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
7915860 7929121 F 7915860-7 20110322 20111109 20111115 EXP US-ROCHE-GNE317210 ROCHE 88 YR F Y 54.071 KG 20111115 OT 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
7915860 1018053300 PS LUCENTIS 1 OTHER NOTREPORTED
7915860 1018053305 C OMEPRAZOLE 1
7915860 1018053303 C CODEINE PHOSPHATE 2
7915860 1018053301 C AMLODIPINE 1
7915860 1018053302 C ARICEPT 1
7915860 1018053304 C HALOPERIDOL 1
7915860 1018053306 C ACETAMINOPHEN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
7915860 1018053300 PRODUCT USED FOR UNKNOWN INDICATION
7915860 1018053305 PRODUCT USED FOR UNKNOWN INDICATION
7915860 1018053303 PRODUCT USED FOR UNKNOWN INDICATION
7915860 1018053301 PRODUCT USED FOR UNKNOWN INDICATION
7915860 1018053302 PRODUCT USED FOR UNKNOWN INDICATION
7915860 1018053304 PRODUCT USED FOR UNKNOWN INDICATION
7915860 1018053306 PRODUCT USED FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
7915860 DE
7915860 OT

Reactions reported

Event ID PT
7915860 IRON DEFICIENCY
7915860 ARTERIOSCLEROSIS CORONARY ARTERY
7915860 LOWER RESPIRATORY TRACT INFECTION
7915860 BRONCHOPNEUMONIA
7915860 CEREBROVASCULAR DISORDER
7915860 ANAEMIA

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

no results found

Therapies reported

no results found