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

NAUSEA ( 1212 FDA reports)
DYSPNOEA ( 1202 FDA reports)
MYOCARDIAL INFARCTION ( 1114 FDA reports)
PAIN ( 1078 FDA reports)
DIZZINESS ( 999 FDA reports)
FATIGUE ( 923 FDA reports)
ASTHENIA ( 886 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 848 FDA reports)
ANXIETY ( 835 FDA reports)
CHEST PAIN ( 816 FDA reports)
DIARRHOEA ( 814 FDA reports)
VOMITING ( 799 FDA reports)
HYPOTENSION ( 765 FDA reports)
RENAL FAILURE ACUTE ( 739 FDA reports)
DRUG INEFFECTIVE ( 729 FDA reports)
HEADACHE ( 714 FDA reports)
HYPERTENSION ( 692 FDA reports)
OEDEMA PERIPHERAL ( 658 FDA reports)
WEIGHT DECREASED ( 642 FDA reports)
BLOOD GLUCOSE INCREASED ( 634 FDA reports)
FALL ( 630 FDA reports)
CORONARY ARTERY DISEASE ( 621 FDA reports)
COUGH ( 614 FDA reports)
DEPRESSION ( 602 FDA reports)
CEREBROVASCULAR ACCIDENT ( 589 FDA reports)
DEHYDRATION ( 579 FDA reports)
RENAL FAILURE ( 568 FDA reports)
INJURY ( 566 FDA reports)
ANAEMIA ( 563 FDA reports)
ARTHRALGIA ( 559 FDA reports)
PAIN IN EXTREMITY ( 547 FDA reports)
ATRIAL FIBRILLATION ( 514 FDA reports)
BACK PAIN ( 496 FDA reports)
BLOOD PRESSURE INCREASED ( 451 FDA reports)
ABDOMINAL PAIN ( 450 FDA reports)
PNEUMONIA ( 444 FDA reports)
INSOMNIA ( 439 FDA reports)
MALAISE ( 429 FDA reports)
DRUG INTERACTION ( 428 FDA reports)
MYALGIA ( 394 FDA reports)
CONFUSIONAL STATE ( 389 FDA reports)
RASH ( 378 FDA reports)
SYNCOPE ( 371 FDA reports)
EMOTIONAL DISTRESS ( 369 FDA reports)
PYREXIA ( 367 FDA reports)
WEIGHT INCREASED ( 365 FDA reports)
BLOOD CREATININE INCREASED ( 352 FDA reports)
URINARY TRACT INFECTION ( 346 FDA reports)
DIABETES MELLITUS ( 342 FDA reports)
DECREASED APPETITE ( 336 FDA reports)
PALPITATIONS ( 335 FDA reports)
PRURITUS ( 329 FDA reports)
DEATH ( 317 FDA reports)
ABDOMINAL PAIN UPPER ( 313 FDA reports)
HYPOAESTHESIA ( 313 FDA reports)
SOMNOLENCE ( 313 FDA reports)
CONSTIPATION ( 309 FDA reports)
HYPERKALAEMIA ( 306 FDA reports)
FEELING ABNORMAL ( 305 FDA reports)
CARDIAC DISORDER ( 295 FDA reports)
LOSS OF CONSCIOUSNESS ( 289 FDA reports)
MUSCLE SPASMS ( 289 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 281 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 278 FDA reports)
DYSPHAGIA ( 276 FDA reports)
ANHEDONIA ( 271 FDA reports)
HYPERHIDROSIS ( 263 FDA reports)
UNEVALUABLE EVENT ( 263 FDA reports)
PARAESTHESIA ( 258 FDA reports)
MITRAL VALVE INCOMPETENCE ( 257 FDA reports)
GAIT DISTURBANCE ( 254 FDA reports)
CARDIOMEGALY ( 252 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 250 FDA reports)
BRADYCARDIA ( 246 FDA reports)
PLEURAL EFFUSION ( 245 FDA reports)
TREMOR ( 243 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 242 FDA reports)
OSTEOARTHRITIS ( 236 FDA reports)
ANGINA PECTORIS ( 234 FDA reports)
NEUROPATHY PERIPHERAL ( 232 FDA reports)
CHEST DISCOMFORT ( 231 FDA reports)
HAEMOGLOBIN DECREASED ( 229 FDA reports)
HYPERLIPIDAEMIA ( 228 FDA reports)
CONDITION AGGRAVATED ( 227 FDA reports)
HYPONATRAEMIA ( 227 FDA reports)
FLUSHING ( 226 FDA reports)
ERYTHEMA ( 225 FDA reports)
OSTEONECROSIS OF JAW ( 222 FDA reports)
CONVULSION ( 220 FDA reports)
HYPOGLYCAEMIA ( 217 FDA reports)
RENAL IMPAIRMENT ( 216 FDA reports)
CARDIAC ARREST ( 215 FDA reports)
MUSCULAR WEAKNESS ( 213 FDA reports)
ECONOMIC PROBLEM ( 212 FDA reports)
HYPERGLYCAEMIA ( 207 FDA reports)
SINUSITIS ( 207 FDA reports)
VISION BLURRED ( 205 FDA reports)
BRONCHITIS ( 204 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 202 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 200 FDA reports)
CARDIAC FAILURE ( 199 FDA reports)
CONTUSION ( 196 FDA reports)
TACHYCARDIA ( 196 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 196 FDA reports)
ABDOMINAL DISTENSION ( 195 FDA reports)
HEART RATE INCREASED ( 193 FDA reports)
THROMBOCYTOPENIA ( 193 FDA reports)
PULMONARY OEDEMA ( 191 FDA reports)
RESPIRATORY FAILURE ( 191 FDA reports)
STRESS ( 190 FDA reports)
OEDEMA ( 187 FDA reports)
DYSPNOEA EXERTIONAL ( 184 FDA reports)
FEAR ( 182 FDA reports)
DYSPEPSIA ( 178 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 178 FDA reports)
SPINAL OSTEOARTHRITIS ( 177 FDA reports)
SWELLING ( 176 FDA reports)
HYPOKALAEMIA ( 171 FDA reports)
NECK PAIN ( 171 FDA reports)
BLOOD GLUCOSE DECREASED ( 169 FDA reports)
DEEP VEIN THROMBOSIS ( 169 FDA reports)
BLOOD PRESSURE DECREASED ( 168 FDA reports)
BLOOD UREA INCREASED ( 168 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 168 FDA reports)
BONE DISORDER ( 166 FDA reports)
CHILLS ( 165 FDA reports)
TYPE 2 DIABETES MELLITUS ( 165 FDA reports)
GASTRITIS ( 163 FDA reports)
INFECTION ( 162 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 162 FDA reports)
BALANCE DISORDER ( 158 FDA reports)
PULMONARY EMBOLISM ( 158 FDA reports)
CELLULITIS ( 157 FDA reports)
MUSCULOSKELETAL PAIN ( 157 FDA reports)
DYSGEUSIA ( 154 FDA reports)
AMNESIA ( 153 FDA reports)
ARTHRITIS ( 152 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 151 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 150 FDA reports)
ARRHYTHMIA ( 150 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 150 FDA reports)
ALOPECIA ( 148 FDA reports)
MYOCARDIAL ISCHAEMIA ( 147 FDA reports)
RENAL INJURY ( 147 FDA reports)
HYPERSENSITIVITY ( 146 FDA reports)
ABDOMINAL DISCOMFORT ( 145 FDA reports)
OSTEOMYELITIS ( 145 FDA reports)
ARTERIOSCLEROSIS ( 144 FDA reports)
ASTHMA ( 144 FDA reports)
RHABDOMYOLYSIS ( 143 FDA reports)
SEPSIS ( 142 FDA reports)
URTICARIA ( 140 FDA reports)
IMPAIRED HEALING ( 139 FDA reports)
MULTIPLE INJURIES ( 138 FDA reports)
ANOREXIA ( 137 FDA reports)
HEART RATE IRREGULAR ( 137 FDA reports)
PANCREATITIS ( 136 FDA reports)
CARDIAC MURMUR ( 133 FDA reports)
MEMORY IMPAIRMENT ( 132 FDA reports)
CARDIOMYOPATHY ( 131 FDA reports)
PLATELET COUNT DECREASED ( 131 FDA reports)
ATELECTASIS ( 130 FDA reports)
VENTRICULAR TACHYCARDIA ( 130 FDA reports)
ANGIOEDEMA ( 129 FDA reports)
WHEEZING ( 129 FDA reports)
CORONARY ARTERY OCCLUSION ( 128 FDA reports)
SLEEP APNOEA SYNDROME ( 128 FDA reports)
LETHARGY ( 127 FDA reports)
PULMONARY HYPERTENSION ( 126 FDA reports)
CATARACT ( 125 FDA reports)
TOOTH EXTRACTION ( 125 FDA reports)
HIATUS HERNIA ( 123 FDA reports)
SWELLING FACE ( 122 FDA reports)
ARTHROPATHY ( 121 FDA reports)
FLUID RETENTION ( 120 FDA reports)
MULTI-ORGAN FAILURE ( 119 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 118 FDA reports)
CHOLELITHIASIS ( 117 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 117 FDA reports)
EJECTION FRACTION DECREASED ( 116 FDA reports)
ERECTILE DYSFUNCTION ( 115 FDA reports)
HAEMORRHAGE ( 115 FDA reports)
HYPERCHOLESTEROLAEMIA ( 115 FDA reports)
HYPOPHAGIA ( 115 FDA reports)
MOBILITY DECREASED ( 114 FDA reports)
RENAL FAILURE CHRONIC ( 114 FDA reports)
ORTHOSTATIC HYPOTENSION ( 113 FDA reports)
CARPAL TUNNEL SYNDROME ( 112 FDA reports)
OBESITY ( 112 FDA reports)
RECTAL HAEMORRHAGE ( 112 FDA reports)
DEFORMITY ( 111 FDA reports)
FLATULENCE ( 111 FDA reports)
HEART RATE DECREASED ( 111 FDA reports)
URINARY INCONTINENCE ( 111 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 108 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 108 FDA reports)
AGITATION ( 107 FDA reports)
OSTEONECROSIS ( 107 FDA reports)
SUICIDAL IDEATION ( 107 FDA reports)
EPISTAXIS ( 105 FDA reports)
HAEMORRHOIDS ( 105 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 105 FDA reports)
NERVOUSNESS ( 103 FDA reports)
SPINAL COLUMN STENOSIS ( 103 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 103 FDA reports)
EXOSTOSIS ( 102 FDA reports)
POLLAKIURIA ( 102 FDA reports)
ROTATOR CUFF SYNDROME ( 102 FDA reports)
THROMBOSIS ( 102 FDA reports)
VISUAL IMPAIRMENT ( 102 FDA reports)
DRUG HYPERSENSITIVITY ( 101 FDA reports)
OROPHARYNGEAL PAIN ( 101 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 100 FDA reports)
DISORIENTATION ( 100 FDA reports)
HERPES ZOSTER ( 100 FDA reports)
VERTIGO ( 99 FDA reports)
DRY MOUTH ( 98 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 98 FDA reports)
PAIN IN JAW ( 98 FDA reports)
ROAD TRAFFIC ACCIDENT ( 98 FDA reports)
ABASIA ( 97 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 97 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 97 FDA reports)
BREAST MASS ( 96 FDA reports)
BURNING SENSATION ( 96 FDA reports)
DYSARTHRIA ( 96 FDA reports)
MENTAL STATUS CHANGES ( 96 FDA reports)
MIGRAINE ( 96 FDA reports)
PERICARDIAL EFFUSION ( 96 FDA reports)
PRIMARY SEQUESTRUM ( 96 FDA reports)
STAPHYLOCOCCAL INFECTION ( 96 FDA reports)
DIABETIC NEUROPATHY ( 95 FDA reports)
TREATMENT NONCOMPLIANCE ( 94 FDA reports)
VISUAL ACUITY REDUCED ( 94 FDA reports)
AORTIC VALVE INCOMPETENCE ( 93 FDA reports)
GOUT ( 93 FDA reports)
JOINT SWELLING ( 93 FDA reports)
RENAL CYST ( 93 FDA reports)
ANGINA UNSTABLE ( 92 FDA reports)
FLUID OVERLOAD ( 92 FDA reports)
OSTEOPOROSIS ( 92 FDA reports)
URINARY RETENTION ( 92 FDA reports)
GASTRIC ULCER ( 91 FDA reports)
HAEMATURIA ( 91 FDA reports)
TINNITUS ( 91 FDA reports)
UNRESPONSIVE TO STIMULI ( 91 FDA reports)
DYSPHONIA ( 90 FDA reports)
HYPOXIA ( 90 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 90 FDA reports)
FEELING HOT ( 89 FDA reports)
LUNG DISORDER ( 89 FDA reports)
LYMPHADENOPATHY ( 89 FDA reports)
CARDIO-RESPIRATORY ARREST ( 88 FDA reports)
EMPHYSEMA ( 88 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 87 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 87 FDA reports)
HYPOTHYROIDISM ( 87 FDA reports)
JAUNDICE ( 87 FDA reports)
BLOOD POTASSIUM DECREASED ( 86 FDA reports)
BURSITIS ( 86 FDA reports)
HAEMATOCHEZIA ( 86 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 85 FDA reports)
HAEMATOCRIT DECREASED ( 85 FDA reports)
PANCREATITIS ACUTE ( 85 FDA reports)
SINUS BRADYCARDIA ( 85 FDA reports)
SURGERY ( 85 FDA reports)
TOOTH ABSCESS ( 85 FDA reports)
DIVERTICULITIS ( 84 FDA reports)
NEPHROLITHIASIS ( 84 FDA reports)
SKIN ULCER ( 84 FDA reports)
SLEEP DISORDER ( 84 FDA reports)
ABSCESS ( 82 FDA reports)
DIVERTICULUM ( 82 FDA reports)
HALLUCINATION ( 82 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 82 FDA reports)
SWOLLEN TONGUE ( 82 FDA reports)
TOOTHACHE ( 82 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 82 FDA reports)
OVERDOSE ( 81 FDA reports)
SINUS TACHYCARDIA ( 81 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 81 FDA reports)
BLINDNESS ( 79 FDA reports)
DENTAL CARIES ( 79 FDA reports)
NASOPHARYNGITIS ( 78 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 78 FDA reports)
ILL-DEFINED DISORDER ( 77 FDA reports)
LIP SWELLING ( 77 FDA reports)
TOOTH LOSS ( 77 FDA reports)
AGGRESSION ( 76 FDA reports)
SKIN DISCOLOURATION ( 76 FDA reports)
BONE LESION ( 75 FDA reports)
COLONIC POLYP ( 75 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 74 FDA reports)
LOOSE TOOTH ( 74 FDA reports)
LUNG INFILTRATION ( 74 FDA reports)
RESTLESSNESS ( 74 FDA reports)
TENDONITIS ( 74 FDA reports)
DISTURBANCE IN ATTENTION ( 73 FDA reports)
PANIC ATTACK ( 73 FDA reports)
ADVERSE EVENT ( 72 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 72 FDA reports)
GASTROINTESTINAL DISORDER ( 72 FDA reports)
JAW DISORDER ( 72 FDA reports)
ORAL DISORDER ( 72 FDA reports)
BLOOD POTASSIUM INCREASED ( 71 FDA reports)
DECREASED INTEREST ( 70 FDA reports)
DYSURIA ( 70 FDA reports)
METASTASES TO BONE ( 70 FDA reports)
OCULAR HYPERAEMIA ( 70 FDA reports)
PANCYTOPENIA ( 70 FDA reports)
PRODUCTIVE COUGH ( 70 FDA reports)
PULMONARY FIBROSIS ( 70 FDA reports)
BLOOD SODIUM DECREASED ( 69 FDA reports)
CORONARY ARTERY STENOSIS ( 69 FDA reports)
VENTRICULAR FIBRILLATION ( 69 FDA reports)
INJECTION SITE PAIN ( 68 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 68 FDA reports)
OXYGEN SATURATION DECREASED ( 68 FDA reports)
RESPIRATORY DISTRESS ( 68 FDA reports)
ACUTE CORONARY SYNDROME ( 67 FDA reports)
COMA ( 67 FDA reports)
RIB FRACTURE ( 67 FDA reports)
DIPLOPIA ( 66 FDA reports)
HEPATIC ENZYME INCREASED ( 66 FDA reports)
HEPATIC STEATOSIS ( 66 FDA reports)
PULMONARY CONGESTION ( 66 FDA reports)
SPEECH DISORDER ( 66 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 65 FDA reports)
IRRITABLE BOWEL SYNDROME ( 65 FDA reports)
MEDICATION ERROR ( 65 FDA reports)
RASH GENERALISED ( 65 FDA reports)
CARDIOVASCULAR DISORDER ( 64 FDA reports)
HAEMATOMA ( 64 FDA reports)
HIP FRACTURE ( 64 FDA reports)
MUSCLE STRAIN ( 64 FDA reports)
SKIN EXFOLIATION ( 64 FDA reports)
VISUAL DISTURBANCE ( 64 FDA reports)
FAECAL INCONTINENCE ( 63 FDA reports)
LIFE EXPECTANCY SHORTENED ( 63 FDA reports)
MOUTH ULCERATION ( 63 FDA reports)
MYOSITIS ( 63 FDA reports)
NASAL CONGESTION ( 63 FDA reports)
PHARYNGITIS ( 63 FDA reports)
PROTHROMBIN TIME PROLONGED ( 63 FDA reports)
SINUS DISORDER ( 63 FDA reports)
BONE DENSITY DECREASED ( 62 FDA reports)
INFLUENZA LIKE ILLNESS ( 62 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 62 FDA reports)
NEUTROPENIA ( 62 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 61 FDA reports)
ATRIAL FLUTTER ( 61 FDA reports)
CARDIOGENIC SHOCK ( 61 FDA reports)
PHARYNGEAL OEDEMA ( 61 FDA reports)
PRESYNCOPE ( 61 FDA reports)
AORTIC STENOSIS ( 60 FDA reports)
BLOOD BILIRUBIN INCREASED ( 60 FDA reports)
BONE PAIN ( 60 FDA reports)
CARDIAC VALVE DISEASE ( 60 FDA reports)
HAEMATEMESIS ( 60 FDA reports)
IRRITABILITY ( 60 FDA reports)
MENTAL DISORDER ( 60 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 60 FDA reports)
THIRST ( 60 FDA reports)
ANGIONEUROTIC OEDEMA ( 59 FDA reports)
ATRIOVENTRICULAR BLOCK ( 59 FDA reports)
DISABILITY ( 59 FDA reports)
MALNUTRITION ( 59 FDA reports)
STOMACH DISCOMFORT ( 59 FDA reports)
ABNORMAL DREAMS ( 58 FDA reports)
CAROTID ARTERY STENOSIS ( 58 FDA reports)
CEREBRAL INFARCTION ( 58 FDA reports)
FIBROMYALGIA ( 58 FDA reports)
HAEMOPTYSIS ( 58 FDA reports)
INFLAMMATION ( 58 FDA reports)
NEOPLASM MALIGNANT ( 58 FDA reports)
PALLOR ( 58 FDA reports)
POST PROCEDURAL COMPLICATION ( 58 FDA reports)
RENAL DISORDER ( 58 FDA reports)
BLOOD CALCIUM DECREASED ( 57 FDA reports)
CIRCULATORY COLLAPSE ( 57 FDA reports)
DISEASE PROGRESSION ( 57 FDA reports)
DIVERTICULUM INTESTINAL ( 57 FDA reports)
DRUG EFFECT DECREASED ( 57 FDA reports)
HOT FLUSH ( 57 FDA reports)
OSTEITIS ( 57 FDA reports)
RHINORRHOEA ( 57 FDA reports)
HEAD INJURY ( 56 FDA reports)
HYPOVOLAEMIA ( 56 FDA reports)
ORAL PAIN ( 56 FDA reports)
RESTLESS LEGS SYNDROME ( 56 FDA reports)
VENTRICULAR HYPERTROPHY ( 56 FDA reports)
ASCITES ( 55 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 55 FDA reports)
COLD SWEAT ( 55 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 55 FDA reports)
DRY SKIN ( 55 FDA reports)
FEBRILE NEUTROPENIA ( 55 FDA reports)
MASS ( 55 FDA reports)
MELAENA ( 55 FDA reports)
ORTHOPNOEA ( 55 FDA reports)
PRODUCT QUALITY ISSUE ( 55 FDA reports)
TOOTH DISORDER ( 55 FDA reports)
DRUG TOXICITY ( 54 FDA reports)
INCORRECT DOSE ADMINISTERED ( 54 FDA reports)
OSTEOLYSIS ( 54 FDA reports)
TOOTH FRACTURE ( 54 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 53 FDA reports)
BLISTER ( 53 FDA reports)
DIALYSIS ( 53 FDA reports)
DIFFICULTY IN WALKING ( 53 FDA reports)
LEFT ATRIAL DILATATION ( 53 FDA reports)
RESPIRATORY ARREST ( 53 FDA reports)
COAGULOPATHY ( 52 FDA reports)
EMOTIONAL DISORDER ( 52 FDA reports)
HEPATIC FAILURE ( 52 FDA reports)
OFF LABEL USE ( 52 FDA reports)
RHINITIS ALLERGIC ( 52 FDA reports)
SKIN LESION ( 52 FDA reports)
BASAL CELL CARCINOMA ( 51 FDA reports)
ELECTROLYTE IMBALANCE ( 51 FDA reports)
GASTROENTERITIS ( 51 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 51 FDA reports)
MUSCLE DISORDER ( 51 FDA reports)
OESOPHAGITIS ( 51 FDA reports)
RADICULOPATHY ( 51 FDA reports)
RETCHING ( 51 FDA reports)
THYROID DISORDER ( 51 FDA reports)
TYPE 1 DIABETES MELLITUS ( 51 FDA reports)
IRON DEFICIENCY ANAEMIA ( 50 FDA reports)
PSORIASIS ( 50 FDA reports)
SEPTIC SHOCK ( 50 FDA reports)
AZOTAEMIA ( 49 FDA reports)
DEMENTIA ( 49 FDA reports)
DRUG INTOLERANCE ( 49 FDA reports)
DRY EYE ( 49 FDA reports)
DYSKINESIA ( 49 FDA reports)
ECCHYMOSIS ( 49 FDA reports)
GALLBLADDER DISORDER ( 49 FDA reports)
HEPATITIS ( 49 FDA reports)
JOINT INJURY ( 49 FDA reports)
LEUKOCYTOSIS ( 49 FDA reports)
MOVEMENT DISORDER ( 49 FDA reports)
RHINITIS ( 49 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 49 FDA reports)
BLINDNESS UNILATERAL ( 48 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 48 FDA reports)
INTERSTITIAL LUNG DISEASE ( 48 FDA reports)
LACERATION ( 48 FDA reports)
MITRAL VALVE CALCIFICATION ( 48 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 48 FDA reports)
VITREOUS FLOATERS ( 48 FDA reports)
CATARACT OPERATION ( 47 FDA reports)
GASTRIC DISORDER ( 47 FDA reports)
LUNG NEOPLASM ( 47 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 47 FDA reports)
PNEUMONITIS ( 47 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 47 FDA reports)
COMPRESSION FRACTURE ( 46 FDA reports)
CYST ( 46 FDA reports)
DECUBITUS ULCER ( 46 FDA reports)
DELIRIUM ( 46 FDA reports)
GLAUCOMA ( 46 FDA reports)
HEART INJURY ( 46 FDA reports)
HYPOMAGNESAEMIA ( 46 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 46 FDA reports)
MUSCLE ATROPHY ( 46 FDA reports)
PNEUMONIA ASPIRATION ( 46 FDA reports)
PRURITUS GENERALISED ( 46 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 46 FDA reports)
AORTIC VALVE DISEASE ( 45 FDA reports)
DRUG DOSE OMISSION ( 45 FDA reports)
ERUCTATION ( 45 FDA reports)
INJECTION SITE ERYTHEMA ( 45 FDA reports)
RHEUMATOID ARTHRITIS ( 45 FDA reports)
SUICIDE ATTEMPT ( 45 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 45 FDA reports)
BLOOD ALBUMIN DECREASED ( 44 FDA reports)
EAR PAIN ( 44 FDA reports)
HEMIPARESIS ( 44 FDA reports)
NOCTURIA ( 44 FDA reports)
PANCREATIC CARCINOMA ( 44 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 44 FDA reports)
RASH PRURITIC ( 44 FDA reports)
SUDDEN DEATH ( 44 FDA reports)
CHOKING ( 43 FDA reports)
DIABETIC KETOACIDOSIS ( 43 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 43 FDA reports)
METABOLIC ACIDOSIS ( 43 FDA reports)
MOOD SWINGS ( 43 FDA reports)
PERIODONTITIS ( 43 FDA reports)
PHYSICAL DISABILITY ( 43 FDA reports)
PURULENT DISCHARGE ( 43 FDA reports)
ACCIDENTAL OVERDOSE ( 42 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 42 FDA reports)
BRONCHOSPASM ( 42 FDA reports)
DILATATION ATRIAL ( 42 FDA reports)
ENDODONTIC PROCEDURE ( 42 FDA reports)
FAECES DISCOLOURED ( 42 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 42 FDA reports)
JAW FRACTURE ( 42 FDA reports)
LIVER DISORDER ( 42 FDA reports)
PERIPHERAL ISCHAEMIA ( 42 FDA reports)
PETECHIAE ( 42 FDA reports)
SPINAL DISORDER ( 42 FDA reports)
ACUTE RESPIRATORY FAILURE ( 41 FDA reports)
CARDIAC PACEMAKER INSERTION ( 41 FDA reports)
DIABETIC RETINOPATHY ( 41 FDA reports)
INJECTION SITE HAEMORRHAGE ( 41 FDA reports)
MUSCLE INJURY ( 41 FDA reports)
PATHOLOGICAL FRACTURE ( 41 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 41 FDA reports)
RASH MACULAR ( 41 FDA reports)
RASH MACULO-PAPULAR ( 41 FDA reports)
ANAPHYLACTIC REACTION ( 40 FDA reports)
APHASIA ( 40 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 40 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 40 FDA reports)
DYSLIPIDAEMIA ( 40 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 40 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 40 FDA reports)
ODYNOPHAGIA ( 40 FDA reports)
PNEUMOTHORAX ( 40 FDA reports)
SCAR ( 40 FDA reports)
SCOLIOSIS ( 40 FDA reports)
SYNOVIAL CYST ( 40 FDA reports)
URINE OUTPUT DECREASED ( 40 FDA reports)
BLOOD URINE PRESENT ( 39 FDA reports)
COLITIS ISCHAEMIC ( 39 FDA reports)
CYSTITIS ( 39 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 39 FDA reports)
EYE DISORDER ( 39 FDA reports)
INFLUENZA ( 39 FDA reports)
MENISCUS LESION ( 39 FDA reports)
MYOPATHY ( 39 FDA reports)
PYURIA ( 39 FDA reports)
TENDERNESS ( 39 FDA reports)
THROAT IRRITATION ( 39 FDA reports)
TROPONIN INCREASED ( 39 FDA reports)
BREAST CANCER ( 38 FDA reports)
CEREBRAL HAEMORRHAGE ( 38 FDA reports)
CEREBROVASCULAR DISORDER ( 38 FDA reports)
CHOLECYSTITIS ( 38 FDA reports)
COGNITIVE DISORDER ( 38 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 38 FDA reports)
EXCORIATION ( 38 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 38 FDA reports)
GASTROENTERITIS VIRAL ( 38 FDA reports)
GINGIVAL BLEEDING ( 38 FDA reports)
GLOSSODYNIA ( 38 FDA reports)
LARYNGEAL OEDEMA ( 38 FDA reports)
PERIPHERAL COLDNESS ( 38 FDA reports)
SCIATICA ( 38 FDA reports)
SKIN DISORDER ( 38 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 37 FDA reports)
DISCOMFORT ( 37 FDA reports)
DRY THROAT ( 37 FDA reports)
EYE PAIN ( 37 FDA reports)
HEARING IMPAIRED ( 37 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 37 FDA reports)
NEURALGIA ( 37 FDA reports)
SKIN INDURATION ( 37 FDA reports)
CORONARY ARTERY BYPASS ( 36 FDA reports)
DEBRIDEMENT ( 36 FDA reports)
GENERALISED OEDEMA ( 36 FDA reports)
HEPATIC CYST ( 36 FDA reports)
HYPERTENSIVE CRISIS ( 36 FDA reports)
MAJOR DEPRESSION ( 36 FDA reports)
METASTASES TO LIVER ( 36 FDA reports)
MUCOSAL INFLAMMATION ( 36 FDA reports)
NERVOUS SYSTEM DISORDER ( 36 FDA reports)
NIGHTMARE ( 36 FDA reports)
RASH ERYTHEMATOUS ( 36 FDA reports)
RESPIRATORY DISORDER ( 36 FDA reports)
SHOCK ( 36 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 36 FDA reports)
THROAT TIGHTNESS ( 36 FDA reports)
UROSEPSIS ( 36 FDA reports)
ACTINOMYCOSIS ( 35 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 35 FDA reports)
CANDIDIASIS ( 35 FDA reports)
HEPATIC CIRRHOSIS ( 35 FDA reports)
LACTIC ACIDOSIS ( 35 FDA reports)
LUNG NEOPLASM MALIGNANT ( 35 FDA reports)
MACULAR DEGENERATION ( 35 FDA reports)
PERIODONTAL DISEASE ( 35 FDA reports)
PULSE ABSENT ( 35 FDA reports)
STOMATITIS ( 35 FDA reports)
SUBDURAL HAEMATOMA ( 35 FDA reports)
TACHYARRHYTHMIA ( 35 FDA reports)
UPPER LIMB FRACTURE ( 35 FDA reports)
AGEUSIA ( 34 FDA reports)
COLITIS ( 34 FDA reports)
DIASTOLIC DYSFUNCTION ( 34 FDA reports)
ENCEPHALOPATHY ( 34 FDA reports)
FRACTURE ( 34 FDA reports)
INTERMITTENT CLAUDICATION ( 34 FDA reports)
LEUKOPENIA ( 34 FDA reports)
OSTEOPENIA ( 34 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 34 FDA reports)
WRIST FRACTURE ( 34 FDA reports)
ABNORMAL BEHAVIOUR ( 33 FDA reports)
ACTINIC KERATOSIS ( 33 FDA reports)
FEMUR FRACTURE ( 33 FDA reports)
FLANK PAIN ( 33 FDA reports)
HALLUCINATION, VISUAL ( 33 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 33 FDA reports)
HEPATOMEGALY ( 33 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 33 FDA reports)
PERIARTHRITIS ( 33 FDA reports)
PHOTOSENSITIVITY REACTION ( 33 FDA reports)
RENAL TUBULAR NECROSIS ( 33 FDA reports)
STENT PLACEMENT ( 33 FDA reports)
VENTRICULAR HYPOKINESIA ( 33 FDA reports)
AGRANULOCYTOSIS ( 32 FDA reports)
BACK DISORDER ( 32 FDA reports)
CAROTID ARTERY OCCLUSION ( 32 FDA reports)
CHROMATURIA ( 32 FDA reports)
COORDINATION ABNORMAL ( 32 FDA reports)
FACE OEDEMA ( 32 FDA reports)
FAILURE TO THRIVE ( 32 FDA reports)
GASTRIC POLYPS ( 32 FDA reports)
HYPOCALCAEMIA ( 32 FDA reports)
INJECTION SITE BRUISING ( 32 FDA reports)
LOBAR PNEUMONIA ( 32 FDA reports)
MENTAL IMPAIRMENT ( 32 FDA reports)
MUSCLE TWITCHING ( 32 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 32 FDA reports)
RALES ( 32 FDA reports)
SINUS CONGESTION ( 32 FDA reports)
SPONDYLOLISTHESIS ( 32 FDA reports)
APNOEA ( 31 FDA reports)
BODY TEMPERATURE INCREASED ( 31 FDA reports)
CARDIAC OPERATION ( 31 FDA reports)
CEREBRAL ATROPHY ( 31 FDA reports)
CERVICAL SPINAL STENOSIS ( 31 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 31 FDA reports)
CONJUNCTIVITIS ( 31 FDA reports)
DEAFNESS ( 31 FDA reports)
EROSIVE OESOPHAGITIS ( 31 FDA reports)
INCREASED TENDENCY TO BRUISE ( 31 FDA reports)
INTENTIONAL OVERDOSE ( 31 FDA reports)
LABORATORY TEST ABNORMAL ( 31 FDA reports)
LIBIDO DECREASED ( 31 FDA reports)
LUMBAR SPINAL STENOSIS ( 31 FDA reports)
MICTURITION URGENCY ( 31 FDA reports)
MULTIPLE MYELOMA ( 31 FDA reports)
NEUTROPHIL COUNT DECREASED ( 31 FDA reports)
RASH PAPULAR ( 31 FDA reports)
RESPIRATORY RATE INCREASED ( 31 FDA reports)
SENSORY DISTURBANCE ( 31 FDA reports)
SKIN CANCER ( 31 FDA reports)
SKIN HYPERTROPHY ( 31 FDA reports)
VIRAL INFECTION ( 31 FDA reports)
ACUTE PULMONARY OEDEMA ( 30 FDA reports)
ANGER ( 30 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 30 FDA reports)
COMPLETED SUICIDE ( 30 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 30 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 30 FDA reports)
ECZEMA ( 30 FDA reports)
FEELING JITTERY ( 30 FDA reports)
GINGIVITIS ( 30 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 30 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 30 FDA reports)
LEG AMPUTATION ( 30 FDA reports)
LOCALISED INFECTION ( 30 FDA reports)
MIDDLE INSOMNIA ( 30 FDA reports)
RENAL ARTERY STENOSIS ( 30 FDA reports)
TOOTH INFECTION ( 30 FDA reports)
ULCER ( 30 FDA reports)
AORTIC VALVE STENOSIS ( 29 FDA reports)
BACTERIAL INFECTION ( 29 FDA reports)
BEDRIDDEN ( 29 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 29 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 29 FDA reports)
BONE DEBRIDEMENT ( 29 FDA reports)
CHOLESTASIS ( 29 FDA reports)
CRYING ( 29 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 29 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 29 FDA reports)
EYE SWELLING ( 29 FDA reports)
HAEMODIALYSIS ( 29 FDA reports)
HYDRONEPHROSIS ( 29 FDA reports)
HYSTERECTOMY ( 29 FDA reports)
INTRACARDIAC THROMBUS ( 29 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 29 FDA reports)
OCULAR HYPERTENSION ( 29 FDA reports)
OESOPHAGITIS ULCERATIVE ( 29 FDA reports)
PARALYSIS ( 29 FDA reports)
SKIN BURNING SENSATION ( 29 FDA reports)
TIBIA FRACTURE ( 29 FDA reports)
TONGUE OEDEMA ( 29 FDA reports)
ACUTE PRERENAL FAILURE ( 28 FDA reports)
BREAST CANCER METASTATIC ( 28 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 28 FDA reports)
DIABETIC NEPHROPATHY ( 28 FDA reports)
FOOT DEFORMITY ( 28 FDA reports)
HYPERSOMNIA ( 28 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 28 FDA reports)
INCONTINENCE ( 28 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 28 FDA reports)
NIGHT SWEATS ( 28 FDA reports)
OEDEMA MOUTH ( 28 FDA reports)
PARANOIA ( 28 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 28 FDA reports)
SPINAL COMPRESSION FRACTURE ( 28 FDA reports)
AORTIC ANEURYSM ( 27 FDA reports)
BACK INJURY ( 27 FDA reports)
BIPOLAR DISORDER ( 27 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 27 FDA reports)
DILATATION VENTRICULAR ( 27 FDA reports)
DIZZINESS POSTURAL ( 27 FDA reports)
DYSSTASIA ( 27 FDA reports)
FACIAL PAIN ( 27 FDA reports)
GOITRE ( 27 FDA reports)
HEPATITIS C ( 27 FDA reports)
HYPERKERATOSIS ( 27 FDA reports)
ILEUS ( 27 FDA reports)
LACRIMATION INCREASED ( 27 FDA reports)
LUNG INFECTION ( 27 FDA reports)
METASTASES TO LYMPH NODES ( 27 FDA reports)
NODULE ( 27 FDA reports)
OLIGURIA ( 27 FDA reports)
ORAL INTAKE REDUCED ( 27 FDA reports)
ORAL SURGERY ( 27 FDA reports)
POLYP ( 27 FDA reports)
SKIN LACERATION ( 27 FDA reports)
SPLENOMEGALY ( 27 FDA reports)
TENDON RUPTURE ( 27 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 26 FDA reports)
ANURIA ( 26 FDA reports)
ARTERIAL DISORDER ( 26 FDA reports)
CARDIAC FLUTTER ( 26 FDA reports)
DEPRESSED MOOD ( 26 FDA reports)
DEVICE FAILURE ( 26 FDA reports)
EOSINOPHILIA ( 26 FDA reports)
FEELING COLD ( 26 FDA reports)
IMPAIRED WORK ABILITY ( 26 FDA reports)
ISCHAEMIA ( 26 FDA reports)
JOINT STIFFNESS ( 26 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 26 FDA reports)
METASTASES TO LUNG ( 26 FDA reports)
ORAL FIBROMA ( 26 FDA reports)
PERICARDITIS ( 26 FDA reports)
PYELONEPHRITIS ( 26 FDA reports)
SEDATION ( 26 FDA reports)
SHOULDER PAIN ( 26 FDA reports)
SQUAMOUS CELL CARCINOMA ( 26 FDA reports)
TONGUE INJURY ( 26 FDA reports)
VITAMIN D DEFICIENCY ( 26 FDA reports)
ANAPHYLACTIC SHOCK ( 25 FDA reports)
ANEURYSM ( 25 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 25 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 25 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 25 FDA reports)
DENTAL FISTULA ( 25 FDA reports)
DISEASE RECURRENCE ( 25 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 25 FDA reports)
HEPATOCELLULAR DAMAGE ( 25 FDA reports)
HYPOACUSIS ( 25 FDA reports)
LARYNGITIS ( 25 FDA reports)
LEUKOENCEPHALOPATHY ( 25 FDA reports)
MACULAR OEDEMA ( 25 FDA reports)
MUSCLE CRAMP ( 25 FDA reports)
ORAL CANDIDIASIS ( 25 FDA reports)
ORAL INFECTION ( 25 FDA reports)
SENSORY LOSS ( 25 FDA reports)
SKIN HYPERPIGMENTATION ( 25 FDA reports)
SKIN TIGHTNESS ( 25 FDA reports)
SOCIAL PROBLEM ( 25 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 25 FDA reports)
TRANSAMINASES INCREASED ( 25 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 24 FDA reports)
BARRETT'S OESOPHAGUS ( 24 FDA reports)
BLOOD AMYLASE INCREASED ( 24 FDA reports)
CARDIAC ANEURYSM ( 24 FDA reports)
CYANOSIS ( 24 FDA reports)
DRUG DEPENDENCE ( 24 FDA reports)
EDENTULOUS ( 24 FDA reports)
ERYSIPELAS ( 24 FDA reports)
EYE HAEMORRHAGE ( 24 FDA reports)
FAECALOMA ( 24 FDA reports)
FOOT FRACTURE ( 24 FDA reports)
GASTROINTESTINAL PAIN ( 24 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 24 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 24 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 24 FDA reports)
