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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5689611 | 6602483 | I | 5689611-3 | 20080306 | 20080331 | PER | US-BOEHRINGER INGELHEIM GMBH, GERMANY-2008-BP-03608BP | BOEHRINGER INGELHEIM GMBH, GERMANY | M | Y | 20080331 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5689611 | 1009730156 | PS | SPIRIVA | 1 | ORAL | NOT REPORTED | 021395 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
5689611 | INCORRECT ROUTE OF DRUG ADMINISTRATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |