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
90099513 9009951 3 F 2000 20160909 20130110 20160914 EXP US-009507513-1301USA002312 MERCK 0.00 F Y 0.00000 20160914 PH 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
90099513 9009951 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, UNK 20560 70 MG TABLET
90099513 9009951 2 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Unknown 70 MG, UNK 0 70 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
90099513 9009951 1 Osteoporosis
90099513 9009951 2 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
90099513 9009951 OT
90099513 9009951 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
90099513 9009951 Ankle fracture
90099513 9009951 Appendicectomy
90099513 9009951 Back pain
90099513 9009951 Blood cholesterol increased
90099513 9009951 Bone pain
90099513 9009951 Deep vein thrombosis
90099513 9009951 Depression
90099513 9009951 Emotional disorder
90099513 9009951 Fall
90099513 9009951 Femur fracture
90099513 9009951 Haemorrhagic anaemia
90099513 9009951 Hyperlipidaemia
90099513 9009951 Hysterectomy
90099513 9009951 Osteoarthritis

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
90099513 9009951 1 1995 20101011 0
90099513 9009951 2 20081201 0