Pseudoephedrine

Pseudoephedrine
Clinical data
Trade names Afrinol, Sudafed, Sinutab(UK)
AHFS/Drugs.com Monograph
MedlinePlus a682619
Pregnancy
category
  • AU: B2
  • US: C (Risk not ruled out)
Dependence
liability		 Low
Routes of
administration		 oral, insufflation
ATC code
Legal status
Legal status
  • AU: S3 (Pharmacist only)
  • CA: OTC; NDS Schedule II (BTC) for single-drug products, NDS Schedule III (OTC) when part of a combination product
  • UK: P (Pharmacy medicines)
  • US: Behind the Counter (BTC); Rx-only in Oregon and Mississippi
Pharmacokinetic data
Bioavailability ~100%[1]
Metabolism hepatic (10–30%)
Biological half-life 4.3–8 hours[1]
Excretion 43–96% renal[1]
Identifiers
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
ECHA InfoCard 100.001.835
Chemical and physical data
Formula C10H15NO
Molar mass 165.23
3D model (JSmol)
  (verify)

Pseudoephedrine (/ˌsjuːdoʊ.ɪˈfɛdrɪn/ or /ˌsjuːdoʊˈɛfɪdriːn/; PSE) is a sympathomimetic drug of the phenethylamine and amphetamine chemical classes. It may be used as a nasal/sinus decongestant, as a stimulant, or as a wakefulness-promoting agent[2] in higher doses.[3]

The salts pseudoephedrine hydrochloride and pseudoephedrine sulfate are found in many over-the-counter preparations, either as a single ingredient or (more commonly) in combination with antihistamines, guaifenesin, dextromethorphan, and/or paracetamol (acetaminophen) or an NSAID (such as aspirin or ibuprofen).

Chemistry

Pseudoephedrine is a diastereomer of ephedrine and is readily reduced into methamphetamine or oxidized into methcathinone.

Two pairs of enantiomers: ephedrine (top) and pseudoephedrine (bottom)

Nomenclatures

The dextrorotary (+)- or d- enantiomer is (1S,2S)-pseudoephedrine, whereas the levorotating (−)- or l- form is (1R,2R)-pseudoephedrine.

In the outdated d/l system (+)-pseudoephedrine is also referred to as l-pseudoephedrine and (−)-pseudoephedrine as d-pseudoephedrine (in the Fisher projection then the phenyl ring is drawn at bottom).[4][5]

Often the d/l system (with small caps) and the d/l system (with lower-case) are confused. The result is that the dextrorotary d-pseudoephedrine is wrongly named d-pseudoephedrine and the levorotary l-ephedrine (the diastereomer) wrongly l-ephedrine.

The IUPAC names of the two enantiomers are (1S,2S)- respectively (1R,2R)-2-methylamino-1-phenylpropan-1-ol. Synonyms for both are psi-ephedrine and threo-ephedrine.

Pseudoephedrine is the International Nonproprietary Name of the (+)-form, when used as pharmaceutical substance.[6]

Synthesis

Although pseudoephedrine occurs naturally as an alkaloid in certain plant species (for example, as a constituent of extracts from the Ephedra species, also known as ma huang, in which it occurs together with other isomers of ephedrine), the majority of pseudoephedrine produced for commercial use is derived from yeast fermentation of dextrose in the presence of benzaldehyde. In this process, specialized strains of yeast (typically a variety of Candida utilis or Saccharomyces cerevisiae) are added to large vats containing water, dextrose and the enzyme pyruvate decarboxylase (such as found in beets and other plants). After the yeast has begun fermenting the dextrose, the benzaldehyde is added to the vats, and in this environment the yeast converts the ingredients to the precursor l-phenylacetylcarbinol (L-PAC). L-PAC is then chemically converted to pseudoephedrine via reductive amination.[7]

The bulk of pseudoephedrine is produced by commercial pharmaceutical manufacturers in India and China, where economic and industrial conditions favor its mass production for export.[8]

Mechanism of action

Pseudoephedrine is a sympathomimetic amine. Its principal mechanism of action relies on its direct action on the adrenergic receptor system.[9][10] The vasoconstriction that pseudoephedrine produces is believed to be principally an α-adrenergic receptor response.[11]

Pseudoephedrine acts on α- and β2-adrenergic receptors, to cause vasoconstriction and relaxation of smooth muscle in the bronchi, respectively.[9][10] α-adrenergic receptors are located on the muscles lining the walls of blood vessels. When these receptors are activated, the muscles contract, causing the blood vessels to constrict (vasoconstriction). The constricted blood vessels now allow less fluid to leave the blood vessels and enter the nose, throat and sinus linings, which results in decreased inflammation of nasal membranes, as well as decreased mucus production. Thus, by constriction of blood vessels, mainly those located in the nasal passages, pseudoephedrine causes a decrease in the symptoms of nasal congestion. Activation of β2-adrenergic receptors produces relaxation of smooth muscle of the bronchi,[9] causing bronchial dilation and in turn decreasing congestion (although not fluid) and difficulty breathing.

Medical uses

A selection of over-counter medications, including Contac, which contains pseudoephedrine.

Pseudoephedrine is a stimulant, but it is well known for shrinking swollen nasal mucous membranes, so it is often used as a decongestant. It reduces tissue hyperemia, edema, and nasal congestion commonly associated with colds or allergies. Other beneficial effects may include increasing the drainage of sinus secretions, and opening of obstructed Eustachian tubes. The same vasoconstriction action can also result in hypertension, which is a noted side effect of pseudoephedrine.

Pseudoephedrine can be used either as oral or as topical decongestant. The advantage of oral pseudoephedrine over topical nasal preparations is that it does not cause rebound congestion (rhinitis medicamentosa). However, due to its stimulating qualities, it is more likely to cause adverse effects, including hypertension, sweating, insomnia, anxiety, and urinary retention.[12][13] According to one study, pseudoephedrine may show effectiveness as an antitussive drug (suppression of cough).[14]

Indications

Pseudoephedrine is indicated for the treatment of nasal congestion, sinus congestion and Eustachian tube congestion.[15] Pseudoephedrine is also indicated for vasomotor rhinitis, and as an adjunct to other agents in the optimum treatment of allergic rhinitis, croup, sinusitis, otitis media, and tracheobronchitis.[15]

Pseudoephedrine is also used as a first-line prophylactic for recurrent priapism. Erection is largely a parasympathetic response, so the sympathetic action of pseudoephedrine may serve to relieve this condition. Treatment for urinary incontinence is an off-label use ("unlabeled use") for these medications.[16]

Adverse effects

Common adverse drug reactions (ADRs) associated with pseudoephedrine therapy include central nervous system stimulation, insomnia, nervousness, excitability, dizziness and anxiety. Infrequent ADRs include tachycardia or palpitations. Rarely, pseudoephedrine therapy may be associated with mydriasis (dilated pupils), hallucinations, arrhythmias, hypertension, seizures and ischemic colitis;[17] as well as severe skin reactions known as recurrent pseudo-scarlatina, systemic contact dermatitis, and nonpigmenting fixed drug eruption.[18] Pseudoephedrine, particularly when combined with other drugs including narcotics, may also play a role in the precipitation of episodes of paranoid psychosis.[19] It has also been reported that pseudoephedrine, among other sympathomimetic agents, may be associated with the occurrence of stroke.[20]

Precautions and contraindications

Pseudoephedrine is contraindicated in patients with diabetes mellitus, cardiovascular disease, severe or uncontrolled hypertension, severe coronary artery disease, prostatic hypertrophy, hyperthyroidism, closed angle glaucoma, or by pregnant women.[17] The safety and effectiveness of nasal decongestant use in children is unclear.[21]

Interactions

Concomitant or recent (previous fourteen days) monoamine oxidase inhibitor use can lead to hypertensive reactions, including hypertensive crises.[17]

The antihypertensive effects of methyldopa, mecamylamine, reserpine and veratrum alkaloids may be reduced by sympathomimetics. Beta-adrenergic antagonists may also interact with sympathomimetics. Increase of ectopic pacemaker activity can occur when pseudoephedrine is used concomitantly with digitalis. Antacids increase the rate of pseudoephedrine absorption, while kaolin decreases it.

Common brand names

The following is a list of consumer medicines that either contain pseudoephedrine or have switched to an alternative such as phenylephrine.

Other uses

There have been reports of off-label uses of pseudoephedrine for its stimulant properties. Long-distance truck drivers and athletes, for example, have reportedly used pseudoephedrine as a stimulant to increase their state of alertness/awareness.

Manufacture of methamphetamine and methcathinone

Its membership in the amphetamine class has made pseudoephedrine a sought-after chemical precursor in the illicit manufacture of methamphetamine and methcathinone. As a result of the increasing regulatory restrictions on the sale and distribution of pseudoephedrine, many pharmaceutical firms have reformulated, or are in the process of reformulating medications to use alternative, but less effective,[22] decongestants, such as phenylephrine.

