Abstract #1098 A Curious Case of Persistently Elevated TSH Associated with High Dose Over the Counter Biotin Supplementation

2018 ◽  
Vol 24 ◽  
pp. 271-272
Author(s):  
Thomas Varghese ◽  
Faisal Qureshi
Author(s):  
G.A. Miranda ◽  
M.A. Arroyo ◽  
C.A. Lucio ◽  
M. Mongeotti ◽  
S.S. Poolsawat

Exposure to drugs and toxic chemicals, during late pregnancy, is a common occurrence in childbearing women. Some studies have reported that more than 90% of pregnant women use at least 1 prescription; of this, 60% used more than one. Another study indicated that 80% of the consumed drugs were not prescribed, and of this figure, 95% were “over-the-counter” drugs. Acetaminophen, the safest of all over-the-counter drugs, has been reported to induce fetal liver necrosis in man and animals and to have abortifacient and embryocidal action in mice. This study examines the degree to which acetaminophen affects the neonatal liver and kidney, when a fatty diet is simultaneously fed to the mother during late pregnancy.Timed Swiss Webster female mice were gavaged during late pregnancy (days 16-19) with fat suspended acetaminophen at a high dose, HD = 84.50 mg/kg, and a low dose, LD = 42.25 mg/kg; a control group received fat alone.


Author(s):  
Pamayyagari Kalpana

Self-medication is a wide spread behavior, particularly among elderly patients. Self-medication involves not only the consumption of over-the-counter products but also the re-use of formerly prescribed drugs without medical supervision. This practice may lead to severe adverse health events. Here we report a case of old female, presented with cushingoid face and hyperglycemia due to self-medication of high dose Prednisolone for longer duration. Symptomatic treatment was given to stabilize the patient. Patient was warned regarding the adverse effects of drugs and strictly advised to use medication only under medical supervision.


Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 1961-1961
Author(s):  
Susan A Oliveria ◽  
Nancy Brandenburg ◽  
Syd Phillips ◽  
Kimberley J Woodcroft ◽  
Karen Wells ◽  
...  

Abstract Patients with multiple myeloma (MM) are at increased risk for venous thromboembolism (VTE) due to patient, disease, and treatment-related factors. Current National Comprehensive Cancer Network (NCCN) guidelines for VTE suggest that patients with MM receiving thalidomide or lenalidomide in combination with high-dose dexamethasone (480 mg per month) receive VTE prophylaxis. For MM patients at high risk for VTE (≥2 risk factors), low molecular weight heparin or full-dose warfarin is recommended. For MM patients at low risk for VTE (0-1 risk factor), aspirin 81-325 mg once daily is recommended for VTE prophylaxis. Eighty-five percent of patients diagnosed with MM are aged ≥55 and many of them are prescribed aspirin for primary or secondary prevention of cardiovascular or cerebrovascular disease, independent of their MM diagnosis. According to the 2010 National Health Interview survey, the prevalence of regular aspirin use among persons in the United States ≥50 years of age is 35.9%. Because aspirin use may provide effective prophylaxis of venous events in MM patients at low risk for VTE, it is important to understand the prevalence of aspirin use among MM patients. As part of a larger study examining the risk of VTE among patients diagnosed with MM and treated with thalidomide or lenalidomide, the objective of this study was to estimate the prevalence of over-the-counter (OTC) aspirin use among MM patients. Patients ≥18 years of age diagnosed with MM between January 1, 2005 and September 30, 2012 were identified from the tumor registry at the Henry Ford Health System (HFHS), a large integrated health care delivery system located in southeastern Michigan; whose data are included in the Surveillance, Epidemiology, and End Results (SEER) Program of the National Cancer Institute. We developed a telephone survey, and then contacted all eligible patients (i.e. they were alive and/or not documented as deceased) to quantify OTC aspirin use. Data analyses included descriptive statistics to assess the demographic, clinical, and aspirin use characteristics. We identified 381 patients diagnosed with MM; of those, 177 were eligible for the survey. We contacted these patients and achieved a 67% (n=119) response rate. The median age of survey respondents was 64 years (range 41-93) and 93 (78%) were aged ≥55. Sixty-two (52%) of the survey responders were female, 82 (69%) were African American, and 36 (30%) were white. Of the respondents, 46 (39%) reported weekly aspirin use and 43 of the 46 (94%) reported daily aspirin use. The average daily dose was 114 mg/day (standard deviation 93) and most patients (n=39 of 46; 85%) reported taking an 81 mg dose. The reason for daily aspirin use was cited as “Other reason for prophylaxis” by 36 (of 43; 84%) of the patients. In this case, patients indicated that they were taking aspirin for prophylaxis, but did not provide enough information to determine the reason for daily aspirin use. Only 5 patients (12%) reported taking aspirin for heart disease prophylaxis. Roughly one-quarter of the MM patients (n=31 of 119; 26%) indicated that they had a health problem that made aspirin use unsafe. Twenty-seven (23%) reported that they had a parent or sibling who had a heart attack before the age of 60; fourteen patients (12%) reported that they had a parent or sibling who has or ever had a VTE. Seventeen patients (14%) reported a history of ever having a VTE event themselves. Our data indicate that over one-third of patients diagnosed with MM use OTC aspirin daily. When treating patients diagnosed with MM, assessing risk for VTE and determining an appropriate VTE prophylaxis therapy is of the utmost importance. Disclosures: Brandenburg: Celgene Corporation: Employment, Equity Ownership.


2019 ◽  
Vol 151 (5) ◽  
pp. 486-493 ◽  
Author(s):  
Ithiel J Frame ◽  
Parag H Joshi ◽  
Caroline Mwangi ◽  
Ian Gunsolus ◽  
James A De Lemos ◽  
...  

Abstract Objectives To investigate biotin interference on three cardiac troponin (cTn) assays and demonstrate a method to overcome biotin interference. Methods cTn levels were measured in (1) plasma from healthy volunteers on 10-mg daily biotin supplementation mixed with a plasma with known elevated troponin, (2) plasmas with known elevated cTn after mixing in reagent biotin to simulate supplementation, and (3) biotin-spiked plasma specimens pretreated with streptavidin-agarose beads. Results Daily biotin ingestion (10 mg) and studies simulating daily biotin use resulted in significant interference in the Gen5 cardiac troponin T (cTnT) assay; the contemporary Gen 4 cTnT and high-sensitivity cardiac troponin I (hs-cTnI) assays were unaffected. The biotin interference threshold was 31, 315, and more than 2,000 ng/mL for Gen5 cTnT, cTnT, and hs-cTnI assays, respectively. Streptavidin pretreatment blocked biotin interference in cTn assays. Conclusions Biotin interference is possible at plasma concentrations achievable by ingestion of over-the-counter supplements that may lead to delayed or missed diagnosis of myocardial injury with the Gen5 cTnT assay.


2019 ◽  
Vol 1 (1) ◽  
pp. 25-29
Author(s):  
Uzma Daud ◽  
Qasim Muneer ◽  
Javeria Noor ◽  
Fahad Raza ◽  
Sarah Khalid

Background: The versatile and dynamic activities of Panax Ginseng are attributed to its active components. They are readily available over the counter and are known for their effects as an aphrodisiac & health building; in addition, they are given rather generously during pregnancy, as they are considered virtuous for the baby and mother. Despite its easy availability and excess usage, little is known about its effects on the fetus. The current experimental design was focused towards the lack of differentiation and inhibition of cell growth of mesodermal derivatives inflicted by PanaxGingex. Methods:18 pregnant albino dams were randomly divided into three groups; Group A was control, Group B was Low dose and Group C was labeled as High dose groups. Tissues (bone, kidney and blood) were selected as derivatives of paraxial, intermediate and lateral plate mesoderm respectively and were used for light microscopic study. Results and Conclusion: The light microscopic examination demonstrated extensive apoptosis and an escalation of angiogenesis. Both the histological findings were not only statistically significant but was clearly indicative of dysmorphogenesis. The results of present study raise a finger towards the unsupervised practice of over the counter preparations especially during the vital antenatal period of development.


2021 ◽  
Author(s):  
David Scheim ◽  
Jennifer A. Hibberd ◽  
Juan Chamie-Quintero

A randomized controlled trial for treatment of mild cases of COVID-19 conducted in Cali, Colombia reported no statistically significant differences in outcomes for its ivermectin (IVM) and placebo arms. A striking anomaly, however, was that certain adverse events (AEs) that are distinctive for the study’s high-dose IVM use occurred at nearly identical rates in its IVM and placebo arms. The backdrop for these indicators of IVM use in study controls was widespread sales of IVM for COVID-19 in the Cali area during the study period, with 1.6 IVM doses sold over the counter for each case of COVID-19. The study compounded these risks of contamination of the control arm with critical errors in blinding and segregation of IVM v. placebo doses. A labeling error substituted IVM for placebo doses of 38 patients. Also, 5% dextrose solution was used for several weeks as a placebo, easily distinguishable from bitter tasting IVM. Given widespread availability and sales of IVM in Cali, lapses in segregation and blinding of IVM and control doses, and IVM-characteristic AEs in controls, the integrity of the study’s control arm was violated. Some useful information can nevertheless be salvaged from outcomes of this study’s IVM treatment arm, which had 0 deaths and generally mild symptoms, with AEs typical for high-dose IVM (replicated in the control group) that were generally mild and transient.


2003 ◽  
Vol 38 (3) ◽  
pp. 199-270 ◽  
Author(s):  
Joel Shuster

The purpose of this feature is to heighten awareness of specific adverse drug reactions (ADRs), to discuss methods of prevention, and to promote reporting of ADRs to the FDA's medWatch program (800-FDA-1088). If you have reported an interesting preventable ADR to medWatch, please consider sharing the account with our readers.


Author(s):  
Turki M. Al-Shaikh ◽  
Mahmoud M. E. Mudawi ◽  
Abdelhadi Y. A. Yassin ◽  
Rami S. Habeballa ◽  
Vijay R. Chidrawar

Many patients may administered medications like captopril (ACE inhibitor) for treatment of chronic diseases and may also take Paracetamol as an Over The Counter (OTC) drug which may interact with captopril. Therefore, the aim of this study is to evaluate of the hepatoprotective effect of captopril on liver toxicity induced by low and high dose of paracetamol in rats. This study was conducted in two phases: first study for low dose of paracetamol (300 mg/kg); animals were divided into 4 groups of 6 rats each (n = 6); all groups were treated orally either 0.9 % Normal Saline (NS), captopril 20 mg/kg, paracetamol 300 mg/kg or captopril 20 mg/kg plus paracetamol 300 mg/kg for 10 consecutive days. Second study for single high dose of paracetamol (3000 mg/kg); animals were divided into 4 groups of 6 rats each (n = 6); all groups were pretreated orally either 0.9 % Normal Saline (NS) or captopril 20 mg/kg for 7 consecutive days followed by single oral administration of Paracetamol 3000 mg/kg or normal saline. The administration of Paracetamol or normal saline was performed 24 hours after the last administration of captopril. After 48 hours of hepatic injury induction, the animals were then sacrificed and the liver was removed for histopathological studies. Low dose (300 mg/kg) for 10 days and high single dose (3000 mg/kg) of paracetamol produced hepatotoxic effects. While captopril 20 mg/kg showed marked protection against changes induced by low and high dose of paracetamol on the liver.


2004 ◽  
Vol 23 (5) ◽  
pp. 235-244 ◽  
Author(s):  
F Burdan

The aim of the study was to determine the influence of an over-the-counter (OTC) mixture of propyphenazone with caffeine or paracetamol on prenatal development. Propyphenazone:caffeine and propyphenazone:paracetamol mixtures were prepared with constant 3:1 and 3:5 ratios, respectively. Three dose levels of each of the mixtures were administered separately in Tween-80 water suspension once a day to pregnant Wistar rats on gestation days 8-14. The low dose was similar to the OTC preparations, 2.1 mg/kg of propyphenazone, 0.7 mg/kg of caffeine or 3.5 mg/kg of paracetamol. The middle dose was 21.0, 7.0 or 35.0 mg/kg, and the highest 210.0, 70.0 or 350.0 mg/kg for propyphenazone, caffeine or paracetamol, respectively. On day 21 of gestation the fetuses were delivered by hysterectomy. Dead or live fetuses, resorptions and the number of implantation sites were counted. Live fetuses were examined for external, visceral and skeletal malformation. Postimplantation mortality was calculated. Dose-dependent effects in the middle and high dose groups on fetal body weight/length and placental weight were found. No increase in external or internal congenital anomalies was found in any of the mixture-exposed groups. Prenatal coadministration of propyphenazone with caffeine or paracetamol caused intrauterine growth retardation but did not increase external or internal congenital anomalies. The risk of midline defects (umbilical hernia and gastroschisis) is discussed.


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