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

PAIN ( 278 FDA reports)
DIARRHOEA ( 259 FDA reports)
NAUSEA ( 247 FDA reports)
ARTHRALGIA ( 218 FDA reports)
DRUG INEFFECTIVE ( 211 FDA reports)
FALL ( 196 FDA reports)
DYSPNOEA ( 187 FDA reports)
DIZZINESS ( 176 FDA reports)
FATIGUE ( 173 FDA reports)
BACK PAIN ( 165 FDA reports)
ANAEMIA ( 161 FDA reports)
VOMITING ( 159 FDA reports)
ANXIETY ( 158 FDA reports)
DEPRESSION ( 155 FDA reports)
ASTHENIA ( 151 FDA reports)
HEADACHE ( 151 FDA reports)
MYOCARDIAL INFARCTION ( 148 FDA reports)
WEIGHT DECREASED ( 147 FDA reports)
PAIN IN EXTREMITY ( 145 FDA reports)
CHEST PAIN ( 138 FDA reports)
PYREXIA ( 136 FDA reports)
OEDEMA PERIPHERAL ( 134 FDA reports)
ABDOMINAL PAIN UPPER ( 131 FDA reports)
PNEUMONIA ( 114 FDA reports)
RENAL FAILURE ( 110 FDA reports)
MALAISE ( 108 FDA reports)
MYALGIA ( 108 FDA reports)
PARAESTHESIA ( 103 FDA reports)
HYPERTENSION ( 100 FDA reports)
ARTHRITIS ( 99 FDA reports)
RASH ( 99 FDA reports)
CEREBROVASCULAR ACCIDENT ( 98 FDA reports)
ABDOMINAL PAIN ( 95 FDA reports)
OSTEOARTHRITIS ( 95 FDA reports)
HYPOAESTHESIA ( 94 FDA reports)
INSOMNIA ( 94 FDA reports)
DRUG INTERACTION ( 93 FDA reports)
HYPOTENSION ( 93 FDA reports)
RENAL FAILURE ACUTE ( 93 FDA reports)
ABDOMINAL DISCOMFORT ( 92 FDA reports)
WEIGHT INCREASED ( 85 FDA reports)
CONDITION AGGRAVATED ( 82 FDA reports)
MUSCLE SPASMS ( 81 FDA reports)
GAIT DISTURBANCE ( 78 FDA reports)
CONSTIPATION ( 77 FDA reports)
INJURY ( 76 FDA reports)
URINARY TRACT INFECTION ( 74 FDA reports)
COUGH ( 73 FDA reports)
VISION BLURRED ( 73 FDA reports)
HYPERSENSITIVITY ( 72 FDA reports)
DEHYDRATION ( 71 FDA reports)
ARTHROPATHY ( 69 FDA reports)
EMOTIONAL DISTRESS ( 69 FDA reports)
JOINT SWELLING ( 66 FDA reports)
CONFUSIONAL STATE ( 65 FDA reports)
BRONCHITIS ( 64 FDA reports)
CHILLS ( 64 FDA reports)
HYPOKALAEMIA ( 64 FDA reports)
PULMONARY EMBOLISM ( 64 FDA reports)
RHEUMATOID ARTHRITIS ( 64 FDA reports)
CONVULSION ( 63 FDA reports)
CORONARY ARTERY DISEASE ( 63 FDA reports)
HYPERHIDROSIS ( 62 FDA reports)
SYNCOPE ( 62 FDA reports)
AMNESIA ( 61 FDA reports)
BLOOD PRESSURE INCREASED ( 61 FDA reports)
DEATH ( 60 FDA reports)
DECREASED APPETITE ( 60 FDA reports)
FEELING ABNORMAL ( 60 FDA reports)
SOMNOLENCE ( 59 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 57 FDA reports)
SEPSIS ( 57 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 56 FDA reports)
PALPITATIONS ( 56 FDA reports)
CONTUSION ( 55 FDA reports)
PRURITUS ( 55 FDA reports)
LOSS OF CONSCIOUSNESS ( 54 FDA reports)
MUSCULAR WEAKNESS ( 54 FDA reports)
COLITIS ( 53 FDA reports)
TREMOR ( 53 FDA reports)
ALOPECIA ( 51 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 51 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 50 FDA reports)
DIABETES MELLITUS ( 50 FDA reports)
NEUROPATHY PERIPHERAL ( 50 FDA reports)
DYSPHAGIA ( 49 FDA reports)
HAEMOGLOBIN DECREASED ( 49 FDA reports)
HOT FLUSH ( 49 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 49 FDA reports)
DYSPEPSIA ( 48 FDA reports)
DRUG HYPERSENSITIVITY ( 47 FDA reports)
ABDOMINAL DISTENSION ( 46 FDA reports)
DIVERTICULUM ( 46 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 45 FDA reports)
IMPAIRED HEALING ( 45 FDA reports)
CELLULITIS ( 44 FDA reports)
OSTEONECROSIS OF JAW ( 44 FDA reports)
ATRIAL FIBRILLATION ( 43 FDA reports)
DEEP VEIN THROMBOSIS ( 43 FDA reports)
DYSPNOEA EXERTIONAL ( 43 FDA reports)
NECK PAIN ( 43 FDA reports)
PLEURAL EFFUSION ( 43 FDA reports)
GASTRIC DISORDER ( 42 FDA reports)
OSTEOMYELITIS ( 42 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 41 FDA reports)
NEPHROLITHIASIS ( 41 FDA reports)
ANOREXIA ( 40 FDA reports)
LYMPHADENOPATHY ( 40 FDA reports)
URTICARIA ( 40 FDA reports)
CATARACT ( 39 FDA reports)
MUSCULOSKELETAL PAIN ( 39 FDA reports)
RECTAL HAEMORRHAGE ( 39 FDA reports)
SLEEP APNOEA SYNDROME ( 39 FDA reports)
DYSGEUSIA ( 38 FDA reports)
NASOPHARYNGITIS ( 38 FDA reports)
DRUG EFFECT DECREASED ( 37 FDA reports)
DYSARTHRIA ( 37 FDA reports)
FLUSHING ( 37 FDA reports)
HAEMATURIA ( 37 FDA reports)
HIATUS HERNIA ( 37 FDA reports)
OEDEMA ( 37 FDA reports)
PULMONARY OEDEMA ( 37 FDA reports)
SHOCK ( 37 FDA reports)
MIGRAINE ( 36 FDA reports)
PANCYTOPENIA ( 36 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 35 FDA reports)
INFLUENZA LIKE ILLNESS ( 35 FDA reports)
ROAD TRAFFIC ACCIDENT ( 35 FDA reports)
BONE DISORDER ( 34 FDA reports)
BONE PAIN ( 34 FDA reports)
INFECTION ( 34 FDA reports)
MULTI-ORGAN FAILURE ( 34 FDA reports)
RENAL IMPAIRMENT ( 34 FDA reports)
DIVERTICULITIS ( 33 FDA reports)
DRUG TOXICITY ( 33 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 33 FDA reports)
UNEVALUABLE EVENT ( 33 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 33 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 32 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 32 FDA reports)
ERYTHEMA ( 32 FDA reports)
HYPERLIPIDAEMIA ( 32 FDA reports)
LARGE INTESTINAL ULCER ( 32 FDA reports)
GASTRITIS ( 31 FDA reports)
INJECTION SITE PAIN ( 31 FDA reports)
LUMBAR SPINAL STENOSIS ( 31 FDA reports)
MEMORY IMPAIRMENT ( 31 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 30 FDA reports)
BLOOD GLUCOSE INCREASED ( 30 FDA reports)
HAEMORRHAGE ( 30 FDA reports)
HYPOMAGNESAEMIA ( 30 FDA reports)
SUICIDAL IDEATION ( 30 FDA reports)
WHEEZING ( 30 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 29 FDA reports)
MITRAL VALVE INCOMPETENCE ( 29 FDA reports)
SCAR ( 29 FDA reports)
ANHEDONIA ( 28 FDA reports)
BALANCE DISORDER ( 28 FDA reports)
BODY HEIGHT DECREASED ( 28 FDA reports)
CHEST DISCOMFORT ( 28 FDA reports)
CORONARY ARTERY OCCLUSION ( 28 FDA reports)
DISORIENTATION ( 28 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 28 FDA reports)
DRY MOUTH ( 28 FDA reports)
HAEMORRHOIDS ( 28 FDA reports)
OSTEOPENIA ( 28 FDA reports)
PNEUMONIA ASPIRATION ( 28 FDA reports)
TACHYCARDIA ( 28 FDA reports)
ANGINA PECTORIS ( 27 FDA reports)
BLOOD CREATININE INCREASED ( 27 FDA reports)
CARDIAC DISORDER ( 27 FDA reports)
CIRCULATORY COLLAPSE ( 27 FDA reports)
HEPATIC ENZYME INCREASED ( 27 FDA reports)
LUNG NEOPLASM ( 27 FDA reports)
METABOLIC ACIDOSIS ( 27 FDA reports)
OSTEONECROSIS ( 27 FDA reports)
TOOTH DISORDER ( 27 FDA reports)
TOOTH EXTRACTION ( 27 FDA reports)
TYPE 2 DIABETES MELLITUS ( 27 FDA reports)
BLOOD PRESSURE DECREASED ( 26 FDA reports)
CARDIO-RESPIRATORY ARREST ( 26 FDA reports)
DYSSTASIA ( 26 FDA reports)
JAW DISORDER ( 26 FDA reports)
MYOCARDIAL ISCHAEMIA ( 26 FDA reports)
SPINAL OSTEOARTHRITIS ( 26 FDA reports)
ARRHYTHMIA ( 25 FDA reports)
BRADYCARDIA ( 25 FDA reports)
DYSPHONIA ( 25 FDA reports)
FLATULENCE ( 25 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 25 FDA reports)
LETHARGY ( 25 FDA reports)
STAPHYLOCOCCAL INFECTION ( 25 FDA reports)
SWELLING ( 25 FDA reports)
SWELLING FACE ( 25 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 24 FDA reports)
HAEMATEMESIS ( 24 FDA reports)
HEART RATE INCREASED ( 24 FDA reports)
HERPES ZOSTER ( 24 FDA reports)
HYPERGLYCAEMIA ( 24 FDA reports)
HYPOGLYCAEMIA ( 24 FDA reports)
MOOD SWINGS ( 24 FDA reports)
NERVOUSNESS ( 24 FDA reports)
OSTEOPOROSIS ( 24 FDA reports)
SINUSITIS ( 24 FDA reports)
VAGINAL HAEMORRHAGE ( 24 FDA reports)
ASTHMA ( 23 FDA reports)
CANDIDIASIS ( 23 FDA reports)
DYSKINESIA ( 23 FDA reports)
FEELING HOT ( 23 FDA reports)
HYPERKALAEMIA ( 23 FDA reports)
HYPOTHYROIDISM ( 23 FDA reports)
LEUKOCYTOSIS ( 23 FDA reports)
MEDICATION ERROR ( 23 FDA reports)
ORTHOSTATIC HYPOTENSION ( 23 FDA reports)
PANIC ATTACK ( 23 FDA reports)
PLEURITIC PAIN ( 23 FDA reports)
PULMONARY HYPERTENSION ( 23 FDA reports)
CHOLESTASIS ( 22 FDA reports)
DEAFNESS ( 22 FDA reports)
DENTAL CARIES ( 22 FDA reports)
FIBROMYALGIA ( 22 FDA reports)
HEART RATE IRREGULAR ( 22 FDA reports)
OVERDOSE ( 22 FDA reports)
PALLOR ( 22 FDA reports)
PANCREATITIS ( 22 FDA reports)
TOOTHACHE ( 22 FDA reports)
ANOXIC ENCEPHALOPATHY ( 21 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 21 FDA reports)
BLOOD POTASSIUM DECREASED ( 21 FDA reports)
BLOOD UREA INCREASED ( 21 FDA reports)
BREAST CANCER ( 21 FDA reports)
BURNING SENSATION ( 21 FDA reports)
CARDIAC ARREST ( 21 FDA reports)
CARDIOMEGALY ( 21 FDA reports)
CYST ( 21 FDA reports)
DYSURIA ( 21 FDA reports)
FAECES DISCOLOURED ( 21 FDA reports)
FOOT FRACTURE ( 21 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 21 FDA reports)
GASTRIC ULCER ( 21 FDA reports)
GASTROENTERITIS ( 21 FDA reports)
HYPOCALCAEMIA ( 21 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 21 FDA reports)
LUNG NEOPLASM MALIGNANT ( 21 FDA reports)
MELAENA ( 21 FDA reports)
NEURALGIA ( 21 FDA reports)
OROPHARYNGEAL PAIN ( 21 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 21 FDA reports)
POLLAKIURIA ( 21 FDA reports)
POSTOPERATIVE ILEUS ( 21 FDA reports)
RESPIRATORY FAILURE ( 21 FDA reports)
SYPHILIS ( 21 FDA reports)
THROMBOCYTOPENIA ( 21 FDA reports)
BASAL CELL CARCINOMA ( 20 FDA reports)
BLISTER ( 20 FDA reports)
CARPAL TUNNEL SYNDROME ( 20 FDA reports)
DRUG DEPENDENCE ( 20 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 20 FDA reports)
INTESTINAL OBSTRUCTION ( 20 FDA reports)
NEOPLASM MALIGNANT ( 20 FDA reports)
OFF LABEL USE ( 20 FDA reports)
POLYNEUROPATHY ( 20 FDA reports)
RASH GENERALISED ( 20 FDA reports)
RETROPERITONEAL FIBROSIS ( 20 FDA reports)
TREATMENT NONCOMPLIANCE ( 20 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 19 FDA reports)
DISCOMFORT ( 19 FDA reports)
DRY EYE ( 19 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 19 FDA reports)
HEPATIC STEATOSIS ( 19 FDA reports)
HYPOXIA ( 19 FDA reports)
INCORRECT DOSE ADMINISTERED ( 19 FDA reports)
INJECTION SITE ERYTHEMA ( 19 FDA reports)
JAUNDICE ( 19 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 19 FDA reports)
PAIN IN JAW ( 19 FDA reports)
RHABDOMYOLYSIS ( 19 FDA reports)
RHINORRHOEA ( 19 FDA reports)
SPEECH DISORDER ( 19 FDA reports)
SPINAL COLUMN STENOSIS ( 19 FDA reports)
SURGERY ( 19 FDA reports)
URINARY INCONTINENCE ( 19 FDA reports)
VASCULITIS ( 19 FDA reports)
ARTERIOSCLEROSIS ( 18 FDA reports)
BACK DISORDER ( 18 FDA reports)
CARDIAC FAILURE ( 18 FDA reports)
CHOLELITHIASIS ( 18 FDA reports)
CYSTITIS ( 18 FDA reports)
DIFFICULTY IN WALKING ( 18 FDA reports)
GASTROINTESTINAL DISORDER ( 18 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 18 FDA reports)
IMPAIRED DRIVING ABILITY ( 18 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 18 FDA reports)
IRRITABILITY ( 18 FDA reports)
KNEE ARTHROPLASTY ( 18 FDA reports)
ORAL HERPES ( 18 FDA reports)
SEPTIC SHOCK ( 18 FDA reports)
THYROID DISORDER ( 18 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 18 FDA reports)
ULCER ( 18 FDA reports)
VERTIGO ( 18 FDA reports)
VISUAL DISTURBANCE ( 18 FDA reports)
AGGRESSION ( 17 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 17 FDA reports)
CHROMATURIA ( 17 FDA reports)
CRYING ( 17 FDA reports)
DEPRESSED MOOD ( 17 FDA reports)
GINGIVAL PAIN ( 17 FDA reports)
HAEMATOCHEZIA ( 17 FDA reports)
HEART RATE DECREASED ( 17 FDA reports)
INFLAMMATION ( 17 FDA reports)
JOINT STIFFNESS ( 17 FDA reports)
LUNG DISORDER ( 17 FDA reports)
MENTAL DISORDER ( 17 FDA reports)
METASTASES TO LUNG ( 17 FDA reports)
MOUTH ULCERATION ( 17 FDA reports)
NERVOUS SYSTEM DISORDER ( 17 FDA reports)
NOCTURIA ( 17 FDA reports)
SPINAL FRACTURE ( 17 FDA reports)
SPONDYLOLISTHESIS ( 17 FDA reports)
STRESS FRACTURE ( 17 FDA reports)
SUICIDE ATTEMPT ( 17 FDA reports)
TOOTH INFECTION ( 17 FDA reports)
VISUAL ACUITY REDUCED ( 17 FDA reports)
ADVERSE EVENT ( 16 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 16 FDA reports)
BONE MARROW FAILURE ( 16 FDA reports)
CARDIOGENIC SHOCK ( 16 FDA reports)
DEFORMITY ( 16 FDA reports)
DRUG LEVEL INCREASED ( 16 FDA reports)
GOUT ( 16 FDA reports)
HAEMODIALYSIS ( 16 FDA reports)
HEPATIC FAILURE ( 16 FDA reports)
IRRITABLE BOWEL SYNDROME ( 16 FDA reports)
JOINT DISLOCATION ( 16 FDA reports)
NEUROPATHY ( 16 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 16 FDA reports)
PERONEAL NERVE PALSY ( 16 FDA reports)
PRODUCT QUALITY ISSUE ( 16 FDA reports)
PSORIASIS ( 16 FDA reports)
PULMONARY FIBROSIS ( 16 FDA reports)
RENAL DISORDER ( 16 FDA reports)
RESPIRATORY DISORDER ( 16 FDA reports)
ROTATOR CUFF SYNDROME ( 16 FDA reports)
STRESS ( 16 FDA reports)
TOOTH ABSCESS ( 16 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 16 FDA reports)
URINARY RETENTION ( 16 FDA reports)
VENTRICULAR FIBRILLATION ( 16 FDA reports)
ABASIA ( 15 FDA reports)
ABSCESS ( 15 FDA reports)
ATELECTASIS ( 15 FDA reports)
COLONIC POLYP ( 15 FDA reports)
DECUBITUS ULCER ( 15 FDA reports)
EAR PAIN ( 15 FDA reports)
ENDODONTIC PROCEDURE ( 15 FDA reports)
ERECTILE DYSFUNCTION ( 15 FDA reports)
FACE INJURY ( 15 FDA reports)
FLUID RETENTION ( 15 FDA reports)
HAEMATOCRIT DECREASED ( 15 FDA reports)
HAEMOPTYSIS ( 15 FDA reports)
HYPERTHYROIDISM ( 15 FDA reports)
HYPONATRAEMIA ( 15 FDA reports)
HYPOPHOSPHATAEMIA ( 15 FDA reports)
INFUSION RELATED REACTION ( 15 FDA reports)
MOBILITY DECREASED ( 15 FDA reports)
NASAL CONGESTION ( 15 FDA reports)
RASH PRURITIC ( 15 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 15 FDA reports)
RENAL CYST ( 15 FDA reports)
SKIN LESION ( 15 FDA reports)
AGITATION ( 14 FDA reports)
ANAPHYLACTIC REACTION ( 14 FDA reports)
ANAPHYLACTIC SHOCK ( 14 FDA reports)
BACK INJURY ( 14 FDA reports)
