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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126032831 | 12603283 | 1 | I | 20160726 | 20160727 | 20160728 | 20160728 | PER | US-BAYER-2016-146874 | BAYER | 84.00 | YR | E | M | Y | 74.83000 | KG | 20160728 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126032831 | 12603283 | 1 | PS | CLARITIN | LORATADINE | 1 | Oral | 1 DF, QD | CVM0AUA | 19658 | 1 | DF | TABLET | QD | |||||
126032831 | 12603283 | 2 | SS | CLARITIN | LORATADINE | 1 | 19658 | TABLET | |||||||||||
126032831 | 12603283 | 3 | C | CHLOR-TRIMETON | CHLORPHENIRAMINE MALEATE | 1 | UNK | 0 | |||||||||||
126032831 | 12603283 | 4 | C | LISINOPRIL. | LISINOPRIL | 1 | 1 DF, BID | 0 | 1 | DF | BID | ||||||||
126032831 | 12603283 | 5 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | 1 DF, QD | 0 | 1 | DF | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126032831 | 12603283 | 1 | Arthropod bite |
126032831 | 12603283 | 2 | Swelling |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126032831 | 12603283 | Product use issue |
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 |
---|---|---|---|---|---|---|
126032831 | 12603283 | 1 | 20160726 | 20160728 | 0 |