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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5329796 | 6317677 | I | 5329796-1 | 20070401 | 20070517 | DIR | 42 | YR | M | N | 185 | LBS | 20070516 | CN | N | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5329796 | 1008497768 | PS | CONCERTA | 1 | ORAL | 1 TABLET DAILY PO | D | D |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5329796 | 1008497768 | ATTENTION DEFICIT/HYPERACTIVITY DISORDER |
Outcome of event
Event ID | OUTC COD |
---|---|
5329796 | HO |
Reactions reported
Event ID | PT |
---|---|
5329796 | ANGINA PECTORIS |
5329796 | CHEST PAIN |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5329796 | 1008497768 | 20050701 | 20070516 |