CARDIOMYOPATHY ( 14 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 14 FDA reports)
CHEST X-RAY ABNORMAL ( 14 FDA reports)
CHOKING ( 14 FDA reports)
CORONARY ARTERY STENOSIS ( 14 FDA reports)
DENTURE WEARER ( 14 FDA reports)
DIABETIC COMA ( 14 FDA reports)
DISTURBANCE IN ATTENTION ( 14 FDA reports)
FEELING COLD ( 14 FDA reports)
FEMUR FRACTURE ( 14 FDA reports)
FIBROSIS ( 14 FDA reports)
GASTRIC HAEMORRHAGE ( 14 FDA reports)
GLAUCOMA ( 14 FDA reports)
GLOSSODYNIA ( 14 FDA reports)
HALLUCINATION ( 14 FDA reports)
HEAD INJURY ( 14 FDA reports)
HYPOPHAGIA ( 14 FDA reports)
INJECTION SITE REACTION ( 14 FDA reports)
LOWER LIMB FRACTURE ( 14 FDA reports)
MACULOPATHY ( 14 FDA reports)
NEUTROPENIA ( 14 FDA reports)
NIGHT SWEATS ( 14 FDA reports)
POST PROCEDURAL COMPLICATION ( 14 FDA reports)
SINUS DISORDER ( 14 FDA reports)
SLEEP DISORDER ( 14 FDA reports)
STOMATITIS ( 14 FDA reports)
TINNITUS ( 14 FDA reports)
TOOTH FRACTURE ( 14 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 13 FDA reports)
BLOOD SODIUM DECREASED ( 13 FDA reports)
DISEASE PROGRESSION ( 13 FDA reports)
ECONOMIC PROBLEM ( 13 FDA reports)
EPISTAXIS ( 13 FDA reports)
EYE DISORDER ( 13 FDA reports)
FRACTURE NONUNION ( 13 FDA reports)
HIP FRACTURE ( 13 FDA reports)
HYPERVENTILATION ( 13 FDA reports)
ILL-DEFINED DISORDER ( 13 FDA reports)
IMPAIRED WORK ABILITY ( 13 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 13 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 13 FDA reports)
MENISCUS LESION ( 13 FDA reports)
MUSCLE STRAIN ( 13 FDA reports)
PERITONEAL TUBERCULOSIS ( 13 FDA reports)
SKIN DISORDER ( 13 FDA reports)
STOMACH DISCOMFORT ( 13 FDA reports)
VISUAL IMPAIRMENT ( 13 FDA reports)
ACTINIC KERATOSIS ( 12 FDA reports)
APHASIA ( 12 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 12 FDA reports)
BONE DEBRIDEMENT ( 12 FDA reports)
BURSITIS ( 12 FDA reports)
CARDIAC FIBRILLATION ( 12 FDA reports)
COLON CANCER ( 12 FDA reports)
COMA ( 12 FDA reports)
DECREASED INTEREST ( 12 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 12 FDA reports)
EYE SWELLING ( 12 FDA reports)
FEAR ( 12 FDA reports)
HEPATITIS ( 12 FDA reports)
HIP ARTHROPLASTY ( 12 FDA reports)
INFLUENZA ( 12 FDA reports)
INJECTION SITE HAEMORRHAGE ( 12 FDA reports)
INTENTIONAL OVERDOSE ( 12 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 12 FDA reports)
MALIGNANT MELANOMA ( 12 FDA reports)
MASS ( 12 FDA reports)
MULTIPLE FRACTURES ( 12 FDA reports)
MULTIPLE SCLEROSIS ( 12 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 12 FDA reports)
MYOSITIS ( 12 FDA reports)
OBESITY ( 12 FDA reports)
PERIODONTITIS ( 12 FDA reports)
PLATELET AGGREGATION INCREASED ( 12 FDA reports)
SWOLLEN TONGUE ( 12 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 12 FDA reports)
TENDERNESS ( 12 FDA reports)
THROMBOSIS ( 12 FDA reports)
TONGUE DISORDER ( 12 FDA reports)
UPPER LIMB FRACTURE ( 12 FDA reports)
UTERINE LEIOMYOMA ( 12 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 12 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 12 FDA reports)
ABNORMAL DREAMS ( 11 FDA reports)
ABSCESS JAW ( 11 FDA reports)
ACCIDENTAL OVERDOSE ( 11 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 11 FDA reports)
ANEURYSM ( 11 FDA reports)
APLASTIC ANAEMIA ( 11 FDA reports)
BLOOD ALBUMIN DECREASED ( 11 FDA reports)
BLOOD BILIRUBIN INCREASED ( 11 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 11 FDA reports)
BLOOD URINE PRESENT ( 11 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 11 FDA reports)
CATARACT OPERATION ( 11 FDA reports)
COMPRESSION FRACTURE ( 11 FDA reports)
COSTOCHONDRITIS ( 11 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 11 FDA reports)
DIPLOPIA ( 11 FDA reports)
DYSLIPIDAEMIA ( 11 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 11 FDA reports)
GASTROINTESTINAL PAIN ( 11 FDA reports)
HERNIA ( 11 FDA reports)
INJECTION SITE HAEMATOMA ( 11 FDA reports)
JOINT SPRAIN ( 11 FDA reports)
LEUKOPENIA ( 11 FDA reports)
LIMB INJURY ( 11 FDA reports)
LIVER DISORDER ( 11 FDA reports)
MYOPATHY ( 11 FDA reports)
ORAL PAIN ( 11 FDA reports)
PARKINSON'S DISEASE ( 11 FDA reports)
PNEUMOTHORAX ( 11 FDA reports)
RENAL FAILURE CHRONIC ( 11 FDA reports)
SCIATICA ( 11 FDA reports)
SKIN DISCOLOURATION ( 11 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 11 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 11 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 11 FDA reports)
VITAMIN D DEFICIENCY ( 11 FDA reports)
ABDOMINAL PAIN LOWER ( 10 FDA reports)
ANURIA ( 10 FDA reports)
BEDRIDDEN ( 10 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 10 FDA reports)
CALCULUS BLADDER ( 10 FDA reports)
CARDIAC OPERATION ( 10 FDA reports)
CARDIOPULMONARY FAILURE ( 10 FDA reports)
CEREBRAL INFARCTION ( 10 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 10 FDA reports)
DIABETIC RETINOPATHY ( 10 FDA reports)
DRUG ADMINISTRATION ERROR ( 10 FDA reports)
DUODENAL ULCER ( 10 FDA reports)
EXOSTOSIS ( 10 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 10 FDA reports)
FOOT DEFORMITY ( 10 FDA reports)
GINGIVAL DISORDER ( 10 FDA reports)
GINGIVAL SWELLING ( 10 FDA reports)
HEMIPARESIS ( 10 FDA reports)
HERPES SIMPLEX ( 10 FDA reports)
INGROWING NAIL ( 10 FDA reports)
INTESTINAL PERFORATION ( 10 FDA reports)
IRON DEFICIENCY ANAEMIA ( 10 FDA reports)
LIBIDO DECREASED ( 10 FDA reports)
LYMPHOMA ( 10 FDA reports)
MUCOSAL INFLAMMATION ( 10 FDA reports)
MUSCLE INJURY ( 10 FDA reports)
NEPHROPATHY TOXIC ( 10 FDA reports)
NEURITIS ( 10 FDA reports)
OSTEOLYSIS ( 10 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 10 FDA reports)
POST POLIO SYNDROME ( 10 FDA reports)
POSTNASAL DRIP ( 10 FDA reports)
PRESYNCOPE ( 10 FDA reports)
PSORIATIC ARTHROPATHY ( 10 FDA reports)
PULMONARY TUBERCULOSIS ( 10 FDA reports)
PUNCTATE KERATITIS ( 10 FDA reports)
PURPURA ( 10 FDA reports)
RAYNAUD'S PHENOMENON ( 10 FDA reports)
TONGUE BITING ( 10 FDA reports)
ANDROGENS ABNORMAL ( 9 FDA reports)
ANKLE FRACTURE ( 9 FDA reports)
B-CELL LYMPHOMA ( 9 FDA reports)
BLINDNESS ( 9 FDA reports)
BLOOD POTASSIUM INCREASED ( 9 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 9 FDA reports)
BONE DENSITY DECREASED ( 9 FDA reports)
BREAST CALCIFICATIONS ( 9 FDA reports)
CARDIAC MURMUR ( 9 FDA reports)
CAROTID BRUIT ( 9 FDA reports)
DRUG DOSE OMISSION ( 9 FDA reports)
EJECTION FRACTION DECREASED ( 9 FDA reports)
EMPHYSEMA ( 9 FDA reports)
EUPHORIC MOOD ( 9 FDA reports)
EYELID PTOSIS ( 9 FDA reports)
FUNGAL INFECTION ( 9 FDA reports)
FURUNCLE ( 9 FDA reports)
HEART INJURY ( 9 FDA reports)
HYPERAEMIA ( 9 FDA reports)
HYPERCALCAEMIA ( 9 FDA reports)
IMMUNOSUPPRESSION ( 9 FDA reports)
INJECTION SITE URTICARIA ( 9 FDA reports)
LARYNGOSPASM ( 9 FDA reports)
LIP SWELLING ( 9 FDA reports)
LOOSE TOOTH ( 9 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 9 FDA reports)
MARROW HYPERPLASIA ( 9 FDA reports)
MOVEMENT DISORDER ( 9 FDA reports)
OESOPHAGITIS ( 9 FDA reports)
ORAL DISCOMFORT ( 9 FDA reports)
OSTEITIS ( 9 FDA reports)
PANCREATITIS ACUTE ( 9 FDA reports)
PATHOLOGICAL GAMBLING ( 9 FDA reports)
PEPTIC ULCER ( 9 FDA reports)
POLYURIA ( 9 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 9 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 9 FDA reports)
RADICULITIS LUMBOSACRAL ( 9 FDA reports)
RASH MACULAR ( 9 FDA reports)
RECTAL FISSURE ( 9 FDA reports)
RENAL INJURY ( 9 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 9 FDA reports)
RIB FRACTURE ( 9 FDA reports)
ROSACEA ( 9 FDA reports)
SPINAL CORD DISORDER ( 9 FDA reports)
SPINAL LAMINECTOMY ( 9 FDA reports)
TARSAL TUNNEL SYNDROME ( 9 FDA reports)
TENDON RUPTURE ( 9 FDA reports)
THIRST ( 9 FDA reports)
TONGUE INJURY ( 9 FDA reports)
TOOTH LOSS ( 9 FDA reports)
UNRESPONSIVE TO STIMULI ( 9 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 9 FDA reports)
ANGIONEUROTIC OEDEMA ( 8 FDA reports)
ANKYLOSING SPONDYLITIS ( 8 FDA reports)
ANXIETY DISORDER ( 8 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 8 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 8 FDA reports)
ARTHROPOD BITE ( 8 FDA reports)
BLINDNESS UNILATERAL ( 8 FDA reports)
BLOOD CALCIUM DECREASED ( 8 FDA reports)
BLOOD PRESSURE ABNORMAL ( 8 FDA reports)
BONE LESION ( 8 FDA reports)
BONE LOSS ( 8 FDA reports)
BRAIN NEOPLASM ( 8 FDA reports)
BREATH ODOUR ( 8 FDA reports)
BRONCHOPNEUMONIA ( 8 FDA reports)
CHEST INJURY ( 8 FDA reports)
CHOLECYSTECTOMY ( 8 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 8 FDA reports)
DENTAL OPERATION ( 8 FDA reports)
DRESSLER'S SYNDROME ( 8 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 8 FDA reports)
ENZYME ABNORMALITY ( 8 FDA reports)
EXPIRED DRUG ADMINISTERED ( 8 FDA reports)
FASCIITIS ( 8 FDA reports)
FOOT OPERATION ( 8 FDA reports)
GASTRIC INFECTION ( 8 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 8 FDA reports)
HIP SURGERY ( 8 FDA reports)
HYDRONEPHROSIS ( 8 FDA reports)
HYPERPHAGIA ( 8 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 8 FDA reports)
INCISIONAL DRAINAGE ( 8 FDA reports)
INJECTION SITE PRURITUS ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 8 FDA reports)
JOINT INJURY ( 8 FDA reports)
KNEE OPERATION ( 8 FDA reports)
LIFE EXPECTANCY SHORTENED ( 8 FDA reports)
LOCAL SWELLING ( 8 FDA reports)
LUMBAR RADICULOPATHY ( 8 FDA reports)
LUPUS-LIKE SYNDROME ( 8 FDA reports)
METASTASIS ( 8 FDA reports)
METRORRHAGIA ( 8 FDA reports)
NERVE INJURY ( 8 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 8 FDA reports)
ORAL CAVITY FISTULA ( 8 FDA reports)
POST PROCEDURAL OEDEMA ( 8 FDA reports)
POSTURE ABNORMAL ( 8 FDA reports)
RASH MACULO-PAPULAR ( 8 FDA reports)
SEQUESTRECTOMY ( 8 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 8 FDA reports)
TENOSYNOVITIS ( 8 FDA reports)
VERTEBROPLASTY ( 8 FDA reports)
VIITH NERVE PARALYSIS ( 8 FDA reports)
WRIST FRACTURE ( 8 FDA reports)
ACCIDENTAL EXPOSURE ( 7 FDA reports)
ACCOMMODATION DISORDER ( 7 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 7 FDA reports)
ACUTE SINUSITIS ( 7 FDA reports)
ASPIRATION ( 7 FDA reports)
BLOOD GLUCOSE DECREASED ( 7 FDA reports)
BLOOD UREA DECREASED ( 7 FDA reports)
BREAST ENLARGEMENT ( 7 FDA reports)
BRONCHOSPASM ( 7 FDA reports)
CATARACT OPERATION COMPLICATION ( 7 FDA reports)
CHOLECYSTITIS ( 7 FDA reports)
CHONDROPATHY ( 7 FDA reports)
COLD SWEAT ( 7 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 7 FDA reports)
CYANOSIS ( 7 FDA reports)
DEBRIDEMENT ( 7 FDA reports)
DENTAL IMPLANTATION ( 7 FDA reports)
DEVICE MALFUNCTION ( 7 FDA reports)
DIASTOLIC DYSFUNCTION ( 7 FDA reports)
DILATATION ATRIAL ( 7 FDA reports)
DISEASE RECURRENCE ( 7 FDA reports)
DRUG ABUSER ( 7 FDA reports)
DRUG ERUPTION ( 7 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 7 FDA reports)
DUODENAL ULCER PERFORATION ( 7 FDA reports)
ENCEPHALITIS ( 7 FDA reports)
EYE HAEMORRHAGE ( 7 FDA reports)
FRACTURE ( 7 FDA reports)
GRANULOMA ( 7 FDA reports)
HAND FRACTURE ( 7 FDA reports)
HYPERCHOLESTEROLAEMIA ( 7 FDA reports)
INCONTINENCE ( 7 FDA reports)
INCREASED TENDENCY TO BRUISE ( 7 FDA reports)
INJECTION SITE EXTRAVASATION ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
ISCHAEMIA ( 7 FDA reports)
LEUKAEMIA ( 7 FDA reports)
LITHOTRIPSY ( 7 FDA reports)
LUNG HYPERINFLATION ( 7 FDA reports)
LUNG INFILTRATION ( 7 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 7 FDA reports)
MANIA ( 7 FDA reports)
MEDICAL DEVICE COMPLICATION ( 7 FDA reports)
METASTASES TO BONE ( 7 FDA reports)
MICTURITION URGENCY ( 7 FDA reports)
MUSCLE CRAMP ( 7 FDA reports)
MYELODYSPLASTIC SYNDROME ( 7 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 7 FDA reports)
NASAL DISORDER ( 7 FDA reports)
NASAL ULCER ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
NOSOCOMIAL INFECTION ( 7 FDA reports)
ODYNOPHAGIA ( 7 FDA reports)
OEDEMA MOUTH ( 7 FDA reports)
PANCREATIC CARCINOMA ( 7 FDA reports)
PATHOLOGICAL FRACTURE ( 7 FDA reports)
PERITONITIS ( 7 FDA reports)
PHYSICAL DISABILITY ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 7 FDA reports)
PROSTATE CANCER ( 7 FDA reports)
PSEUDOMONAS INFECTION ( 7 FDA reports)
PURPURA SENILE ( 7 FDA reports)
RADICULITIS ( 7 FDA reports)
RASH ERYTHEMATOUS ( 7 FDA reports)
REFLUX OESOPHAGITIS ( 7 FDA reports)
RESPIRATORY DISTRESS ( 7 FDA reports)
RHEUMATOID NODULE ( 7 FDA reports)
SEBORRHOEIC KERATOSIS ( 7 FDA reports)
SEDATION ( 7 FDA reports)
SHOULDER OPERATION ( 7 FDA reports)
SINUS BRADYCARDIA ( 7 FDA reports)
SINUS TACHYCARDIA ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
SKIN LACERATION ( 7 FDA reports)
SKIN OPERATION ( 7 FDA reports)
SPINAL COMPRESSION FRACTURE ( 7 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 7 FDA reports)
THROAT IRRITATION ( 7 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 7 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
VAGINAL INFECTION ( 7 FDA reports)
VITAMIN D DECREASED ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ADVERSE DRUG REACTION ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 6 FDA reports)
ANAL ABSCESS ( 6 FDA reports)
AORTIC VALVE INCOMPETENCE ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
BACTERIAL INFECTION ( 6 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 6 FDA reports)
BIPOLAR I DISORDER ( 6 FDA reports)
BLOOD CULTURE POSITIVE ( 6 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 6 FDA reports)
CEREBRAL ATROPHY ( 6 FDA reports)
COGNITIVE DISORDER ( 6 FDA reports)
CORNEAL SCAR ( 6 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 6 FDA reports)
DENTAL FISTULA ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DIABETIC FOOT INFECTION ( 6 FDA reports)
DIABETIC NEUROPATHY ( 6 FDA reports)
DIVERTICULUM INTESTINAL ( 6 FDA reports)
DRUG INTOLERANCE ( 6 FDA reports)
DRUG LEVEL DECREASED ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
DYSAESTHESIA ( 6 FDA reports)
DYSMENORRHOEA ( 6 FDA reports)
EATING DISORDER ( 6 FDA reports)
ELECTROPHORESIS ABNORMAL ( 6 FDA reports)
EMOTIONAL DISORDER ( 6 FDA reports)
ENDOMETRIOSIS ( 6 FDA reports)
ENTEROVESICAL FISTULA ( 6 FDA reports)
GALLBLADDER DISORDER ( 6 FDA reports)
GANGRENE ( 6 FDA reports)
GASTRIC ULCER PERFORATION ( 6 FDA reports)
GASTROENTERITIS SALMONELLA ( 6 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 6 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 6 FDA reports)
GROIN PAIN ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HEPATIC CIRRHOSIS ( 6 FDA reports)
HEPATIC LESION ( 6 FDA reports)
HUMERUS FRACTURE ( 6 FDA reports)
HUNGER ( 6 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 6 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 6 FDA reports)
HYPERPLASIA ( 6 FDA reports)
HYPERTONIC BLADDER ( 6 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
INJECTION SITE SWELLING ( 6 FDA reports)
INTENTIONAL DRUG MISUSE ( 6 FDA reports)
INTENTIONAL SELF-INJURY ( 6 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 6 FDA reports)
ISCHAEMIC STROKE ( 6 FDA reports)
JOINT ARTHROPLASTY ( 6 FDA reports)
LABILE HYPERTENSION ( 6 FDA reports)
LEFT ATRIAL DILATATION ( 6 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 6 FDA reports)
LIGAMENT RUPTURE ( 6 FDA reports)
MAJOR DEPRESSION ( 6 FDA reports)
MENOPAUSE ( 6 FDA reports)
METASTASES TO LYMPH NODES ( 6 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 6 FDA reports)
MIDDLE INSOMNIA ( 6 FDA reports)
MIGRAINE WITH AURA ( 6 FDA reports)
MITRAL VALVE REPAIR ( 6 FDA reports)
MULTIPLE ALLERGIES ( 6 FDA reports)
MYELOMA RECURRENCE ( 6 FDA reports)
NEPHROSCLEROSIS ( 6 FDA reports)
NEUROMYOPATHY ( 6 FDA reports)
NIGHTMARE ( 6 FDA reports)
OESOPHAGEAL DISORDER ( 6 FDA reports)
PARALYSIS ( 6 FDA reports)
PELVIC PAIN ( 6 FDA reports)
PHOTOSENSITIVITY REACTION ( 6 FDA reports)
PLATELET COUNT INCREASED ( 6 FDA reports)
POLYP ( 6 FDA reports)
POOR QUALITY SLEEP ( 6 FDA reports)
PRURITUS GENERALISED ( 6 FDA reports)
PSEUDOPOLYPOSIS ( 6 FDA reports)
PSYCHOTIC DISORDER ( 6 FDA reports)
PULMONARY INFARCTION ( 6 FDA reports)
RADICULOPATHY ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
RESORPTION BONE INCREASED ( 6 FDA reports)
RESTLESSNESS ( 6 FDA reports)
RHINITIS ALLERGIC ( 6 FDA reports)
SENSORY DISTURBANCE ( 6 FDA reports)
SINOBRONCHITIS ( 6 FDA reports)
SINUS ARRHYTHMIA ( 6 FDA reports)
SKELETAL INJURY ( 6 FDA reports)
SKIN ULCER ( 6 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 6 FDA reports)
SPINAL FUSION SURGERY ( 6 FDA reports)
SPINAL LIGAMENT OSSIFICATION ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
TEMPERATURE INTOLERANCE ( 6 FDA reports)
TESTICULAR ATROPHY ( 6 FDA reports)
THROAT TIGHTNESS ( 6 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 6 FDA reports)
TONGUE ULCERATION ( 6 FDA reports)
VERTIGO POSITIONAL ( 6 FDA reports)
VESTIBULAR DISORDER ( 6 FDA reports)
WALKING AID USER ( 6 FDA reports)
WHEELCHAIR USER ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
ANAEMIA POSTOPERATIVE ( 5 FDA reports)
ANGINA UNSTABLE ( 5 FDA reports)
APPLICATION SITE ERYTHEMA ( 5 FDA reports)
APPLICATION SITE RASH ( 5 FDA reports)
ATRIAL FLUTTER ( 5 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
BLADDER SPASM ( 5 FDA reports)
BLOOD COUNT ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
BURNS THIRD DEGREE ( 5 FDA reports)
CHOKING SENSATION ( 5 FDA reports)
COLITIS ISCHAEMIC ( 5 FDA reports)
COLITIS ULCERATIVE ( 5 FDA reports)
CULTURE URINE ( 5 FDA reports)
DELIRIUM ( 5 FDA reports)
DEMYELINATION ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
DISABILITY ( 5 FDA reports)
DRUG ABUSE ( 5 FDA reports)
DUODENAL STENOSIS ( 5 FDA reports)
ELECTROLYTE IMBALANCE ( 5 FDA reports)
ERUCTATION ( 5 FDA reports)
ESCHERICHIA INFECTION ( 5 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 5 FDA reports)
EXTRASYSTOLES ( 5 FDA reports)
EYE IRRITATION ( 5 FDA reports)
EYE PAIN ( 5 FDA reports)
FACET JOINT SYNDROME ( 5 FDA reports)
GASTRITIS EROSIVE ( 5 FDA reports)
GASTROENTERITIS VIRAL ( 5 FDA reports)
GENERALISED ERYTHEMA ( 5 FDA reports)
GINGIVITIS ( 5 FDA reports)
HAEMANGIOMA OF LIVER ( 5 FDA reports)
HAEMORRHAGIC ANAEMIA ( 5 FDA reports)
HEPATOCELLULAR INJURY ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HOARSENESS ( 5 FDA reports)
HYPOVOLAEMIA ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
INJECTION SITE IRRITATION ( 5 FDA reports)
INJECTION SITE RASH ( 5 FDA reports)
LACERATION ( 5 FDA reports)
LIVER INJURY ( 5 FDA reports)
MACULAR DEGENERATION ( 5 FDA reports)
MENORRHAGIA ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
MULTIPLE MYELOMA ( 5 FDA reports)
MUSCLE DISORDER ( 5 FDA reports)
MUSCLE TIGHTNESS ( 5 FDA reports)
NARCOLEPSY ( 5 FDA reports)
NEPHROTIC SYNDROME ( 5 FDA reports)
NEUROGENIC BLADDER ( 5 FDA reports)
NIGHT BLINDNESS ( 5 FDA reports)
OPEN WOUND ( 5 FDA reports)
OSTEOSCLEROSIS ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PERIODONTAL DISEASE ( 5 FDA reports)
PERIPHERAL COLDNESS ( 5 FDA reports)
PNEUMONIA LEGIONELLA ( 5 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 5 FDA reports)
PRIMARY SEQUESTRUM ( 5 FDA reports)
PROCTALGIA ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
PULMONARY CONGESTION ( 5 FDA reports)
PULMONARY MASS ( 5 FDA reports)
RALES ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 5 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
RENAL TUBULAR ATROPHY ( 5 FDA reports)
RESTLESS LEGS SYNDROME ( 5 FDA reports)
RETINAL ARTERY THROMBOSIS ( 5 FDA reports)
SHOULDER PAIN ( 5 FDA reports)
SKIN BURNING SENSATION ( 5 FDA reports)
SMALL INTESTINAL PERFORATION ( 5 FDA reports)
SNEEZING ( 5 FDA reports)
SOFT TISSUE DISORDER ( 5 FDA reports)
SPINAL CORD COMPRESSION ( 5 FDA reports)
SPINAL DISORDER ( 5 FDA reports)
STREPTOCOCCAL INFECTION ( 5 FDA reports)
SYNOVITIS ( 5 FDA reports)
TARDIVE DYSKINESIA ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 5 FDA reports)
THINKING ABNORMAL ( 5 FDA reports)
THYROID NEOPLASM ( 5 FDA reports)
TIBIA FRACTURE ( 5 FDA reports)
TONGUE DISCOLOURATION ( 5 FDA reports)
TOXIC SKIN ERUPTION ( 5 FDA reports)
TUBERCULOSIS ( 5 FDA reports)
TYPE 1 DIABETES MELLITUS ( 5 FDA reports)
URETERIC STENOSIS ( 5 FDA reports)
