The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
88341845 8834184 5 F 200707 20160916 20121010 20160920 EXP US-009507513-1210USA004457 MERCK 0.00 F Y 65.76000 KG 20160920 MD US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
88341845 8834184 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, UNK D 20560 70 MG TABLET
88341845 8834184 2 SS FOSAMAX PLUS D ALENDRONATE SODIUMCHOLECALCIFEROL 1 Oral 70 MG/2800, QW D 0 TABLET /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
88341845 8834184 1 Osteoporosis
88341845 8834184 2 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
88341845 8834184 HO
88341845 8834184 OT
88341845 8834184 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
88341845 8834184 Abdominal panniculectomy
88341845 8834184 Adenotonsillectomy
88341845 8834184 Anaemia
88341845 8834184 Antinuclear antibody positive
88341845 8834184 Autoimmune disorder
88341845 8834184 Basal cell carcinoma
88341845 8834184 Blood cholesterol increased
88341845 8834184 Bone metabolism disorder
88341845 8834184 Carpal tunnel syndrome
88341845 8834184 Chest pain
88341845 8834184 Compression fracture
88341845 8834184 Connective tissue disorder
88341845 8834184 Depression
88341845 8834184 Device failure
88341845 8834184 Dyspnoea exertional
88341845 8834184 Electrocardiogram T wave inversion
88341845 8834184 Femur fracture
88341845 8834184 Foot fracture
88341845 8834184 Fracture nonunion
88341845 8834184 Gastrooesophageal reflux disease
88341845 8834184 Hypokalaemia
88341845 8834184 Intervertebral disc operation
88341845 8834184 Lithotripsy
88341845 8834184 Low turnover osteopathy
88341845 8834184 Nausea
88341845 8834184 Nephrolithiasis
88341845 8834184 Oedema peripheral
88341845 8834184 Osteoarthritis
88341845 8834184 Skin disorder
88341845 8834184 Stomatitis
88341845 8834184 Tooth extraction
88341845 8834184 Vitamin D abnormal
88341845 8834184 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
88341845 8834184 1 200706 200903 0
88341845 8834184 2 200607 200812 0