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

NAUSEA ( 1080 FDA reports)
DRUG INEFFECTIVE ( 746 FDA reports)
DIZZINESS ( 585 FDA reports)
FATIGUE ( 516 FDA reports)
VOMITING ( 499 FDA reports)
DYSPNOEA ( 476 FDA reports)
DRUG INTERACTION ( 474 FDA reports)
HEADACHE ( 447 FDA reports)
DIARRHOEA ( 438 FDA reports)
DEPRESSION ( 423 FDA reports)
PAIN ( 418 FDA reports)
MALAISE ( 417 FDA reports)
INSOMNIA ( 404 FDA reports)
MYALGIA ( 384 FDA reports)
ASTHENIA ( 368 FDA reports)
FEELING ABNORMAL ( 345 FDA reports)
ANXIETY ( 332 FDA reports)
OEDEMA PERIPHERAL ( 323 FDA reports)
CONSTIPATION ( 320 FDA reports)
PAIN IN EXTREMITY ( 317 FDA reports)
HYPOTENSION ( 313 FDA reports)
HYPERTENSION ( 306 FDA reports)
WEIGHT INCREASED ( 299 FDA reports)
CHEST PAIN ( 296 FDA reports)
FALL ( 295 FDA reports)
SOMNOLENCE ( 292 FDA reports)
WEIGHT DECREASED ( 286 FDA reports)
RENAL FAILURE ACUTE ( 281 FDA reports)
ABNORMAL DREAMS ( 276 FDA reports)
MYOCARDIAL INFARCTION ( 275 FDA reports)
ARTHRALGIA ( 253 FDA reports)
PYREXIA ( 249 FDA reports)
CONFUSIONAL STATE ( 243 FDA reports)
ABDOMINAL PAIN UPPER ( 239 FDA reports)
ANAEMIA ( 231 FDA reports)
PNEUMONIA ( 225 FDA reports)
PRURITUS ( 221 FDA reports)
DEHYDRATION ( 217 FDA reports)
DECREASED APPETITE ( 213 FDA reports)
ATRIAL FIBRILLATION ( 208 FDA reports)
CEREBROVASCULAR ACCIDENT ( 206 FDA reports)
TREMOR ( 205 FDA reports)
GAIT DISTURBANCE ( 200 FDA reports)
MUSCULAR WEAKNESS ( 196 FDA reports)
RASH ( 195 FDA reports)
SYNCOPE ( 193 FDA reports)
BACK PAIN ( 190 FDA reports)
MUSCLE SPASMS ( 189 FDA reports)
VISION BLURRED ( 187 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 176 FDA reports)
BLOOD PRESSURE INCREASED ( 172 FDA reports)
LOSS OF CONSCIOUSNESS ( 168 FDA reports)
BLOOD GLUCOSE INCREASED ( 165 FDA reports)
DEATH ( 161 FDA reports)
BLOOD CREATININE INCREASED ( 159 FDA reports)
ABDOMINAL DISCOMFORT ( 158 FDA reports)
URINARY TRACT INFECTION ( 157 FDA reports)
RENAL FAILURE ( 156 FDA reports)
PARAESTHESIA ( 155 FDA reports)
FLATULENCE ( 154 FDA reports)
DYSGEUSIA ( 150 FDA reports)
NERVOUSNESS ( 149 FDA reports)
HYPERHIDROSIS ( 148 FDA reports)
THROMBOCYTOPENIA ( 142 FDA reports)
CARDIAC FAILURE ( 141 FDA reports)
CONVULSION ( 141 FDA reports)
HYPERSENSITIVITY ( 140 FDA reports)
CONDITION AGGRAVATED ( 139 FDA reports)
HYPOAESTHESIA ( 138 FDA reports)
MEMORY IMPAIRMENT ( 136 FDA reports)
RHABDOMYOLYSIS ( 134 FDA reports)
ABDOMINAL PAIN ( 131 FDA reports)
BREAST CANCER FEMALE ( 126 FDA reports)
AGITATION ( 123 FDA reports)
HAEMOGLOBIN DECREASED ( 122 FDA reports)
PALPITATIONS ( 122 FDA reports)
COUGH ( 121 FDA reports)
CARDIAC ARREST ( 120 FDA reports)
DRY MOUTH ( 120 FDA reports)
SEPSIS ( 119 FDA reports)
AMNESIA ( 118 FDA reports)
SUICIDAL IDEATION ( 117 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 114 FDA reports)
DYSPEPSIA ( 114 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 113 FDA reports)
NIGHTMARE ( 113 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 111 FDA reports)
CHILLS ( 111 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 111 FDA reports)
RESPIRATORY FAILURE ( 111 FDA reports)
SLEEP DISORDER ( 111 FDA reports)
ERYTHEMA ( 108 FDA reports)
HYPOGLYCAEMIA ( 107 FDA reports)
HYPONATRAEMIA ( 107 FDA reports)
BALANCE DISORDER ( 104 FDA reports)
HEART RATE INCREASED ( 104 FDA reports)
BRADYCARDIA ( 103 FDA reports)
ABDOMINAL DISTENSION ( 102 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 100 FDA reports)
CARDIAC DISORDER ( 99 FDA reports)
DIABETES MELLITUS ( 99 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 98 FDA reports)
INFECTION ( 98 FDA reports)
AGGRESSION ( 97 FDA reports)
SUICIDE ATTEMPT ( 97 FDA reports)
IRRITABILITY ( 96 FDA reports)
URTICARIA ( 95 FDA reports)
CHEST DISCOMFORT ( 94 FDA reports)
OVERDOSE ( 94 FDA reports)
CONTUSION ( 93 FDA reports)
DRUG EFFECT DECREASED ( 93 FDA reports)
DYSPHAGIA ( 93 FDA reports)
BREAST CANCER ( 92 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 92 FDA reports)
LETHARGY ( 91 FDA reports)
ALOPECIA ( 90 FDA reports)
JOINT SWELLING ( 90 FDA reports)
STRESS ( 89 FDA reports)
SWELLING FACE ( 87 FDA reports)
VISUAL IMPAIRMENT ( 86 FDA reports)
PLEURAL EFFUSION ( 85 FDA reports)
ABNORMAL BEHAVIOUR ( 83 FDA reports)
HAEMORRHAGE ( 83 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 81 FDA reports)
BLOOD PRESSURE DECREASED ( 81 FDA reports)
NEUROPATHY PERIPHERAL ( 81 FDA reports)
PULMONARY OEDEMA ( 81 FDA reports)
CORONARY ARTERY DISEASE ( 80 FDA reports)
INCORRECT DOSE ADMINISTERED ( 80 FDA reports)
ANGINA PECTORIS ( 79 FDA reports)
HALLUCINATION ( 79 FDA reports)
POLLAKIURIA ( 79 FDA reports)
ARRHYTHMIA ( 78 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 78 FDA reports)
DISTURBANCE IN ATTENTION ( 78 FDA reports)
HYPERGLYCAEMIA ( 77 FDA reports)
EPISTAXIS ( 76 FDA reports)
HEART RATE DECREASED ( 76 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 75 FDA reports)
OEDEMA ( 75 FDA reports)
PLATELET COUNT DECREASED ( 75 FDA reports)
VENTRICULAR TACHYCARDIA ( 75 FDA reports)
HYPOKALAEMIA ( 74 FDA reports)
MUSCULOSKELETAL PAIN ( 74 FDA reports)
RENAL IMPAIRMENT ( 73 FDA reports)
BLOOD UREA INCREASED ( 72 FDA reports)
DRUG HYPERSENSITIVITY ( 71 FDA reports)
MULTI-ORGAN FAILURE ( 71 FDA reports)
HYPERKALAEMIA ( 70 FDA reports)
PULMONARY EMBOLISM ( 69 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 68 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 67 FDA reports)
PANIC ATTACK ( 67 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 67 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 66 FDA reports)
DEPRESSED MOOD ( 66 FDA reports)
DISORIENTATION ( 66 FDA reports)
FLUSHING ( 66 FDA reports)
STEVENS-JOHNSON SYNDROME ( 65 FDA reports)
ANGER ( 63 FDA reports)
BURNING SENSATION ( 63 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 63 FDA reports)
THROMBOSIS ( 63 FDA reports)
LEUKOPENIA ( 62 FDA reports)
BRONCHITIS ( 60 FDA reports)
HYPERTENSIVE EMERGENCY ( 60 FDA reports)
INTENTIONAL OVERDOSE ( 59 FDA reports)
NEUTROPENIA ( 59 FDA reports)
RESTLESSNESS ( 59 FDA reports)
SPEECH DISORDER ( 59 FDA reports)
DRUG INTOLERANCE ( 58 FDA reports)
HAEMATURIA ( 57 FDA reports)
HYPERSOMNIA ( 57 FDA reports)
ABASIA ( 56 FDA reports)
ARTHRITIS ( 56 FDA reports)
HEPATIC ENZYME INCREASED ( 56 FDA reports)
NASOPHARYNGITIS ( 56 FDA reports)
TACHYCARDIA ( 56 FDA reports)
ASTHMA ( 55 FDA reports)
BONE PAIN ( 55 FDA reports)
COMA ( 55 FDA reports)
RENAL FAILURE CHRONIC ( 55 FDA reports)
ERECTILE DYSFUNCTION ( 54 FDA reports)
MENTAL STATUS CHANGES ( 54 FDA reports)
SWOLLEN TONGUE ( 54 FDA reports)
TINNITUS ( 54 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 53 FDA reports)
CRYING ( 52 FDA reports)
EYE PAIN ( 52 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 51 FDA reports)
HOT FLUSH ( 51 FDA reports)
IMPAIRED HEALING ( 51 FDA reports)
JAUNDICE ( 51 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 51 FDA reports)
VERTIGO ( 51 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 50 FDA reports)
BLISTER ( 49 FDA reports)
BLOOD POTASSIUM DECREASED ( 49 FDA reports)
DISEASE PROGRESSION ( 49 FDA reports)
DYSKINESIA ( 49 FDA reports)
SWELLING ( 49 FDA reports)
TOBACCO USER ( 49 FDA reports)
ANGIOEDEMA ( 48 FDA reports)
BODY HEIGHT DECREASED ( 48 FDA reports)
CORONARY ARTERY OCCLUSION ( 48 FDA reports)
MENTAL IMPAIRMENT ( 48 FDA reports)
MIDDLE INSOMNIA ( 48 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 48 FDA reports)
LIP SWELLING ( 47 FDA reports)
RENAL DISORDER ( 47 FDA reports)
CARDIOGENIC SHOCK ( 46 FDA reports)
CIRCULATORY COLLAPSE ( 46 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 46 FDA reports)
HYPOTHYROIDISM ( 46 FDA reports)
MENTAL DISORDER ( 46 FDA reports)
METABOLIC ACIDOSIS ( 46 FDA reports)
MOBILITY DECREASED ( 46 FDA reports)
MUSCLE ATROPHY ( 46 FDA reports)
MUSCLE TWITCHING ( 46 FDA reports)
OROPHARYNGEAL PAIN ( 46 FDA reports)
ANOREXIA ( 45 FDA reports)
APHASIA ( 45 FDA reports)
DRUG DOSE OMISSION ( 45 FDA reports)
EMOTIONAL DISORDER ( 45 FDA reports)
RECTAL HAEMORRHAGE ( 45 FDA reports)
STENT PLACEMENT ( 45 FDA reports)
URINARY INCONTINENCE ( 45 FDA reports)
VISUAL ACUITY REDUCED ( 45 FDA reports)
WITHDRAWAL SYNDROME ( 45 FDA reports)
ARTHROPATHY ( 44 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 44 FDA reports)
CEREBRAL HAEMORRHAGE ( 44 FDA reports)
DYSURIA ( 44 FDA reports)
BLOOD BILIRUBIN INCREASED ( 43 FDA reports)
COMPLETED SUICIDE ( 43 FDA reports)
FEELING HOT ( 43 FDA reports)
FIBROMYALGIA ( 43 FDA reports)
NEURALGIA ( 43 FDA reports)
PANCREATITIS ( 43 FDA reports)
SINUS BRADYCARDIA ( 43 FDA reports)
CATARACT ( 42 FDA reports)
DRUG TOXICITY ( 42 FDA reports)
DYSARTHRIA ( 42 FDA reports)
HAEMOPTYSIS ( 42 FDA reports)
INFLUENZA LIKE ILLNESS ( 42 FDA reports)
LACTIC ACIDOSIS ( 42 FDA reports)
OCULAR HYPERAEMIA ( 42 FDA reports)
PANCYTOPENIA ( 42 FDA reports)
URINARY RETENTION ( 42 FDA reports)
NECK PAIN ( 41 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 41 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 41 FDA reports)
GASTRIC DISORDER ( 40 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 40 FDA reports)
IMPAIRED WORK ABILITY ( 40 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 39 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 39 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 39 FDA reports)
MYOCARDIAL ISCHAEMIA ( 39 FDA reports)
PERIPHERAL COLDNESS ( 39 FDA reports)
CARDIAC MURMUR ( 38 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 38 FDA reports)
LIVER DISORDER ( 38 FDA reports)
MOOD SWINGS ( 38 FDA reports)
OSTEOARTHRITIS ( 38 FDA reports)
SINUSITIS ( 38 FDA reports)
SKIN EXFOLIATION ( 38 FDA reports)
THINKING ABNORMAL ( 38 FDA reports)
WHEEZING ( 38 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 37 FDA reports)
EYE DISORDER ( 37 FDA reports)
HAEMATEMESIS ( 37 FDA reports)
UNEVALUABLE EVENT ( 37 FDA reports)
BLINDNESS ( 36 FDA reports)
FLUID RETENTION ( 36 FDA reports)
GASTRITIS ( 36 FDA reports)
INCREASED APPETITE ( 36 FDA reports)
PARANOIA ( 36 FDA reports)
RESTLESS LEGS SYNDROME ( 36 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 35 FDA reports)
DRY SKIN ( 35 FDA reports)
GASTROINTESTINAL DISORDER ( 35 FDA reports)
MITRAL VALVE INCOMPETENCE ( 35 FDA reports)
MYOSITIS ( 35 FDA reports)
RASH PRURITIC ( 35 FDA reports)
BLOOD SODIUM DECREASED ( 34 FDA reports)
CHROMATURIA ( 34 FDA reports)
HEART RATE IRREGULAR ( 34 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 34 FDA reports)
INFLUENZA ( 34 FDA reports)
MEDICATION ERROR ( 34 FDA reports)
SEPTIC SHOCK ( 34 FDA reports)
VENTRICULAR FIBRILLATION ( 34 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 33 FDA reports)
BLOOD POTASSIUM INCREASED ( 33 FDA reports)
CORONARY ARTERY BYPASS ( 33 FDA reports)
DRY EYE ( 33 FDA reports)