UTERINE HAEMORRHAGE ( 5 FDA reports)
VENTRICULAR HYPOKINESIA ( 5 FDA reports)
ABDOMINAL HERNIA ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ABSCESS ORAL ( 4 FDA reports)
ACCIDENT ( 4 FDA reports)
ACTINOMYCOSIS ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ADENOTONSILLECTOMY ( 4 FDA reports)
ADNEXA UTERI PAIN ( 4 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ANGER ( 4 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 4 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 4 FDA reports)
APNOEA ( 4 FDA reports)
APPENDICITIS ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 4 FDA reports)
BLOOD ALBUMIN INCREASED ( 4 FDA reports)
BLOOD MAGNESIUM DECREASED ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BLOOD PRESSURE ( 4 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BONE GRAFT ( 4 FDA reports)
BONE SCAN ABNORMAL ( 4 FDA reports)
CARDIAC PACEMAKER INSERTION ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CARDITIS ( 4 FDA reports)
CATARACT DIABETIC ( 4 FDA reports)
CATHETERISATION CARDIAC ( 4 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 4 FDA reports)
CERVICOBRACHIAL SYNDROME ( 4 FDA reports)
CHANGE OF BOWEL HABIT ( 4 FDA reports)
CHEILITIS ( 4 FDA reports)
CHOLECYSTITIS CHRONIC ( 4 FDA reports)
CHRONIC HEPATITIS ( 4 FDA reports)
CHRONIC SINUSITIS ( 4 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 4 FDA reports)
CLAVICLE FRACTURE ( 4 FDA reports)
CLOSTRIDIAL INFECTION ( 4 FDA reports)
COELIAC DISEASE ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
CONNECTIVE TISSUE DISORDER ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
DEAFNESS UNILATERAL ( 4 FDA reports)
DERMATITIS CONTACT ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DIARRHOEA INFECTIOUS ( 4 FDA reports)
DILATATION VENTRICULAR ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
EAR DISORDER ( 4 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
ERYTHEMA NODOSUM ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 4 FDA reports)
EYE INFECTION ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
EYE PROSTHESIS INSERTION ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 4 FDA reports)
FIBULA FRACTURE ( 4 FDA reports)
FOREIGN BODY ( 4 FDA reports)
FORMICATION ( 4 FDA reports)
FRACTURED SACRUM ( 4 FDA reports)
GASTRECTOMY ( 4 FDA reports)
GASTRIC BYPASS ( 4 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 4 FDA reports)
GASTROINTESTINAL PERFORATION ( 4 FDA reports)
GENITAL PRURITUS FEMALE ( 4 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 4 FDA reports)
HAEMANGIOMA ( 4 FDA reports)
HAEMOCHROMATOSIS ( 4 FDA reports)
HEAD DISCOMFORT ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HEPATIC TRAUMA ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HEPATITIS TOXIC ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HEPATOTOXICITY ( 4 FDA reports)
HORMONE LEVEL ABNORMAL ( 4 FDA reports)
HYDROURETER ( 4 FDA reports)
HYPERSEXUALITY ( 4 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 4 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
ILEUS ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INJECTION SITE BURNING ( 4 FDA reports)
INJECTION SITE WARMTH ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 4 FDA reports)
JOINT CREPITATION ( 4 FDA reports)
JOINT EFFUSION ( 4 FDA reports)
JOINT INSTABILITY ( 4 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 4 FDA reports)
KYPHOSIS ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
LARYNGITIS ( 4 FDA reports)
LEUKOARAIOSIS ( 4 FDA reports)
LIMB OPERATION ( 4 FDA reports)
LOCALISED INFECTION ( 4 FDA reports)
LOOSE STOOLS ( 4 FDA reports)
LYMPHANGIOMA ( 4 FDA reports)
MACROCYTOSIS ( 4 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 4 FDA reports)
MAMMOGRAM ABNORMAL ( 4 FDA reports)
MASTICATION DISORDER ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
MENINGITIS ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
METAPLASIA ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
MITRAL VALVE PROLAPSE ( 4 FDA reports)
MOTOR DYSFUNCTION ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
MYELOPATHY ( 4 FDA reports)
NASAL MUCOSAL DISORDER ( 4 FDA reports)
NECROTISING FASCIITIS ( 4 FDA reports)
NERVE COMPRESSION ( 4 FDA reports)
NEURODERMATITIS ( 4 FDA reports)
NO ADVERSE EFFECT ( 4 FDA reports)
NODULE ( 4 FDA reports)
NON-CARDIAC CHEST PAIN ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OESOPHAGEAL ULCER ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
ORAL INFECTION ( 4 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 4 FDA reports)
ORTHOSIS USER ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PAROSMIA ( 4 FDA reports)
PERIARTHRITIS ( 4 FDA reports)
PHLEBITIS ( 4 FDA reports)
POLYARTHRITIS ( 4 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 4 FDA reports)
POSTOPERATIVE INFECTION ( 4 FDA reports)
PROCEDURAL HYPERTENSION ( 4 FDA reports)
PROSTATE CANCER METASTATIC ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
RETINAL DETACHMENT ( 4 FDA reports)
SENSORY LOSS ( 4 FDA reports)
SKIN CANCER ( 4 FDA reports)
SKIN PAPILLOMA ( 4 FDA reports)
SLEEP TALKING ( 4 FDA reports)
STRESS URINARY INCONTINENCE ( 4 FDA reports)
TABLET ISSUE ( 4 FDA reports)
TEMPOROMANDIBULAR JOINT SURGERY ( 4 FDA reports)
TENDON INJURY ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 4 FDA reports)
URINE ODOUR ABNORMAL ( 4 FDA reports)
UROSEPSIS ( 4 FDA reports)
UVEITIS ( 4 FDA reports)
VAGINAL BURNING SENSATION ( 4 FDA reports)
VASODILATION PROCEDURE ( 4 FDA reports)
VENOUS THROMBOSIS LIMB ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
WISDOM TEETH REMOVAL ( 4 FDA reports)
WOUND INFECTION ( 4 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 3 FDA reports)
ALVEOLITIS FIBROSING ( 3 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
AORTIC OCCLUSION ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
APATHY ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
ARACHNOID CYST ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ARTHRITIS BACTERIAL ( 3 FDA reports)
ATHEROSCLEROSIS ( 3 FDA reports)
BENIGN LUNG NEOPLASM ( 3 FDA reports)
BENIGN MESOTHELIOMA ( 3 FDA reports)
BENIGN NEOPLASM OF SKIN ( 3 FDA reports)
BLADDER PROLAPSE ( 3 FDA reports)
BLOOD CREATININE DECREASED ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
BLOOD PROLACTIN INCREASED ( 3 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 3 FDA reports)
BONE NEOPLASM MALIGNANT ( 3 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
BUTTOCK PAIN ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CALCIUM DEFICIENCY ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CARTILAGE INJURY ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CLEFT LIP ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
