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
127080041 12708004 1 I 20160819 20160901 20160901 EXP DE-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-070005 BRISTOL MYERS SQUIBB 39.00 YR F Y 120.00000 KG 20160901 CN DE DE

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
127080041 12708004 1 PS ABILIFY ARIPIPRAZOLE 1 Oral 10 MG, QD U 21436 10 MG QD
127080041 12708004 2 SS L-THYROXIN LEVOTHYROXINE SODIUM 1 Oral 275 ?G, QD U 0 275 UG QD
127080041 12708004 3 SS FOLIO /00349401/ CYANOCOBALAMINFOLIC ACID 1 Oral 0.4 MG, QD U 0 .4 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127080041 12708004 1 Bipolar disorder
127080041 12708004 2 Hypothyroidism
127080041 12708004 3 Prophylaxis of neural tube defect

Outcome of event

Event ID CASEID OUTC COD
127080041 12708004 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127080041 12708004 Caesarean section
127080041 12708004 Gestational diabetes
127080041 12708004 Maternal exposure during pregnancy
127080041 12708004 Pre-eclampsia
127080041 12708004 Product use issue

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
127080041 12708004 1 20150605 20160226 0