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

PAIN ( 97 FDA reports)
ANXIETY ( 84 FDA reports)
HYPERTENSION ( 79 FDA reports)
ANAEMIA ( 73 FDA reports)
PNEUMONIA ( 65 FDA reports)
INJURY ( 63 FDA reports)
CEREBROVASCULAR ACCIDENT ( 54 FDA reports)
ARTHRALGIA ( 53 FDA reports)
RENAL FAILURE ( 53 FDA reports)
HEADACHE ( 52 FDA reports)
PAIN IN EXTREMITY ( 51 FDA reports)
DIZZINESS ( 50 FDA reports)
FALL ( 50 FDA reports)
URINARY TRACT INFECTION ( 49 FDA reports)
PYREXIA ( 48 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 47 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 46 FDA reports)
FATIGUE ( 46 FDA reports)
CHEST PAIN ( 45 FDA reports)
DEPRESSION ( 44 FDA reports)
DYSPNOEA ( 43 FDA reports)
CARDIOMEGALY ( 42 FDA reports)
OSTEOARTHRITIS ( 42 FDA reports)
BONE DISORDER ( 41 FDA reports)
OEDEMA PERIPHERAL ( 41 FDA reports)
FEELING ABNORMAL ( 40 FDA reports)
OSTEOPENIA ( 40 FDA reports)
BACK PAIN ( 39 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 39 FDA reports)
OSTEONECROSIS OF JAW ( 38 FDA reports)
ANHEDONIA ( 37 FDA reports)
ASTHENIA ( 37 FDA reports)
ATRIAL FIBRILLATION ( 37 FDA reports)
SEPSIS ( 37 FDA reports)
DIARRHOEA ( 36 FDA reports)
SPINAL COMPRESSION FRACTURE ( 36 FDA reports)
GAIT DISTURBANCE ( 35 FDA reports)
OSTEOMYELITIS ( 35 FDA reports)
COUGH ( 34 FDA reports)
MENTAL DISORDER ( 34 FDA reports)
CHOLELITHIASIS ( 33 FDA reports)
NAUSEA ( 33 FDA reports)
RENAL FAILURE ACUTE ( 33 FDA reports)
ROTATOR CUFF SYNDROME ( 32 FDA reports)
BLOOD PRESSURE INCREASED ( 31 FDA reports)
DYSPHAGIA ( 31 FDA reports)
PANCYTOPENIA ( 31 FDA reports)
ATELECTASIS ( 30 FDA reports)
DIPLOPIA ( 30 FDA reports)
EMOTIONAL DISTRESS ( 30 FDA reports)
HYPERHIDROSIS ( 30 FDA reports)
MUSCLE SPASMS ( 30 FDA reports)
PLEURAL EFFUSION ( 30 FDA reports)
RENAL IMPAIRMENT ( 30 FDA reports)
UNEVALUABLE EVENT ( 29 FDA reports)
UNRESPONSIVE TO STIMULI ( 29 FDA reports)
VISION BLURRED ( 29 FDA reports)
CONFUSIONAL STATE ( 28 FDA reports)
FEAR ( 28 FDA reports)
CAESAREAN SECTION ( 27 FDA reports)
RESPIRATORY FAILURE ( 27 FDA reports)
SPINAL OSTEOARTHRITIS ( 27 FDA reports)
VENTRICULAR TACHYCARDIA ( 27 FDA reports)
WEIGHT DECREASED ( 27 FDA reports)
NEUROPATHY PERIPHERAL ( 26 FDA reports)
RADICULOPATHY ( 26 FDA reports)
VOMITING ( 26 FDA reports)
CORONARY ARTERY DISEASE ( 25 FDA reports)
HYPOAESTHESIA ( 25 FDA reports)
HYPOTENSION ( 25 FDA reports)
OVERDOSE ( 25 FDA reports)
PAIN IN JAW ( 25 FDA reports)
TOOTH FRACTURE ( 25 FDA reports)
MALNUTRITION ( 24 FDA reports)
PERIODONTAL DISEASE ( 24 FDA reports)
BLOOD GLUCOSE INCREASED ( 23 FDA reports)
CARDIAC DISORDER ( 23 FDA reports)
DEHYDRATION ( 23 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 23 FDA reports)
NEPHROLITHIASIS ( 23 FDA reports)
ARTHRITIS ( 22 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 22 FDA reports)
URINARY RETENTION ( 22 FDA reports)
BLOOD CREATININE INCREASED ( 21 FDA reports)
MALAISE ( 21 FDA reports)
MUSCULOSKELETAL PAIN ( 21 FDA reports)
OSTEOPOROSIS ( 21 FDA reports)
PREMATURE BABY ( 21 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 20 FDA reports)
DEVICE MALFUNCTION ( 20 FDA reports)
ENCEPHALOPATHY ( 20 FDA reports)
ENDODONTIC PROCEDURE ( 20 FDA reports)
ILEUS ( 20 FDA reports)
LUNG INFILTRATION ( 20 FDA reports)
LYMPHADENOPATHY ( 20 FDA reports)
MULTIPLE MYELOMA ( 20 FDA reports)
MUSCULAR WEAKNESS ( 20 FDA reports)
NECK PAIN ( 20 FDA reports)
OEDEMA ( 20 FDA reports)
PULMONARY HYPERTENSION ( 20 FDA reports)
RENAL INJURY ( 20 FDA reports)
SINUS DISORDER ( 20 FDA reports)
TACHYCARDIA ( 20 FDA reports)
TREMOR ( 20 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 19 FDA reports)
CARDIOMYOPATHY ( 19 FDA reports)
CEREBRAL ATROPHY ( 19 FDA reports)
COMPRESSION FRACTURE ( 19 FDA reports)
DEATH ( 19 FDA reports)
LEFT ATRIAL DILATATION ( 19 FDA reports)
MYALGIA ( 19 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 19 FDA reports)
APNOEA ( 18 FDA reports)
ARTERIOSCLEROSIS ( 18 FDA reports)
CONTUSION ( 18 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 18 FDA reports)
HAEMOPTYSIS ( 18 FDA reports)
HIATUS HERNIA ( 18 FDA reports)
NERVOUSNESS ( 18 FDA reports)
ARTHROPATHY ( 17 FDA reports)
BONE PAIN ( 17 FDA reports)
BRONCHIAL SECRETION RETENTION ( 17 FDA reports)
BRONCHITIS ( 17 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 17 FDA reports)
CERVICAL CORD COMPRESSION ( 17 FDA reports)
CHILLS ( 17 FDA reports)
CHONDROMALACIA ( 17 FDA reports)
DECREASED INTEREST ( 17 FDA reports)
DENTAL CARIES ( 17 FDA reports)
DENTAL PULP DISORDER ( 17 FDA reports)
DIABETES MELLITUS ( 17 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 17 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 17 FDA reports)
EMPHYSEMA ( 17 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 17 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 17 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 17 FDA reports)
KYPHOSIS ( 17 FDA reports)
LOSS OF CONSCIOUSNESS ( 17 FDA reports)
LUDWIG ANGINA ( 17 FDA reports)
MASTICATION DISORDER ( 17 FDA reports)
MOVEMENT DISORDER ( 17 FDA reports)
MULTI-ORGAN FAILURE ( 17 FDA reports)
MYASTHENIA GRAVIS ( 17 FDA reports)
NEUTROPENIC SEPSIS ( 17 FDA reports)
ORAL PAIN ( 17 FDA reports)
PULMONARY OEDEMA ( 17 FDA reports)
SENSITIVITY OF TEETH ( 17 FDA reports)
SPINAL FUSION ACQUIRED ( 17 FDA reports)
SPUTUM DISCOLOURED ( 17 FDA reports)
SUBCUTANEOUS NODULE ( 17 FDA reports)
ABSCESS DRAINAGE ( 16 FDA reports)
ABSCESS ORAL ( 16 FDA reports)
COLITIS ( 16 FDA reports)
DECREASED APPETITE ( 16 FDA reports)
ERB'S PALSY ( 16 FDA reports)
FACIAL BONES FRACTURE ( 16 FDA reports)
GASTRINOMA ( 16 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 16 FDA reports)
METASTASES TO BONE ( 16 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 16 FDA reports)
MYOCARDIAL INFARCTION ( 16 FDA reports)
OESOPHAGEAL STENOSIS ( 16 FDA reports)
RECTAL PROLAPSE ( 16 FDA reports)
RENAL FAILURE CHRONIC ( 16 FDA reports)
THROMBOCYTOSIS ( 16 FDA reports)
TOOTH EXTRACTION ( 16 FDA reports)
ULCER HAEMORRHAGE ( 16 FDA reports)
VENOUS THROMBOSIS ( 16 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 16 FDA reports)
ABDOMINAL PAIN ( 15 FDA reports)
ADENOMA BENIGN ( 15 FDA reports)
CONDITION AGGRAVATED ( 15 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 15 FDA reports)
DRUG INEFFECTIVE ( 15 FDA reports)
DRUG TOXICITY ( 15 FDA reports)
HYPERLIPIDAEMIA ( 15 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 15 FDA reports)
RIB FRACTURE ( 15 FDA reports)
STRESS ( 15 FDA reports)
SYNCOPE ( 15 FDA reports)
ALOPECIA ( 14 FDA reports)
BILIARY DILATATION ( 14 FDA reports)
BLINDNESS TRANSIENT ( 14 FDA reports)
CANDIDIASIS ( 14 FDA reports)
CHOLECYSTECTOMY ( 14 FDA reports)
CHOLECYSTITIS ( 14 FDA reports)
EXTRASYSTOLES ( 14 FDA reports)
FACIAL PAIN ( 14 FDA reports)
GLAUCOMA ( 14 FDA reports)
HAEMOGLOBIN DECREASED ( 14 FDA reports)
LUMBAR SPINAL STENOSIS ( 14 FDA reports)
