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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126541611 | 12654161 | 1 | I | 20160803 | 20160803 | 20160816 | 20160816 | PER | US-BAYER-2016-151780 | BAYER | 0.00 | F | Y | 0.00000 | 20160816 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126541611 | 12654161 | 1 | PS | CLARITIN-D 24 HOUR | LORATADINEPSEUDOEPHEDRINE SULFATE | 1 | Oral | 1 DF, QD | CVM081N | 20470 | 1 | DF | PROLONGED-RELEASE TABLET | QD | |||||
| 126541611 | 12654161 | 2 | SS | CLARITIN-D 24 HOUR | LORATADINEPSEUDOEPHEDRINE SULFATE | 1 | 2 DF, UNK | 20470 | 2 | DF | PROLONGED-RELEASE TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126541611 | 12654161 | 1 | Multiple allergies |
| 126541611 | 12654161 | 2 | Multiple allergies |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126541611 | 12654161 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |