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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
107830082 | 10783008 | 2 | F | 2015 | 20160722 | 20150210 | 20160808 | EXP | US-GLAXOSMITHKLINE-A1079919A | GLAXOSMITHKLINE | 0.00 | F | Y | 0.00000 | 20160808 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
107830082 | 10783008 | 1 | PS | VALTREX | VALACYCLOVIR HYDROCHLORIDE | 1 | Unknown | 500 MG | U | UNKNOWN | 20487 | 500 | MG | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
107830082 | 10783008 | 1 | Herpes virus infection |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
107830082 | 10783008 | Drug administration error | |
107830082 | 10783008 | Headache | |
107830082 | 10783008 | Ill-defined disorder | |
107830082 | 10783008 | Joint injury | |
107830082 | 10783008 | Treatment noncompliance |
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 |
---|---|---|---|---|---|---|
107830082 | 10783008 | 1 | 20040219 | 0 |