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
121922203 12192220 3 F 20160629 20160318 20160705 PER US-PFIZER INC-2016153889 PFIZER 57.00 YR F Y 0.00000 20160705 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
121922203 12192220 1 PS BENZYLPENICILLIN POTASSIUM PENICILLIN G POTASSIUM 1 UNK U 60657
121922203 12192220 2 SS ASPIRIN /00002701/ ASPIRIN 1 UNK U 0
121922203 12192220 3 SS GLUTEN WHEAT GLUTEN 1 UNK U 0
121922203 12192220 4 SS TOPROL XL METOPROLOL SUCCINATE 1 UNK U 0
121922203 12192220 5 SS TORADOL KETOROLAC TROMETHAMINE 1 UNK U 0
121922203 12192220 6 SS NITROFURANTOIN. NITROFURANTOIN 1 UNK U 0
121922203 12192220 7 SS MOBIC MELOXICAM 1 UNK U 0
121922203 12192220 8 SS ZINC ZINCINC CHLORIDE 1 UNK U 0
121922203 12192220 9 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 UNK U 0
121922203 12192220 10 SS KEFLEX CEPHALEXIN 1 UNK U 0
121922203 12192220 11 SS CRESTOR ROSUVASTATIN CALCIUM 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
121922203 12192220 Drug hypersensitivity

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

no results found

Therapies reported

no results found