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

FALL ( 37 FDA reports)
DYSPNOEA ( 34 FDA reports)
PAIN ( 31 FDA reports)
DEPRESSION ( 29 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 28 FDA reports)
COUGH ( 27 FDA reports)
DIZZINESS ( 27 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 26 FDA reports)
FATIGUE ( 26 FDA reports)
HYPERTENSION ( 24 FDA reports)
INJURY ( 22 FDA reports)
ASTHMA ( 20 FDA reports)
BONE DISORDER ( 18 FDA reports)
CATARACT ( 18 FDA reports)
NAUSEA ( 17 FDA reports)
PNEUMONIA ( 17 FDA reports)
RESPIRATORY FAILURE ( 17 FDA reports)
SINUSITIS ( 17 FDA reports)
BACK PAIN ( 16 FDA reports)
CONVULSION ( 16 FDA reports)
ERYTHEMA ( 16 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 16 FDA reports)
HEADACHE ( 16 FDA reports)
LOSS OF CONSCIOUSNESS ( 16 FDA reports)
RECTAL HAEMORRHAGE ( 16 FDA reports)
ARTHRALGIA ( 15 FDA reports)
RENAL FAILURE CHRONIC ( 15 FDA reports)
ASTHENIA ( 14 FDA reports)
DRY MOUTH ( 14 FDA reports)
EMOTIONAL DISTRESS ( 14 FDA reports)
SYNCOPE ( 14 FDA reports)
TACHYCARDIA ( 14 FDA reports)
CHEST PAIN ( 13 FDA reports)
DRUG INEFFECTIVE ( 13 FDA reports)
HEART RATE IRREGULAR ( 13 FDA reports)
TREMOR ( 13 FDA reports)
URINARY TRACT INFECTION ( 13 FDA reports)
ANGINA PECTORIS ( 12 FDA reports)
ANXIETY ( 12 FDA reports)
CELLULITIS ( 12 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 12 FDA reports)
CORONARY ARTERY DISEASE ( 12 FDA reports)
HAEMOGLOBIN DECREASED ( 12 FDA reports)
HEART VALVE CALCIFICATION ( 12 FDA reports)
HEART VALVE INCOMPETENCE ( 12 FDA reports)
HYPOGLYCAEMIA ( 12 FDA reports)
LABILE BLOOD PRESSURE ( 12 FDA reports)
MEMORY IMPAIRMENT ( 12 FDA reports)
PAIN IN EXTREMITY ( 12 FDA reports)
RADIOTHERAPY ( 12 FDA reports)
URINE ODOUR ABNORMAL ( 12 FDA reports)
WEIGHT DECREASED ( 12 FDA reports)
ANAEMIA ( 11 FDA reports)
ATRIAL FIBRILLATION ( 11 FDA reports)
CEREBROVASCULAR ACCIDENT ( 11 FDA reports)
DEATH ( 11 FDA reports)
DIARRHOEA ( 11 FDA reports)
DRUG HYPERSENSITIVITY ( 11 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 11 FDA reports)
GINGIVAL INFECTION ( 11 FDA reports)
HEPATIC STEATOSIS ( 11 FDA reports)
PLEURAL EFFUSION ( 11 FDA reports)
SWELLING ( 11 FDA reports)
TENDERNESS ( 11 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 10 FDA reports)
ANGINA UNSTABLE ( 10 FDA reports)
ATAXIA ( 10 FDA reports)
BASAL CELL CARCINOMA ( 10 FDA reports)
BONE DEBRIDEMENT ( 10 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 10 FDA reports)
CEREBRAL ARTERY STENOSIS ( 10 FDA reports)
CEREBROSCLEROSIS ( 10 FDA reports)
CERUMEN IMPACTION ( 10 FDA reports)
COLONOSCOPY ABNORMAL ( 10 FDA reports)
DENTAL CARIES ( 10 FDA reports)
DIVERTICULUM INTESTINAL ( 10 FDA reports)
EAR PAIN ( 10 FDA reports)
EATING DISORDER ( 10 FDA reports)
FISTULA ( 10 FDA reports)
GINGIVAL ULCERATION ( 10 FDA reports)
HAEMATOCHEZIA ( 10 FDA reports)
HYPOAESTHESIA ( 10 FDA reports)
IMPAIRED HEALING ( 10 FDA reports)
INCISIONAL DRAINAGE ( 10 FDA reports)
INCONTINENCE ( 10 FDA reports)
MASTICATION DISORDER ( 10 FDA reports)
NEUROPATHY PERIPHERAL ( 10 FDA reports)
NIGHT SWEATS ( 10 FDA reports)
OSTEOMYELITIS ( 10 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 10 FDA reports)
PALPITATIONS ( 10 FDA reports)
PRIMARY SEQUESTRUM ( 10 FDA reports)
PURULENCE ( 10 FDA reports)
PYELONEPHRITIS ( 10 FDA reports)
RENAL FAILURE ( 10 FDA reports)
SOFT TISSUE INFECTION ( 10 FDA reports)
TOOTH DISCOLOURATION ( 10 FDA reports)
TOOTH EXTRACTION ( 10 FDA reports)
TOOTH FRACTURE ( 10 FDA reports)
TOOTH LOSS ( 10 FDA reports)
VISUAL IMPAIRMENT ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
ADVERSE DRUG REACTION ( 9 FDA reports)
BRONCHITIS ( 9 FDA reports)
CARDIAC DISORDER ( 9 FDA reports)
FEMUR FRACTURE ( 9 FDA reports)
HYPERLIPIDAEMIA ( 9 FDA reports)
HYPOXIA ( 9 FDA reports)
LACUNAR INFARCTION ( 9 FDA reports)
NOCTURIA ( 9 FDA reports)
VOMITING ( 9 FDA reports)
ABSCESS JAW ( 8 FDA reports)
BLINDNESS ( 8 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 8 FDA reports)
CORONARY ARTERY EMBOLISM ( 8 FDA reports)
DIABETIC NEPHROPATHY ( 8 FDA reports)
DIABETIC NEUROPATHY ( 8 FDA reports)
DIABETIC RETINAL OEDEMA ( 8 FDA reports)
DIABETIC RETINOPATHY ( 8 FDA reports)
