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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 106954083 | 10695408 | 3 | F | 20020827 | 20160825 | 20150107 | 20160908 | EXP | US-JNJFOC-20150101724 | JANSSEN | 7.98 | YR | C | M | Y | 0.00000 | 20160908 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 106954083 | 10695408 | 1 | PS | RISPERDAL | RISPERIDONE | 1 | Oral | 0.25 MG AND 1 MG | U | U | 20272 | TABLETS | |||||||
| 106954083 | 10695408 | 2 | C | STRATTERA | ATOMOXETINE HYDROCHLORIDE | 1 | Unknown | 40MG- 60 MG | U | 0 | UNSPECIFIED | ||||||||
| 106954083 | 10695408 | 3 | C | CLONIDINE. | CLONIDINE | 1 | Unknown | 0 | 1 | MG | UNSPECIFIED | ||||||||
| 106954083 | 10695408 | 4 | C | CLONIDINE. | CLONIDINE | 1 | Unknown | 0 | 1 | MG | UNSPECIFIED | ||||||||
| 106954083 | 10695408 | 5 | C | ADDERALL | AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE | 1 | Unknown | 5 MG- 2MG | 0 | 5 | MG | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 106954083 | 10695408 | 1 | Attention deficit/hyperactivity disorder |
| 106954083 | 10695408 | 2 | Product used for unknown indication |
| 106954083 | 10695408 | 3 | Product used for unknown indication |
| 106954083 | 10695408 | 4 | Product used for unknown indication |
| 106954083 | 10695408 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 106954083 | 10695408 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 106954083 | 10695408 | Gynaecomastia | |
| 106954083 | 10695408 | Obesity | |
| 106954083 | 10695408 | Product use issue |
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 |
|---|---|---|---|---|---|---|
| 106954083 | 10695408 | 1 | 20020827 | 20060518 | 0 | |
| 106954083 | 10695408 | 2 | 2004 | 2006 | 0 | |
| 106954083 | 10695408 | 3 | 2002 | 2008 | 0 | |
| 106954083 | 10695408 | 4 | 2011 | 2014 | 0 | |
| 106954083 | 10695408 | 5 | 2000 | 2002 | 0 |