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
126887741 12688774 1 I 20160310 0 20160825 20160825 DIR 50.00 YR F N 220.00000 LBS 20160824 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
126887741 12688774 1 PS RECLAST ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) INTO A VEIN N D 0
126887741 12688774 3 C LAMICTAL LAMOTRIGINE 1 0
126887741 12688774 5 C GEODON ZIPRASIDONE HYDROCHLORIDEIPRASIDONE MESYLATE 1 0
126887741 12688774 7 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 0
126887741 12688774 9 C ADDERALL AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE 1 0
126887741 12688774 11 C BACLOFEN. BACLOFEN 1 0
126887741 12688774 13 C DILAUDED 2 0
126887741 12688774 15 C VITAMIN D CHOLECALCIFEROL 1 0
126887741 12688774 17 C VITAMIN B VITAMIN B 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126887741 12688774 1 Osteoporosis postmenopausal

Outcome of event

Event ID CASEID OUTC COD
126887741 12688774 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126887741 12688774 Cardiac disorder
126887741 12688774 Pain

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
126887741 12688774 1 20160310 20160310 0