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
117780732 11778073 2 F 20160818 20151125 20160823 PER US-PFIZER INC-2015382877 PFIZER 0.00 F Y 0.00000 20160823 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
117780732 11778073 1 SS NEXIUM 24HR ESOMEPRAZOLE MAGNESIUM 1 UNK U 0 PROLONGED-RELEASE CAPSULE
117780732 11778073 2 PS PROTONIX PANTOPRAZOLE SODIUM 1 UNK 20987
117780732 11778073 3 SS DIAZEPAM. DIAZEPAM 1 GENERIC U 71583
117780732 11778073 4 SS DIAZEPAM. DIAZEPAM 1 U 71583
117780732 11778073 5 SS DIAZEPAM. DIAZEPAM 1 U 71583
117780732 11778073 6 SS ZANTAC RANITIDINE HYDROCHLORIDE 1 UNK U 0
117780732 11778073 7 SS PEPCID FAMOTIDINE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117780732 11778073 3 Back injury
117780732 11778073 4 Muscle tightness
117780732 11778073 5 Anxiety

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
117780732 11778073 Drug ineffective
117780732 11778073 Intentional product misuse

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

no results found

Therapies reported

no results found