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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124315482 | 12431548 | 2 | F | 20131222 | 20160628 | 20160603 | 20160706 | EXP | US-JAZZ-2015-US-017406 | JAZZ | 61.41 | YR | F | Y | 0.00000 | 20160706 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124315482 | 12431548 | 1 | PS | XYREM | SODIUM OXYBATE | 1 | Oral | 3 G, BID | Y | 21196 | 3 | G | ORAL SOLUTION | ||||||
124315482 | 12431548 | 2 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | 3 G, BID | Y | 21196 | 3 | G | ORAL SOLUTION | ||||||
124315482 | 12431548 | 3 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | 3 G, BID | Y | 21196 | 3 | G | ORAL SOLUTION | ||||||
124315482 | 12431548 | 4 | C | DEXEDRINE | DEXTROAMPHETAMINE SULFATE | 1 | UNK | 0 | TABLET | ||||||||||
124315482 | 12431548 | 5 | C | BUSPIRONE HYDROCHLORIDE. | BUSPIRONE HYDROCHLORIDE | 1 | UNK | 0 | TABLET | ||||||||||
124315482 | 12431548 | 6 | C | AMERGE | NARATRIPTAN HYDROCHLORIDE | 1 | UNK | 0 | TABLET | ||||||||||
124315482 | 12431548 | 7 | C | Diamox er | 2 | UNK | 0 | CAPSULE | |||||||||||
124315482 | 12431548 | 8 | C | Amiloride | AMILORIDE | 1 | U | 0 | |||||||||||
124315482 | 12431548 | 9 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | U | 0 | |||||||||||
124315482 | 12431548 | 10 | C | Potassium | POTASSIUM | 1 | U | 0 | |||||||||||
124315482 | 12431548 | 11 | C | Omega 3 | OMEGA-3 FATTY ACIDS | 1 | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124315482 | 12431548 | 1 | Narcolepsy |
124315482 | 12431548 | 4 | Product used for unknown indication |
124315482 | 12431548 | 5 | Product used for unknown indication |
124315482 | 12431548 | 6 | Product used for unknown indication |
124315482 | 12431548 | 7 | Product used for unknown indication |
124315482 | 12431548 | 8 | Product used for unknown indication |
124315482 | 12431548 | 9 | Product used for unknown indication |
124315482 | 12431548 | 10 | Product used for unknown indication |
124315482 | 12431548 | 11 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124315482 | 12431548 | HO |
124315482 | 12431548 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124315482 | 12431548 | Drug ineffective | |
124315482 | 12431548 | Fall | |
124315482 | 12431548 | Humerus fracture | |
124315482 | 12431548 | Jaw fracture | |
124315482 | 12431548 | Pre-existing condition improved | |
124315482 | 12431548 | Therapeutic response unexpected | |
124315482 | 12431548 | Tooth injury |
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 |
---|---|---|---|---|---|---|
124315482 | 12431548 | 1 | 200209 | 2009 | 0 | |
124315482 | 12431548 | 2 | 201205 | 2013 | 0 | |
124315482 | 12431548 | 3 | 201407 | 0 | ||
124315482 | 12431548 | 4 | 20151015 | 0 | ||
124315482 | 12431548 | 5 | 20150707 | 0 | ||
124315482 | 12431548 | 6 | 20000501 | 0 | ||
124315482 | 12431548 | 7 | 20000501 | 0 |