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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6194993 | 6997729 | I | 6194993-2 | 20080101 | 20090512 | 20090519 | EXP | A0783747A | GLAXOSMITHKLINE | 63 | YR | F | Y | 20090519 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6194993 | 1011592775 | PS | ADVAIR HFA | 1 | RESPIRATORY (INHALATION) | 1PUFF TWICE PER DAY | UNKNOWN | 021077 | |||
6194993 | 1011592776 | C | OTC VITAMINS | 2 | |||||||
6194993 | 1011592777 | C | CALCIUM | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6194993 | 1011592775 | ASTHMA |
Outcome of event
Event ID | OUTC COD |
---|---|
6194993 | OT |
Reactions reported
Event ID | PT |
---|---|
6194993 | BONE DISORDER |
6194993 | VISUAL ACUITY REDUCED |
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 |
---|---|---|---|---|---|
6194993 | 1011592775 | 20050101 |