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
126699532 12669953 2 F 201607 20160809 20160820 20160829 PER US-ASTRAZENECA-2016SE87036 ASTRAZENECA 52.00 YR F Y 0.00000 20160829 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
126699532 12669953 1 PS PRILOSEC OTC OMEPRAZOLE MAGNESIUM 1 Oral Y 6145171972 21229 1 DF MODIFIED-RELEASE TABLET QD
126699532 12669953 2 C PENICILLIN PENICILLIN 1 0
126699532 12669953 3 C CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126699532 12669953 2 Product used for unknown indication
126699532 12669953 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126699532 12669953 Abdominal discomfort
126699532 12669953 Diarrhoea
126699532 12669953 Hypersensitivity
126699532 12669953 Pruritus
126699532 12669953 Reaction to drug excipients
126699532 12669953 Skin irritation

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
126699532 12669953 1 201607 0