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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
95308212 | 9530821 | 2 | F | 20160715 | 20130918 | 20160722 | EXP | CA-009507513-1309CAN006054 | MERCK | 0.00 | C | F | Y | 0.00000 | 20160722 | OT | CA | CA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
95308212 | 9530821 | 1 | PS | SINGULAIR | MONTELUKAST SODIUM | 1 | Unknown | 5 MG, UNK | U | 20830 | 5 | MG | CHEWABLE TABLET | ||||||
95308212 | 9530821 | 2 | SS | SINGULAIR | MONTELUKAST SODIUM | 1 | Unknown | 4 MG, UNK | U | 20830 | 4 | MG | CHEWABLE TABLET |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
95308212 | 9530821 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
95308212 | 9530821 | Abnormal behaviour |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |