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
126364391 12636439 1 I 20160805 20160809 20160809 EXP US-SCIEGEN PHARMACEUTICALS INC-2016SCILIT00348 SCIEGEN 57.00 YR F Y 0.00000 20160809 MD 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
126364391 12636439 1 PS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 Unknown UNK U U 204165 TABLET
126364391 12636439 2 I Etravirine ETRAVIRINE 1 Unknown UNK U U 0
126364391 12636439 3 C Fosamprenavir FOSAMPRENAVIR 1 Unknown UNK 0
126364391 12636439 4 C Tenofovir TENOFOVIR 1 Unknown UNK U 0
126364391 12636439 5 C Andacabavir 2 Unknown UNK U 0
126364391 12636439 6 C LAMIVUDINE. LAMIVUDINE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126364391 12636439 1 Product used for unknown indication
126364391 12636439 2 HIV infection
126364391 12636439 3 HIV infection
126364391 12636439 4 HIV infection
126364391 12636439 5 HIV infection
126364391 12636439 6 HIV infection

Outcome of event

Event ID CASEID OUTC COD
126364391 12636439 OT
126364391 12636439 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126364391 12636439 Chest pain
126364391 12636439 Coronary artery disease
126364391 12636439 Drug interaction
126364391 12636439 Vascular stent restenosis

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
126364391 12636439 2 201209 0