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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6767312 | 7418170 | I | 6767312-8 | 20100601 | 20100608 | 20100614 | PER | US-BAYER-201016514BCC | BAYER HEALTHCARE LLC | 62 | YR | M | Y | 82 | KG | 20100614 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6767312 | 1013856267 | PS | ALEVE | 1 | ORAL | TOTAL DAILY DOSE: 880 MG UNIT DOSE: 220 MG | 296249K | 020204 | |||
6767312 | 1013856268 | C | STRATTERA | 1 | UNKNOWN | UNKNOWN | |||||
6767312 | 1013856269 | C | LISINOPRIL | 1 | UNKNOWN | UNKNOWN | |||||
6767312 | 1013856270 | C | LUPRON | 1 | UNKNOWN | UNKNOWN | |||||
6767312 | 1013856271 | C | VITAMIN D | 1 | UNKNOWN | UNKNOWN | |||||
6767312 | 1013856272 | C | VITAMIN E | 1 | UNKNOWN | UNKNOWN | |||||
6767312 | 1013856273 | C | FISH OIL | 2 | UNKNOWN | UNKNOWN | |||||
6767312 | 1013856274 | C | CALCIUM CARBONATE | 1 | UNKNOWN | UNKNOWN | |||||
6767312 | 1013856275 | C | CHROMIUM | 2 | UNKNOWN | UNKNOWN | |||||
6767312 | 1013856276 | C | CRANBERRY EXTRACT | 2 | UNKNOWN | UNKNOWN |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6767312 | 1013856267 | ARTHRALGIA |
Outcome of event
Event ID | OUTC COD |
---|---|
6767312 | OT |
Reactions reported
Event ID | PT |
---|---|
6767312 | HAEMATOCHEZIA |
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 |
---|---|---|---|---|---|
6767312 | 1013856267 | 20100526 | 20100601 | 7 | DAY |