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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127992471 | 12799247 | 1 | I | 20160920 | 20160922 | 20160930 | 20160930 | EXP | US-SA-2016SA177267 | AVENTIS | 0.00 | A | M | Y | 0.00000 | 20160930 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127992471 | 12799247 | 1 | PS | ALLEGRA | FEXOFENADINE HYDROCHLORIDE | 1 | Oral | START DATE : 05 SEPTEMBER, STOP DATE 08SEPTEMBER?ON SEPT. 5,6,7,8 | Y | UNK | 20872 | 2 | DF | TABLET | QD | ||||
| 127992471 | 12799247 | 2 | SS | ALLEGRA | FEXOFENADINE HYDROCHLORIDE | 1 | Oral | START DATE : 12 SEPTEMBER, STOP DATE 14SEPTEMBER?ON SEPT.12, 13,14. | Y | UNK | 20872 | 2 | DF | TABLET | QD |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127992471 | 12799247 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127992471 | 12799247 | Agitation | |
| 127992471 | 12799247 | Mania | |
| 127992471 | 12799247 | Seizure |
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 |
|---|---|---|---|---|---|---|
| 127992471 | 12799247 | 1 | 20160905 | 20160908 | 0 | |
| 127992471 | 12799247 | 2 | 20160912 | 20160914 | 0 |