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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126891201 | 12689120 | 1 | I | 20160811 | 20160826 | 20160826 | PER | US-BAYER-2016-158689 | BAYER | 59.00 | YR | A | F | Y | 61.22000 | KG | 20160826 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126891201 | 12689120 | 1 | PS | CLARITIN-D 24 HOUR | LORATADINEPSEUDOEPHEDRINE SULFATE | 1 | Oral | 1 DF, QD | 20470 | 1 | DF | PROLONGED-RELEASE TABLET | QD | ||||||
126891201 | 12689120 | 2 | SS | CHILDREN CLARITIN ALLERGY | LORATADINE | 1 | Oral | 1 DF, QD | 0 | 1 | DF | SYRUP | QD | ||||||
126891201 | 12689120 | 3 | C | RILUZOLE. | RILUZOLE | 1 | UNK | 0 | |||||||||||
126891201 | 12689120 | 4 | C | LEXAPRO | ESCITALOPRAM OXALATE | 1 | UNK | 0 | |||||||||||
126891201 | 12689120 | 5 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | UNK | 0 | |||||||||||
126891201 | 12689120 | 6 | C | MOBIC | MELOXICAM | 1 | 0 | ||||||||||||
126891201 | 12689120 | 7 | C | ALBUTEROL. | ALBUTEROL | 1 | 0 | ||||||||||||
126891201 | 12689120 | 8 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | 0 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126891201 | 12689120 | Drug ineffective | |
126891201 | 12689120 | Drug prescribing error | |
126891201 | 12689120 | Product use issue | |
126891201 | 12689120 | Therapeutic response unexpected | |
126891201 | 12689120 | Wrong technique in product usage process |
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 |
---|---|---|---|---|---|---|
126891201 | 12689120 | 1 | 201608 | 0 | ||
126891201 | 12689120 | 2 | 201608 | 0 |