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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 83511204 | 8351120 | 4 | F | 20111227 | 0 | 20120124 | 20120320 | DIR | 69.00 | YR | F | N | 0.00000 | 20120316 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 83511204 | 8351120 | 1 | PS | VIMPAT | 1 | ORAL | 22253 | 100 | MG | TABLET | |||||||||
| 83511204 | 8351120 | 2 | SS | KEPPRA | 1 | ORAL | 0 | 750 | MG | ||||||||||
| 83511204 | 8351120 | 3 | SS | ALPRAZOLAM | 1 | ORAL | 0 | 1 | MG | ||||||||||
| 83511204 | 8351120 | 4 | C | METOCLOPRAMIDE | 1 | 0 | 25 | MG | |||||||||||
| 83511204 | 8351120 | 5 | C | KALETRA | 1 | 200MG/50MGX2TABS BID | 0 | TABLET | |||||||||||
| 83511204 | 8351120 | 6 | C | LAMIVUDINEIDOVUDINE | 1 | ORAL | DAILY | 0 | |||||||||||
| 83511204 | 8351120 | 7 | C | ETODOLAC | 1 | ORAL | DAILY:400MG | 0 | |||||||||||
| 83511204 | 8351120 | 8 | C | FERROUS SULFATE | 1 | DAILY :325 MG | 0 | ||||||||||||
| 83511204 | 8351120 | 9 | C | VITIS VINIFERA SEED | 2 | ORAL | DAILY: 100MG | 0 | |||||||||||
| 83511204 | 8351120 | 10 | C | DILANTIN | 1 | ON TAB DAILY | 0 | ||||||||||||
| 83511204 | 8351120 | 11 | C | MAGNESIUM OXIDE | 1 | 0 | |||||||||||||
| 83511204 | 8351120 | 12 | C | ARICEPT | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 83511204 | 8351120 | 5 | HIV infection |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 83511204 | 8351120 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 83511204 | 8351120 | Blood pressure inadequately controlled | |
| 83511204 | 8351120 | Blood pressure increased | |
| 83511204 | 8351120 | Death | |
| 83511204 | 8351120 | Product substitution issue | |
| 83511204 | 8351120 | Toxic epidermal necrolysis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | CASEID | RPSR COD |
|---|---|---|
| 83511204 | 8351120 | HP |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 83511204 | 8351120 | 1 | 20111215 | 20111227 | 0 | |
| 83511204 | 8351120 | 2 | 20100326 | 0 |