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
126398041 12639804 1 I 20110712 0 20160809 20160809 DIR 79.00 YR F N 85.00000 LBS 20160728 Y 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
126398041 12639804 1 PS RECLAST ZOLEDRONIC ACID 1 0
126398041 12639804 2 SS PROLIA DENOSUMAB 1 ABOUT 2 YRS AGO 0
126398041 12639804 4 C SYNTHROID LEVOTHYROXINE SODIUM 1 0
126398041 12639804 6 C CALCIUM CALCIUM 1 0
126398041 12639804 8 C FOLTABS 2 0
126398041 12639804 10 C MIRALAX POLYETHYLENE GLYCOL 3350 1 0
126398041 12639804 12 C TYLENOL ACETAMINOPHEN 1 0
126398041 12639804 14 C VITAMIN D CHOLECALCIFEROL 1 0
126398041 12639804 16 C LUNESTA ESZOPICLONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126398041 12639804 1 Osteoporosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126398041 12639804 Headache
126398041 12639804 Pruritus generalised
126398041 12639804 Throat irritation
126398041 12639804 Vulvovaginal pruritus

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
126398041 12639804 1 20110712 0