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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126139711 | 12613971 | 1 | I | 20160726 | 20160802 | 20160802 | PER | US-PFIZER INC-2016364245 | PFIZER | 0.00 | M | Y | 0.00000 | 20160802 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126139711 | 12613971 | 1 | PS | ZOLOFT | SERTRALINE HYDROCHLORIDE | 1 | 125 MG, UNK | 19839 | 125 | MG | |||||||||
126139711 | 12613971 | 2 | SS | ZOLOFT | SERTRALINE HYDROCHLORIDE | 1 | 112.5 MG, UNK | 19839 | 112.5 | MG | |||||||||
126139711 | 12613971 | 3 | SS | ZOLOFT | SERTRALINE HYDROCHLORIDE | 1 | 125 MG, UNK | 19839 | 125 | MG |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126139711 | 12613971 | Depression | |
126139711 | 12613971 | Malaise | |
126139711 | 12613971 | Nausea | |
126139711 | 12613971 | Nightmare |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |