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

NAUSEA ( 1129 FDA reports)
PAIN ( 953 FDA reports)
DIZZINESS ( 798 FDA reports)
ANXIETY ( 797 FDA reports)
DYSPNOEA ( 763 FDA reports)
FATIGUE ( 752 FDA reports)
HEADACHE ( 701 FDA reports)
DIARRHOEA ( 652 FDA reports)
CHEST PAIN ( 650 FDA reports)
VOMITING ( 643 FDA reports)
ARTHRALGIA ( 600 FDA reports)
DRUG INEFFECTIVE ( 594 FDA reports)
ASTHENIA ( 576 FDA reports)
DEPRESSION ( 550 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 537 FDA reports)
FALL ( 526 FDA reports)
WEIGHT DECREASED ( 495 FDA reports)
PAIN IN EXTREMITY ( 476 FDA reports)
BACK PAIN ( 472 FDA reports)
HYPERTENSION ( 470 FDA reports)
INSOMNIA ( 461 FDA reports)
ABDOMINAL PAIN ( 457 FDA reports)
OEDEMA PERIPHERAL ( 441 FDA reports)
INJURY ( 437 FDA reports)
MYOCARDIAL INFARCTION ( 401 FDA reports)
ABDOMINAL PAIN UPPER ( 375 FDA reports)
CONSTIPATION ( 363 FDA reports)
ANAEMIA ( 347 FDA reports)
DYSPEPSIA ( 345 FDA reports)
CEREBROVASCULAR ACCIDENT ( 327 FDA reports)
PNEUMONIA ( 327 FDA reports)
PYREXIA ( 322 FDA reports)
HYPOAESTHESIA ( 298 FDA reports)
COUGH ( 289 FDA reports)
EMOTIONAL DISTRESS ( 281 FDA reports)
DYSPHAGIA ( 277 FDA reports)
OSTEOARTHRITIS ( 277 FDA reports)
PALPITATIONS ( 276 FDA reports)
DEHYDRATION ( 272 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 269 FDA reports)
URINARY TRACT INFECTION ( 268 FDA reports)
MYALGIA ( 265 FDA reports)
PARAESTHESIA ( 264 FDA reports)
PRURITUS ( 263 FDA reports)
VISION BLURRED ( 262 FDA reports)
CORONARY ARTERY DISEASE ( 256 FDA reports)
HIATUS HERNIA ( 250 FDA reports)
BONE DISORDER ( 249 FDA reports)
CHOLELITHIASIS ( 247 FDA reports)
MUSCLE SPASMS ( 243 FDA reports)
OSTEONECROSIS OF JAW ( 241 FDA reports)
CHOLECYSTITIS CHRONIC ( 232 FDA reports)
MALAISE ( 232 FDA reports)
FEELING ABNORMAL ( 231 FDA reports)
WEIGHT INCREASED ( 229 FDA reports)
BLOOD GLUCOSE INCREASED ( 227 FDA reports)
DECREASED APPETITE ( 225 FDA reports)
TREMOR ( 222 FDA reports)
CHEST DISCOMFORT ( 220 FDA reports)
GASTRITIS ( 220 FDA reports)
RASH ( 220 FDA reports)
HYPOTENSION ( 217 FDA reports)
ATRIAL FIBRILLATION ( 214 FDA reports)
BRONCHITIS ( 210 FDA reports)
SYNCOPE ( 209 FDA reports)
CONFUSIONAL STATE ( 208 FDA reports)
PAIN IN JAW ( 206 FDA reports)
SPINAL OSTEOARTHRITIS ( 203 FDA reports)
OSTEONECROSIS ( 201 FDA reports)
NECK PAIN ( 199 FDA reports)
BLOOD PRESSURE INCREASED ( 196 FDA reports)
ASTHMA ( 194 FDA reports)
GAIT DISTURBANCE ( 194 FDA reports)
PULMONARY EMBOLISM ( 190 FDA reports)
MUSCULAR WEAKNESS ( 189 FDA reports)
GALLBLADDER DISORDER ( 186 FDA reports)
PLEURAL EFFUSION ( 186 FDA reports)
DRY MOUTH ( 185 FDA reports)
SINUSITIS ( 184 FDA reports)
RENAL FAILURE ( 183 FDA reports)
DEEP VEIN THROMBOSIS ( 180 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 179 FDA reports)
AMNESIA ( 177 FDA reports)
ANHEDONIA ( 177 FDA reports)
INFECTION ( 175 FDA reports)
ABDOMINAL DISTENSION ( 171 FDA reports)
CONDITION AGGRAVATED ( 171 FDA reports)
HYPERHIDROSIS ( 171 FDA reports)
OSTEOMYELITIS ( 171 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 170 FDA reports)
MUSCULOSKELETAL PAIN ( 169 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 165 FDA reports)
RENAL FAILURE ACUTE ( 163 FDA reports)
CONTUSION ( 162 FDA reports)
MITRAL VALVE INCOMPETENCE ( 162 FDA reports)
HAEMORRHOIDS ( 160 FDA reports)
HYPERLIPIDAEMIA ( 159 FDA reports)
SOMNOLENCE ( 159 FDA reports)
FLATULENCE ( 154 FDA reports)
DIVERTICULUM ( 153 FDA reports)
DIABETES MELLITUS ( 151 FDA reports)
LOSS OF CONSCIOUSNESS ( 150 FDA reports)
BONE PAIN ( 143 FDA reports)
CELLULITIS ( 143 FDA reports)
DYSURIA ( 143 FDA reports)
OSTEOPOROSIS ( 143 FDA reports)
HEART RATE INCREASED ( 142 FDA reports)
BALANCE DISORDER ( 139 FDA reports)
CARDIAC DISORDER ( 139 FDA reports)
DEATH ( 138 FDA reports)
STRESS ( 138 FDA reports)
OSTEOPENIA ( 137 FDA reports)
HYPERSENSITIVITY ( 136 FDA reports)
IMPAIRED HEALING ( 136 FDA reports)
ERYTHEMA ( 135 FDA reports)
HAEMOGLOBIN DECREASED ( 135 FDA reports)
ABDOMINAL DISCOMFORT ( 133 FDA reports)
FLUSHING ( 133 FDA reports)
CONVULSION ( 132 FDA reports)
NEUROPATHY PERIPHERAL ( 131 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 131 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 129 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 129 FDA reports)
SWELLING ( 129 FDA reports)
JOINT SWELLING ( 128 FDA reports)
FEMUR FRACTURE ( 125 FDA reports)
SUICIDAL IDEATION ( 125 FDA reports)
CHILLS ( 123 FDA reports)
EPISTAXIS ( 123 FDA reports)
RESPIRATORY FAILURE ( 123 FDA reports)
TOOTH EXTRACTION ( 122 FDA reports)
ATELECTASIS ( 121 FDA reports)
MOUTH ULCERATION ( 121 FDA reports)
DYSGEUSIA ( 119 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 117 FDA reports)
MIGRAINE ( 115 FDA reports)
ALOPECIA ( 114 FDA reports)
HIP FRACTURE ( 114 FDA reports)
INJECTION SITE PAIN ( 114 FDA reports)
CATARACT ( 113 FDA reports)
LYMPHADENOPATHY ( 113 FDA reports)
ROAD TRAFFIC ACCIDENT ( 113 FDA reports)
POLLAKIURIA ( 110 FDA reports)
ROTATOR CUFF SYNDROME ( 110 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 109 FDA reports)
OEDEMA ( 108 FDA reports)
ARTHRITIS ( 107 FDA reports)
ARTHROPATHY ( 107 FDA reports)
HERPES ZOSTER ( 107 FDA reports)
HOT FLUSH ( 107 FDA reports)
NEPHROLITHIASIS ( 106 FDA reports)
BURNING SENSATION ( 105 FDA reports)
CARDIOMEGALY ( 105 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 105 FDA reports)
HYPOTHYROIDISM ( 105 FDA reports)
VERTIGO ( 105 FDA reports)
ANGINA PECTORIS ( 104 FDA reports)
DEFORMITY ( 104 FDA reports)
OESOPHAGITIS ( 103 FDA reports)
OROPHARYNGEAL PAIN ( 103 FDA reports)
HYPERKERATOSIS ( 102 FDA reports)
URTICARIA ( 101 FDA reports)
MENTAL DISORDER ( 99 FDA reports)
SCOLIOSIS ( 99 FDA reports)
BURSITIS ( 98 FDA reports)
HYPOKALAEMIA ( 98 FDA reports)
GASTROINTESTINAL DISORDER ( 97 FDA reports)
PANCREATITIS ( 97 FDA reports)
SLEEP APNOEA SYNDROME ( 97 FDA reports)
SPINAL COLUMN STENOSIS ( 97 FDA reports)
STOMATITIS ( 97 FDA reports)
RHEUMATOID ARTHRITIS ( 96 FDA reports)
FOOT FRACTURE ( 94 FDA reports)
TOOTHACHE ( 94 FDA reports)
HYPERGLYCAEMIA ( 93 FDA reports)
PRIMARY SEQUESTRUM ( 93 FDA reports)
RHINITIS ALLERGIC ( 92 FDA reports)
ENDODONTIC PROCEDURE ( 91 FDA reports)
WHEEZING ( 91 FDA reports)
DYSPHONIA ( 90 FDA reports)
JOINT EFFUSION ( 90 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 90 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 89 FDA reports)
URINARY INCONTINENCE ( 89 FDA reports)
ANOREXIA ( 87 FDA reports)
CHOLECYSTITIS ( 87 FDA reports)
CYSTITIS ( 87 FDA reports)
ERECTILE DYSFUNCTION ( 87 FDA reports)
GASTRIC DISORDER ( 87 FDA reports)
INFLUENZA LIKE ILLNESS ( 87 FDA reports)
CARPAL TUNNEL SYNDROME ( 86 FDA reports)
SEPSIS ( 86 FDA reports)
TINNITUS ( 86 FDA reports)
DRUG HYPERSENSITIVITY ( 85 FDA reports)
HAEMORRHAGE ( 85 FDA reports)
HEPATIC STEATOSIS ( 84 FDA reports)
LETHARGY ( 84 FDA reports)
RECTAL HAEMORRHAGE ( 84 FDA reports)
THROMBOSIS ( 84 FDA reports)
URINARY RETENTION ( 84 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 83 FDA reports)
DENTAL CARIES ( 83 FDA reports)
DYSARTHRIA ( 83 FDA reports)
EYE PAIN ( 83 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 83 FDA reports)
SYNOVIAL CYST ( 83 FDA reports)
MEMORY IMPAIRMENT ( 82 FDA reports)
DENTAL FISTULA ( 81 FDA reports)
SLEEP DISORDER ( 81 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 81 FDA reports)
ECONOMIC PROBLEM ( 80 FDA reports)
HEPATIC CYST ( 80 FDA reports)
AORTIC VALVE INCOMPETENCE ( 79 FDA reports)
DRUG DOSE OMISSION ( 79 FDA reports)
IRRITABLE BOWEL SYNDROME ( 79 FDA reports)
ARTERIOSCLEROSIS ( 78 FDA reports)
COLONIC POLYP ( 78 FDA reports)
HEART RATE IRREGULAR ( 78 FDA reports)
MYOCARDIAL ISCHAEMIA ( 78 FDA reports)
RIB FRACTURE ( 78 FDA reports)
DISCOMFORT ( 77 FDA reports)
GASTRIC ULCER ( 77 FDA reports)
NEURALGIA ( 77 FDA reports)
TACHYCARDIA ( 77 FDA reports)
VISUAL IMPAIRMENT ( 77 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 76 FDA reports)
NERVOUSNESS ( 76 FDA reports)
STAPHYLOCOCCAL INFECTION ( 76 FDA reports)
AGITATION ( 75 FDA reports)
HYPERCHOLESTEROLAEMIA ( 75 FDA reports)
METASTASES TO LIVER ( 75 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 74 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 74 FDA reports)
LUNG DISORDER ( 74 FDA reports)
LUNG INFILTRATION ( 74 FDA reports)
NASAL CONGESTION ( 74 FDA reports)
ADVERSE EVENT ( 73 FDA reports)
CARDIAC ARREST ( 73 FDA reports)
DEPRESSED MOOD ( 73 FDA reports)
DIPLOPIA ( 73 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 73 FDA reports)
HAEMATURIA ( 73 FDA reports)
PULMONARY OEDEMA ( 73 FDA reports)
SINUS TACHYCARDIA ( 73 FDA reports)
THROMBOCYTOPENIA ( 73 FDA reports)
HYPOGLYCAEMIA ( 72 FDA reports)
METASTASES TO LUNG ( 72 FDA reports)
RESTLESS LEGS SYNDROME ( 72 FDA reports)
ARRHYTHMIA ( 71 FDA reports)
COLITIS ( 71 FDA reports)
DYSPNOEA EXERTIONAL ( 71 FDA reports)
INJECTION SITE ERYTHEMA ( 71 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 71 FDA reports)
ANGINA UNSTABLE ( 70 FDA reports)
EXOSTOSIS ( 70 FDA reports)
METASTASES TO SPINE ( 70 FDA reports)
PULMONARY HYPERTENSION ( 70 FDA reports)
TYPE 2 DIABETES MELLITUS ( 70 FDA reports)
FACIAL BONES FRACTURE ( 69 FDA reports)
SPEECH DISORDER ( 69 FDA reports)
BLOOD CALCIUM INCREASED ( 68 FDA reports)
MENISCUS LESION ( 68 FDA reports)
MENTAL STATUS CHANGES ( 68 FDA reports)
METASTASES TO BONE ( 68 FDA reports)
SPINAL COMPRESSION FRACTURE ( 68 FDA reports)
EMOTIONAL DISORDER ( 67 FDA reports)
GINGIVAL PAIN ( 67 FDA reports)
UNEVALUABLE EVENT ( 67 FDA reports)
GLAUCOMA ( 66 FDA reports)
GLOSSODYNIA ( 66 FDA reports)
HYPOPHAGIA ( 66 FDA reports)
LUMBAR SPINAL STENOSIS ( 66 FDA reports)
LUNG NEOPLASM ( 66 FDA reports)
OVERDOSE ( 66 FDA reports)
BLOOD GLUCOSE DECREASED ( 65 FDA reports)
BONE LESION ( 65 FDA reports)
BRADYCARDIA ( 65 FDA reports)
PLATELET COUNT DECREASED ( 65 FDA reports)
PULMONARY CONGESTION ( 65 FDA reports)
RESPIRATORY DISTRESS ( 65 FDA reports)
SWELLING FACE ( 65 FDA reports)
TENDONITIS ( 65 FDA reports)
TOOTH FRACTURE ( 65 FDA reports)
TENDERNESS ( 64 FDA reports)
VITAMIN D DEFICIENCY ( 64 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 63 FDA reports)
NEOPLASM MALIGNANT ( 63 FDA reports)
TOOTH LOSS ( 63 FDA reports)
ABASIA ( 62 FDA reports)
BLOOD POTASSIUM DECREASED ( 62 FDA reports)
ERUCTATION ( 62 FDA reports)
GROIN PAIN ( 62 FDA reports)
RENAL IMPAIRMENT ( 62 FDA reports)
BILIARY DYSKINESIA ( 61 FDA reports)
BONE DEBRIDEMENT ( 61 FDA reports)
HYPONATRAEMIA ( 61 FDA reports)
THROAT IRRITATION ( 61 FDA reports)
CYST ( 60 FDA reports)
HAEMATOCRIT DECREASED ( 60 FDA reports)
HEPATIC ENZYME INCREASED ( 60 FDA reports)
INFLAMMATION ( 60 FDA reports)
BACK INJURY ( 59 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 59 FDA reports)
CORONARY ARTERY OCCLUSION ( 59 FDA reports)
DRUG INTERACTION ( 59 FDA reports)
INJECTION SITE HAEMORRHAGE ( 59 FDA reports)
MASS ( 59 FDA reports)
PEPTIC ULCER ( 59 FDA reports)
RENAL CYST ( 59 FDA reports)
RHINORRHOEA ( 59 FDA reports)
BASAL CELL CARCINOMA ( 58 FDA reports)
CARDIAC FAILURE ( 58 FDA reports)
CARDIAC MURMUR ( 58 FDA reports)
CHOLECYSTECTOMY ( 58 FDA reports)
GINGIVITIS ( 58 FDA reports)
RADICULOPATHY ( 58 FDA reports)
CAROTID ARTERY STENOSIS ( 57 FDA reports)
DIVERTICULITIS ( 57 FDA reports)
DYSKINESIA ( 57 FDA reports)
FLANK PAIN ( 57 FDA reports)
FLUID RETENTION ( 57 FDA reports)
NASOPHARYNGITIS ( 57 FDA reports)
PANCREATITIS ACUTE ( 56 FDA reports)
EAR PAIN ( 55 FDA reports)
EMPHYSEMA ( 55 FDA reports)
HALLUCINATION ( 55 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 55 FDA reports)
OFF LABEL USE ( 55 FDA reports)
PANIC ATTACK ( 55 FDA reports)
VIRAL INFECTION ( 55 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 55 FDA reports)
BLOOD PRESSURE DECREASED ( 54 FDA reports)
DECREASED INTEREST ( 54 FDA reports)
STRESS FRACTURE ( 54 FDA reports)
ABSCESS JAW ( 53 FDA reports)
MUSCLE ATROPHY ( 53 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 53 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 53 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 53 FDA reports)
COMPRESSION FRACTURE ( 52 FDA reports)
DRY EYE ( 52 FDA reports)
HYPERTONIC BLADDER ( 52 FDA reports)
PURULENT DISCHARGE ( 52 FDA reports)
DRUG EFFECT DECREASED ( 51 FDA reports)
FEELING HOT ( 51 FDA reports)
FIBROMYALGIA ( 51 FDA reports)
GINGIVAL SWELLING ( 51 FDA reports)
HAEMATOCHEZIA ( 51 FDA reports)
HYPERSOMNIA ( 51 FDA reports)
JOINT INJURY ( 51 FDA reports)
PRODUCT QUALITY ISSUE ( 51 FDA reports)
TARDIVE DYSKINESIA ( 51 FDA reports)
ASCITES ( 50 FDA reports)
SINUS DISORDER ( 50 FDA reports)
SKIN LACERATION ( 50 FDA reports)
TOOTH ABSCESS ( 50 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 49 FDA reports)
ENCEPHALOPATHY ( 49 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 49 FDA reports)
MUSCLE TWITCHING ( 49 FDA reports)
OESOPHAGEAL STENOSIS ( 49 FDA reports)
ORAL DISORDER ( 49 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 49 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 48 FDA reports)
CEREBRAL ATROPHY ( 48 FDA reports)
DISTURBANCE IN ATTENTION ( 48 FDA reports)
FEAR ( 48 FDA reports)
LEUKOCYTOSIS ( 48 FDA reports)
MOBILITY DECREASED ( 48 FDA reports)
ORAL PAIN ( 48 FDA reports)
SINUS BRADYCARDIA ( 48 FDA reports)
ANAPHYLACTIC REACTION ( 47 FDA reports)
DRY SKIN ( 47 FDA reports)
INCONTINENCE ( 47 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 47 FDA reports)
LIBIDO DECREASED ( 47 FDA reports)
MELAENA ( 47 FDA reports)
MULTIPLE INJURIES ( 47 FDA reports)
PERIODONTITIS ( 47 FDA reports)
RENAL DISORDER ( 47 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 47 FDA reports)
CARDIOMYOPATHY ( 46 FDA reports)
DEAFNESS ( 46 FDA reports)
INCORRECT DOSE ADMINISTERED ( 46 FDA reports)
ULCER ( 46 FDA reports)
WOUND DEHISCENCE ( 46 FDA reports)
BACK DISORDER ( 45 FDA reports)
HEAD INJURY ( 45 FDA reports)
HYPOXIA ( 45 FDA reports)
PERICARDIAL EFFUSION ( 45 FDA reports)
SPINAL DISORDER ( 45 FDA reports)
TOOTH INFECTION ( 45 FDA reports)
VISUAL ACUITY REDUCED ( 45 FDA reports)
VITAMIN B12 DEFICIENCY ( 45 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 44 FDA reports)
BLINDNESS ( 44 FDA reports)
BLOOD UREA INCREASED ( 44 FDA reports)
FRACTURE NONUNION ( 44 FDA reports)
INFLUENZA ( 44 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 44 FDA reports)
INTESTINAL OBSTRUCTION ( 44 FDA reports)
LOOSE TOOTH ( 44 FDA reports)
MICTURITION URGENCY ( 44 FDA reports)
OSTEOSCLEROSIS ( 44 FDA reports)
RASH PRURITIC ( 44 FDA reports)
BLOOD CREATININE INCREASED ( 43 FDA reports)
CORONARY ARTERY STENOSIS ( 43 FDA reports)
FEELING JITTERY ( 43 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 43 FDA reports)
KYPHOSIS ( 43 FDA reports)
MUCOSAL INFLAMMATION ( 43 FDA reports)
OSTEITIS ( 43 FDA reports)
PANCYTOPENIA ( 43 FDA reports)
PELVIC PAIN ( 43 FDA reports)
PULMONARY FIBROSIS ( 43 FDA reports)
RASH GENERALISED ( 43 FDA reports)
TREATMENT NONCOMPLIANCE ( 43 FDA reports)
ABDOMINAL PAIN LOWER ( 42 FDA reports)
ABNORMAL DREAMS ( 42 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 42 FDA reports)
CARDIO-RESPIRATORY ARREST ( 42 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 42 FDA reports)
CHROMATURIA ( 42 FDA reports)
FUNGAL INFECTION ( 42 FDA reports)
HYPOCALCAEMIA ( 42 FDA reports)
PRESYNCOPE ( 42 FDA reports)
TOOTH DISORDER ( 42 FDA reports)
VENTRICULAR TACHYCARDIA ( 42 FDA reports)
CARDIOVASCULAR DISORDER ( 41 FDA reports)
DISORIENTATION ( 41 FDA reports)
GALLBLADDER INJURY ( 41 FDA reports)
JAW DISORDER ( 41 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 41 FDA reports)
LEFT ATRIAL DILATATION ( 41 FDA reports)
NOCTURIA ( 41 FDA reports)
ODYNOPHAGIA ( 41 FDA reports)
ORAL HERPES ( 41 FDA reports)
ORAL INFECTION ( 41 FDA reports)
OXYGEN SATURATION DECREASED ( 41 FDA reports)
POOR QUALITY SLEEP ( 41 FDA reports)
POST PROCEDURAL COMPLICATION ( 41 FDA reports)
SKIN LESION ( 41 FDA reports)
SWOLLEN TONGUE ( 41 FDA reports)
TONGUE ULCERATION ( 41 FDA reports)
ACUTE SINUSITIS ( 40 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 40 FDA reports)
HEPATITIS ( 40 FDA reports)
IRRITABILITY ( 40 FDA reports)
SINUS HEADACHE ( 40 FDA reports)
ACCIDENTAL OVERDOSE ( 39 FDA reports)
BREAST CANCER RECURRENT ( 39 FDA reports)
HAEMATEMESIS ( 39 FDA reports)
LIGAMENT SPRAIN ( 39 FDA reports)
MEDICATION ERROR ( 39 FDA reports)
MITRAL VALVE CALCIFICATION ( 39 FDA reports)
MYOPATHY ( 39 FDA reports)
PERIODONTAL DISEASE ( 39 FDA reports)
RHABDOMYOLYSIS ( 39 FDA reports)
TRIGGER FINGER ( 39 FDA reports)
CEREBRAL INFARCTION ( 38 FDA reports)
DYSLIPIDAEMIA ( 38 FDA reports)
FACE OEDEMA ( 38 FDA reports)
GOITRE ( 38 FDA reports)
JOINT STIFFNESS ( 38 FDA reports)
LACUNAR INFARCTION ( 38 FDA reports)
MASTICATION DISORDER ( 38 FDA reports)
MENTAL IMPAIRMENT ( 38 FDA reports)
PSORIASIS ( 38 FDA reports)
SICK SINUS SYNDROME ( 38 FDA reports)
CANDIDIASIS ( 37 FDA reports)
DRUG DEPENDENCE ( 37 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 37 FDA reports)
GINGIVAL INFECTION ( 37 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 37 FDA reports)
IRON DEFICIENCY ANAEMIA ( 37 FDA reports)
LACRIMATION INCREASED ( 37 FDA reports)
NIGHT SWEATS ( 37 FDA reports)
NIGHTMARE ( 37 FDA reports)
PHARYNGITIS ( 37 FDA reports)
RESPIRATORY DISORDER ( 37 FDA reports)
SUICIDE ATTEMPT ( 37 FDA reports)
THINKING ABNORMAL ( 37 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 37 FDA reports)
ADVERSE DRUG REACTION ( 36 FDA reports)
AGGRESSION ( 36 FDA reports)
BARRETT'S OESOPHAGUS ( 36 FDA reports)
BLOOD SODIUM DECREASED ( 36 FDA reports)
BONE DENSITY DECREASED ( 36 FDA reports)
BREAST CANCER ( 36 FDA reports)
COMA ( 36 FDA reports)
EAR INFECTION ( 36 FDA reports)
EYE HAEMORRHAGE ( 36 FDA reports)
FOOT DEFORMITY ( 36 FDA reports)
ISCHAEMIA ( 36 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 36 FDA reports)
NEUTROPENIA ( 36 FDA reports)
PELVIC FRACTURE ( 36 FDA reports)
RENAL FAILURE CHRONIC ( 36 FDA reports)
RHINITIS ( 36 FDA reports)
SPLENOMEGALY ( 36 FDA reports)
STOMACH DISCOMFORT ( 36 FDA reports)
ANGER ( 35 FDA reports)
APHASIA ( 35 FDA reports)
BLOOD CALCIUM DECREASED ( 35 FDA reports)
COLON CANCER ( 35 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 35 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 35 FDA reports)
EJECTION FRACTION DECREASED ( 35 FDA reports)
EXTRASYSTOLES ( 35 FDA reports)
EYE INFECTION ( 35 FDA reports)
MULTIPLE SCLEROSIS ( 35 FDA reports)
PNEUMOTHORAX ( 35 FDA reports)
VISUAL DISTURBANCE ( 35 FDA reports)
ASPIRATION ( 34 FDA reports)
BRUXISM ( 34 FDA reports)
CHOLECYSTITIS ACUTE ( 34 FDA reports)
COGNITIVE DISORDER ( 34 FDA reports)
DIABETIC NEUROPATHY ( 34 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 34 FDA reports)
HAND FRACTURE ( 34 FDA reports)
KNEE ARTHROPLASTY ( 34 FDA reports)
LOW TURNOVER OSTEOPATHY ( 34 FDA reports)
MENORRHAGIA ( 34 FDA reports)
MOVEMENT DISORDER ( 34 FDA reports)
OBESITY ( 34 FDA reports)
SINUS CONGESTION ( 34 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 34 FDA reports)
ACUTE CORONARY SYNDROME ( 33 FDA reports)
ANAEMIA POSTOPERATIVE ( 33 FDA reports)
BREAST PAIN ( 33 FDA reports)
DIVERTICULUM INTESTINAL ( 33 FDA reports)
FAECES DISCOLOURED ( 33 FDA reports)
GOUT ( 33 FDA reports)
SKIN ULCER ( 33 FDA reports)
SURGERY ( 33 FDA reports)
THROAT TIGHTNESS ( 33 FDA reports)
TONGUE DISORDER ( 33 FDA reports)
WRIST FRACTURE ( 33 FDA reports)
DRUG TOXICITY ( 32 FDA reports)
ESSENTIAL HYPERTENSION ( 32 FDA reports)
EYE SWELLING ( 32 FDA reports)
LARYNGEAL OEDEMA ( 32 FDA reports)
PRURITUS GENERALISED ( 32 FDA reports)
SNORING ( 32 FDA reports)
THYROID DISORDER ( 32 FDA reports)
BILE DUCT STENOSIS ( 31 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 31 FDA reports)
GASTROENTERITIS ( 31 FDA reports)
HAEMOLYTIC ANAEMIA ( 31 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 31 FDA reports)
INJECTION SITE REACTION ( 31 FDA reports)
MITRAL VALVE PROLAPSE ( 31 FDA reports)
ORAL DISCOMFORT ( 31 FDA reports)
PALLOR ( 31 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 31 FDA reports)
PHOTOPHOBIA ( 31 FDA reports)
SCAR ( 31 FDA reports)
SKIN DISORDER ( 31 FDA reports)
SPINAL FRACTURE ( 31 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 31 FDA reports)
TOOTH REPAIR ( 31 FDA reports)
ABNORMAL BEHAVIOUR ( 30 FDA reports)
ABSCESS ORAL ( 30 FDA reports)
ACTINIC KERATOSIS ( 30 FDA reports)
ANEURYSM ( 30 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 30 FDA reports)
CHONDROMALACIA ( 30 FDA reports)
DISABILITY ( 30 FDA reports)
DRUG INTOLERANCE ( 30 FDA reports)
FACIAL PALSY ( 30 FDA reports)
GASTRITIS EROSIVE ( 30 FDA reports)
GINGIVAL BLEEDING ( 30 FDA reports)
GLOSSITIS ( 30 FDA reports)
HEART RATE DECREASED ( 30 FDA reports)
HEMIPARESIS ( 30 FDA reports)
HERNIA ( 30 FDA reports)
ILL-DEFINED DISORDER ( 30 FDA reports)
INJECTION SITE HAEMATOMA ( 30 FDA reports)
INTENTIONAL DRUG MISUSE ( 30 FDA reports)
LUMBAR RADICULOPATHY ( 30 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 30 FDA reports)
SCIATICA ( 30 FDA reports)
SKIN BURNING SENSATION ( 30 FDA reports)
SPONDYLOLISTHESIS ( 30 FDA reports)
WITHDRAWAL SYNDROME ( 30 FDA reports)
ANKLE FRACTURE ( 29 FDA reports)
BLISTER ( 29 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 29 FDA reports)
CROHN'S DISEASE ( 29 FDA reports)
CRYING ( 29 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 29 FDA reports)
EROSIVE OESOPHAGITIS ( 29 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 29 FDA reports)
HYPOAESTHESIA ORAL ( 29 FDA reports)
IMPAIRED WORK ABILITY ( 29 FDA reports)
JAUNDICE ( 29 FDA reports)
MIDDLE INSOMNIA ( 29 FDA reports)
PROCEDURAL PAIN ( 29 FDA reports)
RASH ERYTHEMATOUS ( 29 FDA reports)
SEQUESTRECTOMY ( 29 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 29 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 28 FDA reports)
BREAST MASS ( 28 FDA reports)
DELIRIUM ( 28 FDA reports)
DISEASE PROGRESSION ( 28 FDA reports)
DRUG ADMINISTRATION ERROR ( 28 FDA reports)
ELECTROLYTE IMBALANCE ( 28 FDA reports)
GINGIVAL ULCERATION ( 28 FDA reports)
HAEMATOMA ( 28 FDA reports)
HEPATIC FAILURE ( 28 FDA reports)
HYPERKALAEMIA ( 28 FDA reports)
MEDICAL DEVICE COMPLICATION ( 28 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 28 FDA reports)
PARKINSON'S DISEASE ( 28 FDA reports)
RECTAL PROLAPSE ( 28 FDA reports)
RENAL INJURY ( 28 FDA reports)
SEBORRHOEIC KERATOSIS ( 28 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 28 FDA reports)
BONE SWELLING ( 27 FDA reports)
BRAIN NEOPLASM ( 27 FDA reports)
COLITIS ULCERATIVE ( 27 FDA reports)
DYSSTASIA ( 27 FDA reports)
DYSTONIA ( 27 FDA reports)
EXCORIATION ( 27 FDA reports)
EYE PRURITUS ( 27 FDA reports)
FEBRILE NEUTROPENIA ( 27 FDA reports)
GENITAL HERPES ( 27 FDA reports)
GINGIVAL ERYTHEMA ( 27 FDA reports)
GINGIVAL OEDEMA ( 27 FDA reports)
HYPOKINESIA ( 27 FDA reports)
MOOD ALTERED ( 27 FDA reports)
MULTI-ORGAN FAILURE ( 27 FDA reports)
NERVE COMPRESSION ( 27 FDA reports)
NERVOUS SYSTEM DISORDER ( 27 FDA reports)
OEDEMA MOUTH ( 27 FDA reports)
OTORRHOEA ( 27 FDA reports)
OVARIAN CYST ( 27 FDA reports)
PANCREATITIS CHRONIC ( 27 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 27 FDA reports)
SKIN INDURATION ( 27 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 27 FDA reports)
UPPER LIMB FRACTURE ( 27 FDA reports)
VENTRICULAR HYPERTROPHY ( 27 FDA reports)
ABSCESS ( 26 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 26 FDA reports)
ANXIETY DISORDER ( 26 FDA reports)
CHOKING ( 26 FDA reports)
COLITIS ISCHAEMIC ( 26 FDA reports)
DEAFNESS NEUROSENSORY ( 26 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 26 FDA reports)
DILATATION VENTRICULAR ( 26 FDA reports)
EARLY SATIETY ( 26 FDA reports)
EATING DISORDER ( 26 FDA reports)
FAECAL INCONTINENCE ( 26 FDA reports)
FRACTURE DELAYED UNION ( 26 FDA reports)
GASTRIC POLYPS ( 26 FDA reports)
GASTROENTERITIS VIRAL ( 26 FDA reports)
HAEMORRHAGIC ANAEMIA ( 26 FDA reports)
HEPATIC CIRRHOSIS ( 26 FDA reports)
IMPAIRED DRIVING ABILITY ( 26 FDA reports)
MAJOR DEPRESSION ( 26 FDA reports)
METASTATIC NEOPLASM ( 26 FDA reports)
MOOD SWINGS ( 26 FDA reports)
NEURITIS ( 26 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 26 FDA reports)
ONYCHOMYCOSIS ( 26 FDA reports)
ORAL CANDIDIASIS ( 26 FDA reports)
PULMONARY MASS ( 26 FDA reports)
SEPTIC SHOCK ( 26 FDA reports)
SKIN EXFOLIATION ( 26 FDA reports)
STASIS DERMATITIS ( 26 FDA reports)
SUBCUTANEOUS ABSCESS ( 26 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 26 FDA reports)
SYNOVITIS ( 26 FDA reports)
THYROID CANCER ( 26 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 26 FDA reports)
URETHRAL STENOSIS ( 26 FDA reports)
BLOOD BILIRUBIN INCREASED ( 25 FDA reports)
BODY HEIGHT DECREASED ( 25 FDA reports)
COAGULOPATHY ( 25 FDA reports)
DIFFICULTY IN WALKING ( 25 FDA reports)
EAR CONGESTION ( 25 FDA reports)
EXPOSED BONE IN JAW ( 25 FDA reports)
FACIAL PAIN ( 25 FDA reports)
HUMERUS FRACTURE ( 25 FDA reports)
MUSCLE CRAMP ( 25 FDA reports)
MUSCLE TIGHTNESS ( 25 FDA reports)
ORTHOSTATIC HYPOTENSION ( 25 FDA reports)
PLEURAL FIBROSIS ( 25 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 25 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 25 FDA reports)
RESPIRATORY TRACT CONGESTION ( 25 FDA reports)
RESTLESSNESS ( 25 FDA reports)
ACTINOMYCOSIS ( 24 FDA reports)
CHRONIC SINUSITIS ( 24 FDA reports)
DERMATITIS ( 24 FDA reports)
DIASTOLIC DYSFUNCTION ( 24 FDA reports)
DISEASE RECURRENCE ( 24 FDA reports)
EYE DISORDER ( 24 FDA reports)
FEELING COLD ( 24 FDA reports)
HERPES VIRUS INFECTION ( 24 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 24 FDA reports)
IMPETIGO ( 24 FDA reports)
INFUSION RELATED REACTION ( 24 FDA reports)
JOINT DISLOCATION ( 24 FDA reports)
JOINT SPRAIN ( 24 FDA reports)
LENTIGO ( 24 FDA reports)
LIVER DISORDER ( 24 FDA reports)
LUNG NEOPLASM MALIGNANT ( 24 FDA reports)
MUSCLE STRAIN ( 24 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 24 FDA reports)
PROTEINURIA ( 24 FDA reports)
PYURIA ( 24 FDA reports)
REFLUX OESOPHAGITIS ( 24 FDA reports)
RESPIRATORY ARREST ( 24 FDA reports)
THIRST ( 24 FDA reports)
ACNE ( 23 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 23 FDA reports)
APHONIA ( 23 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 23 FDA reports)
BREAST CANCER FEMALE ( 23 FDA reports)
CIRCULATORY COLLAPSE ( 23 FDA reports)
COLD SWEAT ( 23 FDA reports)
COORDINATION ABNORMAL ( 23 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 23 FDA reports)
FISTULA ( 23 FDA reports)
HISTOPLASMOSIS ( 23 FDA reports)
INCREASED APPETITE ( 23 FDA reports)
JAW OPERATION ( 23 FDA reports)
LIMB INJURY ( 23 FDA reports)
MALNUTRITION ( 23 FDA reports)
NEOPLASM PROGRESSION ( 23 FDA reports)
NEPHRITIS INTERSTITIAL ( 23 FDA reports)
POLYP ( 23 FDA reports)
PROSTATE CANCER ( 23 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 23 FDA reports)
STOMATITIS NECROTISING ( 23 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 23 FDA reports)
BODY TEMPERATURE INCREASED ( 22 FDA reports)
DECUBITUS ULCER ( 22 FDA reports)
FRACTURE ( 22 FDA reports)
GENERALISED OEDEMA ( 22 FDA reports)
HYPOVOLAEMIA ( 22 FDA reports)
ILEUS ( 22 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 22 FDA reports)
KIDNEY INFECTION ( 22 FDA reports)
LACERATION ( 22 FDA reports)
LOCAL SWELLING ( 22 FDA reports)
LYMPHOEDEMA ( 22 FDA reports)
MANIA ( 22 FDA reports)
OESOPHAGEAL PAIN ( 22 FDA reports)
PERIPHERAL COLDNESS ( 22 FDA reports)
PHOTOSENSITIVITY REACTION ( 22 FDA reports)
PLASMACYTOMA ( 22 FDA reports)
PROTHROMBIN TIME PROLONGED ( 22 FDA reports)
SENSORY LOSS ( 22 FDA reports)
THYROID NEOPLASM ( 22 FDA reports)
ADENOMA BENIGN ( 21 FDA reports)
ATAXIA ( 21 FDA reports)
ATRIOVENTRICULAR BLOCK ( 21 FDA reports)
BILIARY COLIC ( 21 FDA reports)
DEBRIDEMENT ( 21 FDA reports)
DIABETIC KETOACIDOSIS ( 21 FDA reports)
DUODENAL ULCER ( 21 FDA reports)
ECCHYMOSIS ( 21 FDA reports)
EOSINOPHIL COUNT INCREASED ( 21 FDA reports)
FACET JOINT SYNDROME ( 21 FDA reports)
FISTULA DISCHARGE ( 21 FDA reports)
HAEMATOCRIT INCREASED ( 21 FDA reports)
HAEMORRHAGIC STROKE ( 21 FDA reports)
HEARING IMPAIRED ( 21 FDA reports)
HELICOBACTER GASTRITIS ( 21 FDA reports)
HEPATITIS C ( 21 FDA reports)
INCREASED TENDENCY TO BRUISE ( 21 FDA reports)
LIMB DISCOMFORT ( 21 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 21 FDA reports)
NEUROPATHY ( 21 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 21 FDA reports)
OPEN WOUND ( 21 FDA reports)
ORTHOPNOEA ( 21 FDA reports)
PARANOIA ( 21 FDA reports)
PATHOLOGICAL GAMBLING ( 21 FDA reports)
PHYSICAL DISABILITY ( 21 FDA reports)
PRODUCTIVE COUGH ( 21 FDA reports)
RADIUS FRACTURE ( 21 FDA reports)
RASH MACULAR ( 21 FDA reports)
RETCHING ( 21 FDA reports)
TONSILLAR DISORDER ( 21 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 20 FDA reports)
ADRENAL INSUFFICIENCY ( 20 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 20 FDA reports)
APPLICATION SITE ERYTHEMA ( 20 FDA reports)
APPLICATION SITE PRURITUS ( 20 FDA reports)
BLEPHARITIS ( 20 FDA reports)
BLINDNESS TRANSIENT ( 20 FDA reports)
BLINDNESS UNILATERAL ( 20 FDA reports)
BLOOD ALBUMIN DECREASED ( 20 FDA reports)
BONE LOSS ( 20 FDA reports)
COSTOCHONDRITIS ( 20 FDA reports)
DEMENTIA ( 20 FDA reports)
DIABETIC RETINOPATHY ( 20 FDA reports)
FIBULA FRACTURE ( 20 FDA reports)
GINGIVAL DISORDER ( 20 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 20 FDA reports)
METASTASES TO THORAX ( 20 FDA reports)
SEDATION ( 20 FDA reports)
SKIN PLAQUE ( 20 FDA reports)
SNEEZING ( 20 FDA reports)
VASCULAR ANOMALY ( 20 FDA reports)
VENTRICULAR DYSFUNCTION ( 20 FDA reports)
VITREOUS FLOATERS ( 20 FDA reports)
ABDOMINAL TENDERNESS ( 19 FDA reports)
AGEUSIA ( 19 FDA reports)
BLADDER OPERATION ( 19 FDA reports)
BLOOD PRESSURE ABNORMAL ( 19 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 19 FDA reports)
CARDIAC VALVE DISEASE ( 19 FDA reports)
CYANOSIS ( 19 FDA reports)
DERMATITIS CONTACT ( 19 FDA reports)
DUODENITIS ( 19 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 19 FDA reports)
EYE INJURY ( 19 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 19 FDA reports)
INJECTION SITE SWELLING ( 19 FDA reports)
INTERSTITIAL LUNG DISEASE ( 19 FDA reports)
INTESTINAL PERFORATION ( 19 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 19 FDA reports)
ORAL SURGERY ( 19 FDA reports)
PERIARTHRITIS ( 19 FDA reports)
SHOULDER PAIN ( 19 FDA reports)
SINUS OPERATION ( 19 FDA reports)
SKIN PAPILLOMA ( 19 FDA reports)
ULCER HAEMORRHAGE ( 19 FDA reports)
UNRESPONSIVE TO STIMULI ( 19 FDA reports)
URINARY HESITATION ( 19 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 19 FDA reports)
ACUTE RESPIRATORY FAILURE ( 18 FDA reports)
ADHESION ( 18 FDA reports)
APATHY ( 18 FDA reports)
BACTERIAL INFECTION ( 18 FDA reports)
BONE MARROW TRANSPLANT ( 18 FDA reports)
BONE METABOLISM DISORDER ( 18 FDA reports)
CARDIAC PACEMAKER INSERTION ( 18 FDA reports)
CATHETERISATION CARDIAC ( 18 FDA reports)
CERVICOBRACHIAL SYNDROME ( 18 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 18 FDA reports)
EJACULATION DISORDER ( 18 FDA reports)
HAEMOPTYSIS ( 18 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 18 FDA reports)
HEART INJURY ( 18 FDA reports)
HEPATOMEGALY ( 18 FDA reports)
HYPOMANIA ( 18 FDA reports)
JAW FRACTURE ( 18 FDA reports)
KNEE OPERATION ( 18 FDA reports)
LACTOSE INTOLERANCE ( 18 FDA reports)
LEUKOPENIA ( 18 FDA reports)
LIPOMA ( 18 FDA reports)
NON-CARDIAC CHEST PAIN ( 18 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 18 FDA reports)
OSTEOLYSIS ( 18 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 18 FDA reports)
SACROILIITIS ( 18 FDA reports)
SEASONAL ALLERGY ( 18 FDA reports)
SKIN HYPERTROPHY ( 18 FDA reports)
VENTRICULAR FIBRILLATION ( 18 FDA reports)
VISUAL FIELD DEFECT ( 18 FDA reports)
VITREOUS DETACHMENT ( 18 FDA reports)
VULVOVAGINAL DRYNESS ( 18 FDA reports)
WHEELCHAIR USER ( 18 FDA reports)
ABSCESS DRAINAGE ( 17 FDA reports)
ALVEOLOPLASTY ( 17 FDA reports)
AZOTAEMIA ( 17 FDA reports)
BLADDER DISORDER ( 17 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 17 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 17 FDA reports)
BREAST DISORDER ( 17 FDA reports)
CARDIOGENIC SHOCK ( 17 FDA reports)
CAROTID BRUIT ( 17 FDA reports)
CATARACT OPERATION ( 17 FDA reports)
CHARLES BONNET SYNDROME ( 17 FDA reports)
COLECTOMY ( 17 FDA reports)
DILATATION ATRIAL ( 17 FDA reports)
EAR NEOPLASM ( 17 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 17 FDA reports)
EYE INFLAMMATION ( 17 FDA reports)
EYE IRRITATION ( 17 FDA reports)
FAMILY STRESS ( 17 FDA reports)
FIBROMA ( 17 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 17 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 17 FDA reports)
HEPATIC LESION ( 17 FDA reports)
HOSPITALISATION ( 17 FDA reports)
HYPERPARATHYROIDISM ( 17 FDA reports)
HYPERTENSIVE HEART DISEASE ( 17 FDA reports)
HYPOACUSIS ( 17 FDA reports)
HYPOMAGNESAEMIA ( 17 FDA reports)
INTRACRANIAL ANEURYSM ( 17 FDA reports)
JAW CYST ( 17 FDA reports)
LOCALISED OEDEMA ( 17 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 17 FDA reports)
MACROGLOSSIA ( 17 FDA reports)
MENOPAUSAL SYMPTOMS ( 17 FDA reports)
MULTIPLE FRACTURES ( 17 FDA reports)
NODAL OSTEOARTHRITIS ( 17 FDA reports)
PNEUMONIA ASPIRATION ( 17 FDA reports)
PNEUMONITIS ( 17 FDA reports)
RETINAL DETACHMENT ( 17 FDA reports)
SCAPULA FRACTURE ( 17 FDA reports)
SLUGGISHNESS ( 17 FDA reports)
SQUAMOUS CELL CARCINOMA ( 17 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 17 FDA reports)
THERAPY NON-RESPONDER ( 17 FDA reports)
TIBIA FRACTURE ( 17 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 17 FDA reports)
UTERINE LEIOMYOMA ( 17 FDA reports)
VAGINAL DISCHARGE ( 17 FDA reports)
VENOUS INSUFFICIENCY ( 17 FDA reports)
VENTRICULAR HYPOKINESIA ( 17 FDA reports)
ACUTE PULMONARY OEDEMA ( 16 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 16 FDA reports)
ANGIOPATHY ( 16 FDA reports)
APPENDICITIS ( 16 FDA reports)
BILIARY DILATATION ( 16 FDA reports)
BLOOD IRON DECREASED ( 16 FDA reports)
BREAST TENDERNESS ( 16 FDA reports)
BRONCHOSPASM ( 16 FDA reports)
CAROTID ARTERY OCCLUSION ( 16 FDA reports)
CEREBRAL ISCHAEMIA ( 16 FDA reports)
CYST ASPIRATION ( 16 FDA reports)
EOSINOPHILIA ( 16 FDA reports)
EYELID OEDEMA ( 16 FDA reports)
HYPERCALCAEMIA ( 16 FDA reports)
INFECTED SEBACEOUS CYST ( 16 FDA reports)
LUNG HYPERINFLATION ( 16 FDA reports)
MENISCUS REMOVAL ( 16 FDA reports)
MENSTRUATION IRREGULAR ( 16 FDA reports)
OESOPHAGEAL ULCER ( 16 FDA reports)
OPEN REDUCTION OF FRACTURE ( 16 FDA reports)
OSTEOMYELITIS ACUTE ( 16 FDA reports)
PATHOLOGICAL FRACTURE ( 16 FDA reports)
PERINEAL PAIN ( 16 FDA reports)
PHARYNGEAL OEDEMA ( 16 FDA reports)
POLYNEUROPATHY ( 16 FDA reports)
PROSTATE TENDERNESS ( 16 FDA reports)
PROTEIN URINE PRESENT ( 16 FDA reports)
PYELONEPHRITIS ( 16 FDA reports)
RASH PAPULAR ( 16 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 16 FDA reports)
SENSATION OF HEAVINESS ( 16 FDA reports)
SENSORY DISTURBANCE ( 16 FDA reports)
SHOULDER ARTHROPLASTY ( 16 FDA reports)
SHOULDER OPERATION ( 16 FDA reports)
SKIN DISCOLOURATION ( 16 FDA reports)
SKIN TIGHTNESS ( 16 FDA reports)
TENDON RUPTURE ( 16 FDA reports)
TENOSYNOVITIS ( 16 FDA reports)
THYROIDECTOMY ( 16 FDA reports)
VAGINAL HAEMORRHAGE ( 16 FDA reports)
ABDOMINAL HERNIA ( 15 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 15 FDA reports)
AMENORRHOEA ( 15 FDA reports)
ANGIOEDEMA ( 15 FDA reports)
APHTHOUS STOMATITIS ( 15 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 15 FDA reports)
BIPOLAR DISORDER ( 15 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 15 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 15 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 15 FDA reports)
BONE OPERATION ( 15 FDA reports)
CALCIUM DEFICIENCY ( 15 FDA reports)
CEREBRAL HAEMORRHAGE ( 15 FDA reports)
CHEST WALL MASS ( 15 FDA reports)
CHOKING SENSATION ( 15 FDA reports)
CRANIOTOMY ( 15 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 15 FDA reports)
DEVICE FAILURE ( 15 FDA reports)
DIZZINESS POSTURAL ( 15 FDA reports)
DRUG PRESCRIBING ERROR ( 15 FDA reports)
ENCEPHALOMALACIA ( 15 FDA reports)
EPIGASTRIC DISCOMFORT ( 15 FDA reports)
ERB'S PALSY ( 15 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 15 FDA reports)
GASTRINOMA ( 15 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 15 FDA reports)
JOINT INSTABILITY ( 15 FDA reports)
LARYNGITIS ( 15 FDA reports)
LIP SWELLING ( 15 FDA reports)
LOCALISED INFECTION ( 15 FDA reports)
MACULAR DEGENERATION ( 15 FDA reports)
MENINGIOMA ( 15 FDA reports)
MULTIPLE MYELOMA ( 15 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 15 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 15 FDA reports)
OTITIS MEDIA ACUTE ( 15 FDA reports)
PAINFUL RESPIRATION ( 15 FDA reports)
PLATELET COUNT INCREASED ( 15 FDA reports)
PLEURISY ( 15 FDA reports)
SENSATION OF FOREIGN BODY ( 15 FDA reports)
STENT PLACEMENT ( 15 FDA reports)
TENDON DISORDER ( 15 FDA reports)
THROMBOCYTOSIS ( 15 FDA reports)
UTERINE HAEMORRHAGE ( 15 FDA reports)
VEIN DISORDER ( 15 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 15 FDA reports)
AORTIC ANEURYSM ( 14 FDA reports)
BLOOD CORTISOL ABNORMAL ( 14 FDA reports)
BREAST CANCER METASTATIC ( 14 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 14 FDA reports)
CALCINOSIS ( 14 FDA reports)
CERVICAL SPINAL STENOSIS ( 14 FDA reports)
CHAPPED LIPS ( 14 FDA reports)
CHOROIDAL DETACHMENT ( 14 FDA reports)
CORONARY ARTERY RESTENOSIS ( 14 FDA reports)
DIAPHRAGMATIC HERNIA ( 14 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 14 FDA reports)
DRY THROAT ( 14 FDA reports)
DUODENAL ULCER PERFORATION ( 14 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 14 FDA reports)
EATING DISORDER SYMPTOM ( 14 FDA reports)
ECZEMA ( 14 FDA reports)
EMBOLIC STROKE ( 14 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 14 FDA reports)
HEPATIC NEOPLASM ( 14 FDA reports)
HICCUPS ( 14 FDA reports)
HIP ARTHROPLASTY ( 14 FDA reports)
HYSTERECTOMY ( 14 FDA reports)
INADEQUATE ANALGESIA ( 14 FDA reports)
INGROWING NAIL ( 14 FDA reports)
INJECTION SITE PRURITUS ( 14 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 14 FDA reports)
JOINT CREPITATION ( 14 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 14 FDA reports)
MYOSITIS ( 14 FDA reports)
OESOPHAGEAL DISORDER ( 14 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 14 FDA reports)
ORAL MUCOSAL HYPERTROPHY ( 14 FDA reports)
OSTEORADIONECROSIS ( 14 FDA reports)
PANCREATIC NEOPLASM ( 14 FDA reports)
PARALYSIS ( 14 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 14 FDA reports)
PERITONITIS BACTERIAL ( 14 FDA reports)
