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
126482472 12648247 2 F 20160805 20160829 20160812 20160831 PER US-BAYER-2016-156992 BAYER 35.00 YR A F Y 81.63000 KG 20160831 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
126482472 12648247 1 PS MAGNEVIST GADOPENTETATE DIMEGLUMINE 1 Intravenous (not otherwise specified) 13 ML, ONCE (LEFT ANTERIOR WRIST) 53043B 19596 13 ML SOLUTION FOR INJECTION 1X
126482472 12648247 2 SS MAGNEVIST GADOPENTETATE DIMEGLUMINE 1 19596 SOLUTION FOR INJECTION
126482472 12648247 3 C DEXAMETHASONE. DEXAMETHASONE 1 2 MG, UNK 0 2 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126482472 12648247 1 Nuclear magnetic resonance imaging brain
126482472 12648247 2 Meningioma

Outcome of event

Event ID CASEID OUTC COD
126482472 12648247 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126482472 12648247 Lip swelling
126482472 12648247 Nausea
126482472 12648247 Swelling face
126482472 12648247 Urticaria
126482472 12648247 Vomiting

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126482472 12648247 1 20160805 20160805 0