LACUNAR INFARCTION ( 24 FDA reports)
LOWER LIMB FRACTURE ( 24 FDA reports)
METASTATIC NEOPLASM ( 24 FDA reports)
MUSCLE TIGHTNESS ( 24 FDA reports)
ORAL CAVITY FISTULA ( 24 FDA reports)
PROSTATE CANCER ( 24 FDA reports)
PROTEINURIA ( 24 FDA reports)
SENSATION OF HEAVINESS ( 24 FDA reports)
SICK SINUS SYNDROME ( 24 FDA reports)
UTERINE LEIOMYOMA ( 24 FDA reports)
WOUND ( 24 FDA reports)
ABSCESS JAW ( 23 FDA reports)
ADVERSE DRUG REACTION ( 23 FDA reports)
ANGIOPATHY ( 23 FDA reports)
BLOOD PRESSURE ABNORMAL ( 23 FDA reports)
CATHETERISATION CARDIAC ( 23 FDA reports)
CEREBRAL ISCHAEMIA ( 23 FDA reports)
CORONARY ARTERY THROMBOSIS ( 23 FDA reports)
CREPITATIONS ( 23 FDA reports)
DRUG ADMINISTRATION ERROR ( 23 FDA reports)
EYE IRRITATION ( 23 FDA reports)
FAMILY STRESS ( 23 FDA reports)
HYPOKINESIA ( 23 FDA reports)
INTENTIONAL DRUG MISUSE ( 23 FDA reports)
LIPASE INCREASED ( 23 FDA reports)
MUSCLE SWELLING ( 23 FDA reports)
OCCULT BLOOD POSITIVE ( 23 FDA reports)
ONYCHOMYCOSIS ( 23 FDA reports)
ORAL DISCOMFORT ( 23 FDA reports)
PANCREATIC DISORDER ( 23 FDA reports)
PLEURITIC PAIN ( 23 FDA reports)
POOR QUALITY SLEEP ( 23 FDA reports)
STEVENS-JOHNSON SYNDROME ( 23 FDA reports)
ABDOMINAL PAIN LOWER ( 22 FDA reports)
ABDOMINAL TENDERNESS ( 22 FDA reports)
BRADYARRHYTHMIA ( 22 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 22 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 22 FDA reports)
EMPYEMA ( 22 FDA reports)
EXPOSED BONE IN JAW ( 22 FDA reports)
HOSPITALISATION ( 22 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 22 FDA reports)
ILEUS PARALYTIC ( 22 FDA reports)
JOINT EFFUSION ( 22 FDA reports)
JUGULAR VEIN THROMBOSIS ( 22 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 22 FDA reports)
MITRAL VALVE PROLAPSE ( 22 FDA reports)
MOUTH HAEMORRHAGE ( 22 FDA reports)
NEUROPATHY ( 22 FDA reports)
PANIC DISORDER ( 22 FDA reports)
RIGHT ATRIAL DILATATION ( 22 FDA reports)
SOMNAMBULISM ( 22 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 22 FDA reports)
SUBCUTANEOUS ABSCESS ( 22 FDA reports)
TARDIVE DYSKINESIA ( 22 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 22 FDA reports)
VASCULITIS ( 22 FDA reports)
WOUND INFECTION ( 22 FDA reports)
ACUTE SINUSITIS ( 21 FDA reports)
ATRIAL TACHYCARDIA ( 21 FDA reports)
BRONCHIECTASIS ( 21 FDA reports)
CHEST X-RAY ABNORMAL ( 21 FDA reports)
CHRONIC SINUSITIS ( 21 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 21 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 21 FDA reports)
EXTRASYSTOLES ( 21 FDA reports)
GINGIVAL SWELLING ( 21 FDA reports)
LIMB INJURY ( 21 FDA reports)
MASTICATION DISORDER ( 21 FDA reports)
MENINGIOMA ( 21 FDA reports)
MENOPAUSE ( 21 FDA reports)
MIOSIS ( 21 FDA reports)
PURPURA ( 21 FDA reports)
RETINAL DETACHMENT ( 21 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 21 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 21 FDA reports)
VENOUS INSUFFICIENCY ( 21 FDA reports)
VENTRICULAR DYSFUNCTION ( 21 FDA reports)
VISUAL FIELD DEFECT ( 21 FDA reports)
ASPIRATION ( 20 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 20 FDA reports)
DERMATITIS ( 20 FDA reports)
DIABETIC COMA ( 20 FDA reports)
FUNGAL INFECTION ( 20 FDA reports)
HAEMODYNAMIC INSTABILITY ( 20 FDA reports)
HYPERCALCAEMIA ( 20 FDA reports)
HYPOTONIA ( 20 FDA reports)
IMPETIGO ( 20 FDA reports)
INFUSION RELATED REACTION ( 20 FDA reports)
KLEBSIELLA INFECTION ( 20 FDA reports)
NERVE INJURY ( 20 FDA reports)
OCCIPITAL NEURALGIA ( 20 FDA reports)
OSTEORADIONECROSIS ( 20 FDA reports)
POLYURIA ( 20 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 20 FDA reports)
PRESCRIBED OVERDOSE ( 20 FDA reports)
PROCEDURAL COMPLICATION ( 20 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 20 FDA reports)
PULMONARY AIR LEAKAGE ( 20 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 20 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 20 FDA reports)
RETINAL HAEMORRHAGE ( 20 FDA reports)
SYNOVIAL RUPTURE ( 20 FDA reports)
TACHYPNOEA ( 20 FDA reports)
TONGUE DISORDER ( 20 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 20 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 20 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 20 FDA reports)
ABDOMINAL HERNIA ( 19 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 19 FDA reports)
ANXIETY DISORDER ( 19 FDA reports)
APHAGIA ( 19 FDA reports)
APLASTIC ANAEMIA ( 19 FDA reports)
BARTHOLIN'S CYST ( 19 FDA reports)
BLADDER CANCER ( 19 FDA reports)
BONE GIANT CELL TUMOUR ( 19 FDA reports)
CERVICOBRACHIAL SYNDROME ( 19 FDA reports)
DERMAL CYST ( 19 FDA reports)
DUODENAL ULCER ( 19 FDA reports)
EYE DISCHARGE ( 19 FDA reports)
FACIAL PALSY ( 19 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 19 FDA reports)
GASTRITIS EROSIVE ( 19 FDA reports)
GINGIVAL INFECTION ( 19 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 19 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 19 FDA reports)
HYPERTENSIVE HEART DISEASE ( 19 FDA reports)
INTESTINAL ISCHAEMIA ( 19 FDA reports)
INTRACRANIAL ANEURYSM ( 19 FDA reports)
ISCHAEMIC STROKE ( 19 FDA reports)
JAUNDICE CHOLESTATIC ( 19 FDA reports)
LIVEDO RETICULARIS ( 19 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 19 FDA reports)
NASAL SEPTUM DEVIATION ( 19 FDA reports)
NON-CARDIAC CHEST PAIN ( 19 FDA reports)
PANCREATITIS NECROTISING ( 19 FDA reports)
PARAPLEGIA ( 19 FDA reports)
PATHOLOGICAL GAMBLING ( 19 FDA reports)
POLYCYTHAEMIA ( 19 FDA reports)
RADIUS FRACTURE ( 19 FDA reports)
THINKING ABNORMAL ( 19 FDA reports)
VAGINAL HAEMORRHAGE ( 19 FDA reports)
VITAMIN B12 DEFICIENCY ( 19 FDA reports)
WHEELCHAIR USER ( 19 FDA reports)
WOUND DEHISCENCE ( 19 FDA reports)
ACIDOSIS ( 18 FDA reports)
ANKLE FRACTURE ( 18 FDA reports)
AORTIC VALVE SCLEROSIS ( 18 FDA reports)
BLINDNESS TRANSIENT ( 18 FDA reports)
BLOOD CREATINE INCREASED ( 18 FDA reports)
BONE MARROW FAILURE ( 18 FDA reports)
BREATH SOUNDS ABNORMAL ( 18 FDA reports)
CATHETER PLACEMENT ( 18 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 18 FDA reports)
COSTOCHONDRITIS ( 18 FDA reports)
DERMATITIS BULLOUS ( 18 FDA reports)
DRUG DISPENSING ERROR ( 18 FDA reports)
EAR INFECTION ( 18 FDA reports)
ESCHERICHIA INFECTION ( 18 FDA reports)
FLUID INTAKE REDUCED ( 18 FDA reports)
GANGRENE ( 18 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 18 FDA reports)
HEART RATE ABNORMAL ( 18 FDA reports)
HEPATIC NEOPLASM ( 18 FDA reports)
HERPES SIMPLEX ( 18 FDA reports)
HIP ARTHROPLASTY ( 18 FDA reports)
HYDROPNEUMOTHORAX ( 18 FDA reports)
INJURY CORNEAL ( 18 FDA reports)
LOSS OF LIBIDO ( 18 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 18 FDA reports)
MELANOCYTIC NAEVUS ( 18 FDA reports)
MULTIPLE SCLEROSIS ( 18 FDA reports)
NECROSIS ( 18 FDA reports)
NEOPLASM ( 18 FDA reports)
PEPTIC ULCER ( 18 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 18 FDA reports)
PUBIS FRACTURE ( 18 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 18 FDA reports)
TENSION ( 18 FDA reports)
URINE COLOUR ABNORMAL ( 18 FDA reports)
APHTHOUS STOMATITIS ( 17 FDA reports)
ATAXIA ( 17 FDA reports)
BACTERIAL DISEASE CARRIER ( 17 FDA reports)
BLOOD URIC ACID INCREASED ( 17 FDA reports)
BREAST CANCER FEMALE ( 17 FDA reports)
BRONCHITIS ACUTE ( 17 FDA reports)
BRONCHOPLEURAL FISTULA ( 17 FDA reports)
BUNDLE BRANCH BLOCK ( 17 FDA reports)
CHOLECYSTECTOMY ( 17 FDA reports)
CLOSTRIDIAL INFECTION ( 17 FDA reports)
CYTOLYTIC HEPATITIS ( 17 FDA reports)
DIABETIC ULCER ( 17 FDA reports)
DRUG LEVEL INCREASED ( 17 FDA reports)
DYSTHYMIC DISORDER ( 17 FDA reports)
EATING DISORDER ( 17 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 17 FDA reports)
ENGRAFTMENT SYNDROME ( 17 FDA reports)
FIBULA FRACTURE ( 17 FDA reports)
FISTULA ( 17 FDA reports)
GRANULOMA ( 17 FDA reports)
HAEMOLYSIS ( 17 FDA reports)
INJECTION SITE SWELLING ( 17 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 17 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 17 FDA reports)
LIP DISCOLOURATION ( 17 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 17 FDA reports)
PERSONALITY CHANGE ( 17 FDA reports)
SEQUESTRECTOMY ( 17 FDA reports)
SNEEZING ( 17 FDA reports)
THERAPY NON-RESPONDER ( 17 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 17 FDA reports)
VASCULAR CALCIFICATION ( 17 FDA reports)
VENTRICULAR ARRHYTHMIA ( 17 FDA reports)
WOUND DRAINAGE ( 17 FDA reports)
ABNORMAL SENSATION IN EYE ( 16 FDA reports)
ABORTION SPONTANEOUS ( 16 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 16 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 16 FDA reports)
BODY HEIGHT DECREASED ( 16 FDA reports)
BONE LOSS ( 16 FDA reports)
BRAIN NEOPLASM ( 16 FDA reports)
BRUXISM ( 16 FDA reports)
CAROTID ARTERY DISEASE ( 16 FDA reports)
CHONDROMALACIA ( 16 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 16 FDA reports)
CROHN'S DISEASE ( 16 FDA reports)
DEVICE RELATED INFECTION ( 16 FDA reports)
EMBOLIC STROKE ( 16 FDA reports)
ESSENTIAL HYPERTENSION ( 16 FDA reports)
GINGIVAL DISORDER ( 16 FDA reports)
HAEMORRHAGIC DIATHESIS ( 16 FDA reports)
HAEMORRHAGIC STROKE ( 16 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 16 FDA reports)
IMPAIRED DRIVING ABILITY ( 16 FDA reports)
INITIAL INSOMNIA ( 16 FDA reports)
JAW OPERATION ( 16 FDA reports)
KYPHOSIS ( 16 FDA reports)
LIPIDS INCREASED ( 16 FDA reports)
LOCAL SWELLING ( 16 FDA reports)
MEDICAL DEVICE COMPLICATION ( 16 FDA reports)
MYOCLONUS ( 16 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 16 FDA reports)
PARKINSON'S DISEASE ( 16 FDA reports)
PELVIC PAIN ( 16 FDA reports)
PROSTHESIS USER ( 16 FDA reports)
PULMONARY MASS ( 16 FDA reports)
QUALITY OF LIFE DECREASED ( 16 FDA reports)
RENAL MASS ( 16 FDA reports)
RETINOPATHY ( 16 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 16 FDA reports)
SCHIZOPHRENIA ( 16 FDA reports)
SEBORRHOEIC KERATOSIS ( 16 FDA reports)
SHOCK HYPOGLYCAEMIC ( 16 FDA reports)
SNORING ( 16 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 16 FDA reports)
ULNA FRACTURE ( 16 FDA reports)
UTERINE CANCER ( 16 FDA reports)
VASCULAR PSEUDOANEURYSM ( 16 FDA reports)
BIPOLAR I DISORDER ( 15 FDA reports)
BLEPHARITIS ( 15 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 15 FDA reports)
BREAST PAIN ( 15 FDA reports)
BURNS THIRD DEGREE ( 15 FDA reports)
CACHEXIA ( 15 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 15 FDA reports)
CAROTID BRUIT ( 15 FDA reports)
CHOLECYSTITIS ACUTE ( 15 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 15 FDA reports)
CLAVICLE FRACTURE ( 15 FDA reports)
CUBITAL TUNNEL SYNDROME ( 15 FDA reports)
DEMYELINATION ( 15 FDA reports)
DEVICE MALFUNCTION ( 15 FDA reports)
DIABETIC COMPLICATION ( 15 FDA reports)
DRUG ERUPTION ( 15 FDA reports)
EAR DISCOMFORT ( 15 FDA reports)
EARLY SATIETY ( 15 FDA reports)
ENTEROCOCCAL INFECTION ( 15 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 15 FDA reports)
FACIAL PARESIS ( 15 FDA reports)
GOUTY ARTHRITIS ( 15 FDA reports)
HAEMOLYTIC ANAEMIA ( 15 FDA reports)
HAND FRACTURE ( 15 FDA reports)
HERNIA ( 15 FDA reports)
HYPOALBUMINAEMIA ( 15 FDA reports)
HYPOGLYCAEMIC COMA ( 15 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 15 FDA reports)
INJECTION SITE HAEMATOMA ( 15 FDA reports)
INJECTION SITE IRRITATION ( 15 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 15 FDA reports)
LABILE BLOOD PRESSURE ( 15 FDA reports)
MITRAL VALVE DISEASE ( 15 FDA reports)
MYELODYSPLASTIC SYNDROME ( 15 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 15 FDA reports)
OSTEOSCLEROSIS ( 15 FDA reports)
PIGMENTATION DISORDER ( 15 FDA reports)
RECTAL POLYP ( 15 FDA reports)
SENSATION OF FOREIGN BODY ( 15 FDA reports)
STREPTOCOCCAL INFECTION ( 15 FDA reports)
WALKING AID USER ( 15 FDA reports)
APLASIA PURE RED CELL ( 14 FDA reports)
ARTERIAL THROMBOSIS ( 14 FDA reports)
ATHEROSCLEROSIS ( 14 FDA reports)
BLADDER DISORDER ( 14 FDA reports)
BLOOD PH DECREASED ( 14 FDA reports)
BODY TEMPERATURE DECREASED ( 14 FDA reports)
BONE MARROW OEDEMA ( 14 FDA reports)
BREAST CALCIFICATIONS ( 14 FDA reports)
CONTRAST MEDIA REACTION ( 14 FDA reports)
DRUG ABUSER ( 14 FDA reports)
ENDOMETRIAL CANCER ( 14 FDA reports)
EPIGASTRIC DISCOMFORT ( 14 FDA reports)
ERYTHEMA MULTIFORME ( 14 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 14 FDA reports)
EYELID PTOSIS ( 14 FDA reports)
FIBRIN D DIMER INCREASED ( 14 FDA reports)
GRAND MAL CONVULSION ( 14 FDA reports)
HEMIPLEGIA ( 14 FDA reports)
HEPATIC ENCEPHALOPATHY ( 14 FDA reports)
HEPATOSPLENOMEGALY ( 14 FDA reports)
HICCUPS ( 14 FDA reports)
HUMERUS FRACTURE ( 14 FDA reports)
HYPERTONIC BLADDER ( 14 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 14 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 14 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 14 FDA reports)
INTESTINAL OBSTRUCTION ( 14 FDA reports)
KNEE ARTHROPLASTY ( 14 FDA reports)
LICHEN PLANUS ( 14 FDA reports)
METABOLIC ENCEPHALOPATHY ( 14 FDA reports)
NERVE COMPRESSION ( 14 FDA reports)
OESOPHAGEAL STENOSIS ( 14 FDA reports)
ORGAN FAILURE ( 14 FDA reports)
OROPHARYNGEAL BLISTERING ( 14 FDA reports)
PERITONITIS BACTERIAL ( 14 FDA reports)
PHOTOPHOBIA ( 14 FDA reports)
PLEURAL FIBROSIS ( 14 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 14 FDA reports)
PSEUDOMONAS INFECTION ( 14 FDA reports)
PSYCHOTIC DISORDER ( 14 FDA reports)
RADICULITIS CERVICAL ( 14 FDA reports)
SKIN PLAQUE ( 14 FDA reports)
SPUTUM DISCOLOURED ( 14 FDA reports)
VASCULAR OCCLUSION ( 14 FDA reports)
AORTIC DILATATION ( 13 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 13 FDA reports)
CEREBRAL DISORDER ( 13 FDA reports)
COLON CANCER METASTATIC ( 13 FDA reports)
COR PULMONALE ( 13 FDA reports)
DEAFNESS UNILATERAL ( 13 FDA reports)
DENTAL OPERATION ( 13 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 13 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 13 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 13 FDA reports)
ENDOCARDITIS ( 13 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 13 FDA reports)
EYELID OEDEMA ( 13 FDA reports)
GASTROENTERITIS RADIATION ( 13 FDA reports)
GINGIVAL RECESSION ( 13 FDA reports)
HEPATIC LESION ( 13 FDA reports)
HEPATITIS CHOLESTATIC ( 13 FDA reports)
HYPERTHYROIDISM ( 13 FDA reports)
HYPERVENTILATION ( 13 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 13 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 13 FDA reports)
INCREASED APPETITE ( 13 FDA reports)
INTESTINAL POLYP ( 13 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 13 FDA reports)
LEFT VENTRICULAR FAILURE ( 13 FDA reports)
LOSS OF EMPLOYMENT ( 13 FDA reports)
MALIGNANT HYPERTENSION ( 13 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 13 FDA reports)
NASAL DISORDER ( 13 FDA reports)
NEPHROSCLEROSIS ( 13 FDA reports)
NEURITIS ( 13 FDA reports)
NEUROLOGICAL SYMPTOM ( 13 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 13 FDA reports)
PANIC REACTION ( 13 FDA reports)
PARKINSONISM ( 13 FDA reports)
PAROSMIA ( 13 FDA reports)
PELVIC FRACTURE ( 13 FDA reports)
PLATELET COUNT INCREASED ( 13 FDA reports)
PROTEIN URINE PRESENT ( 13 FDA reports)
PSYCHIATRIC SYMPTOM ( 13 FDA reports)
REFLUX OESOPHAGITIS ( 13 FDA reports)
SCAPULA FRACTURE ( 13 FDA reports)
SECONDARY SEQUESTRUM ( 13 FDA reports)
TENDON DISORDER ( 13 FDA reports)
THERMAL BURN ( 13 FDA reports)
TORSADE DE POINTES ( 13 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 13 FDA reports)
TRAUMATIC BRAIN INJURY ( 13 FDA reports)
VAGINAL DISCHARGE ( 13 FDA reports)
VERBAL ABUSE ( 13 FDA reports)
VITREOUS HAEMORRHAGE ( 13 FDA reports)
WEIGHT FLUCTUATION ( 13 FDA reports)
ADHESION ( 12 FDA reports)
ALLERGIC COUGH ( 12 FDA reports)
ANGIOPLASTY ( 12 FDA reports)
AORTIC BRUIT ( 12 FDA reports)
AORTIC DISORDER ( 12 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 12 FDA reports)
BIOPSY BONE ( 12 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 12 FDA reports)
BLOOD MAGNESIUM DECREASED ( 12 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 12 FDA reports)
BREAST DISORDER ( 12 FDA reports)
CALCULUS URETERIC ( 12 FDA reports)
CARDIAC VALVE SCLEROSIS ( 12 FDA reports)
CARDIOPULMONARY FAILURE ( 12 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 12 FDA reports)
CERUMEN IMPACTION ( 12 FDA reports)
CHRONIC FATIGUE SYNDROME ( 12 FDA reports)
COLON CANCER ( 12 FDA reports)
COMPULSIONS ( 12 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 12 FDA reports)
CONDUCTION DISORDER ( 12 FDA reports)
CULTURE URINE POSITIVE ( 12 FDA reports)
DRUG PRESCRIBING ERROR ( 12 FDA reports)
ENDOTRACHEAL INTUBATION ( 12 FDA reports)
EPILEPSY ( 12 FDA reports)
FRACTURE NONUNION ( 12 FDA reports)
GINGIVAL PAIN ( 12 FDA reports)
GUN SHOT WOUND ( 12 FDA reports)
HAEMANGIOMA ( 12 FDA reports)
HUNGER ( 12 FDA reports)
HYPERAESTHESIA ( 12 FDA reports)
HYPOAESTHESIA ORAL ( 12 FDA reports)
HYPOTHERMIA ( 12 FDA reports)
HYPOVOLAEMIC SHOCK ( 12 FDA reports)
INJECTION SITE PRURITUS ( 12 FDA reports)
JUGULAR VEIN DISTENSION ( 12 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 12 FDA reports)
LABYRINTHITIS ( 12 FDA reports)
LIMB DISCOMFORT ( 12 FDA reports)
LIPOMA ( 12 FDA reports)
LIVER OPERATION ( 12 FDA reports)
LUMBAR RADICULOPATHY ( 12 FDA reports)
MANIA ( 12 FDA reports)
METASTASES TO SPINE ( 12 FDA reports)
MOOD ALTERED ( 12 FDA reports)
NEUROGENIC BLADDER ( 12 FDA reports)
NODAL RHYTHM ( 12 FDA reports)
OCCULT BLOOD ( 12 FDA reports)
OCULAR ICTERUS ( 12 FDA reports)
PERFORMANCE STATUS DECREASED ( 12 FDA reports)
POLYNEUROPATHY ( 12 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 12 FDA reports)
POSTNASAL DRIP ( 12 FDA reports)
PROSTATITIS ( 12 FDA reports)
RAYNAUD'S PHENOMENON ( 12 FDA reports)
RESORPTION BONE INCREASED ( 12 FDA reports)
SINUS HEADACHE ( 12 FDA reports)
SPINAL FRACTURE ( 12 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 12 FDA reports)
STENT OCCLUSION ( 12 FDA reports)
SUDDEN CARDIAC DEATH ( 12 FDA reports)
SYNOVITIS ( 12 FDA reports)
TOOTH IMPACTED ( 12 FDA reports)
TRIGEMINAL NEURALGIA ( 12 FDA reports)
VARICOSE VEIN ( 12 FDA reports)
XEROSIS ( 12 FDA reports)
ACNE ( 11 FDA reports)
ADJUSTMENT DISORDER ( 11 FDA reports)
ANORECTAL DISORDER ( 11 FDA reports)
ANOSMIA ( 11 FDA reports)
APPENDICECTOMY ( 11 FDA reports)
ASPHYXIA ( 11 FDA reports)
ASTIGMATISM ( 11 FDA reports)
BENIGN RENAL NEOPLASM ( 11 FDA reports)
BLADDER MASS ( 11 FDA reports)
BLADDER SPASM ( 11 FDA reports)
BLOOD CHLORIDE DECREASED ( 11 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 11 FDA reports)
BRAIN SCAN ABNORMAL ( 11 FDA reports)
CAESAREAN SECTION ( 11 FDA reports)
CALCULUS URINARY ( 11 FDA reports)
CATHETER RELATED INFECTION ( 11 FDA reports)
CHEST TUBE INSERTION ( 11 FDA reports)
CORONARY ARTERY RESTENOSIS ( 11 FDA reports)
DENTAL CARE ( 11 FDA reports)
DIABETIC GASTROPARESIS ( 11 FDA reports)
EYE OEDEMA ( 11 FDA reports)
FACET JOINT SYNDROME ( 11 FDA reports)
FEELING DRUNK ( 11 FDA reports)
FIBROSIS ( 11 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 11 FDA reports)
GYNAECOMASTIA ( 11 FDA reports)
HAEMANGIOMA OF LIVER ( 11 FDA reports)
HEPATOTOXICITY ( 11 FDA reports)
HERNIA REPAIR ( 11 FDA reports)
HYPOAESTHESIA FACIAL ( 11 FDA reports)
HYPOCHLORAEMIA ( 11 FDA reports)
KIDNEY INFECTION ( 11 FDA reports)
LENTIGO ( 11 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 11 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 11 FDA reports)
LYMPHOPENIA ( 11 FDA reports)
MENORRHAGIA ( 11 FDA reports)
METASTASIS ( 11 FDA reports)
MICROCYTIC ANAEMIA ( 11 FDA reports)
NEPHRITIS INTERSTITIAL ( 11 FDA reports)
NEPHROPATHY ( 11 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 11 FDA reports)
OESOPHAGEAL SPASM ( 11 FDA reports)
OPEN FRACTURE ( 11 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 11 FDA reports)
PARAESTHESIA ORAL ( 11 FDA reports)
PAROTID GLAND ENLARGEMENT ( 11 FDA reports)
PARTNER STRESS ( 11 FDA reports)
PEAU D'ORANGE ( 11 FDA reports)
PERONEAL NERVE PALSY ( 11 FDA reports)
PERSONALITY DISORDER ( 11 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 11 FDA reports)
PROTEIN TOTAL INCREASED ( 11 FDA reports)
PSORIATIC ARTHROPATHY ( 11 FDA reports)
PUPIL FIXED ( 11 FDA reports)
PUPILS UNEQUAL ( 11 FDA reports)
RASH PUSTULAR ( 11 FDA reports)
RENAL CANCER ( 11 FDA reports)
RESPIRATORY TRACT INFECTION ( 11 FDA reports)
SERUM FERRITIN INCREASED ( 11 FDA reports)
SEXUAL DYSFUNCTION ( 11 FDA reports)
SKIN NODULE ( 11 FDA reports)
SOFT TISSUE DISORDER ( 11 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 11 FDA reports)
SYNCOPE VASOVAGAL ( 11 FDA reports)
VASCULAR GRAFT OCCLUSION ( 11 FDA reports)
WITHDRAWAL SYNDROME ( 11 FDA reports)
WRONG DRUG ADMINISTERED ( 11 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 10 FDA reports)
AFFECTIVE DISORDER ( 10 FDA reports)
ANOXIC ENCEPHALOPATHY ( 10 FDA reports)
AORTIC CALCIFICATION ( 10 FDA reports)
APPLICATION SITE RASH ( 10 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 10 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 10 FDA reports)
BREATH ODOUR ( 10 FDA reports)
BULIMIA NERVOSA ( 10 FDA reports)
CARDIAC ENZYMES INCREASED ( 10 FDA reports)
CARDIAC FAILURE ACUTE ( 10 FDA reports)
CARDIAC FAILURE CHRONIC ( 10 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 10 FDA reports)
CHOLECYSTITIS CHRONIC ( 10 FDA reports)
COLITIS ULCERATIVE ( 10 FDA reports)
COLON POLYPECTOMY ( 10 FDA reports)
CORONARY ANGIOPLASTY ( 10 FDA reports)
CORONARY ARTERY SURGERY ( 10 FDA reports)
CUTIS LAXA ( 10 FDA reports)
DELUSION ( 10 FDA reports)
DERMOID CYST ( 10 FDA reports)
DROOLING ( 10 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 10 FDA reports)
EMBOLISM ( 10 FDA reports)
EPIDERMAL NECROSIS ( 10 FDA reports)
EROSIVE DUODENITIS ( 10 FDA reports)
ESCHERICHIA SEPSIS ( 10 FDA reports)
EXOPHTHALMOS ( 10 FDA reports)
FIBROUS DYSPLASIA OF JAW ( 10 FDA reports)
FOLLICULITIS ( 10 FDA reports)
GASTRIC HAEMORRHAGE ( 10 FDA reports)
HAEMOGLOBIN ABNORMAL ( 10 FDA reports)
HALLUCINATION, AUDITORY ( 10 FDA reports)
HEPATIC CONGESTION ( 10 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 10 FDA reports)
HIGH FREQUENCY ABLATION ( 10 FDA reports)
HYPOVENTILATION ( 10 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 10 FDA reports)
INGROWING NAIL ( 10 FDA reports)
INTENTIONAL SELF-INJURY ( 10 FDA reports)
INTESTINAL PERFORATION ( 10 FDA reports)
JOINT CONTRACTURE ( 10 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 10 FDA reports)
LICHENOID KERATOSIS ( 10 FDA reports)
LIGAMENT DISORDER ( 10 FDA reports)
LIVER INJURY ( 10 FDA reports)
LYMPHOMA ( 10 FDA reports)
MALLORY-WEISS SYNDROME ( 10 FDA reports)
MEDIASTINITIS ( 10 FDA reports)
MICTURITION DISORDER ( 10 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 10 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 10 FDA reports)
MYOPIA ( 10 FDA reports)
NASAL OEDEMA ( 10 FDA reports)
NASAL TURBINATE ABNORMALITY ( 10 FDA reports)
NEPHROPATHY TOXIC ( 10 FDA reports)
NEUROMYOPATHY ( 10 FDA reports)
NIPPLE EXUDATE BLOODY ( 10 FDA reports)
OESOPHAGEAL RUPTURE ( 10 FDA reports)
OPEN ANGLE GLAUCOMA ( 10 FDA reports)
PAIN OF SKIN ( 10 FDA reports)
PCO2 DECREASED ( 10 FDA reports)
PERITONITIS ( 10 FDA reports)
POST PROCEDURAL FISTULA ( 10 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 10 FDA reports)
PREGNANCY ( 10 FDA reports)
PREGNANCY TEST POSITIVE ( 10 FDA reports)
PREMATURE BABY ( 10 FDA reports)
PROCEDURAL HYPOTENSION ( 10 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 10 FDA reports)
RADIOTHERAPY ( 10 FDA reports)
RENAL PAIN ( 10 FDA reports)
RENAL TRANSPLANT ( 10 FDA reports)
RESPIRATORY ACIDOSIS ( 10 FDA reports)
RETROPERITONEAL HAEMATOMA ( 10 FDA reports)
SHOCK HAEMORRHAGIC ( 10 FDA reports)
SINUS OPERATION ( 10 FDA reports)
SKIN PAPILLOMA ( 10 FDA reports)
SLEEP WALKING ( 10 FDA reports)
SPINAL CORD COMPRESSION ( 10 FDA reports)
STRESS URINARY INCONTINENCE ( 10 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 10 FDA reports)
TRACHEOBRONCHITIS ( 10 FDA reports)
UTERINE DISORDER ( 10 FDA reports)
WEIGHT LOSS POOR ( 10 FDA reports)
ALVEOLITIS ( 9 FDA reports)
ALVEOLOPLASTY ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 9 FDA reports)
APICECTOMY ( 9 FDA reports)
APPENDICITIS ( 9 FDA reports)
APPLICATION SITE ERYTHEMA ( 9 FDA reports)
APPLICATION SITE REACTION ( 9 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 9 FDA reports)
ARTERIOSPASM CORONARY ( 9 FDA reports)
BACTERAEMIA ( 9 FDA reports)
BITE ( 9 FDA reports)
BLOOD CULTURE POSITIVE ( 9 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 9 FDA reports)
BRAIN STEM INFARCTION ( 9 FDA reports)
CALCIUM DEFICIENCY ( 9 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 9 FDA reports)
CATHETER SITE HAEMORRHAGE ( 9 FDA reports)
CLAUSTROPHOBIA ( 9 FDA reports)
COLON ADENOMA ( 9 FDA reports)
CONCUSSION ( 9 FDA reports)
DECREASED ACTIVITY ( 9 FDA reports)
DENTURE WEARER ( 9 FDA reports)
DERMATITIS ALLERGIC ( 9 FDA reports)
DERMATITIS EXFOLIATIVE ( 9 FDA reports)
DRUG ABUSE ( 9 FDA reports)
DRUG RESISTANCE ( 9 FDA reports)
DYSPNOEA EXACERBATED ( 9 FDA reports)
EAR DISORDER ( 9 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 9 FDA reports)
EUPHORIC MOOD ( 9 FDA reports)
EXPIRED DRUG ADMINISTERED ( 9 FDA reports)
EYE MOVEMENT DISORDER ( 9 FDA reports)
EYE PRURITUS ( 9 FDA reports)
FACET JOINT BLOCK ( 9 FDA reports)
FEAR OF DEATH ( 9 FDA reports)
FOLATE DEFICIENCY ( 9 FDA reports)
FURUNCLE ( 9 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 9 FDA reports)
GASTROINTESTINAL INFECTION ( 9 FDA reports)
GENERALISED ERYTHEMA ( 9 FDA reports)
GLOSSITIS ( 9 FDA reports)
GROIN PAIN ( 9 FDA reports)
HEART SOUNDS ABNORMAL ( 9 FDA reports)
HEPATIC ENZYME ABNORMAL ( 9 FDA reports)
HEPATIC NECROSIS ( 9 FDA reports)
HYDROCEPHALUS ( 9 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 9 FDA reports)
HYPERPLASIA ( 9 FDA reports)
HYPOPNOEA ( 9 FDA reports)
IMMOBILE ( 9 FDA reports)
INCISIONAL DRAINAGE ( 9 FDA reports)
INGUINAL HERNIA ( 9 FDA reports)
INJECTION SITE NODULE ( 9 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 9 FDA reports)
JAW LESION EXCISION ( 9 FDA reports)
JOINT DISLOCATION ( 9 FDA reports)
KETOACIDOSIS ( 9 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 9 FDA reports)
LIGAMENT RUPTURE ( 9 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 9 FDA reports)
MAMMOPLASTY ( 9 FDA reports)
MEIBOMIANITIS ( 9 FDA reports)
MENSTRUATION IRREGULAR ( 9 FDA reports)
MONARTHRITIS ( 9 FDA reports)
MOTOR DYSFUNCTION ( 9 FDA reports)
MUSCLE ENZYME INCREASED ( 9 FDA reports)
NEOPLASM PROGRESSION ( 9 FDA reports)
NERVE ROOT COMPRESSION ( 9 FDA reports)
NO ADVERSE EVENT ( 9 FDA reports)
OOPHORECTOMY ( 9 FDA reports)
OPTIC NEUROPATHY ( 9 FDA reports)
OROPHARYNGEAL SWELLING ( 9 FDA reports)
OSTEOARTHROPATHY ( 9 FDA reports)
OVERWEIGHT ( 9 FDA reports)
PERIORBITAL HAEMATOMA ( 9 FDA reports)
PHLEBITIS ( 9 FDA reports)
PINGUECULA ( 9 FDA reports)
PLEURODESIS ( 9 FDA reports)
PNEUMONIA KLEBSIELLA ( 9 FDA reports)
POSTOPERATIVE INFECTION ( 9 FDA reports)
PRESBYOPIA ( 9 FDA reports)
RADIAL NERVE PALSY ( 9 FDA reports)
RHONCHI ( 9 FDA reports)
RIGHT VENTRICULAR FAILURE ( 9 FDA reports)
SCRATCH ( 9 FDA reports)
SICCA SYNDROME ( 9 FDA reports)
SLUGGISHNESS ( 9 FDA reports)
SUBDURAL HAEMORRHAGE ( 9 FDA reports)
TESTICULAR SWELLING ( 9 FDA reports)
THORACOSTOMY ( 9 FDA reports)
THORACOTOMY ( 9 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 9 FDA reports)
THROMBOSIS IN DEVICE ( 9 FDA reports)
TUMOUR EXCISION ( 9 FDA reports)
ULCER HAEMORRHAGE ( 9 FDA reports)
VENOUS STENOSIS ( 9 FDA reports)
VIITH NERVE PARALYSIS ( 9 FDA reports)
VOLUME BLOOD DECREASED ( 9 FDA reports)
ABDOMINAL MASS ( 8 FDA reports)
ABNORMAL FAECES ( 8 FDA reports)
ACCIDENT ( 8 FDA reports)
ACCIDENT AT WORK ( 8 FDA reports)
ADRENAL DISORDER ( 8 FDA reports)
ANAEMIA MACROCYTIC ( 8 FDA reports)
ANAPHYLACTOID REACTION ( 8 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 8 FDA reports)
APATHY ( 8 FDA reports)
APPETITE DISORDER ( 8 FDA reports)
BENIGN BREAST LUMP REMOVAL ( 8 FDA reports)
BILE DUCT STONE ( 8 FDA reports)
BIOPSY GINGIVAL ( 8 FDA reports)
BLEEDING TIME PROLONGED ( 8 FDA reports)
BLOOD BLISTER ( 8 FDA reports)
BLOOD CALCIUM INCREASED ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MM INCREASED ( 8 FDA reports)
BLOOD DISORDER ( 8 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 8 FDA reports)
BLOOD IRON DECREASED ( 8 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 8 FDA reports)
BONE EROSION ( 8 FDA reports)
BONE TRIMMING ( 8 FDA reports)
BRACHIAL PLEXOPATHY ( 8 FDA reports)
BREAST ENLARGEMENT ( 8 FDA reports)
BRONCHITIS CHRONIC ( 8 FDA reports)
BUTTOCK PAIN ( 8 FDA reports)
CATHETER RELATED COMPLICATION ( 8 FDA reports)
CHOLANGITIS ( 8 FDA reports)
DEAFNESS NEUROSENSORY ( 8 FDA reports)
DIABETIC EYE DISEASE ( 8 FDA reports)
DRESSLER'S SYNDROME ( 8 FDA reports)
EAR CONGESTION ( 8 FDA reports)
EJACULATION FAILURE ( 8 FDA reports)
EUTHYROID SICK SYNDROME ( 8 FDA reports)
FACE INJURY ( 8 FDA reports)
FACIAL BONES FRACTURE ( 8 FDA reports)
FAECES PALE ( 8 FDA reports)
HELICOBACTER INFECTION ( 8 FDA reports)
HYPEROSMOLAR STATE ( 8 FDA reports)
HYPERSEXUALITY ( 8 FDA reports)
IMMUNOGLOBULINS DECREASED ( 8 FDA reports)
INCOHERENT ( 8 FDA reports)
LARGE INTESTINAL ULCER ( 8 FDA reports)
LARYNGOSPASM ( 8 FDA reports)
LIGAMENT INJURY ( 8 FDA reports)
