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
88159753 8815975 3 F 1999 20160805 20120928 20160810 EXP US-009507513-1209USA010322 MERCK 0.00 F Y 0.00000 20160810 CN 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
88159753 8815975 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 10 MG, UNK 20560 10 MG TABLET
88159753 8815975 2 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, UNK 20560 70 MG TABLET
88159753 8815975 3 SS BONIVA IBANDRONATE SODIUM 1 Oral 150 MG, UNK 0 150 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
88159753 8815975 1 Osteoporosis
88159753 8815975 3 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
88159753 8815975 HO
88159753 8815975 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
88159753 8815975 Arthralgia
88159753 8815975 Blood cholesterol increased
88159753 8815975 Cardiac pacemaker insertion
88159753 8815975 Cholecystectomy
88159753 8815975 Deep vein thrombosis
88159753 8815975 Femur fracture
88159753 8815975 Hypertension
88159753 8815975 Hypothyroidism
88159753 8815975 Pain in extremity
88159753 8815975 Upper limb 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
88159753 8815975 1 1998 2001 0
88159753 8815975 2 20010131 200506 0
88159753 8815975 3 2005 20110510 0