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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126820772 | 12682077 | 2 | F | 20150413 | 20160804 | 20160824 | 20160831 | EXP | ZA-GILEAD-2016-0230242 | GILEAD | 47.00 | YR | A | F | Y | 0.00000 | 20160831 | OT | ZA | ZA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126820772 | 12682077 | 1 | PS | EFAVIRENZ | EFAVIRENZ | 1 | Unknown | 600 MG, QD | 0 | 600 | MG | QD | |||||||
| 126820772 | 12682077 | 2 | SS | ZIDOVUDINE. | ZIDOVUDINE | 1 | Unknown | 300 MG, BID | 0 | 300 | MG | BID | |||||||
| 126820772 | 12682077 | 3 | SS | LAMIVUDINE. | LAMIVUDINE | 1 | Unknown | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126820772 | 12682077 | 1 | HIV infection |
| 126820772 | 12682077 | 2 | HIV infection |
| 126820772 | 12682077 | 3 | HIV infection |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126820772 | 12682077 | LT |
| 126820772 | 12682077 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126820772 | 12682077 | Anaemia |
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 |
|---|---|---|---|---|---|---|
| 126820772 | 12682077 | 1 | 20140611 | 0 |