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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127422331 | 12742233 | 1 | I | 20160911 | 0 | 20160914 | 20160914 | DIR | US-FDA-350535 | FDA-CTU | 59.00 | YR | F | N | 81.00000 | KG | 20160914 | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127422331 | 12742233 | 1 | PS | MISOPROSTOL. | MISOPROSTOL | 1 | Oral | OTHER STRENGTH:MCG;OTHER DOSE:;OTHER FREQUENCY:TAKE 2 TABLETS;OTHER ROUTE: | Y | D | 20170909 | 0 | 2 | DF | COATED TABLET | ||||
127422331 | 12742233 | 3 | C | CENTRUM IROBN | 2 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127422331 | 12742233 | 1 | Medical procedure |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127422331 | 12742233 | Blood pressure increased | |
127422331 | 12742233 | Heart rate increased | |
127422331 | 12742233 | Muscle spasms | |
127422331 | 12742233 | Nausea | |
127422331 | 12742233 | Pain |
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 |
---|---|---|---|---|---|---|
127422331 | 12742233 | 1 | 20160911 | 20160911 | 0 |