Cinnamon – Cinnamomi cortex (Cinnamomum verum J. S. Presl, (Cinnamomum zeylanicum Nees))
|Latin name of the genus:||Cinnamomi cortex|
|Latin name of herbal substance:||Cinnamomum verum j. s. presl|
|Botanical name of plant:||Cinnamon|
|English common name of herbal substance:||(cinnamomum zeylanicum nees)|
Latin name of the genus: Cinnamomi cortex
Botanical name of plant: Cinnamomum verum J. S. Presl, (Cinnamomum zeylanicum Nees)
English common name of herbal substance: Cinnamon
2.2.Information on traditional/current indications and specified substances/preparations . 10
2.3.Specified strength/posology/route of administration/duration of use for relevant
1.1. Description of the herbal substance(s), herbal preparation(s) or combinations thereof
1.Cinnamomum verum J. S. Presl. (=Cinnamomum zeylanicum Nees), dried bark, freed from the outer cork and the underlying parenchyma (ESCOP, 2003; European Pharmacopoeia 6.2, 2009).
2.Cinnamomum verum J. S. Presl. is also known by the synonym Cinnamomum zeylanicum Blume and is member of Lauraceae family (Keller et al., 1992).
This assessment report does not evaluate Cinnamomum aromaticum Nees (synonym: Cinnamomum cassia Blume), cortex although they are both comparable in composition and widely used in flavouring agents in foods and in pharmaceutical and cosmetic preparations (Kommission E, 1990; Barnes et al., 2007).
The drug consists of the dried bark, freed from the outer cork and the underlying parenchyma, of the shoots grown cut stock of Cinnamomum verum J. S. Presl. The matt pieces of bark,
Cinnamon bark contains up to 4% of essential oil consisting primarily of cinnamaldehyde
Other constituents are oligopolymeric procyanidins, cinnamic acid, phenolic acids, pentacyclic diterpenes cinnzeylanol and it’s acetyl derivative cinnzeylanine and the sugars mannitol,
The essential oil of the bark is described in the European Pharmacopoeia (6.2, 2009).
There exists a summary report on the essential oil of cinnamon bark by the Committee for Veterinary Medicinal Products. According to this information, the oil mainly contains cinnamaldehyde
Cinnamon bark oil may be adulterated with cinnamon leaf oil and oil of cassia (Price & Price, 2007).
Figure 1: cinnamaldehyde
Figure 2: eugenol
a)Comminuted herbal substance
b)Liquid extract (DER 1:1) extraction solvent: 70% ethanol
c)Tincture (ratio of herbal substance to extraction solvent 1:5) extraction solvent: 70% ethanol
d)Essential oil obtained by steam distillation from the cortex
Combinations of herbal substance(s) and/or herbal preparation(s) including a description of vitamin(s) and/or mineral(s) as ingredients of traditional combination herbal medicinal products assessed, where applicable.
See section 1.2 ‘Information about products on the market in the Member States’
The drug contains per 100 g:
–vitamin A: 260 IU
–thiamine: 0.02 mg
–riboflavin: 0.14 mg
–niacin: 1.3 mg
–ascorbic acid: 28 mg
The drug contains per 100 g:
–Ca: 1.228 mg
–P: 61 mg
–Fe: 38 mg
–Mg: 56 mg
–Na: 26 mg
–K: 500 mg
–Zn: 2 mg
1.2. Information about products on the market in the Member States
Regulatory status overview
MA: Marketing Authorisation TRAD: Traditional Use Registration
Other TRAD: Other national Traditional systems of registration
This regulatory overview is not legally binding and does not necessarily reflect the legal status of the products in the MSs concerned.
Specific information about preparations in the EU
several liquid extracts of the drug in combination products for gastrointestinal complaints or as a flavouring excipient
solution for oral or external use containing extracts from Melissae folium, Inulae radix, Angelicae radix, Zingiberis radix, Caryophylli flos, Galangae radix, Piperis nigri fructus, Gentianae radix, Myristicae semen, Aurantii pericarpium, Cinnamomi cortex, Cassiae flos, Cardamomi fructus
Cinnamon is one of the 13 ingredients of a solution for oral or external use (see above).
the same combination preparation as mentioned above
the same combination preparation as mentioned above and Cinnamomi aetheroleum in a nother product
combined preparation containing Melissae aetheroleum, Caryophylli aetheroleum, Cinnamoni aetheroleum, Citri limoni aetheroleum, Menthae piperitae aetheroleum, Lavandulae aetheroleum and menthol in ethanol
1.3. Search and assessment methodology
Basic sources searched for Cinnamomum verum and Cinnamomum zeylanicum
Barnes J, Anderson LA, Philipson JD. Herbal medicines. 3rd edition. Pharmaceutical press; 2007
Bisset NG. Cinnamomi cortex. In: Herbal drugs and phytopharmaceuticals. Medpharm Scientific Pulishers, Stuttgart; 1994
Delfosse M. Drogues végétales plants médicinales. Service Scientifique de l’Association Pharmaceutique Belge; 1998
Duke JA. Cinnamomum verum. In: Handbook of medicinal herbs. CRC Press; 1988
E/S/C/O/P Monographs. The scientific foundation for herbal medicinal products. 2nd ed. Thieme, 2003
European Pharmacopoeia 6.0. Cinnamon. 2009
European Pharmacopoeia 6.2. Cinnamon bark oil, Ceylon. 2009
Hänsel R, Keller K, Rimpler H, Schneider G. editors. Cinnamomi cortex. In: Hagers Handbuch der Pharmazeutischen Praxis. Berlin.
Keller K, Hänsel R, Chandler RF. Adverse Effects of Herbal Drugs: Cinnamomum species. Volume 1 by P.A.G.M. De Smet. Springer Verlag, Heidelberg 1992
Kommission E. Cinnamoni ceylanici cortex. Deutscher Apotheker Verlag; 1990
Madaus: http://www.henriettesherbal.com/eclectic/madaus/cinnamomum.html 1938
Price S, Price L. Aromatherapy for health professionals. 3rd edition. Churchill Livingstone Elsevier; 2007
Todd G. Extra Pharmacopoeia Martindale. The Pharmaceutical Press, London 1967
WHO monographs on selected medicinal plants. volume1. World health Organisation Geneva; 1999
EMA documents retrieved
CVMP Committee for Veterinary Medicinal Products. Cinnamomi ceylanici cortex. Summary report. The European Agency for the Evaluation of Medicinal Products. Evaluation of Medicines For Veterinary Use.
Search in databases:
International Pharmaceutical Abstracts
Keywords: cinnamomum, cinnamon, cinnamomum verum cinnamomum zeylanicum alone or combined with volatile oil, essential oil, cortex, bark.
2. Historical data on medicinal use
2.1. Information on period of medicinal use in the Community
Cinnamon has been used as a spice for thousands of years. In Egypt, cinnamon was a spice used in embalming fluids. In Ayurvedic medicine, cinnamon bark was used as an antiemetic, antidiarrheal, antiflatulent and as a general stimulant. The Portuguese found cinnamon trees growing in Sri Lanka (Ceylon) in the early 16th century; they subsequently imported cinnamon to Europe during the 16th and 17th centuries. The Dutch occupied Sri Lanka in the
Cinnamon belongs to the herbal substances with one of the longest medicinal traditions. It has been mentioned in the Bible, as well as by Greek and Roman literature (amongst others Theophrast, Herodot, Dioskurides, Galenus and Plinius). There is however no real reference to Ceylon as its original source. Dioskorides described 5 cassia and 7 cinnamon species. The latter ones were reported as possessing diuretic and digestive properties. From the 8th century, cinnamon was introduced in Europe as an expensive spice that only could be used by kings and popes. There is a written report on the use of cinnamon in an Arabian source from around 1275. In 1310, Johannes of Montevino confirmed the existence of cinnamon trees in Ceylon. About 100 years later, Nicolo Conit provided a real description of the cinnamon tree.
