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
126796842 12679684 2 F 20160913 20160824 20160916 PER US-PFIZER INC-2016398350 PFIZER 63.00 YR M Y 0.00000 20160916 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
126796842 12679684 1 PS AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 Oral 500 MG, (DAY 1) Y 50670 500 MG
126796842 12679684 2 SS AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 Oral 250 MG, (DAYS 2 - 5) Y 50670 250 MG
126796842 12679684 3 SS DOXYCYCLINE HYCLATE. DOXYCYCLINE HYCLATE 1 Oral UNK U 50007
126796842 12679684 4 SS ETODOLAC. ETODOLAC 1 UNK U 0
126796842 12679684 5 SS NAPROXEN SODIUM. NAPROXEN SODIUM 1 UNK U 0
126796842 12679684 6 SS DESIPRAMINE DESIPRAMINE 1 UNK U 0
126796842 12679684 7 SS MELOXICAM. MELOXICAM 1 UNK U 0
126796842 12679684 8 SS PROZAC FLUOXETINE HYDROCHLORIDE 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
126796842 12679684 Abdominal pain
126796842 12679684 Drug hypersensitivity

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

no results found

Therapies reported

no results found