MEDICATION RESIDUE ( 8 FDA reports)
MICROALBUMINURIA ( 8 FDA reports)
MYASTHENIA GRAVIS ( 8 FDA reports)
NAIL DISORDER ( 8 FDA reports)
NECK INJURY ( 8 FDA reports)
NEUTROPHIL COUNT INCREASED ( 8 FDA reports)
NO THERAPEUTIC RESPONSE ( 8 FDA reports)
OBSTRUCTIVE UROPATHY ( 8 FDA reports)
OESOPHAGEAL ULCER ( 8 FDA reports)
ORAL SOFT TISSUE DISORDER ( 8 FDA reports)
PARTIAL SEIZURES ( 8 FDA reports)
PLASMACYTOSIS ( 8 FDA reports)
POLYTRAUMATISM ( 8 FDA reports)
PULMONARY HAEMORRHAGE ( 8 FDA reports)
RADICULITIS LUMBOSACRAL ( 8 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 8 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 8 FDA reports)
RETINAL VEIN OCCLUSION ( 8 FDA reports)
ROTATOR CUFF REPAIR ( 8 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 8 FDA reports)
SKIN INFECTION ( 8 FDA reports)
SKIN IRRITATION ( 8 FDA reports)
SKIN WARM ( 8 FDA reports)
STRESS FRACTURE ( 8 FDA reports)
STRESS SYMPTOMS ( 8 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 8 FDA reports)
THROMBOPHLEBITIS ( 8 FDA reports)
TOBACCO USER ( 8 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 8 FDA reports)
TRAUMATIC ARTHRITIS ( 8 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 8 FDA reports)
URINARY HESITATION ( 8 FDA reports)
URINE CYTOLOGY ABNORMAL ( 8 FDA reports)
UTERINE PROLAPSE ( 8 FDA reports)
VITAMIN B12 INCREASED ( 8 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 8 FDA reports)
WOUND SECRETION ( 8 FDA reports)
ACCIDENTAL EXPOSURE ( 7 FDA reports)
ACUTE HEPATIC FAILURE ( 7 FDA reports)
ALCOHOL ABUSE ( 7 FDA reports)
ALCOHOL USE ( 7 FDA reports)
AMMONIA INCREASED ( 7 FDA reports)
AORTIC VALVE REPLACEMENT ( 7 FDA reports)
APPLICATION SITE PAIN ( 7 FDA reports)
APPLICATION SITE PRURITUS ( 7 FDA reports)
ARTERIAL INSUFFICIENCY ( 7 FDA reports)
ARTHRITIS INFECTIVE ( 7 FDA reports)
ARTHROPOD BITE ( 7 FDA reports)
B-CELL LYMPHOMA ( 7 FDA reports)
BILE DUCT STENOSIS ( 7 FDA reports)
BLOOD BICARBONATE DECREASED ( 7 FDA reports)
BLOOD LACTIC ACID INCREASED ( 7 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 7 FDA reports)
BREAST SWELLING ( 7 FDA reports)
CARDIAC OUTPUT DECREASED ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 7 FDA reports)
CARDIORENAL SYNDROME ( 7 FDA reports)
CARNITINE DECREASED ( 7 FDA reports)
CATARACT NUCLEAR ( 7 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 7 FDA reports)
CHEILITIS ( 7 FDA reports)
CHOKING SENSATION ( 7 FDA reports)
CLOSTRIDIUM COLITIS ( 7 FDA reports)
COELIAC DISEASE ( 7 FDA reports)
COLLAPSE OF LUNG ( 7 FDA reports)
COLOUR BLINDNESS ( 7 FDA reports)
CUSHINGOID ( 7 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 7 FDA reports)
DERMATOMYOSITIS ( 7 FDA reports)
DRUG EFFECT INCREASED ( 7 FDA reports)
DYSTONIA ( 7 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 7 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 7 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 7 FDA reports)
ENTERITIS ( 7 FDA reports)
ENTEROBACTER INFECTION ( 7 FDA reports)
ENTEROCELE ( 7 FDA reports)
EOSINOPHIL COUNT INCREASED ( 7 FDA reports)
ERYTHEMA NODOSUM ( 7 FDA reports)
EXERCISE TOLERANCE DECREASED ( 7 FDA reports)
FOOD CRAVING ( 7 FDA reports)
FOOT AMPUTATION ( 7 FDA reports)
FOREIGN BODY TRAUMA ( 7 FDA reports)
GASTRIC CANCER ( 7 FDA reports)
GASTRODUODENITIS ( 7 FDA reports)
GLUCOSE URINE PRESENT ( 7 FDA reports)
HAIR GROWTH ABNORMAL ( 7 FDA reports)
HOARSENESS ( 7 FDA reports)
HOMICIDAL IDEATION ( 7 FDA reports)
HYPERCAPNIA ( 7 FDA reports)
HYPERKINESIA ( 7 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 7 FDA reports)
INJECTION SITE EXTRAVASATION ( 7 FDA reports)
INSULIN RESISTANCE ( 7 FDA reports)
IODINE ALLERGY ( 7 FDA reports)
JOINT SPRAIN ( 7 FDA reports)
LOCALISED OEDEMA ( 7 FDA reports)
LYMPHOEDEMA ( 7 FDA reports)
MALIGNANT MELANOMA ( 7 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 7 FDA reports)
METABOLIC SYNDROME ( 7 FDA reports)
MIXED INCONTINENCE ( 7 FDA reports)
MULTIPLE FRACTURES ( 7 FDA reports)
MUSCLE HAEMORRHAGE ( 7 FDA reports)
MUSCLE NECROSIS ( 7 FDA reports)
NARCOTIC INTOXICATION ( 7 FDA reports)
NEUROPATHIC PAIN ( 7 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 7 FDA reports)
NON-SMALL CELL LUNG CANCER ( 7 FDA reports)
OESOPHAGEAL DISORDER ( 7 FDA reports)
ONYCHOMADESIS ( 7 FDA reports)
OPEN WOUND ( 7 FDA reports)
PANCREATIC CYST ( 7 FDA reports)
PERICARDIAL HAEMORRHAGE ( 7 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 7 FDA reports)
PLANTAR FASCIITIS ( 7 FDA reports)
POOR PERIPHERAL CIRCULATION ( 7 FDA reports)
POST HERPETIC NEURALGIA ( 7 FDA reports)
PROCTALGIA ( 7 FDA reports)
PROSTATE CANCER RECURRENT ( 7 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 7 FDA reports)
PROSTATIC OBSTRUCTION ( 7 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 7 FDA reports)
PULMONARY HILUM MASS ( 7 FDA reports)
RECTOCELE ( 7 FDA reports)
RESPIRATORY TRACT OEDEMA ( 7 FDA reports)
RETICULOCYTOSIS ( 7 FDA reports)
RETINAL ARTERY OCCLUSION ( 7 FDA reports)
RETINAL TEAR ( 7 FDA reports)
SCOTOMA ( 7 FDA reports)
SEASONAL ALLERGY ( 7 FDA reports)
SEPSIS SYNDROME ( 7 FDA reports)
SINUS ARREST ( 7 FDA reports)
SKIN ULCER HAEMORRHAGE ( 7 FDA reports)
SPLENIC INFARCTION ( 7 FDA reports)
SPONDYLOLYSIS ( 7 FDA reports)
SPUTUM CULTURE POSITIVE ( 7 FDA reports)
STEM CELL TRANSPLANT ( 7 FDA reports)
SUBCUTANEOUS NODULE ( 7 FDA reports)
SUPERINFECTION ( 7 FDA reports)
TOBACCO ABUSE ( 7 FDA reports)
TONGUE DRY ( 7 FDA reports)
TOXIC ENCEPHALOPATHY ( 7 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 7 FDA reports)
TROPONIN I INCREASED ( 7 FDA reports)
TUBERCULIN TEST POSITIVE ( 7 FDA reports)
URETERIC OBSTRUCTION ( 7 FDA reports)
URETHRAL SPASM ( 7 FDA reports)
URINE KETONE BODY PRESENT ( 7 FDA reports)
UTERINE ATONY ( 7 FDA reports)
VAGINAL PROLAPSE ( 7 FDA reports)
VASCULAR BYPASS GRAFT ( 7 FDA reports)
VASCULAR GRAFT ( 7 FDA reports)
VERTIGO POSITIONAL ( 7 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
ABDOMINAL INFECTION ( 6 FDA reports)
ABSCESS INTESTINAL ( 6 FDA reports)
ACROCHORDON ( 6 FDA reports)
ACUTE PSYCHOSIS ( 6 FDA reports)
ALLODYNIA ( 6 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 6 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 6 FDA reports)
ANAEMIA POSTOPERATIVE ( 6 FDA reports)
ANOXIA ( 6 FDA reports)
APHONIA ( 6 FDA reports)
ARTHROSCOPIC SURGERY ( 6 FDA reports)
ASTHMA LATE ONSET ( 6 FDA reports)
ATROPHIC VULVOVAGINITIS ( 6 FDA reports)
AURICULAR SWELLING ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
BILE DUCT OBSTRUCTION ( 6 FDA reports)
BILIARY CIRRHOSIS ( 6 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 6 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 6 FDA reports)
BONE LESION EXCISION ( 6 FDA reports)
BRAIN COMPRESSION ( 6 FDA reports)
BREAST DISCHARGE ( 6 FDA reports)
BREAST TENDERNESS ( 6 FDA reports)
CANCER PAIN ( 6 FDA reports)
CARTILAGE INJURY ( 6 FDA reports)
CATARACT CORTICAL ( 6 FDA reports)
CHANGE OF BOWEL HABIT ( 6 FDA reports)
CHEST WALL PAIN ( 6 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 6 FDA reports)
CYSTOCELE ( 6 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 6 FDA reports)
DERMATITIS CONTACT ( 6 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 6 FDA reports)
DIVERTICULAR PERFORATION ( 6 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 6 FDA reports)
DUODENITIS ( 6 FDA reports)
DYSPHASIA ( 6 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 6 FDA reports)
EPICONDYLITIS ( 6 FDA reports)
EPIDERMOID CYST EXCISION ( 6 FDA reports)
EXANTHEM ( 6 FDA reports)
FATTY LIVER ALCOHOLIC ( 6 FDA reports)
FOAMING AT MOUTH ( 6 FDA reports)
FOOD ALLERGY ( 6 FDA reports)
FOREARM FRACTURE ( 6 FDA reports)
FOREIGN BODY ( 6 FDA reports)
FORMICATION ( 6 FDA reports)
FRACTURED SACRUM ( 6 FDA reports)
GASTROINTESTINAL OEDEMA ( 6 FDA reports)
GLOBAL AMNESIA ( 6 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 6 FDA reports)
HAEMOTHORAX ( 6 FDA reports)
HEART TRANSPLANT ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
HEPATIC HAEMORRHAGE ( 6 FDA reports)
HIP SURGERY ( 6 FDA reports)
HYPERNATRAEMIA ( 6 FDA reports)
HYPERURICAEMIA ( 6 FDA reports)
HYPOAESTHESIA EYE ( 6 FDA reports)
HYPOPHOSPHATAEMIA ( 6 FDA reports)
INADEQUATE ANALGESIA ( 6 FDA reports)
INCISION SITE COMPLICATION ( 6 FDA reports)
INFARCTION ( 6 FDA reports)
INFERTILITY ( 6 FDA reports)
INJECTION SITE URTICARIA ( 6 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 6 FDA reports)
INTERCOSTAL NEURALGIA ( 6 FDA reports)
JOINT CREPITATION ( 6 FDA reports)
JOINT INSTABILITY ( 6 FDA reports)
JUDGEMENT IMPAIRED ( 6 FDA reports)
KNEE DEFORMITY ( 6 FDA reports)
LEUKAEMIA ( 6 FDA reports)
LIBIDO INCREASED ( 6 FDA reports)
LOCALISED OSTEOARTHRITIS ( 6 FDA reports)
LUNG INJURY ( 6 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 6 FDA reports)
LYMPHADENITIS ( 6 FDA reports)
MAGNESIUM DEFICIENCY ( 6 FDA reports)
MECHANICAL VENTILATION ( 6 FDA reports)
MONOPLEGIA ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE ( 6 FDA reports)
MUSCLE FLAP OPERATION ( 6 FDA reports)
MUSCULOSKELETAL DISORDER ( 6 FDA reports)
NAIL DISCOLOURATION ( 6 FDA reports)
NEPHROTIC SYNDROME ( 6 FDA reports)
NEUROSIS ( 6 FDA reports)
NIPPLE PAIN ( 6 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 6 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 6 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 6 FDA reports)
ONYCHOLYSIS ( 6 FDA reports)
OVARIAN CANCER ( 6 FDA reports)
PANCREATITIS CHRONIC ( 6 FDA reports)
PETIT MAL EPILEPSY ( 6 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 6 FDA reports)
PLEURISY ( 6 FDA reports)
POLYCYSTIC OVARIES ( 6 FDA reports)
PORTAL HYPERTENSION ( 6 FDA reports)
POST PROCEDURAL HAEMATOMA ( 6 FDA reports)
PROCEDURAL PAIN ( 6 FDA reports)
PROSTATE INFECTION ( 6 FDA reports)
PROSTATOMEGALY ( 6 FDA reports)
PROTEIN TOTAL DECREASED ( 6 FDA reports)
PSYCHOMOTOR RETARDATION ( 6 FDA reports)
PULMONARY GRANULOMA ( 6 FDA reports)
PULMONARY THROMBOSIS ( 6 FDA reports)
PYELONEPHRITIS ACUTE ( 6 FDA reports)
RADICULITIS BRACHIAL ( 6 FDA reports)
RASH VESICULAR ( 6 FDA reports)
RENAL CELL CARCINOMA ( 6 FDA reports)
RESPIRATORY RATE DECREASED ( 6 FDA reports)
RESPIRATORY TRACT CONGESTION ( 6 FDA reports)
SCAB ( 6 FDA reports)
SELF-MEDICATION ( 6 FDA reports)
SINOATRIAL BLOCK ( 6 FDA reports)
SINUS ARRHYTHMIA ( 6 FDA reports)
SKIN HAEMORRHAGE ( 6 FDA reports)
SKIN HYPOPIGMENTATION ( 6 FDA reports)
SKIN REACTION ( 6 FDA reports)
SKULL FRACTURED BASE ( 6 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 6 FDA reports)
SMOKER ( 6 FDA reports)
SPLENECTOMY ( 6 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 6 FDA reports)
STATUS EPILEPTICUS ( 6 FDA reports)
STUPOR ( 6 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 6 FDA reports)
TEMPERATURE INTOLERANCE ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 6 FDA reports)
TINEA PEDIS ( 6 FDA reports)
TONGUE DISCOLOURATION ( 6 FDA reports)
TONGUE ULCERATION ( 6 FDA reports)
TRIGGER FINGER ( 6 FDA reports)
UMBILICAL HERNIA ( 6 FDA reports)
URAEMIC GASTROPATHY ( 6 FDA reports)
URINARY TRACT DISORDER ( 6 FDA reports)
URINE FLOW DECREASED ( 6 FDA reports)
VARICES OESOPHAGEAL ( 6 FDA reports)
VASCULAR DEMENTIA ( 6 FDA reports)
VASCULAR PURPURA ( 6 FDA reports)
VISUAL MIDLINE SHIFT SYNDROME ( 6 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 6 FDA reports)
X-RAY ABNORMAL ( 6 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 5 FDA reports)
ADENOCARCINOMA ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
AMAUROSIS FUGAX ( 5 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 5 FDA reports)
ANIMAL BITE ( 5 FDA reports)
ANION GAP INCREASED ( 5 FDA reports)
ARTERIAL STENOSIS ( 5 FDA reports)
ASEPTIC NECROSIS BONE ( 5 FDA reports)
ATRIAL HYPERTROPHY ( 5 FDA reports)
ATROPHY ( 5 FDA reports)
AUTOIMMUNE HEPATITIS ( 5 FDA reports)
BLOOD CHLORIDE INCREASED ( 5 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 5 FDA reports)
BLOOD URINE ( 5 FDA reports)
BONE MARROW DEPRESSION ( 5 FDA reports)
BRAIN CONTUSION ( 5 FDA reports)
BREAST ABSCESS ( 5 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 5 FDA reports)
BURSITIS INFECTIVE ( 5 FDA reports)
CARDIAC DISCOMFORT ( 5 FDA reports)
CARDIAC TAMPONADE ( 5 FDA reports)
CARDIOVERSION ( 5 FDA reports)
CORONARY ARTERY REOCCLUSION ( 5 FDA reports)
CORONARY OSTIAL STENOSIS ( 5 FDA reports)
CUSHING'S SYNDROME ( 5 FDA reports)
CUTANEOUS VASCULITIS ( 5 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 5 FDA reports)
DERMATITIS ACNEIFORM ( 5 FDA reports)
DIABETIC FOOT ( 5 FDA reports)
DRUG CLEARANCE DECREASED ( 5 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 5 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENDOCARDITIS CANDIDA ( 5 FDA reports)
ENURESIS ( 5 FDA reports)
EXCESSIVE EYE BLINKING ( 5 FDA reports)
FEMORAL PULSE DECREASED ( 5 FDA reports)
FOOD INTOLERANCE ( 5 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 5 FDA reports)
GASTRIC OPERATION ( 5 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 5 FDA reports)
GASTROINTESTINAL ULCER ( 5 FDA reports)
GESTATIONAL DIABETES ( 5 FDA reports)
GINGIVAL HYPERPLASIA ( 5 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 5 FDA reports)
HAIR TEXTURE ABNORMAL ( 5 FDA reports)
HEPATOJUGULAR REFLUX ( 5 FDA reports)
HODGKIN'S DISEASE ( 5 FDA reports)
HYDROURETER ( 5 FDA reports)
HYPERCOAGULATION ( 5 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 5 FDA reports)
HYPOPERFUSION ( 5 FDA reports)
HYPOTRICHOSIS ( 5 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 5 FDA reports)
IMMUNOSUPPRESSION ( 5 FDA reports)
IMPAIRED SELF-CARE ( 5 FDA reports)
INCISIONAL HERNIA ( 5 FDA reports)
INJECTION SITE ABSCESS ( 5 FDA reports)
INJECTION SITE RASH ( 5 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 5 FDA reports)
INTUBATION ( 5 FDA reports)
IRIS DISORDER ( 5 FDA reports)
KERATOACANTHOMA ( 5 FDA reports)
LABILE HYPERTENSION ( 5 FDA reports)
LACTOSE INTOLERANCE ( 5 FDA reports)
LIP OEDEMA ( 5 FDA reports)
LIP PAIN ( 5 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 5 FDA reports)
LISTLESS ( 5 FDA reports)
LIVIDITY ( 5 FDA reports)
LOW TURNOVER OSTEOPATHY ( 5 FDA reports)
LUNG OPERATION ( 5 FDA reports)
MADAROSIS ( 5 FDA reports)
MASTITIS ( 5 FDA reports)
MEAN CELL VOLUME INCREASED ( 5 FDA reports)
MEGAKARYOCYTES INCREASED ( 5 FDA reports)
MENIERE'S DISEASE ( 5 FDA reports)
MITRAL VALVE REPAIR ( 5 FDA reports)
MITRAL VALVE REPLACEMENT ( 5 FDA reports)
MONOCYTE COUNT INCREASED ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 5 FDA reports)
MYCOSIS FUNGOIDES ( 5 FDA reports)
MYDRIASIS ( 5 FDA reports)
NEOVASCULARISATION ( 5 FDA reports)
