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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125575882 | 12557588 | 2 | F | 2015 | 20160822 | 20160714 | 20160826 | EXP | BR-PFIZER INC-2016339616 | PFIZER | 80.00 | YR | F | Y | 60.00000 | KG | 20160826 | CN | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125575882 | 12557588 | 1 | PS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | Oral | 50 MG, UNK | U | 21992 | 50 | MG | PROLONGED-RELEASE TABLET | ||||||
| 125575882 | 12557588 | 2 | SS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | Oral | 100 MG, UNK | U | 99769 | 21992 | 100 | MG | PROLONGED-RELEASE TABLET | |||||
| 125575882 | 12557588 | 3 | C | SOMALIUM | BROMAZEPAM | 1 | Oral | 3MG, 1 TABLET PER DAY | 0 | 3 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125575882 | 12557588 | 1 | Depression |
| 125575882 | 12557588 | 3 | Sleep disorder |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125575882 | 12557588 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125575882 | 12557588 | Activities of daily living impaired | |
| 125575882 | 12557588 | Blood cholesterol abnormal | |
| 125575882 | 12557588 | Brain hypoxia | |
| 125575882 | 12557588 | Confusional state | |
| 125575882 | 12557588 | Dementia Alzheimer's type | |
| 125575882 | 12557588 | Drug dependence | |
| 125575882 | 12557588 | Drug dose omission | |
| 125575882 | 12557588 | Drug effect decreased | |
| 125575882 | 12557588 | Fatigue | |
| 125575882 | 12557588 | Nervousness | |
| 125575882 | 12557588 | Rheumatoid arthritis | |
| 125575882 | 12557588 | Slow speech | |
| 125575882 | 12557588 | Somnolence |
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 |
|---|---|---|---|---|---|---|
| 125575882 | 12557588 | 2 | 2011 | 0 |