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
126127992 12612799 2 F 2016 20160804 20160801 20160803 PER US-009507513-1607USA008867 MERCK 0.00 M Y 0.00000 20160803 PH 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
126127992 12612799 1 PS INTRON A INTERFERON ALFA-2B 1 Subcutaneous 23 MU, EVERY MONDAY, WEDNESDAY AND FRIDAY U 103132 23 DF POWDER FOR INJECTION
126127992 12612799 2 SS INTRON A INTERFERON ALFA-2B 1 Subcutaneous 23 MU, EVERY MONDAY, WEDNESDAY AND FRIDAY U 103132 23 DF POWDER FOR INJECTION
126127992 12612799 3 C INDOCIN INDOMETHACININDOMETHACIN SODIUM 1 0 INTRAVENOUS INJECTION
126127992 12612799 4 C CELEXA CITALOPRAM HYDROBROMIDE 1 0
126127992 12612799 5 C NAPROXEN. NAPROXEN 1 0
126127992 12612799 6 C RESTORIL TEMAZEPAM 1 0
126127992 12612799 7 C COMPAZINE PROCHLORPERAZINE MALEATE 1 0
126127992 12612799 8 C ALLOPURINOL. ALLOPURINOL 1 0
126127992 12612799 9 C PRINIVIL LISINOPRIL 1 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126127992 12612799 1 Oncologic complication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126127992 12612799 Headache
126127992 12612799 Vomiting

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
126127992 12612799 1 20160324 2016 0
126127992 12612799 2 2016 0