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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127445621 | 12744562 | 1 | I | 20160520 | 20160914 | 20160914 | PER | US-JAZZ-2016-US-009555 | JAZZ | 0.00 | F | Y | 0.00000 | 20160914 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127445621 | 12744562 | 1 | PS | XYREM | SODIUM OXYBATE | 1 | Oral | 2.25 G, BID | U | 21196 | 2.25 | G | ORAL SOLUTION | ||||||
| 127445621 | 12744562 | 2 | SS | BENADRYL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | U | 0 | |||||||||||
| 127445621 | 12744562 | 3 | C | LINZESS | LINACLOTIDE | 1 | U | 0 | |||||||||||
| 127445621 | 12744562 | 4 | C | ACCOLATE | ZAFIRLUKAST | 1 | U | 0 | |||||||||||
| 127445621 | 12744562 | 5 | C | ALBUTEROL SULFATE. | ALBUTEROL SULFATE | 1 | U | 0 | |||||||||||
| 127445621 | 12744562 | 6 | C | BREO ELLIPTA | FLUTICASONE FUROATEVILANTEROL TRIFENATATE | 1 | U | 0 | |||||||||||
| 127445621 | 12744562 | 7 | C | CYANOCOBALAMIN. | CYANOCOBALAMIN | 1 | U | 0 | |||||||||||
| 127445621 | 12744562 | 8 | C | DEXILANT | DEXLANSOPRAZOLE | 1 | U | 0 | |||||||||||
| 127445621 | 12744562 | 9 | C | IBUPROFEN. | IBUPROFEN | 1 | U | 0 | |||||||||||
| 127445621 | 12744562 | 10 | C | NUVIGIL | ARMODAFINIL | 1 | U | 0 | |||||||||||
| 127445621 | 12744562 | 11 | C | Paroxetine Hcl | PAROXETINE HYDROCHLORIDE | 1 | U | 0 | |||||||||||
| 127445621 | 12744562 | 12 | C | VITAMIN D2 | ERGOCALCIFEROL | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127445621 | 12744562 | 1 | Narcolepsy |
| 127445621 | 12744562 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127445621 | 12744562 | Condition aggravated | |
| 127445621 | 12744562 | Unevaluable event |
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 |
|---|---|---|---|---|---|---|
| 127445621 | 12744562 | 1 | 201602 | 0 |