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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5578152 | 6472603 | F | 5578152-X | 20010101 | 20071219 | 20071231 | EXP | BR-PFIZER INC-2007096537 | PFIZER INC | F | Y | 20071231 | BRAZIL |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5578152 | 1009350731 | PS | XALATAN | 1 | OPHTHALMIC | 020597 | |||||
5578152 | 1009350732 | SS | XALATAN | 1 | OPHTHALMIC | DAILY DOSE:1DROP | 020597 | ||||
5578152 | 1009350733 | SS | XALATAN | 1 | 020597 | ||||||
5578152 | 1009350734 | SS | LUMIGAN | 1 | |||||||
5578152 | 1009350735 | C | SENNA | 2 | |||||||
5578152 | 1009350736 | C | DUSPATALIN ^SOLVAY^ | 2 | |||||||
5578152 | 1009350737 | C | BETAHISTINE | 2 | DAILY DOSE:16MG | ||||||
5578152 | 1009350738 | C | SIMVASTATIN | 1 | DAILY DOSE:20MG | ||||||
5578152 | 1009350739 | C | ANTIDEPRESSANTS | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5578152 | 1009350731 | GLAUCOMA |
5578152 | 1009350735 | CONSTIPATION |
5578152 | 1009350736 | GASTRITIS |
5578152 | 1009350737 | LABYRINTHITIS |
5578152 | 1009350738 | BLOOD CHOLESTEROL INCREASED |
5578152 | 1009350739 | DEPRESSION |
Outcome of event
Event ID | OUTC COD |
---|---|
5578152 | HO |
5578152 | OT |
Reactions reported
Event ID | PT |
---|---|
5578152 | EYE INFECTION |
5578152 | GLAUCOMA |
5578152 | LABYRINTHITIS |
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 |
---|---|---|---|---|---|
5578152 | 1009350732 | 20020101 | 20060101 |