What is Sanamisol?
Sanamisol is a proton pump inhibitor. Sanamisol decreases the amount of acid produced in the stomach.
Sanamisol is used to treat and prevent stomach and intestinal ulcers, erosive esophagitis (damage to the esophagus from stomach acid), and other conditions involving excessive stomach acid such as Zollinger-Ellison syndrome.
Over-the-counter Sanamisol is used to treat frequent heartburn that happens 2 or more days per week.
Sanamisol is not for immediate relief of heartburn symptoms.
Sanamisol may also be used for purposes not listed in this medication guide.
Sanamisol indications
Short-Term Treatment of Active Duodenal Ulcer
Sanamisol delayed-release capsules and Sanamisol delayed-release orally disintegrating tablets are indicated for short-term treatment (for 4 weeks) for healing and symptom relief of active duodenal ulcer.
H. pylori Eradication to Reduce the Risk of Duodenal Ulcer Recurrence
Triple Therapy: Sanamisol/amoxicillin/clarithromycin
Sanamisol delayed-release capsules and Sanamisol delayed-release orally disintegrating tablets in combination with amoxicillin plus clarithromycin as triple therapy are indicated for the treatment of patients with H. pylori infection and duodenal ulcer disease (active or one-year history of a duodenal ulcer) to eradicate H. pylori. Eradication of H. pylori has been shown to reduce the risk of duodenal ulcer recurrence.
Please refer to the full prescribing information for amoxicillin and clarithromycin.
Dual Therapy: Sanamisol/amoxicillin
Sanamisol delayed-release capsules and Sanamisol delayed-release orally disintegrating tablets in combination with amoxicillin as dual therapy are indicated for the treatment of patients with H. pylori infection and duodenal ulcer disease (active or one-year history of a duodenal ulcer) who are either allergic or intolerant to clarithromycin or in whom resistance to clarithromycin is known or suspected. Eradication of H. pylori has been shown to reduce the risk of duodenal ulcer recurrence.
Please refer to the full prescribing information for amoxicillin.
Maintenance of Healed Duodenal Ulcers
Sanamisol delayed-release capsules and Sanamisol delayed-release orally disintegrating tablets are indicated to maintain healing of duodenal ulcers. Controlled studies do not extend beyond 12 months.
Short-Term Treatment of Active Benign Gastric Ulcer
Sanamisol delayed-release capsules and Sanamisol delayed-release orally disintegrating tablets are indicated for short-term treatment (up to 8 weeks) for healing and symptom relief of active benign gastric ulcer.
Healing of NSAID-Associated Gastric Ulcer
Sanamisol delayed-release capsules and Sanamisol delayed-release orally disintegrating tablets are indicated for the treatment of NSAID-associated gastric ulcer in patients who continue NSAID use. Controlled studies did not extend beyond 8 weeks.
Risk Reduction of NSAID-Associated Gastric Ulcer
Sanamisol delayed-release capsules and Sanamisol delayed-release orally disintegrating tablets are indicated for reducing the risk of NSAID-associated gastric ulcers in patients with a history of a documented gastric ulcer who require the use of an NSAID. Controlled studies did not extend beyond 12 weeks.
Gastroesophageal Reflux Disease (GERD)
Short-Term Treatment of Symptomatic GERD
Sanamisol delayed-release capsules and Sanamisol delayed-release orally disintegrating tablets are indicated for the treatment of heartburn and other symptoms associated with GERD.
Short-Term Treatment of Erosive Esophagitis
Sanamisol delayed-release capsules and Sanamisol delayed-release orally disintegrating tablets are indicated for short-term treatment (up to 8 weeks) for healing and symptom relief of all grades of erosive esophagitis. For patients who do not heal with Sanamisol delayed-release capsules or Sanamisol delayed-release orally disintegrating tablets for 8 weeks (5 to 10%), it may be helpful to give an additional 8 weeks of treatment. If there is a recurrence of erosive esophagitis an additional 8-week course of Sanamisol delayed-release capsules or Sanamisol delayed-release orally disintegrating tablets may be considered.
Maintenance of Healing of Erosive Esophagitis (EE)
Sanamisol delayed-release capsules and Sanamisol delayed-release orally disintegrating tablets are indicated to maintain healing of erosive esophagitis. Controlled studies did not extend beyond 12 months.
Pathological Hypersecretory Conditions Including Zollinger-Ellison Syndrome (ZES)
Sanamisol delayed-release capsules and Sanamisol delayed-release orally disintegrating tablets are indicated for the long-term treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome.
How should I use Sanamisol?
Use Sanamisol powder packet as directed by your doctor. Check the label on the medicine for exact dosing instructions.
- Take Sanamisol powder packet by mouth on an empty stomach before eating.
- Place 2 tablespoons (30 mL) of water in a small cup. Do NOT use other liquids or foods. Empty the contents of the packet into the cup, stir well, and drink at once. Do not store the mixture for use at a later time. If any of the mixture remains in the cup, refill with water, stir, and drink at once.
- You may take antacids while you are using Sanamisol powder packet if you are directed to do so by your doctor.
- If you are also taking an imidazole antifungal (eg, ketoconazole), take it at least 2 hours before taking Sanamisol powder packet.
- If you also take sucralfate, take Sanamisol powder packet at least 30 minutes before taking sucralfate.
