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

HYPERTENSION ( 22 FDA reports)
ANXIETY ( 19 FDA reports)
DEPRESSION ( 19 FDA reports)
FALL ( 19 FDA reports)
INJURY ( 19 FDA reports)
JAUNDICE ( 19 FDA reports)
MALNUTRITION ( 19 FDA reports)
PAIN ( 19 FDA reports)
HYPOAESTHESIA ( 18 FDA reports)
WEIGHT DECREASED ( 18 FDA reports)
ABDOMINAL PAIN UPPER ( 17 FDA reports)
AGITATION ( 17 FDA reports)
ANHEDONIA ( 17 FDA reports)
ANKLE FRACTURE ( 17 FDA reports)
ASCITES ( 17 FDA reports)
BREATH ODOUR ( 17 FDA reports)
CACHEXIA ( 17 FDA reports)
COMPRESSION FRACTURE ( 17 FDA reports)
DISABILITY ( 17 FDA reports)
DRY EYE ( 17 FDA reports)
DRY MOUTH ( 17 FDA reports)
DUODENITIS ( 17 FDA reports)
DYSPNOEA ( 17 FDA reports)
FACIAL PAIN ( 17 FDA reports)
GASTRITIS ( 17 FDA reports)
HEART RATE IRREGULAR ( 17 FDA reports)
HEPATITIS ( 17 FDA reports)
HYPERTHYROIDISM ( 17 FDA reports)
HYPOVOLAEMIA ( 17 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 17 FDA reports)
INSOMNIA ( 17 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 17 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 17 FDA reports)
KYPHOSIS ( 17 FDA reports)
MIGRAINE ( 17 FDA reports)
MUCOSAL INFLAMMATION ( 17 FDA reports)
MUSCLE STRAIN ( 17 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 17 FDA reports)
OSTEOMYELITIS CHRONIC ( 17 FDA reports)
OSTEONECROSIS OF JAW ( 17 FDA reports)
OSTEOPENIA ( 17 FDA reports)
OSTEOPOROSIS ( 17 FDA reports)
PARAESTHESIA ( 17 FDA reports)
PERIODONTAL DISEASE ( 17 FDA reports)
RENAL FAILURE CHRONIC ( 17 FDA reports)
RIB FRACTURE ( 17 FDA reports)
SINUS CONGESTION ( 17 FDA reports)
SINUS TACHYCARDIA ( 17 FDA reports)
STOMATITIS ( 17 FDA reports)
SWELLING FACE ( 17 FDA reports)
TINNITUS ( 17 FDA reports)
VITAMIN A DEFICIENCY ( 17 FDA reports)
DEAFNESS ( 16 FDA reports)
DEHYDRATION ( 16 FDA reports)
EAR PAIN ( 16 FDA reports)
EPISTAXIS ( 16 FDA reports)
TOOTH INFECTION ( 16 FDA reports)
VISION BLURRED ( 16 FDA reports)
ALOPECIA ( 15 FDA reports)
ANOREXIA NERVOSA ( 15 FDA reports)
BONE DENSITY DECREASED ( 15 FDA reports)
BONE MARROW FAILURE ( 15 FDA reports)
CEREBROVASCULAR ACCIDENT ( 15 FDA reports)
CRANIAL NERVE DISORDER ( 15 FDA reports)
DENTAL CARIES ( 15 FDA reports)
ENDOCRINE DISORDER ( 15 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 15 FDA reports)
FACET JOINT SYNDROME ( 15 FDA reports)
FAILURE TO THRIVE ( 15 FDA reports)
FEELING ABNORMAL ( 15 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 15 FDA reports)
HYPERALDOSTERONISM ( 15 FDA reports)
HYPOGLYCAEMIA ( 15 FDA reports)
HYPOMETABOLISM ( 15 FDA reports)
IMMUNODEFICIENCY ( 15 FDA reports)
JOINT SWELLING ( 15 FDA reports)
NASAL ULCER ( 15 FDA reports)
PALPITATIONS ( 15 FDA reports)
PINEAL GLAND CYST ( 15 FDA reports)
RAYNAUD'S PHENOMENON ( 15 FDA reports)
RHINITIS ( 15 FDA reports)
SCOLIOSIS ( 15 FDA reports)
SIALOADENITIS ( 15 FDA reports)
TIBIA FRACTURE ( 15 FDA reports)
VITAMIN C DEFICIENCY ( 15 FDA reports)
VITAMIN D DEFICIENCY ( 15 FDA reports)
ANAEMIA ( 14 FDA reports)
BONE MARROW OEDEMA ( 14 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 14 FDA reports)
VERTEBRAL WEDGING ( 14 FDA reports)
BONE PAIN ( 13 FDA reports)
HYPERCORTICOIDISM ( 13 FDA reports)
KIDNEY MALROTATION ( 13 FDA reports)
OSTEOCHONDROSIS ( 13 FDA reports)
OSTEOMALACIA ( 13 FDA reports)
RIGHT ATRIAL DILATATION ( 13 FDA reports)
BACK PAIN ( 12 FDA reports)
NECK PAIN ( 12 FDA reports)
PAIN IN EXTREMITY ( 12 FDA reports)
HEADACHE ( 11 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ACUTE PULMONARY OEDEMA ( 6 FDA reports)
ANAL FISTULA ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
CROHN'S DISEASE ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
GASTRIC NEOPLASM ( 5 FDA reports)
LEFT VENTRICULAR FAILURE ( 5 FDA reports)
SPLENIC INJURY ( 5 FDA reports)
AMENORRHOEA ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
VOMITING ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
PERIRECTAL ABSCESS ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
SCAR ( 3 FDA reports)
SPASTIC DIPLEGIA ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
ABDOMINAL INJURY ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DIAPHRAGMATIC INJURY ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
INTERCOSTAL NEURALGIA ( 2 FDA reports)
KLEPTOMANIA ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PHYSICAL DISABILITY ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
TRAUMATIC LIVER INJURY ( 2 FDA reports)
TRAUMATIC SHOCK ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ACNE ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HYPERCHROMIC ANAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OSTEOMA CUTIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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