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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125833481 | 12583348 | 1 | I | 20160718 | 20160719 | 20160722 | 20160722 | PER | US-BAYER-2016-141558 | BAYER | 73.00 | YR | E | F | Y | 76.19000 | KG | 20160722 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125833481 | 12583348 | 1 | PS | CLARITIN REDITABS | LORATADINE | 1 | Oral | 1 DF, QD | 7RXF102 | 21993 | 1 | DF | ORODISPERSIBLE TABLET | QD | |||||
125833481 | 12583348 | 2 | C | METHYLPREDNISOLONE. | METHYLPREDNISOLONE | 1 | UNK | 0 | |||||||||||
125833481 | 12583348 | 3 | C | RAMIPRIL. | RAMIPRIL | 1 | UNK | 0 | |||||||||||
125833481 | 12583348 | 4 | C | HYDROCHLORZIDE | HYDROCHLOROTHIAZIDE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125833481 | 12583348 | 1 | Seasonal allergy |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125833481 | 12583348 | Expired product administered |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |