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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127203061 | 12720306 | 1 | I | 20160616 | 20160907 | 20160907 | EXP | JP-GLAXOSMITHKLINE-JP2016JPN086067 | GLAXOSMITHKLINE | 90.00 | YR | F | Y | 0.00000 | 20160907 | CN | JP | JP |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127203061 | 12720306 | 1 | PS | VALTREX | VALACYCLOVIR HYDROCHLORIDE | 1 | Oral | U | 20487 | TABLET | |||||||||
127203061 | 12720306 | 2 | C | UNKNOWN DRUG | UNSPECIFIED INGREDIENT | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127203061 | 12720306 | 1 | Herpes zoster |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127203061 | 12720306 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127203061 | 12720306 | Decreased appetite | |
127203061 | 12720306 | Hyponatraemia | |
127203061 | 12720306 | Urine output decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |