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
87162723 8716272 3 F 2006 20160803 20120810 20160808 EXP US-MERCK-1208USA000749 MERCK 0.00 F Y 76.19000 KG 20160808 OT 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
87162723 8716272 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW 20560 70 MG TABLET /wk
87162723 8716272 2 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, QW 0 70 MG TABLET /wk
87162723 8716272 3 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 50 MG, UNK U 0 50 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
87162723 8716272 1 Osteoporosis
87162723 8716272 2 Osteoporosis
87162723 8716272 3 Nephrolithiasis

Outcome of event

Event ID CASEID OUTC COD
87162723 8716272 OT
87162723 8716272 HO
87162723 8716272 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
87162723 8716272 Abdominal pain
87162723 8716272 Device fastener issue
87162723 8716272 Ear infection
87162723 8716272 Faeces pale
87162723 8716272 Fatigue
87162723 8716272 Femur fracture
87162723 8716272 High density lipoprotein decreased
87162723 8716272 Hypokalaemia
87162723 8716272 Insomnia
87162723 8716272 Intramedullary rod insertion
87162723 8716272 Osteopenia
87162723 8716272 Pollakiuria
87162723 8716272 Rosacea
87162723 8716272 Soft tissue disorder

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
87162723 8716272 1 20040108 200709 0
87162723 8716272 2 200804 201009 0
87162723 8716272 3 1990 0