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

FATIGUE ( 10 FDA reports)
HEADACHE ( 7 FDA reports)
PAIN ( 7 FDA reports)
ANXIETY ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
INJURY ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
BLISTER ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DYSPHONIA ( 5 FDA reports)
METRORRHAGIA ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ACTINIC KERATOSIS ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
CHORIORETINITIS ( 4 FDA reports)
COMA ( 4 FDA reports)
CYST ( 4 FDA reports)
DEBRIDEMENT ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
OESOPHAGEAL MASS ( 4 FDA reports)
OESOPHAGITIS ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
OSTEONECROSIS OF JAW ( 4 FDA reports)
OSTEOPENIA ( 4 FDA reports)
PAIN IN JAW ( 4 FDA reports)
PHYSICAL DISABILITY ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
RASH ( 4 FDA reports)
SCAR ( 4 FDA reports)
SERUM SEROTONIN INCREASED ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
UTERINE LEIOMYOMA ( 4 FDA reports)
ASTHENIA ( 3 FDA reports)
BONE LESION ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIASTOLIC DYSFUNCTION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
MALAISE ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
SYNOVIAL CYST ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
THYROID NEOPLASM ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PHYTOTHERAPY ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
SELENIUM DEFICIENCY ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TENSION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
ZINC DEFICIENCY ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use