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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126509821 | 12650982 | 1 | I | 20160316 | 20160815 | 20160815 | PER | US-JAZZ-2016-US-005231 | JAZZ | 0.00 | F | Y | 0.00000 | 20160815 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126509821 | 12650982 | 1 | PS | XYREM | SODIUM OXYBATE | 1 | Oral | 2.25 G, BID | U | 21196 | 2.25 | G | ORAL SOLUTION | ||||||
| 126509821 | 12650982 | 2 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | 3 G, BID | U | 21196 | 3 | G | ORAL SOLUTION | ||||||
| 126509821 | 12650982 | 3 | SS | KLONOPIN | CLONAZEPAM | 1 | UNK | 0 | |||||||||||
| 126509821 | 12650982 | 4 | C | WELLBUTRIN | BUPROPION HYDROCHLORIDE | 1 | U | 0 | |||||||||||
| 126509821 | 12650982 | 5 | C | TRAMADOL. | TRAMADOL | 1 | U | 0 | |||||||||||
| 126509821 | 12650982 | 6 | C | ADDERALL | AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE | 1 | U | 0 | |||||||||||
| 126509821 | 12650982 | 7 | C | Multivitamins | VITAMINS | 1 | U | 0 | |||||||||||
| 126509821 | 12650982 | 8 | C | XANAX | ALPRAZOLAM | 1 | U | 0 | |||||||||||
| 126509821 | 12650982 | 9 | C | ALBUTEROL SULFATE. | ALBUTEROL SULFATE | 1 | U | 0 | |||||||||||
| 126509821 | 12650982 | 10 | C | ALBUTEROL SULFATE. | ALBUTEROL SULFATE | 1 | U | 0 | |||||||||||
| 126509821 | 12650982 | 11 | C | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126509821 | 12650982 | 1 | Narcolepsy |
| 126509821 | 12650982 | 2 | Cataplexy |
| 126509821 | 12650982 | 3 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126509821 | 12650982 | Dyspnoea | |
| 126509821 | 12650982 | Narcolepsy |
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 |
|---|---|---|---|---|---|---|
| 126509821 | 12650982 | 1 | 201504 | 201504 | 0 | |
| 126509821 | 12650982 | 2 | 201504 | 2015 | 0 | |
| 126509821 | 12650982 | 3 | 20141116 | 20141216 | 0 |