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
125379731 12537973 1 I 20160623 20160707 20160707 PER US-PFIZER INC-2016318401 PFIZER 0.00 F Y 0.00000 20160707 OT 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
125379731 12537973 1 PS ZITHROMAX AZITHROMYCIN DIHYDRATE 1 UNK U 50670
125379731 12537973 2 SS ZOLOFT SERTRALINE HYDROCHLORIDE 1 UNK U 19839
125379731 12537973 3 SS MEDENT GUAIFENESINPSEUDOEPHEDRINE 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
125379731 12537973 Drug hypersensitivity

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

no results found

Therapies reported

no results found