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
127566101 12756610 1 I 20160914 20160917 20160917 PER PHEH2016US023690 NOVARTIS 0.00 F Y 0.00000 20160917 CN 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
127566101 12756610 1 PS VOLTAREN DICLOFENAC SODIUM 1 Unknown UNK U 19201
127566101 12756610 2 SS DARVOCET ACETAMINOPHENPROPOXYPHENE HYDROCHLORIDE 1 Unknown UNK U 0
127566101 12756610 3 SS DARVON PROPOXYPHENE HYDROCHLORIDE 1 Unknown UNK U 0
127566101 12756610 4 SS TYLENOL ACETAMINOPHEN 1 Unknown UNK U 0
127566101 12756610 5 SS CODEINE CODEINE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127566101 12756610 1 Product used for unknown indication
127566101 12756610 2 Product used for unknown indication
127566101 12756610 3 Product used for unknown indication
127566101 12756610 4 Product used for unknown indication
127566101 12756610 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127566101 12756610 Hypersensitivity

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

no results found

Therapies reported

no results found