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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8610981 | 8747232 | I | 8610981-8 | 20040701 | 20110401 | 20120420 | PER | WAES 1104UAS00219 | MERCK + CO., INC. | 13 | YR | F | N | 115 | LBS | 20120419 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8610981 | 1020673059 | C | PREDNISONE | 1 | |||||||
8610981 | 1020622756 | PS | SINGULAIR | 1 | ORAL | PO | N | D | 20830 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8610981 | 1020622756 | ASTHMA |
Outcome of event
Event ID | OUTC COD |
---|---|
8610981 | HO |
Reactions reported
Event ID | PT |
---|---|
8610981 | DEPRESSION |
8610981 | TREMOR |
8610981 | AUTOIMMUNE DISORDER |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
8610981 | CSM |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
8610981 | 1020622756 | 19970101 | 20041001 |