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
89410072 8941007 2 F 20110308 20160908 20121203 20160914 EXP US-009507513-0501USA04273 MERCK 0.00 F Y 0.00000 20160914 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
89410072 8941007 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW U 20560 70 MG TABLET /wk
89410072 8941007 2 SS FOSAMAX ALENDRONATE SODIUM 1 U 20560 TABLET
89410072 8941007 3 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, QW 7140 MG 0 70 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
89410072 8941007 1 Osteopenia
89410072 8941007 2 Osteoporosis prophylaxis
89410072 8941007 3 Osteopenia

Outcome of event

Event ID CASEID OUTC COD
89410072 8941007 HO
89410072 8941007 DS
89410072 8941007 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
89410072 8941007 Abdominal pain upper
89410072 8941007 Dizziness
89410072 8941007 Femur fracture
89410072 8941007 Hypertension
89410072 8941007 Hypokalaemia
89410072 8941007 Low turnover osteopathy
89410072 8941007 Osteoarthritis
89410072 8941007 Osteoporosis
89410072 8941007 Scoliosis
89410072 8941007 Stress fracture

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
89410072 8941007 1 20050121 0
89410072 8941007 3 20090109 20101221 0