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

MIGRAINE ( 5 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
PRURITUS ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CARBOHYDRATE TOLERANCE DECREASED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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