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

DIZZINESS ( 646 FDA reports)
DRUG INEFFECTIVE ( 603 FDA reports)
HYPERTENSION ( 592 FDA reports)
DYSPNOEA ( 579 FDA reports)
BLOOD PRESSURE INCREASED ( 565 FDA reports)
FATIGUE ( 518 FDA reports)
NAUSEA ( 492 FDA reports)
MALAISE ( 466 FDA reports)
HEADACHE ( 464 FDA reports)
ASTHENIA ( 439 FDA reports)
DIARRHOEA ( 434 FDA reports)
FALL ( 411 FDA reports)
HYPOTENSION ( 396 FDA reports)
OEDEMA PERIPHERAL ( 368 FDA reports)
PAIN ( 363 FDA reports)
VOMITING ( 345 FDA reports)
RENAL FAILURE ACUTE ( 344 FDA reports)
CHEST PAIN ( 334 FDA reports)
WEIGHT DECREASED ( 329 FDA reports)
ANAEMIA ( 318 FDA reports)
CEREBROVASCULAR ACCIDENT ( 318 FDA reports)
DRUG INTERACTION ( 306 FDA reports)
MYOCARDIAL INFARCTION ( 297 FDA reports)
RENAL FAILURE ( 292 FDA reports)
COUGH ( 291 FDA reports)
ANXIETY ( 289 FDA reports)
ARTHRALGIA ( 285 FDA reports)
INSOMNIA ( 273 FDA reports)
PYREXIA ( 253 FDA reports)
PAIN IN EXTREMITY ( 248 FDA reports)
ATRIAL FIBRILLATION ( 235 FDA reports)
DEHYDRATION ( 233 FDA reports)
LOSS OF CONSCIOUSNESS ( 232 FDA reports)
BACK PAIN ( 231 FDA reports)
DEPRESSION ( 230 FDA reports)
PNEUMONIA ( 217 FDA reports)
SYNCOPE ( 214 FDA reports)
PRURITUS ( 213 FDA reports)
BLOOD CREATININE INCREASED ( 207 FDA reports)
DEATH ( 200 FDA reports)
MYALGIA ( 200 FDA reports)
CONFUSIONAL STATE ( 198 FDA reports)
FEELING ABNORMAL ( 194 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 192 FDA reports)
HYPERKALAEMIA ( 191 FDA reports)
HYPONATRAEMIA ( 189 FDA reports)
WEIGHT INCREASED ( 188 FDA reports)
BLOOD GLUCOSE INCREASED ( 181 FDA reports)
ABDOMINAL PAIN ( 180 FDA reports)
DRUG DOSE OMISSION ( 180 FDA reports)
SOMNOLENCE ( 179 FDA reports)
PALPITATIONS ( 173 FDA reports)
CARDIAC FAILURE ( 171 FDA reports)
HYPOAESTHESIA ( 165 FDA reports)
BRADYCARDIA ( 163 FDA reports)
VISION BLURRED ( 163 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 162 FDA reports)
GAIT DISTURBANCE ( 160 FDA reports)
ABDOMINAL PAIN UPPER ( 159 FDA reports)
MUSCLE SPASMS ( 157 FDA reports)
DIABETES MELLITUS ( 155 FDA reports)
RASH ( 151 FDA reports)
CONSTIPATION ( 147 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 147 FDA reports)
BLOOD PRESSURE DECREASED ( 144 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 141 FDA reports)
HAEMOGLOBIN DECREASED ( 139 FDA reports)
INJURY ( 138 FDA reports)
CARDIAC DISORDER ( 137 FDA reports)
BURNING SENSATION ( 136 FDA reports)
OSTEOARTHRITIS ( 133 FDA reports)
HYPERHIDROSIS ( 129 FDA reports)
CONDITION AGGRAVATED ( 126 FDA reports)
PARAESTHESIA ( 125 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 125 FDA reports)
TREMOR ( 124 FDA reports)
URINARY TRACT INFECTION ( 124 FDA reports)
DECREASED APPETITE ( 121 FDA reports)
FLUSHING ( 121 FDA reports)
RENAL IMPAIRMENT ( 116 FDA reports)
DYSPEPSIA ( 115 FDA reports)
ARRHYTHMIA ( 114 FDA reports)
ASTHMA ( 114 FDA reports)
BALANCE DISORDER ( 114 FDA reports)
ABDOMINAL DISTENSION ( 108 FDA reports)
CORONARY ARTERY DISEASE ( 107 FDA reports)
MUSCULAR WEAKNESS ( 107 FDA reports)
BRONCHITIS ( 106 FDA reports)
ERYTHEMA ( 105 FDA reports)
OFF LABEL USE ( 105 FDA reports)
ORTHOSTATIC HYPOTENSION ( 103 FDA reports)
JOINT SWELLING ( 102 FDA reports)
TACHYCARDIA ( 102 FDA reports)
PLEURAL EFFUSION ( 101 FDA reports)
AMNESIA ( 99 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 98 FDA reports)
CATARACT ( 98 FDA reports)
DYSPHAGIA ( 98 FDA reports)
THROMBOCYTOPENIA ( 97 FDA reports)
ALOPECIA ( 95 FDA reports)
SINUSITIS ( 94 FDA reports)
VERTIGO ( 94 FDA reports)
HYPERSENSITIVITY ( 93 FDA reports)
RENAL FAILURE CHRONIC ( 93 FDA reports)
ANHEDONIA ( 92 FDA reports)
CHEST DISCOMFORT ( 92 FDA reports)
CYSTITIS ( 92 FDA reports)
BLOOD UREA INCREASED ( 91 FDA reports)
CARDIAC ARREST ( 90 FDA reports)
GASTRITIS ( 88 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 88 FDA reports)
HAEMORRHAGE ( 88 FDA reports)
DRY MOUTH ( 87 FDA reports)
EPISTAXIS ( 87 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 86 FDA reports)
HEART RATE INCREASED ( 86 FDA reports)
SWELLING ( 86 FDA reports)
HYPOGLYCAEMIA ( 84 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 84 FDA reports)
OSTEONECROSIS OF JAW ( 83 FDA reports)
POLLAKIURIA ( 83 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 82 FDA reports)
CONVULSION ( 80 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 79 FDA reports)
DRUG HYPERSENSITIVITY ( 78 FDA reports)
RESPIRATORY FAILURE ( 78 FDA reports)
SEPSIS ( 78 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 77 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 77 FDA reports)
NEUROPATHY PERIPHERAL ( 75 FDA reports)
OEDEMA ( 75 FDA reports)
OSTEOMYELITIS ( 75 FDA reports)
STRESS ( 75 FDA reports)
DYSGEUSIA ( 74 FDA reports)
EMOTIONAL DISTRESS ( 74 FDA reports)
HYPERLIPIDAEMIA ( 74 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 73 FDA reports)
INGROWING NAIL ( 73 FDA reports)
MEMORY IMPAIRMENT ( 73 FDA reports)
HYPOKALAEMIA ( 72 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 71 FDA reports)
HEART RATE DECREASED ( 71 FDA reports)
NEOPLASM MALIGNANT ( 71 FDA reports)
PLATELET COUNT DECREASED ( 71 FDA reports)
VISUAL ACUITY REDUCED ( 71 FDA reports)
ARTHRITIS ( 70 FDA reports)
DYSPHONIA ( 70 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 70 FDA reports)
HAEMATOMA ( 70 FDA reports)
PULMONARY EMBOLISM ( 70 FDA reports)
URINARY INCONTINENCE ( 69 FDA reports)
ANGINA PECTORIS ( 68 FDA reports)
NERVOUSNESS ( 68 FDA reports)
URTICARIA ( 68 FDA reports)
THROMBOSIS ( 67 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 66 FDA reports)
FLATULENCE ( 66 FDA reports)
INTENTIONAL DRUG MISUSE ( 66 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 66 FDA reports)
ABDOMINAL DISCOMFORT ( 65 FDA reports)
ASCITES ( 65 FDA reports)
MITRAL VALVE INCOMPETENCE ( 65 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 64 FDA reports)
CHOLECYSTECTOMY ( 64 FDA reports)
LEUKOPENIA ( 64 FDA reports)
NASOPHARYNGITIS ( 64 FDA reports)
OVERDOSE ( 64 FDA reports)
PULMONARY OEDEMA ( 64 FDA reports)
BLOOD COUNT ABNORMAL ( 63 FDA reports)
CARDIOMEGALY ( 63 FDA reports)
MULTI-ORGAN FAILURE ( 63 FDA reports)
NECK PAIN ( 63 FDA reports)
NEPHROLITHIASIS ( 62 FDA reports)
PANCREATITIS ( 62 FDA reports)
MUSCULOSKELETAL PAIN ( 61 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 59 FDA reports)
CARDIOMYOPATHY ( 59 FDA reports)
INFLAMMATION ( 59 FDA reports)
SPEECH DISORDER ( 59 FDA reports)
GASTRIC DISORDER ( 58 FDA reports)
RENAL DISORDER ( 58 FDA reports)
TINNITUS ( 58 FDA reports)
JAUNDICE ( 57 FDA reports)
ROAD TRAFFIC ACCIDENT ( 57 FDA reports)
ADVERSE EVENT ( 56 FDA reports)
HOT FLUSH ( 56 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 56 FDA reports)
RHEUMATOID ARTHRITIS ( 56 FDA reports)
CHILLS ( 55 FDA reports)
LETHARGY ( 55 FDA reports)
OSTEONECROSIS ( 55 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 55 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 54 FDA reports)
HEART RATE IRREGULAR ( 54 FDA reports)
HYPERGLYCAEMIA ( 54 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 54 FDA reports)
OSTEOPOROSIS ( 54 FDA reports)
PANCYTOPENIA ( 54 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 54 FDA reports)
VENTRICULAR TACHYCARDIA ( 54 FDA reports)
VISUAL IMPAIRMENT ( 54 FDA reports)
ANOREXIA ( 53 FDA reports)
BONE DISORDER ( 53 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 53 FDA reports)
DYSPNOEA EXERTIONAL ( 53 FDA reports)
ECONOMIC PROBLEM ( 53 FDA reports)
GOUT ( 53 FDA reports)
HAEMATURIA ( 53 FDA reports)
IMPAIRED HEALING ( 53 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 53 FDA reports)
OROPHARYNGEAL PAIN ( 53 FDA reports)
RHABDOMYOLYSIS ( 53 FDA reports)
DEEP VEIN THROMBOSIS ( 52 FDA reports)
HEPATIC STEATOSIS ( 52 FDA reports)
HERPES ZOSTER ( 52 FDA reports)
INCORRECT DOSE ADMINISTERED ( 52 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 52 FDA reports)
ANGIOEDEMA ( 51 FDA reports)
FACE OEDEMA ( 51 FDA reports)
HYPERTENSIVE CRISIS ( 51 FDA reports)
LUNG DISORDER ( 51 FDA reports)
MACULAR DEGENERATION ( 51 FDA reports)
SPINAL OSTEOARTHRITIS ( 51 FDA reports)
TOE OPERATION ( 51 FDA reports)
BLOOD SODIUM DECREASED ( 50 FDA reports)
DISORIENTATION ( 50 FDA reports)
FLUID RETENTION ( 50 FDA reports)
SEPTIC SHOCK ( 50 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 49 FDA reports)
HYPOTHYROIDISM ( 49 FDA reports)
PULMONARY HYPERTENSION ( 49 FDA reports)
UNEVALUABLE EVENT ( 49 FDA reports)
CYTOLYTIC HEPATITIS ( 48 FDA reports)
INFLUENZA ( 48 FDA reports)
SLEEP APNOEA SYNDROME ( 48 FDA reports)
APHASIA ( 47 FDA reports)
DYSURIA ( 47 FDA reports)
FEELING HOT ( 47 FDA reports)
BLOOD POTASSIUM INCREASED ( 46 FDA reports)
CORONARY ARTERY OCCLUSION ( 46 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 46 FDA reports)
GALLBLADDER DISORDER ( 46 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 45 FDA reports)
ARTERIOSCLEROSIS ( 45 FDA reports)
BLOOD GLUCOSE DECREASED ( 45 FDA reports)
DIVERTICULITIS ( 45 FDA reports)
HEPATIC ENZYME INCREASED ( 45 FDA reports)
ATELECTASIS ( 44 FDA reports)
FEAR ( 44 FDA reports)
HAEMATOCRIT DECREASED ( 44 FDA reports)
METASTASES TO BONE ( 44 FDA reports)
NEUTROPENIA ( 44 FDA reports)
SUICIDAL IDEATION ( 44 FDA reports)
THROAT IRRITATION ( 44 FDA reports)
TYPE 2 DIABETES MELLITUS ( 44 FDA reports)
CARDIAC MURMUR ( 43 FDA reports)
FEMUR FRACTURE ( 43 FDA reports)
SWELLING FACE ( 43 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 42 FDA reports)
HAEMATOCHEZIA ( 42 FDA reports)
ILL-DEFINED DISORDER ( 42 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 42 FDA reports)
OSTEOPENIA ( 42 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 42 FDA reports)
PULMONARY FIBROSIS ( 42 FDA reports)
URINARY RETENTION ( 42 FDA reports)
FULL BLOOD COUNT DECREASED ( 41 FDA reports)
INFECTION ( 41 FDA reports)
METASTASES TO LIVER ( 41 FDA reports)
MIGRAINE ( 41 FDA reports)
RECTAL HAEMORRHAGE ( 41 FDA reports)
UPPER LIMB FRACTURE ( 41 FDA reports)
ATRIOVENTRICULAR BLOCK ( 40 FDA reports)
CARDIO-RESPIRATORY ARREST ( 40 FDA reports)
CELLULITIS ( 40 FDA reports)
CHOLESTASIS ( 40 FDA reports)
HEPATITIS ( 40 FDA reports)
WHEEZING ( 40 FDA reports)
BLOOD PRESSURE ABNORMAL ( 39 FDA reports)
BURSITIS ( 39 FDA reports)
ENCEPHALOPATHY ( 39 FDA reports)
RENAL CYST ( 39 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 39 FDA reports)
DRUG INTOLERANCE ( 38 FDA reports)
HEPATIC FAILURE ( 38 FDA reports)
HIP FRACTURE ( 38 FDA reports)
HYPERCHOLESTEROLAEMIA ( 38 FDA reports)
MOBILITY DECREASED ( 38 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 38 FDA reports)
TENDONITIS ( 38 FDA reports)
ABASIA ( 37 FDA reports)
ANKLE FRACTURE ( 37 FDA reports)
COLITIS ( 37 FDA reports)
CYST ( 37 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 37 FDA reports)
EJECTION FRACTION DECREASED ( 37 FDA reports)
EYE DISORDER ( 37 FDA reports)
HAEMORRHOIDS ( 37 FDA reports)
LYMPHADENOPATHY ( 37 FDA reports)
SKIN DISCOLOURATION ( 37 FDA reports)
SLEEP DISORDER ( 37 FDA reports)
BLINDNESS ( 36 FDA reports)
CHOLELITHIASIS ( 36 FDA reports)
INTERSTITIAL LUNG DISEASE ( 36 FDA reports)
LIVER DISORDER ( 36 FDA reports)
LUNG NEOPLASM ( 36 FDA reports)
METABOLIC ACIDOSIS ( 36 FDA reports)
NASAL CONGESTION ( 36 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 36 FDA reports)
RIB FRACTURE ( 36 FDA reports)
SUICIDE ATTEMPT ( 36 FDA reports)
SWOLLEN TONGUE ( 36 FDA reports)
BLOOD POTASSIUM DECREASED ( 35 FDA reports)
CIRCULATORY COLLAPSE ( 35 FDA reports)
CONTUSION ( 35 FDA reports)
DEAFNESS ( 35 FDA reports)
DRY SKIN ( 35 FDA reports)
DYSARTHRIA ( 35 FDA reports)
LIMB DISCOMFORT ( 35 FDA reports)
PRESYNCOPE ( 35 FDA reports)
PROSTATE CANCER ( 35 FDA reports)
TOOTH ABSCESS ( 35 FDA reports)
ANURIA ( 34 FDA reports)
AORTIC VALVE INCOMPETENCE ( 34 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 34 FDA reports)
BREAST CANCER ( 34 FDA reports)
DENTAL CARIES ( 34 FDA reports)
EMOTIONAL DISORDER ( 34 FDA reports)
HALLUCINATION ( 34 FDA reports)
INFLUENZA LIKE ILLNESS ( 34 FDA reports)
OBESITY ( 34 FDA reports)
SCAR ( 34 FDA reports)
TOOTH DISORDER ( 34 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 34 FDA reports)
VISUAL DISTURBANCE ( 34 FDA reports)
BLOOD BILIRUBIN INCREASED ( 33 FDA reports)
DEAFNESS NEUROSENSORY ( 33 FDA reports)
EMPHYSEMA ( 33 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 33 FDA reports)
IRRITABILITY ( 33 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 33 FDA reports)
MEDICATION ERROR ( 33 FDA reports)
NIGHTMARE ( 33 FDA reports)
PAIN IN JAW ( 33 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 33 FDA reports)
ROTATOR CUFF SYNDROME ( 33 FDA reports)
TRANSAMINASES INCREASED ( 33 FDA reports)
TREATMENT NONCOMPLIANCE ( 33 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 33 FDA reports)
ARTHROPATHY ( 32 FDA reports)
BLOOD URINE PRESENT ( 32 FDA reports)
BONE PAIN ( 32 FDA reports)
CORONARY ARTERY STENOSIS ( 32 FDA reports)
HALLUCINATION, VISUAL ( 32 FDA reports)
HIATUS HERNIA ( 32 FDA reports)
MELAENA ( 32 FDA reports)
RENAL INJURY ( 32 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 32 FDA reports)
AGITATION ( 31 FDA reports)
ANGINA UNSTABLE ( 31 FDA reports)
BRONCHOSPASM ( 31 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 31 FDA reports)
GASTRIC ULCER ( 31 FDA reports)
GINGIVITIS ( 31 FDA reports)
HYPERCALCAEMIA ( 31 FDA reports)
HYPERTHYROIDISM ( 31 FDA reports)
MASS ( 31 FDA reports)
OESOPHAGITIS ( 31 FDA reports)
PALLOR ( 31 FDA reports)
PULMONARY CONGESTION ( 31 FDA reports)
RASH MACULAR ( 31 FDA reports)
TOOTH EXTRACTION ( 31 FDA reports)
WRIST FRACTURE ( 31 FDA reports)
DIVERTICULUM INTESTINAL ( 30 FDA reports)
ERECTILE DYSFUNCTION ( 30 FDA reports)
GLAUCOMA ( 30 FDA reports)
HAEMOPTYSIS ( 30 FDA reports)
HEMIPLEGIA ( 30 FDA reports)
HYPOXIA ( 30 FDA reports)
PANIC ATTACK ( 30 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 30 FDA reports)
POST PROCEDURAL COMPLICATION ( 30 FDA reports)
SICK SINUS SYNDROME ( 30 FDA reports)
VENTRICULAR HYPERTROPHY ( 30 FDA reports)
CEREBRAL INFARCTION ( 29 FDA reports)
FEELING JITTERY ( 29 FDA reports)
GASTROENTERITIS ( 29 FDA reports)
HEMIPARESIS ( 29 FDA reports)
NOCTURIA ( 29 FDA reports)
PRURITUS GENERALISED ( 29 FDA reports)
PSORIASIS ( 29 FDA reports)
ACUTE PULMONARY OEDEMA ( 28 FDA reports)
BLISTER ( 28 FDA reports)
COLON CANCER ( 28 FDA reports)
DIALYSIS ( 28 FDA reports)
DIVERTICULUM ( 28 FDA reports)
DRUG EFFECT DECREASED ( 28 FDA reports)
FOOT FRACTURE ( 28 FDA reports)
GINGIVAL SWELLING ( 28 FDA reports)
IRON DEFICIENCY ANAEMIA ( 28 FDA reports)
JAW FRACTURE ( 28 FDA reports)
LACRIMATION INCREASED ( 28 FDA reports)
MUSCLE TWITCHING ( 28 FDA reports)
OLIGOHYDRAMNIOS ( 28 FDA reports)
PANCREATITIS ACUTE ( 28 FDA reports)
PHARYNGEAL OEDEMA ( 28 FDA reports)
PROTEINURIA ( 28 FDA reports)
RASH PRURITIC ( 28 FDA reports)
SPINAL COMPRESSION FRACTURE ( 28 FDA reports)
BASAL CELL CARCINOMA ( 27 FDA reports)
CEREBRAL ATROPHY ( 27 FDA reports)
DELIRIUM ( 27 FDA reports)
ECZEMA ( 27 FDA reports)
LACERATION ( 27 FDA reports)
MENTAL STATUS CHANGES ( 27 FDA reports)
POLYNEUROPATHY ( 27 FDA reports)
PROSTATE CANCER METASTATIC ( 27 FDA reports)
RHINORRHOEA ( 27 FDA reports)
SINUS DISORDER ( 27 FDA reports)
SKIN EXFOLIATION ( 27 FDA reports)
SPINAL COLUMN STENOSIS ( 27 FDA reports)
ADVERSE DRUG REACTION ( 26 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 26 FDA reports)
CARDIAC PACEMAKER INSERTION ( 26 FDA reports)
CEREBRAL HAEMORRHAGE ( 26 FDA reports)
DIPLOPIA ( 26 FDA reports)
EXTRASYSTOLES ( 26 FDA reports)
INJECTION SITE PAIN ( 26 FDA reports)
JOINT INJURY ( 26 FDA reports)
LUNG INFILTRATION ( 26 FDA reports)
PERIODONTAL DISEASE ( 26 FDA reports)
SKIN ULCER ( 26 FDA reports)
TOXIC SKIN ERUPTION ( 26 FDA reports)
AGGRESSION ( 25 FDA reports)
ATRIAL FLUTTER ( 25 FDA reports)
COLD SWEAT ( 25 FDA reports)
DRY EYE ( 25 FDA reports)
EXOSTOSIS ( 25 FDA reports)
EXPOSED BONE IN JAW ( 25 FDA reports)
FEBRILE NEUTROPENIA ( 25 FDA reports)
HUNGER ( 25 FDA reports)
JOINT STIFFNESS ( 25 FDA reports)
LACTIC ACIDOSIS ( 25 FDA reports)
MULTIPLE INJURIES ( 25 FDA reports)
MYOCARDIAL ISCHAEMIA ( 25 FDA reports)
PHLEBITIS ( 25 FDA reports)
STOMATITIS ( 25 FDA reports)
TENDON RUPTURE ( 25 FDA reports)
VENOUS OCCLUSION ( 25 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 25 FDA reports)
BACK DISORDER ( 24 FDA reports)
BACTERIAL INFECTION ( 24 FDA reports)
BLEPHARITIS ( 24 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 24 FDA reports)
DRUG TOXICITY ( 24 FDA reports)
INFARCTION ( 24 FDA reports)
RALES ( 24 FDA reports)
RESTLESSNESS ( 24 FDA reports)
SINUS TACHYCARDIA ( 24 FDA reports)
SPINAL FRACTURE ( 24 FDA reports)
STENT PLACEMENT ( 24 FDA reports)
ABNORMAL DREAMS ( 23 FDA reports)
CAROTID ARTERY STENOSIS ( 23 FDA reports)
CARPAL TUNNEL SYNDROME ( 23 FDA reports)
CHROMATURIA ( 23 FDA reports)
DEMENTIA ( 23 FDA reports)
DEPRESSED MOOD ( 23 FDA reports)
DISTURBANCE IN ATTENTION ( 23 FDA reports)
EYE SWELLING ( 23 FDA reports)
FEELING COLD ( 23 FDA reports)
INJECTION SITE HAEMORRHAGE ( 23 FDA reports)
LYMPHOEDEMA ( 23 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 23 FDA reports)
MENTAL DISORDER ( 23 FDA reports)
OLIGURIA ( 23 FDA reports)
PNEUMOTHORAX ( 23 FDA reports)
PROTEIN URINE PRESENT ( 23 FDA reports)
RESPIRATORY DISTRESS ( 23 FDA reports)
SHOCK ( 23 FDA reports)
SURGERY ( 23 FDA reports)
TACHYARRHYTHMIA ( 23 FDA reports)
BRAIN STEM INFARCTION ( 22 FDA reports)
CAROTID ARTERY OCCLUSION ( 22 FDA reports)
COMA ( 22 FDA reports)
EYE HAEMORRHAGE ( 22 FDA reports)
FUNGAL INFECTION ( 22 FDA reports)
GLOSSODYNIA ( 22 FDA reports)
HEPATIC ENCEPHALOPATHY ( 22 FDA reports)
HEPATITIS TOXIC ( 22 FDA reports)
LACUNAR INFARCTION ( 22 FDA reports)
MOUTH ULCERATION ( 22 FDA reports)
ORAL INFECTION ( 22 FDA reports)
STAPHYLOCOCCAL INFECTION ( 22 FDA reports)
SUDDEN DEATH ( 22 FDA reports)
VIRAL INFECTION ( 22 FDA reports)
ANAPHYLACTIC REACTION ( 21 FDA reports)
BLINDNESS UNILATERAL ( 21 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 21 FDA reports)
CARDIOVASCULAR DISORDER ( 21 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 21 FDA reports)
DISEASE PROGRESSION ( 21 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 21 FDA reports)
EOSINOPHILIA ( 21 FDA reports)
GINGIVAL PAIN ( 21 FDA reports)
HAEMATEMESIS ( 21 FDA reports)
HYPERSOMNIA ( 21 FDA reports)
HYPOKINESIA ( 21 FDA reports)
INFUSION RELATED REACTION ( 21 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 21 FDA reports)
LIP SWELLING ( 21 FDA reports)
OCULAR HYPERAEMIA ( 21 FDA reports)
OEDEMA MOUTH ( 21 FDA reports)
PARALYSIS ( 21 FDA reports)
PEMPHIGOID ( 21 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 21 FDA reports)
SPINAL DISORDER ( 21 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 21 FDA reports)
SYNOVIAL CYST ( 21 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 20 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 20 FDA reports)
BLOOD CALCIUM DECREASED ( 20 FDA reports)
COGNITIVE DISORDER ( 20 FDA reports)
COORDINATION ABNORMAL ( 20 FDA reports)
DIFFICULTY IN WALKING ( 20 FDA reports)
DISABILITY ( 20 FDA reports)
DRUG ADMINISTRATION ERROR ( 20 FDA reports)
FAECAL INCONTINENCE ( 20 FDA reports)
GINGIVAL BLEEDING ( 20 FDA reports)
GOITRE ( 20 FDA reports)
HEAD INJURY ( 20 FDA reports)
HOSPITALISATION ( 20 FDA reports)
HYDRONEPHROSIS ( 20 FDA reports)
INJECTION SITE ERYTHEMA ( 20 FDA reports)
ISCHAEMIA ( 20 FDA reports)
JOINT EFFUSION ( 20 FDA reports)
LIBIDO DECREASED ( 20 FDA reports)
LIPOMA ( 20 FDA reports)
MALIGNANT MELANOMA ( 20 FDA reports)
MOVEMENT DISORDER ( 20 FDA reports)
MULTIPLE MYELOMA ( 20 FDA reports)
PERIPHERAL COLDNESS ( 20 FDA reports)
RADICULOPATHY ( 20 FDA reports)
SKIN DISORDER ( 20 FDA reports)
THYROID DISORDER ( 20 FDA reports)
WOUND ( 20 FDA reports)
ABNORMAL BEHAVIOUR ( 19 FDA reports)
ACCIDENTAL OVERDOSE ( 19 FDA reports)
AORTIC ANEURYSM ( 19 FDA reports)
DEFORMITY ( 19 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 19 FDA reports)
DILATATION VENTRICULAR ( 19 FDA reports)
DYSSTASIA ( 19 FDA reports)
ECCHYMOSIS ( 19 FDA reports)
FACIAL BONES FRACTURE ( 19 FDA reports)
HEPATOMEGALY ( 19 FDA reports)
HYPOPHAGIA ( 19 FDA reports)
IMPAIRED WORK ABILITY ( 19 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 19 FDA reports)
KIDNEY INFECTION ( 19 FDA reports)
LABORATORY TEST ABNORMAL ( 19 FDA reports)
MUSCLE ATROPHY ( 19 FDA reports)
MYOCLONUS ( 19 FDA reports)
POLYURIA ( 19 FDA reports)
PRODUCT QUALITY ISSUE ( 19 FDA reports)
RASH ERYTHEMATOUS ( 19 FDA reports)
SKIN CANCER ( 19 FDA reports)
SKIN HYPERTROPHY ( 19 FDA reports)
STOMACH DISCOMFORT ( 19 FDA reports)
SUBDURAL HAEMATOMA ( 19 FDA reports)
TENDON DISORDER ( 19 FDA reports)
AGEUSIA ( 18 FDA reports)
BAROTRAUMA ( 18 FDA reports)
BLOOD ALBUMIN DECREASED ( 18 FDA reports)
CANDIDIASIS ( 18 FDA reports)
CARDIOGENIC SHOCK ( 18 FDA reports)
COLITIS ULCERATIVE ( 18 FDA reports)
CYANOSIS ( 18 FDA reports)
DECUBITUS ULCER ( 18 FDA reports)
DIASTOLIC DYSFUNCTION ( 18 FDA reports)
DRUG PRESCRIBING ERROR ( 18 FDA reports)
EPILEPSY ( 18 FDA reports)
EYE IRRITATION ( 18 FDA reports)
EYE PAIN ( 18 FDA reports)
GENERALISED OEDEMA ( 18 FDA reports)
HYPOACUSIS ( 18 FDA reports)
INGUINAL HERNIA ( 18 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 18 FDA reports)
LEUKOCYTOSIS ( 18 FDA reports)
LIVER INJURY ( 18 FDA reports)
MENISCUS LESION ( 18 FDA reports)
MENTAL IMPAIRMENT ( 18 FDA reports)
ORAL SURGERY ( 18 FDA reports)
RESPIRATORY ARREST ( 18 FDA reports)
RESPIRATORY DISORDER ( 18 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 18 FDA reports)
THINKING ABNORMAL ( 18 FDA reports)
TONGUE DISORDER ( 18 FDA reports)
VENTRICULAR FIBRILLATION ( 18 FDA reports)
BLOOD CREATINE INCREASED ( 17 FDA reports)
CARBUNCLE ( 17 FDA reports)
CARDIAC FLUTTER ( 17 FDA reports)
COAGULOPATHY ( 17 FDA reports)
CONJUNCTIVITIS ( 17 FDA reports)
DEAFNESS UNILATERAL ( 17 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 17 FDA reports)
FLUID OVERLOAD ( 17 FDA reports)
GASTROINTESTINAL DISORDER ( 17 FDA reports)
GLIOSIS ( 17 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 17 FDA reports)
HEPATIC LESION ( 17 FDA reports)
HYPOVOLAEMIA ( 17 FDA reports)
INTRACRANIAL ANEURYSM ( 17 FDA reports)
KNEE ARTHROPLASTY ( 17 FDA reports)
LOWER LIMB FRACTURE ( 17 FDA reports)
LUNG INFECTION ( 17 FDA reports)
MASTICATION DISORDER ( 17 FDA reports)
PETECHIAE ( 17 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 17 FDA reports)
PRODUCTIVE COUGH ( 17 FDA reports)
SHOCK HYPOGLYCAEMIC ( 17 FDA reports)
SHOULDER PAIN ( 17 FDA reports)
SQUAMOUS CELL CARCINOMA ( 17 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 17 FDA reports)
TENSION ( 17 FDA reports)
THIRST ( 17 FDA reports)
URINE OUTPUT DECREASED ( 17 FDA reports)
ANOSMIA ( 16 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 16 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 16 FDA reports)
CHOLECYSTITIS ( 16 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 16 FDA reports)
CORONARY ARTERY BYPASS ( 16 FDA reports)
CROHN'S DISEASE ( 16 FDA reports)
DERMATITIS ALLERGIC ( 16 FDA reports)
DERMATITIS BULLOUS ( 16 FDA reports)
DISEASE RECURRENCE ( 16 FDA reports)
DRUG DISPENSING ERROR ( 16 FDA reports)
DRUG ERUPTION ( 16 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 16 FDA reports)
DRY THROAT ( 16 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 16 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 16 FDA reports)
FIBROMYALGIA ( 16 FDA reports)
HEARING IMPAIRED ( 16 FDA reports)
HERNIA ( 16 FDA reports)
HERPES VIRUS INFECTION ( 16 FDA reports)
HUMERUS FRACTURE ( 16 FDA reports)
ISCHAEMIC STROKE ( 16 FDA reports)
LABYRINTHITIS ( 16 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 16 FDA reports)
MICTURITION FREQUENCY DECREASED ( 16 FDA reports)
MITRAL VALVE CALCIFICATION ( 16 FDA reports)
MUSCLE DISORDER ( 16 FDA reports)
ORAL DISCOMFORT ( 16 FDA reports)
OVARIAN CANCER ( 16 FDA reports)
PANCREATITIS CHRONIC ( 16 FDA reports)
PNEUMONITIS ( 16 FDA reports)
THROAT TIGHTNESS ( 16 FDA reports)
THYROID NEOPLASM ( 16 FDA reports)
UROSEPSIS ( 16 FDA reports)
ACUTE CORONARY SYNDROME ( 15 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 15 FDA reports)
BACK INJURY ( 15 FDA reports)
BLOOD CALCIUM INCREASED ( 15 FDA reports)
BLOOD IRON DECREASED ( 15 FDA reports)
CAROTID ARTERY DISEASE ( 15 FDA reports)
COLONIC POLYP ( 15 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 15 FDA reports)
DISCOMFORT ( 15 FDA reports)
DYSKINESIA ( 15 FDA reports)
ELECTROLYTE IMBALANCE ( 15 FDA reports)
ERYSIPELAS ( 15 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 15 FDA reports)
HEPATIC CYST ( 15 FDA reports)
HYPOCALCAEMIA ( 15 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 15 FDA reports)
INTESTINAL STENOSIS ( 15 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 15 FDA reports)
JOINT CONTRACTURE ( 15 FDA reports)
MULTIPLE ALLERGIES ( 15 FDA reports)
OSTEITIS ( 15 FDA reports)
OXYGEN SATURATION DECREASED ( 15 FDA reports)
PAIN OF SKIN ( 15 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 15 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 15 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 15 FDA reports)
PHOTOPHOBIA ( 15 FDA reports)
POLYMYALGIA RHEUMATICA ( 15 FDA reports)
POLYP ( 15 FDA reports)
PREMATURE BABY ( 15 FDA reports)
RAYNAUD'S PHENOMENON ( 15 FDA reports)
RENAL COLIC ( 15 FDA reports)
SKULL MALFORMATION ( 15 FDA reports)
TENDERNESS ( 15 FDA reports)
URETHRAL OBSTRUCTION ( 15 FDA reports)
ATAXIA ( 14 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 14 FDA reports)
BONE MARROW FAILURE ( 14 FDA reports)
CEREBROVASCULAR DISORDER ( 14 FDA reports)
DECREASED ACTIVITY ( 14 FDA reports)
DUODENAL ULCER ( 14 FDA reports)
HEPATITIS CHOLESTATIC ( 14 FDA reports)
HYPOVOLAEMIC SHOCK ( 14 FDA reports)
INCONTINENCE ( 14 FDA reports)
LARGE INTESTINE PERFORATION ( 14 FDA reports)
LIMB INJURY ( 14 FDA reports)
MANIA ( 14 FDA reports)
MUSCLE STRAIN ( 14 FDA reports)
MYOPATHY ( 14 FDA reports)
NEPHRITIS ( 14 FDA reports)
NEURALGIA ( 14 FDA reports)
PERIODONTITIS ( 14 FDA reports)
PERITONITIS ( 14 FDA reports)
RETINAL HAEMORRHAGE ( 14 FDA reports)
RHINITIS ALLERGIC ( 14 FDA reports)
SPLENOMEGALY ( 14 FDA reports)
SPUTUM INCREASED ( 14 FDA reports)
THROMBOPHLEBITIS ( 14 FDA reports)
TONGUE OEDEMA ( 14 FDA reports)
TOOTHACHE ( 14 FDA reports)
URINE FLOW DECREASED ( 14 FDA reports)
ABSCESS JAW ( 13 FDA reports)
ACUTE HEPATIC FAILURE ( 13 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 13 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 13 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 13 FDA reports)
APLASTIC ANAEMIA ( 13 FDA reports)
AUTOIMMUNE HEPATITIS ( 13 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 13 FDA reports)
BREAST MASS ( 13 FDA reports)
CALCULUS URETERIC ( 13 FDA reports)
CARDIAC VALVE DISEASE ( 13 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 13 FDA reports)
CRYING ( 13 FDA reports)
DENTAL FISTULA ( 13 FDA reports)
EAR PAIN ( 13 FDA reports)
FEELING DRUNK ( 13 FDA reports)
GASTRIC HAEMORRHAGE ( 13 FDA reports)
GENERALISED ERYTHEMA ( 13 FDA reports)
GINGIVAL INFECTION ( 13 FDA reports)
GRAND MAL CONVULSION ( 13 FDA reports)
GROIN PAIN ( 13 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 13 FDA reports)
HEPATIC CIRRHOSIS ( 13 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 13 FDA reports)
HEPATITIS C ( 13 FDA reports)
HEPATOTOXICITY ( 13 FDA reports)
METASTASES TO SPINE ( 13 FDA reports)
METASTATIC NEOPLASM ( 13 FDA reports)
MICTURITION URGENCY ( 13 FDA reports)
MYOSITIS ( 13 FDA reports)
NERVOUS SYSTEM DISORDER ( 13 FDA reports)
OCULAR ICTERUS ( 13 FDA reports)
ORTHOPNOEA ( 13 FDA reports)
PURULENT DISCHARGE ( 13 FDA reports)
RASH PUSTULAR ( 13 FDA reports)
RESPIRATORY TRACT INFECTION ( 13 FDA reports)
SEROTONIN SYNDROME ( 13 FDA reports)
SKIN LESION ( 13 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 13 FDA reports)
ACIDOSIS ( 12 FDA reports)
ACTINOMYCOSIS ( 12 FDA reports)
AGRANULOCYTOSIS ( 12 FDA reports)
AZOTAEMIA ( 12 FDA reports)
BILE DUCT CANCER ( 12 FDA reports)
BRUXISM ( 12 FDA reports)
CARDIAC TAMPONADE ( 12 FDA reports)
CEREBRAL ISCHAEMIA ( 12 FDA reports)
CHARLES BONNET SYNDROME ( 12 FDA reports)
CONDUCTION DISORDER ( 12 FDA reports)
DIABETIC KETOACIDOSIS ( 12 FDA reports)
DRUG DEPENDENCE ( 12 FDA reports)
EAR NEOPLASM ( 12 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 12 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 12 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 12 FDA reports)
EYE PRURITUS ( 12 FDA reports)
EYELID OEDEMA ( 12 FDA reports)
EYELID PTOSIS ( 12 FDA reports)
FAECES DISCOLOURED ( 12 FDA reports)
FAILURE TO THRIVE ( 12 FDA reports)
FIBROMA ( 12 FDA reports)
FIBULA FRACTURE ( 12 FDA reports)
GINGIVAL ULCERATION ( 12 FDA reports)
HEPATIC CONGESTION ( 12 FDA reports)
HEPATIC INFARCTION ( 12 FDA reports)
HEPATOCELLULAR INJURY ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 12 FDA reports)
JAW OPERATION ( 12 FDA reports)
LARYNGEAL OEDEMA ( 12 FDA reports)
LARYNGITIS ( 12 FDA reports)
LIP HAEMORRHAGE ( 12 FDA reports)
LOBAR PNEUMONIA ( 12 FDA reports)
LOCALISED INFECTION ( 12 FDA reports)
LUMBAR SPINAL STENOSIS ( 12 FDA reports)
MACROGLOSSIA ( 12 FDA reports)
PARONYCHIA ( 12 FDA reports)
PHYSICAL DISABILITY ( 12 FDA reports)
PROSTATOMEGALY ( 12 FDA reports)
PSYCHOTIC DISORDER ( 12 FDA reports)
RASH MACULO-PAPULAR ( 12 FDA reports)
RASH PAPULAR ( 12 FDA reports)
RENAL ATROPHY ( 12 FDA reports)
RESTLESS LEGS SYNDROME ( 12 FDA reports)
SCOLIOSIS ( 12 FDA reports)
SEQUESTRECTOMY ( 12 FDA reports)
SKIN TIGHTNESS ( 12 FDA reports)
VASCULITIS ( 12 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 12 FDA reports)
VOCAL CORD THICKENING ( 12 FDA reports)
WITHDRAWAL SYNDROME ( 12 FDA reports)
ADDISON'S DISEASE ( 11 FDA reports)
ANGIONEUROTIC OEDEMA ( 11 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 11 FDA reports)
AORTIC DILATATION ( 11 FDA reports)
BEDRIDDEN ( 11 FDA reports)
BIOPSY BONE ABNORMAL ( 11 FDA reports)
BLOOD CHLORIDE DECREASED ( 11 FDA reports)
BLOOD URIC ACID INCREASED ( 11 FDA reports)
BONE FRAGMENTATION ( 11 FDA reports)
BONE SWELLING ( 11 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 11 FDA reports)
CHOKING ( 11 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 11 FDA reports)
COMPRESSION FRACTURE ( 11 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 11 FDA reports)
ENDOCARDITIS ( 11 FDA reports)
ENTEROCOCCAL INFECTION ( 11 FDA reports)
ESCHERICHIA INFECTION ( 11 FDA reports)
FISTULA ( 11 FDA reports)
FLANK PAIN ( 11 FDA reports)
GASTROINTESTINAL CARCINOMA ( 11 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 11 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 11 FDA reports)
HAEMODIALYSIS ( 11 FDA reports)
HAND FRACTURE ( 11 FDA reports)
HEART INJURY ( 11 FDA reports)
HEPATIC ENZYME ABNORMAL ( 11 FDA reports)
HEPATIC MASS ( 11 FDA reports)
HYDROCELE ( 11 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 11 FDA reports)
INTESTINAL OBSTRUCTION ( 11 FDA reports)
LACTOBACILLUS INFECTION ( 11 FDA reports)
LARYNGEAL CYST ( 11 FDA reports)
LYMPHOPENIA ( 11 FDA reports)
MEDICATION RESIDUE ( 11 FDA reports)
METASTASES TO LUNG ( 11 FDA reports)
MIOSIS ( 11 FDA reports)
MITRAL VALVE PROLAPSE ( 11 FDA reports)
MUCOSAL INFLAMMATION ( 11 FDA reports)
MUSCLE RIGIDITY ( 11 FDA reports)
MUSCULAR DYSTROPHY ( 11 FDA reports)
NAIL DISORDER ( 11 FDA reports)
PARANOIA ( 11 FDA reports)
PAROSMIA ( 11 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 11 FDA reports)
RASH GENERALISED ( 11 FDA reports)
RETCHING ( 11 FDA reports)
ROSACEA ( 11 FDA reports)
SENSATION OF FOREIGN BODY ( 11 FDA reports)
SENSORY DISTURBANCE ( 11 FDA reports)
SEXUAL DYSFUNCTION ( 11 FDA reports)
SINUS BRADYCARDIA ( 11 FDA reports)
SPLEEN DISORDER ( 11 FDA reports)
STRESS FRACTURE ( 11 FDA reports)
TESTICULAR PAIN ( 11 FDA reports)
TOOTH INFECTION ( 11 FDA reports)
TORSADE DE POINTES ( 11 FDA reports)
TROPONIN INCREASED ( 11 FDA reports)
WRONG DRUG ADMINISTERED ( 11 FDA reports)
ABNORMAL FAECES ( 10 FDA reports)
ABSCESS ( 10 FDA reports)
ACUTE RESPIRATORY FAILURE ( 10 FDA reports)
ANAL FISTULA ( 10 FDA reports)
ANGER ( 10 FDA reports)
APHAGIA ( 10 FDA reports)
APPLICATION SITE PRURITUS ( 10 FDA reports)
ASPIRATION ( 10 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 10 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 10 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 10 FDA reports)
BODY HEIGHT DECREASED ( 10 FDA reports)
BONE DEBRIDEMENT ( 10 FDA reports)
BONE EROSION ( 10 FDA reports)
BREAST CANCER RECURRENT ( 10 FDA reports)
BREAST PAIN ( 10 FDA reports)
CATHETERISATION CARDIAC ( 10 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 10 FDA reports)
DERMATITIS PSORIASIFORM ( 10 FDA reports)
DEVICE MALFUNCTION ( 10 FDA reports)
DISSOCIATION ( 10 FDA reports)
DIZZINESS POSTURAL ( 10 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 10 FDA reports)
ENDOMETRIAL CANCER ( 10 FDA reports)
ESSENTIAL HYPERTENSION ( 10 FDA reports)
FOETAL DISORDER ( 10 FDA reports)
GASTRIC POLYPS ( 10 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 10 FDA reports)
GYNAECOMASTIA ( 10 FDA reports)
HALLUCINATION, AUDITORY ( 10 FDA reports)
HEAD DISCOMFORT ( 10 FDA reports)
HEPATIC NEOPLASM ( 10 FDA reports)
HYPERBILIRUBINAEMIA ( 10 FDA reports)
HYPOMAGNESAEMIA ( 10 FDA reports)
HYPOTHERMIA ( 10 FDA reports)
ILEUS PARALYTIC ( 10 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 10 FDA reports)
INITIAL INSOMNIA ( 10 FDA reports)
INTRACARDIAC THROMBUS ( 10 FDA reports)
LACTOSE INTOLERANCE ( 10 FDA reports)
LIGAMENT RUPTURE ( 10 FDA reports)
LYMPHOMA ( 10 FDA reports)
MONOPARESIS ( 10 FDA reports)
MOOD ALTERED ( 10 FDA reports)
MOOD SWINGS ( 10 FDA reports)
MOTOR DYSFUNCTION ( 10 FDA reports)
MULTIPLE DRUG OVERDOSE ( 10 FDA reports)
MUSCLE RUPTURE ( 10 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 10 FDA reports)
MYDRIASIS ( 10 FDA reports)
NECROSIS ( 10 FDA reports)
NODULE ( 10 FDA reports)
NON-CARDIAC CHEST PAIN ( 10 FDA reports)
OVERWEIGHT ( 10 FDA reports)
PATHOLOGICAL FRACTURE ( 10 FDA reports)
PERICARDIAL EFFUSION ( 10 FDA reports)
PNEUMONIA ASPIRATION ( 10 FDA reports)
PULMONARY HYPOPLASIA ( 10 FDA reports)
QUALITY OF LIFE DECREASED ( 10 FDA reports)
RENAL ARTERY STENOSIS ( 10 FDA reports)
RENAL TUBULAR NECROSIS ( 10 FDA reports)
RESPIRATORY RATE DECREASED ( 10 FDA reports)
RHINITIS ( 10 FDA reports)
ROTATOR CUFF REPAIR ( 10 FDA reports)
SEDATION ( 10 FDA reports)
SERUM FERRITIN INCREASED ( 10 FDA reports)
SKIN BURNING SENSATION ( 10 FDA reports)
SKIN WARM ( 10 FDA reports)
STEVENS-JOHNSON SYNDROME ( 10 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 10 FDA reports)
SYNOVITIS ( 10 FDA reports)
TIBIA FRACTURE ( 10 FDA reports)
TOOTH LOSS ( 10 FDA reports)
URETERAL NEOPLASM ( 10 FDA reports)
UTERINE LEIOMYOMA ( 10 FDA reports)
VENTRICULAR HYPOKINESIA ( 10 FDA reports)
VIRAL LABYRINTHITIS ( 10 FDA reports)
VITAMIN D DECREASED ( 10 FDA reports)
ABNORMAL SENSATION IN EYE ( 9 FDA reports)
ABORTION INDUCED ( 9 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 9 FDA reports)
APHONIA ( 9 FDA reports)
APHTHOUS STOMATITIS ( 9 FDA reports)
BASAL GANGLIA INFARCTION ( 9 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 9 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 9 FDA reports)
BLOOD DISORDER ( 9 FDA reports)
BONE DENSITY DECREASED ( 9 FDA reports)
BULLOUS LUNG DISEASE ( 9 FDA reports)
CATARACT OPERATION ( 9 FDA reports)
CHOLANGITIS SCLEROSING ( 9 FDA reports)
CHONDROPATHY ( 9 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 9 FDA reports)
CLOSTRIDIUM COLITIS ( 9 FDA reports)
CREPITATIONS ( 9 FDA reports)
DECREASED INTEREST ( 9 FDA reports)
DERMATITIS EXFOLIATIVE ( 9 FDA reports)
DEVICE DISLOCATION ( 9 FDA reports)
EAR DISCOMFORT ( 9 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 9 FDA reports)
EOSINOPHIL COUNT INCREASED ( 9 FDA reports)
ERUCTATION ( 9 FDA reports)
FACIAL PAIN ( 9 FDA reports)
FACIAL PALSY ( 9 FDA reports)
FAMILY STRESS ( 9 FDA reports)
FOETAL GROWTH RETARDATION ( 9 FDA reports)
FOOT DEFORMITY ( 9 FDA reports)
FRACTURE ( 9 FDA reports)
GASTROENTERITIS RADIATION ( 9 FDA reports)
HEPATITIS ACUTE ( 9 FDA reports)
HILAR LYMPHADENOPATHY ( 9 FDA reports)
HYDROURETER ( 9 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 9 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 9 FDA reports)
INJECTION SITE HAEMATOMA ( 9 FDA reports)
INJECTION SITE SWELLING ( 9 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 9 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 9 FDA reports)
LEUKOENCEPHALOPATHY ( 9 FDA reports)
LIMB CRUSHING INJURY ( 9 FDA reports)
LIP DRY ( 9 FDA reports)
LUNG NEOPLASM MALIGNANT ( 9 FDA reports)
MALABSORPTION ( 9 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 9 FDA reports)
MIDDLE INSOMNIA ( 9 FDA reports)
MUSCLE HAEMORRHAGE ( 9 FDA reports)
NERVE COMPRESSION ( 9 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 9 FDA reports)
OSTEOMYELITIS CHRONIC ( 9 FDA reports)
OSTEOPOROTIC FRACTURE ( 9 FDA reports)
PENILE INFECTION ( 9 FDA reports)
PROCEDURAL COMPLICATION ( 9 FDA reports)
PURPURA ( 9 FDA reports)
QRS AXIS ABNORMAL ( 9 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 9 FDA reports)
RENAL PAIN ( 9 FDA reports)
SELF-MEDICATION ( 9 FDA reports)
SENSATION OF HEAVINESS ( 9 FDA reports)
SINUS OPERATION ( 9 FDA reports)
SKIN NECROSIS ( 9 FDA reports)
SNEEZING ( 9 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 9 FDA reports)
THERAPY NON-RESPONDER ( 9 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
UTERINE MASS ( 9 FDA reports)
ADRENAL MASS ( 8 FDA reports)
ALCOHOL POISONING ( 8 FDA reports)
ANGIOPLASTY ( 8 FDA reports)
AORTIC STENOSIS ( 8 FDA reports)
APNOEA ( 8 FDA reports)
ARTERIAL DISORDER ( 8 FDA reports)
ARTERIAL INJURY ( 8 FDA reports)
ATHEROSCLEROSIS ( 8 FDA reports)
AUTONOMIC NEUROPATHY ( 8 FDA reports)
BACTERAEMIA ( 8 FDA reports)
BARRETT'S OESOPHAGUS ( 8 FDA reports)
BLOOD OSMOLARITY DECREASED ( 8 FDA reports)
BONE MARROW TRANSPLANT ( 8 FDA reports)
BUNDLE BRANCH BLOCK ( 8 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 8 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 8 FDA reports)
CERVICOBRACHIAL SYNDROME ( 8 FDA reports)
COMPLETED SUICIDE ( 8 FDA reports)
CYSTOCELE ( 8 FDA reports)
DILATATION ATRIAL ( 8 FDA reports)
DRUG LEVEL INCREASED ( 8 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 8 FDA reports)
DYSLIPIDAEMIA ( 8 FDA reports)
ENDODONTIC PROCEDURE ( 8 FDA reports)
ENDOTRACHEAL INTUBATION ( 8 FDA reports)
EUPHORIC MOOD ( 8 FDA reports)
FRUSTRATION ( 8 FDA reports)
GASTRITIS EROSIVE ( 8 FDA reports)
GASTROINTESTINAL INFECTION ( 8 FDA reports)
GINGIVAL HYPERPLASIA ( 8 FDA reports)
HAEMOLYTIC ANAEMIA ( 8 FDA reports)
HAEMORRHAGIC STROKE ( 8 FDA reports)
HEPATIC FIBROSIS ( 8 FDA reports)
HYPERKERATOSIS ( 8 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 8 FDA reports)
HYPERTHERMIA ( 8 FDA reports)
HYPOAESTHESIA ORAL ( 8 FDA reports)
HYPOCHLORAEMIA ( 8 FDA reports)
HYPOPHOSPHATAEMIA ( 8 FDA reports)
HYPOPNOEA ( 8 FDA reports)
HYPOTONIA ( 8 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 8 FDA reports)
ILEITIS ( 8 FDA reports)
ILEUS ( 8 FDA reports)
INCREASED APPETITE ( 8 FDA reports)
INJECTION SITE BRUISING ( 8 FDA reports)
INJECTION SITE CELLULITIS ( 8 FDA reports)
INJECTION SITE WARMTH ( 8 FDA reports)
INTESTINAL POLYP ( 8 FDA reports)
IRON DEFICIENCY ( 8 FDA reports)
JOINT LOCK ( 8 FDA reports)
LARGE INTESTINAL ULCER ( 8 FDA reports)
MACULAR OEDEMA ( 8 FDA reports)
MECHANICAL VENTILATION ( 8 FDA reports)
METASTASES TO SPLEEN ( 8 FDA reports)
MICROCYTIC ANAEMIA ( 8 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 8 FDA reports)
NERVE INJURY ( 8 FDA reports)
NEURITIS ( 8 FDA reports)
NEUROLOGICAL SYMPTOM ( 8 FDA reports)
NIGHT SWEATS ( 8 FDA reports)
ORAL PAIN ( 8 FDA reports)
OSTEOLYSIS ( 8 FDA reports)
PARKINSON'S DISEASE ( 8 FDA reports)
PLEURISY ( 8 FDA reports)
PULMONARY MASS ( 8 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 8 FDA reports)
RETINAL DETACHMENT ( 8 FDA reports)
RIGHT VENTRICULAR FAILURE ( 8 FDA reports)
SCAB ( 8 FDA reports)
SENSORY LOSS ( 8 FDA reports)
SKIN IRRITATION ( 8 FDA reports)
SKIN LACERATION ( 8 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 8 FDA reports)
SOCIAL PROBLEM ( 8 FDA reports)
STRESS INCONTINENCE ( 8 FDA reports)
SUDDEN CARDIAC DEATH ( 8 FDA reports)
TENDON INJURY ( 8 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 8 FDA reports)
TOOTH FRACTURE ( 8 FDA reports)
ULCER ( 8 FDA reports)
URETERIC OBSTRUCTION ( 8 FDA reports)
URINE OUTPUT INCREASED ( 8 FDA reports)
VASCULAR GRAFT ( 8 FDA reports)
WALKING AID USER ( 8 FDA reports)
YELLOW SKIN ( 8 FDA reports)
ACCIDENTAL EXPOSURE ( 7 FDA reports)
ALVEOLITIS ( 7 FDA reports)
AMAUROSIS FUGAX ( 7 FDA reports)
ANAPHYLACTIC SHOCK ( 7 FDA reports)
ANGIOPATHY ( 7 FDA reports)
ANORECTAL DISCOMFORT ( 7 FDA reports)
AORTIC DISSECTION ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 7 FDA reports)
AUTOIMMUNE DISORDER ( 7 FDA reports)
BILE DUCT OBSTRUCTION ( 7 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 7 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 7 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 7 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 7 FDA reports)
BREAST CANCER FEMALE ( 7 FDA reports)
BRONCHIECTASIS ( 7 FDA reports)
CARDIAC OUTPUT DECREASED ( 7 FDA reports)
CEREBRAL HAEMATOMA ( 7 FDA reports)
CHEMOTHERAPY ( 7 FDA reports)
COLECTOMY ( 7 FDA reports)
CONCUSSION ( 7 FDA reports)
CULTURE URINE POSITIVE ( 7 FDA reports)
DENTAL CLEANING ( 7 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 7 FDA reports)
DIABETIC NEPHROPATHY ( 7 FDA reports)
DIABETIC NEUROPATHY ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 7 FDA reports)
ENERGY INCREASED ( 7 FDA reports)
EPIDIDYMITIS ( 7 FDA reports)
EXCORIATION ( 7 FDA reports)
EXPIRED DRUG ADMINISTERED ( 7 FDA reports)
FIBROSIS ( 7 FDA reports)
FISTULA REPAIR ( 7 FDA reports)
FOREIGN BODY TRAUMA ( 7 FDA reports)
GASTRIC CANCER ( 7 FDA reports)
GASTROENTERITIS VIRAL ( 7 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 7 FDA reports)
GASTROINTESTINAL TOXICITY ( 7 FDA reports)
GLUCOSE URINE PRESENT ( 7 FDA reports)
HAEMOTHORAX ( 7 FDA reports)
HEART VALVE INCOMPETENCE ( 7 FDA reports)
HEPATITIS FULMINANT ( 7 FDA reports)
HICCUPS ( 7 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 7 FDA reports)
HYPERURICAEMIA ( 7 FDA reports)
INTESTINAL ISCHAEMIA ( 7 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 7 FDA reports)
KIDNEY MALFORMATION ( 7 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 7 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 7 FDA reports)
LOSS OF LIBIDO ( 7 FDA reports)
METABOLIC ENCEPHALOPATHY ( 7 FDA reports)
METABOLIC SYNDROME ( 7 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 7 FDA reports)
METASTASES TO ADRENALS ( 7 FDA reports)
MONOCYTE COUNT INCREASED ( 7 FDA reports)
MOUTH HAEMORRHAGE ( 7 FDA reports)
MUCOSAL NECROSIS ( 7 FDA reports)
MUSCLE INJURY ( 7 FDA reports)
MUSCLE TIGHTNESS ( 7 FDA reports)
MYELODYSPLASTIC SYNDROME ( 7 FDA reports)
NEPHRITIS INTERSTITIAL ( 7 FDA reports)
NEPHROTIC SYNDROME ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 7 FDA reports)
ORAL HERPES ( 7 FDA reports)
ORAL INTAKE REDUCED ( 7 FDA reports)
ORTHOPEDIC PROCEDURE ( 7 FDA reports)
PANCREATIC DISORDER ( 7 FDA reports)
PHOTOPSIA ( 7 FDA reports)
POLYDIPSIA ( 7 FDA reports)
PREGNANCY ( 7 FDA reports)
PROTEIN TOTAL DECREASED ( 7 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 7 FDA reports)
PSEUDOMONAS INFECTION ( 7 FDA reports)
RADICULAR PAIN ( 7 FDA reports)
RADIUS FRACTURE ( 7 FDA reports)
RECTOCELE ( 7 FDA reports)
RENAL HAEMORRHAGE ( 7 FDA reports)
RENAL TUBULAR DISORDER ( 7 FDA reports)
RETINOPATHY OF PREMATURITY ( 7 FDA reports)
SCIATICA ( 7 FDA reports)
SENSATION OF PRESSURE ( 7 FDA reports)
SHOCK HAEMORRHAGIC ( 7 FDA reports)
SINUS CONGESTION ( 7 FDA reports)
SKIN REACTION ( 7 FDA reports)
SPUTUM DISCOLOURED ( 7 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 7 FDA reports)
STREPTOCOCCAL INFECTION ( 7 FDA reports)
SUBILEUS ( 7 FDA reports)
TEMPERATURE INTOLERANCE ( 7 FDA reports)
TENDON PAIN ( 7 FDA reports)
THERMAL BURN ( 7 FDA reports)
THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
TUBERCULOSIS ( 7 FDA reports)
TYPE 1 DIABETES MELLITUS ( 7 FDA reports)
UNDERDOSE ( 7 FDA reports)
UNEMPLOYMENT ( 7 FDA reports)
URINE ANALYSIS ABNORMAL ( 7 FDA reports)
VARICOSE VEIN ( 7 FDA reports)
VENA CAVA FILTER INSERTION ( 7 FDA reports)
WEGENER'S GRANULOMATOSIS ( 7 FDA reports)
WOUND DRAINAGE ( 7 FDA reports)
WOUND INFECTION ( 7 FDA reports)
ABDOMINAL PAIN LOWER ( 6 FDA reports)
ABDOMINAL TENDERNESS ( 6 FDA reports)
ACCOMMODATION DISORDER ( 6 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 6 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 6 FDA reports)
ADVERSE REACTION ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 6 FDA reports)
ANXIETY DISORDER ( 6 FDA reports)
AORTIC CALCIFICATION ( 6 FDA reports)
AORTIC VALVE REPLACEMENT ( 6 FDA reports)
APLASIA PURE RED CELL ( 6 FDA reports)
APPARENT DEATH ( 6 FDA reports)
APRAXIA ( 6 FDA reports)
B-CELL LYMPHOMA STAGE I ( 6 FDA reports)
BIPOLAR DISORDER ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 6 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 6 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 6 FDA reports)
BRADYARRHYTHMIA ( 6 FDA reports)
BRAIN HERNIATION ( 6 FDA reports)
BRAIN INJURY ( 6 FDA reports)
BRAIN OEDEMA ( 6 FDA reports)
CALCINOSIS ( 6 FDA reports)
CALCULUS URINARY ( 6 FDA reports)
CERVICAL SPINAL STENOSIS ( 6 FDA reports)
CHEST X-RAY ABNORMAL ( 6 FDA reports)
CHOLECYSTITIS INFECTIVE ( 6 FDA reports)
CLAVICLE FRACTURE ( 6 FDA reports)
COAGULATION TIME PROLONGED ( 6 FDA reports)
COLITIS ISCHAEMIC ( 6 FDA reports)
COLONIC STENOSIS ( 6 FDA reports)
DYSPNOEA EXACERBATED ( 6 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 6 FDA reports)
EATING DISORDER ( 6 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 6 FDA reports)
EPIGASTRIC DISCOMFORT ( 6 FDA reports)
EPIGLOTTITIS ( 6 FDA reports)
EYE INFECTION ( 6 FDA reports)
EYE INFLAMMATION ( 6 FDA reports)
EYE MOVEMENT DISORDER ( 6 FDA reports)
FRACTURED COCCYX ( 6 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 6 FDA reports)
GASTROINTESTINAL PAIN ( 6 FDA reports)
GINGIVAL HYPERTROPHY ( 6 FDA reports)
GOUTY ARTHRITIS ( 6 FDA reports)
HAEMORRHAGIC ANAEMIA ( 6 FDA reports)
HAEMORRHAGIC DISORDER ( 6 FDA reports)
HEPATOCELLULAR DAMAGE ( 6 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 6 FDA reports)
HYPERPARATHYROIDISM ( 6 FDA reports)
HYPOAESTHESIA FACIAL ( 6 FDA reports)
HYPOALBUMINAEMIA ( 6 FDA reports)
HYPOSPADIAS ( 6 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 6 FDA reports)
INJECTION SITE INDURATION ( 6 FDA reports)
INJECTION SITE REACTION ( 6 FDA reports)
INTENTIONAL OVERDOSE ( 6 FDA reports)
INTERMITTENT CLAUDICATION ( 6 FDA reports)
INTESTINAL HAEMORRHAGE ( 6 FDA reports)
INTESTINAL PERFORATION ( 6 FDA reports)
JAW DISORDER ( 6 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 6 FDA reports)
LEFT ATRIAL DILATATION ( 6 FDA reports)
LIFE EXPECTANCY SHORTENED ( 6 FDA reports)
LIP OEDEMA ( 6 FDA reports)
LOOSE TOOTH ( 6 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
MAJOR DEPRESSION ( 6 FDA reports)
MALNUTRITION ( 6 FDA reports)
METASTASES TO BONE MARROW ( 6 FDA reports)
MICROALBUMINURIA ( 6 FDA reports)
MONOPLEGIA ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 6 FDA reports)
MUSCLE CRAMP ( 6 FDA reports)
NEONATAL HYPOTENSION ( 6 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
NEPHROANGIOSCLEROSIS ( 6 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 6 FDA reports)
OCCULT BLOOD POSITIVE ( 6 FDA reports)
ODYNOPHAGIA ( 6 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 6 FDA reports)
ONYCHOMYCOSIS ( 6 FDA reports)
OOPHORECTOMY ( 6 FDA reports)
ORTHOSTATIC HYPERTENSION ( 6 FDA reports)
PERITONEAL HAEMORRHAGE ( 6 FDA reports)
PERSONALITY CHANGE ( 6 FDA reports)
POLYCYTHAEMIA ( 6 FDA reports)
POOR QUALITY SLEEP ( 6 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 6 FDA reports)
PULMONARY GRANULOMA ( 6 FDA reports)
PULMONARY TUBERCULOSIS ( 6 FDA reports)
PURULENCE ( 6 FDA reports)
RAPID CORRECTION OF HYPONATRAEMIA ( 6 FDA reports)
RENAL APLASIA ( 6 FDA reports)
RENAL CANCER ( 6 FDA reports)
RENAL MASS ( 6 FDA reports)
RHINITIS SEASONAL ( 6 FDA reports)
SKIN ATROPHY ( 6 FDA reports)
SKIN INDURATION ( 6 FDA reports)
SNORING ( 6 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 6 FDA reports)
STRABISMUS ( 6 FDA reports)
STUPOR ( 6 FDA reports)
TESTICULAR SWELLING ( 6 FDA reports)
TETANY ( 6 FDA reports)
THROMBOCYTOSIS ( 6 FDA reports)
TINEA CRURIS ( 6 FDA reports)
TOE AMPUTATION ( 6 FDA reports)
TRANSFERRIN DECREASED ( 6 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 6 FDA reports)
TYPE I HYPERSENSITIVITY ( 6 FDA reports)
VASCULAR CALCIFICATION ( 6 FDA reports)
VASCULAR PSEUDOANEURYSM ( 6 FDA reports)
VISUAL FIELD DEFECT ( 6 FDA reports)
ACCIDENT ( 5 FDA reports)
ACOUSTIC NEUROMA ( 5 FDA reports)
ACUTE PRERENAL FAILURE ( 5 FDA reports)
ALBUMIN URINE PRESENT ( 5 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 5 FDA reports)
AORTIC VALVE SCLEROSIS ( 5 FDA reports)
APPLICATION SITE ERYTHEMA ( 5 FDA reports)
ARACHNOID CYST ( 5 FDA reports)
AREFLEXIA ( 5 FDA reports)
ASPIRATION PLEURAL CAVITY ( 5 FDA reports)
BEREAVEMENT REACTION ( 5 FDA reports)
BILIARY DYSKINESIA ( 5 FDA reports)
BLADDER AGENESIS ( 5 FDA reports)
BLOOD ALBUMIN INCREASED ( 5 FDA reports)
BLOOD CHLORIDE INCREASED ( 5 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 5 FDA reports)
BLOOD SODIUM INCREASED ( 5 FDA reports)
BLOOD TEST ABNORMAL ( 5 FDA reports)
BODY TEMPERATURE DECREASED ( 5 FDA reports)
BRAIN HYPOXIA ( 5 FDA reports)
BRAIN NEOPLASM ( 5 FDA reports)
BREATH SOUNDS ABNORMAL ( 5 FDA reports)
BRONCHIAL DISORDER ( 5 FDA reports)
BRONCHITIS CHRONIC ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 5 FDA reports)
CAESAREAN SECTION ( 5 FDA reports)
CAROTID BRUIT ( 5 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 5 FDA reports)
CHOREA ( 5 FDA reports)
CLONUS ( 5 FDA reports)
CLOSTRIDIAL INFECTION ( 5 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 5 FDA reports)
CONGENITAL ANOMALY ( 5 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 5 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 5 FDA reports)
CRANIAL SUTURES WIDENING ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
DIABETIC COMPLICATION ( 5 FDA reports)
DISTRACTIBILITY ( 5 FDA reports)
DIVERTICULAR PERFORATION ( 5 FDA reports)
DRUG SCREEN POSITIVE ( 5 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 5 FDA reports)
DYSGRAPHIA ( 5 FDA reports)
EAR INFECTION ( 5 FDA reports)
EAR OPERATION ( 5 FDA reports)
EARLY SATIETY ( 5 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 5 FDA reports)
EMBOLISM ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
EYE ALLERGY ( 5 FDA reports)
EYE INJURY ( 5 FDA reports)
EYE ROLLING ( 5 FDA reports)
FAILURE TO ANASTOMOSE ( 5 FDA reports)
GINGIVAL RECESSION ( 5 FDA reports)
HAIR TEXTURE ABNORMAL ( 5 FDA reports)
HEAD DEFORMITY ( 5 FDA reports)
HEART SOUNDS ABNORMAL ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HIP ARTHROPLASTY ( 5 FDA reports)
HYDROCEPHALUS ( 5 FDA reports)
HYPERACUSIS ( 5 FDA reports)
HYPERAESTHESIA ( 5 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 5 FDA reports)
HYPERTONIC BLADDER ( 5 FDA reports)
HYPERVENTILATION ( 5 FDA reports)
IMMUNODEFICIENCY ( 5 FDA reports)
IMPAIRED DRIVING ABILITY ( 5 FDA reports)
IMPLANT SITE INDURATION ( 5 FDA reports)
INCISION SITE INFECTION ( 5 FDA reports)
INJECTION SITE CALCIFICATION ( 5 FDA reports)
INTESTINAL INFARCTION ( 5 FDA reports)
IRRITABLE BOWEL SYNDROME ( 5 FDA reports)
JOINT DISLOCATION ( 5 FDA reports)
LICHENOID KERATOSIS ( 5 FDA reports)
LIGAMENT INJURY ( 5 FDA reports)
LISTLESS ( 5 FDA reports)
LOCAL SWELLING ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 5 FDA reports)
LUMBAR RADICULOPATHY ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 5 FDA reports)
MUSCLE SPASTICITY ( 5 FDA reports)
MUSCULOSKELETAL DISORDER ( 5 FDA reports)
NASAL DISCOMFORT ( 5 FDA reports)
NEPHROSCLEROSIS ( 5 FDA reports)
NERVE ROOT COMPRESSION ( 5 FDA reports)
NO THERAPEUTIC RESPONSE ( 5 FDA reports)
OPERATIVE HAEMORRHAGE ( 5 FDA reports)
ORAL CANDIDIASIS ( 5 FDA reports)
ORAL DISORDER ( 5 FDA reports)
OTITIS EXTERNA ( 5 FDA reports)
PATHOLOGICAL GAMBLING ( 5 FDA reports)
PELVIC FRACTURE ( 5 FDA reports)
PELVIC MASS ( 5 FDA reports)
PELVIC PROLAPSE ( 5 FDA reports)
PEPTIC ULCER ( 5 FDA reports)
PERICARDIAL HAEMORRHAGE ( 5 FDA reports)
PERICARDITIS ( 5 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
PLATELET COUNT INCREASED ( 5 FDA reports)
PLATELET DISORDER ( 5 FDA reports)
PNEUMONIA BACTERIAL ( 5 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 5 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 5 FDA reports)
POSTOPERATIVE ABSCESS ( 5 FDA reports)
PRESCRIBED OVERDOSE ( 5 FDA reports)
PROSTATIC OPERATION ( 5 FDA reports)
PROSTATITIS ( 5 FDA reports)
PROTEIN TOTAL INCREASED ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 5 FDA reports)
PSEUDOPHAKIA ( 5 FDA reports)
PUPIL FIXED ( 5 FDA reports)
REFLUX OESOPHAGITIS ( 5 FDA reports)
RENAL CELL CARCINOMA ( 5 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 5 FDA reports)
ROTAVIRUS TEST POSITIVE ( 5 FDA reports)
SARCOIDOSIS ( 5 FDA reports)
SCOTOMA ( 5 FDA reports)
SEBORRHOEIC KERATOSIS ( 5 FDA reports)
SKELETAL INJURY ( 5 FDA reports)
SLEEP-RELATED EATING DISORDER ( 5 FDA reports)
STARING ( 5 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 5 FDA reports)
SUFFOCATION FEELING ( 5 FDA reports)
TACHYPNOEA ( 5 FDA reports)
TARDIVE DYSKINESIA ( 5 FDA reports)
TENOSYNOVITIS ( 5 FDA reports)
TESTICULAR SEMINOMA (PURE) ( 5 FDA reports)
THORACIC OUTLET SYNDROME ( 5 FDA reports)
THYROID CANCER METASTATIC ( 5 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 5 FDA reports)
TONGUE BITING ( 5 FDA reports)
TONGUE DISCOLOURATION ( 5 FDA reports)
TRAUMATIC BRAIN INJURY ( 5 FDA reports)
TREATMENT FAILURE ( 5 FDA reports)
ULNA FRACTURE ( 5 FDA reports)
UMBILICAL HERNIA ( 5 FDA reports)
URINE COLOUR ABNORMAL ( 5 FDA reports)
VAGINAL HAEMORRHAGE ( 5 FDA reports)
VITAMIN B12 DEFICIENCY ( 5 FDA reports)
VULVAL ABSCESS ( 5 FDA reports)
WEIGHT FLUCTUATION ( 5 FDA reports)
ABDOMINAL MASS ( 4 FDA reports)
AKATHISIA ( 4 FDA reports)
ALBUMINURIA ( 4 FDA reports)
ANAL HAEMORRHAGE ( 4 FDA reports)
ANASTOMOTIC COMPLICATION ( 4 FDA reports)
ANGIOGRAM ( 4 FDA reports)
ANOXIC ENCEPHALOPATHY ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 4 FDA reports)
APATHY ( 4 FDA reports)
APLASIA ( 4 FDA reports)
APPLICATION SITE RASH ( 4 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 4 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
ATRIAL TACHYCARDIA ( 4 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 4 FDA reports)
BILE DUCT STENOSIS ( 4 FDA reports)
BILE DUCT STONE ( 4 FDA reports)
BILIARY DILATATION ( 4 FDA reports)
BLOOD LACTIC ACID INCREASED ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BONE LESION ( 4 FDA reports)
BREAST CANCER IN SITU ( 4 FDA reports)
BREAST LUMP REMOVAL ( 4 FDA reports)
CARDIAC OPERATION ( 4 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 4 FDA reports)
CARDIAC VENTRICULOGRAM ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CHEST TUBE INSERTION ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CHOLANGITIS ( 4 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 4 FDA reports)
CHROMATOPSIA ( 4 FDA reports)
COLLAPSE OF LUNG ( 4 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 4 FDA reports)
CONJUNCTIVAL OEDEMA ( 4 FDA reports)
CORONARY ANGIOPLASTY ( 4 FDA reports)
CORONARY ARTERY ANEURYSM ( 4 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 4 FDA reports)
CYANOPSIA ( 4 FDA reports)
DEPRESSION SUICIDAL ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
DERMATITIS CONTACT ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DUODENITIS ( 4 FDA reports)
DYSPNOEA AT REST ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 4 FDA reports)
FACIAL PARESIS ( 4 FDA reports)
FAECALOMA ( 4 FDA reports)
FAECES PALE ( 4 FDA reports)
FAMILIAL TREMOR ( 4 FDA reports)
FAT NECROSIS ( 4 FDA reports)
FEMORAL NECK FRACTURE ( 4 FDA reports)
FLUID INTAKE REDUCED ( 4 FDA reports)
FORMICATION ( 4 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 4 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
HAEMARTHROSIS ( 4 FDA reports)
HAEMOGLOBIN INCREASED ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
HAIR GROWTH ABNORMAL ( 4 FDA reports)
HALO VISION ( 4 FDA reports)
HANGOVER ( 4 FDA reports)
HELICOBACTER INFECTION ( 4 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 4 FDA reports)
HERNIA REPAIR ( 4 FDA reports)
HIP SURGERY ( 4 FDA reports)
HODGKIN'S DISEASE ( 4 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 4 FDA reports)
HYPERPHOSPHATAEMIA ( 4 FDA reports)
HYPERPROTEINAEMIA ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 4 FDA reports)
HYPOPROTHROMBINAEMIA ( 4 FDA reports)
HYPOVENTILATION ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
ILLUSION ( 4 FDA reports)
IMMUNE SYSTEM DISORDER ( 4 FDA reports)
IMPULSIVE BEHAVIOUR ( 4 FDA reports)
INCISION SITE HAEMORRHAGE ( 4 FDA reports)
INCISIONAL HERNIA ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 4 FDA reports)
INJECTION SITE NODULE ( 4 FDA reports)
INTESTINAL DILATATION ( 4 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
KIDNEY ENLARGEMENT ( 4 FDA reports)
KYPHOSIS ( 4 FDA reports)
LONG QT SYNDROME ( 4 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
LYME DISEASE ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
MASKED FACIES ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MENORRHAGIA ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 4 FDA reports)
NEOPLASM ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
NEPHROPATHY TOXIC ( 4 FDA reports)
NEUROPATHY ( 4 FDA reports)
NEUTROPENIC COLITIS ( 4 FDA reports)
NEUTROPENIC SEPSIS ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
NO ADVERSE EVENT ( 4 FDA reports)
NOCTURNAL DYSPNOEA ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 4 FDA reports)
NYSTAGMUS ( 4 FDA reports)
OCCULT BLOOD ( 4 FDA reports)
ORAL DYSAESTHESIA ( 4 FDA reports)
OROANTRAL FISTULA ( 4 FDA reports)
OROPHARYNGEAL BLISTERING ( 4 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 4 FDA reports)
PANIC DISORDER ( 4 FDA reports)
PERICARDIAL FIBROSIS ( 4 FDA reports)
PERIORBITAL OEDEMA ( 4 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 4 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 4 FDA reports)
PLANTAR FASCIITIS ( 4 FDA reports)
PNEUMONIA VIRAL ( 4 FDA reports)
POISONING ( 4 FDA reports)
POLYCHONDRITIS ( 4 FDA reports)
POLYSUBSTANCE ABUSE ( 4 FDA reports)
PORTAL HYPERTENSION ( 4 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 4 FDA reports)
POSTOPERATIVE ILEUS ( 4 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 4 FDA reports)
PROSTATIC DISORDER ( 4 FDA reports)
PSYCHOMOTOR RETARDATION ( 4 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
REGURGITATION ( 4 FDA reports)
RENAL AGENESIS ( 4 FDA reports)
RENAL DYSPLASIA ( 4 FDA reports)
RENAL HYPERTROPHY ( 4 FDA reports)
RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
RETINAL ARTERY THROMBOSIS ( 4 FDA reports)
RETINOPATHY ( 4 FDA reports)
RHEUMATIC FEVER ( 4 FDA reports)
SEPSIS SYNDROME ( 4 FDA reports)
SEROSITIS ( 4 FDA reports)
SINUS HEADACHE ( 4 FDA reports)
SJOGREN'S SYNDROME ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN HYPERPIGMENTATION ( 4 FDA reports)
SOPOR ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
STILLBIRTH ( 4 FDA reports)
SUNBURN ( 4 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 4 FDA reports)
TESTICULAR MASS ( 4 FDA reports)
THALAMIC INFARCTION ( 4 FDA reports)
THERAPY CESSATION ( 4 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
TONGUE COATED ( 4 FDA reports)
TONGUE HAEMORRHAGE ( 4 FDA reports)
TRICHOPHYTON INFECTION ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
URETHRAL STENOSIS ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
VAGINAL DISCHARGE ( 4 FDA reports)
VAGINITIS ATROPHIC ( 4 FDA reports)
VASCULAR PURPURA ( 4 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 4 FDA reports)
VENOUS INSUFFICIENCY ( 4 FDA reports)
VENTRICULAR DYSFUNCTION ( 4 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 4 FDA reports)
WOUND DEHISCENCE ( 4 FDA reports)
ABDOMINAL HERNIA ( 3 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 3 FDA reports)
ACCELERATED HYPERTENSION ( 3 FDA reports)
ACUTE ABDOMEN ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ADENOCARCINOMA ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
ANAL SPHINCTER ATONY ( 3 FDA reports)
ANASTOMOTIC STENOSIS ( 3 FDA reports)
ANEURYSM ( 3 FDA reports)
ANION GAP INCREASED ( 3 FDA reports)
ANKYLOSING SPONDYLITIS ( 3 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 3 FDA reports)
AORTIC DISORDER ( 3 FDA reports)
AORTIC OCCLUSION ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ASTERIXIS ( 3 FDA reports)
ATROPHY ( 3 FDA reports)
AURICULAR SWELLING ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
BENIGN COLONIC NEOPLASM ( 3 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 3 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
BLADDER PROLAPSE ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ( 3 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD INSULIN INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BLOODY AIRWAY DISCHARGE ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BREAST OPERATION ( 3 FDA reports)
BREATH ODOUR ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
BRONCHOSCOPY ABNORMAL ( 3 FDA reports)
BULIMIA NERVOSA ( 3 FDA reports)
BURNING SENSATION MUCOSAL ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 3 FDA reports)
CARDIAC ANEURYSM ( 3 FDA reports)
CARDIAC HYPERTROPHY ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CEREBELLAR SYNDROME ( 3 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 3 FDA reports)
CEREBRAL THROMBOSIS ( 3 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 3 FDA reports)
CHEST WALL PAIN ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHRONIC HEPATITIS ( 3 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 3 FDA reports)
COLITIS COLLAGENOUS ( 3 FDA reports)
COLORECTAL CANCER ( 3 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 3 FDA reports)
CONGENITAL FOOT MALFORMATION ( 3 FDA reports)
CONGENITAL MULTIPLEX ARTHROGRYPOSIS ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 3 FDA reports)
DENGUE FEVER ( 3 FDA reports)
DERMATOMYOSITIS ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DISLOCATION OF VERTEBRA ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG LEVEL DECREASED ( 3 FDA reports)
DRUG TOLERANCE DECREASED ( 3 FDA reports)
DYSENTERY ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 3 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 3 FDA reports)
ENDOMETRIOSIS ( 3 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 3 FDA reports)
EPINEPHRINE INCREASED ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
ESCHERICHIA TEST POSITIVE ( 3 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 3 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
EYE DISCHARGE ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
FAECES HARD ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FRUCTOSAMINE INCREASED ( 3 FDA reports)
FUNGAL SKIN INFECTION ( 3 FDA reports)
GASTRIC DILATATION ( 3 FDA reports)
GASTROENTERITIS NOROVIRUS ( 3 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 3 FDA reports)
GERSTMANN'S SYNDROME ( 3 FDA reports)
GESTATIONAL DIABETES ( 3 FDA reports)
GINGIVAL ABSCESS ( 3 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 3 FDA reports)
GLOBAL AMNESIA ( 3 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
HAEMANGIOMA ( 3 FDA reports)
HAEMANGIOMA OF SKIN ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMORRHAGIC INFARCTION ( 3 FDA reports)
HAIR COLOUR CHANGES ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 3 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPERTENSIVE EMERGENCY ( 3 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPOVITAMINOSIS ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
HYSTERECTOMY ( 3 FDA reports)
IMPAIRED SELF-CARE ( 3 FDA reports)
INFUSION SITE INFLAMMATION ( 3 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 3 FDA reports)
INJECTION SITE INFLAMMATION ( 3 FDA reports)
INJECTION SITE MASS ( 3 FDA reports)
INJECTION SITE NECROSIS ( 3 FDA reports)
INJECTION SITE STINGING ( 3 FDA reports)
INTENTIONAL MISUSE ( 3 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 3 FDA reports)
INVESTIGATION ( 3 FDA reports)
IODINE UPTAKE INCREASED ( 3 FDA reports)
JUGULAR VEIN DISTENSION ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
KLEBSIELLA BACTERAEMIA ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LEUKOCYTURIA ( 3 FDA reports)
LIMB DEFORMITY ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LUNG ADENOCARCINOMA ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MALIGNANT HYPERTENSION ( 3 FDA reports)
MALIGNANT TUMOUR EXCISION ( 3 FDA reports)
MENIERE'S DISEASE ( 3 FDA reports)
MENINGIOMA ( 3 FDA reports)
MENSTRUAL DISORDER ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
METASTASES TO PERITONEUM ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
MITRAL VALVE REPLACEMENT ( 3 FDA reports)
MIXED LIVER INJURY ( 3 FDA reports)
MUCOSAL HAEMORRHAGE ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MYASTHENIA GRAVIS ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
MYOCARDIAL CALCIFICATION ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
MYOPIA ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NECK DEFORMITY ( 3 FDA reports)
NECK INJURY ( 3 FDA reports)
NEONATAL DISORDER ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
OCULAR DISCOMFORT ( 3 FDA reports)
OCULAR NEOPLASM ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
OESOPHAGEAL SPASM ( 3 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
OPHTHALMOPLEGIA ( 3 FDA reports)
ORAL FUNGAL INFECTION ( 3 FDA reports)
ORCHITIS ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
OTITIS MEDIA ( 3 FDA reports)
OTITIS MEDIA CHRONIC ( 3 FDA reports)
OVARIAN MASS ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PARATHYROID DISORDER ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 3 FDA reports)
PERIORBITAL CELLULITIS ( 3 FDA reports)
PERIPHERAL EMBOLISM ( 3 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 3 FDA reports)
PERITONITIS BACTERIAL ( 3 FDA reports)
PERONEAL NERVE PALSY ( 3 FDA reports)
PLASMACYTOMA ( 3 FDA reports)
PLASMACYTOSIS ( 3 FDA reports)
PLEURAL FIBROSIS ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
POOR PERSONAL HYGIENE ( 3 FDA reports)
POST PROCEDURAL HAEMATURIA ( 3 FDA reports)
POTENTIATING DRUG INTERACTION ( 3 FDA reports)
PROCTOCOLITIS ( 3 FDA reports)
PRODUCT TASTE ABNORMAL ( 3 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
PROSTATECTOMY ( 3 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 3 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 3 FDA reports)
PRURIGO ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
PULMONARY INFARCTION ( 3 FDA reports)
PULMONARY TOXICITY ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
RADIATION INJURY ( 3 FDA reports)
RECTAL DISCHARGE ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RENAL VASCULITIS ( 3 FDA reports)
RENIN INCREASED ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
RETROPERITONEAL HAEMATOMA ( 3 FDA reports)
RIGHT ATRIAL DILATATION ( 3 FDA reports)
SACROILIITIS ( 3 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SINOATRIAL BLOCK ( 3 FDA reports)
SINUS ARRHYTHMIA ( 3 FDA reports)
SKIN NEOPLASM EXCISION ( 3 FDA reports)
SKIN PLAQUE ( 3 FDA reports)
SKIN TOXICITY ( 3 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
SMALL FOR DATES BABY ( 3 FDA reports)
SMALL INTESTINE CARCINOMA ( 3 FDA reports)
SOFT TISSUE INFECTION ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SPLENIC RUPTURE ( 3 FDA reports)
SPUTUM ABNORMAL ( 3 FDA reports)
STRESS URINARY INCONTINENCE ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 3 FDA reports)
TACHYCARDIA PAROXYSMAL ( 3 FDA reports)
TEMPERATURE REGULATION DISORDER ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
THROAT CANCER ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
THYROIDECTOMY ( 3 FDA reports)
TONGUE BLISTERING ( 3 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TRICHORRHEXIS ( 3 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
UREA URINE INCREASED ( 3 FDA reports)
URETERIC HAEMORRHAGE ( 3 FDA reports)
URGE INCONTINENCE ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
VEIN PAIN ( 3 FDA reports)
VENOUS THROMBOSIS LIMB ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VESICOURETERIC REFLUX ( 3 FDA reports)
VITAMIN B6 DEFICIENCY ( 3 FDA reports)
VITREOUS DETACHMENT ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
VOCAL CORD DISORDER ( 3 FDA reports)
VOCAL CORD PARALYSIS ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
5-HYDROXYINDOLACETIC ACID IN URINE INCREASED ( 2 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ADRENAL NEOPLASM ( 2 FDA reports)
ALCOHOL INDUCED PERSISTING DEMENTIA ( 2 FDA reports)
ALLERGIC BRONCHITIS ( 2 FDA reports)
AMNIOTIC CAVITY DISORDER ( 2 FDA reports)
AMPUTATION ( 2 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ANAL SPHINCTEROTOMY ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANGIOLIPOMA ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ANTIGLIADIN ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC BRUIT ( 2 FDA reports)
AORTIC RUPTURE ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
AORTIC VALVE CALCIFICATION ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASBESTOSIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ATONIC URINARY BLADDER ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATROPHIC VULVOVAGINITIS ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BEHCET'S SYNDROME ( 2 FDA reports)
BICYTOPENIA ( 2 FDA reports)
BIOPSY LIVER ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLADDER REPAIR ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD COPPER INCREASED ( 2 FDA reports)
BLOOD CREATINE ABNORMAL ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BLOOD UREA ABNORMAL ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE FISTULA ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BOVINE TUBERCULOSIS ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BREAST CANCER STAGE I ( 2 FDA reports)
BREAST DISCOMFORT ( 2 FDA reports)
BREAST DISORDER ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
CALCIUM IONISED INCREASED ( 2 FDA reports)
CANDIDA PNEUMONIA ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC SEPTAL DEFECT ( 2 FDA reports)
CARDIAC VALVE SCLEROSIS ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 2 FDA reports)
CAROTID ARTERY ATHEROMA ( 2 FDA reports)
CATARACT CORTICAL ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CATHETERISATION VENOUS ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CELLULITIS STREPTOCOCCAL ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 2 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 2 FDA reports)
CERVICAL CORD COMPRESSION ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHOLESTATIC LIVER INJURY ( 2 FDA reports)
CHOROIDAL INFARCTION ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
COCCYDYNIA ( 2 FDA reports)
COLITIS MICROSCOPIC ( 2 FDA reports)
COLON ADENOMA ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLON NEOPLASM ( 2 FDA reports)
COLONOSCOPY ABNORMAL ( 2 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORNEAL THICKENING ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYST RUPTURE ( 2 FDA reports)
DEAFNESS TRANSITORY ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEFORMITY THORAX ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DERMATOSIS ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIABETIC ULCER ( 2 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DIZZINESS EXERTIONAL ( 2 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DRUG SCREEN NEGATIVE ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EJACULATION DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
ENURESIS ( 2 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
ESSENTIAL TREMOR ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTREMITY CONTRACTURE ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
EYELID PAIN ( 2 FDA reports)
FABRY'S DISEASE ( 2 FDA reports)
FACIAL DYSMORPHISM ( 2 FDA reports)
FACIAL NERVE DISORDER ( 2 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FINE MOTOR DELAY ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
FOETAL ARRHYTHMIA ( 2 FDA reports)
FOETAL HYPOKINESIA ( 2 FDA reports)
FOETAL MALFORMATION ( 2 FDA reports)
FOETAL MOVEMENTS DECREASED ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRITIS ATROPHIC ( 2 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GINGIVAL ERYTHEMA ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 2 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 2 FDA reports)
GROIN INFECTION ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMOBILIA ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HAND DEFORMITY ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART VALVE OPERATION ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEPATECTOMY ( 2 FDA reports)
HEPATIC PAIN ( 2 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 2 FDA reports)
HERNIA OBSTRUCTIVE ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HISTIOCYTOSIS ( 2 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE III ( 2 FDA reports)
HODGKIN'S DISEASE STAGE III ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HORMONE LEVEL ABNORMAL ( 2 FDA reports)
HYPERALDOSTERONISM ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOTONIA NEONATAL ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
IGA NEPHROPATHY ( 2 FDA reports)
ILEAL GANGRENE ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
IMPINGEMENT SYNDROME ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR REMOVAL ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INSULIN RESISTANCE SYNDROME ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRAOCULAR LENS IMPLANT ( 2 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
IVTH NERVE PARALYSIS ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LDL/HDL RATIO INCREASED ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LENTIGO ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LIMB PROSTHESIS USER ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIVER SCAN ABNORMAL ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 2 FDA reports)
LOW TENSION GLAUCOMA ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG CREPITATION ( 2 FDA reports)
LYMPH NODE CANCER METASTATIC ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
MACULOPATHY ( 2 FDA reports)
MANTLE CELL LYMPHOMA ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MEDICAL INDUCTION OF COMA ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENINGORRHAGIA ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METAMORPHOPSIA ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MINERAL DEFICIENCY ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
NASAL NEOPLASM ( 2 FDA reports)
NASAL OPERATION ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NASAL SEPTUM DEVIATION ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NEONATAL ANURIA ( 2 FDA reports)
NEPHRECTOMY ( 2 FDA reports)
NEPHRITIS ALLERGIC ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEURODERMATITIS ( 2 FDA reports)
NEUROPATHIC PAIN ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OEDEMA DUE TO RENAL DISEASE ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OESOPHAGEAL LESION EXCISION ( 2 FDA reports)
OESOPHAGEAL MASS ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OSTEOSYNTHESIS ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
OVARIAN DISORDER ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PAPILLOMA ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARANEOPLASTIC SYNDROME ( 2 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PELIOSIS HEPATIS ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PERINEAL OPERATION ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 2 FDA reports)
PERIVASCULAR DERMATITIS ( 2 FDA reports)
PH URINE DECREASED ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PHOBIA ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLEUROTHOTONUS ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POLYCYSTIC LIVER DISEASE ( 2 FDA reports)
POLYP COLORECTAL ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROGRESSIVE MASSIVE FIBROSIS ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PSORIATIC ARTHROPATHY ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PULMONARY MALFORMATION ( 2 FDA reports)
PULMONARY VALVE STENOSIS ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RECTAL CANCER STAGE III ( 2 FDA reports)
RECTAL POLYP ( 2 FDA reports)
RECTAL PROLAPSE REPAIR ( 2 FDA reports)
RECTOSIGMOID CANCER ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL CANCER METASTATIC ( 2 FDA reports)
RENAL SURGERY ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL SCAR ( 2 FDA reports)
RETINAL VEIN THROMBOSIS ( 2 FDA reports)
RETINOPATHY HYPERTENSIVE ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SALIVARY GLAND CALCULUS ( 2 FDA reports)
SCAN ABNORMAL ( 2 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SEROLOGY ABNORMAL ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SHUNT THROMBOSIS ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 2 FDA reports)
SKIN FIBROSIS ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN TEST POSITIVE ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SOFT TISSUE INJURY ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 2 FDA reports)
STOMACH MASS ( 2 FDA reports)
STOOL ANALYSIS ABNORMAL ( 2 FDA reports)
SUBACUTE ENDOCARDITIS ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUDDEN ONSET OF SLEEP ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SUPERINFECTION LUNG ( 2 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
SYSTOLIC DYSFUNCTION ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TEMPORAL ARTERITIS ( 2 FDA reports)
TESTICULAR HYPERTROPHY ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THOUGHT BLOCKING ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
TONGUE BLACK HAIRY ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TOTAL BILE ACIDS INCREASED ( 2 FDA reports)
TRACHEOBRONCHITIS ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 2 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
URETERIC INJURY ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URINARY BLADDER ATROPHY ( 2 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 2 FDA reports)
URINE POTASSIUM DECREASED ( 2 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 2 FDA reports)
URINE URIC ACID ( 2 FDA reports)
URINOMA ( 2 FDA reports)
VAGINAL CYST ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
VANISHING BILE DUCT SYNDROME ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VARICOSE VEINS SUBLINGUAL ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VASCULAR RESISTANCE SYSTEMIC ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VENOUS STENOSIS ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULAR HYPERKINESIA ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VOCAL CORD POLYP ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
VULVAL CANCER STAGE 0 ( 2 FDA reports)
VULVAL ULCERATION ( 2 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 2 FDA reports)
WATER INTOXICATION ( 2 FDA reports)
WEIGHT LOSS POOR ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
WOUND INFECTION BACTERIAL ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALLERGY TO METALS ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAESTHETIC COMPLICATION PULMONARY ( 1 FDA reports)
ANAL PROLAPSE ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INHIBITOR FOETOPATHY ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANTERIOR CHAMBER DISORDER ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY NEGATIVE ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTA HYPOPLASIA ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE DISCHARGE ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE PUSTULES ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR CANAL ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BARIUM ENEMA ( 1 FDA reports)
BARTTER'S SYNDROME ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BED REST ( 1 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BETA 2 MICROGLOBULIN DECREASED ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIOPANCREATIC BYPASS ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY BRONCHUS NORMAL ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BITE ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE ABNORMAL ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD HOMOCYSTEINE ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD INSULIN ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID ( 1 FDA reports)
BLOOD PH ABNORMAL ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRACHIAL PLEXOPATHY ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOGRAM ABNORMAL ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BUNION ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARCINOMA IN SITU ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC IMAGING PROCEDURE ABNORMAL ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CARNITINE INCREASED ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CEPHALHAEMATOMA ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CIRCULATORY FAILURE NEONATAL ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
COAGULATION FACTOR INCREASED ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLLAGEN ANTIGEN TYPE 1 ( 1 FDA reports)
COLON CANCER STAGE I ( 1 FDA reports)
COLON CANCER STAGE III ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONGENITAL BLADDER ANOMALY ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL JOINT MALFORMATION ( 1 FDA reports)
CONGENITAL OSTEODYSTROPHY ( 1 FDA reports)
CONGENITAL URETERIC ANOMALY ( 1 FDA reports)
CONGENITAL VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVAL NEOPLASM ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTOURETHROCELE ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOREDUCTIVE SURGERY ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DAWN PHENOMENON ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DELAYED FONTANELLE CLOSURE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DEPRESSION POSTOPERATIVE ( 1 FDA reports)
DEPRESSIVE DELUSION ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DERMO-HYPODERMITIS ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DIVERTICULAR HERNIA ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULUM DUODENAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENECTOMY ( 1 FDA reports)
DUODENITIS HAEMORRHAGIC ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR LOBE INFECTION ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE BIPHASIC ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHEMA INDURATUM ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FALLOPIAN TUBE DISORDER ( 1 FDA reports)
FAMILIAL RISK FACTOR ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FEMORAL HERNIA ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLAT FEET ( 1 FDA reports)
FLUCTUANCE ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FONTANELLE BULGING ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC HYPERMOTILITY ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRIC PH INCREASED ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL CYST ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL GRAFT ( 1 FDA reports)
GLAUCOMATOUS OPTIC DISC ATROPHY ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAIR METAL TEST ABNORMAL ( 1 FDA reports)
HAPTOGLOBIN ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEART VALVE STENOSIS ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEPATIC CYST INFECTION ( 1 FDA reports)
HEPATIC CYST RUPTURED ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERNIAL EVENTRATION ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCAPNIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSION NEONATAL ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPETIGO HERPETIFORMIS ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INCREASED INSULIN REQUIREMENT ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRIS ATROPHY ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRIS NEOVASCULARISATION ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LACTATE PYRUVATE RATIO ABNORMAL ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARYNGEAL DISCOMFORT ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIMB SALVAGE THERAPY ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIPOMA OF BREAST ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUMBAR HERNIA ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROSCOPIC POLYANGIITIS ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYXOEDEMA ( 1 FDA reports)
MYXOEDEMA COMA ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL SEPTAL OPERATION ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NECROBIOSIS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEOLOGISM ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL INJURY ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGOGASTROSTOMY ( 1 FDA reports)
OLFACTORY TEST ABNORMAL ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL CAVITY FISTULA ( 1 FDA reports)
ORAL DISCHARGE ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORAL NEOPLASM ( 1 FDA reports)
ORAL TORUS ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTEOCALCIN DECREASED ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OTOSCLEROSIS ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PAPILLARY MUSCLE INFARCTION ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PAROTID GLAND INFLAMMATION ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERIARTICULAR DISORDER ( 1 FDA reports)
PERIDIVERTICULITIS ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERIPHERAL REVASCULARISATION ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERISTALSIS VISIBLE ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PHARYNGEAL CYST ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL OPERATION ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHLEBOTOMY ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHOTOKERATITIS ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLACENTAL HYPERTROPHY ( 1 FDA reports)
PLATELET ADHESIVENESS INCREASED ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRESBYACUSIS ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRESUMED OCULAR HISTOPLASMOSIS SYNDROME ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PRODUCT TAMPERING ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN BOUND IODINE INCREASED ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN TOTAL ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPERTENSIVE CRISIS ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULMONARY VENOUS THROMBOSIS ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYODERMA ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RADIAL PULSE DECREASED ( 1 FDA reports)
RADIATION INTERACTION ( 1 FDA reports)
RADIATION OESOPHAGITIS ( 1 FDA reports)
RADICULAR SYNDROME ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL ADENOMA ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RED BLOOD CELL ELLIPTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL CANCER STAGE IV ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL HYPOPLASIA ( 1 FDA reports)
RENAL OSTEODYSTROPHY ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL OPERATION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINOPEXY ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SCARLET FEVER ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEPTAL PANNICULITIS ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN TEST NEGATIVE ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLEEP STUDY ABNORMAL ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL INTESTINE OPERATION ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOCIAL FEAR ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SOLAR URTICARIA ( 1 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL VASCULAR DISORDER ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 1 FDA reports)
STENT MALAPPOSITION ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STRANGULATED HERNIA REPAIR ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUBDURAL EFFUSION ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TEMPERATURE PERCEPTION TEST ABNORMAL ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
TESTICULAR SEMINOMA (PURE) STAGE II ( 1 FDA reports)
TESTIS CANCER ( 1 FDA reports)
THERAPEUTIC AGENT URINE POSITIVE ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOSIS PROPHYLAXIS ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
THYROID GLAND SCAN ABNORMAL ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOBACCO POISONING ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE CYST ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRICUSPID VALVE REPAIR ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TUMOUR RUPTURE ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETHRAL STRICTURE POSTOPERATIVE ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINARY TRACT INFLAMMATION ( 1 FDA reports)
URINARY TRACT PAIN ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE PHOSPHATE INCREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENOUS STENT INSERTION ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VIRUS STOOL TEST POSITIVE ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVAL OEDEMA ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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