The Safety Rates Drug Report

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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
126785501 12678550 1 I 20160801 20160823 20160823 PER US-PFIZER INC-2016370157 PFIZER 0.00 F Y 0.00000 20160823 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
126785501 12678550 1 PS FUROSEMIDE. FUROSEMIDE 1 UNK U 18667
126785501 12678550 2 SS OXYCODONE OXYCODONE 1 UNK U 0
126785501 12678550 3 SS ASPIRIN. ASPIRIN 1 UNK U 0
126785501 12678550 4 SS CODEINE CODEINE 1 UNK U 0
126785501 12678550 5 SS SIMVASTATIN. SIMVASTATIN 1 UNK U 0
126785501 12678550 6 SS BACLOFEN. BACLOFEN 1 UNK U 0
126785501 12678550 7 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 UNK U 0
126785501 12678550 8 SS LAMOTRIGINE. LAMOTRIGINE 1 UNK U 0
126785501 12678550 9 SS METHOCARBAMOL. METHOCARBAMOL 1 UNK U 0
126785501 12678550 10 SS LACTOSE LACTOSE 1 UNK U 0
126785501 12678550 11 SS SULFACETAMIDE. SULFACETAMIDE 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
126785501 12678550 Drug hypersensitivity

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

no results found

Therapies reported

no results found