Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7487223 | 7618270 | F | 7487223-2 | 20100310 | 20110414 | 20110518 | PER | US-BAYER-201035672NA | BAYER HEALTHCARE PHARMACEUTICALS INC. | 16 | YR | F | Y | 54 | KG | 20110518 | CN | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7487223 | 1016524428 | PS | YAZ | 1 | ORAL | UNK UNK, UNK | 021676 | ||||
| 7487223 | 1016524429 | SS | YASMIN | 1 | ORAL | ||||||
| 7487223 | 1016524430 | C | ZANTAC | 1 | |||||||
| 7487223 | 1016524431 | C | LO/OVRAL | 1 | UNK UNK, CONT | ||||||
| 7487223 | 1016524433 | C | IBUPROFEN | 1 | |||||||
| 7487223 | 1016524432 | C | CLARITIN | 1 | UNK | ||||||
| 7487223 | 1016524435 | C | RANITIDINE | 1 | |||||||
| 7487223 | 1016524434 | C | ADVIL LIQUI-GELS | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7487223 | 1016524428 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7487223 | 1016524429 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7487223 | HO |
| 7487223 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7487223 | CHOLELITHIASIS |
| 7487223 | GALLBLADDER DISORDER |
| 7487223 | PAIN |
| 7487223 | CHOLECYSTITIS |
| 7487223 | ABDOMINAL PAIN |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7487223 | 1016524428 | 20080501 | 20100201 | 608 | DAY |
| 7487223 | 1016524429 | 20080501 | 20100101 | 608 | DAY |