POLYTRAUMATISM ( 14 FDA reports)
PSYCHOTIC DISORDER ( 14 FDA reports)
RESORPTION BONE INCREASED ( 14 FDA reports)
SEXUAL DYSFUNCTION ( 14 FDA reports)
SKIN ODOUR ABNORMAL ( 14 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 14 FDA reports)
SUBCUTANEOUS NODULE ( 14 FDA reports)
TEMPORAL ARTERITIS ( 14 FDA reports)
TYPE 1 DIABETES MELLITUS ( 14 FDA reports)
VITREOUS HAEMORRHAGE ( 14 FDA reports)
ADJUSTMENT DISORDER ( 13 FDA reports)
ALVEOLAR OSTEITIS ( 13 FDA reports)
APHAGIA ( 13 FDA reports)
APNOEA ( 13 FDA reports)
APPLICATION SITE RASH ( 13 FDA reports)
ATRIAL FLUTTER ( 13 FDA reports)
BACTERIAL TEST POSITIVE ( 13 FDA reports)
BALANITIS ( 13 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 13 FDA reports)
BLADDER CANCER ( 13 FDA reports)
BLADDER DIVERTICULUM ( 13 FDA reports)
BLOOD DISORDER ( 13 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 13 FDA reports)
CARDIAC OUTPUT DECREASED ( 13 FDA reports)
CHEST X-RAY ABNORMAL ( 13 FDA reports)
CHOLANGITIS SCLEROSING ( 13 FDA reports)
COELIAC DISEASE ( 13 FDA reports)
CUBITAL TUNNEL SYNDROME ( 13 FDA reports)
DEPENDENCE ( 13 FDA reports)
DERMATITIS ACNEIFORM ( 13 FDA reports)
DEVICE BREAKAGE ( 13 FDA reports)
DIALYSIS ( 13 FDA reports)
GENITAL RASH ( 13 FDA reports)
HAEMANGIOMA ( 13 FDA reports)
HAEMANGIOMA OF LIVER ( 13 FDA reports)
HAEMORRHOID OPERATION ( 13 FDA reports)
HEPATOCELLULAR DAMAGE ( 13 FDA reports)
HERPES SIMPLEX ( 13 FDA reports)
HYDRONEPHROSIS ( 13 FDA reports)
HYPERTHYROIDISM ( 13 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 13 FDA reports)
INJECTION SITE IRRITATION ( 13 FDA reports)
ISCHAEMIC STROKE ( 13 FDA reports)
LABORATORY TEST ABNORMAL ( 13 FDA reports)
LIVER INJURY ( 13 FDA reports)
LOBAR PNEUMONIA ( 13 FDA reports)
LOWER LIMB FRACTURE ( 13 FDA reports)
MAMMOGRAM ABNORMAL ( 13 FDA reports)
MASTECTOMY ( 13 FDA reports)
METABOLIC ACIDOSIS ( 13 FDA reports)
METASTASES TO SPLEEN ( 13 FDA reports)
MOUTH HAEMORRHAGE ( 13 FDA reports)
MYOPIA ( 13 FDA reports)
NEUROLOGICAL SYMPTOM ( 13 FDA reports)
NIGHT BLINDNESS ( 13 FDA reports)
ORAL INTAKE REDUCED ( 13 FDA reports)
PALATAL DISORDER ( 13 FDA reports)
PANIC DISORDER ( 13 FDA reports)
PATELLA FRACTURE ( 13 FDA reports)
PERSONALITY CHANGE ( 13 FDA reports)
PHOTODERMATOSIS ( 13 FDA reports)
PNEUMONIA VIRAL ( 13 FDA reports)
POST PROCEDURAL HAEMATOMA ( 13 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 13 FDA reports)
PROCEDURAL HYPERTENSION ( 13 FDA reports)
PROSTATITIS ( 13 FDA reports)
SALIVARY GLAND MASS ( 13 FDA reports)
SKIN NEOPLASM EXCISION ( 13 FDA reports)
SPINAL CORD COMPRESSION ( 13 FDA reports)
SPLENIC ARTERY ANEURYSM ( 13 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 13 FDA reports)
TUBERCULOSIS ( 13 FDA reports)
UMBILICAL HERNIA ( 13 FDA reports)
VERTIGO POSITIONAL ( 13 FDA reports)
WOUND ( 13 FDA reports)
ABNORMAL SENSATION IN EYE ( 12 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 12 FDA reports)
AKATHISIA ( 12 FDA reports)
ANGIOMYOLIPOMA ( 12 FDA reports)
APPLICATION SITE REACTION ( 12 FDA reports)
BEDRIDDEN ( 12 FDA reports)
BIPOLAR I DISORDER ( 12 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 12 FDA reports)
BUNION ( 12 FDA reports)
CARDIAC FLUTTER ( 12 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 12 FDA reports)
CLOSTRIDIAL INFECTION ( 12 FDA reports)
CYSTOCELE ( 12 FDA reports)
DROOLING ( 12 FDA reports)
ECTROPION ( 12 FDA reports)
ENDOCARDITIS ( 12 FDA reports)
EPIDIDYMITIS ( 12 FDA reports)
FEELING OF DESPAIR ( 12 FDA reports)
FISTULA REPAIR ( 12 FDA reports)
FRACTURE DISPLACEMENT ( 12 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 12 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 12 FDA reports)
HYPOPNOEA ( 12 FDA reports)
HYPOTONY OF EYE ( 12 FDA reports)
ILIUM FRACTURE ( 12 FDA reports)
INITIAL INSOMNIA ( 12 FDA reports)
INTESTINAL ISCHAEMIA ( 12 FDA reports)
KERATITIS ( 12 FDA reports)
LIGAMENT RUPTURE ( 12 FDA reports)
LUPUS-LIKE SYNDROME ( 12 FDA reports)
MASTOCYTOSIS ( 12 FDA reports)
MECHANICAL VENTILATION ( 12 FDA reports)
MOTOR DYSFUNCTION ( 12 FDA reports)
MUSCULOSKELETAL DISORDER ( 12 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 12 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 12 FDA reports)
PARATHYROID TUMOUR BENIGN ( 12 FDA reports)
PLEURITIC PAIN ( 12 FDA reports)
POOR DENTAL CONDITION ( 12 FDA reports)
PSEUDOMONAS INFECTION ( 12 FDA reports)
PULMONARY THROMBOSIS ( 12 FDA reports)
RAYNAUD'S PHENOMENON ( 12 FDA reports)
RECTOCELE ( 12 FDA reports)
RENAL ARTERY STENOSIS ( 12 FDA reports)
SELF ESTEEM DECREASED ( 12 FDA reports)
SHOCK ( 12 FDA reports)
SKIN REACTION ( 12 FDA reports)
SPINAL LAMINECTOMY ( 12 FDA reports)
URINE OUTPUT DECREASED ( 12 FDA reports)
VASCULITIS ( 12 FDA reports)
VENA CAVA FILTER INSERTION ( 12 FDA reports)
WOUND DRAINAGE ( 12 FDA reports)
ATRIAL THROMBOSIS ( 11 FDA reports)
AUTOIMMUNE HEPATITIS ( 11 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 11 FDA reports)
BILE DUCT STONE ( 11 FDA reports)
BLOOD CHLORIDE DECREASED ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 11 FDA reports)
BLOOD MAGNESIUM DECREASED ( 11 FDA reports)
BLOOD POTASSIUM INCREASED ( 11 FDA reports)
CAECUM OPERATION ( 11 FDA reports)
CATARACT NUCLEAR ( 11 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 11 FDA reports)
COLON POLYPECTOMY ( 11 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 11 FDA reports)
CONJUNCTIVITIS ( 11 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 11 FDA reports)
DEVICE MALFUNCTION ( 11 FDA reports)
DIABETIC NEPHROPATHY ( 11 FDA reports)
DRUG ABUSE ( 11 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 11 FDA reports)
EAR DISCOMFORT ( 11 FDA reports)
EXTRASKELETAL OSSIFICATION ( 11 FDA reports)
HEMIPLEGIA ( 11 FDA reports)
HOSTILITY ( 11 FDA reports)
IMMUNE SYSTEM DISORDER ( 11 FDA reports)
INGUINAL HERNIA ( 11 FDA reports)
INJECTION SITE BRUISING ( 11 FDA reports)
INJECTION SITE RASH ( 11 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 11 FDA reports)
LABYRINTHITIS ( 11 FDA reports)
LARGE INTESTINE PERFORATION ( 11 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 11 FDA reports)
LIP ULCERATION ( 11 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 11 FDA reports)
METABOLIC ENCEPHALOPATHY ( 11 FDA reports)
NASAL DISORDER ( 11 FDA reports)
NERVE INJURY ( 11 FDA reports)
OTITIS MEDIA ( 11 FDA reports)
OVARIAN MASS ( 11 FDA reports)
PERICARDITIS ( 11 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 11 FDA reports)
PHOTOPSIA ( 11 FDA reports)
PLANTAR FASCIITIS ( 11 FDA reports)
POLYMYALGIA RHEUMATICA ( 11 FDA reports)
POLYP COLORECTAL ( 11 FDA reports)
POSTNASAL DRIP ( 11 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 11 FDA reports)
PROSTATOMEGALY ( 11 FDA reports)
RADIOTHERAPY TO BRAIN ( 11 FDA reports)
RECTAL PROLAPSE REPAIR ( 11 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 11 FDA reports)
SKIN CANCER ( 11 FDA reports)
SKIN FISSURES ( 11 FDA reports)
SKIN HYPERPIGMENTATION ( 11 FDA reports)
SPLENIC LESION ( 11 FDA reports)
STERNOTOMY ( 11 FDA reports)
TENSION HEADACHE ( 11 FDA reports)
TESTICULAR PAIN ( 11 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 11 FDA reports)
ACIDOSIS ( 10 FDA reports)
ANOSMIA ( 10 FDA reports)
AORTIC STENOSIS ( 10 FDA reports)
BACTERAEMIA ( 10 FDA reports)
BILE DUCT OBSTRUCTION ( 10 FDA reports)
BLADDER OBSTRUCTION ( 10 FDA reports)
BLOOD CORTISOL DECREASED ( 10 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 10 FDA reports)
BLOOD URINE PRESENT ( 10 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 10 FDA reports)
BRONCHITIS ACUTE ( 10 FDA reports)
BRONCHITIS CHRONIC ( 10 FDA reports)
CAROTID ARTERY DISEASE ( 10 FDA reports)
CHOLESTEROSIS ( 10 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 10 FDA reports)
DECREASED ACTIVITY ( 10 FDA reports)
ENDOMETRIOSIS ( 10 FDA reports)
ENDOTRACHEAL INTUBATION ( 10 FDA reports)
EUPHORIC MOOD ( 10 FDA reports)
FAECES PALE ( 10 FDA reports)
FLUID OVERLOAD ( 10 FDA reports)
FOOT OPERATION ( 10 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 10 FDA reports)
GASTRIC HAEMORRHAGE ( 10 FDA reports)
GASTROINTESTINAL ULCER ( 10 FDA reports)
HAEMARTHROSIS ( 10 FDA reports)
HAEMOLYSIS ( 10 FDA reports)
HELICOBACTER INFECTION ( 10 FDA reports)
HEPATIC FIBROSIS ( 10 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 10 FDA reports)
HIGH FREQUENCY ABLATION ( 10 FDA reports)
HIP SURGERY ( 10 FDA reports)
HOARSENESS ( 10 FDA reports)
HYPOAESTHESIA FACIAL ( 10 FDA reports)
HYPOPHOSPHATAEMIA ( 10 FDA reports)
HYPOTONIA ( 10 FDA reports)
INJECTION SITE URTICARIA ( 10 FDA reports)
INTESTINAL HAEMORRHAGE ( 10 FDA reports)
LIMB DEFORMITY ( 10 FDA reports)
LUNG CONSOLIDATION ( 10 FDA reports)
LUNG INFECTION ( 10 FDA reports)
LYMPHADENITIS ( 10 FDA reports)
MAXILLOFACIAL OPERATION ( 10 FDA reports)
MEDICATION RESIDUE ( 10 FDA reports)
METASTASES TO ADRENALS ( 10 FDA reports)
METASTASES TO NECK ( 10 FDA reports)
METASTASES TO THE MEDIASTINUM ( 10 FDA reports)
MUSCLE DISORDER ( 10 FDA reports)
NASAL DRYNESS ( 10 FDA reports)
NO THERAPEUTIC RESPONSE ( 10 FDA reports)
OCULAR ICTERUS ( 10 FDA reports)
ONYCHOCLASIS ( 10 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 10 FDA reports)
OPTIC NEURITIS ( 10 FDA reports)
OROANTRAL FISTULA ( 10 FDA reports)
PAPILLOEDEMA ( 10 FDA reports)
PARAESTHESIA ORAL ( 10 FDA reports)
PENIS DISORDER ( 10 FDA reports)
PERIODONTAL INFECTION ( 10 FDA reports)
PERIODONTAL OPERATION ( 10 FDA reports)
PERONEAL NERVE PALSY ( 10 FDA reports)
POLYURIA ( 10 FDA reports)
PREMATURE LABOUR ( 10 FDA reports)
PROTEIN TOTAL DECREASED ( 10 FDA reports)
PULMONARY INFARCTION ( 10 FDA reports)
PULPITIS DENTAL ( 10 FDA reports)
RADICULAR SYNDROME ( 10 FDA reports)
RED BLOOD CELL ABNORMALITY ( 10 FDA reports)
SCAB ( 10 FDA reports)
SCREAMING ( 10 FDA reports)
SECRETION DISCHARGE ( 10 FDA reports)
SINUS RHYTHM ( 10 FDA reports)
SKIN IRRITATION ( 10 FDA reports)
STEVENS-JOHNSON SYNDROME ( 10 FDA reports)
SUBSTANCE ABUSE ( 10 FDA reports)
SUDDEN DEATH ( 10 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 10 FDA reports)
THERMAL BURN ( 10 FDA reports)
TOOTH IMPACTED ( 10 FDA reports)
URETHRAL STRICTURE ( 10 FDA reports)
VASCULAR OCCLUSION ( 10 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 10 FDA reports)
VITAMIN D ABNORMAL ( 10 FDA reports)
VITAMIN D DECREASED ( 10 FDA reports)
ABSCESS LIMB ( 9 FDA reports)
ACANTHOLYSIS ( 9 FDA reports)
ADNEXA UTERI MASS ( 9 FDA reports)
AFFECTIVE DISORDER ( 9 FDA reports)
APLASTIC ANAEMIA ( 9 FDA reports)
ARTERIOSPASM CORONARY ( 9 FDA reports)
ARTHRITIS BACTERIAL ( 9 FDA reports)
ARTHROPOD BITE ( 9 FDA reports)
AXILLARY MASS ( 9 FDA reports)
BLADDER NECK SCLEROSIS ( 9 FDA reports)
BODY TEMPERATURE DECREASED ( 9 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 9 FDA reports)
BRADYKINESIA ( 9 FDA reports)
BREAST ENLARGEMENT ( 9 FDA reports)
BRONCHOPNEUMONIA ( 9 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 9 FDA reports)
CARTILAGE ATROPHY ( 9 FDA reports)
CERVICAL DYSPLASIA ( 9 FDA reports)
CHOLESTASIS ( 9 FDA reports)
CONTRAST MEDIA REACTION ( 9 FDA reports)
CYSTOPEXY ( 9 FDA reports)
DERMATITIS ALLERGIC ( 9 FDA reports)
DIVERTICULAR PERFORATION ( 9 FDA reports)
DRUG SCREEN POSITIVE ( 9 FDA reports)
ENCEPHALITIS ( 9 FDA reports)
EPICONDYLITIS ( 9 FDA reports)
ESCHERICHIA BACTERAEMIA ( 9 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 9 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 9 FDA reports)
GENERALISED ANXIETY DISORDER ( 9 FDA reports)
HALLUCINATION, VISUAL ( 9 FDA reports)
HEPATIC ENCEPHALOPATHY ( 9 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 9 FDA reports)
HYPOCOAGULABLE STATE ( 9 FDA reports)
INCOHERENT ( 9 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 9 FDA reports)
INFUSION SITE IRRITATION ( 9 FDA reports)
INJECTION SITE WARMTH ( 9 FDA reports)
INTRAOCULAR LENS IMPLANT ( 9 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 9 FDA reports)
JOINT CONTRACTURE ( 9 FDA reports)
MUCOUS STOOLS ( 9 FDA reports)
MULTIPLE DRUG OVERDOSE ( 9 FDA reports)
MUSCLE FATIGUE ( 9 FDA reports)
MYELOPATHY ( 9 FDA reports)
MYOMECTOMY ( 9 FDA reports)
NAIL DISORDER ( 9 FDA reports)
NASAL SEPTUM DEVIATION ( 9 FDA reports)
NEUROGENIC BLADDER ( 9 FDA reports)
NICOTINE DEPENDENCE ( 9 FDA reports)
NO ADVERSE EVENT ( 9 FDA reports)
NODULE ( 9 FDA reports)
OCULAR HYPERAEMIA ( 9 FDA reports)
OSTEOMYELITIS CHRONIC ( 9 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 9 FDA reports)
PANCREATIC CARCINOMA ( 9 FDA reports)
POLYPECTOMY ( 9 FDA reports)
POSTURE ABNORMAL ( 9 FDA reports)
PRESBYACUSIS ( 9 FDA reports)
PRESCRIBED OVERDOSE ( 9 FDA reports)
PURULENCE ( 9 FDA reports)
RALES ( 9 FDA reports)
RASH MACULO-PAPULAR ( 9 FDA reports)
RECTAL POLYP ( 9 FDA reports)
RESPIRATORY TRACT INFECTION ( 9 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 9 FDA reports)
SALPINGITIS ( 9 FDA reports)
SERUM SICKNESS ( 9 FDA reports)
SKIN INFECTION ( 9 FDA reports)
SPINAL HAEMANGIOMA ( 9 FDA reports)
STREPTOCOCCAL INFECTION ( 9 FDA reports)
SUBRETINAL FIBROSIS ( 9 FDA reports)
TENDON INJURY ( 9 FDA reports)
TINEA CRURIS ( 9 FDA reports)
TONGUE INJURY ( 9 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 9 FDA reports)
UROSEPSIS ( 9 FDA reports)
VARICOSE VEIN ( 9 FDA reports)
ABDOMINAL ADHESIONS ( 8 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 8 FDA reports)
ACUTE HEPATIC FAILURE ( 8 FDA reports)
AGORAPHOBIA ( 8 FDA reports)
APPENDIX DISORDER ( 8 FDA reports)
ASEPTIC NECROSIS BONE ( 8 FDA reports)
BIOPSY ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 8 FDA reports)
BLOODY DISCHARGE ( 8 FDA reports)
BONE NEOPLASM MALIGNANT ( 8 FDA reports)
BONE SCAN ABNORMAL ( 8 FDA reports)
BRAIN DEATH ( 8 FDA reports)
BRAIN INJURY ( 8 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 8 FDA reports)
CEREBELLAR ATROPHY ( 8 FDA reports)
CHOLECYSTITIS INFECTIVE ( 8 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 8 FDA reports)
CLAUSTROPHOBIA ( 8 FDA reports)
CLUSTER HEADACHE ( 8 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 8 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 8 FDA reports)
CSF SHUNT REMOVAL ( 8 FDA reports)
CYSTITIS INTERSTITIAL ( 8 FDA reports)
DRUG ABUSER ( 8 FDA reports)
DRUG TOLERANCE ( 8 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 8 FDA reports)
EXERCISE LACK OF ( 8 FDA reports)
EXFOLIATIVE RASH ( 8 FDA reports)
EYE DISCHARGE ( 8 FDA reports)
EYELID PTOSIS ( 8 FDA reports)
FRUSTRATION ( 8 FDA reports)
GASTROINTESTINAL PAIN ( 8 FDA reports)
GRAND MAL CONVULSION ( 8 FDA reports)
HEAD DISCOMFORT ( 8 FDA reports)
HEART RATE ABNORMAL ( 8 FDA reports)
HYPERCOAGULATION ( 8 FDA reports)
HYPERCORTICOIDISM ( 8 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 8 FDA reports)
HYPERTRANSAMINASAEMIA ( 8 FDA reports)
IMPAIRED FASTING GLUCOSE ( 8 FDA reports)
INCISIONAL HERNIA ( 8 FDA reports)
INJECTION SITE NODULE ( 8 FDA reports)
INNER EAR DISORDER ( 8 FDA reports)
INTENTIONAL OVERDOSE ( 8 FDA reports)
INTERMITTENT CLAUDICATION ( 8 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 8 FDA reports)
LYMPHADENECTOMY ( 8 FDA reports)
MACULOPATHY ( 8 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 8 FDA reports)
MENIERE'S DISEASE ( 8 FDA reports)
MITRAL VALVE STENOSIS ( 8 FDA reports)
MULTIPLE ALLERGIES ( 8 FDA reports)
MUSCLE RUPTURE ( 8 FDA reports)
NEPHROPATHY TOXIC ( 8 FDA reports)
NEUROPATHIC ARTHROPATHY ( 8 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 8 FDA reports)
OCCULT BLOOD POSITIVE ( 8 FDA reports)
ORAL CAVITY FISTULA ( 8 FDA reports)
PAPILLOMA ( 8 FDA reports)
PARAPROTEINAEMIA ( 8 FDA reports)
PETECHIAE ( 8 FDA reports)
PNEUMONIA BACTERIAL ( 8 FDA reports)
POSTOPERATIVE FEVER ( 8 FDA reports)
PROSTATIC DISORDER ( 8 FDA reports)
PROTEIN S DEFICIENCY ( 8 FDA reports)
PSORIATIC ARTHROPATHY ( 8 FDA reports)
ROTATOR CUFF REPAIR ( 8 FDA reports)
SCOTOMA ( 8 FDA reports)
SHUNT INFECTION ( 8 FDA reports)
SJOGREN'S SYNDROME ( 8 FDA reports)
SKIN ATROPHY ( 8 FDA reports)
SOFT TISSUE MASS ( 8 FDA reports)
SOMNAMBULISM ( 8 FDA reports)
SPINAL FUSION SURGERY ( 8 FDA reports)
SPONDYLITIS ( 8 FDA reports)
SUBDURAL HAEMATOMA ( 8 FDA reports)
TACHYPNOEA ( 8 FDA reports)
TESTICULAR ATROPHY ( 8 FDA reports)
THYROID CYST ( 8 FDA reports)
TONGUE BITING ( 8 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 8 FDA reports)
URINE ODOUR ABNORMAL ( 8 FDA reports)
VAGINAL FISTULA ( 8 FDA reports)
XEROSIS ( 8 FDA reports)
ABNORMAL FAECES ( 7 FDA reports)
ABORTION SPONTANEOUS ( 7 FDA reports)
AEROPHAGIA ( 7 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 7 FDA reports)
AMMONIA INCREASED ( 7 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 7 FDA reports)
AORTIC VALVE SCLEROSIS ( 7 FDA reports)
AREFLEXIA ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 7 FDA reports)
BIOPSY BONE ( 7 FDA reports)
BLADDER DISCOMFORT ( 7 FDA reports)
BLOOD CULTURE POSITIVE ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
BRAIN MASS ( 7 FDA reports)
BREAKTHROUGH PAIN ( 7 FDA reports)
BREAST OPERATION ( 7 FDA reports)
CALCULUS URETERIC ( 7 FDA reports)
CHEST WALL PAIN ( 7 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 7 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 7 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 7 FDA reports)
CUSHINGOID ( 7 FDA reports)
DELUSION ( 7 FDA reports)
DEMYELINATION ( 7 FDA reports)
DRUG DISPENSING ERROR ( 7 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 7 FDA reports)
EAR PRURITUS ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 7 FDA reports)
EXERCISE TOLERANCE DECREASED ( 7 FDA reports)
EXPIRED DRUG ADMINISTERED ( 7 FDA reports)
EXTRAVASATION ( 7 FDA reports)
FLUID INTAKE REDUCED ( 7 FDA reports)
FOREIGN BODY ( 7 FDA reports)
GASTRIC BYPASS ( 7 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 7 FDA reports)
GASTROINTESTINAL INFECTION ( 7 FDA reports)
GRIEF REACTION ( 7 FDA reports)
GRIMACING ( 7 FDA reports)
GUN SHOT WOUND ( 7 FDA reports)
HAEMOGLOBIN INCREASED ( 7 FDA reports)
HALLUCINATION, AUDITORY ( 7 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 7 FDA reports)
HORMONE LEVEL ABNORMAL ( 7 FDA reports)
HYDROCEPHALUS ( 7 FDA reports)
HYPERBILIRUBINAEMIA ( 7 FDA reports)
HYPERCHLORHYDRIA ( 7 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 7 FDA reports)
HYPERREFLEXIA ( 7 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 7 FDA reports)
HYPERVENTILATION ( 7 FDA reports)
IMPAIRED REASONING ( 7 FDA reports)
INTENTIONAL MISUSE ( 7 FDA reports)
JAUNDICE CHOLESTATIC ( 7 FDA reports)
KIDNEY MALROTATION ( 7 FDA reports)
LACTIC ACIDOSIS ( 7 FDA reports)
LARGE INTESTINAL ULCER ( 7 FDA reports)
LEFT VENTRICULAR FAILURE ( 7 FDA reports)
LEUKAEMIA ( 7 FDA reports)
LIBIDO INCREASED ( 7 FDA reports)
LIPIDS INCREASED ( 7 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 7 FDA reports)
LYMPHOMA ( 7 FDA reports)
MASTOIDITIS ( 7 FDA reports)
MENINGITIS ( 7 FDA reports)
MENOPAUSE ( 7 FDA reports)
METRORRHAGIA ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 7 FDA reports)
MUSCLE INJURY ( 7 FDA reports)
MYDRIASIS ( 7 FDA reports)
MYELOMA RECURRENCE ( 7 FDA reports)
NEOPLASM ( 7 FDA reports)
NEPHROSCLEROSIS ( 7 FDA reports)
NONSPECIFIC REACTION ( 7 FDA reports)
OESOPHAGEAL SPASM ( 7 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 7 FDA reports)
OSTEOCHONDROSIS ( 7 FDA reports)
OTITIS EXTERNA ( 7 FDA reports)
PAIN OF SKIN ( 7 FDA reports)
PANCREATIC INSUFFICIENCY ( 7 FDA reports)
PARESIS ( 7 FDA reports)
PHLEBITIS ( 7 FDA reports)
PITTING OEDEMA ( 7 FDA reports)
POST HERPETIC NEURALGIA ( 7 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 7 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 7 FDA reports)
PROCEDURAL HAEMORRHAGE ( 7 FDA reports)
PROCEDURAL NAUSEA ( 7 FDA reports)
PROCEDURAL VOMITING ( 7 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 7 FDA reports)
QRS AXIS ABNORMAL ( 7 FDA reports)
RADICULITIS ( 7 FDA reports)
REFLUX LARYNGITIS ( 7 FDA reports)
RENAL CELL CARCINOMA ( 7 FDA reports)
RESUSCITATION ( 7 FDA reports)
RHONCHI ( 7 FDA reports)
RIGHT VENTRICULAR FAILURE ( 7 FDA reports)
SEBORRHOEA ( 7 FDA reports)
SINUS ARRHYTHMIA ( 7 FDA reports)
SKIN WRINKLING ( 7 FDA reports)
SPONDYLITIC MYELOPATHY ( 7 FDA reports)
STEM CELL TRANSPLANT ( 7 FDA reports)
THROMBOCYTHAEMIA ( 7 FDA reports)
TONGUE DISCOLOURATION ( 7 FDA reports)
ULCERATIVE KERATITIS ( 7 FDA reports)
VAGINAL LEUKOPLAKIA ( 7 FDA reports)
VAGINAL ULCERATION ( 7 FDA reports)
VITREOUS DEGENERATION ( 7 FDA reports)
VOCAL CORD CYST ( 7 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 7 FDA reports)
WOUND INFECTION ( 7 FDA reports)
ABSCESS NECK ( 6 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 6 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 6 FDA reports)
ALCOHOL ABUSE ( 6 FDA reports)
ALCOHOL USE ( 6 FDA reports)
ANAL FISSURE ( 6 FDA reports)
ANAL SPHINCTER ATONY ( 6 FDA reports)
ANOXIC ENCEPHALOPATHY ( 6 FDA reports)
AORTIC DILATATION ( 6 FDA reports)
AORTIC VALVE CALCIFICATION ( 6 FDA reports)
APPLICATION SITE IRRITATION ( 6 FDA reports)
ATRIAL TACHYCARDIA ( 6 FDA reports)
ATROPHIC VULVOVAGINITIS ( 6 FDA reports)
BIPOLAR II DISORDER ( 6 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 6 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 6 FDA reports)
BONE CYST ( 6 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CARTILAGE INJURY ( 6 FDA reports)
CEREBRAL HAEMATOMA ( 6 FDA reports)
CHEILITIS ( 6 FDA reports)
COLLAPSE OF LUNG ( 6 FDA reports)
CONJUNCTIVAL ABRASION ( 6 FDA reports)
DENTAL DISCOMFORT ( 6 FDA reports)
DENTAL OPERATION ( 6 FDA reports)
DEVICE RELATED INFECTION ( 6 FDA reports)
DISEASE COMPLICATION ( 6 FDA reports)
DRUG EFFECT INCREASED ( 6 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
DRUG LEVEL INCREASED ( 6 FDA reports)
DYSGRAPHIA ( 6 FDA reports)
EAR DISORDER ( 6 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 6 FDA reports)
ELECTROPHORESIS ABNORMAL ( 6 FDA reports)
ENDARTERECTOMY ( 6 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 6 FDA reports)
ESCHERICHIA INFECTION ( 6 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 6 FDA reports)
FEELINGS OF WORTHLESSNESS ( 6 FDA reports)
FIBRIN D DIMER INCREASED ( 6 FDA reports)
FOOD INTOLERANCE ( 6 FDA reports)
FOREIGN BODY TRAUMA ( 6 FDA reports)
FRACTURED COCCYX ( 6 FDA reports)
FUNGAL SKIN INFECTION ( 6 FDA reports)
FURUNCLE ( 6 FDA reports)
GALLBLADDER OPERATION ( 6 FDA reports)
GLIOSIS ( 6 FDA reports)
GRANULOMA ( 6 FDA reports)
HANGOVER ( 6 FDA reports)
HEPATITIS VIRAL ( 6 FDA reports)
HEPATOTOXICITY ( 6 FDA reports)
HERNIA REPAIR ( 6 FDA reports)
HODGKIN'S DISEASE ( 6 FDA reports)
HYPERTENSIVE CRISIS ( 6 FDA reports)
HYPOREFLEXIA ( 6 FDA reports)
HYPOVOLAEMIC SHOCK ( 6 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 6 FDA reports)
INCISIONAL DRAINAGE ( 6 FDA reports)
INJECTION SITE CELLULITIS ( 6 FDA reports)
INJECTION SITE DISCOLOURATION ( 6 FDA reports)
KLEBSIELLA TEST POSITIVE ( 6 FDA reports)
LATEX ALLERGY ( 6 FDA reports)
LIMB OPERATION ( 6 FDA reports)
LIPASE INCREASED ( 6 FDA reports)
LIVER TRANSPLANT REJECTION ( 6 FDA reports)
LOCALISED OSTEOARTHRITIS ( 6 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 6 FDA reports)
MACULAR OEDEMA ( 6 FDA reports)
MACULAR SCAR ( 6 FDA reports)
MALABSORPTION ( 6 FDA reports)
MALIGNANT MELANOMA ( 6 FDA reports)
MERALGIA PARAESTHETICA ( 6 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 6 FDA reports)
MONARTHRITIS ( 6 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 6 FDA reports)
MUSCLE RIGIDITY ( 6 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 6 FDA reports)
NEUROTOXICITY ( 6 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 6 FDA reports)
OESOPHAGITIS ULCERATIVE ( 6 FDA reports)
OSTECTOMY ( 6 FDA reports)
OSTEOPOROTIC FRACTURE ( 6 FDA reports)
OVARIAN CANCER ( 6 FDA reports)
PANCREATIC DISORDER ( 6 FDA reports)
PERITONITIS ( 6 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 6 FDA reports)
PO2 DECREASED ( 6 FDA reports)
PORTAL HYPERTENSION ( 6 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 6 FDA reports)
POST PROCEDURAL CONSTIPATION ( 6 FDA reports)
PREGNANCY ( 6 FDA reports)
PROCEDURAL COMPLICATION ( 6 FDA reports)
PROSTATIC OBSTRUCTION ( 6 FDA reports)
PSYCHOLOGICAL TRAUMA ( 6 FDA reports)
PUBIS FRACTURE ( 6 FDA reports)
PUPIL FIXED ( 6 FDA reports)
RADICULAR PAIN ( 6 FDA reports)
RECTAL ABSCESS ( 6 FDA reports)
RECURRENT CANCER ( 6 FDA reports)
RETICULOCYTE COUNT INCREASED ( 6 FDA reports)
RETINOPATHY HYPERTENSIVE ( 6 FDA reports)
RHEUMATIC HEART DISEASE ( 6 FDA reports)
SENSATION OF PRESSURE ( 6 FDA reports)
SERUM FERRITIN INCREASED ( 6 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 6 FDA reports)
SKIN DISCOMFORT ( 6 FDA reports)
SLEEP WALKING ( 6 FDA reports)
SOCIAL PROBLEM ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
SUBMANDIBULAR MASS ( 6 FDA reports)
SUDDEN CARDIAC DEATH ( 6 FDA reports)
SUICIDAL BEHAVIOUR ( 6 FDA reports)
SYNCOPE VASOVAGAL ( 6 FDA reports)
TENDON PAIN ( 6 FDA reports)
TENSION ( 6 FDA reports)
TRANSAMINASES INCREASED ( 6 FDA reports)
TUNNEL VISION ( 6 FDA reports)
URETHRAL DISORDER ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
VARICES OESOPHAGEAL ( 6 FDA reports)
VASCULAR PSEUDOANEURYSM ( 6 FDA reports)
VASOSPASM ( 6 FDA reports)
VENOUS THROMBOSIS ( 6 FDA reports)
VIITH NERVE PARALYSIS ( 6 FDA reports)
VOCAL CORD DISORDER ( 6 FDA reports)
WOUND SECRETION ( 6 FDA reports)
X-RAY ABNORMAL ( 6 FDA reports)
ABDOMINAL INFECTION ( 5 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 5 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 5 FDA reports)
ABSCESS INTESTINAL ( 5 FDA reports)
ACETABULUM FRACTURE ( 5 FDA reports)
ACUTE PRERENAL FAILURE ( 5 FDA reports)
AMYLOIDOSIS ( 5 FDA reports)
ANGIONEUROTIC OEDEMA ( 5 FDA reports)
ANKYLOSING SPONDYLITIS ( 5 FDA reports)
AORTIC CALCIFICATION ( 5 FDA reports)
AORTIC DISORDER ( 5 FDA reports)
ARTHRITIS INFECTIVE ( 5 FDA reports)
ATHEROSCLEROSIS ( 5 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 5 FDA reports)
AURICULAR SWELLING ( 5 FDA reports)
AUTOIMMUNE DISORDER ( 5 FDA reports)
BIOPSY BONE ABNORMAL ( 5 FDA reports)
BLADDER PAIN ( 5 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 5 FDA reports)
BLOOD IRON INCREASED ( 5 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 5 FDA reports)
BLOOD SODIUM INCREASED ( 5 FDA reports)
BONE DENSITY INCREASED ( 5 FDA reports)
BONE TRIMMING ( 5 FDA reports)
BOTULISM ( 5 FDA reports)
BRONCHIOLITIS ( 5 FDA reports)
CALCIUM METABOLISM DISORDER ( 5 FDA reports)
CALCULUS URETHRAL ( 5 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 5 FDA reports)
CATARACT CORTICAL ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 5 FDA reports)
CEREBROVASCULAR DISORDER ( 5 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 5 FDA reports)
CHONDROPLASTY ( 5 FDA reports)
CHONDROSARCOMA ( 5 FDA reports)
CITROBACTER INFECTION ( 5 FDA reports)
CLOSTRIDIUM COLITIS ( 5 FDA reports)
COMMUNICATION DISORDER ( 5 FDA reports)
CONCUSSION ( 5 FDA reports)
CRANIAL NERVE PARALYSIS ( 5 FDA reports)
CREPITATIONS ( 5 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
DEVICE DISLOCATION ( 5 FDA reports)
DISSEMINATED TUBERCULOSIS ( 5 FDA reports)
DYSAESTHESIA ( 5 FDA reports)
DYSKINESIA OESOPHAGEAL ( 5 FDA reports)
DYSTHYMIC DISORDER ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 5 FDA reports)
EMBOLISM VENOUS ( 5 FDA reports)
ENCEPHALITIS HERPES ( 5 FDA reports)
ENTEROCOCCAL INFECTION ( 5 FDA reports)
EROSIVE DUODENITIS ( 5 FDA reports)
ERYTHEMA MULTIFORME ( 5 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 5 FDA reports)
EXCESSIVE EYE BLINKING ( 5 FDA reports)
EYELID DISORDER ( 5 FDA reports)
FACE INJURY ( 5 FDA reports)
FASCIITIS ( 5 FDA reports)
FEELING DRUNK ( 5 FDA reports)
FINGER DEFORMITY ( 5 FDA reports)
FOOD ALLERGY ( 5 FDA reports)
FRACTURED SACRUM ( 5 FDA reports)
GALLBLADDER PAIN ( 5 FDA reports)
GINGIVAL HYPERPLASIA ( 5 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 5 FDA reports)
HAIR TEXTURE ABNORMAL ( 5 FDA reports)
HEAT RASH ( 5 FDA reports)
HELICOBACTER TEST POSITIVE ( 5 FDA reports)
HEPATITIS ACUTE ( 5 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 5 FDA reports)
HUNGER ( 5 FDA reports)
HYPERADRENOCORTICISM ( 5 FDA reports)
HYPERAESTHESIA ( 5 FDA reports)
HYPERSEXUALITY ( 5 FDA reports)
HYPERTENSIVE EMERGENCY ( 5 FDA reports)
HYPOVENTILATION ( 5 FDA reports)
IMMUNOSUPPRESSION ( 5 FDA reports)
IMPAIRED SELF-CARE ( 5 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
INFECTED DERMAL CYST ( 5 FDA reports)
INJECTION SITE MASS ( 5 FDA reports)
INJECTION SITE VESICLES ( 5 FDA reports)
INTENTIONAL SELF-INJURY ( 5 FDA reports)
KIDNEY ENLARGEMENT ( 5 FDA reports)
KLEBSIELLA INFECTION ( 5 FDA reports)
LIMB CRUSHING INJURY ( 5 FDA reports)
LIPOMATOSIS ( 5 FDA reports)
LOOSE STOOLS ( 5 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
LUPUS PNEUMONITIS ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
MELANOCYTIC NAEVUS ( 5 FDA reports)
MENINGITIS ASEPTIC ( 5 FDA reports)
METABOLIC SYNDROME ( 5 FDA reports)
MICROCYTIC ANAEMIA ( 5 FDA reports)
MIGRAINE WITH AURA ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MORTON'S NEUROMA ( 5 FDA reports)
MUCOSAL ULCERATION ( 5 FDA reports)
MUSCLE HAEMORRHAGE ( 5 FDA reports)
MYELITIS ( 5 FDA reports)
NAIL BED BLEEDING ( 5 FDA reports)
NARCOLEPSY ( 5 FDA reports)
NECK INJURY ( 5 FDA reports)
NEPHROPATHY ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
NEUTROPHIL COUNT INCREASED ( 5 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 5 FDA reports)
OESOPHAGEAL RUPTURE ( 5 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 5 FDA reports)
ORAL MUCOSAL BLISTERING ( 5 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 5 FDA reports)
ORGAN FAILURE ( 5 FDA reports)
OSTEITIS DEFORMANS ( 5 FDA reports)
OVERWEIGHT ( 5 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 5 FDA reports)
PANCREATIC CYST ( 5 FDA reports)
PANCREATITIS RELAPSING ( 5 FDA reports)
PARASITE BLOOD TEST POSITIVE ( 5 FDA reports)
PARKINSONISM ( 5 FDA reports)
PCO2 DECREASED ( 5 FDA reports)
PENILE HAEMORRHAGE ( 5 FDA reports)
PERIRECTAL ABSCESS ( 5 FDA reports)
PEYRONIE'S DISEASE ( 5 FDA reports)
PHARYNGEAL ERYTHEMA ( 5 FDA reports)
POLYARTHRITIS ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 5 FDA reports)
POST LAMINECTOMY SYNDROME ( 5 FDA reports)
POST PROCEDURAL INFECTION ( 5 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 5 FDA reports)
PROCEDURAL SITE REACTION ( 5 FDA reports)
PRODUCT ADHESION ISSUE ( 5 FDA reports)
PROSTHESIS USER ( 5 FDA reports)
QUALITY OF LIFE DECREASED ( 5 FDA reports)
RASH VESICULAR ( 5 FDA reports)
RECTAL ADENOMA ( 5 FDA reports)
REGURGITATION ( 5 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 5 FDA reports)
RESPIRATION ABNORMAL ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
RICKETTSIOSIS ( 5 FDA reports)
SALIVARY HYPERSECRETION ( 5 FDA reports)
SELF-INJURIOUS IDEATION ( 5 FDA reports)
SLOW SPEECH ( 5 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 5 FDA reports)
SOFT TISSUE INJURY ( 5 FDA reports)
SPINAL CORD INFECTION ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 5 FDA reports)
STRESS INCONTINENCE ( 5 FDA reports)
STRESS SYMPTOMS ( 5 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 5 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 5 FDA reports)
TEARFULNESS ( 5 FDA reports)
TEMPERATURE INTOLERANCE ( 5 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 5 FDA reports)
TOE OPERATION ( 5 FDA reports)
TOTAL LUNG CAPACITY INCREASED ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 5 FDA reports)
URINE CALCIUM INCREASED ( 5 FDA reports)
UTERINE POLYP ( 5 FDA reports)
VOCAL CORD INFLAMMATION ( 5 FDA reports)
WALKING AID USER ( 5 FDA reports)
WRONG DRUG ADMINISTERED ( 5 FDA reports)
ABDOMINAL MASS ( 4 FDA reports)
ABDOMINAL SYMPTOM ( 4 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 4 FDA reports)
ABORTION ( 4 FDA reports)
ACROCHORDON ( 4 FDA reports)
ADRENAL ADENOMA ( 4 FDA reports)
ADRENAL DISORDER ( 4 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
ANGIOPLASTY ( 4 FDA reports)
ANIMAL BITE ( 4 FDA reports)
ANION GAP INCREASED ( 4 FDA reports)
ANKLE OPERATION ( 4 FDA reports)
ANORECTAL DISCOMFORT ( 4 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
AORTIC ATHEROSCLEROSIS ( 4 FDA reports)
APLASIA PURE RED CELL ( 4 FDA reports)
APPLICATION SITE PAIN ( 4 FDA reports)
ATROPHY ( 4 FDA reports)
BACTERIA URINE IDENTIFIED ( 4 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 4 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
BINGE EATING ( 4 FDA reports)
BIOPSY BREAST ( 4 FDA reports)
BLADDER PROLAPSE ( 4 FDA reports)
BLEPHAROSPASM ( 4 FDA reports)
BLOOD CHLORIDE INCREASED ( 4 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 4 FDA reports)
BLOOD PROLACTIN INCREASED ( 4 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BLOOD URINE ( 4 FDA reports)
BONE GRAFT ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
BREAST CANCER IN SITU ( 4 FDA reports)
BREAST CELLULITIS ( 4 FDA reports)
BREAST DISCHARGE ( 4 FDA reports)
BREAST FIBROSIS ( 4 FDA reports)
BREAST LUMP REMOVAL ( 4 FDA reports)
BREATH SOUNDS ABNORMAL ( 4 FDA reports)
BRONCHIECTASIS ( 4 FDA reports)
CARCINOID TUMOUR ( 4 FDA reports)
CARCINOMA ( 4 FDA reports)
CARDIAC AMYLOIDOSIS ( 4 FDA reports)
CARDIAC ENZYMES INCREASED ( 4 FDA reports)
CARDIAC INFECTION ( 4 FDA reports)
CARDIAC OPERATION ( 4 FDA reports)
CAROTID ENDARTERECTOMY ( 4 FDA reports)
CATHETER RELATED COMPLICATION ( 4 FDA reports)
CENTRAL LINE INFECTION ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM MASS ( 4 FDA reports)
CHANGE OF BOWEL HABIT ( 4 FDA reports)
CHONDROLYSIS ( 4 FDA reports)
CHOREA ( 4 FDA reports)
CHRONIC FATIGUE SYNDROME ( 4 FDA reports)
CLONUS ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 4 FDA reports)
COR PULMONALE ( 4 FDA reports)
CORONARY ARTERY BYPASS ( 4 FDA reports)
DENTURE WEARER ( 4 FDA reports)
DERMATITIS PSORIASIFORM ( 4 FDA reports)
DERMOID CYST ( 4 FDA reports)
DEVICE MISUSE ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
DIARRHOEA INFECTIOUS ( 4 FDA reports)
DISINHIBITION ( 4 FDA reports)
DISLOCATION OF VERTEBRA ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 4 FDA reports)
DYSMENORRHOEA ( 4 FDA reports)
DYSPHASIA ( 4 FDA reports)
DYSPNOEA AT REST ( 4 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 4 FDA reports)
ENZYME ABNORMALITY ( 4 FDA reports)
EXCESSIVE MASTURBATION ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
FACIAL NERVE DISORDER ( 4 FDA reports)
FACIAL SPASM ( 4 FDA reports)
FAILURE TO THRIVE ( 4 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 4 FDA reports)
FORMICATION ( 4 FDA reports)
FUNGAL RASH ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GASTROINTESTINAL SURGERY ( 4 FDA reports)
GENERAL SYMPTOM ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GINGIVECTOMY ( 4 FDA reports)
GLYCOSURIA ( 4 FDA reports)
GRAVITATIONAL OEDEMA ( 4 FDA reports)
GYNAECOMASTIA ( 4 FDA reports)
H1N1 INFLUENZA ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HAIR GROWTH ABNORMAL ( 4 FDA reports)
HEART VALVE INCOMPETENCE ( 4 FDA reports)
HEAT STROKE ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATIC ENZYME ABNORMAL ( 4 FDA reports)
HEPATIC HAEMATOMA ( 4 FDA reports)
HOMICIDAL IDEATION ( 4 FDA reports)
HYPERPROLACTINAEMIA ( 4 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 4 FDA reports)
HYPOPROTEINAEMIA ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
INFUSION SITE ERYTHEMA ( 4 FDA reports)
INFUSION SITE PAIN ( 4 FDA reports)
INJECTION SITE BURNING ( 4 FDA reports)
INJECTION SITE EXTRAVASATION ( 4 FDA reports)
INJECTION SITE INDURATION ( 4 FDA reports)
INJECTION SITE INFECTION ( 4 FDA reports)
INJECTION SITE NECROSIS ( 4 FDA reports)
INTESTINAL FISTULA ( 4 FDA reports)
INTESTINAL HYPOMOTILITY ( 4 FDA reports)
INTESTINAL MUCOSAL ATROPHY ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
ISCHAEMIC NEPHROPATHY ( 4 FDA reports)
ISCHAEMIC ULCER ( 4 FDA reports)
JOINT ARTHROPLASTY ( 4 FDA reports)
JOINT LOCK ( 4 FDA reports)
KYPHOSCOLIOSIS ( 4 FDA reports)
LIP DRY ( 4 FDA reports)
LIP HAEMORRHAGE ( 4 FDA reports)
LIPOHYPERTROPHY ( 4 FDA reports)
LOGORRHOEA ( 4 FDA reports)
LOOSE BODY IN JOINT ( 4 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 4 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 4 FDA reports)
MASKED FACIES ( 4 FDA reports)
MENSTRUAL DISORDER ( 4 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 4 FDA reports)
METASTASES TO LYMPH NODES ( 4 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 4 FDA reports)
MIDDLE EAR EFFUSION ( 4 FDA reports)
MONOPLEGIA ( 4 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 4 FDA reports)
MULTI-ORGAN DISORDER ( 4 FDA reports)
MUSCLE SPASTICITY ( 4 FDA reports)
MYOCLONUS ( 4 FDA reports)
NAIL INFECTION ( 4 FDA reports)
NASAL DISCOMFORT ( 4 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
NEGATIVE THOUGHTS ( 4 FDA reports)
NEUROMYELITIS OPTICA ( 4 FDA reports)
NODULE ON EXTREMITY ( 4 FDA reports)
NORMAL NEWBORN ( 4 FDA reports)
OBSTRUCTION ( 4 FDA reports)
OBSTRUCTIVE UROPATHY ( 4 FDA reports)
OESOPHAGEAL ACHALASIA ( 4 FDA reports)
OESTROGEN DEFICIENCY ( 4 FDA reports)
OPTIC ATROPHY ( 4 FDA reports)
OPTIC NEUROPATHY ( 4 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 4 FDA reports)
PAINFUL DEFAECATION ( 4 FDA reports)
PANCREATIC PSEUDOCYST ( 4 FDA reports)
PANCREATITIS NECROTISING ( 4 FDA reports)
PAPILLARY THYROID CANCER ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PAROSMIA ( 4 FDA reports)
PENILE PAIN ( 4 FDA reports)
PERICARDITIS LUPUS ( 4 FDA reports)
PERIORBITAL HAEMATOMA ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PHAGOPHOBIA ( 4 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 4 FDA reports)
PLATYBASIA ( 4 FDA reports)
PNEUMONIA KLEBSIELLA ( 4 FDA reports)
POOR PERIPHERAL CIRCULATION ( 4 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 4 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 4 FDA reports)
POSTOPERATIVE INFECTION ( 4 FDA reports)
PROLONGED LABOUR ( 4 FDA reports)
PROTRUSION TONGUE ( 4 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 4 FDA reports)
PULMONARY GRANULOMA ( 4 FDA reports)
RADIOTHERAPY ( 4 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 4 FDA reports)
RENAL CANCER METASTATIC ( 4 FDA reports)
RENAL MASS ( 4 FDA reports)
RENAL TRANSPLANT ( 4 FDA reports)
RESPIRATORY ACIDOSIS ( 4 FDA reports)
RESPIRATORY TRACT IRRITATION ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
RETINOPATHY ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
ROSACEA ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SCLERODERMA ( 4 FDA reports)
SKELETAL INJURY ( 4 FDA reports)
SKIN INJURY ( 4 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 4 FDA reports)
SMEAR CERVIX ABNORMAL ( 4 FDA reports)
SPLENIC VEIN THROMBOSIS ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
STOOL ANALYSIS ABNORMAL ( 4 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 4 FDA reports)
STUBBORNNESS ( 4 FDA reports)
SURGICAL FAILURE ( 4 FDA reports)
SYNOVIAL DISORDER ( 4 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 4 FDA reports)
TINEL'S SIGN ( 4 FDA reports)
TONGUE BLACK HAIRY ( 4 FDA reports)
TOOTH EROSION ( 4 FDA reports)
TOXIC ENCEPHALOPATHY ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
UNDERDOSE ( 4 FDA reports)
URINE FLOW DECREASED ( 4 FDA reports)
UTERINE CANCER ( 4 FDA reports)
VASCULAR CALCIFICATION ( 4 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 4 FDA reports)
VENA CAVA THROMBOSIS ( 4 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 4 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
ABDOMINAL ABSCESS ( 3 FDA reports)
ACCIDENT AT WORK ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ADDISON'S DISEASE ( 3 FDA reports)
ADENOCARCINOMA ( 3 FDA reports)
ADRENAL HAEMORRHAGE ( 3 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 3 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ALVEOLITIS ALLERGIC ( 3 FDA reports)
ANAEMIA MACROCYTIC ( 3 FDA reports)
ANAL PRURITUS ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANISOCYTOSIS ( 3 FDA reports)
ANOGENITAL WARTS ( 3 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
ANORGASMIA ( 3 FDA reports)
ANTIANDROGEN THERAPY ( 3 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 3 FDA reports)
AORTIC VALVE DISEASE ( 3 FDA reports)
APPARENT DEATH ( 3 FDA reports)
APPLICATION SITE BURNING ( 3 FDA reports)
ARTHROSCOPY ( 3 FDA reports)
ASTHENOPIA ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
BACTERIA URINE ( 3 FDA reports)
BELLIGERENCE ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
BILIARY TRACT DISORDER ( 3 FDA reports)
BLADDER NECK SUSPENSION ( 3 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 3 FDA reports)
BLOOD BLISTER ( 3 FDA reports)
BLOOD CREATINE ABNORMAL ( 3 FDA reports)
BLOOD IRON ABNORMAL ( 3 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
BONE LESION EXCISION ( 3 FDA reports)
BONE MARROW DISORDER ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BONE NEOPLASM ( 3 FDA reports)
BRACHIAL PLEXUS INJURY ( 3 FDA reports)
BRAIN CANCER METASTATIC ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BREAST CALCIFICATIONS ( 3 FDA reports)
BREAST CYST ( 3 FDA reports)
BREAST MICROCALCIFICATION ( 3 FDA reports)
BREAST SWELLING ( 3 FDA reports)
BUDD-CHIARI SYNDROME ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CARDIAC FIBRILLATION ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CAROTID ARTERY DISSECTION ( 3 FDA reports)
CATATONIA ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CEREBRAL DISORDER ( 3 FDA reports)
CEREBRAL THROMBOSIS ( 3 FDA reports)
CERVICAL POLYP ( 3 FDA reports)
CHEST WALL OPERATION ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
CHOLESTEATOMA ( 3 FDA reports)
COLLAGEN DISORDER ( 3 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 3 FDA reports)
CONGENITAL TONGUE ANOMALY ( 3 FDA reports)
CONJUNCTIVITIS VIRAL ( 3 FDA reports)
CONVERSION DISORDER ( 3 FDA reports)
CORNEAL OEDEMA ( 3 FDA reports)
CORNEAL OPERATION ( 3 FDA reports)
CORONARY ANGIOPLASTY ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
CORRECTIVE LENS USER ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CRYPTOCOCCOSIS ( 3 FDA reports)
CULTURE URINE POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DERMAL CYST ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
DIABETIC GASTROPARESIS ( 3 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DYSPLASIA ( 3 FDA reports)
DYSPLASTIC NAEVUS ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
ENERGY INCREASED ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
FEAR OF DISEASE ( 3 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 3 FDA reports)
FOLLICULITIS ( 3 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GASTROINTESTINAL NECROSIS ( 3 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 3 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 3 FDA reports)
GENITAL LESION ( 3 FDA reports)
GINGIVAL ABSCESS ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
HAEMOCHROMATOSIS ( 3 FDA reports)
HAIR COLOUR CHANGES ( 3 FDA reports)
HALO VISION ( 3 FDA reports)
HEART VALVE REPLACEMENT ( 3 FDA reports)
HEMIANOPIA ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 3 FDA reports)
HEPATIC HAEMORRHAGE ( 3 FDA reports)
HEPATIC MASS ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HEPATIC VEIN OCCLUSION ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
HIP DEFORMITY ( 3 FDA reports)
HYPERMETABOLISM ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
IATROGENIC INJURY ( 3 FDA reports)
ICHTHYOSIS ( 3 FDA reports)
ILEITIS ( 3 FDA reports)
INDURATION ( 3 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 3 FDA reports)
INSULIN RESISTANCE ( 3 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL STENOSIS ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
ISCHAEMIC HEPATITIS ( 3 FDA reports)
LEARNING DISORDER ( 3 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 3 FDA reports)
LIGAMENT DISORDER ( 3 FDA reports)
LIPIDS ABNORMAL ( 3 FDA reports)
LIVEDO RETICULARIS ( 3 FDA reports)
LIVER OPERATION ( 3 FDA reports)
LORDOSIS ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LOWER EXTREMITY MASS ( 3 FDA reports)
LUNG OPERATION ( 3 FDA reports)
MACROCYTOSIS ( 3 FDA reports)
MANTLE CELL LYMPHOMA ( 3 FDA reports)
MARITAL PROBLEM ( 3 FDA reports)
MEDICAL DIET ( 3 FDA reports)
MENINGITIS VIRAL ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
METASTASIS ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MYCOBACTERIAL INFECTION ( 3 FDA reports)
MYELITIS TRANSVERSE ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
NIPPLE DISORDER ( 3 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
NOCTURNAL DYSPNOEA ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
OCULAR VASCULAR DISORDER ( 3 FDA reports)
OESOPHAGEAL DILATATION ( 3 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
ONYCHOGRYPHOSIS ( 3 FDA reports)
ORAL PRURITUS ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
OSTEOGENESIS IMPERFECTA ( 3 FDA reports)
OSTEOMALACIA ( 3 FDA reports)
OTITIS MEDIA CHRONIC ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PACEMAKER COMPLICATION ( 3 FDA reports)
PAIN EXACERBATED ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PAPILLITIS ( 3 FDA reports)
PARACENTESIS ( 3 FDA reports)
PARADOXICAL DRUG REACTION ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PERIORBITAL CELLULITIS ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 3 FDA reports)
PHLEBOTHROMBOSIS ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
POST THROMBOTIC SYNDROME ( 3 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 3 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 3 FDA reports)
PRODUCT ODOUR ABNORMAL ( 3 FDA reports)
PRODUCT TASTE ABNORMAL ( 3 FDA reports)
PROSTATIC CALCIFICATION ( 3 FDA reports)
PULMONARY CALCIFICATION ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PULSE ABNORMAL ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
PYODERMA GANGRENOSUM ( 3 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 3 FDA reports)
RECTAL TENESMUS ( 3 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 3 FDA reports)
REGURGITATION OF FOOD ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL ATROPHY ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RETICULOCYTOPENIA ( 3 FDA reports)
RETINAL DISORDER ( 3 FDA reports)
RETROPERITONEAL HAEMATOMA ( 3 FDA reports)
RHINALGIA ( 3 FDA reports)
SALIVARY GLAND CANCER ( 3 FDA reports)
SCAN BONE MARROW ABNORMAL ( 3 FDA reports)
SCINTILLATING SCOTOMA ( 3 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
SEPSIS SYNDROME ( 3 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 3 FDA reports)
SKIN MASS ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SLEEP ATTACKS ( 3 FDA reports)
SPINAL DEFORMITY ( 3 FDA reports)
SPLEEN DISORDER ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
SUDDEN HEARING LOSS ( 3 FDA reports)
SYSTEMIC CANDIDA ( 3 FDA reports)
TESTICULAR DISORDER ( 3 FDA reports)
TETANY ( 3 FDA reports)
THALAMUS HAEMORRHAGE ( 3 FDA reports)
THERAPEUTIC EMBOLISATION ( 3 FDA reports)
THERAPEUTIC PROCEDURE ( 3 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
TIC ( 3 FDA reports)
TINEA INFECTION ( 3 FDA reports)
TOBACCO ABUSE ( 3 FDA reports)
TOBACCO USER ( 3 FDA reports)
TOE AMPUTATION ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TRYPTASE INCREASED ( 3 FDA reports)
TUMOUR FLARE ( 3 FDA reports)
URGE INCONTINENCE ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
URINARY BLADDER POLYP ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
VAGINAL DISORDER ( 3 FDA reports)
VAGINAL MYCOSIS ( 3 FDA reports)
VASCULAR GRAFT ( 3 FDA reports)
VENOUS STENOSIS ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VENTRICULAR FLUTTER ( 3 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
WOUND CLOSURE ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
WOUND TREATMENT ( 3 FDA reports)
ABDOMINAL WALL DISORDER ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO ( 2 FDA reports)
ALCOHOLIC LIVER DISEASE ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
ALLERGY TO CHEMICALS ( 2 FDA reports)
ALOPECIA EFFLUVIUM ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ANGIOGRAM ABNORMAL ( 2 FDA reports)
ANTICOAGULANT THERAPY ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
APPLICATION SITE BURN ( 2 FDA reports)
APPLICATION SITE DRYNESS ( 2 FDA reports)
APPLICATION SITE WARMTH ( 2 FDA reports)
ARACHNOID CYST ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ARTERIOGRAM CORONARY ( 2 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ARTHRODESIS ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AURA ( 2 FDA reports)
AUTONOMIC NEUROPATHY ( 2 FDA reports)
BACTERIAL DISEASE CARRIER ( 2 FDA reports)
BACTERIAL RHINITIS ( 2 FDA reports)
BASOSQUAMOUS CARCINOMA OF SKIN ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BENIGN NEOPLASM ( 2 FDA reports)
BILE OUTPUT ABNORMAL ( 2 FDA reports)
BILE OUTPUT INCREASED ( 2 FDA reports)
BIOPSY LIVER ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 2 FDA reports)
BLADDER PERFORATION ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD CATECHOLAMINES ABNORMAL ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD MERCURY ABNORMAL ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD POTASSIUM ( 2 FDA reports)
BLOOD SODIUM ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BODY TEMPERATURE ( 2 FDA reports)
BONE CALLUS EXCESSIVE ( 2 FDA reports)
BONE FORMATION INCREASED ( 2 FDA reports)
BONE INFECTION ( 2 FDA reports)
BOWEN'S DISEASE ( 2 FDA reports)
BRACHIAL PLEXOPATHY ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREAST CANCER STAGE I ( 2 FDA reports)
BREAST DISORDER FEMALE ( 2 FDA reports)
BREAST MALFORMATION ( 2 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
BURNS FIRST DEGREE ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CAPILLARY FRAGILITY ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 2 FDA reports)
CATARACT OPERATION COMPLICATION ( 2 FDA reports)
CATHETER PLACEMENT ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CATHETER SITE INFLAMMATION ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CATHETER SITE SWELLING ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 2 FDA reports)
CHEMICAL POISONING ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CHOREOATHETOSIS ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CLAVICLE FRACTURE ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLECTOMY PARTIAL ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL ANAEMIA ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CONNECTIVE TISSUE DISORDER ( 2 FDA reports)
CONTRAST MEDIA ALLERGY ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL DEPOSITS ( 2 FDA reports)
CORNEAL REFLEX DECREASED ( 2 FDA reports)
CORONARY ARTERY EMBOLISM ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
CYANOPSIA ( 2 FDA reports)
DECREASED VIBRATORY SENSE ( 2 FDA reports)
DENTAL CARE ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DERMATITIS INFECTED ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DRESSLER'S SYNDROME ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG TOLERANCE INCREASED ( 2 FDA reports)
DUODENAL NEOPLASM ( 2 FDA reports)
ELDERLY ( 2 FDA reports)
ELECTRIC SHOCK ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ELECTROLYTE DEPLETION ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EYE LASER SURGERY ( 2 FDA reports)
EYE OPERATION COMPLICATION ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
EYES SUNKEN ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FACTOR VIII INHIBITION ( 2 FDA reports)
FEELING GUILTY ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FIBROADENOMA OF BREAST ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOETAL DEATH ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GANGLION ( 2 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC PH DECREASED ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GENE MUTATION ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
GROIN INFECTION ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 2 FDA reports)
HERNIA HIATUS REPAIR ( 2 FDA reports)
HERNIA OBSTRUCTIVE ( 2 FDA reports)
HERNIA PAIN ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOACTIVE SEXUAL DESIRE DISORDER ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INCISION SITE PAIN ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INHIBITORY DRUG INTERACTION ( 2 FDA reports)
INJECTION SITE DRYNESS ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE MOVEMENT IMPAIRMENT ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 2 FDA reports)
LIP AND/OR ORAL CAVITY CANCER STAGE IV ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUMBAR PUNCTURE HEADACHE ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MEDIASTINAL MASS ( 2 FDA reports)
MEIBOMIANITIS ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MONOCYTE COUNT ABNORMAL ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MONOCYTOSIS ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MUSCLE HYPERTROPHY ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NERVE ROOT INJURY ( 2 FDA reports)
NEURILEMMOMA BENIGN ( 2 FDA reports)
NEUROMA ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NIGHT CRAMPS ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NODAL ARRHYTHMIA ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OESOPHAGEAL DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OLIGODENDROGLIOMA ( 2 FDA reports)
ONYCHALGIA ( 2 FDA reports)
OOPHORECTOMY ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
ORAL FIBROMA ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OTITIS MEDIA VIRAL ( 2 FDA reports)
PAINFUL ERECTION ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANCREATOLITHIASIS ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PARANEOPLASTIC SYNDROME ( 2 FDA reports)
PARASOMNIA ( 2 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 2 FDA reports)
PERFORATION BILE DUCT ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHARYNGEAL NEOPLASM ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PLICA SYNDROME ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
PORTAL TRIADITIS ( 2 FDA reports)
POST PROCEDURAL DIZZINESS ( 2 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
PROLONGED EXPIRATION ( 2 FDA reports)
PROSTATE CANCER RECURRENT ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PUBIC RAMI FRACTURE ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PURPURA ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
RADIATION INJURY ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
REITER'S SYNDROME ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
REPETITIVE STRAIN INJURY ( 2 FDA reports)
RIFT VALLEY FEVER ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
ROSEOLA ( 2 FDA reports)
SALIVARY GLAND OPERATION ( 2 FDA reports)
SALIVARY GLAND RESECTION ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SCAN BRAIN ( 2 FDA reports)
SCAR PAIN ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCLERITIS ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SEBACEOUS HYPERPLASIA ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SEMEN VOLUME DECREASED ( 2 FDA reports)
SERUM FERRITIN DECREASED ( 2 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN GRAFT FAILURE ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN HYPOPIGMENTATION ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN SWELLING ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SLEEP TERROR ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
SPINAL FUSION ACQUIRED ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
SPLENIC GRANULOMA ( 2 FDA reports)
SPONDYLOARTHROPATHY ( 2 FDA reports)
SPONDYLOLYSIS ( 2 FDA reports)
SPONTANEOUS PENILE ERECTION ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STEAL SYNDROME ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUDDEN ONSET OF SLEEP ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THERMOHYPOAESTHESIA ( 2 FDA reports)
THROAT CANCER ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 2 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TRAUMATIC FRACTURE ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TUMOUR EXCISION ( 2 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 2 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URINARY SEDIMENT PRESENT ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
URTICARIA GENERALISED ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
UTERINE PERFORATION ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VAGINAL LESION ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VASCULAR BYPASS GRAFT ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
VESTIBULOPLASTY ( 2 FDA reports)
VICTIM OF ELDER ABUSE ( 2 FDA reports)
VIRAL DIARRHOEA ( 2 FDA reports)
VIRAL SINUSITIS ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VITAMIN A INCREASED ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
VOCAL CORD PARESIS ( 2 FDA reports)
VOLVULUS OF BOWEL ( 2 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WEIGHT LOSS POOR ( 2 FDA reports)
XANTHELASMA ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCESSORY MUSCLE ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALLERGIC BRONCHITIS ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANORECTAL CELLULITIS ( 1 FDA reports)
ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY NEGATIVE ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE NECROSIS ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTHRITIS ENTEROPATHIC ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
AUTOIMMUNE PANCREATITIS ( 1 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 1 FDA reports)
AUTOPSY ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BASILAR ARTERY STENOSIS ( 1 FDA reports)
BENIGN COLONIC POLYP ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILE OUTPUT ( 1 FDA reports)
BILIARY CANCER METASTATIC ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BIOPSY ARTERY ( 1 FDA reports)
BIOPSY BRAIN ABNORMAL ( 1 FDA reports)
BIOPSY CERVIX ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLEPHAROPLASTY ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD GASTRIN INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD TEST ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 1 FDA reports)
BLOOD TRIGLYCERIDES ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BONE MARROW OEDEMA ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRACHYTHERAPY ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST PROSTHESIS USER ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOLIPIN ANTIBODY ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CATECHOLAMINES URINE INCREASED ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CEREBRAL AMYLOID ANGIOPATHY ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CERULOPLASMIN INCREASED ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CHEST CRUSHING ( 1 FDA reports)
CHEST WALL ABSCESS ( 1 FDA reports)
CHILAIDITI'S SYNDROME ( 1 FDA reports)
CHOLANGIOLITIS ( 1 FDA reports)
CHOLEDOCHOLITHOTOMY ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHOROIDAL EFFUSION ( 1 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA REFRACTORY ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CILIARY BODY DISORDER ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CIRCULATING ANTICOAGULANT POSITIVE ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPLICATED FRACTURE ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
COW'S MILK INTOLERANCE ( 1 FDA reports)
CRANIOPLASTY ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF MYELIN BASIC PROTEIN INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYSTIC FIBROSIS ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEAFNESS CONGENITAL ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DEFORMITY THORAX ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE INFUSION ISSUE ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DIVERTICULAR HERNIA ( 1 FDA reports)
DIVERTICULUM GASTRIC ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
DURAL TEAR ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCONVULSIVE THERAPY ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDERMAL NAEVUS ( 1 FDA reports)
EPIDERMOID CYST EXCISION ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ( 1 FDA reports)
EXPOSURE TO ALLERGEN ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE MUSCLE OPERATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID EROSION ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FALSE NEGATIVE LABORATORY RESULT ( 1 FDA reports)
FALSE NEGATIVE PREGNANCY TEST ( 1 FDA reports)
FASTING ( 1 FDA reports)
FAT INTOLERANCE ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRIC CANCER RECURRENT ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRIC PH INCREASED ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL EROSION ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOMERULONEPHROPATHY ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
HAEMANGIOMA OF SPLEEN ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOPHILUS SEPSIS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEPATECTOMY ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS B CORE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HETEROPHORIA ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOLMES-ADIE PUPIL ( 1 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
ILEAL OPERATION ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPACTED FRACTURE ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE DISCHARGE ( 1 FDA reports)
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IMPRISONMENT ( 1 FDA reports)
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INCISION SITE CELLULITIS ( 1 FDA reports)
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INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
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INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE NERVE DAMAGE ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
IRIS HYPOPIGMENTATION ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JAW LESION EXCISION ( 1 FDA reports)
JOINT ADHESION ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KERATOMILEUSIS ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
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LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
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LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
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LIMB MALFORMATION ( 1 FDA reports)
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LISTERIOSIS ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LOSS OF DREAMING ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
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LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
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LUNG ABSCESS ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 1 FDA reports)
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LYMPH GLAND INFECTION ( 1 FDA reports)
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LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
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LYMPHOCYTIC HYPOPHYSITIS ( 1 FDA reports)
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MACULAR HOLE ( 1 FDA reports)
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MENSTRUATION DELAYED ( 1 FDA reports)
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METHAEMOGLOBINAEMIA ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICROGRAPHIA ( 1 FDA reports)
MICROSPORUM INFECTION ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MIXED INCONTINENCE ( 1 FDA reports)
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MODIFIED RADICAL MASTECTOMY ( 1 FDA reports)
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MOUTH INJURY ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
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MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
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NAEVUS CELL NAEVUS ( 1 FDA reports)
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PARITY ( 1 FDA reports)
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