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
126160593 12616059 3 F 20150217 20160902 20160802 20160906 EXP FR-GUERBET LLC-1055784 GUERBET 67.00 YR F Y 0.00000 20160906 FR FR

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
126160593 12616059 1 PS DOTAREM GADOTERATE MEGLUMINE 1 Intravenous (not otherwise specified) 204781
126160593 12616059 2 SS LOVENOX ENOXAPARIN SODIUM 1 Subcutaneous 0 2000 IU
126160593 12616059 3 SS DROPERIDOL. DROPERIDOL 1 Intravenous (not otherwise specified) 0 1.25 MG
126160593 12616059 4 SS ACUPAN NEFOPAM HYDROCHLORIDE 1 Intravenous (not otherwise specified) 0 20 MG
126160593 12616059 5 SS Paracetamol ACETAMINOPHEN 1 Intravenous (not otherwise specified) 0 1 G
126160593 12616059 6 SS CEFOXITIN CEFOXITIN SODIUM 1 Intravenous (not otherwise specified) 0 2 G

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126160593 12616059 1 Imaging procedure

Outcome of event

Event ID CASEID OUTC COD
126160593 12616059 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126160593 12616059 Chest discomfort
126160593 12616059 Dyspnoea
126160593 12616059 Hypotension
126160593 12616059 Lip oedema
126160593 12616059 Rash maculo-papular
126160593 12616059 Urticaria

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
126160593 12616059 1 20150217 0
126160593 12616059 2 20150217 0
126160593 12616059 3 20150217 0
126160593 12616059 4 20150217 0
126160593 12616059 5 20150217 0
126160593 12616059 6 20150217 0