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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126782061 | 12678206 | 1 | I | 20160816 | 20160823 | 20160823 | EXP | AU-MYLANLABS-2016M1035302 | MYLAN | BOWCOCK E, MORRIS I, LANE A. DEXMEDETOMIDINE FOR ACUTE CLONIDINE WITHDRAWAL FOLLOWING INTRATHECAL PUMP REMOVAL: A DRUG BEGINNING TO FIND ITS EXPANDING NICHE. J-INTENS-CARE-SOC 2016;17(3):271-272. | 0.00 | Y | 0.00000 | 20160823 | OT | AU | AU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126782061 | 12678206 | 1 | PS | CLONIDINE. | CLONIDINE | 1 | Intrathecal | U | 70317 | ||||||||||
| 126782061 | 12678206 | 2 | SS | CLONIDINE. | CLONIDINE | 1 | Oral | TWICE A DAY | U | 70317 | |||||||||
| 126782061 | 12678206 | 3 | SS | CLONIDINE. | CLONIDINE | 1 | Intravenous (not otherwise specified) | U | 70317 | ||||||||||
| 126782061 | 12678206 | 4 | SS | DEXMEDETOMIDINE. | DEXMEDETOMIDINE | 1 | Other | 1 MICROG/KG/H WHICH WAS REDUCED TO 0.4MICROG/KG/H | Y | U | 0 | ||||||||
| 126782061 | 12678206 | 5 | SS | MIDAZOLAM | MIDAZOLAMMIDAZOLAM HYDROCHLORIDE | 1 | Unknown | Y | U | 0 | |||||||||
| 126782061 | 12678206 | 6 | SS | MORPHINE | MORPHINE | 1 | Intrathecal | U | 0 | ||||||||||
| 126782061 | 12678206 | 7 | SS | MORPHINE | MORPHINE | 1 | Intravenous drip | U | 0 | ||||||||||
| 126782061 | 12678206 | 8 | SS | PROPOFOL. | PROPOFOL | 1 | Unknown | Y | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126782061 | 12678206 | 1 | Product used for unknown indication |
| 126782061 | 12678206 | 4 | Drug withdrawal syndrome |
| 126782061 | 12678206 | 5 | Drug withdrawal syndrome |
| 126782061 | 12678206 | 6 | Product used for unknown indication |
| 126782061 | 12678206 | 8 | Drug withdrawal syndrome |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126782061 | 12678206 | LT |
| 126782061 | 12678206 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126782061 | 12678206 | Blood pressure increased | |
| 126782061 | 12678206 | Delirium | |
| 126782061 | 12678206 | Hypotension | |
| 126782061 | 12678206 | Sinus tachycardia | |
| 126782061 | 12678206 | Withdrawal syndrome |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |