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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6532213 | 7546802 | I | 6532213-7 | 20091116 | 20100107 | DIR | 45 | YR | F | N | 250 | LBS | 20100105 | CN | Y | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6532213 | 1012920825 | PS | NAPHAZOLINE HCL | 1 | NASAL | 2 - 3 SPRAYS 12 HOURS -3 DAYS- NASAL | Y | N |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6532213 | 1012920825 | SINUS CONGESTION |
Outcome of event
Event ID | OUTC COD |
---|---|
6532213 | OT |
Reactions reported
Event ID | PT |
---|---|
6532213 | BURNING SENSATION |
6532213 | HEADACHE |
6532213 | NONSPECIFIC REACTION |
6532213 | PAIN |
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 |
---|---|---|---|---|---|
6532213 | 1012920825 | 20091114 | 20091116 |