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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127689821 | 12768982 | 1 | I | 2016 | 20160603 | 20160921 | 20160921 | PER | US-JAZZ-2016-US-010465 | JAZZ | 0.00 | F | Y | 74.83000 | KG | 20160921 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127689821 | 12768982 | 1 | PS | XYREM | SODIUM OXYBATE | 1 | Oral | 3 G, BID | 21196 | 3 | G | ORAL SOLUTION | |||||||
| 127689821 | 12768982 | 2 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | 3.5 G, FIRST DOSE | 21196 | 3.5 | G | ORAL SOLUTION | |||||||
| 127689821 | 12768982 | 3 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | 4 G, SECOND DOSE | 21196 | 4 | G | ORAL SOLUTION | |||||||
| 127689821 | 12768982 | 4 | SS | PROVIGIL | MODAFINIL | 1 | UNK | U | 0 | ||||||||||
| 127689821 | 12768982 | 5 | SS | ADDERALL | AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE | 1 | U | 0 | |||||||||||
| 127689821 | 12768982 | 6 | SS | NUVIGIL | ARMODAFINIL | 1 | U | 0 | |||||||||||
| 127689821 | 12768982 | 7 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | U | 0 | |||||||||||
| 127689821 | 12768982 | 8 | C | Potassium | POTASSIUM | 1 | U | 0 | |||||||||||
| 127689821 | 12768982 | 9 | C | ALEVE | NAPROXEN SODIUM | 1 | U | 0 | |||||||||||
| 127689821 | 12768982 | 10 | C | CELEXA | CITALOPRAM HYDROBROMIDE | 1 | U | 0 | |||||||||||
| 127689821 | 12768982 | 11 | C | TRAMADOL HCL | TRAMADOL HYDROCHLORIDE | 1 | U | 0 | |||||||||||
| 127689821 | 12768982 | 12 | C | TYLENOL | ACETAMINOPHEN | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127689821 | 12768982 | 1 | Narcolepsy |
| 127689821 | 12768982 | 4 | Narcolepsy |
| 127689821 | 12768982 | 5 | Narcolepsy |
| 127689821 | 12768982 | 6 | Product used for unknown indication |
| 127689821 | 12768982 | 7 | Hypothyroidism |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127689821 | 12768982 | Alopecia | |
| 127689821 | 12768982 | Condition aggravated |
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 |
|---|---|---|---|---|---|---|
| 127689821 | 12768982 | 1 | 201604 | 201605 | 0 | |
| 127689821 | 12768982 | 2 | 201605 | 0 | ||
| 127689821 | 12768982 | 3 | 201605 | 0 |