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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126303402 | 12630340 | 2 | F | 20160909 | 20160808 | 20160914 | EXP | US-BAYER-2016-150604 | BAYER | 0.00 | A | F | Y | 0.00000 | 20160914 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126303402 | 12630340 | 1 | PS | CLIMARA PRO | ESTRADIOLLEVONORGESTREL | 1 | Transdermal | UNK | 160105 | 21258 | TRANSDERMAL PATCH | ||||||||
126303402 | 12630340 | 2 | SS | PROGESTERONE. | PROGESTERONE | 1 | Topical | UNKNOWN | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126303402 | 12630340 | 1 | Menopausal symptoms |
126303402 | 12630340 | 2 | Menopausal symptoms |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126303402 | 12630340 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126303402 | 12630340 | Abdominal pain lower | |
126303402 | 12630340 | Discomfort | |
126303402 | 12630340 | Product adhesion issue | |
126303402 | 12630340 | Uterine haemorrhage |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |