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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 98561024 | 9856102 | 4 | F | 20090610 | 20160817 | 20140130 | 20160829 | PER | US-BAYER-2014-013233 | BAYER | 24.00 | YR | A | F | Y | 83.90000 | KG | 20160829 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 98561024 | 9856102 | 1 | PS | MIRENA | LEVONORGESTREL | 1 | Intra-uterine | 20 MCG/24HR, CONT | 21225 | 20 | UG | INTRAUTERINE DELIVERY SYSTEM | |||||||
| 98561024 | 9856102 | 2 | SS | MIRENA | LEVONORGESTREL | 1 | Intra-uterine | 20 MCG/24HR, CONT | TU008XV | 21225 | 20 | UG | INTRAUTERINE DELIVERY SYSTEM | ||||||
| 98561024 | 9856102 | 3 | C | DEPO-PROVERA | MEDROXYPROGESTERONE ACETATE | 1 | UNK | 0 | |||||||||||
| 98561024 | 9856102 | 4 | C | DEPO-PROVERA | MEDROXYPROGESTERONE ACETATE | 1 | UNK | 0 | |||||||||||
| 98561024 | 9856102 | 5 | C | IBUPROFEN. | IBUPROFEN | 1 | 800 MG, UNK | 0 | 800 | MG | |||||||||
| 98561024 | 9856102 | 6 | C | PERCOCET | ACETAMINOPHENOXYCODONE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 98561024 | 9856102 | 7 | C | DOXYCYCLINE. | DOXYCYCLINE | 1 | 100 MG, BID | 0 | 100 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 98561024 | 9856102 | 1 | Contraception |
| 98561024 | 9856102 | 2 | Contraception |
| 98561024 | 9856102 | 3 | Contraception |
| 98561024 | 9856102 | 4 | Contraception |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 98561024 | 9856102 | LT |
| 98561024 | 9856102 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 98561024 | 9856102 | Abdominal pain lower | |
| 98561024 | 9856102 | Device difficult to use | |
| 98561024 | 9856102 | Device expulsion | |
| 98561024 | 9856102 | Device issue | |
| 98561024 | 9856102 | Device physical property issue | |
| 98561024 | 9856102 | General physical health deterioration | |
| 98561024 | 9856102 | Genital haemorrhage | |
| 98561024 | 9856102 | Injury | |
| 98561024 | 9856102 | Medical device discomfort | |
| 98561024 | 9856102 | Metrorrhagia | |
| 98561024 | 9856102 | Pain | |
| 98561024 | 9856102 | 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 |
|---|---|---|---|---|---|---|
| 98561024 | 9856102 | 1 | 20081210 | 20090610 | 0 | |
| 98561024 | 9856102 | 2 | 20110719 | 20121107 | 0 | |
| 98561024 | 9856102 | 3 | 20110525 | 201108 | 0 | |
| 98561024 | 9856102 | 4 | 20120221 | 0 |