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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127018501 | 12701850 | 1 | I | 2016 | 20160421 | 20160831 | 20160831 | PER | US-JAZZ-2016-US-007579 | JAZZ | 0.00 | F | Y | 0.00000 | 20160831 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127018501 | 12701850 | 1 | PS | XYREM | SODIUM OXYBATE | 1 | Oral | 4.5 G, BID | 21196 | 4.5 | G | ORAL SOLUTION | |||||||
| 127018501 | 12701850 | 2 | SS | XYREM | SODIUM OXYBATE | 1 | 21196 | ORAL SOLUTION | |||||||||||
| 127018501 | 12701850 | 3 | SS | DEPAKOTE | DIVALPROEX SODIUM | 1 | UNK | Y | U | 0 | TABLET | ||||||||
| 127018501 | 12701850 | 4 | C | Hydrocodone/acetaminophen | ACETAMINOPHENHYDROCODONE | 1 | U | 0 | |||||||||||
| 127018501 | 12701850 | 5 | C | ADDERALL | AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE | 1 | U | 0 | |||||||||||
| 127018501 | 12701850 | 6 | C | ALBUTEROL SULFATE. | ALBUTEROL SULFATE | 1 | U | 0 | |||||||||||
| 127018501 | 12701850 | 7 | C | CLARITIN | LORATADINE | 1 | U | 0 | |||||||||||
| 127018501 | 12701850 | 8 | C | CLONAZEPAM. | CLONAZEPAM | 1 | U | 0 | |||||||||||
| 127018501 | 12701850 | 9 | C | FOLIC ACID. | FOLIC ACID | 1 | U | 0 | |||||||||||
| 127018501 | 12701850 | 10 | C | Magnesium gluconate | MAGNESIUM GLUCONATE | 1 | U | 0 | |||||||||||
| 127018501 | 12701850 | 11 | C | NUVIGIL | ARMODAFINIL | 1 | U | 0 | |||||||||||
| 127018501 | 12701850 | 12 | C | PROPRANOLOL | PROPRANOLOLPROPRANOLOL HYDROCHLORIDE | 1 | U | 0 | |||||||||||
| 127018501 | 12701850 | 13 | C | ZANTAC | RANITIDINE HYDROCHLORIDE | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127018501 | 12701850 | 1 | Narcolepsy |
| 127018501 | 12701850 | 2 | Cataplexy |
| 127018501 | 12701850 | 3 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127018501 | 12701850 | Depression | |
| 127018501 | 12701850 | Fall | |
| 127018501 | 12701850 | Spinal column 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 |
|---|---|---|---|---|---|---|
| 127018501 | 12701850 | 1 | 201603 | 0 | ||
| 127018501 | 12701850 | 3 | 20160401 | 0 |