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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126940441 | 12694044 | 1 | I | 20160705 | 20160829 | 20160829 | PER | US-JNJFOC-20160704542 | JANSSEN | 0.00 | C | M | Y | 0.00000 | 20160829 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126940441 | 12694044 | 1 | SS | CONCERTA | METHYLPHENIDATE HYDROCHLORIDE | 1 | Oral | U | U | UNKNOWN | 0 | 36 | MG | SUSTAINED RELEASE TABLETS | QD | ||||
126940441 | 12694044 | 2 | PS | CONCERTA | METHYLPHENIDATE HYDROCHLORIDE | 1 | Oral | U | U | UNKNOWN | 21121 | SUSTAINED RELEASE TABLETS |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126940441 | 12694044 | 1 | Attention deficit/hyperactivity disorder |
126940441 | 12694044 | 2 | Attention deficit/hyperactivity disorder |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126940441 | 12694044 | Decreased appetite | |
126940441 | 12694044 | Disturbance in attention | |
126940441 | 12694044 | Drug ineffective | |
126940441 | 12694044 | Fatigue | |
126940441 | 12694044 | Hunger | |
126940441 | 12694044 | Insomnia |
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 |
---|---|---|---|---|---|---|
126940441 | 12694044 | 1 | 2015 | 0 |