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
124935146 12493514 6 F 20160718 20160623 20160725 EXP GB-WATSON-2016-13004 ACTAVIS 0.00 F Y 0.00000 20160725 CN 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
124935146 12493514 1 SS Carboplatin (Unknown) CARBOPLATIN 1 Unknown UNK U UNCONFIRMED 0 UNK
124935146 12493514 2 PS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) UNK U UNCONFIRMED 79160 UNK
124935146 12493514 3 SS VINORELBINE VINORELBINEVINORELBINE TARTRATE 1 Unknown UNK U UNCONFIRMED 0 UNK
124935146 12493514 4 SS Capecitabine (Unknown) CAPECITABINE 1 Unknown UNK U UNCONFIRMED 0 UNK
124935146 12493514 5 SS HERCEPTIN TRASTUZUMAB 1 Subcutaneous 600 MG, UNK U 0 600 MG
124935146 12493514 6 C HEPARIN HEPARIN SODIUM 1 Intravenous (not otherwise specified) UNK U 0
124935146 12493514 7 C LOPERAMIDE LOPERAMIDE 1 Unknown UNK U 0
124935146 12493514 8 C METOCLOPRAMIDE. METOCLOPRAMIDE 1 Unknown UNK U 0
124935146 12493514 9 C ONDANSETRON ONDANSETRON 1 Oral 8 MG, UNK U 0 8 MG
124935146 12493514 10 C TYVERB LAPATINIB 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124935146 12493514 1 Product used for unknown indication
124935146 12493514 2 Product used for unknown indication
124935146 12493514 3 Product used for unknown indication
124935146 12493514 4 Product used for unknown indication
124935146 12493514 5 Product used for unknown indication
124935146 12493514 6 Product used for unknown indication
124935146 12493514 7 Product used for unknown indication
124935146 12493514 8 Product used for unknown indication
124935146 12493514 9 Product used for unknown indication
124935146 12493514 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124935146 12493514 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124935146 12493514 Constipation
124935146 12493514 Cough
124935146 12493514 Depression
124935146 12493514 Diarrhoea
124935146 12493514 Dyspnoea exertional
124935146 12493514 Fatigue
124935146 12493514 Haemoglobin abnormal
124935146 12493514 Herpes zoster
124935146 12493514 Infected skin ulcer
124935146 12493514 Lethargy
124935146 12493514 Malaise
124935146 12493514 Musculoskeletal stiffness
124935146 12493514 Nausea
124935146 12493514 Neutropenia
124935146 12493514 Neutrophil count abnormal
124935146 12493514 Onychalgia
124935146 12493514 Peripheral swelling
124935146 12493514 Plantar erythema
124935146 12493514 Poor quality sleep
124935146 12493514 Rash
124935146 12493514 Tachycardia
124935146 12493514 Vomiting

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

no results found

Therapies reported

no results found