Astragalus image

Overview

Astragalus is a genus of flowering plants that includes herbs and shrubs. Astragalus plants are widely distributed in temperate and arid climates (90663). Astragalus has been used for centuries in traditional Chinese medicine (TCM), in combination with other herbs (303, 114805). It has been traditionally used as an "adaptogen." Adaptogens are theorized to help the body resist physiological and psychological stress.

Some species of astragalus, including Astragalus lentiginosus and Astragalus mollissimus, contain the neurotoxin swainsonine and have been linked to livestock poisonings (10778, 10779). However, these species of astragalus are usually not found in dietary supplements used by humans. Most astragalus supplements contain Astragalus membranaceus.

Coronavirus disease 2019 (COVID-19): Despite claims to the contrary, there is no good evidence to support using astragalus for COVID-19. Recommend healthy lifestyle choices and proven prevention methods instead.

Possibly Safe when used orally and appropriately. Doses of astragalus up to 60 grams daily for up to 4 months have been used without reported adverse effects (32920, 33038, 95909, 114804). ...when used intravenously. Infusion of doses up to 80 grams daily for up to 4 months under the supervision of a medical professional have been used with apparent safety (32811, 32812, 32828, 95909, 114688, 114804).

There is insufficient reliable information available about the safety of astragalus when used topically.

PREGNANCY AND LACTATION: There is insufficient reliable information in humans. However, astragaloside, a constituent of astragalus, has maternal and fetal toxic effects in animals (32881). Avoid using.

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General

Orally and intravenously, astragalus root seems to be well tolerated. Topically, no adverse effects have been reported. However, a thorough evaluation of safety outcomes has not been conducted.

Serious Adverse Effects (Rare)

Orally: A case report raises concerns about liver and kidney cysts with astragalus use.

Cardiovascular

Orally, astragalus has reportedly been associated with lacunar angina in one clinical trial. However, this may not have been caused by astragalus (17355). In addition, rapid intravenous administration of astragalus has resulted in temporary palpitations (32812).

Dermatologic

Intravenously, astragalus may cause rash, eczema, and pruritus (33034).

Gastrointestinal

Orally, astragalus has reportedly been associated with enterocolitis and nausea in one clinical trial. However, these effects may not have been caused by astragalus (17355).

Genitourinary

Orally, astragalus has reportedly been associated with vulvitis in one clinical trial. However, this effect may not have been caused by astragalus (17355).

Hepatic

A case of high serum CA19-9 levels and small liver and kidney cysts has been reported for a 38-year-old woman who drank astragalus tea daily for one month. Levels returned to normal after one month, and cysts disappeared after ten months. Both symptoms returned following a resumption of astragalus use. The authors state that astragalus was the likely cause given the temporal relationship (90658).

Musculoskeletal

Orally, astragalus has been associated with reports of musculoskeletal pain in one clinical trial. However, these effects may not have been caused by astragalus (114803).

Neurologic/CNS

Intravenously, administration of astragalus has been associated with temporary dizziness in patients with heart failure in clinical research (32812, 114804). Orally, astragalus has also been associated with dizziness in one clinical study. However, these effects may not have been caused by astragalus (114803).

Pulmonary/Respiratory

Orally, astragalus has reportedly been associated with rhinosinusitis and pharyngitis in one clinical trial. However, these effects may not have been caused by astragalus (17355).

Renal

A case of high serum CA19-9 levels and small liver and kidney cysts has been reported for a 38-year-old woman who drank astragalus tea daily for one month. Levels returned to normal after one month, and cysts disappeared after ten months. Both symptoms returned following a resumption of astragalus use. The authors state that astragalus was the likely cause given the temporal relationship (90658).

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Insufficient Reliable Evidence to Rate

It is unclear if oral astragalus is beneficial for allergic rhinitis.

Preliminary clinical research shows that taking a specific astragalus root extract standardized to contain 40% polysaccharides (Lectranal, Milsing d.o.o.) 160 mg orally twice daily for 3-6 weeks improves symptoms such as rhinorrhea, sneezing, and itching when compared with placebo in adults with seasonal allergic rhinitis (17355).

Oral astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

One preliminary clinical study shows that taking a liquid decoction containing astragalus 30 grams, dong quai 30 grams, zizyphus 10 fruits, horny goat weed 15 grams, dodder 30 grams, and three slices of ginger, daily in two divided doses for 3 months, can increase menstrual frequency when compared to baseline in patients with amenorrhea (33050). The validity of this finding is limited by the lack of a comparator group. Additionally, it is unclear if this effect is due to astragalus, other ingredients, or the combination.

It is unclear if oral astragalus is beneficial for angina.

A preliminary clinical trial shows that taking astragalus 20 grams orally three times daily for 2 weeks can improve cardiac output, but not diastolic function, when compared to baseline in patients with angina (33063). The validity of these findings is limited by the lack of a comparator group.

It is unclear if intravenous astragalus is beneficial for preventing cardiotoxicity due to anthracyclines. Oral astragalus has not been evaluated for this use.

A large unblinded clinical study in patients with breast cancer or lymphoma receiving a chemotherapy regimen containing epirubicin shows that intravenous use of astragalus 500 mg daily for 14 days during 2 courses of chemotherapy modestly attenuates the decline in left ventricular ejection fraction (LVEF) and reduces the occurrence of cardiotoxicity when compared with standard care (110479). However, this study was conducted in China, which limits the generalizability of its results.

It is unclear if intravenous astragalus is beneficial for aplastic anemia. There is insufficient reliable information about the clinical effects of oral astragalus for this condition.

Preliminary clinical research in patients 15 years and older with chronic aplastic anemia shows that giving intravenous astragalus in combination with stanozolol 2 mg three times daily produces greater improvements in symptoms and blood cell counts than stanozolol alone. Astragalus was given as 80-120 grams daily for repeated 15-day courses at 7-10 day intervals for at least 4 months (32840).

Oral astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

Preliminary clinical research in children with mild asthma shows that taking a combination of astragalus, cordyceps, Radix stemonae (Bai Bu), bulbus fritillariae cirrhosae, and Baikal skullcap orally for 6 months does not improve asthma symptoms, measures of lung function, or total steroid use when compared with placebo (32935).

Although there has been interest in using oral astragalus for beta-thalassemia, there is insufficient reliable information about the clinical effects of astragalus for this condition.

Although there has been interest in using oral astragalus for breast cancer, there is insufficient reliable information about the clinical effects of astragalus for this condition.

Oral astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

A meta-analysis of 19 clinical trials in adults with cervical cancer who are receiving chemotherapy shows that the use of Chinese herbal medicines containing astragalus increases tumor response (complete and partial responses) and Karnofsky performance score and reduces chemotherapy-associated adverse effects when compared with chemotherapy alone (107479). However, most studies included in the meta-analysis were low-quality, and all studies were conducted in China. Higher quality studies in other geographic locations are needed to confirm these findings. Additionally, it is unclear if any effects are due to astragalus, other ingredients, or the combination.

Oral or intravenous astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

A meta-analysis of low-quality clinical trials in patients with colorectal cancer shows that oral or intravenous use of traditional Chinese medicine therapies containing astragalus and other ingredients along with conventional chemotherapy reduces the risk of anemia by 51% when compared with chemotherapy alone (102099). It is unclear if these effects are due to astragalus, the other ingredients, or the combination.

It is unclear if oral or intravenous astragalus is beneficial for chemotherapy-induced diarrhea.

One preliminary clinical study shows that intravenous infusion of astragalus 40 grams in 250 mL of solution, given daily for 21 days during each of four courses of chemotherapy, reduces diarrhea by 59% when compared to chemotherapy alone (32747). Additionally, a meta-analysis of low-quality clinical trials in patients with colorectal cancer shows that oral or intravenous use of traditional Chinese medicine therapies containing astragalus and other ingredients along with conventional chemotherapy reduces the risk of diarrhea by 45% when compared with chemotherapy alone (102099). It is unclear if these effects are due to astragalus, the other ingredients, or the combination.

Oral or intravenous astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

A meta-analysis of low-quality clinical trials in patients with colorectal cancer shows that oral or intravenous use of traditional Chinese medicine therapies containing astragalus and other ingredients along with conventional chemotherapy reduces the risk of thrombocytopenia by 41% when compared with chemotherapy alone (102099). It is unclear if these effects are due to astragalus, the other ingredients, or the combination.

Early research suggests that intravenous astragalus seems to reduce nausea and vomiting associated with chemotherapy use. It is unclear if oral astragalus is beneficial for CINV.

A meta-analysis of low-quality clinical research in Chinese patients with advanced non-small cell lung cancer shows that intravenous infusion of astragalus along with platinum-based chemotherapy reduces the risk of vomiting by 38% when compared with platinum-based chemotherapy alone (100698). Another preliminary clinical study shows that intravenous infusion of astragalus 40 grams in 250 mL of solution, given daily for 21 days during each of four courses of chemotherapy, reduces nausea by 36% and vomiting by 50% when compared with chemotherapy alone (32747). Higher quality studies are needed to confirm these results.

The use of astragalus in combination with other ingredients for prevention of CINV has also been investigated. A meta-analysis of low-quality clinical trials in patients with colorectal cancer shows that oral or intravenous use of traditional Chinese medicine therapies containing astragalus and other ingredients along with conventional chemotherapy reduces the risk of nausea and vomiting by 44% when compared with chemotherapy alone (102099). It is unclear if these effects are due to astragalus, the other ingredients, or the combination.

