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
118415642 11841564 2 F 20160701 20151216 20160711 PER US-009507513-1512USA006609 MERCK 32.00 YR F Y 0.00000 20160709 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
118415642 11841564 1 PS ISENTRESS RALTEGRAVIR POTASSIUM 1 Oral TOTAL DAILY DOSE 800 (UNITS NOT REPORTED), STARTED PRIOR TO CONCEPTION 22145 TABLET
118415642 11841564 2 SS emtricitabine (+) tenofovir disoproxil fumarate EMTRICITABINETENOFOVIR DISOPROXIL 1 Oral TOTAL DAILY DOSE 500 (UNITS NOT REPORTED), STARTED PRIOR TO CONCEPTION 0
118415642 11841564 3 SS DARUNAVIR DARUNAVIR 1 Oral TOTAL DAILY DOSAGE 1600 (UNITS NOT REPORTED), BEGAN AT 9 WEEK GESTATION 0
118415642 11841564 4 SS RITONAVIR. RITONAVIR 1 Oral TOTAL DAILY DOSAGE 200 (UNITS NOT REPORTED), BEGAN AT 9 WEEK GESTATION 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118415642 11841564 Maternal exposure before pregnancy
118415642 11841564 Maternal exposure during pregnancy

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

no results found

Therapies reported

no results found