NEUROPATHIC ARTHROPATHY ( 5 FDA reports)
NOCTURNAL DYSPNOEA ( 5 FDA reports)
NONSPECIFIC REACTION ( 5 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 5 FDA reports)
OBSTRUCTION GASTRIC ( 5 FDA reports)
OESOPHAGEAL PAIN ( 5 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 5 FDA reports)
OTORRHOEA ( 5 FDA reports)
OVARIAN CYST ( 5 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 5 FDA reports)
PARASOMNIA ( 5 FDA reports)
PATELLA FRACTURE ( 5 FDA reports)
PELVIC ABSCESS ( 5 FDA reports)
PERIDIVERTICULAR ABSCESS ( 5 FDA reports)
PERIORBITAL OEDEMA ( 5 FDA reports)
PHOTODERMATOSIS ( 5 FDA reports)
PITYRIASIS ROSEA ( 5 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 5 FDA reports)
POLYARTHRITIS ( 5 FDA reports)
POLYMYALGIA RHEUMATICA ( 5 FDA reports)
POLYMYOSITIS ( 5 FDA reports)
POLYP COLORECTAL ( 5 FDA reports)
POLYPECTOMY ( 5 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 5 FDA reports)
POST PROCEDURAL INFECTION ( 5 FDA reports)
POSTURE ABNORMAL ( 5 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 5 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 5 FDA reports)
QRS AXIS ABNORMAL ( 5 FDA reports)
REFLUX GASTRITIS ( 5 FDA reports)
RENAL COLIC ( 5 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 5 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 5 FDA reports)
RETINAL ANEURYSM ( 5 FDA reports)
RETINAL OEDEMA ( 5 FDA reports)
ROSACEA ( 5 FDA reports)
SECRETION DISCHARGE ( 5 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 5 FDA reports)
SENSATION OF PRESSURE ( 5 FDA reports)
SERUM FERRITIN DECREASED ( 5 FDA reports)
SHOULDER OPERATION ( 5 FDA reports)
SJOGREN'S SYNDROME ( 5 FDA reports)
SKIN ATROPHY ( 5 FDA reports)
SLEEP TERROR ( 5 FDA reports)
SOFT TISSUE NECROSIS ( 5 FDA reports)
SPINAL FUSION SURGERY ( 5 FDA reports)
SPINAL PAIN ( 5 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 5 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 5 FDA reports)
SYSTEMIC CANDIDA ( 5 FDA reports)
THORACIC CAVITY DRAINAGE ( 5 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 5 FDA reports)
THYROID NEOPLASM ( 5 FDA reports)
THYROIDITIS ( 5 FDA reports)
THYROXINE FREE INCREASED ( 5 FDA reports)
TRANSPLANT REJECTION ( 5 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 5 FDA reports)
TUMOUR LYSIS SYNDROME ( 5 FDA reports)
URETHRAL DISORDER ( 5 FDA reports)
URETHRAL STENOSIS ( 5 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 5 FDA reports)
URINE ABNORMALITY ( 5 FDA reports)
URINE ANALYSIS ABNORMAL ( 5 FDA reports)
UTERINE POLYP ( 5 FDA reports)
UVEITIS ( 5 FDA reports)
VENOUS OCCLUSION ( 5 FDA reports)
VENOUS THROMBOSIS ( 5 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 5 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
WOUND DEBRIDEMENT ( 5 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 4 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 4 FDA reports)
ABDOMINAL WALL ABSCESS ( 4 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 4 FDA reports)
ADRENAL ADENOMA ( 4 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
ADRENAL MASS ( 4 FDA reports)
ALCOHOLISM ( 4 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 4 FDA reports)
BENCE JONES PROTEINURIA ( 4 FDA reports)
BILIARY COLIC ( 4 FDA reports)
BIPOLAR II DISORDER ( 4 FDA reports)
BLADDER DISTENSION ( 4 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 4 FDA reports)
BLAST CELL COUNT INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL ( 4 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 4 FDA reports)
BLOOD COUNT ABNORMAL ( 4 FDA reports)
BLOOD CREATININE ABNORMAL ( 4 FDA reports)
BLOOD HOMOCYSTEINE ( 4 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN A ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN G ( 4 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 4 FDA reports)
BLOOD PH INCREASED ( 4 FDA reports)
BLOOD SODIUM INCREASED ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 4 FDA reports)
BONE FRAGMENTATION ( 4 FDA reports)
BONE NEOPLASM MALIGNANT ( 4 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BOWEN'S DISEASE ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
BUNION ( 4 FDA reports)
CALCULUS URETHRAL ( 4 FDA reports)
CARDIAC DEATH ( 4 FDA reports)
CARDIAC FIBRILLATION ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 4 FDA reports)
CEREBRAL HAEMATOMA ( 4 FDA reports)
CERVICAL DYSPLASIA ( 4 FDA reports)
CERVIX INFLAMMATION ( 4 FDA reports)
CHRONIC HEPATITIS ( 4 FDA reports)
CIRCUMORAL OEDEMA ( 4 FDA reports)
CLUSTER HEADACHE ( 4 FDA reports)
COLLAGEN DISORDER ( 4 FDA reports)
COLPORRHAPHY ( 4 FDA reports)
COMPULSIVE SHOPPING ( 4 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 4 FDA reports)
CONGENITAL ANOMALY ( 4 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 4 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 4 FDA reports)
CORNEAL EROSION ( 4 FDA reports)
CYSTOCELE REPAIR ( 4 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 4 FDA reports)
DELAYED SLEEP PHASE ( 4 FDA reports)
DEPENDENCE ( 4 FDA reports)
DEPRESSION SUICIDAL ( 4 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 4 FDA reports)
DIHYDROTESTOSTERONE DECREASED ( 4 FDA reports)
DRUG INTERACTION POTENTIATION ( 4 FDA reports)
DYSGRAPHIA ( 4 FDA reports)
DYSPAREUNIA ( 4 FDA reports)
DYSPNOEA AT REST ( 4 FDA reports)
EAR NEOPLASM MALIGNANT ( 4 FDA reports)
EJACULATION DELAYED ( 4 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ENDOMETRIOSIS ( 4 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 4 FDA reports)
ENTEROBACTER PNEUMONIA ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
EPIGLOTTIC OEDEMA ( 4 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 4 FDA reports)
EXTRADURAL HAEMATOMA ( 4 FDA reports)
FAT NECROSIS ( 4 FDA reports)
FEELING OF RELAXATION ( 4 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 4 FDA reports)
FLIGHT OF IDEAS ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
FROSTBITE ( 4 FDA reports)
FRUSTRATION ( 4 FDA reports)
GALLBLADDER OPERATION ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 4 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 4 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 4 FDA reports)
GENITAL DISCHARGE ( 4 FDA reports)
HAEMOCONCENTRATION ( 4 FDA reports)
HAEMOGLOBIN INCREASED ( 4 FDA reports)
HAEMOGLOBINURIA ( 4 FDA reports)
HANGOVER ( 4 FDA reports)
HELICOBACTER GASTRITIS ( 4 FDA reports)
HEMIANOPIA HOMONYMOUS ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HERPES VIRUS INFECTION ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 4 FDA reports)
HYPERPARATHYROIDISM ( 4 FDA reports)
HYPERTENSIVE EMERGENCY ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPERTROPHY BREAST ( 4 FDA reports)
HYPERVOLAEMIA ( 4 FDA reports)
HYPOREFLEXIA ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
IMPULSE-CONTROL DISORDER ( 4 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
INCISION SITE HAEMORRHAGE ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INCORRECT STORAGE OF DRUG ( 4 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 4 FDA reports)
INJECTION SITE DISCOMFORT ( 4 FDA reports)
INJECTION SITE REACTION ( 4 FDA reports)
INSULIN RESISTANCE SYNDROME ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
JEALOUS DELUSION ( 4 FDA reports)
LARGE INTESTINE PERFORATION ( 4 FDA reports)
LDL/HDL RATIO ( 4 FDA reports)
LIP DRY ( 4 FDA reports)
LIVER ABSCESS ( 4 FDA reports)
LOWER EXTREMITY MASS ( 4 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 4 FDA reports)
LYME DISEASE ( 4 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
MEAN CELL VOLUME DECREASED ( 4 FDA reports)
MEDICAL DEVICE REMOVAL ( 4 FDA reports)
MENINGEAL DISORDER ( 4 FDA reports)
METABOLIC ALKALOSIS ( 4 FDA reports)
METAMORPHOPSIA ( 4 FDA reports)
MITRAL VALVE STENOSIS ( 4 FDA reports)
MONOCLONAL GAMMOPATHY ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
MUCOUS MEMBRANE DISORDER ( 4 FDA reports)
MUCOUS STOOLS ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
MYELOID LEUKAEMIA ( 4 FDA reports)
MYOGLOBINURIA ( 4 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
NEUTROPHILIA ( 4 FDA reports)
NIGHT CRAMPS ( 4 FDA reports)
NODAL ARRHYTHMIA ( 4 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 4 FDA reports)
OPTIC NEURITIS ( 4 FDA reports)
OSTEOMA ( 4 FDA reports)
PAINFUL DEFAECATION ( 4 FDA reports)
PCO2 INCREASED ( 4 FDA reports)
PELVIC DISCOMFORT ( 4 FDA reports)
PEMPHIGOID ( 4 FDA reports)
PENILE HAEMORRHAGE ( 4 FDA reports)
PHARYNGEAL DISORDER ( 4 FDA reports)
PHOTOPSIA ( 4 FDA reports)
PITTING OEDEMA ( 4 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 4 FDA reports)
POLYCHONDRITIS ( 4 FDA reports)
POLYCYTHAEMIA VERA ( 4 FDA reports)
POSTOPERATIVE FEVER ( 4 FDA reports)
PROSTATIC DISORDER ( 4 FDA reports)
PRURIGO ( 4 FDA reports)
PRURITUS GENITAL ( 4 FDA reports)
PULMONARY TOXICITY ( 4 FDA reports)
REBOUND HYPERTENSION ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
RENAL ARTERY THROMBOSIS ( 4 FDA reports)
RENAL ATROPHY ( 4 FDA reports)
REPETITIVE SPEECH ( 4 FDA reports)
RESUSCITATION ( 4 FDA reports)
RETINAL DISORDER ( 4 FDA reports)
SALIVARY HYPERSECRETION ( 4 FDA reports)
SARCOIDOSIS ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 4 FDA reports)
SEBORRHOEIC DERMATITIS ( 4 FDA reports)
SIDEROBLASTIC ANAEMIA ( 4 FDA reports)
SKIN FIBROSIS ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN LESION EXCISION ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SOFT TISSUE INFLAMMATION ( 4 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 4 FDA reports)
SPINAL DEFORMITY ( 4 FDA reports)
SPLEEN DISORDER ( 4 FDA reports)
STASIS DERMATITIS ( 4 FDA reports)
STREPTOCOCCAL SEPSIS ( 4 FDA reports)
STRIDOR ( 4 FDA reports)
SUICIDAL BEHAVIOUR ( 4 FDA reports)
TENDON INJURY ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
TINEA CRURIS ( 4 FDA reports)
TINEA VERSICOLOUR ( 4 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TRANSFUSION REACTION ( 4 FDA reports)
TRAUMATIC HAEMATOMA ( 4 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 4 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 4 FDA reports)
URETERIC STENOSIS ( 4 FDA reports)
URETHRAL HAEMORRHAGE ( 4 FDA reports)
URETHRAL MEATUS STENOSIS ( 4 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 4 FDA reports)
URINARY TRACT OBSTRUCTION ( 4 FDA reports)
URINE ODOUR ABNORMAL ( 4 FDA reports)
URTICARIA GENERALISED ( 4 FDA reports)
UTERINE HAEMORRHAGE ( 4 FDA reports)
VAGINOPLASTY ( 4 FDA reports)
VASODILATATION ( 4 FDA reports)
VASOSPASM ( 4 FDA reports)
VEIN DISORDER ( 4 FDA reports)
VESTIBULAR DISORDER ( 4 FDA reports)
VIRAL SINUSITIS ( 4 FDA reports)
VITAMIN K DECREASED ( 4 FDA reports)
VOCAL CORD PARALYSIS ( 4 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 4 FDA reports)
WRIST SURGERY ( 4 FDA reports)
YELLOW SKIN ( 4 FDA reports)
ABDOMINAL HAEMATOMA ( 3 FDA reports)
ABDOMINAL WALL CYST ( 3 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 3 FDA reports)
ABORTION ( 3 FDA reports)
ABSCESS DRAINAGE ( 3 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ACCIDENTAL NEEDLE STICK ( 3 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ADAMS-STOKES SYNDROME ( 3 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ALKALOSIS ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 3 FDA reports)
ANORGASMIA ( 3 FDA reports)
ANTIBODY TEST POSITIVE ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ANTITHROMBIN III INCREASED ( 3 FDA reports)
AORTIC ATHEROSCLEROSIS ( 3 FDA reports)
AORTIC OCCLUSION ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
APPLICATION SITE BURN ( 3 FDA reports)
APPLICATION SITE VESICLES ( 3 FDA reports)
ARTERIAL INJURY ( 3 FDA reports)
ARTERIAL STENT INSERTION ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 3 FDA reports)
AUTONOMIC NEUROPATHY ( 3 FDA reports)
BILE DUCT CANCER ( 3 FDA reports)
BILIARY DILATATION ( 3 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 3 FDA reports)
BIOPSY COLON ABNORMAL ( 3 FDA reports)
BLADDER CATHETERISATION ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 3 FDA reports)
BLOOD MAGNESIUM INCREASED ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 3 FDA reports)
BLOOD PRESSURE ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 3 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BONE CYST ( 3 FDA reports)
BONE GRAFT ( 3 FDA reports)
BORDERLINE GLAUCOMA ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
BREAST MICROCALCIFICATION ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
BUTTERFLY RASH ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
CANDIDURIA ( 3 FDA reports)
CARCINOID HEART DISEASE ( 3 FDA reports)
CARDIAC HYPERTROPHY ( 3 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 3 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 3 FDA reports)
CATHETER SITE ERYTHEMA ( 3 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 3 FDA reports)
CEREBELLAR ATROPHY ( 3 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CHEYNE-STOKES RESPIRATION ( 3 FDA reports)
CHOROIDAL HAEMORRHAGE ( 3 FDA reports)
CHROMATOPSIA ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 3 FDA reports)
CLONUS ( 3 FDA reports)
COGWHEEL RIGIDITY ( 3 FDA reports)
COLITIS COLLAGENOUS ( 3 FDA reports)
COLONIC HAEMORRHAGE ( 3 FDA reports)
COLONOSCOPY ABNORMAL ( 3 FDA reports)
COMPARTMENT SYNDROME ( 3 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 3 FDA reports)
CONDYLOMA ACUMINATUM ( 3 FDA reports)
CONFUSIONAL AROUSAL ( 3 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 3 FDA reports)
CYANOPSIA ( 3 FDA reports)
CYSTOPEXY ( 3 FDA reports)
DERMATITIS PSORIASIFORM ( 3 FDA reports)
DEVICE OCCLUSION ( 3 FDA reports)
DEVICE RELATED SEPSIS ( 3 FDA reports)
DIASTOLIC HYPERTENSION ( 3 FDA reports)
DIZZINESS EXERTIONAL ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DUODENAL ULCER PERFORATION ( 3 FDA reports)
EAR HAEMORRHAGE ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENCEPHALOMALACIA ( 3 FDA reports)
ENDARTERECTOMY ( 3 FDA reports)
ENDOPHTHALMITIS ( 3 FDA reports)
ENERGY INCREASED ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
ENZYME ABNORMALITY ( 3 FDA reports)
EOSINOPHILIC FASCIITIS ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
EPIDIDYMITIS ( 3 FDA reports)
ERYTHEMA INFECTIOSUM ( 3 FDA reports)
EXFOLIATIVE RASH ( 3 FDA reports)
EYELID DISORDER ( 3 FDA reports)
EYELID INFECTION ( 3 FDA reports)
EYELID INJURY ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
FAT TISSUE INCREASED ( 3 FDA reports)
FEBRILE BONE MARROW APLASIA ( 3 FDA reports)
FEEDING TUBE COMPLICATION ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FEMORAL BRUIT ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
FISTULA DISCHARGE ( 3 FDA reports)
FOETAL GROWTH RETARDATION ( 3 FDA reports)
FOOD INTERACTION ( 3 FDA reports)
FOREIGN BODY ASPIRATION ( 3 FDA reports)
FUNGAL SKIN INFECTION ( 3 FDA reports)
GALLBLADDER PAIN ( 3 FDA reports)
GALLOP RHYTHM PRESENT ( 3 FDA reports)
GANGLION ( 3 FDA reports)
GASTRIC ULCER PERFORATION ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 3 FDA reports)
HAEMOCHROMATOSIS ( 3 FDA reports)
HAEMORRHAGIC DISORDER ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HOSTILITY ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPERTROPHIC ANAL PAPILLA ( 3 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 3 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
ICHTHYOSIS ( 3 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 3 FDA reports)
ILEITIS ( 3 FDA reports)
ILIAC ARTERY STENOSIS ( 3 FDA reports)
IMMUNODEFICIENCY ( 3 FDA reports)
IMPATIENCE ( 3 FDA reports)
IMPLANT SITE ERYTHEMA ( 3 FDA reports)
INCISION SITE ERYTHEMA ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INCREASED INSULIN REQUIREMENT ( 3 FDA reports)
INFUSION SITE PAIN ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INNER EAR DISORDER ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL MASS ( 3 FDA reports)
INTESTINAL OPERATION ( 3 FDA reports)
INTRA-UTERINE DEATH ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
IODINE UPTAKE DECREASED ( 3 FDA reports)
IRITIS ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 3 FDA reports)
ISCHAEMIC HEPATITIS ( 3 FDA reports)
KYPHOSCOLIOSIS ( 3 FDA reports)
LABORATORY TEST INTERFERENCE ( 3 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LIMB DEFORMITY ( 3 FDA reports)
LIVER TRANSPLANT REJECTION ( 3 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LOSS OF CONTROL OF LEGS ( 3 FDA reports)
LOSS OF PROPRIOCEPTION ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
MACULAR HOLE ( 3 FDA reports)
MACULOPATHY ( 3 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 3 FDA reports)
MAMMOGRAM ABNORMAL ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
METAPLASIA ( 3 FDA reports)
METASTASES TO ADRENALS ( 3 FDA reports)
METATARSALGIA ( 3 FDA reports)
METHAEMOGLOBINAEMIA ( 3 FDA reports)
MICTURITION FREQUENCY DECREASED ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 3 FDA reports)
MIXED HYPERLIPIDAEMIA ( 3 FDA reports)
MOUTH BREATHING ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MUSCLE FATIGUE ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
MYOPATHY TOXIC ( 3 FDA reports)
MYOSCLEROSIS ( 3 FDA reports)
NARCOLEPSY ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NASAL MUCOSAL DISORDER ( 3 FDA reports)
NASOPHARYNGEAL DISORDER ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
NIKOLSKY'S SIGN ( 3 FDA reports)
NO ADVERSE EFFECT ( 3 FDA reports)
NODAL OSTEOARTHRITIS ( 3 FDA reports)
NODULE ON EXTREMITY ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE II ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
OEDEMA MUCOSAL ( 3 FDA reports)
OEDEMATOUS PANCREATITIS ( 3 FDA reports)
OLIGOHYDRAMNIOS ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
ORAL PRURITUS ( 3 FDA reports)
OROANTRAL FISTULA ( 3 FDA reports)
OSTEOTOMY ( 3 FDA reports)
OTITIS MEDIA ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 3 FDA reports)
PAPILLARY THYROID CANCER ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PAPULE ( 3 FDA reports)
PARAPARESIS ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PEMPHIGUS ( 3 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 3 FDA reports)
PERINEAL PAIN ( 3 FDA reports)
PERIPHERAL NERVE OPERATION ( 3 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 3 FDA reports)
PHYSICAL ASSAULT ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
POSTOPERATIVE ILEUS ( 3 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 3 FDA reports)
POSTPARTUM DISORDER ( 3 FDA reports)
POTENTIATING DRUG INTERACTION ( 3 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 3 FDA reports)
PRIAPISM ( 3 FDA reports)
PROSTATE CANCER METASTATIC ( 3 FDA reports)
PROSTATIC HAEMORRHAGE ( 3 FDA reports)
PROSTATIC PAIN ( 3 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 3 FDA reports)
PROTHROMBIN TIME SHORTENED ( 3 FDA reports)
PSEUDOEXFOLIATION OF LENS CAPSULE ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
PULMONARY ALVEOLAR MICROLITHIASIS ( 3 FDA reports)
PULSE ABNORMAL ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
PYELONEPHRITIS CHRONIC ( 3 FDA reports)
QUADRIPARESIS ( 3 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
RADIATION OESOPHAGITIS ( 3 FDA reports)
RECTAL ABSCESS ( 3 FDA reports)
RECTAL PROLAPSE ( 3 FDA reports)
RECTAL ULCER ( 3 FDA reports)
REFLEXES ABNORMAL ( 3 FDA reports)
REGURGITATION ( 3 FDA reports)
RENAL AND PANCREAS TRANSPLANT REJECTION ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RESPIRATORY TRACT IRRITATION ( 3 FDA reports)
RETICULOCYTE COUNT DECREASED ( 3 FDA reports)
RETINAL VEIN THROMBOSIS ( 3 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 3 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 3 FDA reports)
SACROILIITIS ( 3 FDA reports)
SALIVA ALTERED ( 3 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SEMEN VOLUME DECREASED ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 3 FDA reports)
SKIN ODOUR ABNORMAL ( 3 FDA reports)
SKIN TURGOR DECREASED ( 3 FDA reports)
SKIN WRINKLING ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SLEEP TALKING ( 3 FDA reports)
SOPOR ( 3 FDA reports)
SPERM COUNT DECREASED ( 3 FDA reports)
SPINAL CORD INFARCTION ( 3 FDA reports)
SPINAL DECOMPRESSION ( 3 FDA reports)
SPLEEN CONGESTION ( 3 FDA reports)
SPLENIC ARTERY ANEURYSM ( 3 FDA reports)
SPLENIC GRANULOMA ( 3 FDA reports)
STAB WOUND ( 3 FDA reports)
STOOL ANALYSIS ABNORMAL ( 3 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
SURGICAL FAILURE ( 3 FDA reports)
SUSPICIOUSNESS ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 3 FDA reports)
TELANGIECTASIA ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
TENDON PAIN ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
TERMINAL STATE ( 3 FDA reports)
THERAPY CESSATION ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
THYROID CANCER ( 3 FDA reports)
TOE AMPUTATION ( 3 FDA reports)
TOE DEFORMITY ( 3 FDA reports)
TOE OPERATION ( 3 FDA reports)
TONGUE BLACK HAIRY ( 3 FDA reports)
TONGUE COATED ( 3 FDA reports)
TONSIL CANCER ( 3 FDA reports)
TONSILLITIS ( 3 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 3 FDA reports)
TRACHEAL OEDEMA ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
TRANSPLANT FAILURE ( 3 FDA reports)
TUMOUR MARKER INCREASED ( 3 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
URETERIC DILATATION ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
URINE OSMOLARITY INCREASED ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
URINE POTASSIUM INCREASED ( 3 FDA reports)
URINE SODIUM INCREASED ( 3 FDA reports)
VAGINAL ABSCESS ( 3 FDA reports)
VAGINAL INFECTION ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 3 FDA reports)
VENOUS STASIS ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 3 FDA reports)
VESTIBULAR NEURONITIS ( 3 FDA reports)
VIRAL MYOCARDITIS ( 3 FDA reports)
VULVOVAGINAL DISCOMFORT ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WOUND ABSCESS ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ALCOHOL INTERACTION ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ALOPECIA EFFLUVIUM ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
AMYOTROPHY ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANAL PRURITUS ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANTASTHMATIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTERIOR CHAMBER DISORDER ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
AORTO-DUODENAL FISTULA ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPENDIX DISORDER ( 2 FDA reports)
APPLICATION SITE EXCORIATION ( 2 FDA reports)
APPLICATION SITE SCAB ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIAL RESTENOSIS ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASBESTOSIS ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ATHETOSIS ( 2 FDA reports)
ATOPY ( 2 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 2 FDA reports)
AUTOIMMUNE PANCREATITIS ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
AXILLARY MASS ( 2 FDA reports)
AZOOSPERMIA ( 2 FDA reports)
BACK CRUSHING ( 2 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BASOSQUAMOUS CARCINOMA OF SKIN ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BILE DUCT STENT INSERTION ( 2 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 2 FDA reports)
BLADDER NECROSIS ( 2 FDA reports)
BLEEDING VARICOSE VEIN ( 2 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 2 FDA reports)
BLOOD CALCIUM ABNORMAL ( 2 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 2 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 2 FDA reports)
BLOOD CREATINE ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLOOD PROLACTIN INCREASED ( 2 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 2 FDA reports)
BONE SWELLING ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
BREAST OEDEMA ( 2 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 2 FDA reports)
BRONCHIAL HAEMORRHAGE ( 2 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 2 FDA reports)
BRONCHIAL NEOPLASM ( 2 FDA reports)
BRONCHIAL OEDEMA ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BURN OESOPHAGEAL ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
CARBON DIOXIDE ABNORMAL ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CARCINOID SYNDROME ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC CIRRHOSIS ( 2 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 2 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CAROTIDYNIA ( 2 FDA reports)
CATARACT DIABETIC ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 2 FDA reports)
CERULOPLASMIN INCREASED ( 2 FDA reports)
CERVICAL CONISATION ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHORIORETINOPATHY ( 2 FDA reports)
CHOROIDAL EFFUSION ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COLON CANCER RECURRENT ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORONARY ARTERY EMBOLISM ( 2 FDA reports)
CORONARY REVASCULARISATION ( 2 FDA reports)
CREATININE URINE DECREASED ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DEPRESSION POSTOPERATIVE ( 2 FDA reports)
DEVICE LEAD DAMAGE ( 2 FDA reports)
DEVICE MATERIAL ISSUE ( 2 FDA reports)
DEVICE STIMULATION ISSUE ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DIABETIC CYSTOPATHY ( 2 FDA reports)
DIAPHRAGMATIC DISORDER ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DIVERTICULUM DUODENAL ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DUODENAL POLYP ( 2 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
ECHOCARDIOGRAM ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
EDUCATIONAL PROBLEM ( 2 FDA reports)
EJACULATION DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ENDOSCOPY ABNORMAL ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
EOSINOPHILS URINE PRESENT ( 2 FDA reports)
EPIDIDYMAL ENLARGEMENT ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
ESSENTIAL TREMOR ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EXTRAVASATION BLOOD ( 2 FDA reports)
EXTREMITY CONTRACTURE ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYE NAEVUS ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
EYELID PAIN ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FAECAL VOLUME INCREASED ( 2 FDA reports)
FALLOPIAN TUBE CYST ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FLASHBACK ( 2 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 2 FDA reports)
FOETAL CEREBROVASCULAR DISORDER ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GENERAL SYMPTOM ( 2 FDA reports)
GENITAL LESION ( 2 FDA reports)
GINGIVAL BLISTER ( 2 FDA reports)
GLOBULINS INCREASED ( 2 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GRANULOMA ANNULARE ( 2 FDA reports)
GRAVITATIONAL OEDEMA ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 2 FDA reports)
HAEMORRHAGE URINARY TRACT ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HALITOSIS ( 2 FDA reports)
HAPTOGLOBIN ( 2 FDA reports)
HEART BLOCK CONGENITAL ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEART TRANSPLANT REJECTION ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HERPES OESOPHAGITIS ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HORNER'S SYNDROME ( 2 FDA reports)
HOSPICE CARE ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERLIPASAEMIA ( 2 FDA reports)
HYPERMETROPIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 2 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
IMMUNOGLOBULINS INCREASED ( 2 FDA reports)
IMPINGEMENT SYNDROME ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCISION SITE OEDEMA ( 2 FDA reports)
INCISIONAL HERNIA REPAIR ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTERNAL INJURY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTESTINAL SPASM ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 2 FDA reports)
LARYNGEAL INFLAMMATION ( 2 FDA reports)
LARYNGEAL OBSTRUCTION ( 2 FDA reports)
LARYNGEAL STENOSIS ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LENS DISORDER ( 2 FDA reports)
LEUKOPLAKIA ( 2 FDA reports)
LICHEN SCLEROSUS ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LIP EXFOLIATION ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPHADENECTOMY ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
MACULAR PSEUDOHOLE ( 2 FDA reports)
MALIGNANT MELANOMA IN SITU ( 2 FDA reports)
MALIGNANT MUSCLE NEOPLASM ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MASS EXCISION ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 2 FDA reports)
MENISCUS REMOVAL ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MICROLITHIASIS ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 2 FDA reports)
MOANING ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MONOCYTOSIS ( 2 FDA reports)
MORAXELLA INFECTION ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUSCLE MASS ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYELOID MATURATION ARREST ( 2 FDA reports)
MYELOMA RECURRENCE ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
MYOCARDIAL CALCIFICATION ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
NASAL DISCHARGE DISCOLOURATION ( 2 FDA reports)
NASAL ODOUR ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NASAL SINUS DRAINAGE ( 2 FDA reports)
NEGATIVE THOUGHTS ( 2 FDA reports)
NEOPLASM PROSTATE ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 2 FDA reports)
NUCLEATED RED CELLS ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OSTEOMYELITIS CHRONIC ( 2 FDA reports)
OVARIAN NEOPLASM ( 2 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PALLIATIVE CARE ( 2 FDA reports)
PANCREATIC DUCT STENOSIS ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERITONITIS SCLEROSING ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PHARYNGEAL CANDIDIASIS ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PHONOPHOBIA ( 2 FDA reports)
PICKWICKIAN SYNDROME ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLASTIC SURGERY ( 2 FDA reports)
PLEURAL CALCIFICATION ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 2 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PSEUDO LYMPHOMA ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULMONARY NECROSIS ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RETINAL INJURY ( 2 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 2 FDA reports)
RETINITIS ( 2 FDA reports)
RETINOPATHY OF PREMATURITY ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 2 FDA reports)
RHEUMATIC HEART DISEASE ( 2 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 2 FDA reports)
SCROTAL ABSCESS ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SENSORY GANGLIONITIS ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SIGMOIDITIS ( 2 FDA reports)
SINGLE UMBILICAL ARTERY ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN NEOPLASM EXCISION ( 2 FDA reports)
SKIN SWELLING ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SMALL INTESTINE OPERATION ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
STAPHYLOCOCCAL MEDIASTINITIS ( 2 FDA reports)
STEREOTYPY ( 2 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 2 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE IV ( 2 FDA reports)
SUPERINFECTION LUNG ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
THALAMUS HAEMORRHAGE ( 2 FDA reports)
THERAPEUTIC EMBOLISATION ( 2 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TOOTH DEPOSIT ( 2 FDA reports)
TOOTH INJURY ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TOXICOLOGIC TEST ( 2 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TROPONIN ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
UBIQUINONE DECREASED ( 2 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 2 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
UPPER EXTREMITY MASS ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
UTERINE PERFORATION ( 2 FDA reports)
VAGINAL DISORDER ( 2 FDA reports)
VAGINAL LESION ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
VIRAL LABYRINTHITIS ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VIRAL PERICARDITIS ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VITREOUS DETACHMENT ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 2 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 2 FDA reports)
WATER INTOXICATION ( 2 FDA reports)
WEIGHT ( 2 FDA reports)
WHITE BLOOD CELL ANALYSIS DECREASED ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOIDAL HYPERTROPHY ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMOEBIASIS ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANOPLASTY ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
ANOTIA ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APHAKIA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL GRAFT ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOSCLEROSIS MOENCKEBERG-TYPE ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTERITIS CORONARY ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASPERMIA ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AURA ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN COLONIC POLYP ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN MUSCLE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILIARY ABSCESS ( 1 FDA reports)
BILIARY CANCER METASTATIC ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIOPSY BREAST ABNORMAL ( 1 FDA reports)
BIOPSY BRONCHUS ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER NECK SUSPENSION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD HOMOCYSTEINE ABNORMAL ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 1 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRACHIAL PLEXUS LESION ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHITIS HAEMOPHILUS ( 1 FDA reports)
BRONCHOMALACIA ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC ANEURYSM REPAIR ( 1 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 1 FDA reports)
CARDIAC ELECTROPHYSIOLOGIC STUDY ABNORMAL ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC PACEMAKER REVISION ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIAC VALVE RUPTURE ( 1 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE PHLEBITIS ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CEREBELLAR ARTERY THROMBOSIS ( 1 FDA reports)
CEREBELLAR ISCHAEMIA ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVIX OPERATION ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHILLBLAINS ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHOROIDAL DETACHMENT ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CIRCUMCISION ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLECTOMY PARTIAL ( 1 FDA reports)
COLLAGEN ANTIGEN TYPE 1 ( 1 FDA reports)
COLON CANCER STAGE I ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPLICATED FRACTURE ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREATININE RENAL CLEARANCE ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CROUP NONINFECTIOUS ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMABRASION ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DERMOGRAPHISM ( 1 FDA reports)
DESQUAMATION MOUTH ( 1 FDA reports)
DEVICE BATTERY ISSUE ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 1 FDA reports)
DIABETIC DERMOPATHY ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DIFFUSE VASCULITIS ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISEASE PRODROMAL STAGE ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENECTOMY ( 1 FDA reports)
DURAL TEAR ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSGLOBULINAEMIA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSTROPHIC CALCIFICATION ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS TOXIC ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENCEPHALOCELE ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTEROSTOMY ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
ENTROPION ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
EXERCISE CAPACITY DECREASED ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYEBALL AVULSION ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FACIAL NERVE DISORDER ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FAMILIAL RISK FACTOR ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GALLSTONE ILEUS ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTRITIS HYPERTROPHIC ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVAL GRAFT ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTE COUNT ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HANGNAIL ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HELMINTHIC INFECTION ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS B DNA ASSAY POSITIVE ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS C RNA INCREASED ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEREDITARY SPHEROCYTOSIS ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPETIC STOMATITIS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOLOPROSENCEPHALY ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYALOSIS ASTEROID ( 1 FDA reports)
HYDRAEMIA ( 1 FDA reports)
HYDROPHOBIA ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERMAGNESAEMIA ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVISCOSITY SYNDROME ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOSPERMIA ( 1 FDA reports)
HYPOTONIC-HYPORESPONSIVE EPISODE ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYPOZINCAEMIA ( 1 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILLITERACY ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE SWELLING ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INNER EAR INFLAMMATION ( 1 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTERVERTEBRAL DISC INJURY ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL HYPERMOTILITY ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
ISCHAEMIC LIMB PAIN ( 1 FDA reports)
IUD MIGRATION ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JOINT INJECTION ( 1 FDA reports)
KERATITIS INTERSTITIAL ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LENS DISLOCATION ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP HAEMATOMA ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPOMA EXCISION ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUMBAR VERTEBRA INJURY ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTE TRANSFORMATION TEST POSITIVE ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHORRHOEA ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MALOCCLUSION ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MASTOPTOSIS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENISCUS OPERATION ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENTAL DISABILITY ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESENTERIC PANNICULITIS ( 1 FDA reports)
METAMYELOCYTE COUNT ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST NEGATIVE ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYELOCYTE COUNT ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOFASCITIS ( 1 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
MYXOEDEMA ( 1 FDA reports)
NAIL BED TENDERNESS ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NEAR DROWNING ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECROBIOSIS LIPOIDICA DIABETICORUM ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NERVE ROOT INJURY CERVICAL ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NITRITOID CRISIS ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
OCULAR SARCOIDOSIS ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
ONYCHOGRYPHOSIS ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEOCALCIN DECREASED ( 1 FDA reports)
OSTEOCHONDROMA ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OVARIAN ADENOMA ( 1 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATIC OPERATION ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARAESTHESIA OF GENITAL MALE ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARAPROTEINAEMIA ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PENILE NECROSIS ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERIARTICULAR DISORDER ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PERITONEAL ADHESIONS DIVISION ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PIGMENTATION BUCCAL ( 1 FDA reports)
PIGMENTATION LIP ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURAL RUB ( 1 FDA reports)
PLICA SYNDROME ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POSITIVE CARDIAC INOTROPIC EFFECT ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST LAMINECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST-TRAUMATIC EPILEPSY ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTINFARCTION ANGINA ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PRADER-WILLI SYNDROME ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PROCALCITONIN ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT COATING ISSUE ( 1 FDA reports)
PRODUCT CONTAINER SEAL ISSUE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT RECONSTITUTION ISSUE ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTATIC MASS ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSEUDOPORPHYRIA ( 1 FDA reports)
PSYCHOSEXUAL DISORDER ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
PYRUVATE KINASE INCREASED ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL FUSION ANOMALY ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DEPTH DECREASED ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL LASER COAGULATION ( 1 FDA reports)
RETINOPATHY HAEMORRHAGIC ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
ROULEAUX FORMATION ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEGMENTED HYALINISING VASCULITIS ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SEMEN VOLUME ABNORMAL ( 1 FDA reports)
SEMINOMA ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SEPTIC PHLEBITIS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERUM SEROTONIN DECREASED ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SNAKE BITE ( 1 FDA reports)
SOLITARY KIDNEY ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPECIFIC GRAVITY URINE DECREASED ( 1 FDA reports)
SPERM COUNT ZERO ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENIC VEIN OCCLUSION ( 1 FDA reports)
SPLINTER ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPONDYLITIC MYELOPATHY ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STARING ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STRESS ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SYMBOLIC DYSFUNCTION ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
TERMINAL DRIBBLING ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTIS CANCER ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THERMOMETRY ABNORMAL ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBOENDARTERECTOMY ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TONGUE GEOGRAPHIC ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRACHEOMALACIA ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TROPONIN I ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR LOCAL INVASION ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNWANTED PREGNANCY ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URETERAL STENT REMOVAL ( 1 FDA reports)
URETEROSCOPY ( 1 FDA reports)
URETHRAL CANCER ( 1 FDA reports)
URETHRAL INJURY ( 1 FDA reports)
URETHRAL MEATOTOMY ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URINARY CALCULUS REMOVAL ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
UTERINE ATROPHY ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VALVULOPLASTY CARDIAC ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASCULITIS GASTROINTESTINAL ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENIPUNCTURE SITE SWELLING ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOUS HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD LIPOINJECTION ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VULVAL HAEMORRHAGE ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)

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