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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126146411 | 12614641 | 1 | I | 201301 | 20130130 | 20160802 | 20160802 | PER | US-JAZZ-JPI-P-029811 | JAZZ | 42.51 | YR | F | Y | 0.00000 | 20160802 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126146411 | 12614641 | 1 | PS | XYREM | SODIUM OXYBATE | 1 | Oral | 2.25 G, BID | 21196 | 2.25 | G | ORAL SOLUTION | |||||||
126146411 | 12614641 | 2 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | DOSE ADJUSTMENTS | 21196 | ORAL SOLUTION | |||||||||
126146411 | 12614641 | 3 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | 4.5 G, BID | 21196 | 4.5 | G | ORAL SOLUTION | |||||||
126146411 | 12614641 | 4 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | 2.25 G, BID | 21196 | 2.25 | G | ORAL SOLUTION | |||||||
126146411 | 12614641 | 5 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | DOSE ADJUSTMENTS | 21196 | ORAL SOLUTION | |||||||||
126146411 | 12614641 | 6 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | 4.5 G, BID | 21196 | 4.5 | G | ORAL SOLUTION | |||||||
126146411 | 12614641 | 7 | SS | XYREM | SODIUM OXYBATE | 1 | UNK | 21196 | ORAL SOLUTION | ||||||||||
126146411 | 12614641 | 8 | SS | FENTANYL. | FENTANYL | 1 | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126146411 | 12614641 | 1 | Narcolepsy |
126146411 | 12614641 | 8 | Pain |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126146411 | 12614641 | Condition aggravated | |
126146411 | 12614641 | Drug effect decreased | |
126146411 | 12614641 | Dyspnoea | |
126146411 | 12614641 | Gastrointestinal disorder | |
126146411 | 12614641 | Gastrooesophageal reflux disease | |
126146411 | 12614641 | Pain | |
126146411 | 12614641 | Psychomotor hyperactivity | |
126146411 | 12614641 | Sleep-related eating disorder |
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 |
---|---|---|---|---|---|---|
126146411 | 12614641 | 1 | 20050117 | 2005 | 0 | |
126146411 | 12614641 | 2 | 2005 | 2005 | 0 | |
126146411 | 12614641 | 3 | 200504 | 2005 | 0 | |
126146411 | 12614641 | 4 | 201301 | 201301 | 0 | |
126146411 | 12614641 | 5 | 2013 | 2013 | 0 | |
126146411 | 12614641 | 6 | 201302 | 0 |