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
5932145 7008840 I 5932145-9 20080412 20081027 DIR 44 F N 125 LBS 20081026 CN N Y 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
5932145 1010627577 PS ZOCOR 1 BUCCAL 1 TABLET ONE DAILY BUCCAL Y N BR3525904 20090404
5932145 1010653718 SS SOLODYN 1 BUCCAL 1 TABLET DAILY BUCCAL Y N BR3525904 20091008
5932145 1010653719 C CLOBETASOL PROPIONATE 1
5932145 1010653720 C METRONIDAZOLE 1
5932145 1010653721 C DESODINE 2
5932145 1010653722 C PROTOPIC 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5932145 1010627577 BLOOD CHOLESTEROL INCREASED
5932145 1010653718 HYPERSENSITIVITY

Outcome of event

Event ID OUTC COD
5932145 LT

Reactions reported

Event ID PT
5932145 ABDOMINAL PAIN UPPER
5932145 ANGINA PECTORIS
5932145 ANXIETY
5932145 CHEST PAIN
5932145 CONSTIPATION
5932145 DRUG INEFFECTIVE
5932145 DYSPNOEA
5932145 ECONOMIC PROBLEM
5932145 EMOTIONAL DISORDER
5932145 HEPATIC PAIN
5932145 HYPERSENSITIVITY
5932145 IMPAIRED WORK ABILITY
5932145 MYALGIA
5932145 ROSACEA

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
5932145 1010627577 20080701 20080910 2 MON
5932145 1010653718 20081008 20081024 20 DAY