LUNG NEOPLASM ( 14 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 14 FDA reports)
NERVE INJURY ( 14 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 14 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 14 FDA reports)
ORAL MUCOSAL HYPERTROPHY ( 14 FDA reports)
PANCREATITIS ACUTE ( 14 FDA reports)
PULMONARY MASS ( 14 FDA reports)
RENAL DISORDER ( 14 FDA reports)
RHABDOMYOLYSIS ( 14 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 14 FDA reports)
ARRHYTHMIA ( 13 FDA reports)
BLOOD BILIRUBIN INCREASED ( 13 FDA reports)
CHOROIDAL DETACHMENT ( 13 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 13 FDA reports)
CONNECTIVE TISSUE DISORDER ( 13 FDA reports)
EJECTION FRACTION DECREASED ( 13 FDA reports)
EYE INJURY ( 13 FDA reports)
FLANK PAIN ( 13 FDA reports)
MENISCUS LESION ( 13 FDA reports)
OSTEOSCLEROSIS ( 13 FDA reports)
PROTEINURIA ( 13 FDA reports)
SOMNOLENCE ( 13 FDA reports)
VITREOUS DETACHMENT ( 13 FDA reports)
VITREOUS HAEMORRHAGE ( 13 FDA reports)
BASAL CELL CARCINOMA ( 12 FDA reports)
BONE OPERATION ( 12 FDA reports)
BRONCHITIS CHRONIC ( 12 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 12 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 12 FDA reports)
ECTROPION ( 12 FDA reports)
FOETAL DISORDER ( 12 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 12 FDA reports)
HEAD INJURY ( 12 FDA reports)
HYPOCALCAEMIA ( 12 FDA reports)
HYPOTONY OF EYE ( 12 FDA reports)
KERATITIS ( 12 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 12 FDA reports)
LUNG CONSOLIDATION ( 12 FDA reports)
MYOPIA ( 12 FDA reports)
OPEN REDUCTION OF FRACTURE ( 12 FDA reports)
RASH ( 12 FDA reports)
RECTAL PROLAPSE REPAIR ( 12 FDA reports)
VITREOUS FLOATERS ( 12 FDA reports)
ASTHMA ( 11 FDA reports)
CAECUM OPERATION ( 11 FDA reports)
CEREBRAL HAEMORRHAGE ( 11 FDA reports)
DISABILITY ( 11 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 11 FDA reports)
GASTROENTERITIS ( 11 FDA reports)
HYPERKALAEMIA ( 11 FDA reports)
HYPONATRAEMIA ( 11 FDA reports)
LETHARGY ( 11 FDA reports)
MITRAL VALVE INCOMPETENCE ( 11 FDA reports)
PARAESTHESIA ( 11 FDA reports)
PRURITUS ( 11 FDA reports)
RESPIRATORY DISORDER ( 11 FDA reports)
SPLENOMEGALY ( 11 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 11 FDA reports)
WEIGHT INCREASED ( 11 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 10 FDA reports)
ADVERSE DRUG REACTION ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 10 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 10 FDA reports)
BLOOD URIC ACID INCREASED ( 10 FDA reports)
CELLULITIS ( 10 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 10 FDA reports)
DEVICE RELATED INFECTION ( 10 FDA reports)
PERIARTHRITIS ( 10 FDA reports)
PROTHROMBIN TIME SHORTENED ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
SKIN ULCER ( 10 FDA reports)
TENDERNESS ( 10 FDA reports)
TENDONITIS ( 10 FDA reports)
URINE OUTPUT DECREASED ( 10 FDA reports)
BACTERAEMIA ( 9 FDA reports)
BLOOD PRESSURE DECREASED ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 9 FDA reports)
CEREBRAL INFARCTION ( 9 FDA reports)
DEEP VEIN THROMBOSIS ( 9 FDA reports)
ELECTROLYTE IMBALANCE ( 9 FDA reports)
ERYTHEMA ( 9 FDA reports)
FEAR OF DEATH ( 9 FDA reports)
FOETAL DISTRESS SYNDROME ( 9 FDA reports)
FUNGAL INFECTION ( 9 FDA reports)
INFECTION ( 9 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 9 FDA reports)
LOW BIRTH WEIGHT BABY ( 9 FDA reports)
MULTIPLE INJURIES ( 9 FDA reports)
MUSCLE DISORDER ( 9 FDA reports)
