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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126756321 | 12675632 | 1 | I | 20160404 | 20160823 | 20160823 | PER | US-JAZZ-2016-US-006396 | JAZZ | 0.00 | F | Y | 0.00000 | 20160823 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126756321 | 12675632 | 1 | PS | XYREM | SODIUM OXYBATE | 1 | Oral | 2 G, BID | U | 21196 | 2 | G | ORAL SOLUTION | ||||||
126756321 | 12675632 | 2 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | DOSE ADJUSTMENTS | U | 21196 | ORAL SOLUTION | ||||||||
126756321 | 12675632 | 3 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | 4.5 G, BID | U | 21196 | 4.5 | G | ORAL SOLUTION | ||||||
126756321 | 12675632 | 4 | SS | PROVIGIL | MODAFINIL | 1 | 0 | ||||||||||||
126756321 | 12675632 | 5 | C | CLARITIN | LORATADINE | 1 | U | 0 | |||||||||||
126756321 | 12675632 | 6 | C | Melatonin | MELATONIN | 1 | U | 0 | |||||||||||
126756321 | 12675632 | 7 | C | MODAFINIL. | MODAFINIL | 1 | U | 0 | |||||||||||
126756321 | 12675632 | 8 | C | NAPROXEN SODIUM. | NAPROXEN SODIUM | 1 | U | 0 | |||||||||||
126756321 | 12675632 | 9 | C | NUVARING | ETHINYL ESTRADIOLETONOGESTREL | 1 | U | 0 | |||||||||||
126756321 | 12675632 | 10 | C | PROAIR HFA | ALBUTEROL SULFATE | 1 | U | 0 | |||||||||||
126756321 | 12675632 | 11 | C | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | U | 0 | |||||||||||
126756321 | 12675632 | 12 | C | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126756321 | 12675632 | 1 | Narcolepsy |
126756321 | 12675632 | 2 | Cataplexy |
126756321 | 12675632 | 4 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126756321 | 12675632 | Drug intolerance | |
126756321 | 12675632 | Feeling abnormal | |
126756321 | 12675632 | Increased appetite | |
126756321 | 12675632 | Wrong technique in product usage process |
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 |
---|---|---|---|---|---|---|
126756321 | 12675632 | 1 | 200612 | 200702 | 0 | |
126756321 | 12675632 | 3 | 201503 | 0 |