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
6250624 6959385 F 6250624-4 20090118 20090618 20090630 EXP US-AMGEN-QUU339993 AMGENSAFETY 77 M Y 91.4 KG 20090630 MD 20090319 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
6250624 1011812012 PS NEULASTA 1 SUBCUTANEOUS UNKNOWN
6250624 1011812013 C DACOGEN 1
6250624 1011812014 C FLOMAX 1
6250624 1011812015 C ASPIRIN 1
6250624 1011812016 C OMEPRAZOLE 1
6250624 1011812017 C SIMVASTATIN 1
6250624 1011812018 C TIMOLOL MALEATE 1
6250624 1011812019 C LUMIGAN 1
6250624 1011812020 C CHONDROITIN 2
6250624 1011812021 C GLUCOSAMINE 2
6250624 1011812022 C MULTI-VITAMINS 1
6250624 1011812023 C STOOL SOFTENER 2
6250624 1011812024 C UNSPECIFIED ANTINEOPLASTIC AGENT 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6250624 1011812012 CHEMOTHERAPY

Outcome of event

Event ID OUTC COD
6250624 DE
6250624 OT

Reactions reported

Event ID PT
6250624 BONE PAIN
6250624 LEUKAEMIA
6250624 PYREXIA
6250624 RASH
6250624 URTICARIA

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
6250624 1011812012 20090118 20090118
6250624 1011812013 20090113 20090227