Presentation on theme: "1 Safety of Dietary Supplements Comments by Daniel Fabricant, Ph.D. Director, Division of Dietary Supplement Programs, ONLDS, CFSAN"— Presentation transcript:
1 Safety of Dietary Supplements Comments by Daniel Fabricant, Ph.D. Director, Division of Dietary Supplement Programs, ONLDS, CFSAN email@example.com February 8, 2013
Safety DSHEA added new adulteration provision Significant or unreasonable risk of injury of illness –Conditions of use –Ordinary conditions of use Didn’t exempt from existing requirements 21 U.S.C. 342(f)
FDA’s Standard Unreasonable risk Met when a product’s risks outweigh its benefits in light of claims and directions for use (or under ordinary conditions) See 69 FR 6787; Feb. 11, 2004
FDA’s Standard Relative weighing of known and reasonably likely risk against known and reasonably likely benefits Doesn’t require showing of causality Seriousness of risks and quality and persuasiveness of the totality of evidence to support the presence of those risks
FDA’s Standard Weight against importance of benefits and quality and persuasiveness of the totality of the evidence to support the existence of those benefits More weight to benefits that –Improve health outcomes –Not temporary –Not rely on subjective measures
Hydroxycut Capsules, drinks/drink powders, liquid shots From 5-20 ingredients/product Varying degrees of ingredient overlap AERs per product from 0 to 31 Formulations changed over time
Basic Facts Liver injury AEs provided the signal Sept. 2008: Physicians contact FDA CAERS search ID’d 18 cases 8 cases were 2002-04 for ephedra- containing products 10 cases with re-formulated product 3 literature reports of 4 patients with acute liver injury
Evidence 67% (n=12) were 20-40 years old Outcomes –Recover: 11 –Liver failure: 2 –Unknown: 5 10 cases provided liver function tests 9 negative drugs, autoantibodies, viruses
Evaluation Adverse events –Temporal relationship of exposure to injury –Exclusion of other causes of liver disease –Resolution upon product discontinuation Unknowns –Responsible ingredient(s)? –Dose-response? Studies of benefit not compelling
Soladek™ Received seven reports of serious health problems occurring in consumers using the product. The problems include decreased renal function, elevated levels of calcium in the blood, fatigue, heart arrhythmia, vomiting, and diarrhea. Symptoms of vitamin D toxicity include weakness, fatigue, headache, nausea, vomiting, diarrhea, changes in mental status, increased blood pressure, abnormal heart rate or rhythm, kidney damage, and coma. Symptoms of vitamin A toxicity include anemia, anorexia, alopecia, joint pain, bone weakness, bulging eyes, liver abnormalities, and birth defects. Other “related” products
Other considerations Contaminants –Intentional –Unintentional
Harm Removal Business What are the major non-compliance problems in the Dietary Supplement Industry? How does the agency address them?
Defining the problem encompassing AERs Invisible Harms - are those which are difficult to discern and analyze because they tend to be under-reported Conscious Opponents - agencies are confronted with individuals or groups of individuals who are engaged in creating a harm (i.e. tainted products) Catastrophic harms - relatively unlikely harmful events that produce enormous levels of victimization Character of Harms – M. Sparrow
Solutions Responsibility (who is?) Process Improvement (which one to choose?)
Let’s go to the numbers Estimates of 1600-2800 DS firms 55,000 + products on the market
Quincy Bioscience WL http://www.fda.gov/ICECI/EnforcementActions/WarningLetters/2012/ucm324557.htm Because your products are labeled as dietary supplements, FDA initially evaluated them under the laws and regulations governing dietary supplements, including the adverse event reporting and recordkeeping requirements for dietary supplements in section 761 of the Act, 21 U.S.C. § 379aa-1, and the current good manufacturing practice (CGMP) regulations for dietary supplements in 21 CFR Part 111. As noted on the list of inspectional observations issued to your headquarters and warehouse facility in Madison, Wisconsin, on December 22, 2011, our inspection of that facility revealed that you failed to report serious adverse events associated with your Prevagen products to FDA, as required by section 761(b)(1) of the Act. Specifically, you failed to report to FDA adverse events like seizures, strokes, and worsening symptoms of multiple sclerosis that had been reported to your firm as being associated with use of Prevagen products. Some of these adverse events resulted in hospitalization. In total, our inspection found records of more than 1000 adverse events and product complaints that had been reported to your firm between May 2008 and December 1, 2011. Some of these involved heart arrhythmias, chest pain, vertigo, tremors, and syncope (fainting), in addition to the seizures, strokes, and worsening of multiple sclerosis already mentioned. As of the beginning of the inspection, only two of these adverse events had been reported to FDA or investigated by your firm.
Evidence of Under-reporting BioSan, Nordimex and Theta Brothers WLs all cited 403(y) ATF/Made Injunction cited a failure to send in SAERs Import refusals for 403(y) Recent OIG exam cited that approx 30% of the firms in it’s sample didn’t have a label compliant with 403(y)
Triggers Safety/Unsafe Statutory Obligations Common ground
Serious Adverse Event Reporting SAER Challenges for addressing Safety –(a) insufficient or inaccurate information in many case reports; –(b) underreporting of adverse events; –(c) data on background rates of adverse events as compared to those that are associated with dietary supplements; –(d) data on extent of exposure to particular dietary supplements within the population. In light of challenges, how does the Agency use SAERs to determine acute, chronic and “mixed/combination” risk to supports the basis for causality, when and where appropriate? What are the triggers?
Because of these limitations, SAE reports are primarily useful for hypothesis generating, rather than hypothesis testing
Safety Triggers for Thought Specific to a Product or Ingredient Labeling/Use Directions/Normal Conditions of Use Pathology of Events Mechanism Food Regulatory Paradigm different than Rx (i.e. Δ in application of numerator and denominators)
Post-Market Surveillance - AERs and Product Complaints Reasonable Corporate Systems are likely Integrated PC are receiving, documenting and tabulating; AERs are the same + reporting requirement If trending and benchmarking are absent and/or deficient in cGMPs regarding product complaints, what might this mean for other requirements? Assessment of a firm’s capabilities
Some of FDA’s Expectations Labels that meet 403(y) SOP’s for AERs and product complaints & related documents/records Training of those that handle AERs How does the firm obtain follow-up? Has the firm ever sent SAERs to FDA? Have you ever received an AER? Does the firm monitor indirect sources of information on AERs? (e.g. social media, news) How does the firm apply medical judgment for those reports they chose not to submit? How are calls & mailed AERs routed if a 24-hr line isn’t available?
Other expectations By rule of construction – SAERs aren’t causal - a failure to submit or a lack of submitting SAERs doesn’t make a product safe! Is your system making your product “better”? Would you know it if it wasn’t?
The take home Safety for dietary supplements is a complex picture Under-reporting is substantial – this must be remedied via responsibility and improved processes Expectations of reporting system may also be flawed, a system that tests hypotheses has limited value, one that develops new ones is preferable The agency will be taking more action in this area, triggered by “both” issues 341 inspections in FY 2012 are there other ways of obtaining a look into AERs?
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