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
74083893 7408389 3 F 201004 20160824 20100603 20160824 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-15120728 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160824 CN 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
74083893 7408389 1 PS SUSTIVA EFAVIRENZ 1 Transplacental 1 DF, QD Y 20972 1 DF CAPSULE QD
74083893 7408389 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNK U 0
74083893 7408389 3 SS KALETRA LOPINAVIRRITONAVIR 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
74083893 7408389 1 Product used for unknown indication
74083893 7408389 2 Product used for unknown indication
74083893 7408389 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
74083893 7408389 OT
74083893 7408389 CA
74083893 7408389 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
74083893 7408389 Foetal exposure during pregnancy
74083893 7408389 Hydrocephalus

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
74083893 7408389 1 20070817 20091202 0
74083893 7408389 2 20070817 0