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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126229321 | 12622932 | 1 | I | 20160726 | 20160804 | 20160804 | EXP | RU-BAYER-2016-147001 | BAYER | 47.00 | YR | A | F | Y | 0.00000 | 20160804 | CN | RU | RU |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126229321 | 12622932 | 1 | PS | YAZ | DROSPIRENONEETHINYL ESTRADIOL | 1 | Oral | UNK | 21676 | FILM-COATED TABLET |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126229321 | 12622932 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126229321 | 12622932 | Abdominal distension | |
126229321 | 12622932 | Abdominal pain lower | |
126229321 | 12622932 | Abnormal withdrawal bleeding | |
126229321 | 12622932 | Back pain | |
126229321 | 12622932 | Breast pain | |
126229321 | 12622932 | Cervical dysplasia | |
126229321 | 12622932 | Metrorrhagia | |
126229321 | 12622932 | Vaginal haemorrhage | |
126229321 | 12622932 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |