Reporting On Adverse Clinical Events
Identifieur interne : 000550 ( Istex/Curation ); précédent : 000549; suivant : 000551Reporting On Adverse Clinical Events
Auteurs :Source :
- Clin-Alert® [ 0069-4770 ] ; 2008-03-15.
English descriptors
- Teeft :
- Acetylsalicylic acid, Acute cerebellitis, Adverse events, Arch dermatol, Blood pressure, Breakthrough reactions, Cell lung cancer, Cetuximab, Children adults, Clin pharmacol, Clopidogrel, Clopidogrel discontinuance, Clopidogrel therapy, Coagulation profile, Concurrent medications, Contrast media, Control phase, Cytosine arabinoside, Drug reactions, Eruption, Erythematous papules, Female patient, First report, Follicular eruptions, Gadolinium contrast agents, Gastroparesis, Gefitinib, Gefitinib therapy, Granulomatous reaction, Heart rate, Higher risk, Human herpesvirus, Hydroxychloroquine, Last dose, Leukoencephalopathy syndrome, Lichenoid drug eruption, Lower extremities, Magnetic resonance imaging, Male patient, Medication, Methadone, Neutrophilic infiltration, Nonsteroidal drugs, Normal limits, Nsaid, Nsaid users, Opioid ingestion, Other medications, Peptic, Perforated peptic ulcer, Pharmacokinetic parameters, Platelet count, Ranelate, Severe gastroparesis, Skin biopsy, Strontium, Strontium ranelate, Subcorneal pustule, Syndrome, Terazosin, Terbinafine, Terbinafine group, Toxic epidermal necrolysis, Tramadol, Tramadol users, Univ, Unknown dose, Unknown name, Unstable angina, Venlafaxine, Venlafaxine administration, Voriconazole, Voriconazole phase, Voriconazole pretreatment, Zonisamide.
Url:
DOI: 10.1177/0069477008317140
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<idno type="ISSN">0069-4770</idno>
<idno type="eISSN">1530-812X</idno>
<imprint><publisher>Sage Publications</publisher>
<pubPlace>Sage CA: Los Angeles, CA</pubPlace>
<date type="published" when="2008-03-15">2008-03-15</date>
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<profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Acetylsalicylic acid</term>
<term>Acute cerebellitis</term>
<term>Adverse events</term>
<term>Arch dermatol</term>
<term>Blood pressure</term>
<term>Breakthrough reactions</term>
<term>Cell lung cancer</term>
<term>Cetuximab</term>
<term>Children adults</term>
<term>Clin pharmacol</term>
<term>Clopidogrel</term>
<term>Clopidogrel discontinuance</term>
<term>Clopidogrel therapy</term>
<term>Coagulation profile</term>
<term>Concurrent medications</term>
<term>Contrast media</term>
<term>Control phase</term>
<term>Cytosine arabinoside</term>
<term>Drug reactions</term>
<term>Eruption</term>
<term>Erythematous papules</term>
<term>Female patient</term>
<term>First report</term>
<term>Follicular eruptions</term>
<term>Gadolinium contrast agents</term>
<term>Gastroparesis</term>
<term>Gefitinib</term>
<term>Gefitinib therapy</term>
<term>Granulomatous reaction</term>
<term>Heart rate</term>
<term>Higher risk</term>
<term>Human herpesvirus</term>
<term>Hydroxychloroquine</term>
<term>Last dose</term>
<term>Leukoencephalopathy syndrome</term>
<term>Lichenoid drug eruption</term>
<term>Lower extremities</term>
<term>Magnetic resonance imaging</term>
<term>Male patient</term>
<term>Medication</term>
<term>Methadone</term>
<term>Neutrophilic infiltration</term>
<term>Nonsteroidal drugs</term>
<term>Normal limits</term>
<term>Nsaid</term>
<term>Nsaid users</term>
<term>Opioid ingestion</term>
<term>Other medications</term>
<term>Peptic</term>
<term>Perforated peptic ulcer</term>
<term>Pharmacokinetic parameters</term>
<term>Platelet count</term>
<term>Ranelate</term>
<term>Severe gastroparesis</term>
<term>Skin biopsy</term>
<term>Strontium</term>
<term>Strontium ranelate</term>
<term>Subcorneal pustule</term>
<term>Syndrome</term>
<term>Terazosin</term>
<term>Terbinafine</term>
<term>Terbinafine group</term>
<term>Toxic epidermal necrolysis</term>
<term>Tramadol</term>
<term>Tramadol users</term>
<term>Univ</term>
<term>Unknown dose</term>
<term>Unknown name</term>
<term>Unstable angina</term>
<term>Venlafaxine</term>
<term>Venlafaxine administration</term>
<term>Voriconazole</term>
<term>Voriconazole phase</term>
<term>Voriconazole pretreatment</term>
<term>Zonisamide</term>
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