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
127169151 12716915 1 I 20160829 20160906 20160906 EXP GB-PFIZER INC-2016412338 PFIZER 0.00 M Y 0.00000 20160906 CN GB GB

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
127169151 12716915 1 PS DOXYCYCLINE MONOHYDRATE DOXYCYCLINE 1 UNK U 50006
127169151 12716915 2 SS ERYTHROMYCIN. ERYTHROMYCIN 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127169151 12716915 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127169151 12716915 Abdominal discomfort
127169151 12716915 Dizziness
127169151 12716915 Facial pain
127169151 12716915 Head discomfort
127169151 12716915 Headache
127169151 12716915 Hyperhidrosis
127169151 12716915 Pyrexia
127169151 12716915 Renal pain

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

no results found

Therapies reported

no results found