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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125558321 | 12555832 | 1 | I | 20150608 | 20160614 | 20160714 | 20160714 | PER | US-009507513-1607USA005536 | MERCK | 0.00 | DY | F | Y | 1.76000 | KG | 20160714 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125558321 | 12555832 | 1 | PS | ISENTRESS | RALTEGRAVIR POTASSIUM | 1 | Transplacental | TOTAL DAILY DOSE: 400 | 22145 | TABLET | |||||||||
| 125558321 | 12555832 | 2 | SS | abacavir sulfate (+) lamivudine | ABACAVIR SULFATELAMIVUDINE | 1 | Transplacental | TOTAL DAILY DOSE: 900 | 0 | ||||||||||
| 125558321 | 12555832 | 3 | SS | DARUNAVIR | DARUNAVIR | 1 | Transplacental | TOTAL DAILY DOSE: 800 | 0 | ||||||||||
| 125558321 | 12555832 | 4 | SS | RITONAVIR. | RITONAVIR | 1 | Transplacental | TOTAL DAILY DOSE: 100 | 0 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125558321 | 12555832 | Low birth weight baby |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |