ( 1 FDA reports)
SOLAR ELASTOSIS ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPINAL CLAUDICATION ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPINAL ROD INSERTION ( 1 FDA reports)
SPINE MALFORMATION ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPLENIC VEIN OCCLUSION ( 1 FDA reports)
SPONDYLOLYSIS ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STERNAL INJURY ( 1 FDA reports)
STERNOTOMY ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS INCONTINENCE ( 1 FDA reports)
STRUCK BY LIGHTNING ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
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T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TANDEM GAIT TEST ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
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TESTICULAR OEDEMA ( 1 FDA reports)
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TETANY ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
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THERAPY REGIMEN CHANGED ( 1 FDA reports)
THERMAL BURNS OF EYE ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBOANGIITIS OBLITERANS ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THYMOMA ( 1 FDA reports)
THYMOMA MALIGNANT RECURRENT ( 1 FDA reports)
THYROID CANCER METASTATIC ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE DESQUAMATION ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
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TONGUE PARALYSIS ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLAR HAEMORRHAGE ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSFUSION-TRANSMITTED INFECTIOUS DISEASE ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TROPICAL ULCER ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
TYMPANOSCLEROSIS ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
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UNINTENDED PREGNANCY ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URETHRAL SYNDROME ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
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URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
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URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
UTERINE ATROPHY ( 1 FDA reports)
UTERINE CERVICAL PAIN ( 1 FDA reports)
UTERINE PROLAPSE REPAIR ( 1 FDA reports)
VAGINAL DYSPLASIA ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
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VAGINAL RELAXATION ( 1 FDA reports)
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VARICELLA ( 1 FDA reports)
VARICOSE VEIN OPERATION ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
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VENOUS RECANALISATION ( 1 FDA reports)
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VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
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VERBAL ABUSE ( 1 FDA reports)
VERTEBRAL ARTERY DISSECTION ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
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VERTIGO LABYRINTHINE ( 1 FDA reports)
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VIRAEMIA ( 1 FDA reports)
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VISCERAL CONGESTION ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)

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