Many retailers in the US have created corporate policies restricting the sale of pseudoephedrine-containing products.[23][24] Their policies restrict sales by limiting purchase quantities and requiring a minimum age with proper identification. These requirements are similar to and sometimes more stringent than existing law. Internationally, pseudoephedrine is listed as a Table I precursor under the United Nations Convention Against Illicit Traffic in Narcotic Drugs and Psychotropic Substances.[25]

Sports

Pseudoephedrine was on the banned substances IOC list until 2004, when the World Anti-Doping Agency (WADA) list replaced the IOC list. Although WADA initially only monitored pseudoephedrine, it is once again on the banned list starting January 1, 2010.[26]

Pseudoephedrine is excreted through urine, and concentration in urine of this drug shows a large inter-individual spread; that is, the same dose can give a vast difference in urine concentration for different individuals.[27] Pseudoephedrine is approved to be taken up to 240 mg per day. In seven healthy male subjects this dose yielded a urine concentration range of 62.8 to 294.4 microgram per milliliter (µg/ml) with mean ± standard deviation 149 ± 72 µg/ml.[28] Thus, normal dosage of 240 mg pseudoephedrine per day can result in urine concentration levels exceeding the limit of 150 µg/ml set by WADA for about half of every user.[29] Furthermore, hydration status does not affect urinary concentration of pseudoephedrine.[30]

Canadian rower Silken Laumann was stripped of her 1995 Pan American Games team gold medal after testing positive for pseudoephedrine.[31]

In February 2000, Elena Berezhnaya and Anton Sikharulidze won gold at the 2000 Europeans but were stripped of their medals after Berezhnaya tested positive. This resulted in a three-month disqualification from the date of the test, and the medal being stripped.[32] She stated that she had taken cold medication approved by a doctor but had failed to inform the ISU as required.[33] The pair missed the World Championships that year as a result of the disqualification.

Romanian gymnast Andreea Răducan was stripped of her gold medal at the 2000 Sydney Olympics after testing positive. She took two pills given to her by the team coach for a cold. Although she was stripped of the overall gold medal, she kept her other medals, and, unlike in most other doping cases, was not banned from competing again; only the team doctor was banned for a number of years. Ion Ţiriac, the president of the Romanian Olympic Committee, resigned over the scandal.[34][35]

In the 2010 Vancouver Olympics, the IOC issued a reprimand against the Slovak ice hockey player Lubomir Visnovsky for usage of pseudoephedrine.[36]

In the 2014 Sochi Olympics the team Sweden and Washington Capitals ice hockey player Nicklas Bäckström was prevented from playing in the final for usage of pseudoephedrine. Bäckström claimed he was using it as allergy medication.[37] In March 2014, the IOC Disciplinary Commission decided that Bäckström would be awarded the silver medal.[38] In January 2015 Bäckström, the IOC, WADA and the IIHF agreed to a settlement in which he accepted a reprimand but was cleared of attempting to enhance his performance.[39]

Detection of use

Pseudoephedrine may be quantitated in blood, plasma or urine to monitor any possible performance-enhancing use by athletes, confirm a diagnosis of poisoning or assist in a medicolegal death investigation. Many commercial immunoassay screening tests directed at the amphetamines cross-react appreciably with pseudoephedrine, but chromatographic techniques can easily distinguish pseudoephedrine from other phenethylamine derivatives. Blood or plasma pseudoephedrine concentrations are typically in the 50–300 µg/l range in persons taking the drug therapeutically, 500–3000 µg/l in abusers or poisoned patients and 10–70 mg/l in cases of acute fatal overdosage.[40][41]

National legislation

Australia

A warning at an Australian pharmacy

Illicit diversion of pseudoephedrine in Australia has caused significant changes to the way the products are regulated. As of 2006, all products containing pseudoephedrine have been rescheduled as either "Pharmacist Only Medicines" (Schedule 3) or "Prescription Only Medicines" (Schedule 4), depending on the amount of pseudoephedrine in the product. A Pharmacist Only Medicine may only be sold to the public if a pharmacist is directly involved in the transaction. These medicines must be kept behind the counter, away from public access.

Pharmacists are also encouraged (and in some states required) to log purchases with the online database Project STOP.[42] This system aims to prevent individuals from purchasing small quantities of pseudoephedrine from many different pharmacies.

As a result, many pharmacies no longer stock Sudafed, the common brand of pseudoephedrine cold/sinus tablets, opting instead to sell Sudafed PE, a phenylephrine product which has not been proven effective in clinical trials.[22][43][44]

Canada

Health Canada has investigated the risks and benefits of pseudoephedrine and ephedrine/ephedra. Near the end of the study, Health Canada issued a warning on their website stating that those who are under the age of 12, or who have heart disease and may suffer from strokes, should avoid taking pseudoephedrine and ephedrine. Also, they warned that everyone should avoid taking ephedrine or pseudoephrine with other stimulants like caffeine. They also banned all products that contain both ephedrine (or pseudoephedrine) and caffeine.[45]

Products whose only medicinal ingredient is pseudoephedrine must be kept behind the pharmacy counter. Products containing pseudoephedrine along with other medicinal ingredients may be displayed on store shelves but may be sold only in a pharmacy when a pharmacist is present.[46][47]

Colombia

The Colombian government prohibited the trade of pseudoephedrine in 2010.[48]

Japan

Medications that contain more than 10% pseudoephedrine are prohibited under the Stimulants Control Law in Japan.[49]

Mexico

On November 23, 2007, the use and trade of pseudoephedrine in Mexico was made illicit, as it was argued that it was extremely popular as a precursor in the synthesis of methamphetamine.[50]

New Zealand

In New Zealand, pseudoephedrine is currently classified as a Class B Part II controlled drug in the Misuse of Drugs Act 1975, making it illegal to supply or possess except on prescription.[51][52].

Pseudoephedrine, ephedrine, and any product containing these substances, e.g. cold and flu medicines, were first classified in October 2004 as Class C Part III (partially exempted) controlled drugs, due to being the principal ingredient in methamphetamine.[53] New Zealand Customs and police officers continued to make large interceptions of precursor substances believed to be destined for methamphetamine production. On 9 October 2009, Prime Minister John Key announced pseudoephedrine-based cold and flu tablets would become prescription-only drugs and reclassified as a class B2 drug.[54] The law was amended by The Misuse of Drugs Amendment Bill 2010, which passed in August 2011.[55]

Turkey

In Turkey, medications containing pseudoephedrine are available with prescription only.[56]

United Kingdom

In the UK, pseudoephedrine is available over the counter under the supervision of a qualified pharmacist, or on prescription. In 2007, the MHRA reacted to concerns over diversion of ephedrine and pseudoephedrine for the illicit manufacture of methamphetamine by introducing voluntary restrictions limiting over the counter sales to one box containing no more than 720 mg of pseudoephedrine in total per transaction. These restrictions became law in April 2008.[57] However no form of ID is required.

United States

Federal

The United States Congress has recognized that pseudoephedrine is used in the illegal manufacture of methamphetamine. In 2005, the Committee on Education and the Workforce heard testimony concerning education programs and state legislation designed to curb this illegal practice.

Attempts to control the sale of the drug date back to 1986, when federal officials at the Drug Enforcement Administration (DEA) first drafted legislation, later proposed by Senator Bob Dole, R-KS, that would have placed a number of chemicals used in the manufacture of illicit drugs under the Controlled Substances Act. The bill would have required each transaction involving pseudoephedrine to be reported to the government, and federal approval of all imports and exports. Fearing this would limit legitimate use of the drug, lobbyists from over the counter drug manufacturing associations sought to stop this legislation from moving forward, and were successful in exempting from the regulations all chemicals that had been turned into a legal final product, such as Sudafed.[58]

Prior to the passage of the Combat Methamphetamine Epidemic Act of 2005, sales of the drug became increasingly regulated, as DEA regulators and pharmaceutical companies continued to fight for their respective positions. The DEA continued to make greater progress in their attempts to control pseudoephedrine as methamphetamine production skyrocketed, becoming a serious problem in the western United States. When purity dropped, so did the number of people in rehab and people admitted to emergency rooms with methamphetamine in their systems. However, this reduction in purity was usually short lived, as methamphetamine producers eventually found a way around the new regulations.[59]

Congress passed the Combat Methamphetamine Epidemic Act of 2005 ("CMEA") as an amendment to the renewal of the USA PATRIOT Act. Signed into law by president George W. Bush on March 6, 2006, the act amended 21 U.S.C. § 830, concerning the sale of pseudoephedrine-containing products. The law mandated two phases, the first needing to be implemented by April 8, 2006, and the second to be completed by September 30, 2006. The first phase dealt primarily with implementing the new buying restrictions based on amount, while the second phase encompassed the requirements of storage, employee training, and record keeping.[60] Though the law was mainly directed at pseudoephedrine products it also applies to all over-the-counter products containing ephedrine, pseudoephedrine, and phenylpropanolamine, their salts, optical isomers, and salts of optical isomers.[60] Pseudoephedrine was defined as a "scheduled listed chemical product" under 21 U.S.C. § 802(45(A)). The act included the following requirements for merchants ("regulated sellers") who sell such products:

In regards to the identification that may be used by an individual buying pseudoephedrine products the following constitute acceptable forms of identification:

State

Most states also have laws regulating pseudoephedrine.[61][62][63]

Alabama, Arizona, Arkansas, California, Colorado, Delaware, Florida, Georgia, Hawaii (as of May 1, 2009) Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana (as of August 15, 2009), Massachusetts, Michigan, Minnesota, Missouri, Montana, Nebraska,[64] Nevada, New Jersey, North Carolina, Ohio, Oklahoma, Pennsylvania, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia and Wisconsin have laws requiring pharmacies to sell pseudoephedrine "behind the counter". Though the drug can be purchased without a prescription, states can limit the number of units sold and can collect personal information from purchasers.[65]

Oregon and Mississippi require a prescription for the purchase of products containing pseudoephedrine.[66][67] Oregon reduced the number of methamphetamine lab seizures from 467 in 2004 (the final full year before implementation of the prescription only law)[68] to a new low of 12 in 2009.[69] However, the decrease in meth lab incidents in Oregon occurred largely before the prescription-only law took effect, according to a NAMSDL report titled Pseudoephedrine Prescription Laws in Oregon and Mississippi[70]. The report posits that the decline in meth lab incidents in both states may be due to other factors: "Mexican traffickers may have contributed to the decline in meth labs in Mississippi and Oregon (and surrounding states) as they were able to provide ample supply of equal or greater quality meth at competitive prices". Additionally, similar decreases in meth lab incidents were seen in surrounding states, according to the report, and meth-related deaths in Oregon have dramatically risen since 2007. Some municipalities in Missouri have enacted similar ordinances, including Washington,[71] Union,[72] New Haven,[73] Cape Girardeau[74] and Ozark.[75] Certain pharmacies in Terre Haute, Indiana do so as well.[76]

Another approach to controlling the drug on the state level which has been mandated by some state governments to control the purchases of their citizens is the use of electronic tracking systems, which require the electronic submission of specified purchaser information by all retailers who sell pseudoephedrine. 32 states now require the National Precursor Log Exchange (NPLEx) to be used for every pseudoephedrine and ephedrine OTC purchase, and ten of the eleven largest pharmacy chains in the US voluntarily contribute all of their similar transactions to NPLEx. These states have seen dramatic results in reducing the number of methamphetamine laboratory seizures. Prior to implementation of the system in Tennessee in 2005, methamphetamine laboratory seizures totaled 1,497 in 2004, but were reduced to 955 in 2005, and 589 in 2009.[69] Kentucky's program was implemented statewide in 2008, and since statewide implementation, the number of laboratory seizures has significantly decreased.[69] Oklahoma initially experienced success with their tracking system after implementation in 2006, as the number of seizures dropped in that year and again in 2007. However, in 2008, seizures began rising again, and have continued to rise in 2009.[69] However, when Oklahoma adopted NPLEx, their lab seizures also dropped significantly.

NPLEx appears to be successful by requiring the real-time submission of transactions, thereby enabling the relevant laws to be enforced at the point of sale. By creating a multi-state database and the ability to compare all transactions quickly, NPLEx enables pharmacies to deny purchases that would be illegal based on gram limits, age, or even to convicted meth offenders in some states. NPLEx also enforces the federal gram limits across state lines, which was impossible with state-operated systems. Access to the records is by law enforcement agencies only, through an online secure portal.[77]

See also

References

  1. 1 2 3 Laurence L Brunton, ed. (2006). Goodman & Gilman's The Pharmacological Basis of Therapeutics (11th ed.). New York: McGraw-Hill Medical Publishing Division. ISBN 0-07-142280-3.
  2. ↑ Hodges, K; Hancock, S; Currell, K; Hamilton, B; Jeukendrup, AE (February 2006). "Pseudoephedrine enhances performance in 1500-m runners". US National Library of Medicine National Institutes of Health. 38 (2): 329–33. PMID 16531903. doi:10.1249/01.mss.0000183201.79330.9c.
  3. ↑ Trinh, KV; Kim, J; Ritsma, A (15 November 2015). "Effect of Pseudoephedrine in Sport: a Systemic Review". BMJ Open Sport & Exercise Medicine. PMID 27900142. doi:10.1136/bmjsem-2015-000066.
  4. ↑ Popat N. Patil, A. Tye and J.B. LaPidus (1965). "A pharmacological study of the ephedrine isomers". JPET. 148 (2): 158–168. PMID 14301006.
  5. ↑ Martindale (1989). Edited by Reynolds JEF, ed. Martindale: The complete drug reference (29th ed.). London: Pharmaceutical Press. ISBN 0-85369-210-6.
  6. ↑ Proposed International Non-Proprietary Names (Prop. I.N.N.): List 11 WHO Chronicle, Vol. 15, No. 8, August 1961, pp. 314–20
  7. ↑ Oliver AL, Anderson BN, Roddick FA (1999). "Factors affecting the production of L-phenylacetylcarbinol by yeast: a case study". Adv. Microb. Physiol. Advances in Microbial Physiology. 41: 1–45. ISBN 978-0-12-027741-4. PMID 10500843. doi:10.1016/S0065-2911(08)60164-2.
  8. ↑ Suo, Steve. Clamp down on shipments of raw ingredients. The Oregonian; 6 October 2004. From a version reprinted on a U.S. congressional caucus website.
  9. 1 2 3 American Medical Association, AMA Department of Drugs (1977). AMA Drug Evaluations. PSG Publishing Co., Inc. p. 627.
  10. 1 2 Thomson/Micromedex (2007). Drug Information for the Health Care Professional, Volume 1,. Greenwood Village, CO. p. 2452.
  11. ↑ Drew, CD; Knight, GT; Hughes, DT; Bush, M (1978). "Comparison of the effects of D-(−)-ephedrine and L-(+)-pseudoephedrine on the cardiovascular and respiratory systems in man". British Journal of Clinical Pharmacology. 6 (3): 221–225. PMC 1429447 Freely accessible. PMID 687500. doi:10.1111/j.1365-2125.1978.tb04588.x.
  12. ↑ "American Urological Association - Medical Student Curriculum - Urinary Incontinence". American Urological Association. Retrieved 2015-08-12.
  13. ↑ "Acute urinary retention due to pseudoephedrine hydrochloride in a 3-year-old child". The Turkish Journal of Pediatrics. Retrieved 2015-08-12.
  14. ↑ Kiyoshi Minamizawa; et al. (2006). "Effect of d-Pseudoephedrine on Cough Reflex and Its Mode of Action in Guinea Pigs". Journal of Pharmacological Sciences. 102 (1): 136–142. PMID 16974066. doi:10.1254/jphs.FP0060526.
  15. 1 2 Bicopoulos D, editor. AusDI: Drug information for the healthcare professional, 2nd edition. Castle Hill: Pharmaceutical Care Information Services; 2002.
  16. ↑ "Selecting Medications for the Treatment of Urinary Incontinence – January 15, 2005 – American Family Physician". Aafp.org. Retrieved 2012-05-06.
  17. 1 2 3 Rossi S, editor. Australian Medicines Handbook 2006. Adelaide: Australian Medicines Handbook; 2006. ISBN 0-9757919-2-3
  18. ↑ Vidal C, Prieto A, Pérez-Carral C, Armisén M (April 1998). "Nonpigmenting fixed drug eruption due to pseudoephedrine". Ann. Allergy Asthma Immunol. 80 (4): 309–10. PMID 9564979. doi:10.1016/S1081-1206(10)62974-2.
  19. ↑ "Adco-Tussend". Home.intekom.com. 1993-03-15. Retrieved 2012-05-06.
  20. ↑ Cantu C, Arauz A, Murillo-Bonilla LM, López M, Barinagarrementeria F (July 2003). "Stroke associated with sympathomimetics contained in over-the-counter cough and cold drugs". Stroke. 34 (7): 1667–72. PMID 12791938. doi:10.1161/01.STR.0000075293.45936.FA.
  21. ↑ Deckx, Laura; De Sutter, An Im; Guo, Linda; Mir, Nabiel A.; van Driel, Mieke L. (17 October 2016). "Nasal decongestants in monotherapy for the common cold". The Cochrane Database of Systematic Reviews. 10: CD009612. PMID 27748955. doi:10.1002/14651858.CD009612.pub2.
  22. 1 2 Hatton RC, Winterstein AG, McKelvey RP, Shuster J, Hendeles L (2007). "Efficacy and safety of oral phenylephrine: systematic review and meta-analysis". Ann Pharmacother. 41 (3): 381–90. PMID 17264159. doi:10.1345/aph.1H679.
  23. ↑ "Pseudoephedrine Compliance". Walgreens. Retrieved 24 January 2016.
  24. ↑ "Target Announces That All Products Containing Pseudoephedrine Will Be Placed Behind Pharmacy Counter". PRNewswire. Retrieved 24 January 2016.
  25. ↑ "Microsoft Word - RedListE2007.doc" (PDF). Retrieved 2012-05-06.
  26. ↑ "WADA 2010 Prohibited List Now Published – World Anti-Doping Agency". Wada-ama.org. Retrieved 2012-05-06.
  27. ↑ "Elimination of ephedrines in urine following multiple dosing the consequences for athletes in relation to doping control". Retrieved 2014-02-24.
  28. ↑ Strano-Rossi, S.; Leone, D.; Torre, X. D. L.; Botrè, F. (2009). "The Relevance of the Urinary Concentration of Ephedrines in Anti-Doping Analysis: Determination of Pseudoephedrine, Cathine, and Ephedrine After Administration of Over-the-Counter Medicaments". Therapeutic Drug Monitoring. 31 (4): 520. doi:10.1097/FTD.0b013e3181ac6006.
  29. ↑ "Ressources" (PDF). Retrieved 18 August 2016.
  30. ↑ Jolley, Daniel; Science, School of Sport; Exercise; Health, and; Australia, University of Western; Crawley; Australia., Western; Dawson, Brian; Maloney, Shane K. "Hydration and Urinary Pseudoephedrine Levels After a Simulated Team Game". International Journal of Sport Nutrition and Exercise Metabolism. 24 (3): 325–332. doi:10.1123/ijsnem.2013-0076.
  31. ↑ "Silken tests positive". Retrieved 2014-02-24.
  32. ↑ Wallechinsky, David (2009). Complete Book of the Winter Olympics. Retrieved 9 July 2010.
  33. ↑ "2000 World Championships – Pairs". Ice Skating International. Retrieved 6 June 2010.
  34. ↑ "Summer Olympics 2000 Raducan tests positive for stimulant". Assets.espn.go.com. 2000-09-26. Retrieved 2012-05-06.
  35. ↑ "Amanar Tops Romanian Money List". International Gymnast Magazine Online. 15 October 2000. Archived from the original on 2001-07-15. Retrieved 2012-05-06.
  36. ↑ "IOC issues a reprimand against Slovakian ice hockey player". Retrieved 2014-02-24.
  37. ↑ "Sweden's Bäckström tests positive for banned substance". Retrieved 2014-02-24.
  38. ↑ "IOC Decision - Swedish ice hockey player Nicklas Backstrom to receive Sochi silver medal.". IOC. 14 March 2014. Retrieved 14 March 2014.
  39. ↑ Prewitt, Alex (15 January 2015). "Nicklas Backstrom’s Olympic doping appeal resolved with reprimand". The Washington Post. Retrieved 18 January 2015.
  40. ↑ Boland DM, Rein J, Lew EO, Hearn WL (2003). "Fatal cold medication intoxication in an infant". J Anal Toxicol. 27 (7): 523–6. PMID 14607011. doi:10.1093/jat/27.7.523.
  41. ↑ R. Baselt (2008). Disposition of Toxic Drugs and Chemicals in Man (8th ed.). Foster City, CA: Biomedical Publications. pp. 1344–1346.
  42. ↑ "Project STOP video – Online Advertising". Innovationrx.com.au. Retrieved 2012-05-06.
  43. ↑ Horak, F; Zieglmayer, P; Zieglmayer, R; Lemell, P; Yao, R; Staudinger, H; Danzig, M (2009). "A placebo-controlled study of the nasal decongestant effect of phenylephrine and pseudoephedrine in the Vienna Challenge Chamber". Annals of Allergy, Asthma & Immunology. 102 (2): 116–20. PMID 19230461. doi:10.1016/S1081-1206(10)60240-2.
  44. ↑ Eccles, R (2007). "Substitution of phenylephrine for pseudoephedrine as a nasal decongeststant. An illogical way to control methamphetamine abuse". British Journal of Clinical Pharmacology. 63 (1): 10–4. PMC 2000711 Freely accessible. PMID 17116124. doi:10.1111/j.1365-2125.2006.02833.x.
  45. ↑ http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2008/13279a-eng.php
  46. ↑ http://pharmacytechniciansletter.therapeuticresearch.com/mobile/Newsletter.aspx?nidchk=1&cs=&s=PTL&vo=1&dd=271114&dt=2&vodd=3
  47. ↑ "Family Health Online - Family Health Magazine -PHARMACY CARE - Over-the-Counter Medication - Why must I ask for that?". Retrieved 18 August 2016.
  48. ↑ "Gobierno prohĂbe antigripales con pseudoefedrina a partir de finales de 2010 – Archivo – Archivo Digital de Noticias de Colombia y el Mundo desde 1.990" [Government Prohibits Flu Pseudoephedrine in Late 2010 - Archive - News Archive Digital Colombia and the World since 1990] (in Spanish). Eltiempo.com. 8 July 2009 [Published 11 August 2009]. Retrieved 2012-05-06.
  49. ↑ "Customs Information". Consulate-General of Japan in Seattle. Retrieved August 27, 2015.
  50. ↑ "Prohibirán definitivamente uso de pseudoefedrina" [A Permanent Ban on Pseudoephedrine] (in Spanish). 23 November 2007 [Published 2 December 2007]. Retrieved 17 December 2013.
  51. ↑ "Controlled drugs". www.health.govt.nz. Retrieved 6 July 2017.
  52. ↑ "Misuse of Drugs Act 1975 No 116, Public Act 8 Exemptions from sections 6 and 7". www.legislation.govt.nz. 22 December 2016. Retrieved 6 July 2017.
  53. ↑ "Ephedrine and Pseudoephedrine to Become Controlled Drugs". Medsafe, New Zealand Medicines and Medical Devices Safety Authority. Archived from the original on 2007-03-08.
  54. ↑ "Chemical Brothers". Listener (New Zealand). Archived from the original on 2010-05-23.
  55. ↑ "Misuse of Drugs Amendment Bill". parliament.nz. Retrieved 6 July 2017.
  56. ↑ "Kontrole Tabi İlaçlar" (PDF). Social Security Institution of Republic of Turkey. July 2013.
  57. ↑ "Drug Safety Update, March 2008" (PDF). The Medicines and Healthcare products Regulatory Agency and the Commission on Human Medicines. 2008-06-30.
  58. ↑ "Search OregonLive.com". The Oregonian.
  59. ↑ "How Legislation Changed Meth Purity" (PDF). The Oregonian.
  60. 1 2 3 "DEA Interim Final Regulation: Ephedrine, Pseudoephedrine, and Phenylpropanolamine Requirements" (PDF). Archived from the original (PDF) on 2006-10-18.
  61. ↑ "State Ephedrine and Pseudoephedrine Single Over-The-Counter Transaction Limits". www.namsdl.org. National Alliance for Model State Drug Laws (NAMSDL). 2013. Archived from the original (PDF) on April 16, 2016. Retrieved December 3, 2016.
  62. ↑ "State Daily Gram Limits for Over-The-Counter Transactions Involving Ephedrine and Pseudoephedrine". www.namsdl.org. National Alliance for Model State Drug Laws (NAMSDL). 2013. Archived from the original (PDF) on August 14, 2016. Retrieved December 3, 2016.
  63. ↑ "State 30 Day Gram Limits for Over-The-Counter Transactions Involving Ephedrine and Pseudoephedrine". www.namsdl.org. National Alliance for Model State Drug Laws (NAMSDL). 2013. Archived from the original (PDF) on August 15, 2016. Retrieved December 3, 2016.
  64. ↑ "Nebraskans to sign for Sudafed". Lincoln Journal-Star. 13 Mar 2006. Retrieved 20 Aug 2012.
  65. ↑ "The National Alliance for Model State Drug Laws (NAMSDL) - Issues and Events". www.namsdl.org. Retrieved 2015-10-24.
  66. ↑ "MS Senate passes bill to restrict pseudoephedrine sales". Associated Content. WLOX. February 2, 2010. Retrieved May 8, 2010.
  67. ↑ Bovett, Rob (November 15, 2010). "How to Kill the Meth Monster". The New York Times. Retrieved November 16, 2010.
  68. ↑ http://www.leg.state.or.us/cgi-bin/searchMeas.pl
  69. 1 2 3 4 "DEA, Maps of Methamphetamine Lab Incidents". Justice.gov. Retrieved 2012-05-06.
  70. ↑ "The National Alliance for Model State Drug Laws (NAMSDL) - Issues and Events". www.namsdl.org. Retrieved 2015-10-24.
  71. ↑ "Council Passes Law Restricting Pseudoephedrine". The Washington Missourian. July 7, 2009. Retrieved December 10, 2010.
  72. ↑ "Union Board Approves Pseudoephedrine Ordinance". The Washington Missourian. October 13, 2009. Retrieved December 10, 2010.
  73. ↑ "New Haven Passes Prescription Law". The Washington Missourian. November 11, 2010. Retrieved December 10, 2010.
  74. ↑ "Cape Girardeau City Council passes prescription requirement for pseudoephedrine". The Southeast Missourian. December 7, 2010. Retrieved December 10, 2010.
  75. ↑ "Ozark passes pseudoephedrine ban: Drug now prescription-only". CCHeadliner.com. June 18, 2013. Retrieved December 17, 2013. (Subscription required (help)).
  76. ↑ Trigg, Lisa (May 20, 2010). "Four Valley pharmacies to require prescriptions for certain products to help fight meth problem". Terre Haute Tribune-Star. (Subscription required, free access for first 30 days)
  77. ↑ "NPLEx - National Precursor Log Exchange". www.nplexservice.com. Retrieved 2015-10-24.
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