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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125630663 | 12563066 | 3 | F | 2010 | 20160830 | 20160715 | 20160912 | EXP | US-009507513-1607USA005552 | MERCK | 0.00 | M | Y | 94.33000 | KG | 20160912 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125630663 | 12563066 | 1 | PS | ISENTRESS | RALTEGRAVIR POTASSIUM | 1 | Oral | 400 MG, BID | 22145 | 400 | MG | TABLET | BID | ||||||
125630663 | 12563066 | 2 | SS | TRUVADA | EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE | 1 | 300/200 MG, QD | U | 0 | QD |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125630663 | 12563066 | OT |
125630663 | 12563066 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125630663 | 12563066 | Atrial fibrillation | |
125630663 | 12563066 | Herpes zoster |
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 |
---|---|---|---|---|---|---|
125630663 | 12563066 | 1 | 20100223 | 0 | ||
125630663 | 12563066 | 2 | 20100223 | 0 |