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
126015081 12601508 1 I 0 20160727 20160727 DIR 54.00 YR M N 155.00000 LBS 20160726 N 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
126015081 12601508 1 PS ACTONEL RISEDRONATE SODIUM 1 N D 0
126015081 12601508 2 SS BONIVA IBANDRONATE SODIUM 1 0
126015081 12601508 3 SS RECLAST ZOLEDRONIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126015081 12601508 1 Osteopenia

Outcome of event

Event ID CASEID OUTC COD
126015081 12601508 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126015081 12601508 Bone pain
126015081 12601508 Cardiovascular insufficiency
126015081 12601508 Dizziness
126015081 12601508 Fear
126015081 12601508 Headache
126015081 12601508 Hypoaesthesia
126015081 12601508 Inflammation
126015081 12601508 Myalgia
126015081 12601508 Neuralgia
126015081 12601508 Pain
126015081 12601508 Pain in extremity
126015081 12601508 Presyncope

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
126015081 12601508 1 20020408 20071023 0