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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5002793 | 6052387 | I | 5002793-1 | 20060428 | 20060512 | EXP | 2006-04-2299 | SCHERING-PLOUGH CORPORATION | 43 | YR | M | N | 20060428 | MD | SPAIN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5002793 | 1007288763 | PS | LORATADINE | 1 | ORAL | ORAL | U | U | 19658 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5002793 | 1007288763 | CONJUNCTIVITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5002793 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5002793 | HEPATIC LESION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5002793 | FGN |
| 5002793 | HP |
| 5002793 | LIT |
Therapies reported
| no results found |