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
126583022 12658302 2 F 201608 20160824 20160817 20160830 EXP US-009507513-1608USA006736 MERCK 43.73 YR M Y 0.00000 20160830 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
126583022 12658302 1 PS INTRON A INTERFERON ALFA-2B 1 Subcutaneous 20 MU, TIW ON MON, WED, FRI FOR 48 WEEKS L041049 103132 20 MIU POWDER FOR INJECTION TIW
126583022 12658302 2 C COMPAZINE PROCHLORPERAZINE MALEATE 1 0
126583022 12658302 3 C CALCIUM (UNSPECIFIED) CALCIUM 1 0
126583022 12658302 4 C CHOLECALCIFEROL CHOLECALCIFEROL 1 0
126583022 12658302 5 C PHOSPHATE (UNSPECIFIED) 2 0
126583022 12658302 6 C TYLENOL ACETAMINOPHEN 1 0
126583022 12658302 7 C IBUPROFEN. IBUPROFEN 1 0
126583022 12658302 8 C MELATONIN MELATONIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126583022 12658302 1 Skin cancer

Outcome of event

Event ID CASEID OUTC COD
126583022 12658302 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126583022 12658302 Fatigue
126583022 12658302 Influenza like illness

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
126583022 12658302 1 20160224 0