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

NAUSEA ( 345 FDA reports)
DIZZINESS ( 294 FDA reports)
FATIGUE ( 268 FDA reports)
HEADACHE ( 232 FDA reports)
DYSPNOEA ( 220 FDA reports)
PAIN ( 213 FDA reports)
DRUG INEFFECTIVE ( 211 FDA reports)
DIARRHOEA ( 188 FDA reports)
HYPERTENSION ( 187 FDA reports)
VOMITING ( 187 FDA reports)
ASTHENIA ( 183 FDA reports)
ANXIETY ( 172 FDA reports)
BLOOD PRESSURE INCREASED ( 169 FDA reports)
CHEST PAIN ( 165 FDA reports)
OEDEMA PERIPHERAL ( 158 FDA reports)
MYOCARDIAL INFARCTION ( 151 FDA reports)
PAIN IN EXTREMITY ( 149 FDA reports)
INSOMNIA ( 140 FDA reports)
ARTHRALGIA ( 133 FDA reports)
WEIGHT DECREASED ( 131 FDA reports)
BACK PAIN ( 130 FDA reports)
DEPRESSION ( 128 FDA reports)
BLOOD GLUCOSE INCREASED ( 127 FDA reports)
ANAEMIA ( 123 FDA reports)
RASH ( 119 FDA reports)
CEREBROVASCULAR ACCIDENT ( 118 FDA reports)
DECREASED APPETITE ( 117 FDA reports)
FALL ( 115 FDA reports)
PYREXIA ( 108 FDA reports)
RENAL FAILURE ACUTE ( 104 FDA reports)
WEIGHT INCREASED ( 104 FDA reports)
COUGH ( 101 FDA reports)
PNEUMONIA ( 101 FDA reports)
FEELING ABNORMAL ( 97 FDA reports)
DEHYDRATION ( 96 FDA reports)
PRURITUS ( 94 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 93 FDA reports)
PARAESTHESIA ( 93 FDA reports)
MALAISE ( 92 FDA reports)
ABDOMINAL PAIN UPPER ( 91 FDA reports)
ABDOMINAL PAIN ( 90 FDA reports)
INJURY ( 86 FDA reports)
MYALGIA ( 86 FDA reports)
RENAL FAILURE ( 86 FDA reports)
VISION BLURRED ( 84 FDA reports)
URINARY TRACT INFECTION ( 83 FDA reports)
DYSPEPSIA ( 81 FDA reports)
CONSTIPATION ( 79 FDA reports)
DIABETES MELLITUS ( 77 FDA reports)
HYPOTENSION ( 76 FDA reports)
FLUSHING ( 75 FDA reports)
PALPITATIONS ( 75 FDA reports)
CORONARY ARTERY DISEASE ( 74 FDA reports)
HYPOAESTHESIA ( 74 FDA reports)
DYSGEUSIA ( 71 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 70 FDA reports)
SYNCOPE ( 70 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 68 FDA reports)
DYSPHAGIA ( 68 FDA reports)
MUSCLE SPASMS ( 68 FDA reports)
ATRIAL FIBRILLATION ( 67 FDA reports)
SOMNOLENCE ( 67 FDA reports)
HYPERHIDROSIS ( 66 FDA reports)
NEUROPATHY PERIPHERAL ( 66 FDA reports)
GAIT DISTURBANCE ( 64 FDA reports)
ABDOMINAL DISTENSION ( 59 FDA reports)
CHEST DISCOMFORT ( 59 FDA reports)
OSTEOARTHRITIS ( 59 FDA reports)
CONFUSIONAL STATE ( 58 FDA reports)
MUSCULOSKELETAL PAIN ( 58 FDA reports)
BRONCHITIS ( 57 FDA reports)
IMPAIRED HEALING ( 55 FDA reports)
SINUSITIS ( 55 FDA reports)
ABDOMINAL DISCOMFORT ( 54 FDA reports)
LOSS OF CONSCIOUSNESS ( 54 FDA reports)
OSTEONECROSIS OF JAW ( 54 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 53 FDA reports)
MUSCULAR WEAKNESS ( 53 FDA reports)
BURSITIS ( 52 FDA reports)
NERVOUSNESS ( 52 FDA reports)
EMOTIONAL DISTRESS ( 51 FDA reports)
DEEP VEIN THROMBOSIS ( 50 FDA reports)
HEART RATE INCREASED ( 50 FDA reports)
CHILLS ( 49 FDA reports)
ERYTHEMA ( 48 FDA reports)
MITRAL VALVE INCOMPETENCE ( 48 FDA reports)
TREMOR ( 48 FDA reports)
BONE DISORDER ( 47 FDA reports)
MEDICATION ERROR ( 47 FDA reports)
ALOPECIA ( 46 FDA reports)
DEATH ( 46 FDA reports)
PLEURAL EFFUSION ( 46 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 46 FDA reports)
JOINT SWELLING ( 45 FDA reports)
CONDITION AGGRAVATED ( 43 FDA reports)
ANOREXIA ( 42 FDA reports)
DRY MOUTH ( 42 FDA reports)
HYPERLIPIDAEMIA ( 42 FDA reports)
NEPHROLITHIASIS ( 42 FDA reports)
BLOOD CREATININE INCREASED ( 40 FDA reports)
BLOOD SODIUM DECREASED ( 40 FDA reports)
ARTHRITIS ( 39 FDA reports)
CYST ( 39 FDA reports)
GASTRITIS ( 39 FDA reports)
OSTEONECROSIS ( 39 FDA reports)
PAIN IN JAW ( 39 FDA reports)
SLEEP APNOEA SYNDROME ( 39 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 39 FDA reports)
CATARACT ( 38 FDA reports)
OEDEMA ( 38 FDA reports)
RENAL FAILURE CHRONIC ( 38 FDA reports)
SWELLING FACE ( 38 FDA reports)
OSTEOPOROSIS ( 37 FDA reports)
HYPERSENSITIVITY ( 36 FDA reports)
SWELLING ( 36 FDA reports)
TINNITUS ( 36 FDA reports)
DYSPHONIA ( 35 FDA reports)
HYPOKALAEMIA ( 35 FDA reports)
DIVERTICULUM ( 34 FDA reports)
FEELING HOT ( 34 FDA reports)
GASTRIC ULCER ( 34 FDA reports)
HEPATIC ENZYME INCREASED ( 34 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 34 FDA reports)
LYMPHADENOPATHY ( 34 FDA reports)
MEMORY IMPAIRMENT ( 34 FDA reports)
PULMONARY EMBOLISM ( 34 FDA reports)
RENAL DISORDER ( 34 FDA reports)
TOOTH EXTRACTION ( 34 FDA reports)
URTICARIA ( 34 FDA reports)
DECREASED INTEREST ( 33 FDA reports)
DRUG INTERACTION ( 33 FDA reports)
DYSURIA ( 33 FDA reports)
EAR PAIN ( 33 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 33 FDA reports)
NECK PAIN ( 33 FDA reports)
OROPHARYNGEAL PAIN ( 33 FDA reports)
ANGINA PECTORIS ( 32 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 32 FDA reports)
INFLAMMATION ( 32 FDA reports)
BRADYCARDIA ( 31 FDA reports)
FLATULENCE ( 31 FDA reports)
NASAL CONGESTION ( 31 FDA reports)
NEUTROPENIA ( 31 FDA reports)
POLLAKIURIA ( 31 FDA reports)
RECTAL HAEMORRHAGE ( 31 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 30 FDA reports)
ASTHMA ( 30 FDA reports)
BLOOD PRESSURE DECREASED ( 30 FDA reports)
GOUT ( 30 FDA reports)
HEPATIC STEATOSIS ( 30 FDA reports)
VERTIGO ( 30 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 29 FDA reports)
BONE DENSITY DECREASED ( 29 FDA reports)
CARDIAC DISORDER ( 29 FDA reports)
EMOTIONAL DISORDER ( 29 FDA reports)
HYPOGLYCAEMIA ( 29 FDA reports)
INFLUENZA ( 29 FDA reports)
RETCHING ( 29 FDA reports)
THROMBOCYTOPENIA ( 29 FDA reports)
ADVERSE EVENT ( 28 FDA reports)
ANHEDONIA ( 28 FDA reports)
BLOOD CALCIUM INCREASED ( 28 FDA reports)
CARDIOMYOPATHY ( 28 FDA reports)
FLUID RETENTION ( 28 FDA reports)
HAEMOGLOBIN DECREASED ( 28 FDA reports)
MASS ( 28 FDA reports)
OSTEOPENIA ( 28 FDA reports)
BLOOD GLUCOSE DECREASED ( 27 FDA reports)
