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
126747992 12674799 2 F 20160620 20160822 20160823 20160831 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-068155 BRISTOL MYERS SQUIBB 0.00 DY F Y 1.05000 KG 20160831 CN US 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
126747992 12674799 1 PS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Transplacental 300 MG, QD 21567 300 MG QD
126747992 12674799 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental 1 DF, UNK 0 1 DF
126747992 12674799 3 SS TIVICAY DOLUTEGRAVIR SODIUM 1 Transplacental 50 MG, QD 0 50 MG QD
126747992 12674799 4 SS NORVIR RITONAVIR 1 Transplacental 100 MG, QD 0 100 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126747992 12674799 1 Product used for unknown indication
126747992 12674799 2 Product used for unknown indication
126747992 12674799 3 Product used for unknown indication
126747992 12674799 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126747992 12674799 OT
126747992 12674799 LT
126747992 12674799 HO
126747992 12674799 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
126747992 12674799 Foetal exposure during pregnancy
126747992 12674799 Patent ductus arteriosus
126747992 12674799 Premature baby
126747992 12674799 Surgery

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
126747992 12674799 1 20160620 0
126747992 12674799 2 20160620 0
126747992 12674799 3 20160425 20160620 0
126747992 12674799 4 20160620 0