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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125804551 | 12580455 | 1 | I | 20160126 | 20160721 | 20160721 | PER | US-JAZZ-2016-US-001431 | JAZZ | 0.00 | F | Y | 0.00000 | 20160721 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125804551 | 12580455 | 1 | PS | XYREM | SODIUM OXYBATE | 1 | Oral | 2.25 G, BID | 21196 | 2.25 | G | ORAL SOLUTION | |||||||
| 125804551 | 12580455 | 2 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | DOSE ADJUSTMENTS | 21196 | ORAL SOLUTION | |||||||||
| 125804551 | 12580455 | 3 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | 3.5 G, BID | 21196 | 3.5 | G | ORAL SOLUTION | |||||||
| 125804551 | 12580455 | 4 | SS | PROVIGIL | MODAFINIL | 1 | UNK | 0 | |||||||||||
| 125804551 | 12580455 | 5 | C | ACETAMINOPHENHYDROCODONE BITARTRATE | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | 2.5-108/5 | U | 0 | ||||||||||
| 125804551 | 12580455 | 6 | C | METHYLPHENIDATE. | METHYLPHENIDATE | 1 | UNK | U | 0 | TABLET | |||||||||
| 125804551 | 12580455 | 7 | C | METHYLPHENIDATE. | METHYLPHENIDATE | 1 | UNK | U | 0 | TABLET | |||||||||
| 125804551 | 12580455 | 8 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | UNK | U | 0 | TABLET | |||||||||
| 125804551 | 12580455 | 9 | C | ADVIL | IBUPROFEN | 1 | UNK | U | 0 | GEL | |||||||||
| 125804551 | 12580455 | 10 | C | ALLEGRA | FEXOFENADINE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
| 125804551 | 12580455 | 11 | C | PROGESTERONE. | PROGESTERONE | 1 | UNK | U | 0 | ||||||||||
| 125804551 | 12580455 | 12 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | UNK | U | 0 | TABLET | |||||||||
| 125804551 | 12580455 | 13 | C | YAZ | DROSPIRENONEETHINYL ESTRADIOL | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125804551 | 12580455 | 1 | Narcolepsy |
| 125804551 | 12580455 | 2 | Cataplexy |
| 125804551 | 12580455 | 4 | Product used for unknown indication |
| 125804551 | 12580455 | 5 | Product used for unknown indication |
| 125804551 | 12580455 | 6 | Product used for unknown indication |
| 125804551 | 12580455 | 7 | Product used for unknown indication |
| 125804551 | 12580455 | 8 | Product used for unknown indication |
| 125804551 | 12580455 | 9 | Product used for unknown indication |
| 125804551 | 12580455 | 10 | Product used for unknown indication |
| 125804551 | 12580455 | 11 | Product used for unknown indication |
| 125804551 | 12580455 | 12 | Product used for unknown indication |
| 125804551 | 12580455 | 13 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125804551 | 12580455 | Anxiety |
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 |
|---|---|---|---|---|---|---|
| 125804551 | 12580455 | 1 | 200810 | 200811 | 0 | |
| 125804551 | 12580455 | 3 | 201106 | 0 | ||
| 125804551 | 12580455 | 4 | 20130101 | 0 | ||
| 125804551 | 12580455 | 5 | 20150223 | 20150302 | 0 | |
| 125804551 | 12580455 | 6 | 20140122 | 20150126 | 0 | |
| 125804551 | 12580455 | 7 | 20130805 | 0 | ||
| 125804551 | 12580455 | 8 | 20130101 | 0 | ||
| 125804551 | 12580455 | 11 | 20130101 | 0 | ||
| 125804551 | 12580455 | 12 | 20130101 | 0 | ||
| 125804551 | 12580455 | 13 | 20130101 | 0 |