Severe Methemoglobinemia and Hemolytic Anemia from Aniline Purchased as 2C-E (4-ethyl-2,5-dimethoxyphenethylamine), a Recreational Drug, on the Internet — Oregon, 2011

In August 2011, two men in Oregon drank a liquid they believed to be 2C-E (4-ethyl-2,5-dimethoxyphenethylamine), a psychoactive stimulant used as a recreational drug, after purchasing it on the Internet. Fifteen minutes after ingestion, the men became cyanotic and subsequently were treated for refractory methemoglobinemia and hemolytic anemia. The Oregon Poison Center, Oregon Public Health Division, Drug Enforcement Administration (DEA), and Food and Drug Administration (FDA) jointly investigated to determine the cause of the poisoning and identify other cases. The Oregon Poison Center and Oregon Public Health Division promptly alerted health-care providers and public health agencies and searched for additional cases. DEA confiscated all product remaining in the men's possession, and FDA identified the substance as aniline, an industrial solvent known to cause methemoglobinemia. One patient reported purchasing the substance from the Internet site of a Chinese chemical company. No additional cases were identified by investigators. Purchase of chemicals from unregulated Internet sources poses a serious risk to purchasers from product contamination and substitution.

Case Reports

Patient A. On August 19, 2011, a man aged 33 years was taken by ambulance to a local emergency department after he collapsed in a fast food restaurant. He reported feeling lightheaded and nauseated 15 minutes after consuming a soft drink with his friend (patient B). When questioned, patient A initially said he had not ingested medications or illicit drugs. On physical examination, he appeared cyanotic with altered mental status, and his blood oxygen saturation measured by pulse oximetry was 86% on 100% supplemental oxygen by nonrebreather mask. Blood drawn for laboratory testing was chocolate-brown. Arterial blood pH was 7.43, the pCO was 35 mm Hg, and the pO was 222 mm Hg. His methemoglobin concentration was 66.7% (normal: 1%–3%), his hemoglobin concentration was 14.3 g/dL (normal: 13.8–17.2 g/dL), and his platelet count was 338,000/mm3 (normal: 150,000–400,000/mm3). The Oregon Poison Center was consulted and recommended administration of 1 mg/kg body weight methylene blue intravenously. The patient was admitted to the hospital intensive-care unit.

After the initial dose of methylene blue, a repeat methemoglobin concentration was 67.2%. A second 1 mg/kg dose was administered 4 hours after arrival. Patient A's methemoglobin concentration peaked at 79.6% at 6 hours after ingestion. The patient ultimately received a total of five 1 mg/kg doses of methylene blue during the next 2 days. By hospital day 3, his methemoglobin concentration had decreased to 11%, and his hemoglobin concentration had decreased to 10.1 g/dL.

On hospital day 5, the patient's hemoglobin concentration was 5.7 g/dL, and he reported fatigue. His blood oxygen saturation measured by pulse oximetry remained at 70%–80% despite supplemental oxygen administration. He received 2 units of packed red blood cells. Other laboratory assessment was significant for haptoglobin <30 mg/dL (normal: 41–165 mg/dL), lactate dehydrogenase (LDH) 2,005 U/L (normal: 105–333 U/L), and platelets 73,000/mm3. Acute oxidant stress-induced hemolysis was suspected, and the patient was transferred to a tertiary-care intensive-care unit.

The patient received an additional unit of packed red blood cells and underwent plasmapheresis, after which his hemoglobin concentration was 5.8 g/dL. During the following 2 days, daily plasmapheresis was performed, as well as one complete exchange transfusion (1). During this process, serum LDH concentration decreased to 428 U/L, and the patient's hemoglobin concentration stabilized at 9.5 g/dL. On hospital day 8, a fourth plasmapheresis was performed; hemoglobin concentration remained stable, and his serum LDH concentration decreased to 158 U/L, suggesting resolution of hemolysis. Glucose-6-phosphate dehydrogenase concentrations were normal (deficiency is a risk factor for hemolytic anemia). On hospital day 12, the patient was discharged home. Subsequently, results of comprehensive toxicology screening of urine by gas chromatography/mass spectroscopy were positive for p-aminophenol, an aniline metabolite.

Patient B. A man aged 34 years (patient B) who had accompanied patient A to the emergency department also appeared cyanotic, but said he had no symptoms. When questioned, patient B also initially said he had not ingested medications or illicit drugs. However, he later reported having consumed the same soft drink as patient A. Patient B's initial blood oxygen saturation measured by pulse oximetry was 80% on 40% supplemental oxygen by nonrebreather mask, and peripheral venous blood drawn for laboratory testing was dark brown. His methemoglobin concentration drawn 45 minutes after ingestion was 49.5%, and his hemoglobin concentration was 16.4 g/dL. Methylene blue 1 mg/kg was administered intravenously, and a repeat methemoglobin concentration was 47.8%. The patient received a second dose of methylene blue, and was admitted to the intensive-care unit overnight. His methemoglobin concentration peaked at 74.4% 8 hours after ingestion.

Patient B received a total of 4 doses of methylene blue and then left the hospital against medical advice 19.5 hours after ingestion. His last methemoglobin concentration was 10%. His glucose-6-phosphate dehydrogenase concentration was not tested.

After patient A was transferred to tertiary care for chemical-induced hemolytic anemia on postexposure day 5, multiple attempts were made to contact patient B. He returned for repeat evaluation on postexposure day 6 and reported fatigue and dyspnea. His hemoglobin concentration had decreased to 10 g/dL at follow-up. A repeat methemoglobin concentration was 1.1%. Despite plans for repeat hemoglobin testing in 1–2 days, he did not return for further evaluation.

Multi-Agency Investigation

During evaluation in the emergency department, the physician questioned patient A and patient B because of concern for possible consumer product contamination of their soft drink by a methemoglobin-inducing substance. After initial denials, they reported buying 2C-E as a recreational chemical from an Internet site. They described ingesting 4 mL of a bitter, yellow-tinted liquid that they had mixed with a soft drink to mask the taste. This description was inconsistent with 2C-E, which is available typically as a capsule or white powder.

Further questioning implicated a company based in Nanjing, China, that produces and sells 2C-E and industrial products manufactured using aniline. Consultation with FDA confirmed that 2C-E was a federally controlled substance, and that, since the product was purchased from an international distributor, the incident was under federal jurisdiction. DEA was notified. DEA obtained the leftover product that the patients had purchased, and FDA determined the liquid was pure aniline, with no evidence of 2C-E. Aniline is a common solvent used in manufacturing processes. Ingestion of aniline can cause methemoglobinemia and hemolytic anemia through the action of its metabolites, phenylhydroxylamine and aminophenol, both strong oxidizing agents (1–4).

The patients said they had not shared the product with others. Nonetheless, public health and poison control investigators conducted active case-finding because of concern that aniline might have been mislabeled and sold to other buyers seeking 2C-E. A case was defined as unexplained methemoglobinemia in a person who had ingested a chemical purchased through the Internet since January, 2011. The Oregon Poison Center queried poison center directors nationally and searched for reports of aniline poisoning in the National Poison Data System. CDC was notified, and investigators conducted supplemental symptom-based case-finding using the Oregon Health Alert Network and CDC's Epidemic Information Exchange (Epi-X)* to query for cases of unexplained methemoglobinemia. No additional cases were identified.

Reported by

Shana Kusin, MD, Jeremy Tesar, MD, Ben Hatten, MD, B. Zane Horowitz, MD, Robert Hendrickson, MD, Oregon Poison Center; Richard Leman, MD, Oregon Public Health Div. Genevieve Buser, MD, EIS Officer, CDC. Corresponding contributor: B. Zane Horowitz, [email protected], 503-494-4833.

Editorial Note

Strong oxidizing agents, such as aniline metabolites, can cause methemoglobinemia or, at higher concentrations, acute red blood cell hemolysis. Symptoms related to increased methemoglobin concentrations reflect declining oxygen delivery. Concentrations above 50% can cause syncope. Concentrations above 70% can be lethal. During venipuncture, the blood usually appears chocolate brown, a clue to the presence of methemoglobin. Standard noninvasive pulse oximetry typically shows a reading of 85% that does not change despite administration of 100% oxygen or the antidote methylene blue.

Hydroxylamine compounds (e.g., aniline metabolites phenylhydroxylamine and aminophenol) often produce methemoglobin that is refractory to conversion back to normal hemoglobin by administration of methylene blue, and can precipitate acute hemolytic anemia (1–4). Paradoxically, methylene blue can be a source of oxidant stress and, in high doses, can cause hemolytic anemia. However, this is more likely with glucose-6-phosphate dehydrogenase deficiency, and patient A's concentrations were normal, whereas patient B's concentrations were not tested.

Use of novel psychoactive chemicals has continued to increase in the United States despite passage of the 1986 Controlled Substances Analogue Enforcement Act (CSAEA) (5,6). The phenethylamines (e.g., 2C-B, 2C-E, and 2C-I), their isomers, and their salts are illegal substances under CSAEA (7). To circumvent such laws, manufacturers produce substances that have chemical structures distinct from regulated substances, yet still produce psychoactive effects. These products pose challenges to both surveillance and regulation because they frequently are advertised for sale as "research chemicals" through international and domestic Internet sites.

Purchase of psychoactive chemicals and other ingestible products from the Internet places the public at risk for obtaining products that are inherently toxic or have been made toxic by adulteration, either inadvertently or deliberately. Persons reporting emergencies involving ingested substances purchased from the Internet should telephone FDA at the 24-hour, toll-free number (1-888-INFO-FDA). Persons reporting nonemergencies should contact the FDA district office consumer complaint coordinator for their geographic area during regular business hours.† Communication and collaboration among health-care, public health, poison control, and law enforcement agencies are crucial to identify adverse events associated with Internet-purchased toxic chemicals and coordinate health messages for health-care providers.

This is the first published report of unintentional aniline intoxication in persons attempting to purchase psychoactive chemicals for recreational use. Whether this potentially lethal incident represents deliberate ingredient substitution or a packaging error by a vendor not subject to industry standards is unknown. This case highlights the danger to the public and the challenges facing public health agencies in an era in which virtually any chemical produced in any country is available through Internet sales.

Acknowledgments

David Farrer, Oregon Public Health Div; Seattle Div, Drug Enforcement Admin; Pacific Region, Food and Drug Admin.

References

1. Mier, RJ. Treatment of aniline poisoning with exchange transfusion. J Toxicol Clin Toxicol 1988;26:357–64.
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3. National Center for Environmental Health/Agency for Toxic Substances and Disease Registry. Medical management guidelines for aniline. Atlanta, GA: US Department of Health and Human Services, CDC; 2011. Available at http://www.atsdr.cdc.gov/mmg/mmg.asp?id=448&tid=79. Accessed February 3, 2012.
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7. US Department of Justice, Drug Enforcement Administration, Office of Diversion Control. Controlled substance schedules. Springfield, VA: Drug Enforcement Administration; 2011. Available at http://www.deadiversion.usdoj.gov/schedules/index.html. Accessed February 8, 2012.