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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125761642 | 12576164 | 2 | F | 20160714 | 20160720 | 20160721 | EXP | GB-GILEAD-2016-0223832 | GILEAD | 68.00 | YR | E | M | Y | 0.00000 | 20160721 | CN | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125761642 | 12576164 | 1 | PS | EMTRIVA | EMTRICITABINE | 1 | Unknown | U | U | UNKNOWN | 21500 | 200 | MG | CAPSULE | |||||
| 125761642 | 12576164 | 2 | SS | TENOFOVIR DISOPROXIL FUMARATE. | TENOFOVIR DISOPROXIL FUMARATE | 1 | Unknown | U | U | UNKNOWN | 0 | 245 | MG | TABLET | |||||
| 125761642 | 12576164 | 3 | SS | ETRAVIRINE | ETRAVIRINE | 1 | Unknown | U | U | UNKNOWN | 0 | 100 | MG | ||||||
| 125761642 | 12576164 | 4 | SS | NORVIR | RITONAVIR | 1 | Oral | U | U | UNKNOWN | 0 | 100 | MG | ||||||
| 125761642 | 12576164 | 5 | SS | PREZISTA | DARUNAVIR ETHANOLATE | 1 | Unknown | U | U | UNKNOWN | 0 | 600 | MG | ||||||
| 125761642 | 12576164 | 6 | SS | RALTEGRAVIR. | RALTEGRAVIR | 1 | Unknown | 400 MG, UNK | U | U | UNKNOWN | 0 | 400 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125761642 | 12576164 | 1 | Product used for unknown indication |
| 125761642 | 12576164 | 2 | Product used for unknown indication |
| 125761642 | 12576164 | 3 | Product used for unknown indication |
| 125761642 | 12576164 | 4 | Product used for unknown indication |
| 125761642 | 12576164 | 5 | Product used for unknown indication |
| 125761642 | 12576164 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125761642 | 12576164 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125761642 | 12576164 | Renal impairment |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |