Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5378422 | 6602890 | I | 5378422-4 | 20070529 | 20070702 | DIR | 24 | YR | F | N | 71 | KG | 20070625 | CN | N | N | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5378422 | 1008662951 | PS | STAVUDINE | 1 | ORAL | 40 MG TWICE A DAY ORAL | D | D | |||
| 5378422 | 1008685158 | SS | LAMIVUDINE | 1 | ORAL | 150 MG TWICE A DAY ORAL | D | D | |||
| 5378422 | 1008685160 | SS | KALETRA | 1 | ORAL | 400MG/100MG TWICE A DAY ORAL | D | D | |||
| 5378422 | 1008685161 | C | COTRIM | 1 | |||||||
| 5378422 | 1008685162 | C | FOLATE | 2 | |||||||
| 5378422 | 1008685163 | C | VITAMIN B | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5378422 | 1008662951 | HIV INFECTION |
| 5378422 | 1008685158 | HIV INFECTION |
| 5378422 | 1008685160 | HIV INFECTION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5378422 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5378422 | ABDOMINAL PAIN LOWER |
| 5378422 | DRUG EXPOSURE DURING PREGNANCY |
| 5378422 | LOWER RESPIRATORY TRACT INFECTION |
| 5378422 | STILLBIRTH |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5378422 | 1008662951 | 20061222 | 20070611 | ||
| 5378422 | 1008685158 | 20061222 | 20070611 | ||
| 5378422 | 1008685160 | 20061222 |