EYE SWELLING ( 33 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 33 FDA reports)
HEMIPARESIS ( 33 FDA reports)
MOOD ALTERED ( 33 FDA reports)
MUSCLE DISORDER ( 33 FDA reports)
MYOPATHY ( 33 FDA reports)
RASH GENERALISED ( 33 FDA reports)
SKIN DISORDER ( 33 FDA reports)
ACCIDENTAL EXPOSURE ( 32 FDA reports)
BLOOD GLUCOSE DECREASED ( 32 FDA reports)
CYANOSIS ( 32 FDA reports)
DELIRIUM ( 32 FDA reports)
DYSPNOEA EXERTIONAL ( 32 FDA reports)
FEELING COLD ( 32 FDA reports)
BLOOD URINE PRESENT ( 31 FDA reports)
FEAR ( 31 FDA reports)
GASTRIC ULCER ( 31 FDA reports)
HALLUCINATION, VISUAL ( 31 FDA reports)
HYPOPHAGIA ( 31 FDA reports)
LIMB DISCOMFORT ( 31 FDA reports)
ORAL PAIN ( 31 FDA reports)
PAIN IN JAW ( 31 FDA reports)
ROAD TRAFFIC ACCIDENT ( 31 FDA reports)
SKIN DISCOLOURATION ( 31 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 31 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 31 FDA reports)
CARDIO-RESPIRATORY ARREST ( 30 FDA reports)
COGNITIVE DISORDER ( 30 FDA reports)
DEAFNESS ( 30 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 30 FDA reports)
GASTROENTERITIS ( 30 FDA reports)
HAEMODIALYSIS ( 30 FDA reports)
NASAL CONGESTION ( 30 FDA reports)
PRODUCT QUALITY ISSUE ( 30 FDA reports)
RASH ERYTHEMATOUS ( 30 FDA reports)
STOMATITIS ( 30 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 29 FDA reports)
DEEP VEIN THROMBOSIS ( 29 FDA reports)
EYE IRRITATION ( 29 FDA reports)
FEELING DRUNK ( 29 FDA reports)
HAEMATOCHEZIA ( 29 FDA reports)
HOMICIDAL IDEATION ( 29 FDA reports)
HYPOKINESIA ( 29 FDA reports)
IMPAIRED DRIVING ABILITY ( 29 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 29 FDA reports)
LUNG DISORDER ( 29 FDA reports)
MIGRAINE ( 29 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 29 FDA reports)
OSTEONECROSIS OF JAW ( 29 FDA reports)
PRESYNCOPE ( 29 FDA reports)
RETCHING ( 29 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 28 FDA reports)
EXTRASYSTOLES ( 28 FDA reports)
HEPATIC FAILURE ( 28 FDA reports)
HYPOVOLAEMIA ( 28 FDA reports)
ISCHAEMIC STROKE ( 28 FDA reports)
RESPIRATORY ARREST ( 28 FDA reports)
STAPHYLOCOCCAL INFECTION ( 28 FDA reports)
BACK INJURY ( 27 FDA reports)
FEELING JITTERY ( 27 FDA reports)
GOUT ( 27 FDA reports)
HEAD INJURY ( 27 FDA reports)
INTERSTITIAL LUNG DISEASE ( 27 FDA reports)
PHARYNGEAL OEDEMA ( 27 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 27 FDA reports)
SKIN ULCER ( 27 FDA reports)
TRANSAMINASES INCREASED ( 27 FDA reports)
UNRESPONSIVE TO STIMULI ( 27 FDA reports)
ASCITES ( 26 FDA reports)
BONE DISORDER ( 26 FDA reports)
DYSSTASIA ( 26 FDA reports)
FRUSTRATION ( 26 FDA reports)
GINGIVAL PAIN ( 26 FDA reports)
HAEMATOCRIT DECREASED ( 26 FDA reports)
INTENTIONAL DRUG MISUSE ( 26 FDA reports)
NEPHROLITHIASIS ( 26 FDA reports)
OFF LABEL USE ( 26 FDA reports)
PRODUCTIVE COUGH ( 26 FDA reports)
RHEUMATOID ARTHRITIS ( 26 FDA reports)
BLADDER DISORDER ( 25 FDA reports)
BLOOD MAGNESIUM DECREASED ( 25 FDA reports)
CELLULITIS ( 25 FDA reports)
CEREBRAL INFARCTION ( 25 FDA reports)
CHOLESTASIS ( 25 FDA reports)
DIPLOPIA ( 25 FDA reports)
GRAND MAL CONVULSION ( 25 FDA reports)
HEPATITIS ( 25 FDA reports)
HYPOCALCAEMIA ( 25 FDA reports)
HYPOXIA ( 25 FDA reports)
INFLAMMATION ( 25 FDA reports)
LEUKOCYTOSIS ( 25 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 25 FDA reports)
LUNG NEOPLASM MALIGNANT ( 25 FDA reports)
SURGERY ( 25 FDA reports)
TOOTH EXTRACTION ( 25 FDA reports)
TREATMENT NONCOMPLIANCE ( 25 FDA reports)
AORTIC STENOSIS ( 24 FDA reports)
BRONCHOPNEUMONIA ( 24 FDA reports)
COLD SWEAT ( 24 FDA reports)
CORONARY ARTERY STENOSIS ( 24 FDA reports)
DYSPHONIA ( 24 FDA reports)
EPILEPSY ( 24 FDA reports)
GASTRITIS EROSIVE ( 24 FDA reports)
LEFT VENTRICULAR FAILURE ( 24 FDA reports)
OEDEMA MOUTH ( 24 FDA reports)
OSTEOPOROSIS ( 24 FDA reports)
POST PROCEDURAL COMPLICATION ( 24 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 24 FDA reports)
RASH MACULAR ( 24 FDA reports)
ANGINA UNSTABLE ( 23 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 23 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 23 FDA reports)
CARDIOMEGALY ( 23 FDA reports)
CHOLELITHIASIS ( 23 FDA reports)
FACE OEDEMA ( 23 FDA reports)
GLOSSODYNIA ( 23 FDA reports)
MULTIPLE MYELOMA ( 23 FDA reports)
OBESITY ( 23 FDA reports)
ORAL DISCOMFORT ( 23 FDA reports)
PROSTATE CANCER ( 23 FDA reports)
RESPIRATORY DISORDER ( 23 FDA reports)
VASCULAR GRAFT ( 23 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 23 FDA reports)
ACUTE CORONARY SYNDROME ( 22 FDA reports)
ACUTE HEPATIC FAILURE ( 22 FDA reports)
AORTIC ANEURYSM ( 22 FDA reports)
APATHY ( 22 FDA reports)
ARTERIOSCLEROSIS ( 22 FDA reports)
ATRIAL FLUTTER ( 22 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 22 FDA reports)
DISCOMFORT ( 22 FDA reports)
DRUG ADMINISTRATION ERROR ( 22 FDA reports)
HYPERLIPIDAEMIA ( 22 FDA reports)
INJECTION SITE ERYTHEMA ( 22 FDA reports)
PERICARDIAL EFFUSION ( 22 FDA reports)
PSYCHOTIC DISORDER ( 22 FDA reports)
PULMONARY HYPERTENSION ( 22 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 22 FDA reports)
SINUS DISORDER ( 22 FDA reports)
SLEEP APNOEA SYNDROME ( 22 FDA reports)
ATRIOVENTRICULAR BLOCK ( 21 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 21 FDA reports)
BICYTOPENIA ( 21 FDA reports)
BLOOD CALCIUM DECREASED ( 21 FDA reports)
COORDINATION ABNORMAL ( 21 FDA reports)
EYE PRURITUS ( 21 FDA reports)
HYPOTONIA ( 21 FDA reports)
MOUTH ULCERATION ( 21 FDA reports)
MOVEMENT DISORDER ( 21 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 21 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 21 FDA reports)
PERITONITIS ( 21 FDA reports)
SEROTONIN SYNDROME ( 21 FDA reports)
SINUS TACHYCARDIA ( 21 FDA reports)
SUDDEN DEATH ( 21 FDA reports)
THROMBOSIS IN DEVICE ( 21 FDA reports)
THYROID DISORDER ( 21 FDA reports)
TYPE 2 DIABETES MELLITUS ( 21 FDA reports)
ANGIOPLASTY ( 20 FDA reports)
BACK DISORDER ( 20 FDA reports)
CARDIOVASCULAR DISORDER ( 20 FDA reports)
CARPAL TUNNEL SYNDROME ( 20 FDA reports)
HAEMATOMA ( 20 FDA reports)
HIATUS HERNIA ( 20 FDA reports)
JAUNDICE CHOLESTATIC ( 20 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 20 FDA reports)
LYMPHADENOPATHY ( 20 FDA reports)
METASTASES TO BONE ( 20 FDA reports)
NERVOUS SYSTEM DISORDER ( 20 FDA reports)
OXYGEN SATURATION DECREASED ( 20 FDA reports)
PARALYSIS ( 20 FDA reports)
RASH MACULO-PAPULAR ( 20 FDA reports)
RESPIRATORY TRACT INFECTION ( 20 FDA reports)
VIRAL INFECTION ( 20 FDA reports)
ANGIOPATHY ( 19 FDA reports)
CARDIAC OPERATION ( 19 FDA reports)
CARDIAC TAMPONADE ( 19 FDA reports)
COLITIS ( 19 FDA reports)
DRUG LEVEL INCREASED ( 19 FDA reports)
FAECES DISCOLOURED ( 19 FDA reports)
HEPATOTOXICITY ( 19 FDA reports)
HERPES ZOSTER ( 19 FDA reports)
HYPOAESTHESIA ORAL ( 19 FDA reports)
ILL-DEFINED DISORDER ( 19 FDA reports)
INJECTION SITE PAIN ( 19 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 19 FDA reports)
JOINT INJURY ( 19 FDA reports)
MELAENA ( 19 FDA reports)
OSTEOMYELITIS ( 19 FDA reports)
PHOTOSENSITIVITY REACTION ( 19 FDA reports)
RESPIRATORY DISTRESS ( 19 FDA reports)
SEDATION ( 19 FDA reports)
SENSORY LOSS ( 19 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 19 FDA reports)
URINE OUTPUT DECREASED ( 19 FDA reports)
ACCIDENT ( 18 FDA reports)
AGEUSIA ( 18 FDA reports)
BONE DENSITY DECREASED ( 18 FDA reports)
BRONCHOSPASM ( 18 FDA reports)
CARDIAC VALVE DISEASE ( 18 FDA reports)
COAGULOPATHY ( 18 FDA reports)
DIVERTICULITIS ( 18 FDA reports)
FEBRILE NEUTROPENIA ( 18 FDA reports)
FLUID OVERLOAD ( 18 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 18 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 18 FDA reports)
NOCTURIA ( 18 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 18 FDA reports)
PROTEINURIA ( 18 FDA reports)
SHOCK HAEMORRHAGIC ( 18 FDA reports)
SKIN LESION ( 18 FDA reports)
THROAT TIGHTNESS ( 18 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 18 FDA reports)
URINE COLOUR ABNORMAL ( 18 FDA reports)
CARDIOMYOPATHY ( 17 FDA reports)
CEREBRAL ATROPHY ( 17 FDA reports)
CHOKING ( 17 FDA reports)
CHOLANGITIS ( 17 FDA reports)
DRUG DEPENDENCE ( 17 FDA reports)
EATING DISORDER ( 17 FDA reports)
ELECTROLYTE IMBALANCE ( 17 FDA reports)
EMOTIONAL DISTRESS ( 17 FDA reports)
EXPIRED DRUG ADMINISTERED ( 17 FDA reports)
HEARING IMPAIRED ( 17 FDA reports)
HIP ARTHROPLASTY ( 17 FDA reports)
HYPERTENSIVE CRISIS ( 17 FDA reports)
INJURY ( 17 FDA reports)
JOINT STIFFNESS ( 17 FDA reports)
MUSCLE RIGIDITY ( 17 FDA reports)
PALLOR ( 17 FDA reports)
PERIPHERAL ISCHAEMIA ( 17 FDA reports)
POLYURIA ( 17 FDA reports)
SELF-INJURIOUS IDEATION ( 17 FDA reports)
SHOCK ( 17 FDA reports)
TENDON RUPTURE ( 17 FDA reports)
WOUND INFECTION ( 17 FDA reports)
ACCIDENTAL OVERDOSE ( 16 FDA reports)
ATAXIA ( 16 FDA reports)
ATELECTASIS ( 16 FDA reports)
BASAL CELL CARCINOMA ( 16 FDA reports)
BIPOLAR DISORDER ( 16 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 16 FDA reports)
CANDIDIASIS ( 16 FDA reports)
CLOSTRIDIAL INFECTION ( 16 FDA reports)
COLITIS ISCHAEMIC ( 16 FDA reports)
DIALYSIS ( 16 FDA reports)
EMBOLISM ( 16 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 16 FDA reports)
HALLUCINATION, AUDITORY ( 16 FDA reports)
HEPATITIS ACUTE ( 16 FDA reports)
HEPATOMEGALY ( 16 FDA reports)
HIP FRACTURE ( 16 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 16 FDA reports)
INJECTION SITE HAEMORRHAGE ( 16 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 16 FDA reports)
LUNG NEOPLASM ( 16 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 16 FDA reports)
MIOSIS ( 16 FDA reports)
MYASTHENIA GRAVIS ( 16 FDA reports)
NERVE INJURY ( 16 FDA reports)
NO ADVERSE EVENT ( 16 FDA reports)
OSTEONECROSIS ( 16 FDA reports)
PANCREATITIS ACUTE ( 16 FDA reports)
PHOTOPHOBIA ( 16 FDA reports)
POOR QUALITY SLEEP ( 16 FDA reports)
RENAL TUBULAR NECROSIS ( 16 FDA reports)
RIB FRACTURE ( 16 FDA reports)
VAGINAL HAEMORRHAGE ( 16 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 15 FDA reports)
APHAGIA ( 15 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 15 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 15 FDA reports)
CHOLECYSTITIS ( 15 FDA reports)
CORONARY ARTERY THROMBOSIS ( 15 FDA reports)
CYSTITIS ( 15 FDA reports)
ECZEMA ( 15 FDA reports)
EMPHYSEMA ( 15 FDA reports)
EXOSTOSIS ( 15 FDA reports)
GINGIVAL BLEEDING ( 15 FDA reports)
GLAUCOMA ( 15 FDA reports)
HEAD DISCOMFORT ( 15 FDA reports)
HEART DISEASE CONGENITAL ( 15 FDA reports)
HEMIPLEGIA ( 15 FDA reports)
HEPATOCELLULAR INJURY ( 15 FDA reports)
HYPOACUSIS ( 15 FDA reports)
HYPOCHONDRIASIS ( 15 FDA reports)
HYPOMAGNESAEMIA ( 15 FDA reports)
KNEE ARTHROPLASTY ( 15 FDA reports)
LIVER TRANSPLANT REJECTION ( 15 FDA reports)
MULTIPLE DRUG OVERDOSE ( 15 FDA reports)
MYOCLONUS ( 15 FDA reports)
NEPHROPATHY TOXIC ( 15 FDA reports)
NIGHT SWEATS ( 15 FDA reports)
OESOPHAGITIS ( 15 FDA reports)
ORTHOSTATIC HYPOTENSION ( 15 FDA reports)
PARAESTHESIA ORAL ( 15 FDA reports)
PARKINSON'S DISEASE ( 15 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 15 FDA reports)
PNEUMONITIS ( 15 FDA reports)
SKIN BURNING SENSATION ( 15 FDA reports)
SKIN IRRITATION ( 15 FDA reports)
TOOTH DISORDER ( 15 FDA reports)
WRONG DRUG ADMINISTERED ( 15 FDA reports)
ANAPHYLACTIC REACTION ( 14 FDA reports)
BACTERIAL INFECTION ( 14 FDA reports)
BLOOD CREATINE INCREASED ( 14 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 14 FDA reports)
BODY TEMPERATURE DECREASED ( 14 FDA reports)
BREAST CANCER METASTATIC ( 14 FDA reports)
CONJUNCTIVITIS ( 14 FDA reports)
DELUSION ( 14 FDA reports)
DENTAL CARIES ( 14 FDA reports)
DIFFICULTY IN WALKING ( 14 FDA reports)
EJECTION FRACTION DECREASED ( 14 FDA reports)
EXCORIATION ( 14 FDA reports)
EXOMPHALOS ( 14 FDA reports)
EYE HAEMORRHAGE ( 14 FDA reports)
EYELID OEDEMA ( 14 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 14 FDA reports)
HYPERCALCAEMIA ( 14 FDA reports)
INFARCTION ( 14 FDA reports)
INTESTINAL ISCHAEMIA ( 14 FDA reports)
ISCHAEMIA ( 14 FDA reports)
LACRIMATION INCREASED ( 14 FDA reports)
LUNG INFECTION ( 14 FDA reports)
LUNG INFILTRATION ( 14 FDA reports)
MEDICATION RESIDUE ( 14 FDA reports)
NEOPLASM MALIGNANT ( 14 FDA reports)
PRODUCT ODOUR ABNORMAL ( 14 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 14 FDA reports)
PSORIASIS ( 14 FDA reports)
PULMONARY FIBROSIS ( 14 FDA reports)
PURULENT DISCHARGE ( 14 FDA reports)
RENAL PAIN ( 14 FDA reports)
RHINORRHOEA ( 14 FDA reports)
TENDERNESS ( 14 FDA reports)
THROAT IRRITATION ( 14 FDA reports)
TROPONIN INCREASED ( 14 FDA reports)
BLOOD PRESSURE ABNORMAL ( 13 FDA reports)
BURSITIS ( 13 FDA reports)
CARDIAC PACEMAKER INSERTION ( 13 FDA reports)
CATARACT OPERATION ( 13 FDA reports)
CATHETERISATION CARDIAC ( 13 FDA reports)
DEMENTIA ( 13 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 13 FDA reports)
EYE MOVEMENT DISORDER ( 13 FDA reports)
FEELING GUILTY ( 13 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 13 FDA reports)
GALLBLADDER DISORDER ( 13 FDA reports)
GANGRENE ( 13 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 13 FDA reports)
HAEMORRHOIDS ( 13 FDA reports)
HEPATIC STEATOSIS ( 13 FDA reports)
INTESTINAL OBSTRUCTION ( 13 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 13 FDA reports)
LIPASE INCREASED ( 13 FDA reports)
LIVER INJURY ( 13 FDA reports)
MACULAR DEGENERATION ( 13 FDA reports)
MALNUTRITION ( 13 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 13 FDA reports)
NON-SMALL CELL LUNG CANCER ( 13 FDA reports)
OLIGURIA ( 13 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 13 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 13 FDA reports)
PROTHROMBIN TIME PROLONGED ( 13 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 13 FDA reports)
RENAL CYST ( 13 FDA reports)
SCIATICA ( 13 FDA reports)
SENSATION OF HEAVINESS ( 13 FDA reports)
SPINAL FRACTURE ( 13 FDA reports)
SUBDURAL HAEMATOMA ( 13 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 13 FDA reports)
TOOTHACHE ( 13 FDA reports)
ACNE ( 12 FDA reports)
ANEURYSM ( 12 FDA reports)
BEDRIDDEN ( 12 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 12 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 12 FDA reports)
CEREBRAL ISCHAEMIA ( 12 FDA reports)
CEREBROVASCULAR DISORDER ( 12 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 12 FDA reports)
DERMATITIS ALLERGIC ( 12 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 12 FDA reports)
EAR PAIN ( 12 FDA reports)
ECCHYMOSIS ( 12 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 12 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 12 FDA reports)
FUNGAL INFECTION ( 12 FDA reports)
GRANULOCYTOPENIA ( 12 FDA reports)
HEPATIC CIRRHOSIS ( 12 FDA reports)
HUNGER ( 12 FDA reports)
HYPERPHAGIA ( 12 FDA reports)
IRRITABLE BOWEL SYNDROME ( 12 FDA reports)
KIDNEY INFECTION ( 12 FDA reports)
LACERATION ( 12 FDA reports)
LEUKOCYTURIA ( 12 FDA reports)
MAJOR DEPRESSION ( 12 FDA reports)
MANIA ( 12 FDA reports)
MUSCLE TIGHTNESS ( 12 FDA reports)
MYDRIASIS ( 12 FDA reports)
PAROSMIA ( 12 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 12 FDA reports)
PROCEDURAL COMPLICATION ( 12 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 12 FDA reports)
PRURITUS GENERALISED ( 12 FDA reports)
RESPIRATORY RATE INCREASED ( 12 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 12 FDA reports)
TACHYPNOEA ( 12 FDA reports)
VAGINAL DISCHARGE ( 12 FDA reports)
VASCULITIC RASH ( 12 FDA reports)
ANURIA ( 11 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 11 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 11 FDA reports)
ASTHENOPIA ( 11 FDA reports)
BLADDER CANCER ( 11 FDA reports)
BLOOD IRON DECREASED ( 11 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 11 FDA reports)
BRADYPHRENIA ( 11 FDA reports)
COELIAC DISEASE ( 11 FDA reports)
COLON CANCER ( 11 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 11 FDA reports)
DERMATITIS EXFOLIATIVE ( 11 FDA reports)
DRUG ERUPTION ( 11 FDA reports)
DRUG LEVEL DECREASED ( 11 FDA reports)
ENCEPHALOPATHY ( 11 FDA reports)
ENTEROCOCCAL INFECTION ( 11 FDA reports)
EOSINOPHIL COUNT INCREASED ( 11 FDA reports)
ESCHERICHIA INFECTION ( 11 FDA reports)
EXANTHEM ( 11 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 11 FDA reports)
GROIN PAIN ( 11 FDA reports)
GROWTH RETARDATION ( 11 FDA reports)
HEPATIC VEIN THROMBOSIS ( 11 FDA reports)
HYPOALBUMINAEMIA ( 11 FDA reports)
INJECTION SITE PRURITUS ( 11 FDA reports)
INJECTION SITE REACTION ( 11 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 11 FDA reports)
INTESTINAL DILATATION ( 11 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 11 FDA reports)
LABILE BLOOD PRESSURE ( 11 FDA reports)
LABORATORY TEST ABNORMAL ( 11 FDA reports)
LOWER LIMB FRACTURE ( 11 FDA reports)
LYMPHOMA ( 11 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 11 FDA reports)
METASTASES TO LYMPH NODES ( 11 FDA reports)
MICTURITION URGENCY ( 11 FDA reports)
MUSCLE INJURY ( 11 FDA reports)
NEUROMYOPATHY ( 11 FDA reports)
NEUTROPHIL COUNT DECREASED ( 11 FDA reports)
PANCREATIC NEOPLASM ( 11 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 11 FDA reports)
PERIODONTAL DISEASE ( 11 FDA reports)
PETECHIAE ( 11 FDA reports)
PNEUMONIA ASPIRATION ( 11 FDA reports)
PREMATURE BABY ( 11 FDA reports)
PURPURA ( 11 FDA reports)
RETROPERITONEAL HAEMATOMA ( 11 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 11 FDA reports)
SALIVARY HYPERSECRETION ( 11 FDA reports)
SENSORY DISTURBANCE ( 11 FDA reports)
SICK SINUS SYNDROME ( 11 FDA reports)
SPINAL OSTEOARTHRITIS ( 11 FDA reports)
TOOTH INFECTION ( 11 FDA reports)
WEIGHT FLUCTUATION ( 11 FDA reports)
YELLOW SKIN ( 11 FDA reports)
ABSCESS JAW ( 10 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 10 FDA reports)
ACUTE RESPIRATORY FAILURE ( 10 FDA reports)
ANAPHYLACTIC SHOCK ( 10 FDA reports)
ANKLE FRACTURE ( 10 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 10 FDA reports)
APPENDICITIS ( 10 FDA reports)
BLADDER CATHETERISATION ( 10 FDA reports)
BLOOD CALCIUM INCREASED ( 10 FDA reports)
BODY TEMPERATURE INCREASED ( 10 FDA reports)
BRAIN INJURY ( 10 FDA reports)
BRAIN OEDEMA ( 10 FDA reports)
DRUG DISPENSING ERROR ( 10 FDA reports)
EJACULATION DISORDER ( 10 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 10 FDA reports)
ENTERITIS ( 10 FDA reports)
ENURESIS ( 10 FDA reports)
ERUCTATION ( 10 FDA reports)
ESSENTIAL HYPERTENSION ( 10 FDA reports)
FAECALOMA ( 10 FDA reports)
FORMICATION ( 10 FDA reports)
GENERALISED OEDEMA ( 10 FDA reports)
HAEMORRHAGIC STROKE ( 10 FDA reports)
HEPATIC ENZYME ABNORMAL ( 10 FDA reports)
HERNIA ( 10 FDA reports)
HYPOTHERMIA ( 10 FDA reports)
INCONTINENCE ( 10 FDA reports)
INITIAL INSOMNIA ( 10 FDA reports)
INJECTION SITE NODULE ( 10 FDA reports)
JAW OPERATION ( 10 FDA reports)
KNEE OPERATION ( 10 FDA reports)
LIMB INJURY ( 10 FDA reports)
LOOSE TOOTH ( 10 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 10 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 10 FDA reports)
OSTEOPENIA ( 10 FDA reports)
OSTEOSYNTHESIS ( 10 FDA reports)
PELVIC PAIN ( 10 FDA reports)
PERFORMANCE STATUS DECREASED ( 10 FDA reports)
PERSONALITY CHANGE ( 10 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 10 FDA reports)
PHOTOPSIA ( 10 FDA reports)
PLATELET COUNT INCREASED ( 10 FDA reports)
POLYNEUROPATHY ( 10 FDA reports)
PRIMARY SEQUESTRUM ( 10 FDA reports)
PULSE ABSENT ( 10 FDA reports)
PYURIA ( 10 FDA reports)
RASH PAPULAR ( 10 FDA reports)
RETINAL HAEMORRHAGE ( 10 FDA reports)
SKIN HYPERPIGMENTATION ( 10 FDA reports)
STOMACH DISCOMFORT ( 10 FDA reports)
TACHYARRHYTHMIA ( 10 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 10 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 10 FDA reports)
THIRST ( 10 FDA reports)
TOBACCO ABUSE ( 10 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 10 FDA reports)
VASCULITIS ( 10 FDA reports)
VENOUS INSUFFICIENCY ( 10 FDA reports)
VITAMIN D DECREASED ( 10 FDA reports)
ABDOMINAL TENDERNESS ( 9 FDA reports)
ABORTION SPONTANEOUS ( 9 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 9 FDA reports)
ADVERSE DRUG REACTION ( 9 FDA reports)
AGRANULOCYTOSIS ( 9 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 9 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 9 FDA reports)
AREFLEXIA ( 9 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 9 FDA reports)
BLOOD ALBUMIN DECREASED ( 9 FDA reports)
BLOOD CHLORIDE DECREASED ( 9 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 9 FDA reports)
BRADYARRHYTHMIA ( 9 FDA reports)
BREAST CANCER IN SITU ( 9 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 9 FDA reports)
CAROTID ARTERY STENOSIS ( 9 FDA reports)
CHEILITIS ( 9 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 9 FDA reports)
CYANOPSIA ( 9 FDA reports)
DEMYELINATION ( 9 FDA reports)
DEVICE OCCLUSION ( 9 FDA reports)
DIABETIC NEUROPATHY ( 9 FDA reports)
DRUG RESISTANCE ( 9 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 9 FDA reports)
DUODENAL ULCER ( 9 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 9 FDA reports)
EUPHORIC MOOD ( 9 FDA reports)
EXERCISE LACK OF ( 9 FDA reports)
FAECAL INCONTINENCE ( 9 FDA reports)
FEAR OF EATING ( 9 FDA reports)
FIBRIN D DIMER INCREASED ( 9 FDA reports)
FOOT OPERATION ( 9 FDA reports)
GASTRIC HAEMORRHAGE ( 9 FDA reports)
GASTROINTESTINAL PAIN ( 9 FDA reports)
GINGIVAL DISORDER ( 9 FDA reports)
HAEMODYNAMIC INSTABILITY ( 9 FDA reports)
HEPATIC ENCEPHALOPATHY ( 9 FDA reports)
HOSPITALISATION ( 9 FDA reports)
HYPERBILIRUBINAEMIA ( 9 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 9 FDA reports)
ILEUS PARALYTIC ( 9 FDA reports)
INFUSION RELATED REACTION ( 9 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 9 FDA reports)
LIPIDS ABNORMAL ( 9 FDA reports)
MALLORY-WEISS SYNDROME ( 9 FDA reports)
MEDICAL DEVICE COMPLICATION ( 9 FDA reports)
MULTI-ORGAN DISORDER ( 9 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 9 FDA reports)
NYSTAGMUS ( 9 FDA reports)
ORAL CANDIDIASIS ( 9 FDA reports)
ORAL DISORDER ( 9 FDA reports)
OROPHARYNGEAL PLAQUE ( 9 FDA reports)
PEPTIC ULCER ( 9 FDA reports)
PERIODONTITIS ( 9 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 9 FDA reports)
POOR PERSONAL HYGIENE ( 9 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 9 FDA reports)
PRODUCT TASTE ABNORMAL ( 9 FDA reports)
PROSTATE CANCER METASTATIC ( 9 FDA reports)
PROSTATIC DISORDER ( 9 FDA reports)
RADIOTHERAPY ( 9 FDA reports)
RESPIRATORY TRACT CONGESTION ( 9 FDA reports)
SCAR ( 9 FDA reports)
SEXUAL DYSFUNCTION ( 9 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 9 FDA reports)
SNEEZING ( 9 FDA reports)
SPINAL COMPRESSION FRACTURE ( 9 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 9 FDA reports)
STREPTOCOCCAL INFECTION ( 9 FDA reports)
TENSION ( 9 FDA reports)
THROMBOPHLEBITIS ( 9 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 9 FDA reports)
TOOTH ABSCESS ( 9 FDA reports)
TRAUMATIC BRAIN INJURY ( 9 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
VIITH NERVE PARALYSIS ( 9 FDA reports)
ABNORMAL FAECES ( 8 FDA reports)
ABORTION INDUCED ( 8 FDA reports)
ACIDOSIS ( 8 FDA reports)
ADVERSE EVENT ( 8 FDA reports)
ALVEOLITIS ( 8 FDA reports)
AORTIC VALVE INCOMPETENCE ( 8 FDA reports)
BLINDNESS TRANSIENT ( 8 FDA reports)
BLOOD AMYLASE INCREASED ( 8 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 8 FDA reports)
BLOOD URIC ACID INCREASED ( 8 FDA reports)
BRAIN NEOPLASM ( 8 FDA reports)
BREAST PAIN ( 8 FDA reports)
CAESAREAN SECTION ( 8 FDA reports)
CHOLECYSTITIS ACUTE ( 8 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 8 FDA reports)
DECREASED INTEREST ( 8 FDA reports)
DISABILITY ( 8 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 8 FDA reports)
EAR DISORDER ( 8 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 8 FDA reports)
FACE INJURY ( 8 FDA reports)
FACIAL BONES FRACTURE ( 8 FDA reports)
GASTROINTESTINAL PERFORATION ( 8 FDA reports)
GENERALISED ERYTHEMA ( 8 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 8 FDA reports)
HAIR GROWTH ABNORMAL ( 8 FDA reports)
HYPERTENSIVE HEART DISEASE ( 8 FDA reports)
ILEUS ( 8 FDA reports)
INJECTION SITE SWELLING ( 8 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 8 FDA reports)
JAW LESION EXCISION ( 8 FDA reports)
LACUNAR INFARCTION ( 8 FDA reports)
LARYNGEAL OEDEMA ( 8 FDA reports)
LIPIDS INCREASED ( 8 FDA reports)
LOCAL SWELLING ( 8 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
MASS ( 8 FDA reports)
MUSCLE CRAMP ( 8 FDA reports)
NARCOTIC INTOXICATION ( 8 FDA reports)
NECROSIS ( 8 FDA reports)
NEURODERMATITIS ( 8 FDA reports)
OCULAR ICTERUS ( 8 FDA reports)
OESOPHAGEAL CARCINOMA ( 8 FDA reports)
ORAL SURGERY ( 8 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 8 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 8 FDA reports)
RETINAL VEIN OCCLUSION ( 8 FDA reports)
ROTATOR CUFF SYNDROME ( 8 FDA reports)
SENSATION OF FOREIGN BODY ( 8 FDA reports)
SKIN WARM ( 8 FDA reports)
SLEEP TERROR ( 8 FDA reports)
SLUGGISHNESS ( 8 FDA reports)
SOMNAMBULISM ( 8 FDA reports)
TARDIVE DYSKINESIA ( 8 FDA reports)
THYROIDITIS ( 8 FDA reports)
TONGUE DISCOLOURATION ( 8 FDA reports)
TORSADE DE POINTES ( 8 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 8 FDA reports)
ULCER ( 8 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 8 FDA reports)
UROSEPSIS ( 8 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 8 FDA reports)
VITAMIN D DEFICIENCY ( 8 FDA reports)
WOUND HAEMORRHAGE ( 8 FDA reports)
ABDOMINAL PAIN LOWER ( 7 FDA reports)
ABSCESS ( 7 FDA reports)
ACUTE PULMONARY OEDEMA ( 7 FDA reports)
AMENORRHOEA ( 7 FDA reports)
ANOSMIA ( 7 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 7 FDA reports)
BLINDNESS UNILATERAL ( 7 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 7 FDA reports)
BLOOD MAGNESIUM INCREASED ( 7 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 7 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 7 FDA reports)
BONE EROSION ( 7 FDA reports)
BREATH SOUNDS ABNORMAL ( 7 FDA reports)
BRONCHIECTASIS ( 7 FDA reports)
CARDIOTOXICITY ( 7 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 7 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 7 FDA reports)
CERVICAL SPINAL STENOSIS ( 7 FDA reports)
COLONIC POLYP ( 7 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 7 FDA reports)
CREPITATIONS ( 7 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 7 FDA reports)
DILATATION VENTRICULAR ( 7 FDA reports)
DIVERTICULUM INTESTINAL ( 7 FDA reports)
DRUG EFFECT INCREASED ( 7 FDA reports)
DYSGRAPHIA ( 7 FDA reports)
EAR DISCOMFORT ( 7 FDA reports)
EAR INFECTION ( 7 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 7 FDA reports)
EOSINOPHILIA ( 7 FDA reports)
ERECTION INCREASED ( 7 FDA reports)
ERYTHEMA MULTIFORME ( 7 FDA reports)
FACIAL PALSY ( 7 FDA reports)
FAILURE TO THRIVE ( 7 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 7 FDA reports)
FRACTURE ( 7 FDA reports)
GASTROENTERITIS VIRAL ( 7 FDA reports)
GASTROINTESTINAL INFECTION ( 7 FDA reports)
GASTROSTOMY TUBE INSERTION ( 7 FDA reports)
GINGIVAL SWELLING ( 7 FDA reports)
GINGIVITIS ( 7 FDA reports)
HAEMORRHAGE URINARY TRACT ( 7 FDA reports)
HAIR COLOUR CHANGES ( 7 FDA reports)
HAIR TEXTURE ABNORMAL ( 7 FDA reports)
HEPATITIS B ( 7 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 7 FDA reports)
HYPERVENTILATION ( 7 FDA reports)
HYPHAEMA ( 7 FDA reports)
HYPOAESTHESIA FACIAL ( 7 FDA reports)
IMMUNE SYSTEM DISORDER ( 7 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 7 FDA reports)
INCREASED TENDENCY TO BRUISE ( 7 FDA reports)
INJECTION SITE RASH ( 7 FDA reports)
INTRACARDIAC THROMBUS ( 7 FDA reports)
JAW DISORDER ( 7 FDA reports)
JOINT SPRAIN ( 7 FDA reports)
JUDGEMENT IMPAIRED ( 7 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 7 FDA reports)
LIBIDO DECREASED ( 7 FDA reports)
LISTLESS ( 7 FDA reports)
LUNG CANCER METASTATIC ( 7 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 7 FDA reports)
MENINGITIS ( 7 FDA reports)
METABOLIC ENCEPHALOPATHY ( 7 FDA reports)
MICTURITION DISORDER ( 7 FDA reports)
MUSCLE ENZYME INCREASED ( 7 FDA reports)
NEGATIVE THOUGHTS ( 7 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 7 FDA reports)
NEPHROTIC SYNDROME ( 7 FDA reports)
NERVE COMPRESSION ( 7 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 7 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 7 FDA reports)
OROPHARYNGEAL BLISTERING ( 7 FDA reports)
PAIN OF SKIN ( 7 FDA reports)
PANCREATIC MASS ( 7 FDA reports)
PANCREATITIS CHRONIC ( 7 FDA reports)
PERICARDIAL HAEMORRHAGE ( 7 FDA reports)
PLANTAR FASCIITIS ( 7 FDA reports)
PNEUMOTHORAX ( 7 FDA reports)
POLYCHROMASIA ( 7 FDA reports)
POLYDIPSIA ( 7 FDA reports)
POLYMYALGIA RHEUMATICA ( 7 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 7 FDA reports)
PSYCHIATRIC SYMPTOM ( 7 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 7 FDA reports)
RALES ( 7 FDA reports)
RASH PUSTULAR ( 7 FDA reports)
REFLUX GASTRITIS ( 7 FDA reports)
RIGHT VENTRICULAR FAILURE ( 7 FDA reports)
SCREAMING ( 7 FDA reports)
SINUS ARRHYTHMIA ( 7 FDA reports)
SINUS CONGESTION ( 7 FDA reports)
SKIN CANCER ( 7 FDA reports)
SKIN LACERATION ( 7 FDA reports)
SKIN NECROSIS ( 7 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 7 FDA reports)
SUDDEN CARDIAC DEATH ( 7 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 7 FDA reports)
TERMINAL INSOMNIA ( 7 FDA reports)
THERAPY NON-RESPONDER ( 7 FDA reports)
TOXIC SKIN ERUPTION ( 7 FDA reports)
TRANSPLANT REJECTION ( 7 FDA reports)
URINE ODOUR ABNORMAL ( 7 FDA reports)
VARICOSE VEIN ( 7 FDA reports)
VENOUS OCCLUSION ( 7 FDA reports)
VISUAL FIELD DEFECT ( 7 FDA reports)
ACUTE PRERENAL FAILURE ( 6 FDA reports)
AFFECT LABILITY ( 6 FDA reports)
ANAL ABSCESS ( 6 FDA reports)
ANHEDONIA ( 6 FDA reports)
ANXIETY DISORDER ( 6 FDA reports)
AORTIC VALVE SCLEROSIS ( 6 FDA reports)
APPARENT DEATH ( 6 FDA reports)
ARTERIAL DISORDER ( 6 FDA reports)
ARTERIAL STENT INSERTION ( 6 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 6 FDA reports)
AZOTAEMIA ( 6 FDA reports)
BILE DUCT OBSTRUCTION ( 6 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 6 FDA reports)
BLOOD TEST ABNORMAL ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 6 FDA reports)
CARDIAC ENZYMES INCREASED ( 6 FDA reports)
CARDIOVERSION ( 6 FDA reports)
CAROTID ARTERY OCCLUSION ( 6 FDA reports)
CEREBRAL CYST ( 6 FDA reports)
CLEFT LIP ( 6 FDA reports)
CLEFT LIP AND PALATE ( 6 FDA reports)
COMA SCALE ABNORMAL ( 6 FDA reports)
COMMUNICATION DISORDER ( 6 FDA reports)
CYST ( 6 FDA reports)
DEAFNESS UNILATERAL ( 6 FDA reports)
DEBRIDEMENT ( 6 FDA reports)
DECUBITUS ULCER ( 6 FDA reports)
DERMATITIS ( 6 FDA reports)
DERMATITIS BULLOUS ( 6 FDA reports)
DERMATOMYOSITIS ( 6 FDA reports)
DEVICE MALFUNCTION ( 6 FDA reports)
DIABETIC KETOACIDOSIS ( 6 FDA reports)
DIABETIC NEPHROPATHY ( 6 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 6 FDA reports)
DIZZINESS POSTURAL ( 6 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 6 FDA reports)
DUODENITIS ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 6 FDA reports)
EMPYEMA ( 6 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 6 FDA reports)
EXERCISE TOLERANCE DECREASED ( 6 FDA reports)
EYE INFECTION ( 6 FDA reports)
FEMORAL NECK FRACTURE ( 6 FDA reports)
FLANK PAIN ( 6 FDA reports)
FOOT DEFORMITY ( 6 FDA reports)
FOOT FRACTURE ( 6 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 6 FDA reports)
GINGIVAL HYPERPLASIA ( 6 FDA reports)
GLYCOSURIA ( 6 FDA reports)
GYNAECOMASTIA ( 6 FDA reports)
HAEMOLYTIC ANAEMIA ( 6 FDA reports)
HEART RATE ABNORMAL ( 6 FDA reports)
HEART VALVE INCOMPETENCE ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 6 FDA reports)
HEPATITIS TOXIC ( 6 FDA reports)
HYPERACUSIS ( 6 FDA reports)
HYPERAESTHESIA ( 6 FDA reports)
HYPERAMMONAEMIA ( 6 FDA reports)
HYPERCHLORHYDRIA ( 6 FDA reports)
HYPERKERATOSIS ( 6 FDA reports)
HYPERREFLEXIA ( 6 FDA reports)
HYPERTHYROIDISM ( 6 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 6 FDA reports)
INDIFFERENCE ( 6 FDA reports)
INJECTION SITE HAEMATOMA ( 6 FDA reports)
IRON DEFICIENCY ANAEMIA ( 6 FDA reports)
JOINT DISLOCATION ( 6 FDA reports)
LEFT ATRIAL DILATATION ( 6 FDA reports)
LOCALISED INFECTION ( 6 FDA reports)
LUPUS-LIKE SYNDROME ( 6 FDA reports)
LYMPHOPENIA ( 6 FDA reports)
MALIGNANT HYPERTENSION ( 6 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 6 FDA reports)
MENORRHAGIA ( 6 FDA reports)
MENSTRUAL DISORDER ( 6 FDA reports)
METASTASES TO LUNG ( 6 FDA reports)
MITRAL VALVE DISEASE ( 6 FDA reports)
MOUTH HAEMORRHAGE ( 6 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 6 FDA reports)
MUSCLE STRAIN ( 6 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 6 FDA reports)
NASAL DISCOMFORT ( 6 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
NEUROPATHY ( 6 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 6 FDA reports)
ONYCHOMYCOSIS ( 6 FDA reports)
OVARIAN CANCER ( 6 FDA reports)
PANCREATIC CARCINOMA ( 6 FDA reports)
PANIC REACTION ( 6 FDA reports)
PARKINSONISM ( 6 FDA reports)
PENILE HAEMORRHAGE ( 6 FDA reports)
PLEURISY ( 6 FDA reports)
POLYMYOSITIS ( 6 FDA reports)
POST PROCEDURAL BILE LEAK ( 6 FDA reports)
PROCTALGIA ( 6 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 6 FDA reports)
PULMONARY CONGESTION ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
PYELONEPHRITIS ( 6 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 6 FDA reports)
SKIN INFECTION ( 6 FDA reports)
SKIN TIGHTNESS ( 6 FDA reports)
SPINAL COLUMN STENOSIS ( 6 FDA reports)
SPINAL DISORDER ( 6 FDA reports)
STUPOR ( 6 FDA reports)
SUBDURAL HAEMORRHAGE ( 6 FDA reports)
SUICIDAL BEHAVIOUR ( 6 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
TEMPERATURE INTOLERANCE ( 6 FDA reports)
TENDON PAIN ( 6 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 6 FDA reports)
TONGUE OEDEMA ( 6 FDA reports)
TRIGGER FINGER ( 6 FDA reports)
TROPONIN I INCREASED ( 6 FDA reports)
TUMOUR HAEMORRHAGE ( 6 FDA reports)
UPPER LIMB FRACTURE ( 6 FDA reports)
VASCULAR OCCLUSION ( 6 FDA reports)
VASCULAR PSEUDOANEURYSM ( 6 FDA reports)
VENTRICULAR HYPOKINESIA ( 6 FDA reports)
VIRAL LOAD INCREASED ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 6 FDA reports)
WOUND ( 6 FDA reports)
ABDOMINAL RIGIDITY ( 5 FDA reports)
ACCIDENT AT WORK ( 5 FDA reports)
ALCOHOL USE ( 5 FDA reports)
ANISOCYTOSIS ( 5 FDA reports)
AORTIC ANEURYSM RUPTURE ( 5 FDA reports)
AORTIC DISORDER ( 5 FDA reports)
AORTIC DISSECTION ( 5 FDA reports)
AORTIC VALVE DISEASE ( 5 FDA reports)
APPLICATION SITE PAIN ( 5 FDA reports)
ASPHYXIA ( 5 FDA reports)
ATRIAL SEPTAL DEFECT ( 5 FDA reports)
BACTERAEMIA ( 5 FDA reports)
BARRETT'S OESOPHAGUS ( 5 FDA reports)
BIPOLAR I DISORDER ( 5 FDA reports)
BLADDER DISCOMFORT ( 5 FDA reports)
BLADDER OBSTRUCTION ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BLOOD CULTURE POSITIVE ( 5 FDA reports)
BLOOD DISORDER ( 5 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 5 FDA reports)
BONE DEBRIDEMENT ( 5 FDA reports)
BONE LOSS ( 5 FDA reports)
CARDIAC ANEURYSM ( 5 FDA reports)
CARDIAC FAILURE CHRONIC ( 5 FDA reports)
CARDIAC FLUTTER ( 5 FDA reports)
CAROTID ARTERY DISEASE ( 5 FDA reports)
CATHETER PLACEMENT ( 5 FDA reports)
CHOLECYSTECTOMY ( 5 FDA reports)
COLITIS ULCERATIVE ( 5 FDA reports)
COLLAPSE OF LUNG ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 5 FDA reports)
CORONARY ARTERY ANEURYSM ( 5 FDA reports)
CROHN'S DISEASE ( 5 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 5 FDA reports)
DARK CIRCLES UNDER EYES ( 5 FDA reports)
DEFORMITY ( 5 FDA reports)
DIARRHOEA INFECTIOUS ( 5 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 5 FDA reports)
DISEASE RECURRENCE ( 5 FDA reports)
DIVERTICULUM ( 5 FDA reports)
DROOLING ( 5 FDA reports)
DRUG ABUSE ( 5 FDA reports)
DRY THROAT ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
ENERGY INCREASED ( 5 FDA reports)
ENZYME ABNORMALITY ( 5 FDA reports)
ERYTHEMA OF EYELID ( 5 FDA reports)
ERYTHROPENIA ( 5 FDA reports)
EXTREMITY NECROSIS ( 5 FDA reports)
EYE INFLAMMATION ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 5 FDA reports)
GASTROINTESTINAL ULCER ( 5 FDA reports)
GASTROSTOMY ( 5 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 5 FDA reports)
HAEMARTHROSIS ( 5 FDA reports)
HAEMOGLOBIN ABNORMAL ( 5 FDA reports)
HAEMOGLOBIN INCREASED ( 5 FDA reports)
HAEMOLYSIS ( 5 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 5 FDA reports)
HALLUCINATION, TACTILE ( 5 FDA reports)
HEART VALVE REPLACEMENT ( 5 FDA reports)
HYDRONEPHROSIS ( 5 FDA reports)
HYPERCHOLESTEROLAEMIA ( 5 FDA reports)
HYPERMAGNESAEMIA ( 5 FDA reports)
HYPOCHROMASIA ( 5 FDA reports)
HYSTERECTOMY ( 5 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 5 FDA reports)
INJECTION SITE WARMTH ( 5 FDA reports)
KAPOSI'S SARCOMA ( 5 FDA reports)
LARGE INTESTINAL ULCER ( 5 FDA reports)
LARGE INTESTINE PERFORATION ( 5 FDA reports)
LIP EROSION ( 5 FDA reports)
LUNG ADENOCARCINOMA ( 5 FDA reports)
MACULAR OEDEMA ( 5 FDA reports)
MALIGNANT MELANOMA ( 5 FDA reports)
METABOLIC DISORDER ( 5 FDA reports)
MICROCYTOSIS ( 5 FDA reports)
MOTOR DYSFUNCTION ( 5 FDA reports)
MULTIPLE SCLEROSIS ( 5 FDA reports)
MUSCULOSKELETAL DISORDER ( 5 FDA reports)
MYELODYSPLASTIC SYNDROME ( 5 FDA reports)
NAIL DISORDER ( 5 FDA reports)
NARCOLEPSY ( 5 FDA reports)
NECK INJURY ( 5 FDA reports)
NEONATAL TACHYPNOEA ( 5 FDA reports)
NEPHROPATHY ( 5 FDA reports)
NO THERAPEUTIC RESPONSE ( 5 FDA reports)
NODAL RHYTHM ( 5 FDA reports)
OESOPHAGEAL OEDEMA ( 5 FDA reports)
ORAL HERPES ( 5 FDA reports)
ORGAN FAILURE ( 5 FDA reports)
OROPHARYNGEAL SWELLING ( 5 FDA reports)
OSTEOSCLEROSIS ( 5 FDA reports)
PARTIAL SEIZURES ( 5 FDA reports)
PELVIC MASS ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
PLEURAL FIBROSIS ( 5 FDA reports)
PLEURITIC PAIN ( 5 FDA reports)
PROSTATISM ( 5 FDA reports)
PROSTATOMEGALY ( 5 FDA reports)
PSYCHOMOTOR RETARDATION ( 5 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 5 FDA reports)
PUPILS UNEQUAL ( 5 FDA reports)
QUADRIPARESIS ( 5 FDA reports)
RAYNAUD'S PHENOMENON ( 5 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 5 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 5 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 5 FDA reports)
RESPIRATORY RATE DECREASED ( 5 FDA reports)
RETINAL DISORDER ( 5 FDA reports)
RHINITIS ALLERGIC ( 5 FDA reports)
ROULEAUX FORMATION ( 5 FDA reports)
SARCOMA ( 5 FDA reports)
SCLERODERMA ( 5 FDA reports)
SCRATCH ( 5 FDA reports)
SINUS HEADACHE ( 5 FDA reports)
SLEEP TALKING ( 5 FDA reports)
SOCIAL PHOBIA ( 5 FDA reports)
SPUTUM DISCOLOURED ( 5 FDA reports)
STERNAL FRACTURE ( 5 FDA reports)
SUBILEUS ( 5 FDA reports)
SUNBURN ( 5 FDA reports)
SUPRAPUBIC PAIN ( 5 FDA reports)
TENDONITIS ( 5 FDA reports)
TETANY ( 5 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TONGUE HAEMORRHAGE ( 5 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 5 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 5 FDA reports)
ULCER HAEMORRHAGE ( 5 FDA reports)
URINARY HESITATION ( 5 FDA reports)
URTICARIA GENERALISED ( 5 FDA reports)
VENTRICULAR DYSFUNCTION ( 5 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 5 FDA reports)
WHITE BLOOD CELL DISORDER ( 5 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
WOUND SECRETION ( 5 FDA reports)
ABDOMINAL HERNIA ( 4 FDA reports)
ABDOMINAL MASS ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 4 FDA reports)
ADJUSTMENT DISORDER ( 4 FDA reports)
AKATHISIA ( 4 FDA reports)
ANEURYSM RUPTURED ( 4 FDA reports)
ANORGASMIA ( 4 FDA reports)
ANTI-INSULIN ANTIBODY ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
APPETITE DISORDER ( 4 FDA reports)
ARTHROPOD BITE ( 4 FDA reports)
BENIGN LUNG NEOPLASM ( 4 FDA reports)
BILIARY TRACT DISORDER ( 4 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 4 FDA reports)
BIOPSY BREAST ABNORMAL ( 4 FDA reports)
BLADDER NEOPLASM ( 4 FDA reports)
BLADDER SPASM ( 4 FDA reports)
BLEPHAROSPASM ( 4 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 4 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 4 FDA reports)
BONE LESION ( 4 FDA reports)
BRAIN DAMAGE ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
BREAKTHROUGH PAIN ( 4 FDA reports)
BREAST SWELLING ( 4 FDA reports)
BRONCHIAL HAEMORRHAGE ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CARDIAC FIBRILLATION ( 4 FDA reports)
CARDIOPULMONARY FAILURE ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 4 FDA reports)
CEREBRAL HAEMATOMA ( 4 FDA reports)
CEREBRAL THROMBOSIS ( 4 FDA reports)
CHOLESTATIC LIVER INJURY ( 4 FDA reports)
CHRONIC SINUSITIS ( 4 FDA reports)
CLAVICLE FRACTURE ( 4 FDA reports)
CLEFT PALATE ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 4 FDA reports)
CONCUSSION ( 4 FDA reports)
CORONARY ANGIOPLASTY ( 4 FDA reports)
CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
CRANIOSYNOSTOSIS ( 4 FDA reports)
CULTURE URINE POSITIVE ( 4 FDA reports)
DEAFNESS NEUROSENSORY ( 4 FDA reports)
DECREASED ACTIVITY ( 4 FDA reports)
DEFAECATION URGENCY ( 4 FDA reports)
DEMENTIA WITH LEWY BODIES ( 4 FDA reports)
DERMATITIS CONTACT ( 4 FDA reports)
DEVICE DISLOCATION ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
DILATATION ATRIAL ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
DUODENAL OBSTRUCTION ( 4 FDA reports)
DYSLIPIDAEMIA ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
EJACULATION FAILURE ( 4 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 4 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
ENDOCARDITIS ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ( 4 FDA reports)
ERYSIPELAS ( 4 FDA reports)
EXFOLIATIVE RASH ( 4 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 4 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 4 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 4 FDA reports)
EYE EXCISION ( 4 FDA reports)
EYELID DISORDER ( 4 FDA reports)
EYELIDS PRURITUS ( 4 FDA reports)
FACIAL PAIN ( 4 FDA reports)
FACIAL PARESIS ( 4 FDA reports)
FAECES PALE ( 4 FDA reports)
FEEDING DISORDER NEONATAL ( 4 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 4 FDA reports)
FEMORAL ARTERY OCCLUSION ( 4 FDA reports)
FEMORAL HERNIA ( 4 FDA reports)
FEMUR FRACTURE ( 4 FDA reports)
FIBROSIS ( 4 FDA reports)
FINGER DEFORMITY ( 4 FDA reports)
FISTULA ( 4 FDA reports)
FOETAL GROWTH RESTRICTION ( 4 FDA reports)
FOETAL GROWTH RETARDATION ( 4 FDA reports)
FOOD CRAVING ( 4 FDA reports)
FOOD INTOLERANCE ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
FUCHS' SYNDROME ( 4 FDA reports)
GALLBLADDER OPERATION ( 4 FDA reports)
GASTROENTERITIS NOROVIRUS ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 4 FDA reports)
GENERALISED ANXIETY DISORDER ( 4 FDA reports)
HAND FRACTURE ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
HERNIA REPAIR ( 4 FDA reports)
HOSTILITY ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPERTONIC BLADDER ( 4 FDA reports)
HYPERVISCOSITY SYNDROME ( 4 FDA reports)
HYPERVOLAEMIA ( 4 FDA reports)
HYPOREFLEXIA ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
ILIAC ARTERY STENOSIS ( 4 FDA reports)
IMPAIRED SELF-CARE ( 4 FDA reports)
IMPATIENCE ( 4 FDA reports)
INADEQUATE ANALGESIA ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INFUSION SITE HAEMORRHAGE ( 4 FDA reports)
INTENTIONAL SELF-INJURY ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 4 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 4 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 4 FDA reports)
INTESTINAL ADENOCARCINOMA ( 4 FDA reports)
INTESTINAL HAEMORRHAGE ( 4 FDA reports)
INTRA-UTERINE DEATH ( 4 FDA reports)
JOINT CONTRACTURE ( 4 FDA reports)
JOINT EFFUSION ( 4 FDA reports)
LARYNGITIS ( 4 FDA reports)
LEG AMPUTATION ( 4 FDA reports)
LESION EXCISION ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LIFE EXPECTANCY SHORTENED ( 4 FDA reports)
LIGHT CHAIN DISEASE ( 4 FDA reports)
LIMB OPERATION ( 4 FDA reports)
LIP BLISTER ( 4 FDA reports)
LIVEDO RETICULARIS ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
LOCALISED OSTEOARTHRITIS ( 4 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 4 FDA reports)
LUNG CONSOLIDATION ( 4 FDA reports)
MACROCYTOSIS ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MECHANICAL VENTILATION ( 4 FDA reports)
MENIERE'S DISEASE ( 4 FDA reports)
MENISCUS LESION ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
MERALGIA PARAESTHETICA ( 4 FDA reports)
MESENTERITIS ( 4 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
METASTASES TO SPINE ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
MITRAL VALVE PROLAPSE ( 4 FDA reports)
MUCOSAL DRYNESS ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
MULTIPLE INJURIES ( 4 FDA reports)
MUSCLE RUPTURE ( 4 FDA reports)
NEPHRITIS INTERSTITIAL ( 4 FDA reports)
NEUROGENIC BLADDER ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NEUTROPENIC SEPSIS ( 4 FDA reports)
NICOTINE DEPENDENCE ( 4 FDA reports)
NODAL ARRHYTHMIA ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 4 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 4 FDA reports)
OPEN WOUND ( 4 FDA reports)
OPTIC ATROPHY ( 4 FDA reports)
ORGANISING PNEUMONIA ( 4 FDA reports)
ORTHOPNOEA ( 4 FDA reports)
OTITIS EXTERNA ( 4 FDA reports)
OVERWEIGHT ( 4 FDA reports)
PARAPARESIS ( 4 FDA reports)
PATHOLOGICAL FRACTURE ( 4 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 4 FDA reports)
PERIORBITAL HAEMATOMA ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PERSONALITY DISORDER ( 4 FDA reports)
PITUITARY TUMOUR BENIGN ( 4 FDA reports)
PLATELET PRODUCTION DECREASED ( 4 FDA reports)
POLYNEUROPATHY IN MALIGNANT DISEASE ( 4 FDA reports)
PROSTHESIS IMPLANTATION ( 4 FDA reports)
PULMONARY THROMBOSIS ( 4 FDA reports)
QUALITY OF LIFE DECREASED ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
RENAL CELL CARCINOMA ( 4 FDA reports)
RENAL COLIC ( 4 FDA reports)
RENAL INJURY ( 4 FDA reports)
RESPIRATORY TRACT OEDEMA ( 4 FDA reports)
RESUSCITATION ( 4 FDA reports)
RETINAL ARTERY EMBOLISM ( 4 FDA reports)
RETINAL ISCHAEMIA ( 4 FDA reports)
SCROTAL INFECTION ( 4 FDA reports)
SEBORRHOEIC DERMATITIS ( 4 FDA reports)
SERUM FERRITIN INCREASED ( 4 FDA reports)
SINUS ARREST ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN HAEMORRHAGE ( 4 FDA reports)
SKIN NEOPLASM EXCISION ( 4 FDA reports)
SKIN WRINKLING ( 4 FDA reports)
SOPOR ( 4 FDA reports)
SPINAL CORD DISORDER ( 4 FDA reports)
SPINAL OPERATION ( 4 FDA reports)
SPLEEN DISORDER ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
STATUS EPILEPTICUS ( 4 FDA reports)
STENT OCCLUSION ( 4 FDA reports)
STREPTOCOCCAL SEPSIS ( 4 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 4 FDA reports)
TALIPES ( 4 FDA reports)
TENDON DISORDER ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 4 FDA reports)
THROAT LESION ( 4 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 4 FDA reports)
TINEA PEDIS ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TOOTH LOSS ( 4 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 4 FDA reports)
VAGINAL INFECTION ( 4 FDA reports)
VASCULAR PURPURA ( 4 FDA reports)
VENOUS HAEMORRHAGE ( 4 FDA reports)
VENOUS THROMBOSIS LIMB ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
VERTEBROPLASTY ( 4 FDA reports)
VULVOVAGINAL DISCOMFORT ( 4 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 4 FDA reports)
WALKING AID USER ( 4 FDA reports)
WEIGHT LOSS POOR ( 4 FDA reports)
WHEELCHAIR USER ( 4 FDA reports)
WOUND COMPLICATION ( 4 FDA reports)
XEROSIS ( 4 FDA reports)
ABDOMINAL ABSCESS ( 3 FDA reports)
ABORTION ( 3 FDA reports)
ACANTHOSIS ( 3 FDA reports)
ACUTE ABDOMEN ( 3 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 3 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
AGORAPHOBIA ( 3 FDA reports)
ALBINISM ( 3 FDA reports)
ALCOHOL ABUSE ( 3 FDA reports)
ALDOLASE INCREASED ( 3 FDA reports)
ALKALOSIS ( 3 FDA reports)
ALVEOLITIS ALLERGIC ( 3 FDA reports)
ANAL HAEMORRHAGE ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANGIOGRAM ABNORMAL ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
ANION GAP INCREASED ( 3 FDA reports)
AORTIC VALVE DISEASE MIXED ( 3 FDA reports)
AORTIC VALVE REPLACEMENT ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
APHONIA ( 3 FDA reports)
APNOEA ( 3 FDA reports)
APPLICATION SITE BURN ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
APPLICATION SITE RASH ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
ARTERIAL HAEMORRHAGE ( 3 FDA reports)
ARTERIAL STENOSIS ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
ARTHROSCOPY ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ATRIAL THROMBOSIS ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 3 FDA reports)
AV DISSOCIATION ( 3 FDA reports)
BACTERIAL TEST ( 3 FDA reports)
BACTERIAL TEST POSITIVE ( 3 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
BIFASCICULAR BLOCK ( 3 FDA reports)
BILE DUCT STONE ( 3 FDA reports)
BILIARY DILATATION ( 3 FDA reports)
BIOPSY LUNG ( 3 FDA reports)
BLADDER OPERATION ( 3 FDA reports)
BLADDER PAIN ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD CREATININE DECREASED ( 3 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD SODIUM ABNORMAL ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BREAST DISCOLOURATION ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
BUNION ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CANDIDA SEPSIS ( 3 FDA reports)
CAPILLARY DISORDER ( 3 FDA reports)
CARBON DIOXIDE ABNORMAL ( 3 FDA reports)
CATARACT NUCLEAR ( 3 FDA reports)
CEREBELLAR HAEMATOMA ( 3 FDA reports)
CEREBELLAR SYNDROME ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
CHAPPED LIPS ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
COLON POLYPECTOMY ( 3 FDA reports)
COLOSTOMY ( 3 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 3 FDA reports)
CONVERSION DISORDER ( 3 FDA reports)
CORONARY ARTERY PERFORATION ( 3 FDA reports)
CORONARY ARTERY SURGERY ( 3 FDA reports)
COSTOCHONDRITIS ( 3 FDA reports)
CUTANEOUS VASCULITIS ( 3 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 3 FDA reports)
DEAFNESS TRANSITORY ( 3 FDA reports)
DENTAL FISTULA ( 3 FDA reports)
DERMATITIS HERPETIFORMIS ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DRUG EFFECT DELAYED ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 3 FDA reports)
DYSPHEMIA ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
EJACULATION DELAYED ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
EMBOLIC STROKE ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
EPIGLOTTITIS ( 3 FDA reports)
EPISCLERITIS ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
ESCHERICHIA BACTERAEMIA ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FEELING OF RELAXATION ( 3 FDA reports)
FEELINGS OF WORTHLESSNESS ( 3 FDA reports)
FIBULA FRACTURE ( 3 FDA reports)
FOOD INTERACTION ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 3 FDA reports)
FRACTURED SACRUM ( 3 FDA reports)
GALLOP RHYTHM PRESENT ( 3 FDA reports)
GAMMOPATHY ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTRIC ULCER PERFORATION ( 3 FDA reports)
GASTROINTESTINAL EROSION ( 3 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 3 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
GOITRE ( 3 FDA reports)
GROWTH OF EYELASHES ( 3 FDA reports)
HAEMATOMA INFECTION ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HAIR DISORDER ( 3 FDA reports)
HEART VALVE CALCIFICATION ( 3 FDA reports)
HEART VALVE OPERATION ( 3 FDA reports)
HEAT RASH ( 3 FDA reports)
HEPATIC HAEMORRHAGE ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HEPATITIS A ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HIDRADENITIS ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
HIP DYSPLASIA ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERTHERMIA MALIGNANT ( 3 FDA reports)
HYPERTRANSAMINASAEMIA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
HYPOVITAMINOSIS ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
IGA NEPHROPATHY ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
INFANTILE SPITTING UP ( 3 FDA reports)
INJECTION SITE BURNING ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 3 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL INFARCTION ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
INTESTINAL RESECTION ( 3 FDA reports)
IRITIS ( 3 FDA reports)
JC VIRUS INFECTION ( 3 FDA reports)
JOINT CREPITATION ( 3 FDA reports)
JUGULAR VEIN THROMBOSIS ( 3 FDA reports)
KAWASAKI'S DISEASE ( 3 FDA reports)
KIDNEY ENLARGEMENT ( 3 FDA reports)
LAPAROTOMY ( 3 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LARYNGEAL DISORDER ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LIMB CRUSHING INJURY ( 3 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 3 FDA reports)
LIP EXFOLIATION ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LONG QT SYNDROME ( 3 FDA reports)
LUMBAR RADICULOPATHY ( 3 FDA reports)
LUMBAR SPINAL STENOSIS ( 3 FDA reports)
MASTECTOMY ( 3 FDA reports)
MENTAL DISABILITY ( 3 FDA reports)
MIGRAINE WITH AURA ( 3 FDA reports)
MITRAL VALVE STENOSIS ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MULTIPLE FRACTURES ( 3 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 3 FDA reports)
MUSCLE FATIGUE ( 3 FDA reports)
MYCOSIS FUNGOIDES ( 3 FDA reports)
MYOCARDIAL RUPTURE ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
NEPHRITIS ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUROPATHIC ARTHROPATHY ( 3 FDA reports)
NEUTROPHILIA ( 3 FDA reports)
NIGHT BLINDNESS ( 3 FDA reports)
NIKOLSKY'S SIGN ( 3 FDA reports)
NIPPLE PAIN ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
OCULAR VASCULAR DISORDER ( 3 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 3 FDA reports)
ONYCHOCLASIS ( 3 FDA reports)
ORAL MUCOSAL BLISTERING ( 3 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
OSTEITIS ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
PAINFUL ERECTION ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PELVIC FRACTURE ( 3 FDA reports)
PENILE CURVATURE ( 3 FDA reports)
PENILE PAIN ( 3 FDA reports)
PENIS DISORDER ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PERIPHERAL NERVE INJURY ( 3 FDA reports)
PERONEAL NERVE PALSY ( 3 FDA reports)
PHLEBITIS ( 3 FDA reports)
PHOTODERMATOSIS ( 3 FDA reports)
PITUITARY TUMOUR ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
PNEUMONIA HAEMOPHILUS ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
