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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121224492 | 12122449 | 2 | F | 20160802 | 20160226 | 20160809 | EXP | US-JAZZ-2016-US-001149 | JAZZ | 0.00 | M | Y | 0.00000 | 20160809 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121224492 | 12122449 | 1 | PS | XYREM | SODIUM OXYBATE | 1 | Oral | 2.25 G, BID | 21196 | 2.25 | G | ORAL SOLUTION | |||||||
121224492 | 12122449 | 2 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | DOSE ADJUSTMENTS | 21196 | ORAL SOLUTION | |||||||||
121224492 | 12122449 | 3 | SS | XYREM | SODIUM OXYBATE | 1 | Oral | 4.5 G, BID | 21196 | 4.5 | G | ORAL SOLUTION | |||||||
121224492 | 12122449 | 4 | SS | NUVIGIL | ARMODAFINIL | 1 | UNK | U | 0 | TABLET | |||||||||
121224492 | 12122449 | 5 | SS | RITALIN | METHYLPHENIDATE HYDROCHLORIDE | 1 | UNK | U | 0 | TABLET | |||||||||
121224492 | 12122449 | 6 | SS | Amphetamine salts | AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE | 1 | U | 0 | |||||||||||
121224492 | 12122449 | 7 | C | ALEVE | NAPROXEN SODIUM | 1 | UNK | U | 0 | TABLET | |||||||||
121224492 | 12122449 | 8 | C | CLARITIN | LORATADINE | 1 | UNK | U | 0 | TABLET | |||||||||
121224492 | 12122449 | 9 | C | Melatonin | MELATONIN | 1 | UNK | U | 0 | TABLET | |||||||||
121224492 | 12122449 | 10 | C | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | UNK | U | 0 | ||||||||||
121224492 | 12122449 | 11 | C | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
121224492 | 12122449 | 12 | C | WELLBUTRIN | BUPROPION HYDROCHLORIDE | 1 | UNK | U | 0 | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
121224492 | 12122449 | 1 | Narcolepsy |
121224492 | 12122449 | 4 | Product used for unknown indication |
121224492 | 12122449 | 5 | Product used for unknown indication |
121224492 | 12122449 | 6 | Product used for unknown indication |
121224492 | 12122449 | 7 | Product used for unknown indication |
121224492 | 12122449 | 8 | Product used for unknown indication |
121224492 | 12122449 | 9 | Product used for unknown indication |
121224492 | 12122449 | 10 | Product used for unknown indication |
121224492 | 12122449 | 11 | Product used for unknown indication |
121224492 | 12122449 | 12 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
121224492 | 12122449 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
121224492 | 12122449 | Condition aggravated | |
121224492 | 12122449 | Prostatic disorder | |
121224492 | 12122449 | Urinary hesitation |
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 |
---|---|---|---|---|---|---|
121224492 | 12122449 | 1 | 201512 | 201512 | 0 | |
121224492 | 12122449 | 2 | 201601 | 201601 | 0 | |
121224492 | 12122449 | 3 | 201601 | 0 | ||
121224492 | 12122449 | 4 | 20151221 | 0 | ||
121224492 | 12122449 | 5 | 20151221 | 0 | ||
121224492 | 12122449 | 7 | 20151222 | 0 | ||
121224492 | 12122449 | 8 | 20151222 | 0 | ||
121224492 | 12122449 | 9 | 20151222 | 0 | ||
121224492 | 12122449 | 10 | 20151222 | 0 | ||
121224492 | 12122449 | 11 | 20151221 | 0 | ||
121224492 | 12122449 | 12 | 20151221 | 0 |