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
125452202 12545220 2 F 201601 20160707 20160711 20160718 PER US-PFIZER INC-2016335919 PFIZER 34.00 YR F Y 0.00000 20160718 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
125452202 12545220 1 PS MEDROXYPROGESTERONE ACETATE. MEDROXYPROGESTERONE ACETATE 1 1 INJECTION, 150MG/1ML U 20246 SUSPENSION FOR INJECTION
125452202 12545220 2 SS MEDROXYPROGESTERONE ACETATE. MEDROXYPROGESTERONE ACETATE 1 UNK U 20246 SUSPENSION FOR INJECTION
125452202 12545220 3 C PROTONIX PANTOPRAZOLE SODIUM 1 40 MG, 1X/DAY 0 40 MG QD
125452202 12545220 4 C CALCIUM + MAGNESIUM 2 1 TABLESPOON LIQUID 0
125452202 12545220 5 C VITAMIN D CHOLECALCIFEROL 1 Oral BY MOUTH DAILY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125452202 12545220 1 Contraception
125452202 12545220 2 Hypermobility syndrome
125452202 12545220 3 Gastrooesophageal reflux disease
125452202 12545220 4 Supplementation therapy
125452202 12545220 5 Vitamin D abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125452202 12545220 Fatigue
125452202 12545220 Neuralgia
125452202 12545220 Pain
125452202 12545220 Pre-existing condition improved
125452202 12545220 Therapeutic response unexpected

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125452202 12545220 1 201601 201601 0
125452202 12545220 2 201607 0