POSTOPERATIVE ILEUS ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 3 FDA reports)
PREVENTIVE SURGERY ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PROSTATECTOMY ( 3 FDA reports)
PROSTATITIS ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PSORIATIC ARTHROPATHY ( 3 FDA reports)
PUBIS FRACTURE ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
PULMONARY SARCOIDOSIS ( 3 FDA reports)
RADIAL PULSE ABNORMAL ( 3 FDA reports)
READING DISORDER ( 3 FDA reports)
REGURGITATION ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RETINAL EXUDATES ( 3 FDA reports)
RETINAL OEDEMA ( 3 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
SCAB ( 3 FDA reports)
SCHIZOPHRENIA ( 3 FDA reports)
SCOTOMA ( 3 FDA reports)
SEASONAL ALLERGY ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
SEROMA ( 3 FDA reports)
SERRATIA BACTERAEMIA ( 3 FDA reports)
SHOULDER OPERATION ( 3 FDA reports)
SKELETAL INJURY ( 3 FDA reports)
SKIN FIBROSIS ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SKIN ODOUR ABNORMAL ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
SPINAL COLUMN INJURY ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
TERATOGENICITY ( 3 FDA reports)
THALASSAEMIA ALPHA ( 3 FDA reports)
THYROID NEOPLASM ( 3 FDA reports)
THYROIDECTOMY ( 3 FDA reports)
TONGUE BLISTERING ( 3 FDA reports)
TONGUE CYST ( 3 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ABNORMAL ( 3 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
URETERIC OBSTRUCTION ( 3 FDA reports)
URINE ANALYSIS ABNORMAL ( 3 FDA reports)
URINE FLOW DECREASED ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VAGINAL DISORDER ( 3 FDA reports)
VASCULAR OPERATION ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
VITAMIN B6 DEFICIENCY ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
WOUND DEHISCENCE ( 3 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABDOMINAL SEPSIS ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACQUIRED HAEMOPHILIA ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
AGITATED DEPRESSION ( 2 FDA reports)
AGNOSIA ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
ALCOHOL PROBLEM ( 2 FDA reports)
ALCOHOLIC ( 2 FDA reports)
ALCOHOLIC LIVER DISEASE ( 2 FDA reports)
ALLERGIC OEDEMA ( 2 FDA reports)
ALLERGY TEST POSITIVE ( 2 FDA reports)
ALPHA HYDROXYBUTYRATE DEHYDROGENASE INCREASED ( 2 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 2 FDA reports)
ANAL ULCER ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
ANTERIOR DISPLACED ANUS ( 2 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
AORTIC CALCIFICATION ( 2 FDA reports)
AORTITIS ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE SCAB ( 2 FDA reports)
APPLICATION SITE VESICLES ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
ASBESTOSIS ( 2 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 2 FDA reports)
ATROPHIC VULVOVAGINITIS ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BIOPSY BONE MARROW ( 2 FDA reports)
BLADDER MASS ( 2 FDA reports)
BLADDER SUSPENSION ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLISTER INFECTED ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD IRON ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 2 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BREAST DISCHARGE ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BREECH PRESENTATION ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BURN OF INTERNAL ORGANS ( 2 FDA reports)
BURSITIS INFECTIVE ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIAC INFECTION ( 2 FDA reports)
CARDIAC MYXOMA ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CEREBELLAR ISCHAEMIA ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 2 FDA reports)
CEREBRAL VASOCONSTRICTION ( 2 FDA reports)
CHEMICAL INJURY ( 2 FDA reports)
CHEST EXPANSION DECREASED ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COLITIS MICROSCOPIC ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL ECTOPIC BLADDER ( 2 FDA reports)
CONGENITAL URETERIC ANOMALY ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
CORONARY ARTERY REOCCLUSION ( 2 FDA reports)
CRACKLES LUNG ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CSF TEST ABNORMAL ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 2 FDA reports)
DENTAL CARE ( 2 FDA reports)
DENTAL PLAQUE ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETIC AMYOTROPHY ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
EAR INJURY ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
EJECTION FRACTION ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENDODONTIC PROCEDURE ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 2 FDA reports)
EPICONDYLITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
EXERCISE TEST ABNORMAL ( 2 FDA reports)
EYE LASER SURGERY ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
EYELID IRRITATION ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
EYELID RETRACTION ( 2 FDA reports)
FACTOR VIII DEFICIENCY ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FLOPPY IRIS SYNDROME ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
FOOD AVERSION ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROOESOPHAGITIS ( 2 FDA reports)
GENITAL BURNING SENSATION ( 2 FDA reports)
GENITALIA EXTERNAL AMBIGUOUS ( 2 FDA reports)
GINGIVAL DISCOLOURATION ( 2 FDA reports)
GINGIVAL RECESSION ( 2 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMATOMA EVACUATION ( 2 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEART TRANSPLANT REJECTION ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HELLP SYNDROME ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 2 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HYDROMETRA ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPONATRAEMIC SYNDROME ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IMPLANT SITE DISCHARGE ( 2 FDA reports)
IMPLANT SITE THROMBOSIS ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INFUSION SITE THROMBOSIS ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE DISCOLOURATION ( 2 FDA reports)
INJECTION SITE DISCOMFORT ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE MOVEMENT IMPAIRMENT ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KIDNEY MALROTATION ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LAZINESS ( 2 FDA reports)
LENTICULAR OPACITIES ( 2 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
LIP INJURY ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 2 FDA reports)
LOWER MOTOR NEURONE LESION ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST NEGATIVE ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
MACULAR PSEUDOHOLE ( 2 FDA reports)
MACULE ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MEDICAL DEVICE REMOVAL ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
METASTATIC GASTRIC CANCER ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
METATARSALGIA ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MILLER FISHER SYNDROME ( 2 FDA reports)
MITRAL VALVE ATRESIA ( 2 FDA reports)
MIXED HYPERLIPIDAEMIA ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MORTON'S NEUROMA ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MUCOSAL ULCERATION ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 2 FDA reports)
MYOGLOBINAEMIA ( 2 FDA reports)
MYOPIA ( 2 FDA reports)
NAEVUS FLAMMEUS ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEONATAL ANURIA ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NODULE ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL OPERATION ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 2 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
OVARIAN ADENOMA ( 2 FDA reports)
PACEMAKER GENERATED RHYTHM ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PALPABLE PURPURA ( 2 FDA reports)
PANCREAS INFECTION ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARENT-CHILD PROBLEM ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARTNER STRESS ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PEDAL PULSE ABNORMAL ( 2 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERIPHERAL NERVE OPERATION ( 2 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PERONEAL NERVE INJURY ( 2 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PEYRONIE'S DISEASE ( 2 FDA reports)
PHANTOM PAIN ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PHARYNGEAL MASS ( 2 FDA reports)
PILOERECTION ( 2 FDA reports)
PITUITARY HAEMORRHAGE ( 2 FDA reports)
PLASMAPHERESIS ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PLEURAL CALCIFICATION ( 2 FDA reports)
PNEUMOBILIA ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
POISONING DELIBERATE ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POLYP ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST LAMINECTOMY SYNDROME ( 2 FDA reports)
POST PROCEDURAL CELLULITIS ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 2 FDA reports)
PROCEDURAL HYPERTENSION ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PRODUCT SIZE ISSUE ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PROSTATIC OPERATION ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PSEUDOLYMPHOMA ( 2 FDA reports)
PSYCHOTIC BEHAVIOUR ( 2 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 2 FDA reports)
PULMONARY GRANULOMA ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
RADICULOPATHY ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 2 FDA reports)
RECTOCELE ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
RENAL APLASIA ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL CANCER METASTATIC ( 2 FDA reports)
RENAL CYST RUPTURED ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
REPERFUSION ARRHYTHMIA ( 2 FDA reports)
REPETITIVE SPEECH ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
ROSACEA ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SALMONELLA SEPSIS ( 2 FDA reports)
SALMONELLOSIS ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
SILICOSIS ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SOMATISATION DISORDER ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
SPONTANEOUS PENILE ERECTION ( 2 FDA reports)
STARING ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
SWEAT GLAND DISORDER ( 2 FDA reports)
SYSTOLIC HYPERTENSION ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THORACIC OPERATION ( 2 FDA reports)
THROMBECTOMY ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
TOE OPERATION ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE COATED ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TRAUMATIC SHOCK ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TRUNCUS ARTERIOSUS PERSISTENT ( 2 FDA reports)
TUMOUR FLARE ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETHRAL HAEMORRHAGE ( 2 FDA reports)
URETHRAL PAIN ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URINARY TRACT NEOPLASM ( 2 FDA reports)
VAGINAL EROSION ( 2 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 2 FDA reports)
VASCULAR ANOMALY ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 2 FDA reports)
VASCULAR INSUFFICIENCY ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VEIN DISCOLOURATION ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VENOUS STENOSIS ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICLE RUPTURE ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR HYPOPLASIA ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VITREOUS DETACHMENT ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABORTION THREATENED ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABSTAINS FROM ALCOHOL ( 1 FDA reports)
ACNE PUSTULAR ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACTINIC ELASTOSIS ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ADRENOGENITAL SYNDROME ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALOPECIA SCARRING ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANDROGEN INSENSITIVITY SYNDROME ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANTERIOR CHAMBER DISORDER ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICIPATORY ANXIETY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS GRAFT ANEURYSM ( 1 FDA reports)
ARTERITIS CORONARY ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BARIUM SWALLOW ABNORMAL ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BED BUG INFESTATION ( 1 FDA reports)
BED REST ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BILATERAL HYDRONEPHROSIS ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BILIARY ISCHAEMIA ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
BLADDER IRRITATION ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD AMYLASE ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CARBON MONOXIDE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MM INCREASED ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD HOMOCYSTEINE ABNORMAL ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY HEIGHT ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BRANCHIAL CLEFT CYST ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST RECONSTRUCTION ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARBON DIOXIDE ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC ANEURYSM REPAIR ( 1 FDA reports)
CARDIAC COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 1 FDA reports)
CAROTID ARTERY BYPASS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CAROTID PULSE ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL AUTOSOMAL DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CERVICAL SPASM ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHEST WALL ABSCESS ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHLOROPSIA ( 1 FDA reports)
CHOLANGIOGRAM ABNORMAL ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLONAL EVOLUTION ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COCHLEA IMPLANT ( 1 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONGENITAL CEREBROVASCULAR ANOMALY ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COR PULMONALE ACUTE ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
CRANIAL NERVE INFECTION ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
CRYSTALLURIA ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DELAYED SLEEP PHASE ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMAL SINUS ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG PHYSIOLOGIC INCOMPATIBILITY ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENAL SCARRING ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSCHEZIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
ENTEROCELE ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIC FASCIITIS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERGOT POISONING ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXERCISE CAPACITY DECREASED ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTRUSION OF DEVICE ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYELASH DISCOLOURATION ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
FACIAL NEURALGIA ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEAR OF CROWDED PLACES ( 1 FDA reports)
FEMORAL NERVE INJURY ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FREE HAEMOGLOBIN PRESENT ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GAMMA RADIATION THERAPY ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTRITIS HYPERTROPHIC ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL GANGRENE ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GENITAL INJURY ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLAUCOMA SURGERY ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATURIA TRAUMATIC ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC ANGIOSARCOMA ( 1 FDA reports)
HEPATIC ARTERY ANEURYSM ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOBILIARY NEOPLASM ( 1 FDA reports)
HETEROPHORIA ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IDEAS OF REFERENCE ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
ILIAC VEIN THROMBOSIS ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFERTILITY MALE ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFUSION SITE ABSCESS ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE ULCER ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERTRIGO CANDIDA ( 1 FDA reports)
INTERVENTRICULAR SEPTUM RUPTURE ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIDOTOMY ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JAUNDICE EXTRAHEPATIC OBSTRUCTIVE ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LANGERHANS' CELL HISTIOCYTOSIS ( 1 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LENTICULAR PIGMENTATION ( 1 FDA reports)
LERICHE SYNDROME ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGAMENT PAIN ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDIASTINUM NEOPLASM ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENISCUS REMOVAL ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
METASTASES TO THORAX ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
METASTATIC UTERINE CANCER ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MICROGRAPHIA ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MIXED HEPATOCELLULAR CHOLANGIOCARCINOMA ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MUSCLE FIBROSIS ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYCOTIC ANEURYSM ( 1 FDA reports)
MYELOCYTOSIS ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYXOEDEMA COMA ( 1 FDA reports)
NAIL BED TENDERNESS ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NASAL SINUS CANCER ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHRITIS HAEMORRHAGIC ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUROMUSCULAR BLOCKADE ( 1 FDA reports)
NEUROMUSCULAR TOXICITY ( 1 FDA reports)
NEUROSYPHILIS ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODAL OSTEOARTHRITIS ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR MYASTHENIA ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OVARIAN HAEMORRHAGE ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OXYGEN CONSUMPTION ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PAINFUL RESPONSE TO NORMAL STIMULI ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENETRATING ABDOMINAL TRAUMA ( 1 FDA reports)
PENILE ERYTHEMA ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERICARDITIS TUBERCULOUS ( 1 FDA reports)
PERIHEPATIC DISCOMFORT ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL REVASCULARISATION ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBITIS DEEP ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHOBIA OF DRIVING ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHYSIOTHERAPY ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PITUITARY INFARCTION ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEUROTHOTONUS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORPHYRINS URINE INCREASED ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)
POSTINFARCTION ANGINA ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRESBYACUSIS ( 1 FDA reports)
PRESBYOPIA ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT CONTAINER ISSUE ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY RADIATION INJURY ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PUNCTURE SITE INFECTION ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PURULENT PERICARDITIS ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYOGENIC GRANULOMA ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIATION NECROSIS ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENIN DECREASED ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY THERAPY ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
ROTAVIRUS TEST POSITIVE ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 1 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 1 FDA reports)
SCROTAL ERYTHEMA ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEPTIC ENCEPHALOPATHY ( 1 FDA reports)
SERUM SEROTONIN DECREASED ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN GRAFT FAILURE ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN SENSITISATION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL CORD HERNIATION ( 1 FDA reports)
SPINAL CORD INJURY CERVICAL ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STENT-GRAFT MALFUNCTION ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TERMINAL DRIBBLING ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
TETANUS ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOSIS PROPHYLAXIS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONSIL CANCER ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TRACHEAL DEVIATION ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSAMINASES ( 1 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRANSIENT PSYCHOSIS ( 1 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TUMOUR PERFORATION ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URAEMIC ENCEPHALOPATHY ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY SEDIMENT ABNORMAL ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VAGINISMUS ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VASCULAR CAUTERISATION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENIPUNCTURE SITE REACTION ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VIROLOGIC FAILURE ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VITAMIN B1 INCREASED ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITREOUS DEGENERATION ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVA CYST ( 1 FDA reports)
VULVAL CANCER ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVAL HAEMORRHAGE ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
WISDOM TEETH REMOVAL ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)

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