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
126304991 12630499 1 I 20160712 20160808 20160808 PER US-PFIZER INC-2016342619 PFIZER 0.00 F Y 0.00000 20160808 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
126304991 12630499 1 PS HEPARIN SODIUM. HEPARIN SODIUM 1 UNK U 89522 SOLUTION FOR INJECTION
126304991 12630499 2 SS PROCARDIA NIFEDIPINE 1 UNK U 18482 CAPSULE, SOFT
126304991 12630499 3 SS CODEINE CODEINE 1 UNK U 0
126304991 12630499 4 SS BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 UNK U 0
126304991 12630499 5 SS BETADINE POVIDONE-IODINE 1 UNK U 0
126304991 12630499 6 SS CLONIDINE. CLONIDINE 1 UNK U 0
126304991 12630499 7 SS IODINE. IODINE 1 UNK U 0
126304991 12630499 8 SS NEORAL CYCLOSPORINE 1 UNK U 0
126304991 12630499 9 SS OXYCODONE OXYCODONE 1 UNK U 0
126304991 12630499 10 SS TEGADERM AG MESH 2-HYDROXYETHYL METHACRYLATE 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
126304991 12630499 Drug hypersensitivity

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

no results found

Therapies reported

no results found