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
118938552 11893855 2 F 20031210 20160826 20160107 20160826 EXP US-BRISTOL-MYERS SQUIBB COMPANY-12511218 BRISTOL MYERS SQUIBB 31.00 YR F Y 0.00000 20160826 OT 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
118938552 11893855 1 PS DIDANOSINE. DIDANOSINE 1 Oral 400 MG, QD 20156 400 MG QD
118938552 11893855 2 SS COMBIVIR LAMIVUDINEIDOVUDINE 1 Oral 300 MG, QD 0 300 MG QD
118938552 11893855 3 SS KALETRA LOPINAVIRRITONAVIR 1 Oral 6 DF, QD 0 6 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118938552 11893855 1 Antiretroviral therapy
118938552 11893855 2 Antiretroviral therapy
118938552 11893855 3 Antiretroviral therapy

Outcome of event

Event ID CASEID OUTC COD
118938552 11893855 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118938552 11893855 Live birth
118938552 11893855 Pregnancy
118938552 11893855 Premature rupture of membranes

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
118938552 11893855 1 20030701 0
118938552 11893855 2 20030701 0
118938552 11893855 3 20030701 0