The Safety Rates Drug Report

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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
126350871 12635087 1 I 20160803 20160808 20160808 EXP US-ELI_LILLY_AND_COMPANY-US201608002667 ELI LILLY AND CO 0.00 E F Y 0.00000 20160808 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
126350871 12635087 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U U 21427 CAPSULE
126350871 12635087 2 C METOPROLOL. METOPROLOL 1 Unknown UNK, UNKNOWN 0
126350871 12635087 3 C LASIX FUROSEMIDE 1 Unknown UNK, UNKNOWN 0
126350871 12635087 4 C POTASSIUM POTASSIUM 1 Unknown UNK, UNKNOWN 0
126350871 12635087 5 C PROSTACYCLIN EPOPROSTENOL 1 Respiratory (inhalation) UNK, UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126350871 12635087 1 Pain in extremity
126350871 12635087 2 Product used for unknown indication
126350871 12635087 3 Product used for unknown indication
126350871 12635087 4 Product used for unknown indication
126350871 12635087 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126350871 12635087 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126350871 12635087 Death
126350871 12635087 Off label use
126350871 12635087 Somnolence

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
126350871 12635087 1 201607 0