Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6768592 | 7409309 | F | 6768592-5 | 20100525 | 20100602 | 20100614 | EXP | JP-PFIZER INC-2010066586 | PFIZERINC | 17 | YR | F | Y | 20100614 | PH | JAPAN |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6768592 | 1013862007 | PS | ZITHROMAC SR | 2 | ORAL | 2 G, SINGLE | 50797 | ||||
| 6768592 | 1013862008 | SS | ZITHROMAC SR | 2 | 050797 | ||||||
| 6768592 | 1013862009 | SS | LOXOPROFEN SODIUM | 2 | ORAL | 180 MG, 1X/DAY | |||||
| 6768592 | 1013862010 | SS | LOXOPROFEN SODIUM | 2 | |||||||
| 6768592 | 1013862011 | C | DASEN | 2 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6768592 | 1013862007 | PYREXIA |
| 6768592 | 1013862008 | OROPHARYNGEAL PAIN |
| 6768592 | 1013862009 | PYREXIA |
| 6768592 | 1013862010 | OROPHARYNGEAL PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6768592 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6768592 | HAEMATURIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6768592 | 1013862007 | 20100524 | 20100524 | 1 | DAY |