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
92006881 9200688 1 I 20130319 20130331 20130331 EXP US-ELI_LILLY_AND_COMPANY-US201303007601 ELI LILLY AND CO 55.00 YR F Y 0.00000 20130328 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
92006881 9200688 1 PS CYMBALTA 1 ORAL 60 MG, QD U 21427 60 MG CAPSULE QD
92006881 9200688 2 C EZETIMIBE 1 UNKNOWN 10 MG, UNKNOWN D 0 10 MG
92006881 9200688 3 C VITAMIN D 1 UNKNOWN UNK, UNKNOWN D 0
92006881 9200688 4 C SYNTHROID 1 UNKNOWN UNK, UNKNOWN D 0
92006881 9200688 5 C OMEPRAZOLE 1 UNKNOWN UNK, UNKNOWN D 0
92006881 9200688 6 C EXFORGE 1 UNKNOWN UNK, UNKNOWN D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92006881 9200688 1 Pain

Outcome of event

Event ID CASEID OUTC COD
92006881 9200688 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
92006881 9200688 Asthenia
92006881 9200688 Diarrhoea
92006881 9200688 Dyspnoea
92006881 9200688 Fatigue
92006881 9200688 Hepatic enzyme increased
92006881 9200688 Hot flush
92006881 9200688 Muscular weakness
92006881 9200688 Nasal congestion
92006881 9200688 Suicidal ideation
92006881 9200688 Weight increased

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
92006881 9200688 1 20121005 20130110 0