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Results 1 - 10 of 1,178 for Adverse drug response
  1. ... particular person and which dose will help prevent adverse drug reactions. Conditions that affect a person’s response to certain drugs include clopidogrel resistance , warfarin sensitivity , ...
  2. Contrast Materials (American College of Radiology) (Radiological Society of North America)  
    X-Rays/Related Issues ... X-Rays ... MRI Scans/Related Issues ... MRI Scans ... Diagnostic Imaging/Learn More ... Diagnostic Imaging ... CT Scans/Related Issues ... CT Scans ... American College ...
  3. Medication/Drug Allergy (National Jewish Health)  
    Drug Reactions/Learn More ... Drug Reactions ... National Jewish Health ... Explore comprehensive insights into Medication/Drug Allergies, including symptoms, causes, ...
  4. Preventing Rejection (United Network for Organ Sharing)  
    Lung Transplantation/Prevention and Risk Factors ... Lung Transplantation ... Organ Transplantation/Living With ... Organ Transplantation ... United Network for Organ Sharing
  5. Skin Cancer/Statistics and Research ... Skin Cancer ... National Cancer Institute ... From the National Institutes of Health ... Two studies reported June 7, 2012, in NEJM ...
  6. ... may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online (http://www.fda.gov/Safety/MedWatch) or by phone (1-800-332-1088).
  7. ... may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online (http://www.fda.gov/Safety/MedWatch) or by phone (1-800-332-1088).
  8. ... may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online (http://www.fda.gov/Safety/MedWatch) or by phone (1-800-332-1088).
  9. ... may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online (http://www.fda.gov/Safety/MedWatch) or by phone (1-800-332-1088).
  10. ... may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online (http://www.fda.gov/Safety/MedWatch) or by phone (1-800-332-1088).
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