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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 98339654 | 9833965 | 4 | F | 20130329 | 20160712 | 20140122 | 20160714 | EXP | IN-BRISTOL-MYERS SQUIBB COMPANY-20068789 | BRISTOL MYERS SQUIBB | JAIN D. FERTILITY AND PREGNANCY OUTCOME IN A WOMAN WITH CLASSIC CONGENITAL ADRENAL HYPERPLASIA. BMJ CASE REP. 2013;1-5 | 0.00 | DY | F | Y | 1.75000 | KG | 20160714 | OT | IN | IN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 98339654 | 9833965 | 1 | PS | METFORMIN HYDROCHLORIDE. | METFORMIN HYDROCHLORIDE | 1 | Transplacental | 500 MG, QD | U | 20357 | 500 | MG | QD | ||||||
| 98339654 | 9833965 | 2 | SS | CLOMIPHENE CITRATE. | CLOMIPHENE CITRATE | 1 | Transplacental | 100 MG, UNK | U | 0 | 100 | MG | |||||||
| 98339654 | 9833965 | 3 | SS | BETAMETHASONE. | BETAMETHASONE | 1 | Transplacental | U | 0 | ||||||||||
| 98339654 | 9833965 | 4 | SS | RITODRINE | RITODRINE | 1 | Transplacental | U | 0 | ||||||||||
| 98339654 | 9833965 | 5 | SS | PROGESTERONE. | PROGESTERONE | 1 | Transplacental | MICRONISED | U | 0 | |||||||||
| 98339654 | 9833965 | 6 | SS | PROGESTERONE. | PROGESTERONE | 1 | Transplacental | 100 MG, UNK | U | 0 | 100 | MG | |||||||
| 98339654 | 9833965 | 7 | SS | PREDNISOLONE. | PREDNISOLONE | 1 | Transplacental | 5 MG, UNK | U | 0 | 5 | MG | |||||||
| 98339654 | 9833965 | 8 | SS | PREDNISOLONE. | PREDNISOLONE | 1 | Transplacental | 6.25 MG, UNK | U | 0 | 6.25 | MG | |||||||
| 98339654 | 9833965 | 9 | SS | PREDNISOLONE. | PREDNISOLONE | 1 | Transplacental | 7.5 MG, UNK | U | 0 | 7.5 | MG | |||||||
| 98339654 | 9833965 | 10 | SS | PREDNISOLONE. | PREDNISOLONE | 1 | Transplacental | 8.75 MG, UNK | U | 0 | 8.75 | MG | |||||||
| 98339654 | 9833965 | 11 | C | FOLIC ACID. | FOLIC ACID | 1 | Transplacental | 5 MG, UNK | U | 0 | 5 | MG | |||||||
| 98339654 | 9833965 | 12 | C | CALCIUM | CALCIUM | 1 | Transplacental | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 98339654 | 9833965 | 1 | Product used for unknown indication |
| 98339654 | 9833965 | 2 | Product used for unknown indication |
| 98339654 | 9833965 | 3 | Product used for unknown indication |
| 98339654 | 9833965 | 4 | Product used for unknown indication |
| 98339654 | 9833965 | 5 | Product used for unknown indication |
| 98339654 | 9833965 | 7 | Product used for unknown indication |
| 98339654 | 9833965 | 11 | Product used for unknown indication |
| 98339654 | 9833965 | 12 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 98339654 | 9833965 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 98339654 | 9833965 | Exposure during breast feeding | |
| 98339654 | 9833965 | Foetal exposure during pregnancy | |
| 98339654 | 9833965 | Premature baby |
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 |
|---|---|---|---|---|---|---|
| 98339654 | 9833965 | 7 | 2012 | 0 | ||
| 98339654 | 9833965 | 8 | 20121121 | 0 | ||
| 98339654 | 9833965 | 9 | 20121214 | 0 | ||
| 98339654 | 9833965 | 10 | 20130221 | 0 |