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
118531922 11853192 2 F 20110728 20160825 20151218 20160825 EXP US-BRISTOL-MYERS SQUIBB COMPANY-16491946 BRISTOL MYERS SQUIBB 18.00 YR F Y 0.00000 20160825 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
118531922 11853192 1 PS EFAVIRENZ EFAVIRENZ 1 Oral 600 MG, QD 541200 MG Y 20972 600 MG QD
118531922 11853192 2 C COMBIVIR LAMIVUDINEIDOVUDINE 1 Oral 1 DF, BID 0 1 DF BID
118531922 11853192 3 C KALETRA LOPINAVIRRITONAVIR 1 Oral NO OF COURSES:1 0 1 DF
118531922 11853192 4 C KALETRA LOPINAVIRRITONAVIR 1 Oral 1 DF, Q4H 0 1 DF
118531922 11853192 5 C TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1 DF, QD Y 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118531922 11853192 1 Antiretroviral therapy
118531922 11853192 2 Antiretroviral therapy
118531922 11853192 3 Antiretroviral therapy
118531922 11853192 5 Antiretroviral therapy

Outcome of event

Event ID CASEID OUTC COD
118531922 11853192 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118531922 11853192 Live birth
118531922 11853192 Maternal exposure during pregnancy
118531922 11853192 Polyhydramnios
118531922 11853192 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
118531922 11853192 1 20081001 20110321 0
118531922 11853192 2 20110321 0
118531922 11853192 3 20110321 0
118531922 11853192 4 20110321 0
118531922 11853192 5 20080724 20110321 0