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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4784081 | 5888603 | I | 4784081-1 | 20050603 | 20050930 | PER | US-GLAXOSMITHKLINE-A0561135A | GLAXOSMITHKLINE | M | Y | 20050929 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4784081 | 1006469495 | PS | FLOVENT | 1 | RESPIRATORY (INHALATION) | 2PUFF TWICE PER DAY | 021433 | ||||
4784081 | 1006469496 | C | SPIRIVA | 1 | |||||||
4784081 | 1006469497 | C | ATENOLOL | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4784081 | 1006469495 | EMPHYSEMA |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
4784081 | HEADACHE |
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 |
---|---|---|---|---|---|
4784081 | 1006469495 | 20050528 |