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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127960731 | 12796073 | 1 | I | 20160926 | 20160929 | 20160929 | EXP | US-WARNER CHILCOTT, LLC-1057853 | WARNER CHILCOTT | 0.00 | F | Y | 68.18000 | KG | 20160929 | CN | COUNTRY NOT SPECIFIED | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127960731 | 12796073 | 1 | PS | ESTRACE | ESTRADIOL | 1 | Vaginal | 90607, 09/--/2017 | 86069 | ||||||||||
| 127960731 | 12796073 | 2 | C | ALLEGRA | FEXOFENADINE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 127960731 | 12796073 | 3 | C | ASPIRIN. | ASPIRIN | 1 | 0 | ||||||||||||
| 127960731 | 12796073 | 4 | C | CITALOPRAM | CITALOPRAM HYDROBROMIDE | 1 | 0 | ||||||||||||
| 127960731 | 12796073 | 5 | C | CITRACAL | CALCIUM CITRATE | 1 | 00751520 | 0 | |||||||||||
| 127960731 | 12796073 | 6 | C | CRANBERRY. | CRANBERRY | 1 | 01512301 | 0 | |||||||||||
| 127960731 | 12796073 | 7 | C | GABAPENTIN. | GABAPENTIN | 1 | 0 | ||||||||||||
| 127960731 | 12796073 | 8 | C | BUPROPION. | BUPROPION | 1 | 0 | ||||||||||||
| 127960731 | 12796073 | 9 | C | MONTELUKAST SODIUM. | MONTELUKAST SODIUM | 1 | 0 | ||||||||||||
| 127960731 | 12796073 | 10 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127960731 | 12796073 | 1 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127960731 | 12796073 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127960731 | 12796073 | Application site discharge | |
| 127960731 | 12796073 | Drug effect decreased | |
| 127960731 | 12796073 | Hospitalisation | |
| 127960731 | 12796073 | Intentional product misuse | |
| 127960731 | 12796073 | Urine abnormality |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |