Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8610954 | 8747139 | I | 8610954-5 | 20111020 | 20120420 | PER | WAES 1110USA03347 | MERCK + CO., INC. | 24 | MON | F | N | 20120419 | MD | UNITED STATES |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
8610954 | 1020622679 | PS | SINGULAIR | 1 | ORAL | 4 MG/DAILY/PO | Y | D | 20830 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8610954 | 1020622679 | ASTHMA |
Outcome of event
Event ID | OUTC COD |
---|---|
8610954 | OT |
Reactions reported
Event ID | PT |
---|---|
8610954 | CONVULSION |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
8610954 | CR |
8610954 | HP |
Therapies reported
no results found |