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
126415651 12641565 1 I 20150524 20160802 20160810 20160810 EXP NL-LRB-223254 NL-FRI-1000086759 FOREST 55.23 YR F Y 78.00000 KG 20160810 OT DK NL

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
126415651 12641565 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral 1 DROP WEEKLY, INCREASED TO 5 DROPS WEEKLY. N 21046 ORAL DROPS /wk
126415651 12641565 2 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 N 21046
126415651 12641565 3 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 N 21046
126415651 12641565 4 C THYRAX DUOTAB LEVOTHYROXINE 1 Oral 150 MICROGRAM 0 150 UG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126415651 12641565 1 Post-traumatic stress disorder
126415651 12641565 2 Anxiety
126415651 12641565 3 Depression
126415651 12641565 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126415651 12641565 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126415651 12641565 Depression
126415651 12641565 Disturbance in attention
126415651 12641565 Feeling abnormal
126415651 12641565 Memory impairment
126415651 12641565 Muscle spasms
126415651 12641565 Muscular weakness
126415651 12641565 Pain
126415651 12641565 Speech disorder
126415651 12641565 Tremor

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
126415651 12641565 1 20150524 20150827 0
126415651 12641565 4 19880321 0