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
7788260 8070729 F 7788260-0 20110601 20110919 20110930 EXP US-ELI_LILLY_AND_COMPANY-US201104006798 ELI LILLY AND COMPANY 85 YR F Y 60 KG 20110930 CN 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
7788260 1017674321 SS FORTEO 1 SUBCUTANEOUS 20 UG, QD 021318
7788260 1017674329 C CENTRUM 2
7788260 1017674320 SS FORTEO 1 SUBCUTANEOUS 20 UG, QD A736415E 021318
7788260 1017674325 C XALATAN 1
7788260 1017674328 C VITAMIN D 1
7788260 1017674330 C CALCIUM CARBONATE 1
7788260 1017674323 C LOTREL 1 UNK, QD
7788260 1017674326 C ASPIRIN 1
7788260 1017674327 C FOLIC ACID 2
7788260 1017674332 C LOZAL 2
7788260 1017674322 C PREDNISONE 1 5 MG, QD
7788260 1017674324 C METHOTREXATE 1 UNK, WEEKLY (1/W)
7788260 1017674333 C NORCO 1
7788260 1017674319 PS FORTEO 1 SUBCUTANEOUS 20 UG, QD A788788K 021318
7788260 1017674331 C FISH OIL 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
7788260 1017674333 PAIN
7788260 1017674319 OSTEOPOROSIS

Outcome of event

Event ID OUTC COD
7788260 OT
7788260 HO

Reactions reported

Event ID PT
7788260 HYPOTENSION
7788260 ARTHRALGIA
7788260 OEDEMA
7788260 HEART RATE DECREASED
7788260 CONSTIPATION

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
7788260 1017674319 20100114