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
126455351 12645535 1 I 20160704 20160802 20160811 20160811 EXP GB-MHRA-EYC 00143055 GB-MYLANLABS-2016M1032406 MYLAN 0.00 Y 0.00000 20160811 OT GB GB

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
126455351 12645535 1 PS ZOLEDRONIC ACID ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) UNK Y U 202650
126455351 12645535 2 C OMEPRAZOLE. OMEPRAZOLE 1 UNK U 0
126455351 12645535 3 C CARBOCISTEINE CARBOCYSTEINE 1 UNK U 0
126455351 12645535 4 C CICLESONIDE CICLESONIDE 1 U 0
126455351 12645535 5 C ZOPICLONE ZOPICLONE 1 U 0
126455351 12645535 6 C SALMETEROL SALMETEROL 1 U 0
126455351 12645535 7 C SOLPHYLLIN 2 U 0
126455351 12645535 8 C TIOTROPIUM TIOTROPIUM 1 U 0
126455351 12645535 9 C AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 U 0
126455351 12645535 10 C COCODAMOL ACETAMINOPHENCODEINE PHOSPHATE 1 UNK U 0
126455351 12645535 11 C SALBUTAMOL ALBUTEROL 1 UNK U 0
126455351 12645535 12 C ZAFIRLUKAST. ZAFIRLUKAST 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126455351 12645535 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126455351 12645535 Chronic obstructive pulmonary disease
126455351 12645535 Dyspnoea
126455351 12645535 Hypersensitivity
126455351 12645535 Malaise
126455351 12645535 Nausea
126455351 12645535 Pain
126455351 12645535 Rash

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
126455351 12645535 1 20160704 20160704 0