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
118777492 11877749 2 F 20160831 20151230 20160902 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-11000437 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160902 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
118777492 11877749 1 PS ZERIT STAVUDINE 1 Oral UNK U 20412 CAPSULE, HARD
118777492 11877749 2 SS VIDEX DIDANOSINE 1 Unknown 400 MG, UNK U 0 400 MG
118777492 11877749 3 SS VIRACEPT NELFINAVIR MESYLATE 1 Unknown 1250 MG, BID Y 0 1250 MG BID
118777492 11877749 4 SS VIRAMUNE NEVIRAPINE 1 Unknown UNK Y 0
118777492 11877749 5 SS RETROVIR ZIDOVUDINE 1 Intravenous (not otherwise specified) 200 MG, UNK Y 0 200 MG
118777492 11877749 6 C I RON FERROUS FUMARATE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118777492 11877749 1 HIV infection
118777492 11877749 2 HIV infection
118777492 11877749 3 HIV infection
118777492 11877749 4 HIV infection
118777492 11877749 5 HIV infection
118777492 11877749 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118777492 11877749 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118777492 11877749 Caesarean section
118777492 11877749 Hepatitis cholestatic
118777492 11877749 Live birth
118777492 11877749 Pregnancy

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
118777492 11877749 2 20000516 0
118777492 11877749 3 20000225 20080418 0
118777492 11877749 4 20000225 20000418 0
118777492 11877749 5 20000823 20000823 0