DRUG DOSE OMISSION ( 8 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 8 FDA reports)
HYPERCAPNIA ( 8 FDA reports)
LIPIDS INCREASED ( 8 FDA reports)
LOW TURNOVER OSTEOPATHY ( 8 FDA reports)
LUNG NEOPLASM ( 8 FDA reports)
MACULAR DEGENERATION ( 8 FDA reports)
MACULOPATHY ( 8 FDA reports)
MASS ( 8 FDA reports)
MENTAL STATUS CHANGES ( 8 FDA reports)
METABOLIC ALKALOSIS ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
NASAL CONGESTION ( 8 FDA reports)
OSTEONECROSIS OF JAW ( 8 FDA reports)
PELVIC FRACTURE ( 8 FDA reports)
PELVIC PAIN ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
PULMONARY HYPERTENSION ( 8 FDA reports)
RADIUS FRACTURE ( 8 FDA reports)
RENAL CYST ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
SCOLIOSIS ( 8 FDA reports)
SEASONAL ALLERGY ( 8 FDA reports)
SKIN LESION ( 8 FDA reports)
SPINAL COLUMN STENOSIS ( 8 FDA reports)
STASIS DERMATITIS ( 8 FDA reports)
VENTRICULAR HYPERTROPHY ( 8 FDA reports)
WRIST FRACTURE ( 8 FDA reports)
ACUTE CORONARY SYNDROME ( 7 FDA reports)
ADRENAL MASS ( 7 FDA reports)
ARTERIOSCLEROSIS ( 7 FDA reports)
AZOTAEMIA ( 7 FDA reports)
BACTERIURIA ( 7 FDA reports)
BLISTER ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CARDIAC MURMUR ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
DYSURIA ( 7 FDA reports)
ECONOMIC PROBLEM ( 7 FDA reports)
GASTROINTESTINAL DISORDER ( 7 FDA reports)
GRAND MAL CONVULSION ( 7 FDA reports)
HEARING IMPAIRED ( 7 FDA reports)
HYPERCALCAEMIA ( 7 FDA reports)
HYPERPARATHYROIDISM ( 7 FDA reports)
HYPOMAGNESAEMIA ( 7 FDA reports)
HYPOPHAGIA ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
NEPHROSCLEROSIS ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
SINUS DISORDER ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
WHEEZING ( 7 FDA reports)
BRONCHITIS ACUTE ( 6 FDA reports)
CONJUNCTIVITIS ( 6 FDA reports)
CYSTITIS ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
ECCHYMOSIS ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
MITRAL VALVE INCOMPETENCE ( 6 FDA reports)
MOBILITY DECREASED ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
PNEUMOTHORAX ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
PRURITUS GENERALISED ( 6 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 6 FDA reports)
RIB FRACTURE ( 6 FDA reports)
TRAUMATIC LUNG INJURY ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 5 FDA reports)
COAGULOPATHY ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HAEMOTHORAX ( 5 FDA reports)
HEPATIC CONGESTION ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
POLLAKIURIA ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 4 FDA reports)
AORTIC STENOSIS ( 4 FDA reports)
AORTIC VALVE INCOMPETENCE ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
BRONCHOSPASM ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CATARACT OPERATION ( 4 FDA reports)
COMA ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DERMATITIS ALLERGIC ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
ESCHAR ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
GASTROENTERITIS VIRAL ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
INTRAOCULAR LENS IMPLANT ( 4 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RASH ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SOCIAL PROBLEM ( 4 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VAGINITIS ( 4 FDA reports)
AGGRESSION ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DROOLING ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
APATHY ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CAROTID ARTERY ATHEROMA ( 2 FDA reports)
CHEST WALL PAIN ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
CONGENITAL CYSTIC LUNG ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEART VALVE STENOSIS ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PROSTATIC PAIN ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
APHONIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EPIPHYSIOLYSIS ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODULE ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
POLYP ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENSION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
ULCER ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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