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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 102253713 | 10225371 | 3 | F | 201006 | 20160630 | 20140609 | 20160705 | PER | US-BAYER-2014-083071 | BAYER | 30.00 | YR | A | F | Y | 81.63000 | KG | 20160705 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 102253713 | 10225371 | 1 | PS | MIRENA | LEVONORGESTREL | 1 | Intra-uterine | 20 MCG/24HR, CONT | N | TU0054P | 21225 | 20 | UG | INTRAUTERINE DELIVERY SYSTEM | |||||
| 102253713 | 10225371 | 2 | SS | MIRENA | LEVONORGESTREL | 1 | N | 21225 | INTRAUTERINE DELIVERY SYSTEM | ||||||||||
| 102253713 | 10225371 | 3 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | 0 | ||||||||||||
| 102253713 | 10225371 | 4 | C | HYDROCORTISONE [HYDROCORTISONE ACETATE] | 2 | 0 | |||||||||||||
| 102253713 | 10225371 | 5 | C | DILAUDID | HYDROMORPHONE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 102253713 | 10225371 | 6 | C | TORADOL | KETOROLAC TROMETHAMINE | 1 | 0 | ||||||||||||
| 102253713 | 10225371 | 7 | C | VYVANSE | LISDEXAMFETAMINE DIMESYLATE | 1 | 0 | ||||||||||||
| 102253713 | 10225371 | 8 | C | PERCOCET | ACETAMINOPHENOXYCODONE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 102253713 | 10225371 | 9 | C | PHENERGAN | PROMETHAZINE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 102253713 | 10225371 | 10 | C | MAXALT | RIZATRIPTAN BENZOATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 102253713 | 10225371 | 1 | Contraception |
| 102253713 | 10225371 | 2 | Menorrhagia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 102253713 | 10225371 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 102253713 | 10225371 | Abdominal pain | |
| 102253713 | 10225371 | Injury | |
| 102253713 | 10225371 | Medical device pain | |
| 102253713 | 10225371 | Post procedural discomfort | |
| 102253713 | 10225371 | Procedural pain | |
| 102253713 | 10225371 | Uterine perforation |
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 |
|---|---|---|---|---|---|---|
| 102253713 | 10225371 | 1 | 20100621 | 20100629 | 0 |