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
126181571 12618157 1 I 20140211 20150206 20160803 20160803 EXP US-VIIV HEALTHCARE LIMITED-US2015GSK019282 VIIV 26.00 YR F Y 0.00000 20160803 CN 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
126181571 12618157 1 SS TENOFOVIR DISOPROXIL FUMARATE. TENOFOVIR DISOPROXIL FUMARATE 1 Oral TOTAL DAILY DOSE OF 300 MG 6900 MG Y 0 300 MG TABLET QD
126181571 12618157 2 PS Maraviroc MARAVIROC 1 Oral TOTAL DAILY DOSE OF 300 MG 6900 MG Y 22128 300 MG TABLET QD
126181571 12618157 3 SS EMTRIVA EMTRICITABINE 1 Oral TOTAL DAILY DOSE OF 200 MG 4600 MG Y 0 200 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126181571 12618157 1 Antiviral prophylaxis
126181571 12618157 2 Antiviral prophylaxis
126181571 12618157 3 Antiviral prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126181571 12618157 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126181571 12618157 Abortion spontaneous
126181571 12618157 Exposure during pregnancy

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
126181571 12618157 1 20140211 20140306 0
126181571 12618157 2 20140211 20140306 0
126181571 12618157 3 20140211 20140306 0