NERVE ROOT COMPRESSION ( 9 FDA reports)
NEUROMYOPATHY ( 9 FDA reports)
NODULE ( 9 FDA reports)
PREMATURE LABOUR ( 9 FDA reports)
SCAR ( 9 FDA reports)
SCOLIOSIS ( 9 FDA reports)
TOOTHACHE ( 9 FDA reports)
VITAMIN D DEFICIENCY ( 9 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
ACUTE PULMONARY OEDEMA ( 8 FDA reports)
ANGINA PECTORIS ( 8 FDA reports)
AORTIC STENOSIS ( 8 FDA reports)
APLASTIC ANAEMIA ( 8 FDA reports)
BLISTER ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 8 FDA reports)
BLOOD UREA INCREASED ( 8 FDA reports)
BONE FRAGMENTATION ( 8 FDA reports)
BREAST CANCER RECURRENT ( 8 FDA reports)
COAGULOPATHY ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
COSTOCHONDRITIS ( 8 FDA reports)
DYSARTHRIA ( 8 FDA reports)
EDENTULOUS ( 8 FDA reports)
ENCEPHALITIS POST MEASLES ( 8 FDA reports)
FEMORAL NECK FRACTURE ( 8 FDA reports)
FUNGAEMIA ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
GESTATIONAL HYPERTENSION ( 8 FDA reports)
GINGIVAL INFECTION ( 8 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 8 FDA reports)
HEPATIC ENCEPHALOPATHY ( 8 FDA reports)
HEPATITIS FULMINANT ( 8 FDA reports)
HYPOPHOSPHATAEMIA ( 8 FDA reports)
HYPOVOLAEMIA ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
IMMUNOSUPPRESSION ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 8 FDA reports)
INTRAOCULAR LENS IMPLANT ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
JOINT PROSTHESIS USER ( 8 FDA reports)
LIVER DISORDER ( 8 FDA reports)
MENINGIOMA ( 8 FDA reports)
NARCOLEPSY ( 8 FDA reports)
NERVE ROOT LESION ( 8 FDA reports)
OEDEMA MOUTH ( 8 FDA reports)
PALLOR ( 8 FDA reports)
PATHOLOGICAL FRACTURE ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
PRE-ECLAMPSIA ( 8 FDA reports)
PREMATURE DELIVERY ( 8 FDA reports)
RENAL CYST ( 8 FDA reports)
SACROILIITIS ( 8 FDA reports)
STREPTOCOCCAL SEPSIS ( 8 FDA reports)
STRESS URINARY INCONTINENCE ( 8 FDA reports)
SYNOVIAL CYST ( 8 FDA reports)
TOOTH LOSS ( 8 FDA reports)
TRACHEOBRONCHITIS ( 8 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 8 FDA reports)
TYPE 1 DIABETES MELLITUS ( 8 FDA reports)
UMBILICAL HERNIA ( 8 FDA reports)
VASCULAR OCCLUSION ( 8 FDA reports)
VENTRICULAR FIBRILLATION ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 7 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 7 FDA reports)
CAECITIS ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 7 FDA reports)
CHOLANGITIS CHRONIC ( 7 FDA reports)
CHOLECYSTITIS ACUTE ( 7 FDA reports)
CIRCULATORY COLLAPSE ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DIABETIC NEUROPATHY ( 7 FDA reports)
DIVERTICULUM ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 7 FDA reports)
FAILURE TO THRIVE ( 7 FDA reports)
FOETAL GROWTH RESTRICTION ( 7 FDA reports)
FOOD AVERSION ( 7 FDA reports)
GOUT ( 7 FDA reports)
HEART RATE IRREGULAR ( 7 FDA reports)
HEPATIC LESION ( 7 FDA reports)
INCORRECT DOSE ADMINISTERED ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
IRON METABOLISM DISORDER ( 7 FDA reports)
LEUKOPENIA ( 7 FDA reports)
LUNG DISORDER ( 7 FDA reports)
MALABSORPTION ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
PANCREATIC INSUFFICIENCY ( 7 FDA reports)
PNEUMATOSIS INTESTINALIS ( 7 FDA reports)
PULMONARY CONGESTION ( 7 FDA reports)
SKIN LESION ( 7 FDA reports)
SKIN NEOPLASM EXCISION ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
STEATORRHOEA ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 7 FDA reports)
VERTIGO ( 7 FDA reports)
