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
127403371 12740337 1 I 20160829 20160913 20160913 PER US-PFIZER INC-2016411474 PFIZER 44.00 YR F Y 0.00000 20160913 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
127403371 12740337 1 PS LIPITOR ATORVASTATIN CALCIUM 1 UNK U 20702 FILM-COATED TABLET
127403371 12740337 2 SS ERYTHROMYCIN. ERYTHROMYCIN 1 UNK U 50609
127403371 12740337 3 SS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 UNK U 74133
127403371 12740337 4 SS ASPIRIN. ASPIRIN 1 UNK U 0
127403371 12740337 5 SS ASA/CAFFEINE/PROPOXYPHENE ASPIRINCAFFEINEPROPOXYPHENE HYDROCHLORIDE 1 UNK U 0
127403371 12740337 6 SS CARVEDILOL. CARVEDILOL 1 UNK U 0
127403371 12740337 7 SS TORADOL KETOROLAC TROMETHAMINE 1 UNK U 0
127403371 12740337 8 SS TAVIST ALLERGY CLEMASTINE FUMARATE 1 UNK U 0
127403371 12740337 9 SS TAVIST-D CLEMASTINE FUMARATEPHENYLPROPANOLAMINE 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
127403371 12740337 Drug hypersensitivity

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

no results found

Therapies reported

no results found