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
126557841 12655784 1 I 20160804 20160816 20160816 PER US-PFIZER INC-2016376157 PFIZER 0.00 F Y 0.00000 20160816 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
126557841 12655784 1 PS AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 UNK U 50670
126557841 12655784 2 SS BUTORPHANOL TARTRATE. BUTORPHANOL TARTRATE 1 UNK U 74626
126557841 12655784 3 SS CODEINE CODEINE 1 UNK U 0
126557841 12655784 4 SS ACETAMINOPHEN W/PROPOXYPHENE NAPSYLATE ACETAMINOPHENPROPOXYPHENE NAPSYLATE 1 UNK U 0
126557841 12655784 5 SS DILAUDID HYDROMORPHONE HYDROCHLORIDE 1 UNK U 0
126557841 12655784 6 SS HYDROCODONE/ACETAMINOPHEN ACETAMINOPHENHYDROCODONE 1 UNK U 0
126557841 12655784 7 SS HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 UNK U 0
126557841 12655784 8 SS NAPROXEN. NAPROXEN 1 UNK U 0
126557841 12655784 9 SS QUINACRINE QUINACRINE 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
126557841 12655784 Drug hypersensitivity

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

no results found

Therapies reported

no results found