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
126251471 12625147 1 I 20160803 0 20160804 20160804 DIR 41.00 YR F N 0.00000 20160803 N PH 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
126251471 12625147 1 PS TIVICAY DOLUTEGRAVIR SODIUM 1 Oral N D 0 50 MG QD
126251471 12625147 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 200-300MG QD PO N D 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126251471 12625147 1 HIV infection
126251471 12625147 2 HIV infection

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126251471 12625147 Constipation
126251471 12625147 Drug dose omission
126251471 12625147 Nausea
126251471 12625147 Vomiting

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

Event ID CASEID RPSR COD
126251471 12625147 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126251471 12625147 1 1 MON
126251471 12625147 2 1 MON