CONTUSION ( 27 FDA reports)
INFECTION ( 27 FDA reports)
IRRITABILITY ( 27 FDA reports)
NASOPHARYNGITIS ( 27 FDA reports)
NEOPLASM MALIGNANT ( 27 FDA reports)
PANCREATITIS ( 27 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 27 FDA reports)
PRODUCTIVE COUGH ( 27 FDA reports)
THROMBOSIS ( 27 FDA reports)
BLOOD POTASSIUM DECREASED ( 26 FDA reports)
CARDIAC MURMUR ( 26 FDA reports)
CELLULITIS ( 26 FDA reports)
DRUG HYPERSENSITIVITY ( 26 FDA reports)
FEMUR FRACTURE ( 26 FDA reports)
HEART RATE IRREGULAR ( 26 FDA reports)
HYPERGLYCAEMIA ( 26 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 26 FDA reports)
MOBILITY DECREASED ( 26 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 26 FDA reports)
STRESS ( 26 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 26 FDA reports)
TOOTH DISORDER ( 26 FDA reports)
ECONOMIC PROBLEM ( 25 FDA reports)
ERECTILE DYSFUNCTION ( 25 FDA reports)
RASH PRURITIC ( 25 FDA reports)
SPINAL OSTEOARTHRITIS ( 25 FDA reports)
SUICIDAL IDEATION ( 25 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 25 FDA reports)
WHEEZING ( 25 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 25 FDA reports)
CONVULSION ( 24 FDA reports)
EXTRASYSTOLES ( 24 FDA reports)
HAEMATURIA ( 24 FDA reports)
HYPERCALCAEMIA ( 24 FDA reports)
LOCALISED INFECTION ( 24 FDA reports)
RENAL IMPAIRMENT ( 24 FDA reports)
ROAD TRAFFIC ACCIDENT ( 24 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 23 FDA reports)
BONE PAIN ( 23 FDA reports)
DEFORMITY ( 23 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 23 FDA reports)
ULCER ( 23 FDA reports)
ABNORMAL DREAMS ( 22 FDA reports)
ARTHROPATHY ( 22 FDA reports)
BLOOD MAGNESIUM DECREASED ( 22 FDA reports)
CARDIOMEGALY ( 22 FDA reports)
DISORIENTATION ( 22 FDA reports)
DRY EYE ( 22 FDA reports)
ERUCTATION ( 22 FDA reports)
EYE PAIN ( 22 FDA reports)
HAEMORRHAGE ( 22 FDA reports)
HIP FRACTURE ( 22 FDA reports)
HYPOXIA ( 22 FDA reports)
SEPSIS ( 22 FDA reports)
SKIN DISCOLOURATION ( 22 FDA reports)
VENTRICULAR HYPERTROPHY ( 22 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 21 FDA reports)
BALANCE DISORDER ( 21 FDA reports)
CARDIAC FAILURE ( 21 FDA reports)
CORONARY ARTERY OCCLUSION ( 21 FDA reports)
DYSPNOEA EXERTIONAL ( 21 FDA reports)
HERPES ZOSTER ( 21 FDA reports)
INJECTION SITE PAIN ( 21 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 21 FDA reports)
LOWER LIMB FRACTURE ( 21 FDA reports)
ORTHOSTATIC HYPOTENSION ( 21 FDA reports)
PANCYTOPENIA ( 21 FDA reports)
THROAT IRRITATION ( 21 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 20 FDA reports)
BONE LESION ( 20 FDA reports)
CANDIDIASIS ( 20 FDA reports)
CAROTID ARTERY STENOSIS ( 20 FDA reports)
DUODENITIS ( 20 FDA reports)
EPISTAXIS ( 20 FDA reports)
HAEMATOCHEZIA ( 20 FDA reports)
LETHARGY ( 20 FDA reports)
PNEUMONITIS ( 20 FDA reports)
PRODUCT QUALITY ISSUE ( 20 FDA reports)
VISUAL IMPAIRMENT ( 20 FDA reports)
ANAPHYLACTIC REACTION ( 19 FDA reports)
ATHEROSCLEROSIS ( 19 FDA reports)
BLISTER ( 19 FDA reports)
BLOOD POTASSIUM INCREASED ( 19 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 19 FDA reports)
BREAST CANCER ( 19 FDA reports)
DIVERTICULITIS ( 19 FDA reports)
DYSARTHRIA ( 19 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 19 FDA reports)
HAEMORRHOIDS ( 19 FDA reports)
HYPOACUSIS ( 19 FDA reports)
JAW DISORDER ( 19 FDA reports)
LEUKOPENIA ( 19 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 19 FDA reports)
MYOCARDIAL ISCHAEMIA ( 19 FDA reports)
OSTEOLYSIS ( 19 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 19 FDA reports)
PRESYNCOPE ( 19 FDA reports)
PRURITUS GENERALISED ( 19 FDA reports)
RHABDOMYOLYSIS ( 19 FDA reports)
SWOLLEN TONGUE ( 19 FDA reports)
TOOTH LOSS ( 19 FDA reports)
TYPE 2 DIABETES MELLITUS ( 19 FDA reports)
BLOOD UREA INCREASED ( 18 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 18 FDA reports)
DRY SKIN ( 18 FDA reports)
EYE SWELLING ( 18 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 18 FDA reports)
HYPOAESTHESIA ORAL ( 18 FDA reports)
HYPOPHAGIA ( 18 FDA reports)
ILL-DEFINED DISORDER ( 18 FDA reports)
LUMBAR SPINAL STENOSIS ( 18 FDA reports)
ODYNOPHAGIA ( 18 FDA reports)
ORAL DISCOMFORT ( 18 FDA reports)
PULMONARY OEDEMA ( 18 FDA reports)
SINUS DISORDER ( 18 FDA reports)
SLEEP DISORDER ( 18 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 18 FDA reports)
UNEVALUABLE EVENT ( 18 FDA reports)
WALKING AID USER ( 18 FDA reports)
ABASIA ( 17 FDA reports)
ARRHYTHMIA ( 17 FDA reports)
BLINDNESS UNILATERAL ( 17 FDA reports)
HAEMOPTYSIS ( 17 FDA reports)
HEPATIC FAILURE ( 17 FDA reports)
HEPATITIS ( 17 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 17 FDA reports)
LOOSE TOOTH ( 17 FDA reports)
LUNG DISORDER ( 17 FDA reports)
NEUTROPHIL COUNT DECREASED ( 17 FDA reports)
NOCTURIA ( 17 FDA reports)
NODULE ( 17 FDA reports)
ORAL INFECTION ( 17 FDA reports)
OVERDOSE ( 17 FDA reports)
PHARYNGEAL OEDEMA ( 17 FDA reports)
RENAL TUBULAR NECROSIS ( 17 FDA reports)
RESPIRATORY FAILURE ( 17 FDA reports)
ROTATOR CUFF SYNDROME ( 17 FDA reports)
TACHYCARDIA ( 17 FDA reports)
URINARY RETENTION ( 17 FDA reports)
WOUND DEHISCENCE ( 17 FDA reports)
ABSCESS DRAINAGE ( 16 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 16 FDA reports)
ARTERIOSCLEROSIS ( 16 FDA reports)
BONE DEBRIDEMENT ( 16 FDA reports)
CARDIAC ARREST ( 16 FDA reports)
CARPAL TUNNEL SYNDROME ( 16 FDA reports)
CHOLELITHIASIS ( 16 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 16 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 16 FDA reports)
DRUG DEPENDENCE ( 16 FDA reports)
DRUG DOSE OMISSION ( 16 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 16 FDA reports)
FIBROMYALGIA ( 16 FDA reports)
GASTROENTERITIS ( 16 FDA reports)
GINGIVAL INFECTION ( 16 FDA reports)
GRANULOMA ( 16 FDA reports)
HAEMATEMESIS ( 16 FDA reports)
HEART RATE DECREASED ( 16 FDA reports)
METABOLIC ACIDOSIS ( 16 FDA reports)
MIGRAINE ( 16 FDA reports)
NASAL MUCOSAL DISORDER ( 16 FDA reports)
OSTEOMYELITIS CHRONIC ( 16 FDA reports)
RENAL INJURY ( 16 FDA reports)
STOMATITIS ( 16 FDA reports)
TONGUE PARALYSIS ( 16 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 15 FDA reports)
BIOPSY BONE ( 15 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 15 FDA reports)
BONE FRAGMENTATION ( 15 FDA reports)
BONE TRIMMING ( 15 FDA reports)
CHROMATURIA ( 15 FDA reports)
CRANIAL NERVE DISORDER ( 15 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 15 FDA reports)
DISTURBANCE IN ATTENTION ( 15 FDA reports)
EJECTION FRACTION ( 15 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 15 FDA reports)
FOREIGN BODY REACTION ( 15 FDA reports)
GRAFT VERSUS HOST DISEASE ( 15 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 15 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 15 FDA reports)
LACRIMATION INCREASED ( 15 FDA reports)
LIMB DISCOMFORT ( 15 FDA reports)
LIVER DISORDER ( 15 FDA reports)
MACROGLOSSIA ( 15 FDA reports)
METASTASES TO BONE MARROW ( 15 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 15 FDA reports)
MOUTH HAEMORRHAGE ( 15 FDA reports)
MUCOSAL EROSION ( 15 FDA reports)
NIGHT SWEATS ( 15 FDA reports)
OESOPHAGITIS ( 15 FDA reports)
ONYCHOMYCOSIS ( 15 FDA reports)
PANCREATIC CYST ( 15 FDA reports)
PROSTHESIS IMPLANTATION ( 15 FDA reports)
SINUS BRADYCARDIA ( 15 FDA reports)
SPONDYLOLISTHESIS ( 15 FDA reports)
STOMACH DISCOMFORT ( 15 FDA reports)
TOOTH RESORPTION ( 15 FDA reports)
UTERINE LEIOMYOMA ( 15 FDA reports)
AMNESIA ( 14 FDA reports)
ANKLE FRACTURE ( 14 FDA reports)
AORTIC VALVE SCLEROSIS ( 14 FDA reports)
BLOOD CALCIUM DECREASED ( 14 FDA reports)
BURNING SENSATION ( 14 FDA reports)
DEVICE RELATED INFECTION ( 14 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 14 FDA reports)
DIABETIC KETOACIDOSIS ( 14 FDA reports)
DRUG EFFECT DECREASED ( 14 FDA reports)
GASTRIC POLYPS ( 14 FDA reports)
HIATUS HERNIA ( 14 FDA reports)
HYPERKALAEMIA ( 14 FDA reports)
HYPOMAGNESAEMIA ( 14 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 14 FDA reports)
MITRAL VALVE PROLAPSE ( 14 FDA reports)
MULTIPLE INJURIES ( 14 FDA reports)
PNEUMONIA ASPIRATION ( 14 FDA reports)
RASH ERYTHEMATOUS ( 14 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 14 FDA reports)
RIB FRACTURE ( 14 FDA reports)
TONGUE ULCERATION ( 14 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 14 FDA reports)
ADVERSE DRUG REACTION ( 13 FDA reports)
AGEUSIA ( 13 FDA reports)
ANGINA UNSTABLE ( 13 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 13 FDA reports)
DEPRESSED MOOD ( 13 FDA reports)
DEVICE FAILURE ( 13 FDA reports)
DRUG ADMINISTRATION ERROR ( 13 FDA reports)
DYSAESTHESIA ( 13 FDA reports)
EYE DISORDER ( 13 FDA reports)
FEAR ( 13 FDA reports)
HOT FLUSH ( 13 FDA reports)
INCORRECT DOSE ADMINISTERED ( 13 FDA reports)
INGROWING NAIL ( 13 FDA reports)
MOOD SWINGS ( 13 FDA reports)
MULTIPLE MYELOMA ( 13 FDA reports)
OCULAR HYPERAEMIA ( 13 FDA reports)
OSTEOMYELITIS ( 13 FDA reports)
PANIC ATTACK ( 13 FDA reports)
PERINEURIAL CYST ( 13 FDA reports)
RADIOTHERAPY ( 13 FDA reports)
SENSORY LOSS ( 13 FDA reports)
SINUS TACHYCARDIA ( 13 FDA reports)
SPINAL COMPRESSION FRACTURE ( 13 FDA reports)
VAGINAL HAEMORRHAGE ( 13 FDA reports)
VISUAL ACUITY REDUCED ( 13 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 13 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 12 FDA reports)
ACUTE CORONARY SYNDROME ( 12 FDA reports)
ASCITES ( 12 FDA reports)
BODY TEMPERATURE INCREASED ( 12 FDA reports)
CEREBRAL HAEMORRHAGE ( 12 FDA reports)
DEAFNESS NEUROSENSORY ( 12 FDA reports)
DRUG DISPENSING ERROR ( 12 FDA reports)
EYE LASER SURGERY ( 12 FDA reports)
FOREIGN BODY TRAUMA ( 12 FDA reports)
HYPERKERATOSIS ( 12 FDA reports)
HYPONATRAEMIA ( 12 FDA reports)
INJECTION SITE BRUISING ( 12 FDA reports)
INJECTION SITE HAEMATOMA ( 12 FDA reports)
JOINT SPRAIN ( 12 FDA reports)
LOCAL SWELLING ( 12 FDA reports)
MUCOSAL INFLAMMATION ( 12 FDA reports)
ORAL HERPES ( 12 FDA reports)
PHARYNGITIS ( 12 FDA reports)
SKIN BURNING SENSATION ( 12 FDA reports)
SPEECH DISORDER ( 12 FDA reports)
STRESS FRACTURE ( 12 FDA reports)
SURGERY ( 12 FDA reports)
THINKING ABNORMAL ( 12 FDA reports)
TREATMENT NONCOMPLIANCE ( 12 FDA reports)
TRIGGER FINGER ( 12 FDA reports)
UNRESPONSIVE TO STIMULI ( 12 FDA reports)
VISUAL DISTURBANCE ( 12 FDA reports)
ANGIOEDEMA ( 11 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 11 FDA reports)
ATELECTASIS ( 11 FDA reports)
BACTERIAL TEST POSITIVE ( 11 FDA reports)
CRYING ( 11 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 11 FDA reports)
DERMATITIS CONTACT ( 11 FDA reports)
DIFFICULTY IN WALKING ( 11 FDA reports)
EJECTION FRACTION DECREASED ( 11 FDA reports)
EYE DISCHARGE ( 11 FDA reports)
FAECES DISCOLOURED ( 11 FDA reports)
FEELING COLD ( 11 FDA reports)
HALLUCINATION ( 11 FDA reports)
HEAD INJURY ( 11 FDA reports)
HYPERCHOLESTEROLAEMIA ( 11 FDA reports)
INFLUENZA LIKE ILLNESS ( 11 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 11 FDA reports)
ISCHAEMIC STROKE ( 11 FDA reports)
KNEE ARTHROPLASTY ( 11 FDA reports)
MENISCUS LESION ( 11 FDA reports)
MENTAL STATUS CHANGES ( 11 FDA reports)
METASTASES TO BONE ( 11 FDA reports)
METASTASES TO LIVER ( 11 FDA reports)
MUSCLE TIGHTNESS ( 11 FDA reports)
OBESITY ( 11 FDA reports)
OSTEORADIONECROSIS ( 11 FDA reports)
PANCREATITIS ACUTE ( 11 FDA reports)
PROTEIN URINE ( 11 FDA reports)
PSORIASIS ( 11 FDA reports)
PULMONARY HYPERTENSION ( 11 FDA reports)
PURULENT DISCHARGE ( 11 FDA reports)
STEVENS-JOHNSON SYNDROME ( 11 FDA reports)
WRIST FRACTURE ( 11 FDA reports)
ACNE ( 10 FDA reports)
AGITATION ( 10 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 10 FDA reports)
