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

DYSPNOEA ( 38 FDA reports)
PAIN ( 35 FDA reports)
INJURY ( 27 FDA reports)
FATIGUE ( 21 FDA reports)
ATRIAL FIBRILLATION ( 17 FDA reports)
ANXIETY ( 16 FDA reports)
ECONOMIC PROBLEM ( 16 FDA reports)
VOMITING ( 15 FDA reports)
COUGH ( 14 FDA reports)
HEADACHE ( 14 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 14 FDA reports)
MUSCLE SPASMS ( 14 FDA reports)
FALL ( 13 FDA reports)
CONVULSION ( 12 FDA reports)
MEMORY IMPAIRMENT ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 12 FDA reports)
ASTHENIA ( 11 FDA reports)
COMPLETED SUICIDE ( 11 FDA reports)
FEELING ABNORMAL ( 11 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 11 FDA reports)
HYPERTENSION ( 11 FDA reports)
URINARY TRACT INFECTION ( 11 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 10 FDA reports)
CHEST PAIN ( 10 FDA reports)
CONFUSIONAL STATE ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
ABDOMINAL PAIN ( 9 FDA reports)
ANAEMIA ( 9 FDA reports)
ANHEDONIA ( 9 FDA reports)
ARTHRALGIA ( 9 FDA reports)
CARDIOMEGALY ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
DIZZINESS ( 9 FDA reports)
FIBROMYALGIA ( 9 FDA reports)
GAIT DISTURBANCE ( 9 FDA reports)
HYPOTENSION ( 9 FDA reports)
ANGINA PECTORIS ( 8 FDA reports)
AORTIC VALVE INCOMPETENCE ( 8 FDA reports)
BACK PAIN ( 8 FDA reports)
CEREBROVASCULAR ACCIDENT ( 8 FDA reports)
DIABETES MELLITUS ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
INJECTION SITE PAIN ( 8 FDA reports)
MALAISE ( 8 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 8 FDA reports)
SYNCOPE ( 8 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 8 FDA reports)
TYPE 2 DIABETES MELLITUS ( 8 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
BRONCHITIS ( 7 FDA reports)
CARDIOMYOPATHY ( 7 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 7 FDA reports)
CORONARY ARTERY DISEASE ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
HAEMATURIA ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 7 FDA reports)
MULTIPLE INJURIES ( 7 FDA reports)
NEPHROLITHIASIS ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
PRODUCT ADHESION ISSUE ( 7 FDA reports)
ROAD TRAFFIC ACCIDENT ( 7 FDA reports)
SLEEP APNOEA SYNDROME ( 7 FDA reports)
TREMOR ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
AGITATION ( 6 FDA reports)
ASTHMA ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DRUG TOXICITY ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
FUNGAL INFECTION ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
NERVE COMPRESSION ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
SCIATICA ( 6 FDA reports)
SPINAL OSTEOARTHRITIS ( 6 FDA reports)
WHEEZING ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
APPLICATION SITE ERYTHEMA ( 5 FDA reports)
ARTERIOSCLEROSIS ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DEATH ( 5 FDA reports)
DRUG ABUSE ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
DRUG PRESCRIBING ERROR ( 5 FDA reports)
EMOTIONAL DISORDER ( 5 FDA reports)
EMOTIONAL DISTRESS ( 5 FDA reports)
ERYTHEMA MULTIFORME ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEART RATE IRREGULAR ( 5 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
INTESTINAL OBSTRUCTION ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
OSTEOARTHRITIS ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 5 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 5 FDA reports)
WOUND INFECTION ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANAL ABSCESS ( 4 FDA reports)
APPLICATION SITE RASH ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DYSPAREUNIA ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
GANGRENE ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
PLEURAL FIBROSIS ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
RALES ( 4 FDA reports)
RASH ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
RETINAL OEDEMA ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SCROTAL ABSCESS ( 4 FDA reports)
SKIN INFECTION ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
WRIST FRACTURE ( 4 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANGER ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
AORTIC STENOSIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CERVICAL SPINAL STENOSIS ( 3 FDA reports)
CHILLS ( 3 FDA reports)
COMA ( 3 FDA reports)
COR PULMONALE ( 3 FDA reports)
CORONARY ARTERY BYPASS ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
COSTOCHONDRITIS ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DIASTOLIC DYSFUNCTION ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
FOETAL GROWTH RETARDATION ( 3 FDA reports)
FOOT AMPUTATION ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LUMBAR SPINAL STENOSIS ( 3 FDA reports)
LUNG HYPERINFLATION ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
METHAEMOGLOBINAEMIA ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
OVARIAN ADHESION ( 3 FDA reports)
PELVIC ADHESIONS ( 3 FDA reports)
PELVIC PAIN ( 3 FDA reports)
PNEUMONIA MYCOPLASMAL ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
RAYNAUD'S PHENOMENON ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
SALPINGITIS ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
SOCIAL PROBLEM ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TREATMENT FAILURE ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ENURESIS ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FAT NECROSIS ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTRASPINAL ABSCESS ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 2 FDA reports)
LIMB OPERATION ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MANIA ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN ( 2 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NASAL SEPTUM DEVIATION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PARASPINAL ABSCESS ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POLYCYSTIC OVARIES ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PULMONARY ARTERY STENOSIS ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VICTIM OF CHILD ABUSE ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACNE PUSTULAR ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GINGIVAL ATROPHY ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC EMBOLISATION ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NODULE ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PHYSICAL ABUSE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
SALPINGECTOMY ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBGALEAL HAEMATOMA ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 1 FDA reports)
THYROID CYST ( 1 FDA reports)
TIC ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTEBRAL COLUMN MASS ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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