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
127818611 12781861 1 I 20160909 20160926 20160926 EXP US-ABBVIE-16P-163-1725877-00 ABBVIE 35.00 YR F Y 0.00000 20160926 OT COUNTRY NOT SPECIFIED 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
127818611 12781861 1 PS NORVIR RITONAVIR 1 Oral SECOND TRIMESTER EXPOSURE D UNKNOWN 22417 200 MG TABLET QD
127818611 12781861 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral FIRST TRIMESTER EXPOSURE; PRIOR TO CONCEPTION D UNKNOWN 0 1 DF
127818611 12781861 3 SS DARUNAVIR ETHANOLATE. DARUNAVIR ETHANOLATE 1 Oral SECOND TRIMESTER EXPOSURE D UNKNOWN 0 1200 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127818611 12781861 1 HIV infection
127818611 12781861 2 HIV infection
127818611 12781861 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
127818611 12781861 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127818611 12781861 Exposure during pregnancy
127818611 12781861 Gestational diabetes

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
127818611 12781861 1 20160121 0
127818611 12781861 3 20160121 0