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
126857191 12685719 1 I 20151208 20160815 20160825 20160825 EXP AT-TEVA-686523ISR TEVA 73.00 YR F Y 57.00000 KG 20160825 CN AT AT

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
126857191 12685719 1 PS GABAPENTIN. GABAPENTIN 1 Y 76017
126857191 12685719 2 SS LYRICA PREGABALIN 1 2X75 Y 0 75 MG CAPSULE, HARD
126857191 12685719 3 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 1X30MG Y 0 30 MG
126857191 12685719 4 C Temesta LORAZEPAM 1 1/2 IN THE AFTERNOON AND 2 FOR SLEEPING Y 0 1 MG
126857191 12685719 5 C Noax uno 100mg Retardtabletten 2 1 DOSAGE FORMS DAILY; 1/2 IN THE MORNING AND 1/2 IN THE AFTERNOON U 0 .5 DF PROLONGED-RELEASE TABLET BID
126857191 12685719 6 C Tramal TRAMADOL 1 U 0 ORAL DROPS
126857191 12685719 7 C Euthyrox 50 Mikrogramm Tabletten 2 U 0
126857191 12685719 8 C Temesta LORAZEPAM 1 Y 0 2 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126857191 12685719 2 Pain
126857191 12685719 4 Sleep disorder
126857191 12685719 6 Pain
126857191 12685719 8 Sleep disorder

Outcome of event

Event ID CASEID OUTC COD
126857191 12685719 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126857191 12685719 Abdominal pain upper
126857191 12685719 Ataxia
126857191 12685719 Blood pressure fluctuation
126857191 12685719 Condition aggravated
126857191 12685719 Cough
126857191 12685719 Depressed mood
126857191 12685719 Dizziness
126857191 12685719 Erythema
126857191 12685719 Fall
126857191 12685719 Gait disturbance
126857191 12685719 Gastrooesophageal reflux disease
126857191 12685719 General physical health deterioration
126857191 12685719 Headache
126857191 12685719 Muscular weakness
126857191 12685719 Nausea
126857191 12685719 Oedema peripheral
126857191 12685719 Pain
126857191 12685719 Pain in extremity
126857191 12685719 Palpitations
126857191 12685719 Pollakiuria
126857191 12685719 Reflux laryngitis
126857191 12685719 Sensory loss
126857191 12685719 Sleep disorder
126857191 12685719 Vomiting

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
126857191 12685719 2 201505 201602 0
126857191 12685719 3 201505 201602 0