VISUAL IMPAIRMENT ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
ACIDOSIS ( 6 FDA reports)
AZOTAEMIA ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
CAROTID ARTERY STENOSIS ( 6 FDA reports)
CATARACT ( 6 FDA reports)
CHORIOAMNIONITIS ( 6 FDA reports)
COMA ( 6 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 6 FDA reports)
DEVELOPMENTAL DELAY ( 6 FDA reports)
DILATATION VENTRICULAR ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
ECONOMIC PROBLEM ( 6 FDA reports)
EXOSTOSIS ( 6 FDA reports)
FEELING HOT ( 6 FDA reports)
FLUID OVERLOAD ( 6 FDA reports)
FRACTURED SACRUM ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
GASTROINTESTINAL INFECTION ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
HAEMOTHORAX ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
HYPOTHYROIDISM ( 6 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 6 FDA reports)
INTERVERTEBRAL DISCITIS ( 6 FDA reports)
MEDIASTINAL HAEMATOMA ( 6 FDA reports)
NEONATAL ASPHYXIA ( 6 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 6 FDA reports)
ORTHOSTATIC HYPOTENSION ( 6 FDA reports)
PLACENTA PRAEVIA ( 6 FDA reports)
POLYDIPSIA ( 6 FDA reports)
POLYURIA ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
RADICULITIS CERVICAL ( 6 FDA reports)
RADICULITIS LUMBOSACRAL ( 6 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 6 FDA reports)
SMALL FOR DATES BABY ( 6 FDA reports)
SPINAL COLUMN STENOSIS ( 6 FDA reports)
ABDOMINAL PAIN LOWER ( 5 FDA reports)
APHASIA ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
BURSITIS INFECTIVE ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
CEREBRAL ISCHAEMIA ( 5 FDA reports)
CHRONIC SINUSITIS ( 5 FDA reports)
DECUBITUS ULCER ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 5 FDA reports)
EMOTIONAL DISORDER ( 5 FDA reports)
ENDOCARDITIS ( 5 FDA reports)
ENDOTRACHEAL INTUBATION ( 5 FDA reports)
EYE SWELLING ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
INGROWING NAIL ( 5 FDA reports)
LORDOSIS ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
OCCULT BLOOD POSITIVE ( 5 FDA reports)
ONYCHOMYCOSIS ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PHAEOCHROMOCYTOMA ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
SKIN DISORDER ( 5 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
VASCULAR GRAFT ( 5 FDA reports)
VERTIGO POSITIONAL ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ABSCESS ( 4 FDA reports)
ANOXIC ENCEPHALOPATHY ( 4 FDA reports)
AORTIC ANEURYSM ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
BRAIN DEATH ( 4 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 4 FDA reports)
CEREBROVASCULAR DISORDER ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
EPIDURAL ANAESTHESIA ( 4 FDA reports)
FISTULA ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
FOOT DEFORMITY ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPERPROTEINAEMIA ( 4 FDA reports)
HYPERTENSIVE CRISIS ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYSTEROTOMY ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INTESTINAL MUCOSAL ATROPHY ( 4 FDA reports)
JOINT INJECTION ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
KNEE OPERATION ( 4 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
LOCALISED INFECTION ( 4 FDA reports)
MECHANICAL VENTILATION ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
PERIPHERAL COLDNESS ( 4 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 4 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PROSTATIC DISORDER ( 4 FDA reports)
PROTEIN TOTAL DECREASED ( 4 FDA reports)
RESTLESS LEGS SYNDROME ( 4 FDA reports)
SHOULDER OPERATION ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SPEECH REHABILITATION ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
TENSION ( 4 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 4 FDA reports)
UMBILICAL HERNIA REPAIR ( 4 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 4 FDA reports)
VASCULAR SHUNT ( 4 FDA reports)
VENOUS INSUFFICIENCY ( 4 FDA reports)
ABNORMAL FAECES ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ANAPHYLACTOID SYNDROME OF PREGNANCY ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
BREATH ODOUR ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC FAILURE CHRONIC ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIAC OPERATION ( 3 FDA reports)
CENTRAL LINE INFECTION ( 3 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HEAD DISCOMFORT ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HELLP SYNDROME ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
IATROGENIC INJURY ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NORMAL NEWBORN ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PARAPROTEINAEMIA ( 3 FDA reports)
PEAU D'ORANGE ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RENAL HAEMORRHAGE ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SCAPULA FRACTURE ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SKIN ATROPHY ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SKIN HYPERTROPHY ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SKIN MASS ( 3 FDA reports)
SKIN PLAQUE ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VITAMIN B12 DECREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ANGER ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
AORTIC VALVE CALCIFICATION ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRADYCARDIA FOETAL ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BREAST FEEDING ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BREECH PRESENTATION ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CHOLURIA ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYSTIC FIBROSIS ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DYSENTERY ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EXTREMITY CONTRACTURE ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FIBRIN DECREASED ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTRIC PH DECREASED ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HIGH RISK PREGNANCY ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPOSTHENURIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
RALES ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SKIN DEGENERATIVE DISORDER ( 2 FDA reports)
SPECIFIC GRAVITY URINE DECREASED ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
ARRHYTHMIA NEONATAL ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL ARRHYTHMIA ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
METATARSAL EXCISION ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYP ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL HYPOPLASIA ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETINOPEXY ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RHEUMATIC HEART DISEASE ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SOLITARY KIDNEY ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICOSE VEIN OPERATION ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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