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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5988651 | 6990055 | I | 5988651-4 | 20081128 | 20081208 | DIR | 53 | YR | F | N | 165 | LBS | 20081129 | PH | N | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5988651 | 1010823638 | PS | PROAIR HFA | 1 | RESPIRATORY (INHALATION) | 2 PUFFS 4 TIMES DAILY | D | D | ADZ41A | 20201118 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5988651 | 1010823638 | ASTHMA |
Outcome of event
Event ID | OUTC COD |
---|---|
5988651 | OT |
Reactions reported
Event ID | PT |
---|---|
5988651 | PRODUCT QUALITY ISSUE |
5988651 | THERAPY CESSATION |
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 |
---|---|---|---|---|---|
5988651 | 1010823638 | 20081124 |