Introduced by the Portuguese, cinnamon of Ceylon remained the preferential substance in Europe. It has been described, that in 1536 cinnamon of Ceylon would have cost 40 times more than the cinnamon from Java or the Philippines. The herbal substance was first collected from wild growing trees. The cultivation of cinnamon started around 1765, when Holland took the lead in the source area. The production was streamlined in the way that a better quality was obtained and Holland could provide enough cinnamon to cover the European needs. When the English took over in 1796, the cinnamon cultivation and trading became a monopoly of the English
Cinnamon oil has been reported as an herbal medicine in case of nerve sensitivity. Higher doses were used to stimulate the cardiovascular system, nerves and muscles, more particularly the uterus. Higher doses could have an abortive effect and could lead to methaemoglobinaemia and nephritis. The oil should also have an antibacterial activity against typhus (Madaus, 1938).
More recent and current use in the Community
See sections 1.2, 2.2 and 2.3
2.2. Information on traditional/current indications and specified substances/preparations
When going back in history, cinnamon was used as stomachic and in case of nerve weakness. As the gastrointestinal use is concerned, cinnamon was used in case of diarrhoeia, dyspepsia, hyperacidity with reflux, vomiting and bloating (Madaus, 1938).
Posologies suggested by Madaus (1938):
Herbal substance: 0.62
Tincture (without specification):
Maximal daily doses are not specified.
The herbal preparations are in traditional medicinal use for over 30 years (Wahrig & Richter, 2009).
The following indications have been reported for cinnamon:
Dyspeptic complaints such as gastrointestinal spasms, bloating and flatulence, loss of appetite and diarrhoea (ESCOP, 2003; BHP, 1983; Bradley, 2006).
Cinnamon is used primarily as a taste enhancer and as a spice, and to some extent also in preparation of liquors.
Indications in folk medicine: diarrhoea, dyspeptic complaints, cold and flu, topical use for wound- cleaning. Except for diarrhoea and dyspeptic complaints, the indications in folk medicine have not been sufficiently documented (Hänsel et al., 1992). The essential oil is used
Another source lists the following indications: application as an astringent, germicide, and antispasmodic. Cinnamon was one of the early treatments for chronic bronchitis, treatment of impotence, frigidity, dyspnea, inflammation of the eye, leukorrhea, vaginitis, rheumatism, and neuralgia, as well as wounds and toothaches (Barceloux, 2009).
Indications for combination preparations:
Czech Republic, Estonia and Lithuania:
solution for oral use as an adjuvant at mild psychovegetative disturbances such as loss of appetite and gastrointestinal complaints, mood changes and headache of different origin, nervosity, restlessness, sleep disorders and as an adjuvant in common cold; externally used as mild remedy in neuritis, muscle pains, lumbago and gingivitis
2.3. Specified strength/posology/route of administration/duration of use for relevant preparations and indications
Posology and method of administration
spiritus: (1 part of oil in 10 of ethanol 90%) 0.3 to 1.2 ml daily, to be given in 3 doses (Todd, 1967) All preparations are orally administered.
Elderly: the same dose as for adults
Method of administration
If the symptoms persist during the use of the medicinal product, a doctor or a qualified health care practitioner should be consulted (Barnes et al., 2007; ESCOP, 2003; Kommission E, 1990).
3.1. Overview of available pharmacological data regarding the herbal substance(s), herbal preparation(s) and relevant constituents thereof
In vitro tests
A foam generator was used as a model of flatulence for generating and assessing foams in digestive fluids in vitro. The effects of volatile oils, including cinnamon oil on gastric and intestinal foams were examined. Reductions in the foam volume were observed in every case, although the effects were not as high as those produced by a combination of dimethicone and silica.
The antifungal activities are mainly contributed to the essential oil (in concentrations ranging from 1% to 0.0025 %) and its active compound cinnamaldehyde inhibiting the growth of fungi and yeasts as well as their mycotoxin production: e.g. Aspergillus clavus, A. niger, A. parasiticus, Candida albicans
(Kalemba & Kunicka, 2003). Cinnamon bark oil also inhibits the growth of several dermatophytes. The inhibitory zone induced by cinnamon bark oil in solid media was 28 mm in diameter, comparable to the
The essential oil was screened against four
The antimicrobial activity against the
Various essential oils, including cinnamon bark oil, used in the treatment of rheumatism and inflammation as well as some of their main constituents and phenolic compounds known for their irritant and pungent properties were screened for activity as inhibitors of prostaglandin biosynthesis. A combination of a
Effects on human spermatozoa:
The effect of cinnamon oil on human spermatozoa in vitro was studied. Fresh ejaculates were obtained from male partners of infertile couples. Cinnamon bark oil showed a spermicidal effect with a minimum concentration of 1:400 V/V. The percentage change in motility over control was calculated. The spermicidal action was confirmed by a
Petroleum ether (25:1) and chloroform (68:1) extracts of cinnamon exhibited cytotoxic effects with respective ED50 values of 60 and 58 µg/ml in human cancer (KB) cells and 24 and 20 µg/ml in mouse leukemia L1210 cells (Chulasiri et al., 1984).
Cinnamaldehyde, also cytotoxic to rat hepatocytes, is the reactive cinnamyl species, since this compound is the most potent intracellular glutathione (GSH) depletor and exhibits the highest cytotoxicity in hepatocyte suspensions with a threshold cytotoxic concentration of
In vivo tests
Spasmolytic and cardiovascular activity:
Effects of cinnamaldehyde on the cardiovascular and digestive systems were examined. A papaverine- like muscolotropic activity of cinnamaldehyde seemed to be involved in the vasodilatation. Cinnamaldehyde, administered intravenously at 5 and 10 mg/kg body weight, moderately inhibited both the rat stomach movement and the mouse intestinal propulsion and had a stimulating effect on the cardiovascular system. Concentrations of
Other studies have shown that cinnamaldehyde is an inhibitor of stomach peristalsis in anaesthetised rats
Dry ethanolic extract of Cinnamomum zeylanicum administered orally to mice at 200 and 400 mg/kg body weight exhibited analgesic effects on the hot plate thermal stimulation and the acetic acid induced writhing tests in a dose dependent manner (Atta & Alkofahi, 1998).
Dry ethanolic extract of Cinnamomum zeylanicum administered orally to rats at 400 mg/kg body weight showed an
3.2. Overview of available pharmacokinetic data regarding the herbal substance(s), herbal preparation(s) and relevant constituents thereof
After application of cinnamaldehyde to rats, benzoic acid and cinnamic acid were found in urine samples (Hänsel et al., 1992).
The pharmacokinetics of cinnamic acid (CA) after oral administration of a decoction of Ramulus Cinnamomi (RC) 7.4 g/kg [containing CA
3.3. Overview of available toxicological data regarding the herbal substance(s)/herbal preparation(s) and constituents thereof
The oral LD50 of cinnamon bark oil in rats has been determined as 4.16 g/kg and 3.4 ml/kg body weight. For cinnamaldehyde the oral LD 50 in rats is 2.22 g/kg body weight. The dermal LD50 of cinnamon bark oil in rabbits has been reported as 0.69 ml/kg and 0.59 mg/kg for cinnamaldehyde. The undiluted oil was severely irritating to the intact skin of rabbits and mildly irritating when applied to the backs of hairless mice; however, when tested at 8% in petrolatum it produced no irritation in 25 human subjects (ESCOP, 2003).
The acceptable daily intake of cinnamaldehyde was set to 700 µg/kg of body weight by the Joint FAO/WHO Expert Committee on Food Additives (JECFA). It was not extended because of inadequate toxicity data. The ADI of eugenol is up to 2.5 mg/kg (CVMP, 2000). Cinnamaldehyde added to the diet of sprague dawley rats for 16 weeks at 10 g/kg resulted in slight swelling of hepatic cells and slight hyperkeratosis of the squamous portion of the stomach; the
Mutagenicity and genotoxitcity:
Cinnamon extracts, cinnamon bark oil and cinnamaldehyde showed no mutagenic potential in several studies using the Ames test. The Ames Salmonella reversion assay was negative for cinnamaldehyde (Sekizawa & Shibamoto, 1982).
On the other hand, other studies, also using the Ames test, have shown mutagenic activity of cinnamon compounds. Cinnamon bark oil and cinnamaldehyde gave positive results in chromosomal aberration tests using Chinese hamster cell cultures as substrate (Ishidate et al., 1984). Positive results in the Ames test were also obtained for alcoholic extracts of cinnamon (Keller et al., 1992).
Cinnamaldehyde and cinnamyl alcohol were positive in the Bacillus subtilis
In the Bacillis subtilis DNA repair test
Cinnamon oil and cinnamaldehyde gave positive results in the chromosomal aberration tests using Chinese hamster cell cultures (Keller et al., 1992). Cinnamaldehyde showed genotoxic effects in Drosophila test systems. In another study an aqueous extract of cinnamon gave a negative result in a similar Drosophila test system (ESCOP, 2003; Keller et al., 1992).
The results of the in vitro bacterial mutagenicity tests must be interpreted with caution because the concentrations used were within the dose range where antimicrobial effects of cinnamaldehyde and cinnamon oil have been proven. Furthermore, growth retardation due to antimicrobial effect is the reason for the reported ‘antimutagenic’ effect of cinnamaldehyde (Keller et al., 1992).
Concentrations of 50, 100, 200, 300, 500, 1000 and 2000 μ/ml of the essential oil of Cinnamomum verum were tested in Salmonella typhymurium strains TA100 with and without rat liver S9 using the Ames Salmonella reversion assay. Results: without S9 fraction, increase in mutant colonies per plate was not observed with any of the used concentrations. Also with the S9 fraction none of the samples caused a significant increase in mutant colonies per plate (Shoeibi et al., 2009).
According to Keller et al. (1992) unspecific cytotoxic effects in vitro are strongly influenced by the culture medium and other experimental conditions. On the other hand, cinnamaldehyde inhibits thioredoxin reductase and can be considered as a candidate for cancer therapy and chemoprevention (see earlier Chew et al., 2009).
Cinnamaldehyde was reported to exhibit teratogenic effects in chick embryos. The teratogenic dose was closely related to the toxic dose of cinnamaldehyde (0.5 mmol/embryo) with 58.2% malformations and 49 % lethality. However, a methanol extract of cinnamon given by gastric intubation was not teratogenic in rats (ESCOP, 2003).
3.4. Overall conclusions on
The in vitro and in vivo tests on the spasmolytic activity of cinnamon bark oil and cinnamaldehyde show clear relaxant effect on the tracheal and ileal smooth muscles. The
The essential oil has antimicrobial activity. It can inhibit the growth of fungi and yeasts like Aspergillus and Candida, including their mycotoxin production. Also the inhibition of dermatophytes has been observed. Inhibitory activity against aflatoxinogenesis is more pronounced than the inhibition of mycelial growth. Cinnamon oil also exhibited inhibitory activity towards both
The in vivo experiments on
In general, the pharmacological effects and the antimicrobial activity described are obtained with high concentrations of cinnamon oil. They partially support the traditional indication but they cannot support a
In vivo data on pharmacokinetics are available on cinnamic acid in cinnamon bark decoction as compared to pure cinnamic acid (Chen et al., 2009). The oral bioavailability of cinnamic acid was higher when administered as the decoction. Cinnamaldehyde seems to be highly susceptible to oxidation. Pharmacokinetic data on the essential oil are absent.
Cinnamon oil contains cinnamaldehyde which is an irritating and sensitizing component that could be the cause of dermatitis. Most of the available data are related to cinnamaldehyde. When using the essential oil or extracts of cinnamon, the results are mostly negative. This makes data on mutagenicity of cinnamon rather contradictory and further investigation as to the beneficial role of the natural matrix is required. Investigations on mutagenicity and genotoxicity are insufficient to fully evaluate the carcinogenic risk of cinnamon. The data on teratogenicity are considered to be of limited value for the risk assessment for use by humans (WHO Monographs, 1999).
In summary, the data on toxicity are insufficient. Therefore a list entry cannot be recommended.
4. Clinical Data
4.1. Clinical Pharmacology
4.1.1. Overview of pharmacodynamic data regarding the herbal substance(s)/preparation(s) including data on relevant constituents
A small scale clinical study by Khan et al. (2003) included 60 patients with type 2 diabetes, randomly divided into groups. As medication capsules contained Cinnamomum cassia 1.3 or 6 g daily (part of the plant not specified). The capsules were given as an
glucose, triglyceride, total cholesterol, HDL cholesterol, and LDL cholesterol levels were measured. After 40 days, all the three levels of cinnamon reduced the mean fasting serum glucose
An aqueous purified extract of Cinnamomum cassia (plant part not specified) was administered to 79 diabetes mellitus type 2 patients three times daily for 4 months. The amount of aqueous cinnamon extract corresponded to 3 g of cinnamon powder daily. There was a higher reduction of fasting plasma glucose level (10.3%) in the cinnamon group than in the placebo group (3.4%). No significant differences were observed regarding glycated haemoglobin (HbA1c), lipid profiles or differences between the pre- and
The influence of Cinnamomum cassia on glucose homeostasis was investigated in 7 lean healthy volunteers (26 + 1 years; BMI 24.5 + 0.3). They underwent an oral glucose tolerance test (OGTT) supplemented with either placebo or 5 g powdered Cinnamomum cassia (most probably bark powder). The cinnamon ingestion reduced total plasma glucose response (AUC) to 75 g glucose orally ingested. When ingested with the glucose, cinnamon reduced the plasma response to glucose with 13%; when ingested 12 hours prior to glucose, this reduction was 10% (both p<0.05). This study proves an immediate and long lasting (12 hours) effect of Cinnamom cassia on glucose in plasma (Solomon & Blannin, 2007).
Eight male volunteers (aged 25 ± 1 years, body mass 76.5 ± 3.0 kg, BMI 24.0 ± 0.7 kg/m²; mean ± SEM) underwent two
A limited number of subjects (N = 22) with impaired fasting blood glucose and a BMI ranging from 25 to 45 were enrolled in a
Plasma malondialdehyde (MDA) concentrations were assessed using high performance liquid chromatography and plasma antioxidant status was evaluated using ferric reducing antioxidant power (FRAP) assay. Erythrocyte
FRAP and plasma thiol (SH) groups increased, while plasma MDA levels decreased in subjects receiving the cinnamon extract. The effects were more pronounced after 12 than 6 weeks. There was also a positive correlation (r = 0.74; p = 0.014) between MDA and plasma glucose. This study supports the hypothesis that the inclusion of water soluble compounds of Cinnamomum cassia reduces risk factors associated with diabetes and cardiovascular disease (Roussel et al., 2009).
Rudowska (2009) made an overview of studies done with Cinnamomum cassia to influence blood glucose. They consider the herbal preparation as a functional food. According to the author, fasting
blood glucose seems to be reduced by cinnamon supplements in men and women with the metabolic syndrome. Also a high dose (6 g/d) of cinnamon with a rice pudding reduces postprandial blood glucose and delays gastric emptying without affecting satiety.
However, other studies could not replicate these findings. Cinnamon supplementation (1.5 g/d) did not improve
22.214.171.124. Overall conclusions on pharmacodynamics
Clinical pharmacological data of Cinnamomum verum preparations do not exist. The plausibility of the efficacy is based on the traditional medicinal use and supported by the
Recent studies with a different Cinnamomum species, C. cassia, showed a hypoglycemic effect (Khan et al., 2003; Mang et al., 2006). The studies are not related to C. verum.
General data on the base of other plant species cannot be considered. From the traditional use of C. verum no clinical hypoglycaemic effects are reported.
4.1.2. Overview of pharmacokinetic data regarding the herbal substance(s)/preparation(s) including data on relevant constituents
No data available.
126.96.36.199. Overall conclusions on pharmacokinetics
Clinical data on absorption, distribution and pharmacokinetic interactions are not available.
4.2. Clinical Efficacy
4.2.1. Dose response studies
Not data available.
4.2.2. Clinical studies (case studies and clinical trials)
Data only available for Cinnamomum cassia (see 4.1.1).
4.2.3. Clinical studies in special populations (e.g. elderly and children)
Not data available.
4.3. Overall conclusions on clinical pharmacology and efficacy
Currently there’s no data available on clinical efficacy.
5. Clinical Safety/Pharmacovigilance
5.1. Overview of toxicological/safety data from clinical trials in humans
No data available.
5.2. Patient exposure
No data available.
5.3. Adverse events and serious adverse events and deaths
Cinnamon bark oil
Undiluted cinnamon bark oil was mildly irritating when applied to the backs of hairless mice and strongly irritating under occlusion to both intact and abraded rabbit skin.
The preparation of 8% in petrolatum did not cause irritation but gave sensitization reactions in humans. Also cases of contact sensitivity to a dentifrice containing the oil have been reported.
It is recommendable to avoid the use of the oil per os in liver conditions, alcoholism and when taking paracetamol because of the glutathione depleting action of cinnamaldehyde (Price & Price, 2007). Cinnamaldehyde, one of the components of the essential oil, 5% in petrolatum is a skin irritant. Cinnamon oil caused
Extensive reporting on side effects of cinnamon is done by Barceloux (2009). Most case reports of toxicity from the cinnamon oil involve local irritation and allergic reactions to the cinnamon oil as a constituent of a personal hygiene (toilet soaps, mouthwash, toothpaste, perfumes, mud baths), beverages (colas, vermouth, bitters), or baking products. Allergic reactions include contact dermatitis, perioral dermatitis, cheilitis, stomatitis, gingivitis, glossitis, chronic lichenoid mucositis, contact urticaria, 24 and rarely immediate hypersensitivity reactions (asthma, urticaria). Clinical manifestations of intraoral reactions include pain, swelling, erythema, ulcerations, fissures, vesicles, and white patches. These reactions are local, and distal skin involvement is rare. Occupational allergic contact dermatitis from spices is rare, and typically involves the hands. More common food sensitizers include carrot, cucumber, tomato, melon, fish, potato, orange, green pepper, onion, red cherry, and garlic. Cinnamon oil contains local mucous membrane irritants such as cinnamaldehyde and cinnamic acid.
Prolonged skin contact (48 hours) from a cinnamon oil spill produced superficial
The severity of the local mucosal reaction depends on the duration of
5.3.1. Serious adverse events and deaths
Severe reactions such as anaphylaxis have not been reported. All cases with side effects recovered when the cinnamon containing preparation was withdrawn. Nevertheless, preparations with more than 0.01% cinnamaldehyde are suspect according to Keller et al. (1992).
5.4. Laboratory findings
No data available.
5.5. Safety in special populations and situations
Patients with an allergy to cinnamon or Peru balsam are contra medicated (WHO monographs, 1999). Cinnamon bark oil must be regarded as a potential sensitizer on the skin. It should not be used on young children and elderly people. Because of the experimentally demonstrated glutathione depleting activity of cinnamaldehyde, it is recommendable to avoid administering cinnamon bark oil per os to patients suffering from liver conditions, in case of alcoholism and when taking paracetamol (Price & Price, 2007).
5.6. Intrinsic (including elderly and children) /extrinsic factors
No special studies about the use in children or elderly exist.
5.7. Drug interactions
No drug interactions are mentioned for Cinnamomum zeylanicum.