CORNEAL DYSTROPHY ( 3 FDA reports)
CORONARY ARTERY BYPASS ( 3 FDA reports)
CROHN'S DISEASE ( 3 FDA reports)
DEAFNESS NEUROSENSORY ( 3 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DIAPHRAGMATIC DISORDER ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DYSPNOEA AT REST ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
ESSENTIAL HYPERTENSION ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FEAR OF DEATH ( 3 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 3 FDA reports)
GAMBLING ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTRIC PERFORATION ( 3 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 3 FDA reports)
GINGIVAL OEDEMA ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HEPATITIS NON-A NON-B NON-C ( 3 FDA reports)
HEPATORENAL FAILURE ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPOCALCIURIA ( 3 FDA reports)
HYPOCHROMIC ANAEMIA ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
IATROGENIC INJURY ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INCISION SITE HAEMORRHAGE ( 3 FDA reports)
INCISION SITE INFECTION ( 3 FDA reports)
INCLUSION BODY MYOSITIS ( 3 FDA reports)
INGUINAL HERNIA ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INTRACRANIAL ANEURYSM ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LOSS OF CONTROL OF LEGS ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MOUTH BREATHING ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
NAIL DISORDER ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NO ADVERSE REACTION ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
OROPHARYNGEAL SWELLING ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
OSTEOMYELITIS CHRONIC ( 3 FDA reports)
OSTEORADIONECROSIS ( 3 FDA reports)
OTORRHOEA ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
OVERWEIGHT ( 3 FDA reports)
PAIN EXACERBATED ( 3 FDA reports)
PANCREATIC PSEUDOCYST ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PATELLA FRACTURE ( 3 FDA reports)
PERFORATED ULCER ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PITTING OEDEMA ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
PLEURISY VIRAL ( 3 FDA reports)
PNEUMOCOCCAL SEPSIS ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
POST LAMINECTOMY SYNDROME ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
POST PROCEDURAL PAIN ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PSYCHOMOTOR RETARDATION ( 3 FDA reports)
PUBIC RAMI FRACTURE ( 3 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
PURULENT DISCHARGE ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RADIATION INJURY ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RECTAL ULCER ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 3 FDA reports)
SCRATCH ( 3 FDA reports)
SEROMA ( 3 FDA reports)
SINUS CONGESTION ( 3 FDA reports)
SKIN INFECTION ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
TEARFULNESS ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
TENDON PAIN ( 3 FDA reports)
THYROIDITIS FIBROUS CHRONIC ( 3 FDA reports)
TOBACCO ABUSE ( 3 FDA reports)
TONGUE COATED ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
TRAUMATIC FRACTURE ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
TYMPANOSCLEROSIS ( 3 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
UTERINE POLYP ( 3 FDA reports)
VAGINITIS BACTERIAL ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
VESSEL PERFORATION ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WOUND TREATMENT ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALCOHOLIC PANCREATITIS ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANAL ULCER ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APPLICATION SITE EXFOLIATION ( 2 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ASTROCYTOMA ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AVULSION FRACTURE ( 2 FDA reports)
AXILLARY MASS ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BASE EXCESS POSITIVE ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BONE CYST ( 2 FDA reports)
BONE FRAGMENTATION ( 2 FDA reports)
BONE LESION EXCISION ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BRONCHIAL HYPERACTIVITY ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BURN OESOPHAGEAL ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CERVIX CARCINOMA ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
CLUBBING ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COAGULATION TIME ABNORMAL ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONGENITAL NOSE MALFORMATION ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEPOSIT EYE ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DISLOCATION OF VERTEBRA ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DRUG TOLERANCE INCREASED ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EJACULATION DISORDER ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 2 FDA reports)
EYE INFECTION FUNGAL ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 2 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FOOD INTERACTION ( 2 FDA reports)
FOREIGN BODY IN EYE ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FRACTURE DELAYED UNION ( 2 FDA reports)
FUNGAL CYSTITIS ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER OBSTRUCTION ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTROENTERITIS BACTERIAL ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GLAUCOMA SURGERY ( 2 FDA reports)
GLOBAL AMNESIA ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GRAFT HAEMORRHAGE ( 2 FDA reports)
GRANULOCYTE COUNT INCREASED ( 2 FDA reports)
GRAVITATIONAL OEDEMA ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HANGOVER ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INCISION SITE ERYTHEMA ( 2 FDA reports)
INCISION SITE OEDEMA ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INGUINAL MASS ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTESTINAL MASS ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
KERATITIS FUNGAL ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LARYNGEAL NEOPLASM ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LIMB ASYMMETRY ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOCALISED OSTEOARTHRITIS ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG CREPITATION ( 2 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 2 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 2 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MONOCYTOSIS ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
MYOPATHY TOXIC ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NO ADVERSE DRUG REACTION ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
