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
87611994 8761199 4 F 2009 20160630 20120830 20160705 EXP US-009507513-1208USA008535 MERCK 0.00 F Y 0.00000 20160705 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
87611994 8761199 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, UNK U 20560 70 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
87611994 8761199 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
87611994 8761199 HO
87611994 8761199 OT
87611994 8761199 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
87611994 8761199 Adverse event
87611994 8761199 Anaemia postoperative
87611994 8761199 Angiopathy
87611994 8761199 Anxiety disorder
87611994 8761199 Cardiac failure congestive
87611994 8761199 Coronary arterial stent insertion
87611994 8761199 Coronary artery disease
87611994 8761199 Deep vein thrombosis
87611994 8761199 Femur fracture
87611994 8761199 Hysterectomy
87611994 8761199 Intestinal resection
87611994 8761199 Oophorectomy bilateral
87611994 8761199 Osteoarthritis
87611994 8761199 Wound dehiscence

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
87611994 8761199 1 2000 2010 0