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
84954993 8495499 3 F 20111013 20160823 20120405 20160823 EXP CH-BRISTOL-MYERS SQUIBB COMPANY-16481152 BRISTOL MYERS SQUIBB 26.00 YR F Y 0.00000 20160823 CN CH CH

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
84954993 8495499 1 PS ABILIFY ARIPIPRAZOLE 1 Oral 20 MG, BID Y 21436 20 MG TABLET BID
84954993 8495499 2 SS METHADONE METHADONE HYDROCHLORIDE 1 Oral 100 MG, QD U 0 100 MG QD
84954993 8495499 3 SS DEPAKINE VALPROATE SODIUM 1 Oral 750 MG, BID Y 0 750 MG BID
84954993 8495499 4 SS HALDOL HALOPERIDOL 1 Oral 1 MG, BID U 0 1 MG BID
84954993 8495499 5 C FOLIC ACID. FOLIC ACID 1 Oral UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
84954993 8495499 1 Product used for unknown indication
84954993 8495499 2 Product used for unknown indication
84954993 8495499 3 Product used for unknown indication
84954993 8495499 4 Product used for unknown indication
84954993 8495499 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
84954993 8495499 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
84954993 8495499 Live birth
84954993 8495499 Maternal exposure during pregnancy
84954993 8495499 Perineal injury

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
84954993 8495499 1 20110217 0
84954993 8495499 2 2010 0
84954993 8495499 3 20110218 0
84954993 8495499 4 2010 0