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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125482781 | 12548278 | 1 | I | 20160630 | 20160712 | 20160712 | PER | US-BAYER-2016-130354 | BAYER | 52.00 | YR | A | F | Y | 77.98000 | KG | 20160712 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125482781 | 12548278 | 1 | PS | CLARITIN | LORATADINE | 1 | Oral | 1 DF, PRN | CVM01K8 | 19658 | 1 | DF | TABLET | ||||||
| 125482781 | 12548278 | 2 | SS | CLARITIN-D 24 HOUR | LORATADINEPSEUDOEPHEDRINE SULFATE | 1 | Oral | 1 DF, UNK | 0 | 1 | DF | PROLONGED-RELEASE TABLET | |||||||
| 125482781 | 12548278 | 3 | C | ULTRACET | ACETAMINOPHENTRAMADOL HYDROCHLORIDE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125482781 | 12548278 | 1 | Seasonal allergy |
| 125482781 | 12548278 | 2 | Seasonal allergy |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125482781 | 12548278 | Drug ineffective | |
| 125482781 | 12548278 | Dyspnoea |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |