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
125495971 12549597 1 I 20160707 20160712 20160712 PER US-PFIZER INC-2016336897 PFIZER 0.00 F Y 0.00000 20160712 OT 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
125495971 12549597 1 PS MORPHINE SULFATE. MORPHINE SULFATE 1 UNK U 19999
125495971 12549597 2 SS AUGMENTIN AMOXICILLINCLAVULANATE POTASSIUM 1 UNK U 0
125495971 12549597 3 SS AZATHIOPRINE. AZATHIOPRINE 1 UNK U 0
125495971 12549597 4 SS HYDROCODONE HYDROCODONE 1 UNK U 0
125495971 12549597 5 SS IMURAN AZATHIOPRINE 1 UNK U 0
125495971 12549597 6 SS INVANZ ERTAPENEM SODIUM 1 UNK U 0
125495971 12549597 7 SS MOBIC MELOXICAM 1 UNK U 0
125495971 12549597 8 SS NUBAIN NALBUPHINE HYDROCHLORIDE 1 UNK U 0
125495971 12549597 9 SS PREDNISONE. PREDNISONE 1 UNK U 0
125495971 12549597 10 SS TRAMADOL. TRAMADOL 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125495971 12549597 Drug hypersensitivity

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

no results found

Therapies reported

no results found