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
126173053 12617305 3 F 201606 20160825 20160803 20160905 EXP US-BAUSCH-BL-2016-017830 BAUSCH AND LOMB 0.00 F Y 0.00000 20160905 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
126173053 12617305 1 PS NIFEDIPINE. NIFEDIPINE 1 Unknown Y 75289
126173053 12617305 2 SS LOSARTAN. LOSARTAN 1 Oral Y 0 25 MG QD
126173053 12617305 3 SS PROCARDIA XL NIFEDIPINE 1 Oral U 0 30 MG QD
126173053 12617305 4 SS PROCARDIA XL NIFEDIPINE 1 Unknown U 0 30 MG QD
126173053 12617305 5 C PREMARIN ESTROGENS, CONJUGATED 1 0 1.25 MG QD
126173053 12617305 6 C SYNTHROID LEVOTHYROXINE SODIUM 1 0 75 UG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126173053 12617305 1 Hypertension
126173053 12617305 2 Hypertension
126173053 12617305 3 Hypertension
126173053 12617305 5 Product used for unknown indication
126173053 12617305 6 Thyroid disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126173053 12617305 Asthenia
126173053 12617305 Dizziness
126173053 12617305 Drug dose omission
126173053 12617305 Product substitution issue

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
126173053 12617305 1 2013 201602 0
126173053 12617305 4 20160610 0
126173053 12617305 6 2013 0