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

WEIGHT DECREASED ( 5 FDA reports)
ASTHENIA ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
HYPOCHONDRIASIS ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN ( 3 FDA reports)
RASH ( 3 FDA reports)
ARTHRITIS ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
POLYMEDICATION ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOREA ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALL ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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