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
125515793 12551579 3 F 20160822 20160713 20160906 EXP US-SUN PHARMACEUTICAL INDUSTRIES LTD-2016US-120050 RANBAXY 50.00 DY F Y 0.00000 20160906 OT GB 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
125515793 12551579 1 PS PROPRANOLOL PROPRANOLOLPROPRANOLOL HYDROCHLORIDE 1 Oral UNK 70321
125515793 12551579 2 SS PROPRANOLOL PROPRANOLOLPROPRANOLOL HYDROCHLORIDE 1 Oral 2 MG/KG, DAILY Y 70321 2 MG/KG
125515793 12551579 3 C TIMOLOL. TIMOLOL 1 Topical 0.52 MG/KG, BID (ONE DROP ON THE EYELID) Y 0 .52 MG/KG GEL Q12H
125515793 12551579 4 C TIMOLOL. TIMOLOL 1 Intraocular 0.52 MG/KG, BID Y 0 .52 MG/KG GEL Q12H
125515793 12551579 5 C TIMOLOL. TIMOLOL 1 Unknown BID Y 0 GEL Q12H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125515793 12551579 1 Product used for unknown indication
125515793 12551579 2 Product used for unknown indication
125515793 12551579 3 Eyelid ptosis
125515793 12551579 5 Haemangioma of skin

Outcome of event

Event ID CASEID OUTC COD
125515793 12551579 HO
125515793 12551579 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125515793 12551579 Bradycardia
125515793 12551579 Hypothermia
125515793 12551579 Lethargy

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

no results found

Therapies reported

no results found