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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5292285 | 6523904 | F | 5292285-7 | 20070207 | 20070323 | 20070403 | EXP | 100#03#2007-00854 | PLIVA - RESEARCH AND DEVELOPMENT LTD. | 43 | YR | M | N | 20070329 | UNITED KINGDOM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5292285 | 1008351904 | PS | AZITHROMYCIN | 1 | ORAL | 1 G ORAL | D | D | 65223 | ||
| 5292285 | 1008393197 | SS | CEFIXIME CHEWABLE | 1 | ORAL | 400 MG ORAL | D | D |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5292285 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5292285 | COUGH |
| 5292285 | DIARRHOEA |
| 5292285 | GASTROINTESTINAL DISORDER |
| 5292285 | LOWER RESPIRATORY TRACT INFECTION |
| 5292285 | PHARYNGOLARYNGEAL PAIN |
| 5292285 | PRODUCTIVE COUGH |
| 5292285 | SWELLING FACE |
| 5292285 | VOMITING |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5292285 | HP |
| 5292285 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5292285 | 1008351904 | 20070208 | 20070208 | 1 | DAY |
| 5292285 | 1008393197 | 20070207 | 20070207 | 1 | DAY |