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
75954073 7595407 3 F 20160711 20100920 20160719 EXP US-ASTRAZENECA-2010SE16497 ASTRAZENECA 0.00 F Y 0.00000 20160720 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
75954073 7595407 1 PS SEROQUEL XR QUETIAPINE FUMARATE 1 Oral 300.0MG UNKNOWN 22047 300 MG PROLONGED-RELEASE TABLET
75954073 7595407 2 SS SEROQUEL XR QUETIAPINE FUMARATE 1 Oral 300.0MG UNKNOWN 22047 300 MG PROLONGED-RELEASE TABLET
75954073 7595407 3 SS SEROQUEL XR QUETIAPINE FUMARATE 1 Oral 2.0DF UNKNOWN 22047 2 DF PROLONGED-RELEASE TABLET QD
75954073 7595407 4 SS SEROQUEL XR QUETIAPINE FUMARATE 1 Oral 2.0DF UNKNOWN 22047 2 DF PROLONGED-RELEASE TABLET QD
75954073 7595407 5 SS UNSPECIFIED MEDICATIONS UNSPECIFIED INGREDIENT 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
75954073 7595407 1 Bipolar disorder
75954073 7595407 2 Depression
75954073 7595407 3 Bipolar disorder
75954073 7595407 4 Depression

Outcome of event

Event ID CASEID OUTC COD
75954073 7595407 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
75954073 7595407 Adverse drug reaction
75954073 7595407 Bite
75954073 7595407 Drug dose omission
75954073 7595407 Feeding disorder
75954073 7595407 Hallucination
75954073 7595407 Insomnia
75954073 7595407 Memory impairment
75954073 7595407 Muscle twitching
75954073 7595407 Withdrawal syndrome

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

no results found

Therapies reported

no results found