The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6251139 7037404 I 6251139-X 20090120 20090420 20090630 PER US-ABBOTT-09P-163-0569250-00 ABBOTT LABORATORIES 58 M Y 20090630 UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6251139 1011814131 PS ZEMPLAR 1 UNKNOWN 021606
6251139 1011814132 C AMLODIPINE 1
6251139 1011814133 C RAMIPRIL 1
6251139 1011814134 C CLONIDINE 1
6251139 1011814135 C DOXAZOSIN MESYLATE 1
6251139 1011814136 C ATENOLOL 1
6251139 1011814137 C ACTOS 1
6251139 1011814138 C GLYBURIDE 1
6251139 1011814139 C FUROSEMIDE INTENSOL 1
6251139 1011814140 C PLAVIX 1
6251139 1011814141 C ASPIRIN 1
6251139 1011814142 C VITAMIN D 1
6251139 1011814143 C ASCORBIC ACID 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6251139 1011814131 HYPERPARATHYROIDISM
6251139 1011814132 HYPERTENSION
6251139 1011814133 HYPERTENSION
6251139 1011814134 HYPERTENSION
6251139 1011814135 HYPERTENSION
6251139 1011814136 HYPERTENSION
6251139 1011814137 DIABETES MELLITUS
6251139 1011814138 DIABETES MELLITUS
6251139 1011814139 FLUID RETENTION
6251139 1011814140 PROPHYLAXIS
6251139 1011814141 PROPHYLAXIS
6251139 1011814142 DRUG USE FOR UNKNOWN INDICATION
6251139 1011814143 DRUG USE FOR UNKNOWN INDICATION

Outcome of event

no results found

Reactions reported

Event ID PT
6251139 DYSGEUSIA

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6251139 1011814131 20090105