Researchers from the Nationwide Children's Hospital in the US found the rate of calls regarding dietary supplement exposures increased 49.3 per cent from 2005 to 2012.
Seventy per cent of dietary supplement exposure calls occurred among children younger than six years old and the majority of these were unintentional.
Most exposures (97.3 per cent) occurred at home, and in more than 97 per cent of the cases, the child swallowed the substance.
"Many consumers believe dietary supplements are held to the same safety and efficacy standards as over-the-counter medications," said Gary Smith, director of the Center of Injury Research and Policy at Nationwide Children's Hospital.
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"However, dietary supplements are not considered drugs, thus they are not required to undergo clinical trials or obtain approval from the FDA prior to sale, unless the product is labelled as intended for therapeutic use," said Smith.
Miscellaneous substances found in commonly used dietary supplements accounted for the majority of exposure calls (43.9 per cent).
Amino acids, cultural medicines and energy products each account for less than two per cent of exposures.
The dietary supplements with the highest proportion of serious medical outcomes were energy products, botanical and cultural medicines.
Energy products, including drinks, advertised to increase energy and mental performance, can cause bad clinical effects as well.
Many energy product exposures were unintentional and occurred among young children, causing heart and breathing problems, seizures, and other clinical problems.
Findings support the need for improved energy product regulation, child-resistant packaging, and caregiver information, researchers said.