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
79014164 7901416 4 F 20110301 20160823 20110415 20160823 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-15529605 BRISTOL MYERS SQUIBB 34.46 YR F Y 95.00000 KG 20160823 MD FR FR

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
79014164 7901416 1 PS ABILIFY ARIPIPRAZOLE 1 Oral 5 MG, QD Y 21436 5 MG TABLET QD
79014164 7901416 2 SS ZOLOFT SERTRALINE HYDROCHLORIDE 1 Oral 50 MG, QD Y 0 50 MG QD
79014164 7901416 3 SS ZYPREXA OLANZAPINE 1 Oral 5 MG, QD Y 0 5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
79014164 7901416 1 Depression
79014164 7901416 2 Depression
79014164 7901416 3 Mood swings

Outcome of event

Event ID CASEID OUTC COD
79014164 7901416 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
79014164 7901416 Caesarean section
79014164 7901416 Gestational diabetes
79014164 7901416 Maternal exposure during pregnancy
79014164 7901416 Nausea
79014164 7901416 Post procedural haemorrhage
79014164 7901416 Premature delivery

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
79014164 7901416 1 20101218 20110301 0
79014164 7901416 2 2006 20100918 0
79014164 7901416 3 2009 20101218 0