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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126683671 | 12668367 | 1 | I | 2001 | 20151105 | 20160819 | 20160819 | EXP | US-PRESTIUM-2015RN000209 | RENAISSANCE | 0.00 | Y | 0.00000 | 20160819 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126683671 | 12668367 | 1 | PS | ACYCLOVIR. | ACYCLOVIR | 1 | Oral | 500 MG | U | UNKNOWN | 20089 | 500 | MG | TABLET | |||||
126683671 | 12668367 | 2 | SS | VALTREX | VALACYCLOVIR HYDROCHLORIDE | 1 | Oral | 1 G, 1 D | Y | 0 | 1 | G | TABLET | ||||||
126683671 | 12668367 | 3 | SS | VALTREX | VALACYCLOVIR HYDROCHLORIDE | 1 | Y | 0 | TABLET | ||||||||||
126683671 | 12668367 | 4 | C | PHENOBARBITAL. | PHENOBARBITAL | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126683671 | 12668367 | 1 | Oral herpes |
126683671 | 12668367 | 2 | Oral herpes |
126683671 | 12668367 | 3 | Herpes simplex |
126683671 | 12668367 | 4 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126683671 | 12668367 | OT |
126683671 | 12668367 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126683671 | 12668367 | Abdominal pain upper | |
126683671 | 12668367 | Arthritis | |
126683671 | 12668367 | Cataract | |
126683671 | 12668367 | Diarrhoea | |
126683671 | 12668367 | Drug ineffective | |
126683671 | 12668367 | Herpes simplex | |
126683671 | 12668367 | Hip arthroplasty | |
126683671 | 12668367 | Hospitalisation | |
126683671 | 12668367 | Hypersensitivity | |
126683671 | 12668367 | Nausea |
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 |
---|---|---|---|---|---|---|
126683671 | 12668367 | 1 | 2001 | 2001 | 0 | |
126683671 | 12668367 | 2 | 2001 | 0 |