Cinnamomum cassia bark (2 g in 100 ml) markedly retarded the in vitro dissolution of tetracycline. HCl from gelatine capsules: only 20% dissolved within 30 minutes in contrast to 97% when only water was used. The effect was attributed to the adsorption of the antibiotic on the particles. There are no further investigations to establish which individual constituents of cassia bark (volatile oil, cinnamaldehyde or mucilage) are responsible for this effect. As a dose of 1 to 2 g cinnamon is not uncommon, it is recommended not to use tetracyclines together with cinnamon at that dose level (Keller et al., 1992).
5.8. Use in pregnancy and lactation
Only limited data are available. The data are not sufficient for an adequate benefit/risk assessment. In accordance with general medicinal practice, Cinnamomi cortex products should not be used during pregnancy and lactation (WHO monographs, 1999).
Cinnamon was used in antiquity and the middle ages as abortifacient. It must be taken into account that in old sources cinnamon (cassia) was confused with Cassia fistulosa which contains anthraquinone (Keller et al., 1992).
An unspecified ‘large amount of cinnamon’ was reported to have caused methemoglobinemia, hematuria, albuminuria and cylindruria in pregnant women. Abortion was not reported. The daily intake of 100 drops of a non specified tincture of cinnamon did not result in abortion (Keller et al., 1992).
Cinnamon bark oil and cinnamaldehyde in doses over 0.2 g/day (equivalent to
A case report of massive ingestion of 60 ml cinnammon oil has been published. The patient, a 7.5-
5.10. Drug abuse
Cases of cinnamon oil abuse were documented in adolescents and children. Sucking on toothpicks or fingers which had been dipped in cinnamon oil was the primary method of abuse. The subjects experienced a rush or sensation of warmth, facial flushing, and oral burning. Some children complained of nausea or abdominal pain but no systemic effects were reported (Perry et al., 1990).
5.11. Withdrawal and rebound
5.12. Effects on ability to drive or operate machinery or impairment of mental ability
5.13. Overall conclusions on clinical safety
The efficacy of Cinnamomum verum is plausible on the basis of long standing use and experience. The traditional use over a long period has shown that C. verum is not harmful when used in the specified conditions. However, a long standing excessive use does not exclude concerns with regard to the product safety. Therefore C. verum should not be used during pregnancy and lactation, in cases of fever of unknown origin, stomach or duodenal ulcers, and in patients with an allergy to cinnamon or Peru balsam. No drug interactions are documented. There is no restriction to the duration of use of the herbal substance.
6. Overall conclusions
Despite of their long tradition, the bark and the essential oil of Cinnamomum verum do not fulfil the requirements of a
The herbal substance or the dried bark of Cinnamomum verum is described in the European Pharmacopoeia. Quality relates to its content of essential oil. There are no cases of contamination or adulteration mentioned in the literature. The odour of the herbal substance can be considered as an important tool in the identification process.
Conclusion: analytical assessment of the quality of Cinnamomum should be made and the
Cinnamon has been used in Europe since the 13th century. Patients with liver pathology should avoid taking cinnamon because there may be a glutathione depleting action of cinnamaldehyde. No serious adverse effects have been reported. Ingestion of supratherapeutic amounts of cinnamon oil (equivalent to 15 to 20 g bark) can lead to
Abuse of the cinnamon oil has been described. Most of the cases reported up to now are not in a
Cinnamaldehyde and other cinnamon compounds were mutagenic in the Ames test and the chromosome aberration test. Cinnamaldehyde was genotoxic in the Drosophila test system. Tests with the isolated compounds, however, are of limited value for the possible risks with the herbal substance.
Conclusion: there is no major concern about the safety of Cinnamomum verum bark preparations under conditions given in the monograph.
Cinnamon bark and essential oil were not adequately tested on genotoxicity where positive effects were obtained for isolated compounds. Therefore a list entry can not be considered.
Cinnamon has been used for centuries for dyspeptic complaints. It has to be considered for symptomatic treatment after serious illness is excluded.
Conclusion: see safety conclusion.