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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124385072 | 12438507 | 2 | F | 20160705 | 20160606 | 20160720 | EXP | NO-GLAXOSMITHKLINE-NO2016GSK067750 | GLAXOSMITHKLINE | 0.00 | M | Y | 0.00000 | 20160720 | MD | NO | NO |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124385072 | 12438507 | 1 | PS | ZOVIRAX | ACYCLOVIR | 1 | Ophthalmic | UNK | 5L904 | 18603 | EYE OINTMENT |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124385072 | 12438507 | 1 | Prophylaxis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124385072 | 12438507 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124385072 | 12438507 | Condition aggravated | |
| 124385072 | 12438507 | Eye irritation | |
| 124385072 | 12438507 | Eye pain | |
| 124385072 | 12438507 | Intraocular pressure increased | |
| 124385072 | 12438507 | Iridocyclitis | |
| 124385072 | 12438507 | Ocular hyperaemia | |
| 124385072 | 12438507 | Photophobia | |
| 124385072 | 12438507 | Product quality issue | |
| 124385072 | 12438507 | Purulent discharge |
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 |
|---|---|---|---|---|---|---|
| 124385072 | 12438507 | 1 | 2012 | 0 |