Incomplete evidence: the inadequacy of databases in tracing published adverse drug reactions in clinical trials - Wikidata - awgldk - TriplyDB

Incomplete evidence: the inadequacy of databases in tracing published adverse drug reactions in clinical trials

Incomplete evidence: the inadequacy of databases in tracing published adverse drug reactions in clinical trials

http://www.wikidata.org/entity/Q24805420

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Vaccines for measles, mumps and rubella in children Assessing harmful effects in systematic reviews The safety of over-the-counter niacin. A randomized placebo-controlled trial [ISRCTN18054903]Room for improvement? A survey of the methods used in systematic reviews of adverse effects Quality of reporting in systematic reviews of adverse events: systematic review Antiepileptic drugs' tolerability and safety--a systematic review and meta-analysis of adverse effects in dogs Systematic reviews of adverse effects: framework for a structured approach Failure or success of search strategies to identify adverse effects of medical devices: a feasibility study using a systematic review Reporting of harms data in RCTs: a systematic review of empirical assessments against the CONSORT harms extension.Comprehensive evaluations of the adverse effects of drugs: importance of appropriate study selection and data sources.Dementia medications and risk of falls, syncope, and related adverse events: meta-analysis of randomized controlled trials.Identifying systematic reviews of the adverse effects of health care interventions.CONSORT for reporting randomized controlled trials in journal and conference abstracts: explanation and elaboration.Meta-analysis of rare and adverse event data.Adverse effects of extra-articular corticosteroid injections: a systematic review.Is there an association between low dose aspirin and anemia (without overt bleeding)? Narrative review.Failure or success of electronic search strategies to identify adverse effects data.Systematic review of methods used in meta-analyses where a primary outcome is an adverse or unintended event Case reports of suspected adverse drug reactions--systematic literature survey of follow-up.Systematic review and meta-analysis of ethnic differences in risks of adverse reactions to drugs used in cardiovascular medicine.Searching the literature for information on traumatic spinal cord injury: the usefulness of abstracts.dRiskKB: a large-scale disease-disease risk relationship knowledge base constructed from biomedical text.Bisphosphonates and risk of cardiovascular events: a meta-analysis.Comparison of Medical Subject Headings and text-word searches in MEDLINE to retrieve studies on sleep in healthy individuals Adverse drug reactions--no farewell to harms.Automatic construction of a large-scale and accurate drug-side-effect association knowledge base from biomedical literature.Assignment of adverse event indexing terms in randomized clinical trials involving spinal manipulative therapy: an audit of records in MEDLINE and EMBASE databases.Topical analgesics for acute and chronic pain in adults - an overview of Cochrane Reviews.Developing efficient search strategies to identify reports of adverse effects in MEDLINE and EMBASE.Efficacy and adverse events of cold vs hot polypectomy: A meta-analysis.Search strategies to identify information on adverse effects: a systematic review.Adverse effects of iodine thyroid blocking: a systematic review.Sensitivity and precision of adverse effects search filters in MEDLINE and EMBASE: a case study of fractures with thiazolidinediones.Optimising the retrieval of information on adverse drug effects.Comparison of search strategies in systematic reviews of adverse effects to other systematic reviews.Toward standardized reporting of drug interactions: the READI checklist for anecdotal reports.Probiotic treatments for induction and maintenance of remission in inflammatory bowel diseases: a meta-analysis of randomized controlled trials.Effectiveness of adverse effects search filters: drugs versus medical devices Metameta-analysis.Balancing benefits and harms in health care.

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P2860

Incomplete evidence: the inadequacy of databases in tracing published adverse drug reactions in clinical trials

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P2860

The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials

Single dose oral ibuprofen and diclofenac for postoperative pain.

Completeness of safety reporting in randomized trials: an evaluation of 7 medical areas.

Risk of gastrointestinal haemorrhage with long term use of aspirin: meta-analysis.

Drug companies should report side effects in terms of frequency.

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