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
41552093 4155209 3 F 19981211 20160826 20040616 20160826 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-10605418 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160826 OT 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
41552093 4155209 1 PS VIDEX DIDANOSINE 1 Oral UNK U 20156
41552093 4155209 2 SS RETROVIR ZIDOVUDINE 1 Unknown U 0
41552093 4155209 3 SS RETROVIR ZIDOVUDINE 1 Parenteral UNK U 0
41552093 4155209 4 C BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Unknown U 0
41552093 4155209 5 C VITAMINS VITAMINS 1 Unknown U 0
41552093 4155209 6 C I RON FERROUS FUMARATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
41552093 4155209 1 HIV infection
41552093 4155209 2 HIV infection
41552093 4155209 3 HIV infection
41552093 4155209 4 Product used for unknown indication
41552093 4155209 5 Product used for unknown indication
41552093 4155209 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
41552093 4155209 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
41552093 4155209 Caesarean section
41552093 4155209 Hyperlactacidaemia
41552093 4155209 Pregnancy
41552093 4155209 Tuberculosis

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
41552093 4155209 3 19981211 19981211 0