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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 97067233 | 9706723 | 3 | F | 20160921 | 20131125 | 20160928 | PER | US-BAYER-2013-141145 | BAYER | 41.00 | YR | A | F | Y | 0.00000 | 20160928 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 97067233 | 9706723 | 1 | PS | MIRENA | LEVONORGESTREL | 1 | Intra-uterine | 20 MCG/24HR, CONT | 21225 | 20 | UG | INTRAUTERINE DELIVERY SYSTEM | |||||||
| 97067233 | 9706723 | 2 | C | LISINOPRIL. | LISINOPRIL | 1 | Oral | 20-25 MG EVERY DAY | 0 | ||||||||||
| 97067233 | 9706723 | 3 | C | CELEXA | CITALOPRAM HYDROBROMIDE | 1 | Oral | 10 MG TAKE 1 TABLET EVERY DAY | 0 | ||||||||||
| 97067233 | 9706723 | 4 | C | NAPROSYN | NAPROXEN | 1 | 0 | ||||||||||||
| 97067233 | 9706723 | 5 | C | VICODIN | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | 0 | ||||||||||||
| 97067233 | 9706723 | 6 | C | ASPIRIN. | ASPIRIN | 1 | 0 | ||||||||||||
| 97067233 | 9706723 | 7 | C | OXYCODONE | OXYCODONE | 1 | 0 | ||||||||||||
| 97067233 | 9706723 | 8 | C | IBUPROFEN. | IBUPROFEN | 1 | 0 | ||||||||||||
| 97067233 | 9706723 | 9 | C | COLACE | DOCUSATE SODIUM | 1 | 0 | ||||||||||||
| 97067233 | 9706723 | 10 | C | PERCOCET | ACETAMINOPHENOXYCODONE HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 97067233 | 9706723 | 1 | Contraception |
| 97067233 | 9706723 | 2 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 97067233 | 9706723 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 97067233 | 9706723 | Abdominal pain | |
| 97067233 | 9706723 | Abdominal pain lower | |
| 97067233 | 9706723 | Device dislocation | |
| 97067233 | 9706723 | Injury | |
| 97067233 | 9706723 | Menorrhagia |
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 |
|---|---|---|---|---|---|---|
| 97067233 | 9706723 | 1 | 200909 | 20120830 | 0 |