BREAST DISCHARGE ( 10 FDA reports)
CATHETERISATION CARDIAC ( 10 FDA reports)
CERUMEN IMPACTION ( 10 FDA reports)
COLD SWEAT ( 10 FDA reports)
COLONIC POLYP ( 10 FDA reports)
CORONARY ARTERY STENOSIS ( 10 FDA reports)
DENTAL CARE ( 10 FDA reports)
DILATATION ATRIAL ( 10 FDA reports)
DISABILITY ( 10 FDA reports)
EXOSTOSIS ( 10 FDA reports)
FEELING JITTERY ( 10 FDA reports)
FOREIGN BODY ( 10 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 10 FDA reports)
GOITRE ( 10 FDA reports)
HAEMANGIOMA OF LIVER ( 10 FDA reports)
HAEMATOCRIT DECREASED ( 10 FDA reports)
HYPOTHYROIDISM ( 10 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 10 FDA reports)
JAW OPERATION ( 10 FDA reports)
MACULAR DEGENERATION ( 10 FDA reports)
MASTICATION DISORDER ( 10 FDA reports)
MENTAL DISORDER ( 10 FDA reports)
MULTI-ORGAN FAILURE ( 10 FDA reports)
MYOSITIS ( 10 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 10 FDA reports)
OESOPHAGEAL ULCER ( 10 FDA reports)
OTITIS MEDIA ( 10 FDA reports)
PALLOR ( 10 FDA reports)
PANCREATIC MASS ( 10 FDA reports)
PERIODONTAL DISEASE ( 10 FDA reports)
PLATELET COUNT DECREASED ( 10 FDA reports)
PROSTATE CANCER ( 10 FDA reports)
RASH GENERALISED ( 10 FDA reports)
RHEUMATOID ARTHRITIS ( 10 FDA reports)
RHINITIS ( 10 FDA reports)
RHINORRHOEA ( 10 FDA reports)
SCAR ( 10 FDA reports)
SEXUAL DYSFUNCTION ( 10 FDA reports)
SKIN EXFOLIATION ( 10 FDA reports)
SKIN LESION ( 10 FDA reports)
SPINAL COLUMN STENOSIS ( 10 FDA reports)
TUBERCULOSIS ( 10 FDA reports)
WOUND INFECTION ( 10 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 9 FDA reports)
BACK DISORDER ( 9 FDA reports)
BACK INJURY ( 9 FDA reports)
BLINDNESS ( 9 FDA reports)
BLOOD URINE PRESENT ( 9 FDA reports)
BONE MARROW TRANSPLANT ( 9 FDA reports)
BONE NEOPLASM MALIGNANT ( 9 FDA reports)
CARDIOVASCULAR DISORDER ( 9 FDA reports)
COMPRESSION FRACTURE ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 9 FDA reports)
DISEASE PROGRESSION ( 9 FDA reports)
DYSKINESIA ( 9 FDA reports)
ECCHYMOSIS ( 9 FDA reports)
ECZEMA ( 9 FDA reports)
FLUID OVERLOAD ( 9 FDA reports)
FOOT DEFORMITY ( 9 FDA reports)
GOUTY ARTHRITIS ( 9 FDA reports)
HYPERTENSIVE CRISIS ( 9 FDA reports)
INJECTION SITE HAEMORRHAGE ( 9 FDA reports)
INTRAOCULAR LENS IMPLANT ( 9 FDA reports)
JOINT SURGERY ( 9 FDA reports)
LIPIDS INCREASED ( 9 FDA reports)
LUMBAR RADICULOPATHY ( 9 FDA reports)
LUNG NEOPLASM ( 9 FDA reports)
LYMPHOMA ( 9 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 9 FDA reports)
ORAL INTAKE REDUCED ( 9 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 9 FDA reports)
PETECHIAE ( 9 FDA reports)
PLEURITIC PAIN ( 9 FDA reports)
PURULENCE ( 9 FDA reports)
RESIDUAL URINE VOLUME ( 9 FDA reports)
SHOCK ( 9 FDA reports)
SKIN HYPERPIGMENTATION ( 9 FDA reports)
TRANSAMINASES INCREASED ( 9 FDA reports)
UMBILICAL HERNIA ( 9 FDA reports)
URINARY INCONTINENCE ( 9 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 9 FDA reports)
ABDOMINAL PAIN LOWER ( 8 FDA reports)
AFFECTIVE DISORDER ( 8 FDA reports)
AORTIC VALVE INCOMPETENCE ( 8 FDA reports)
ATRIAL FLUTTER ( 8 FDA reports)
BLOOD COUNT ABNORMAL ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 8 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 8 FDA reports)
BONE OPERATION ( 8 FDA reports)
BREAST SWELLING ( 8 FDA reports)
CARDIO-RESPIRATORY ARREST ( 8 FDA reports)
COGNITIVE DISORDER ( 8 FDA reports)
COLONOSCOPY ABNORMAL ( 8 FDA reports)
DIABETIC NEPHROPATHY ( 8 FDA reports)
DIASTOLIC DYSFUNCTION ( 8 FDA reports)
DISCOMFORT ( 8 FDA reports)
DYSLIPIDAEMIA ( 8 FDA reports)
EXPIRED DRUG ADMINISTERED ( 8 FDA reports)
EYE HAEMORRHAGE ( 8 FDA reports)
GASTRITIS EROSIVE ( 8 FDA reports)
GENERALISED OEDEMA ( 8 FDA reports)
HEMIPARESIS ( 8 FDA reports)
HYPERVENTILATION ( 8 FDA reports)
HYPOVOLAEMIA ( 8 FDA reports)
INJECTION SITE ERYTHEMA ( 8 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 8 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 8 FDA reports)
IRRITABLE BOWEL SYNDROME ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
JOINT INJURY ( 8 FDA reports)
JOINT STIFFNESS ( 8 FDA reports)
LEUKOCYTOSIS ( 8 FDA reports)
LIP SWELLING ( 8 FDA reports)
LYMPHOEDEMA ( 8 FDA reports)
MALIGNANT MELANOMA ( 8 FDA reports)
MAMMARY DUCT ECTASIA ( 8 FDA reports)
METASTASES TO LUNG ( 8 FDA reports)
MICROALBUMINURIA ( 8 FDA reports)
MOOD ALTERED ( 8 FDA reports)
MULTIPLE SCLEROSIS ( 8 FDA reports)
MUSCLE CRAMP ( 8 FDA reports)
NASAL DISCOMFORT ( 8 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 8 FDA reports)
OFF LABEL USE ( 8 FDA reports)
OTITIS EXTERNA ( 8 FDA reports)
PHOTOSENSITIVITY REACTION ( 8 FDA reports)
RENAL CANCER ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
RESTLESSNESS ( 8 FDA reports)
RHINITIS ALLERGIC ( 8 FDA reports)
SEQUESTRECTOMY ( 8 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 8 FDA reports)
STAPHYLOCOCCAL INFECTION ( 8 FDA reports)
TARDIVE DYSKINESIA ( 8 FDA reports)
TOOTHACHE ( 8 FDA reports)
TOXIC NODULAR GOITRE ( 8 FDA reports)
TRANSFUSION ( 8 FDA reports)
VENTRICULAR HYPOKINESIA ( 8 FDA reports)
VOCAL CORD POLYP ( 8 FDA reports)
WEIGHT BEARING DIFFICULTY ( 8 FDA reports)
AGGRESSION ( 7 FDA reports)
BLOOD PRESSURE ABNORMAL ( 7 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 7 FDA reports)
BONE MARROW DISORDER ( 7 FDA reports)
BREAST CANCER FEMALE ( 7 FDA reports)
BRONCHITIS ACUTE ( 7 FDA reports)
CAROTID BRUIT ( 7 FDA reports)
CHONDROMALACIA ( 7 FDA reports)
CYSTITIS ( 7 FDA reports)
DRUG TOXICITY ( 7 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 7 FDA reports)
EYE IRRITATION ( 7 FDA reports)
EYE PRURITUS ( 7 FDA reports)
FACIAL BONES FRACTURE ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 7 FDA reports)
FRACTURE MALUNION ( 7 FDA reports)
GASTROENTERITIS VIRAL ( 7 FDA reports)
GASTROINTESTINAL DISORDER ( 7 FDA reports)
GINGIVAL SWELLING ( 7 FDA reports)
HAEMATOMA ( 7 FDA reports)
HAEMORRHAGIC ANAEMIA ( 7 FDA reports)
HALLUCINATION, VISUAL ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
HEPATOCELLULAR DAMAGE ( 7 FDA reports)
HEPATOMEGALY ( 7 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 7 FDA reports)
HYPERSOMNIA ( 7 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 7 FDA reports)
INCREASED APPETITE ( 7 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 7 FDA reports)
MALNUTRITION ( 7 FDA reports)
ORTHOPNOEA ( 7 FDA reports)
PANIC DISORDER ( 7 FDA reports)
PARAESTHESIA ORAL ( 7 FDA reports)
PATELLA FRACTURE ( 7 FDA reports)
PEPTIC ULCER ( 7 FDA reports)
POST PROCEDURAL COMPLICATION ( 7 FDA reports)
PRESBYOPIA ( 7 FDA reports)
RASH PAPULAR ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 7 FDA reports)
SENSORY DISTURBANCE ( 7 FDA reports)
SKIN CANCER ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
STENT PLACEMENT ( 7 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 7 FDA reports)
TENDONITIS ( 7 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 7 FDA reports)
THYROID NEOPLASM ( 7 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 7 FDA reports)
TYPE 1 DIABETES MELLITUS ( 7 FDA reports)
UPPER LIMB FRACTURE ( 7 FDA reports)
VITAMIN D DEFICIENCY ( 7 FDA reports)
VITREOUS FLOATERS ( 7 FDA reports)
WRONG DRUG ADMINISTERED ( 7 FDA reports)
ANEURYSM ( 6 FDA reports)
ANGIONEUROTIC OEDEMA ( 6 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 6 FDA reports)
ANOSMIA ( 6 FDA reports)
AORTIC ANEURYSM ( 6 FDA reports)
APHASIA ( 6 FDA reports)
ARTHROPOD BITE ( 6 FDA reports)
ARTHROPOD STING ( 6 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 6 FDA reports)
BEDRIDDEN ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BODY TINEA ( 6 FDA reports)
BURSA CALCIFICATION ( 6 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 6 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 6 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 6 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 6 FDA reports)
DRUG DETOXIFICATION ( 6 FDA reports)
DRY THROAT ( 6 FDA reports)
DYSSTASIA ( 6 FDA reports)
EARLY SATIETY ( 6 FDA reports)
ELECTROLYTE IMBALANCE ( 6 FDA reports)
ENDODONTIC PROCEDURE ( 6 FDA reports)
ENDOMETRIAL ATROPHY ( 6 FDA reports)
EXCORIATION ( 6 FDA reports)
FACE OEDEMA ( 6 FDA reports)
FACET JOINT SYNDROME ( 6 FDA reports)
FIBROUS HISTIOCYTOMA ( 6 FDA reports)
FUNGAL INFECTION ( 6 FDA reports)
GASTRIC DISORDER ( 6 FDA reports)
GINGIVAL BLEEDING ( 6 FDA reports)
GINGIVAL PAIN ( 6 FDA reports)
GYNAECOMASTIA ( 6 FDA reports)
HAEMATOCRIT ABNORMAL ( 6 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 6 FDA reports)
HEPATIC MASS ( 6 FDA reports)
IMMUNOSUPPRESSION ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 6 FDA reports)
INTESTINAL OBSTRUCTION ( 6 FDA reports)
JOINT DISLOCATION ( 6 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 6 FDA reports)
LARYNGITIS ( 6 FDA reports)
LIBIDO DECREASED ( 6 FDA reports)
LIPASE INCREASED ( 6 FDA reports)
LUNG INFILTRATION ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
MEDICAL DEVICE REMOVAL ( 6 FDA reports)
MEDICATION RESIDUE ( 6 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 6 FDA reports)
MUSCLE DISORDER ( 6 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 6 FDA reports)
MYOPATHY ( 6 FDA reports)
NEUROGENIC BLADDER ( 6 FDA reports)
NO ADVERSE EVENT ( 6 FDA reports)
OESOPHAGEAL DISORDER ( 6 FDA reports)
OSTEOSCLEROSIS ( 6 FDA reports)
OVARIAN ADHESION ( 6 FDA reports)
PELVIC ADHESIONS ( 6 FDA reports)
PERIPHERAL COLDNESS ( 6 FDA reports)
POLYURIA ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
PROTHROMBIN TIME PROLONGED ( 6 FDA reports)
PSYCHOTIC DISORDER ( 6 FDA reports)
RASH MACULAR ( 6 FDA reports)
RENAL ATROPHY ( 6 FDA reports)
SICK SINUS SYNDROME ( 6 FDA reports)
SINUS CONGESTION ( 6 FDA reports)
SKIN HYPOPIGMENTATION ( 6 FDA reports)
SKIN INDURATION ( 6 FDA reports)
SPONDYLOLYSIS ( 6 FDA reports)
STEM CELL TRANSPLANT ( 6 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 6 FDA reports)
THYROID MASS ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
ABSCESS LIMB ( 5 FDA reports)
ACTINOMYCOSIS ( 5 FDA reports)
ACUTE PRERENAL FAILURE ( 5 FDA reports)
ALVEOLITIS ( 5 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 5 FDA reports)
ANGER ( 5 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 5 FDA reports)
BASAL CELL CARCINOMA ( 5 FDA reports)
BLEPHAROSPASM ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
CARBON DIOXIDE DECREASED ( 5 FDA reports)
CAROTID ARTERY DISEASE ( 5 FDA reports)
CATHETER REMOVAL ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 5 FDA reports)
CLAVICLE FRACTURE ( 5 FDA reports)
CLOSED FRACTURE MANIPULATION ( 5 FDA reports)
COLITIS ( 5 FDA reports)
COLON ADENOMA ( 5 FDA reports)
CYSTITIS HAEMORRHAGIC ( 5 FDA reports)
DELIRIUM ( 5 FDA reports)
DELUSION ( 5 FDA reports)
DEMENTIA ( 5 FDA reports)
DENTAL TREATMENT ( 5 FDA reports)
DEVICE BREAKAGE ( 5 FDA reports)
DIABETIC NEUROPATHY ( 5 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 5 FDA reports)
DILATATION VENTRICULAR ( 5 FDA reports)
DRUG INTOLERANCE ( 5 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 5 FDA reports)
EAR DISCOMFORT ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 5 FDA reports)
EUPHORIC MOOD ( 5 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 5 FDA reports)
EYE OPERATION ( 5 FDA reports)
FEELING DRUNK ( 5 FDA reports)
FLANK PAIN ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
HEMIPLEGIA ( 5 FDA reports)
HEPATIC LESION ( 5 FDA reports)
HEPATITIS C ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
HYPERPARATHYROIDISM ( 5 FDA reports)
HYPERSPLENISM ( 5 FDA reports)
HYPERTHYROIDISM ( 5 FDA reports)
HYPOPHOSPHATAEMIA ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
INJECTION SITE IRRITATION ( 5 FDA reports)
INJECTION SITE REACTION ( 5 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 5 FDA reports)
LABILE BLOOD PRESSURE ( 5 FDA reports)
LABORATORY TEST ABNORMAL ( 5 FDA reports)
LARYNGEAL OEDEMA ( 5 FDA reports)
LICHEN PLANUS ( 5 FDA reports)
LIMB INJURY ( 5 FDA reports)
LOW TURNOVER OSTEOPATHY ( 5 FDA reports)
LUNG CANCER METASTATIC ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 5 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 5 FDA reports)
MENORRHAGIA ( 5 FDA reports)
METASTASES TO LYMPH NODES ( 5 FDA reports)
MICTURITION URGENCY ( 5 FDA reports)
MIDDLE INSOMNIA ( 5 FDA reports)
MOTOR DYSFUNCTION ( 5 FDA reports)
MUSCULOSKELETAL DISORDER ( 5 FDA reports)
NEPHROPATHY ( 5 FDA reports)
NERVE INJURY ( 5 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 5 FDA reports)
PHOTOPSIA ( 5 FDA reports)
PRESCRIBED OVERDOSE ( 5 FDA reports)
PROSTATIC DISORDER ( 5 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 5 FDA reports)
RADICULOPATHY ( 5 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 5 FDA reports)
REHABILITATION THERAPY ( 5 FDA reports)
RENAL PAIN ( 5 FDA reports)
RESPIRATORY TRACT CONGESTION ( 5 FDA reports)
SARCOIDOSIS ( 5 FDA reports)
SCIATICA ( 5 FDA reports)
SENSATION OF HEAVINESS ( 5 FDA reports)
SKIN HYPERTROPHY ( 5 FDA reports)
SKIN LACERATION ( 5 FDA reports)
SKIN TIGHTNESS ( 5 FDA reports)
SOCIAL PROBLEM ( 5 FDA reports)
SPLENOMEGALY ( 5 FDA reports)
TONSILLAR DISORDER ( 5 FDA reports)
TOOTH ABSCESS ( 5 FDA reports)
TOOTH FRACTURE ( 5 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 5 FDA reports)
TRANSFUSION REACTION ( 5 FDA reports)
URINE ODOUR ABNORMAL ( 5 FDA reports)
URINE OUTPUT DECREASED ( 5 FDA reports)
UROSEPSIS ( 5 FDA reports)
VARICOSE VEIN ( 5 FDA reports)
VEIN DISORDER ( 5 FDA reports)
VENTRICULAR DYSFUNCTION ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
ABDOMINAL MASS ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ACTINIC KERATOSIS ( 4 FDA reports)
ALCOHOL USE ( 4 FDA reports)
ANAEMIA POSTOPERATIVE ( 4 FDA reports)
AORTIC VALVE CALCIFICATION ( 4 FDA reports)
APHONIA ( 4 FDA reports)
APPLICATION SITE RASH ( 4 FDA reports)
ATROPHY ( 4 FDA reports)
BACTERAEMIA ( 4 FDA reports)
BLISTER INFECTED ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BODY HEIGHT DECREASED ( 4 FDA reports)
BREAST CANCER IN SITU ( 4 FDA reports)
BREAST HYPERPLASIA ( 4 FDA reports)
BREAST MASS ( 4 FDA reports)
BREAST OPERATION ( 4 FDA reports)
BREAST TENDERNESS ( 4 FDA reports)
CALCULUS URETERIC ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
CEREBROVASCULAR DISORDER ( 4 FDA reports)
CHOKING ( 4 FDA reports)
CHOLECYSTECTOMY ( 4 FDA reports)
COMA ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 4 FDA reports)
DENTAL FISTULA ( 4 FDA reports)
DIABETIC GASTROPARESIS ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DIVERTICULUM INTESTINAL ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
FLAT AFFECT ( 4 FDA reports)
FOLLICULITIS ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GASTRIC HYPERTONIA ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
HIP ARTHROPLASTY ( 4 FDA reports)
HODGKIN'S DISEASE ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
HYPOTRICHOSIS ( 4 FDA reports)
ILEUS ( 4 FDA reports)
INADEQUATE ANALGESIA ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INITIAL INSOMNIA ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
KYPHOSIS ( 4 FDA reports)
LOCALISED OSTEOARTHRITIS ( 4 FDA reports)
LOWER EXTREMITY MASS ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
METASTATIC LYMPHOMA ( 4 FDA reports)
MITRAL VALVE SCLEROSIS ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
NEPHROPATHY TOXIC ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OESOPHAGEAL PAIN ( 4 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 4 FDA reports)
ORGAN FAILURE ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PANCREATITIS CHRONIC ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
POLYDIPSIA ( 4 FDA reports)
POLYP ( 4 FDA reports)
POLYTRAUMATISM ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
PORPHYRIA NON-ACUTE ( 4 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 4 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
RENAL NEOPLASM ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
RESTLESS LEGS SYNDROME ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
RETINAL VEIN OCCLUSION ( 4 FDA reports)
SCAB ( 4 FDA reports)
SECRETION DISCHARGE ( 4 FDA reports)
SELF-MEDICATION ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 4 FDA reports)
SNEEZING ( 4 FDA reports)
SNORING ( 4 FDA reports)
SPINAL DISORDER ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
STRESS INCONTINENCE ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
VERTIGO POSITIONAL ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
ABNORMAL WEIGHT GAIN ( 3 FDA reports)
ACCIDENT ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
ACUTE SINUSITIS ( 3 FDA reports)
AGORAPHOBIA ( 3 FDA reports)
AMENORRHOEA ( 3 FDA reports)
ANION GAP INCREASED ( 3 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 3 FDA reports)
AORTIC STENOSIS ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
APNOEA ( 3 FDA reports)
APPARENT DEATH ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
APPLICATION SITE IRRITATION ( 3 FDA reports)
APPLICATION SITE PRURITUS ( 3 FDA reports)
APPLICATION SITE REACTION ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
AURICULAR SWELLING ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
CARDIAC PACEMAKER INSERTION ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
CATARACT OPERATION ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CHEMOTHERAPY ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
CULTURE STOOL POSITIVE ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DYSLEXIA ( 3 FDA reports)
DYSTHYMIC DISORDER ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
EJACULATION FAILURE ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
ENERGY INCREASED ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 3 FDA reports)
ESSENTIAL HYPERTENSION ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 3 FDA reports)
FIBROSIS ( 3 FDA reports)
FOOD ALLERGY ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE V ( 3 FDA reports)
GROIN PAIN ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HYPEROSMOLAR STATE ( 3 FDA reports)
HYPERTENSIVE HEART DISEASE ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INJECTION SITE URTICARIA ( 3 FDA reports)
INNER EAR DISORDER ( 3 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
LYMPHADENECTOMY ( 3 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 3 FDA reports)
MARITAL PROBLEM ( 3 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 3 FDA reports)
MICTURITION FREQUENCY DECREASED ( 3 FDA reports)
MITRAL VALVE CALCIFICATION ( 3 FDA reports)
MORTON'S NEUROMA ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
NAIL INFECTION ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
NEPHROCALCINOSIS ( 3 FDA reports)
NEPHROSCLEROSIS ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NEUROFIBROMATOSIS ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
OCULAR VASCULAR DISORDER ( 3 FDA reports)
OESOPHAGEAL DILATATION ( 3 FDA reports)
ORAL DISORDER ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
ORAL TORUS ( 3 FDA reports)
OROPHARYNGEAL SWELLING ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PAPILLARY THYROID CANCER ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PARTNER STRESS ( 3 FDA reports)
PERIODONTITIS ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
PORPHYRIA ( 3 FDA reports)
POST-TRAUMATIC PAIN ( 3 FDA reports)
POSTNASAL DRIP ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PULMONARY INFARCTION ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RESORPTION BONE INCREASED ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESPIRATORY THERAPY ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
RETINAL EXUDATES ( 3 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 3 FDA reports)
RETINOPATHY ( 3 FDA reports)
ROSACEA ( 3 FDA reports)
SEDATION ( 3 FDA reports)
STAG HORN CALCULUS ( 3 FDA reports)
STRESS URINARY INCONTINENCE ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
TENOSYNOVITIS ( 3 FDA reports)
THERAPY CESSATION ( 3 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 3 FDA reports)
THYROID DISORDER ( 3 FDA reports)
THYROXINE FREE INCREASED ( 3 FDA reports)
TIBIA FRACTURE ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
UTERINE HAEMORRHAGE ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
WOUND ( 3 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABDOMINAL OPERATION ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ACROCHORDON ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ALLERGY TO ARTHROPOD STING ( 2 FDA reports)
AMPUTATION ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANGIOSARCOMA ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 2 FDA reports)
BIFASCICULAR BLOCK ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLAST CELL COUNT INCREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEST WALL PAIN ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
CLUSTER HEADACHE ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
COLON CANCER STAGE IV ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
COMPLICATED FRACTURE ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CUTANEOUS SARCOIDOSIS ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYST REMOVAL ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ECTROPION OF CERVIX ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXTERNAL EAR PAIN ( 2 FDA reports)
EXTREMITY CONTRACTURE ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
FRACTURE NONUNION ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GINGIVAL ERYTHEMA ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GLAUCOMA SURGERY ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEART VALVE CALCIFICATION ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HOMICIDE ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOHIDROSIS ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOPERFUSION ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INJECTION SITE ANAESTHESIA ( 2 FDA reports)
INJECTION SITE CALCIFICATION ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJECTION SITE PALLOR ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
IRITIS ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
JOINT CONTRACTURE ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIP DISCOLOURATION ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MUSCLE FIBROSIS ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYASTHENIC SYNDROME ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OPTIC NERVE INJURY ( 2 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL DISCHARGE ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROSTATECTOMY ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PUPILLARY DEFORMITY ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
RALES ( 2 FDA reports)
REGURGITATION OF FOOD ( 2 FDA reports)
RENAL EMBOLISM ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
RHEUMATOID NODULE ( 2 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SEMEN VOLUME DECREASED ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SHIFT TO THE LEFT ( 2 FDA reports)
SHOULDER ARTHROPLASTY ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SKIN WRINKLING ( 2 FDA reports)
SKULL FRACTURE ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SOCIAL PHOBIA ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
TENSION ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THIRST ( 2 FDA reports)
THOUGHT INSERTION ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 2 FDA reports)
THYROIDITIS CHRONIC ( 2 FDA reports)
THYROXINE ABNORMAL ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
TUMOUR ULCERATION ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
UTERINE CERVIX ATROPHY ( 2 FDA reports)
UTERINE DISORDER ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VAGINAL CYST ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VASCULAR GRAFT ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VEIN PAIN ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
VIRAL PHARYNGITIS ( 2 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AUTOTRANSFUSION ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BIOPSY BONE ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DECALCIFICATION ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRANCHIAL CLEFT CYST ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
BURSAL OPERATION ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
DAWN PHENOMENON ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENTAL NECROSIS ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC GLAUCOMA ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
ELBOW DEFORMITY ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENOPHTHALMOS ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTEROSTOMY ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELASH DISCOLOURATION ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FATTY ACID DEFICIENCY ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
FOLLICULAR THYROID CANCER ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC POLYPECTOMY ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HORMONE THERAPY ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYALOSIS ASTEROID ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPOGLOSSAL NERVE DISORDER ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INSPIRATORY CAPACITY ABNORMAL ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
INTRAOCULAR PRESSURE FLUCTUATION ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LESION EXCISION ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MACULE ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MOROSE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECROLYTIC MIGRATORY ERYTHEMA ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN CYSTECTOMY ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENILE PROSTHESIS USER ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIDIVERTICULITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOTOSENSITIVE RASH ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT COMMINGLING ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RADICAL MASTECTOMY ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RHEUMATOID NODULE REMOVAL ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
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SCLERODERMA ( 1 FDA reports)
SCLEROEDEMA ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
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SERUM FERRITIN DECREASED ( 1 FDA reports)
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SKIN EROSION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SPASMODIC DYSPHONIA ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
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SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
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STERNAL FRACTURE ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
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STRESS AT WORK ( 1 FDA reports)
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SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
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SWEATING FEVER ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
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TESTICULAR SWELLING ( 1 FDA reports)
TETANY ( 1 FDA reports)
THALASSAEMIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPY NAIVE ( 1 FDA reports)
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THYROIDECTOMY ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
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TONGUE BLISTERING ( 1 FDA reports)
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TONGUE HAEMORRHAGE ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
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TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TUBAL LIGATION ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULTRASOUND ABDOMEN ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
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UROBILIN URINE PRESENT ( 1 FDA reports)
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VACCINATION FAILURE ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL POLYP ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
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VENOUS INSUFFICIENCY ( 1 FDA reports)
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VIITH NERVE PARALYSIS ( 1 FDA reports)
VIOLENT IDEATION ( 1 FDA reports)
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WEIGHT ABNORMAL ( 1 FDA reports)
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WHEELCHAIR USER ( 1 FDA reports)
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WOUND DRAINAGE ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
X-RAY LIMB ( 1 FDA reports)
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