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
126217281 12621728 1 I 20160727 20160804 20160804 PER US-PFIZER INC-2016364786 PFIZER 0.00 Y 0.00000 20160804 MD 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
126217281 12621728 1 PS MORPHINE SULFATE. MORPHINE SULFATE 1 UNK U 19999
126217281 12621728 2 SS MEPERIDINE HCL MEPERIDINE HYDROCHLORIDE 1 UNK U 21171
126217281 12621728 3 SS LESCOL FLUVASTATIN SODIUM 1 UNK U 0
126217281 12621728 4 SS LIVALO PITAVASTATIN CALCIUM 1 UNK U 0
126217281 12621728 5 SS SULFAMETHOXAZOLE SULFAMETHOXAZOLE 1 UNK U 0
126217281 12621728 6 SS TRIPLE ANTIBIOTIC BACITRACIN ZINCNEOMYCINNEOMYCIN SULFATEPOLYMYXIN B SULFATE 1 UNK U 0 OINTMENT

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126217281 12621728 Drug hypersensitivity

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found