ON AND OFF PHENOMENON ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
OPEN ANGLE GLAUCOMA ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PANCREATIC PHLEGMON ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL NEOPLASM ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PLATELET PRODUCTION DECREASED ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PRODUCT ADHESION ISSUE ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PSEUDODEMENTIA ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSEUDOMENINGOCELE ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
PYURIA ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
REACTION TO COLOURING ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RECTAL POLYP ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
RHEUMATOID LUNG ( 2 FDA reports)
ROSAI-DORFMAN SYNDROME ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCLERAL DISCOLOURATION ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SEMEN VOLUME DECREASED ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TENSION ( 2 FDA reports)
TESTICULAR CANCER METASTATIC ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBOANGIITIS OBLITERANS ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VOCAL CORD THICKENING ( 2 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
WOUND ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED CLAW TOE ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACROMEGALY ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMOEBIC DYSENTERY ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANORECTAL INFECTION BACTERIAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHAKIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ASPIRATION BREAST ( 1 FDA reports)
ASTHMA PROPHYLAXIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
ATYPICAL FEMUR FRACTURE ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARIUM ENEMA ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE ABNORMAL ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BODY HEIGHT ABNORMAL ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARBOHYDRATE TOLERANCE DECREASED ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CARTILAGE ATROPHY ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX CARCINOMA RECURRENT ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL EPITHELIUM DISORDER ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CRANIAL NEUROPATHY ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEATH OF CHILD ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DEPRESSION POSTOPERATIVE ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETIC CARDIOMYOPATHY ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISSOCIATIVE FUGUE ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDEMIC PLEURODYNIA ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPILEPTIC AURA ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACIAL NERVE DISORDER ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLOPPY IRIS SYNDROME ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNCTIONAL RESIDUAL CAPACITY DECREASED ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GASTRIC CANCER STAGE III ( 1 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROSTOMY CLOSURE ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLUTEN FREE DIET ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART VALVE STENOSIS ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST ( 1 FDA reports)
HEPATECTOMY ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS A POSITIVE ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIP DEFORMITY ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOGONADISM MALE ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHOSPHATAEMIC RICKETS ( 1 FDA reports)
HYSTEROSCOPY ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG THERAPY ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 1 FDA reports)
INFERTILITY MALE ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE STINGING ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRA-CEREBRAL ANEURYSM OPERATION ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRITIS ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LEUKAEMIC INFILTRATION ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIPOSARCOMA METASTATIC ( 1 FDA reports)
LIPOSARCOMA RECURRENT ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPH GLAND INFECTION ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
LYMPHOSTASIS ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
MICROSURGERY TO HAND ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NASOPHARYNGEAL CANCER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEOPLASM OF THYMUS ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROPSYCHOLOGICAL TEST ABNORMAL ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NITRITE URINE ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCULOGYRIC CRISIS ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
OSTEOPETROSIS ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
PAIN TRAUMA ACTIVATED ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARATHYROIDECTOMY ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PEPTIC ULCER REACTIVATED ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOPOLYP ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOLOGICAL ABUSE ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYODERMA ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHESUS ANTIBODIES POSITIVE ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SENSORY LEVEL ABNORMAL ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SKIN CYST EXCISION ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SKIN WOUND ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPERM CONCENTRATION DECREASED ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL DECOMPRESSION ( 1 FDA reports)
SPINDLE CELL SARCOMA ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STARING ( 1 FDA reports)
STERNAL INJURY ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMACH MASS ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STRESS POLYCYTHAEMIA ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVIAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENODESIS ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE CANCER METASTATIC ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TUMOUR FLARE ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URAEMIC ENCEPHALOPATHY ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINISMUS ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
XEROSIS ( 1 FDA reports)

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