The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
113366833 11336683 3 F 2008 20160708 20150804 20160713 EXP US-ALLERGAN-1514972US ALLERGAN 79.00 YR F Y 74.83000 KG 20160713 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
113366833 11336683 1 PS RESTASIS CYCLOSPORINE 1 Ophthalmic 2 GTT, BID 86644 50790 2 GTT EYE DROPS BID
113366833 11336683 2 SS SYSTANE (HYPROMELLOSE 2910 (4000 MPA.S)) HYPROMELLOSE 2910 (4000 MPA.S) 1 Ophthalmic IN BETWEEN USING RESTASIS 0
113366833 11336683 3 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral U 0
113366833 11336683 4 C METOPROLOL. METOPROLOL 1 Oral UNK U 0
113366833 11336683 5 C LIPITOR ATORVASTATIN CALCIUM 1 Ophthalmic UNK U 0
113366833 11336683 6 C ZETIA EZETIMIBE 1 Oral UNK U 0
113366833 11336683 7 C LISINOPRIL. LISINOPRIL 1 Oral UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113366833 11336683 1 Dry eye
113366833 11336683 2 Dry eye
113366833 11336683 3 Seasonal allergy
113366833 11336683 4 Cardiac disorder
113366833 11336683 5 Cardiac disorder
113366833 11336683 6 Cardiac disorder
113366833 11336683 7 Cardiac disorder

Outcome of event

Event ID CASEID OUTC COD
113366833 11336683 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113366833 11336683 Aortic aneurysm
113366833 11336683 Drug ineffective
113366833 11336683 Eye pain

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
113366833 11336683 1 2008 0