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
125313394 12531339 4 F 2012 20160923 20160706 20160928 EXP PHHY2016MX087747 NOVARTIS 21.86 YR M Y 72.00000 KG 20160928 CN COUNTRY NOT SPECIFIED MX

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
125313394 12531339 1 PS TEGRETOL CARBAMAZEPINE 1 Oral 1 DF, QHS 16608 1 DF TABLET
125313394 12531339 2 SS TEGRETOL CARBAMAZEPINE 1 16608 TABLET
125313394 12531339 3 C ALBUTEROL. ALBUTEROL 1 Respiratory (inhalation) U 0
125313394 12531339 4 C RINELON 2 Unknown U 0
125313394 12531339 5 C STERIMAR SEA WATER 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125313394 12531339 1 Seizure
125313394 12531339 2 Meningioma
125313394 12531339 3 Product used for unknown indication
125313394 12531339 4 Product used for unknown indication
125313394 12531339 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125313394 12531339 OT
125313394 12531339 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125313394 12531339 Cardiomegaly
125313394 12531339 Dyspnoea
125313394 12531339 Hypoxia
125313394 12531339 Mouth breathing
125313394 12531339 Seizure
125313394 12531339 Tachycardia
125313394 12531339 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
125313394 12531339 1 2010 0