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
126890731 12689073 1 I 20160812 20160826 20160826 EXP TH-CIPLA LTD.-2016TH17523 CIPLA 0.00 Y 0.00000 20160826 OT AU TH

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
126890731 12689073 1 PS Efavirenz EFAVIRENZ 1 Unknown UNK U 0
126890731 12689073 2 SS Efavirenz EFAVIRENZ 1 U 0
126890731 12689073 3 SS ZIDOVUDINE. ZIDOVUDINE 1 Unknown UNK 0
126890731 12689073 4 SS ZIDOVUDINE. ZIDOVUDINE 1 0
126890731 12689073 5 SS LAMIVUDINE. LAMIVUDINE 1 Unknown UNK 0
126890731 12689073 6 SS LAMIVUDINE. LAMIVUDINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126890731 12689073 1 Hepatitis B
126890731 12689073 2 HIV infection
126890731 12689073 3 Hepatitis B
126890731 12689073 4 HIV infection
126890731 12689073 5 Hepatitis B
126890731 12689073 6 HIV infection

Outcome of event

Event ID CASEID OUTC COD
126890731 12689073 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126890731 12689073 Hepatitis B
126890731 12689073 Jaundice
126890731 12689073 Nausea

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found