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
127426592 12742659 2 F 20160906 20160914 20160915 PER US-PFIZER INC-2016422705 PFIZER 0.00 Y 0.00000 20160915 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
127426592 12742659 1 PS ADVIL PM DIPHENHYDRAMINE CITRATEIBUPROFEN 1 UNK U 21393 CAPSULE
127426592 12742659 2 SS BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 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
127426592 12742659 Condition aggravated
127426592 12742659 Restless legs syndrome

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

no results found

Therapies reported

no results found