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
7790822 8164729 I 7790822-1 20110921 20110930 EXP US-ASTRAZENECA-2007UW16054 AZPRODUW00 43 YR F Y 77.1 KG 20110930 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
7790822 1017683792 C NORTRIPTYLINE HCL 1
7790822 1017683793 C BLOOD PRESSURE MEDICATION 2
7790822 1017683786 SS SEROQUEL 1 ORAL 020639
7790822 1017683789 C CYMBALTA 1
7790822 1017683785 PS SEROQUEL 1 ORAL 020639
7790822 1017683787 SS SEROQUEL 1 ORAL 020639
7790822 1017683788 SS SEROQUEL 1 ORAL 020639
7790822 1017683790 C PREMARIN 1
7790822 1017683791 C LOPRESSOR 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
7790822 1017683786 DEPRESSION
7790822 1017683785 BIPOLAR DISORDER

Outcome of event

Event ID OUTC COD
7790822 OT

Reactions reported

Event ID PT
7790822 HYPERHIDROSIS
7790822 CARDIAC DISORDER
7790822 MYOCARDIAL INFARCTION
7790822 ILL-DEFINED DISORDER
7790822 NAUSEA
7790822 DRY MOUTH
7790822 DRUG INEFFECTIVE
7790822 WEIGHT INCREASED
7790822 DEPRESSION

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
7790822 1017683786 20061001
7790822 1017683785 20061001