The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
7023324 7583749 I 7023324-0 20100916 20100930 EXP GB-BAUSCH-2010BL005236 BAUSCH + LOMB INCORPORATED 80 YR F Y 20100930 OT UNITED KINGDOM

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
7023324 1014813758 PS PREDNISOLONE 2 40070
7023324 1014813759 SS PREDNISOLONE 2 040070
7023324 1014813760 SS METHYLPREDNISOLONE 2 INTRAVENOUS
7023324 1014813761 SS ASPIRIN 1
7023324 1014813762 C BENDROFLUMETHIAZIDE 2
7023324 1014813763 C LISINOPRIL 1
7023324 1014813764 C GLICLAZIDE 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
7023324 1014813758 TEMPORAL ARTERITIS
7023324 1014813760 PRODUCT USED FOR UNKNOWN INDICATION
7023324 1014813761 PRODUCT USED FOR UNKNOWN INDICATION
7023324 1014813762 PRODUCT USED FOR UNKNOWN INDICATION
7023324 1014813763 PRODUCT USED FOR UNKNOWN INDICATION
7023324 1014813764 PRODUCT USED FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
7023324 DE

Reactions reported

Event ID PT
7023324 CEREBROVASCULAR ACCIDENT

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

no results found

Therapies reported

no results found