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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125974101 | 12597410 | 1 | I | 20160715 | 20160727 | 20160727 | EXP | GB-WATSON-2016-15958 | WATSON | 0.00 | Y | 0.00000 | 20160727 | CN | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125974101 | 12597410 | 1 | PS | SERTRALINE | SERTRALINE HYDROCHLORIDE | 1 | Oral | UNK | PT00054 | 77663 | UNK |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125974101 | 12597410 | 1 | Depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125974101 | 12597410 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125974101 | 12597410 | Alopecia | |
| 125974101 | 12597410 | Anxiety | |
| 125974101 | 12597410 | Blister | |
| 125974101 | 12597410 | Depressed mood | |
| 125974101 | 12597410 | Disturbance in attention | |
| 125974101 | 12597410 | Drug ineffective | |
| 125974101 | 12597410 | Dry mouth | |
| 125974101 | 12597410 | Dry skin | |
| 125974101 | 12597410 | Fatigue | |
| 125974101 | 12597410 | Hyperhidrosis | |
| 125974101 | 12597410 | Irritable bowel syndrome | |
| 125974101 | 12597410 | Pain in jaw |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |