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 |