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
127542781 12754278 1 I 201604 20160516 20160916 20160916 PER US-ASTRAZENECA-2016SE53289 ASTRAZENECA 71.00 YR F Y 0.00000 20160916 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
127542781 12754278 1 PS PRILOSEC OTC OMEPRAZOLE MAGNESIUM 1 Oral 21229 2 DF MODIFIED-RELEASE TABLET QD
127542781 12754278 2 SS PRILOSEC OTC OMEPRAZOLE MAGNESIUM 1 Oral 6083171972 21229 MODIFIED-RELEASE TABLET
127542781 12754278 3 C FISH OIL FISH OIL 1 0
127542781 12754278 4 C VITAMIN D CHOLECALCIFEROL 1 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127542781 12754278 Arthralgia
127542781 12754278 Arthropathy
127542781 12754278 Dizziness
127542781 12754278 Dizziness postural
127542781 12754278 Dyspnoea
127542781 12754278 Headache
127542781 12754278 Hypoaesthesia
127542781 12754278 Lethargy
127542781 12754278 Muscular weakness
127542781 12754278 Myalgia

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

no results found

Therapies reported

no results found