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
126615771 12661577 1 I 20160810 20160817 20160817 PER US-PFIZER INC-2016383719 PFIZER 0.00 F Y 0.00000 20160817 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
126615771 12661577 1 PS CLINDAMYCIN HCL CLINDAMYCIN HYDROCHLORIDE 1 UNK 50162 CAPSULE, HARD
126615771 12661577 2 SS CLINDAMYCIN HCL CLINDAMYCIN HYDROCHLORIDE 1 50162 CAPSULE, HARD
126615771 12661577 3 SS CLINDAMYCIN HCL CLINDAMYCIN HYDROCHLORIDE 1 50162 CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126615771 12661577 1 Lower respiratory tract infection
126615771 12661577 2 Respiratory tract congestion
126615771 12661577 3 Croup infectious

Outcome of event

Event ID CASEID OUTC COD
126615771 12661577 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126615771 12661577 Hypersensitivity

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

no results found

Therapies reported

no results found