Oral or intravenous astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

A meta-analysis of low-quality clinical trials in patients with colorectal cancer shows that oral or intravenous use of traditional Chinese medicine therapies containing astragalus and other ingredients along with conventional chemotherapy does not reduce the risk of nephrotoxicity when compared with chemotherapy alone (102099). The effects of astragalus when used alone are unclear.

It is unclear if intravenous astragalus is beneficial for chemotherapy-related fatigue. There is insufficient reliable information about the clinical effects of oral astragalus for this condition.

One clinical study in patients with advanced cancer shows that treatment with an intravenous infusion of a partially purified astragalus extract (PG2, Pharmagenesis), 500 mg three times weekly for 4 weeks during chemotherapy, improves fatigue scores after one week, but not after two and four weeks, when compared with placebo (33034).

Oral astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

One preliminary clinical study in adults with CFS shows that taking a 200 mL decoction containing astragalus 30 grams, kudzu 30 grams, codonopsis 15 grams, red sage 10 grams, aizoon stonecrop 15 grams, horny goat weed 10 grams, turmeric 10 grams, and calamus 10 grams, in two divided doses daily for 3 months improves fatigue symptoms when compared to baseline (32920). Another preliminary clinical study shows that taking 1.5 grams of a specific product (Myelophil, Samik Pharmaceutical Company) containing 66% of extracts of astragalus and danshen in a 1:1 ratio twice daily for 4 weeks improves fatigue severity when compared with placebo. However, taking 3 grams of the same product twice daily does not seem to have a benefit (32883). It is unclear if these effects are due to astragalus, the other ingredients, or the combination.

It is unclear if intravenous astragalus is beneficial for CKD. There is insufficient reliable information about the clinical effects of oral astragalus for this condition.

A meta-analysis of preliminary clinical research in patients with CKD shows that using astragalus, usually as an injection, along with conventional treatment modestly improves creatinine clearance by 6 mL/min, serum creatinine by 0.25 mg/dL, and hemoglobin levels by 1 gram/dL when compared with conventional treatment alone (90660). However, the studies included in the meta-analysis were of low quality. Additionally, a moderate-sized clinical study in patients with CKD and type 2 diabetes shows that taking astragalus 15 grams daily for 5 days per week in combination with standard care for 48 weeks ameliorates the decline in glomerular filtration rate, but does not improve the urinary albumin to creatinine ratio, when compared with standard care alone (114803). The validity of these findings is limited by methodological flaws, including inadequate blinding. Also, it is not known if astragalus reduces mortality or attenuates the progression to kidney failure.

Intravenous astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

A meta-analysis of low-quality clinical studies in adults with COPD shows that intravenous astragalus 10-60 mL (concentration not specified) once or twice daily for 2 weeks in combination with ambroxol hydrochloride and other conventional therapies improves COPD clinical symptoms, some measures of pulmonary function, and arterial blood gases when compared with conventional therapies alone (114688). All studies were conducted in China which may limit generalizability of the results. It is unclear if these effects are due to astragalus, ambroxol hydrochloride, or the combination.

Intravenous astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear. There is insufficient reliable information about the clinical effects of oral astragalus for this condition.

A meta-analysis of results from low-quality clinical studies shows that intravenous injection of a combination of astragalus and danshen for up to 90 days might decrease fibrosis when compared with control in patients with liver cirrhosis (90662). However, it is unclear if this is due to astragalus, danshen, or the combination.

Oral or intravenous astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

A meta-analysis of clinical trials in patients with colorectal cancer shows that oral or intravenous use of traditional Chinese medicine therapies containing astragalus and other ingredients along with conventional chemotherapy improves quality of life scores and increases the rate of tumor response by 52% when compared with chemotherapy alone (102099). It is unclear if these effects are due to astragalus, the other ingredients, or the combination.

It is unclear if oral or intravenous astragalus is beneficial for diabetes.

A meta-analysis of preliminary clinical research in Chinese patients with type 2 diabetes shows that astragalus, given as a daily intravenous injection 40-80 grams or taken orally 40-60 grams daily as an aqueous decoction for up to 4 months, modestly improves fasting and postprandial blood glucose levels when compared to a control group. Oral astragalus seems to improve these outcomes slightly more than intravenous astragalus. Orally, astragalus also seems to improve fasting insulin levels and insulin resistance, although its effect on glycated hemoglobin (HbA1c) is inconsistent. (95909). Astragalus has also been evaluated as an adjuvant therapy to metformin. A meta-analysis of several mostly small clinical studies in adults with type 2 diabetes shows that taking astragalus 10-50 grams daily with metformin modestly reduces fasting blood glucose by approximately 12 mg/dL, 2-hour postprandial blood glucose by 12 mg/dL, and HbA1c by 0.9% when compared with metformin monotherapy (112809). A meta-analysis of mostly low-quality clinical studies in patients with diabetes shows that taking astragalus in the form of traditional Chinese medicine, with or without Western medicine, reduces fasting blood glucose, 2-hour postprandial glucose, and glycated hemoglobin when compared with Western medicine alone (114805). However, the clinical studies included in both of these meta-analyses are of low methodological quality and include only Chinese patients, which limits the reliability and generalizability of the results.

Some research has evaluated astragalus in combination with other ingredients. One preliminary clinical study in adults with previously untreated type 2 diabetes shows that taking astragalus 210 mg, goldthread 350 mg, and honeysuckle 840 mg three times daily before meals for 3 months does not improve fasting blood glucose, postprandial blood glucose, or HbA1c when compared with placebo, although glucose disposal rate is modestly improved (32925).

It is unclear if intravenous astragalus is beneficial for diabetic nephropathy.

Meta-analyses of small, low-quality clinical studies including over 4700 patients shows that adding intravenous astragalus to routine therapy for 2-12 weeks modestly improves blood urea nitrogen, serum creatinine, creatinine clearance, urinary protein, urinary albumin, and serum albumin when compared with routine therapy alone in patients with diabetic nephropathy (33019, 102100).

It is unclear if oral astragalus is beneficial for diabetic neuropathy.

A meta-analysis of mostly low-quality clinical studies in patients with diabetic neuropathy shows that taking astragalus in the form of traditional Chinese medicine, with or without Western medicine, modestly reduces signs and symptoms of diabetic neuropathy when compared with Western medicine alone (114805). However, this improvement may not be clinically significant. Additionally, all studies were conducted in China which may limit generalizability of the results.

It is unclear if oral astragalus is beneficial for diabetic retinopathy.

A meta-analysis of results from preliminary clinical research suggests that taking astragalus-containing products for up to 10 months modestly improves visual acuity and fundus manifestations when compared with control in patients with diabetic retinopathy. However, the included studies had methodological limitations, and the results were heterogeneous (90655).

Although there has been interest in using oral astragalus for fibromyalgia, there is insufficient reliable information about the clinical effects of astragalus for this condition.

Oral and intravenous astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

A meta-analysis of 35 randomized, controlled trials involving 2670 patients with advanced gastric cancer shows that taking either intravenous or oral traditional Chinese medicines containing astragalus in conjunction with platinum-based chemotherapy may improve objective response rate, disease control rate, 1-year survival rate, and quality of life, and may also reduce the severity of chemotherapy-associated adverse effects, when compared with chemotherapy alone (107480). The validity of this meta-analysis is limited by potential publication bias, unclear randomization methods, and substantial heterogeneity among the included studies. Additionally, it is unclear if these effects are due to astragalus, other ingredients, or the combination.

It is unclear if intravenous astragalus is beneficial for hearing loss.

Preliminary clinical research shows that injecting 0.5 mL/kg of solution containing astragalus 2 grams/mL daily for 10 days improves hearing in people with sudden deafness or acute acoustic trauma when compared with a control group (33028, 33033).

It is unclear if oral or intravenous astragalus is beneficial for heart failure.

A meta-analysis of small to moderate-sized low quality clinical studies in adults with heart failure with reduced ejection fraction (HFrEF) shows that oral astragalus 30 grams twice daily or intravenous astragalus 20-60 mL (concentration not specified) daily for 2-4 weeks combined with conventional treatment modestly increases left ventricular ejection fraction (LVEF), decreases brain natriuretic peptide levels, and increases 6-minute walking distance when compared with conventional treatment alone (114804). Findings are limited by significant heterogeneity. Additionally, all studies were conducted in China which may limit generalizability of the results.

The conflicting nature of these results are reflected in other small studies. One preliminary clinical study in adults with CHF shows that intravenous infusion of astragalus 60 grams daily for 20 days improves LVEF and left ventricular end-diastolic volume (LVEDV) when compared with conventional treatment (32755). However, another preliminary clinical study shows that intravenous astragalus 60 grams daily for 28 days in combination with conventional treatment for CHF does not improve LVEF, LVEDV, or left ventricular end-systolic volume when compared with conventional treatment alone (32812). Other preliminary clinical research shows that taking oral astragalus 2.25-7.5 grams twice daily for 14-30 days in combination with conventional treatment improves cardiac function, LVEF, and walking distance when compared with conventional treatment alone (33018, 33022). However, each of these studies has methodological problems.

Although there has been interest in using oral astragalus for hepatitis B, there is insufficient reliable information about the clinical effects of astragalus for this condition.

Oral astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

One small clinical study shows that taking a combination containing mainly Baikal skullcap root, glossy privet fruit, astragalus root, and Eupolyphaga et polyphage (Ailing granules) 20 grams twice daily for 4 months improves HIV/AIDS symptoms and CD4 cell counts (32824). However, taking a different combination containing licorice, yin chen, white mulberry, astragalus, and safflower orally for 12 weeks is associated with only a slight decline in viral load and no change in CD4 cell counts (32795). The effects of astragalus alone are unclear.

Although there has been interest in using intravenous astragalus for IgA nephropathy, there is insufficient reliable information about the clinical effects of oral or intravenous astragalus for this condition.

Early research suggests that oral or intravenous astragalus seems to increase the effectiveness of platinum-based chemotherapy or radiotherapy in patients with advanced non-small cell lung cancer (NSCLC).

One meta-analysis in patients with advanced NSCLC shows that intravenous administration of astragalus along with platinum-based chemotherapy increases the rate of one-year survival by 40% when compared with platinum-based chemotherapy alone (100698). Other meta-analyses in these patients show that use of oral or intravenous astragalus-containing herbal products appears to reduce the risk of death at six months by 42%, at one year by 33%, at two years by 27% to 33%, and at three years by 15% to 24% when compared with platinum-based chemotherapy or radiotherapy alone (15001, 90656). Additionally, a network meta-analysis of clinical research in patients with NSCLC ranks intravenous administration of astragalus along with a combination of docetaxel and cisplatin as the most effective of various Chinese herbal medicine injection and docetaxel and cisplatin combinations (114689). However, most studies included in the meta-analyses were low-quality, and all studies were conducted in China. Higher quality studies in other geographic locations are needed to confirm these findings.

Oral astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

A meta-analysis of 48 small, low-quality clinical studies in adults with idiopathic membranous nephropathy conducted in China shows that taking astragalus 20-90 grams per day in combination with a variety of other supplements, in addition to conventional therapy, modestly improves the rate of complete or partial renal remission when compared with conventional therapy (e.g. angiotensin-converting enzyme inhibitors, immunosuppression). Adding astragalus combinations to conventional therapy also modestly reduces proteinuria and serum creatinine (112010). However, the interpretation of these findings is limited by the heterogeneity of the included studies and variable definitions of complete and partial renal remission. Additionally, it is unclear if these effects are due to astragalus, other ingredients, or the combination.

Oral astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

One preliminary clinical study shows that taking Dang Gui Buxue Tang, an herbal decoction containing astragalus and dong quai extract, 3 grams daily for 6 months does not reduce the incidence of menopausal hot flashes (32857). However, another preliminary clinical study shows that taking Dang Gui Buxue Tang 3-6 grams daily for 12 weeks reduces hot flash frequency by up to 40% and night sweat frequency up to 53% when compared to baseline (90659). Each 1.5 grams of Dang gui Buxue Tang contains extract prepared from dong quai 1.5 grams and astragalus 7.5 grams (90659). Another small clinical study in females with moderate or severe menopausal symptoms shows that taking a tablet containing astragalus and Rubus coreanus extract 1000 mg twice daily for 12 weeks modestly improves symptom and quality of life scores when compared with placebo (110478). However, the validity of these findings is limited by a high rate of study participant discontinuation.

Although there has been interest in using intravenous astragalus for MI, there is insufficient reliable information about the clinical effects of oral or intravenous astragalus for this purpose.

It is unclear if oral or injectable astragalus is beneficial for viral myocarditis.

A meta-analysis of 13 mostly small, low-quality clinical studies in adults and children with viral myocarditis shows that astragalus injection may improve the total effective rate and reduce markers of inflammation when compared with conventional treatment (110477). However, most studies included in the meta-analysis were low-quality, dosing was variable, and all studies were conducted in China. Higher quality studies in other geographic locations are needed to confirm these findings. Several clinical studies report improvements in cardiac enzymes, cardiac function, or viral load in peripheral leukocytes with the use of astragalus preparations, but results are inconsistent and the methodological quality of these studies is low (33084, 33105, 33217, 33218, 33220, 33221, 33223). Doses demonstrating benefit include intramuscular astragalus extract, equivalent to 8 grams daily for 3-4 months (33105) and intravenous astragalus extract 40 grams daily for 2 weeks (33218, 33221). It is unclear if astragalus speeds recovery or reduces the risk of mortality due to myocarditis.

It is unclear if oral astragalus is beneficial for preventing infections in patients with nephrotic syndrome.

A meta-analysis of results from two preliminary clinical studies shows that taking astragalus 7.5-15 grams twice daily for 3-6 months reduces the risk of infection by 38% when compared to control in children with nephrotic syndrome (33036).

Oral astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

Preliminary clinical research shows that taking a combination of astragalus, rhubarb, turmeric, red sage root, ginger, and gallic acid concurrently with a reduced-calorie diet does not improve weight loss when compared with a reduced-calorie diet alone in adults who are overweight or obese (20347).

It is unclear if oral astragalus is beneficial for post-stroke fatigue.

A preliminary clinical study shows that taking astragalus extract (Sun Ten Pharmaceutical Co. Ltd.) 2.8 grams three times daily for 28 days improves fatigue and some quality of life measures such as social functioning, role functioning, and physical functioning, when compared with placebo in patients experiencing fatigue following a recent stroke (95908).

It is unclear if intravenous astragalus is beneficial for lupus nephritis. There is insufficient reliable information about the clinical effects of oral astragalus for this condition.

A preliminary clinical study in adults with lupus nephritis shows that intravenous infusions of astragalus 40 grams daily for 12 consecutive days monthly for 3 months, in combination with corticosteroids and cyclophosphamide once monthly as an intravenous drip, can improve symptoms, reduce infections, and reduce urinary protein excretion when compared to treatment with corticosteroids and cyclophosphamide alone (32838).

It is unclear if intravenous astragalus is beneficial for tinnitus.

Preliminary clinical research shows that injecting 0.5 mL/kg of solution containing astragalus 2 grams/mL daily for 10 days reduces tinnitus in patients with acute acoustic trauma when compared to a control group (33028).

Although there has been interest in using oral astragalus for URTI prevention, there is insufficient reliable information about the clinical effects of astragalus for this purpose.

Oral astragalus has only been evaluated in combination with other ingredients; its effect when used alone is unclear.

A moderate-size clinical study in females aged 18-45 with uncomplicated UTIs shows that taking a supplement containing astragalus root extract 100 mg, d-mannose, citric acid, dandelion, and prebiotics as a sachet dissolved in water twice daily for 5 days improves complete resolution of UTI symptoms and clearance of bacteriuria at days 6 and 35 when compared with placebo (111757). However, it is unclear if these effects are due to astragalus, other ingredients, or the combination.

Although there has been interest in using topical astragalus for wound healing, there is insufficient reliable information about the clinical effects of astragalus for this purpose.

More evidence is needed to rate astragalus for these uses.

Adult

Oral:

Astragalus has typically been used as extracts, dried root, or liquid decoctions. See Effectiveness section for condition-specific information

Intravenous/Intramuscular:Astragalus has most often been administered intravenously in doses of 40-80 grams daily for up to 3 months. For intramuscular dosing, research is limited; typical dosing is unavailable.

Many intravenous astragalus solutions used in clinical research have been standardized to contain 2 grams/mL (32742, 32755, 32811, 32812, 32828, 32829, 32838, 32840, 32856).

Children

Oral:

Research is limited; typical dosing is unavailable.

Intravenous/intramuscular:Research is limited; typical dosing is unavailable.

Standardization & Formulation

Astragalus herbal products used in clinical research are prepared from astragalus root and available for intravenous, intramuscular, and oral use. One specific astragalus root extract has been standardized to contain 40% polysaccharides (Lectranal, Milsing d.o.o.) (17355). In many cases, the intravenous astragalus solutions used in clinical research were prepared by Di'Ao JiuHong Pharmaceuticals (China) and standardized to contain 2 grams/mL (32742, 32755, 32811, 32812, 32828, 32829, 32838, 32840, 32856). In one study, prefilled injection syringes manufactured by No. 1 Chinese Medicine Laboratories in Shanghai, China were standardized to contain astragalus 1.5 grams/mL (33049).

In many studies, astragalus is administered in combination with other herbal supplements. One specific product (Myelophil, Samik Pharmaceutical Company), which contains a mixture of equal amounts of astragalus and danshen, is standardized to contain 66% of pure extract and 34% additive (32883).

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ANTIDIABETES DRUGS

Interaction Rating
Moderate Be cautious with this combination.
Severity
MODERATE
Occurrence
PROBABLE
Level of Evidence
A (High-quality meta-analysis (quantitative systematic review))

Theoretically, taking astragalus with antidiabetes drugs might increase the risk of hypoglycemia.

Clinical research in humans shows that astragalus might have hypoglycemic effects (95909, 112809, 114805). Theoretically, taking astragalus, especially in combination with other hypoglycemic agents, might increase the risk of hypoglycemia.


CYCLOPHOSPHAMIDE

Interaction Rating
Moderate Be cautious with this combination.
Severity
HIGH
Occurrence
POSSIBLE
Level of Evidence
D (In vitro or animal study)

Theoretically, astragalus might interfere with cyclophosphamide therapy.

Evidence regarding the effect of astragalus on immunosuppression caused by cyclophosphamide is conflicting. Some animal research suggests that astragalus reverses cyclophosphamide-induced immunosuppression (3713). However, other animal research shows no effect (418).


IMMUNOSUPPRESSANTS

Interaction Rating
Moderate Be cautious with this combination.
Severity
HIGH
Occurrence
POSSIBLE
Level of Evidence
D (In vitro or animal study)

Theoretically, astragalus might interfere with immunosuppressive therapy.

Astragalus seems to stimulate immune function (303, 10777). Theoretically, taking astragalus might decrease the effects of immunosuppressive therapy.


LITHIUM

Interaction Rating
Moderate Be cautious with this combination.
Severity
MODERATE
Occurrence
PROBABLE
Level of Evidence
D (Theoretical based on pharmacology)

Theoretically, astragalus might increase levels and adverse effects of lithium.

Animal research suggests that astragalus has diuretic properties (15103). Theoretically, due to this diuretic effect, astragalus might reduce excretion and increase levels of lithium.

HERBS AND SUPPLEMENTS WITH HYPOGLYCEMIC POTENTIAL

Theoretically, astragalus might have hypoglycemic effects.

Clinical studies in humans show that astragalus has hypoglycemic effects (95909, 112809, 114805). Theoretically, astragalus might have additive effects with supplements that decrease blood glucose levels, increasing the risk of hypoglycemia. See other products with hypoglycemic activity here.

AUTOIMMUNE DISEASES

Theoretically, astragalus might exacerbate certain autoimmune diseases by stimulating disease activity; avoid use or use with caution in patients with autoimmune diseases such as multiple sclerosis, systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), or others. Astragalus seems to stimulate immune function (303, 423, 3713, 10777).

None known.

Presentation

Orally, doses of astragalus greater than 28 grams might cause immunosuppression (303).

Treatment

There is insufficient reliable information available about the treatment of overdose with astragalus.

Absorption

A pharmacokinetic evaluation in a healthy human volunteer suggests that astragalus flavonoids can be absorbed in the gastrointestinal tract. The major metabolites of the flavonoid constituents are glucuronides (15002).

General

The applicable part of astragalus is the root. Astragalus contains a variety of active constituents including more than 40 saponins such as astragaloside, several flavonoids including isoflavones, pterocarpans, and isoflavans, polysaccharides, multiple trace minerals, amino acids, and coumarins (303, 15001, 32784, 32844, 98685).

Anti-inflammatory effects

The anti-inflammatory effects of astragalus may play a role in many of its clinical effects. Mechanisms of action may involve the NF-kappaB pathway modifying gene expression (32771). There is also evidence from laboratory and human research that astragalus and its constituents reduce the formation of various inflammatory cytokines and eicosanoids (12451, 32770, 32858, 32914, 32923, 33013, 110477, 112811). Meta-analyses of clinical studies shows that taking astragalus reduces levels of high-sensitivity C-reactive protein, proinflammatory cytokines such as interleukin-2, interleukin-4, interleukin-6, tumor necrosis factor-alpha, and interferon gamma and reduces levels of the anti-inflammatory cytokine interleukin-10 (112811, 114804, 114805).

Antibacterial effects

Astragalus also seems to have broad-spectrum in vitro antibiotic activity (303). In animal research, the saponin fraction from astragalus protected mice against induced polymicrobial sepsis by inhibiting inflammation and upregulating the protein C pathway (32902).

Anticancer effects

Astragalus is commonly used in individual or multi-ingredient herbal formulations for cancer. In laboratory research, astragalus appears to promote apoptosis (32851, 32867, 32930). Also, astragalus extract appears to reverse Th2 predominant status in peripheral blood mononuclear cells of lung cancer patients. Th2 cytokine production in lung cancer patients has been associated with tumor progression (32758). Lymphocyte activity has also been shown to be improved in laboratory research (419, 423, 10777, 14460, 32836, 33041, 33065, 33068).

Antioxidant effects

Astragalus inhibits free radical production, increases superoxide dismutase, and decreases lipid peroxidation, suggesting antioxidant effects (303, 14462, 32907, 98685). However, not all clinical research has demonstrated antioxidant effects (114805).

Antiviral effects

Astragalus is commonly used as an antiviral agent for various infections. Preliminary clinical research shows that astragalus can increase seroreversion of a hepatitis B viral protein (HBeAg) and hepatitis B virus DNA similarly to interferon-alpha in patients with hepatitis B (32735, 32908). Other laboratory evidence suggests that astragalus can inhibit cytomegalovirus (CMV)-AD169 (32794) and herpes simplex-1 virus (HSV-1) (32778). Possible mechanisms of action may include effects on interferon production (15104, 33079). In mice with viral myocarditis, astragalus resulted in reduced viral load and replication (33055, 33076, 33109). In contrast, astragalus exhibited no in vitro cytotoxic or antiviral activity against HIV infection (32767, 33079).

Bone effects

When administered intravenously, some evidence suggests astragalus extract might increase proliferation and differentiation of bone marrow stem cells and progenitor cells (303). Astragalus extract might also inhibit the development of osteoclasts, increasing bone area (32776). Other laboratory research shows that an isoflavonoid isolated from astragalus, formononetin, increases activity of osteoblasts and differentiation of mesenchymal cells at a fracture site (32919, 32965).

Cardiovascular effects

Astragalus is often promoted for its effects on the cardiovascular system. Astragalus is thought to cause vasodilation and increase cardiac output which might be beneficial in angina, congestive heart failure, and post-myocardial infarction (303). In animal models of heart failure and in humans, astragalus appears to increase myocardial and renal function, possibly due to diuretic and natriuretic effects (15103, 32849). In animal models of coxsackie viral myocarditis, astragalus appears to reduce myocardial lesion size and viral titers (15105).

Fertility effects

There is interest in astragalus for increasing fertility. In vitro, astragalus appears to increase sperm motility (14461, 32785).

Gastrointestinal effects

The anti-inflammatory and antioxidant effects of astragalus may play a role in the gastroprotective effects of astragalus. In an animal model, astragalus reduced symptoms of colitis, possibly by acting as an antioxidant and reducing synthesis of adhesion molecules or cytokine activity (32814, 32900).

Glucose-lowering effects

In animal and human research, astragalus and its constituents have been shown to lower blood glucose (33101, 32805, 114805). This may be due to the effect of constituents on protein tyrosine phosphorylase, protein kinase C, and 5' AMP-activated protein kinase (AMPK) activities, thereby altering insulin sensitivity and glucose uptake and use (32822, 32949, 33107). Also, the isoflavone constituents, formononetin and biochanin A, are potent activators of peroxisome proliferator-activated receptors (PPAR), used to restore glycemic balance (32818). Both human and laboratory research suggests that astragalus may also aid in the protection against the formation of glycated end products, including protein (32854, 32873, 32917).

Hepatoprotective effects

Astragalus is often promoted for its effects on the liver. In individuals with chronic hepatitis, astragalus seems to improve liver function as demonstrated by improvement in serum glutamate pyruvate transaminase (SGPT) levels (303). Laboratory research suggests the liver protective effects of astragalus may be related to the matrix collagen through effects on levels of metalloproteinases and inflammatory or anti-inflammatory cytokines (32931, 32950, 32999).

Immunomodulatory effects

Astragalus is often promoted for its effects on the immune system and seems to improve the immune response. In vitro, the polysaccharide constituents appear to bind and activate B cells and macrophages, but not T cells (14500). Astragalus potentiates the effects of interferon, increases antibody levels of IgA and IgG in nasal secretions and serum, and increases interleukin-2 levels (IL-2) (303, 14464, 15104, 32859). It also seems to improve the response of mononuclear cells and stimulate lymphocyte production (10777). Astragalus seems to potentiate lymphokine-activated killer (LAK) cell activity in vitro when used in combination with IL-2 (14460), as well as natural killer cell activity (32764).

In laboratory research, astragalus may increase the number or activity of T helper cells (32746, 32825, 32837, 32997, 33025), alter cytokine production levels (32746, 32837, 32953, 33069, 112811), and increase the activation of macrophages (33039, 33061). In humans, astragalus may also increase T cell activity and the quantity and activity of dendritic cells (32815, 32831, 32897, 32924). A meta-analysis of 19 clinical studies shows that taking astragalus stimulates the immune system as suggested by increased levels of CD3, a biomarker and activator of T cells, and increased CD4/CD8 ratio, indicating a shift toward favorable immune responses (112811).

There is preliminary evidence that astragalus extracts can restore or improve immune function in cases of immune deficiency (423, 3713, 32841). Astragalus seems to restore in vitro T-cell function which is suppressed in cancer patients (423, 14463). In animal models, an astragalus extract can reverse cyclophosphamide-induced immune deficiency (3713). However, although lower doses of astragalus appear to stimulate the immune system, but doses in excess of 28 grams might suppress immunity (303).

There is also interest in using astragalus to prevent exercise-induced changes in immune function. A very small clinical study in male professional rowers shows that taking astragalus root 1000 mg daily for 6 weeks may attenuate some of the immunologic changes associated with acute and long-term training, such as changes in levels of interleukin (IL)-2, natural killer (NK) cells, and regulatory T cells (107478).

Renoprotective effects

Laboratory research suggests that astragalus may improve microvascular lesions by increasing local renal blood flow and promoting the glomerular filtration rate. Some evidence also suggests that there are improvements in the imbalance of vasoactivators and improving the function of endothelial cells (32862). Renoprotection has been shown in animal models with astragalus alone or in combination with dong quai (32890, 32903).

Vasorelaxant effects

Astragalus is commonly used for its vasorelaxant effects. Its isoflavone constituent formononetin has been shown to have vasorelaxant effects in laboratory research, by a mechanism possibly related to endothelial nitric oxide synthase (eNOS) (32906).

Wound-healing effects

Astragalus is commonly used for its wound-healing effects. The viability of fibroblasts taken from patients with diabetic foot ulcer was found to be enhanced when exposed to a combination of astragalus and rehmannia (32868).

Classes

AdaptogensDiureticsHypoglycemic AgentsImmunomodulatorsImmunostimulantsVasodilators

References

See Monograph References

Literature Review Current Through: 10/2/2025, Last Updated: 12/12/2025

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