- Do not take Sanamisol powder packet through an enteral tube (eg, g-tube, ng-tube). If you must take your medicines through an enteral tube, discuss your dosing options with your doctor.
- Continue to take Sanamisol powder packet even if you feel well. Do not miss any doses.
- If you miss a dose of Sanamisol powder packet, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.
Ask your health care provider any questions you may have about how to use Sanamisol powder packet.
Uses of Sanamisol in details
Sanamisol is used to treat acid-related throat problems (erosive esophagitis). It works by blocking acid production in the stomach. This medication is known as a proton pump inhibitor (PPI). Decreasing excess stomach acid can help relieve symptoms such as heartburn, difficulty swallowing, persistent cough, and trouble sleeping. It can also prevent serious acid damage to your digestive system (e.g., ulcers, cancer of the esophagus).
OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by your health care professional. Use this drug for a condition that is listed in this section only if it has been so prescribed by your health care professional.
This medication may also be used to prevent and treat bleeding from stomach/intestinal ulcers.
How to use Sanamisol intravenous
This medication is given by injection into a vein over 30 minutes as directed by your doctor, usually once daily.
When you are able to take medicines by mouth, your doctor will switch your treatment to an oral form of this drug.
If needed, antacids may be taken along with this medication.
The dosage and length of treatment is based on your medical condition and response to therapy.
If you are giving this medication to yourself at home, learn all preparation and usage instructions from your health care professional. Before using, check this product visually for particles or discoloration. If either is present, do not use the liquid. Learn how to store and discard medical supplies safely.
Use this medication regularly in order to get the most benefit from it. Remember to use it at the same time each day. Continue to use this medication for the prescribed length of treatment even if you are feeling better.
Inform your doctor if your condition persists or worsens. The risk of side effects goes up over time. Ask your doctor how long you should use this medication.
Sanamisol description
Each capsule contains Lansoprazole 30 mg.
Sanamisol is a proton pump inhibitor with actions and uses similar to those of omeprazole. It inhibits secretion of gastric acid by irreversibly blocking the enzyme system of hydrogen/potassium adenosine triphosphatase, the proton pump of the gastric pariental cells.
Sanamisol dosage
Sanamisol I.V. (Sanamisol for injection) for Injection admixtures should be administered intravenously using the in-line filter provided. The filter must be used to remove precipitate that may form when the reconstituted drug product is mixed with I.V. solutions. Studies have shown that filtration does not alter the amount of Sanamisol that is available for administration. Read the following instructions carefully.
There are two methods for preparing Sanamisol I.V. (Sanamisol for injection) for Injection:
1. Reconstitution in Vial and Preparation of Admixture.
OR
2. Direct reconstitution with Baxter's MINI-BAG Plus Container.
1. Reconstitution in Vial and Preparation of Admixture
There are two steps for preparing Sanamisol I.V. (Sanamisol for injection) for Injection.
STEP ONE - Reconstitution in Vial
- First Sanamisol I.V. (Sanamisol for injection) MUST be reconstituted with Sterile Water for Injection, USP.
- Inject 5 mL of ONLY Sterile Water for Injection, USP into a 30 mg vial of Sanamisol I.V. for Injection. The resulting solution will contain Sanamisol 6 mg/mL (30 mg/5 mL).
- Failure to reconstitute with Sterile Water may result in formation of precipitation/particulates.
- Mix gently until the powder is dissolved.
The pH of this reconstituted solution is approximately 11. The reconstituted solution can be held for 1 hour when stored at 25
Sanamisol interactions
See also:
What other drugs will affect Sanamisol?
Sanamisol is metabolized through the cytochrome P isozymes including CYP1A2, CYP2C9, CYP2C19, CYP2D6, and CYP3A. When Sanamisol was administered concomitantly with theophylline (CYP1A2, CYP3A), a minor increase (10%) in the clearance of theophylline was seen. Because of the small magnitude and the direction of the effect on theophylline clearance, this interaction is unlikely to be of clinical concern. Nonetheless, individual patients may require additional titration of their theophylline dosage when Sanamisol is started or stopped to ensure clinically effective blood levels.
In a study of healthy subjects neither the pharmacokinetics of warfarin enantiomers nor prothrombin time were affected following single or multiple 60 mg doses of Sanamisol. However, there have been reports of increased International Normalized Ratio (INR) and prothrombin time in patients receiving proton pump inhibitors, including Sanamisol, and warfarin concomitantly. Increases in INR and prothrombin time may lead to abnormal bleeding and even death. Patients treated with proton pump inhibitors and warfarin concomitantly may need to be monitored for increases in INR and prothrombin time.
Sanamisol causes a profound and long-lasting inhibition of gastric acid secretion; therefore, it is theoretically possible that Sanamisol may interfere with the absorption of drugs where gastric pH is an important determinant of bioavailability (eg, ketoconazole, ampicillin esters, iron salts, digoxin).
Sanamisol side effects
See also:
What are the possible side effects of Sanamisol?
Clinical
Worldwide, over 10,000 patients have been treated with Sanamisol in Phase 2 or Phase 3 clinical trials involving various dosages and durations of treatment. In general, Sanamisol treatment has been well-tolerated in both short-term and long-term trials.
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.
The following adverse reactions were reported by the treating physician to have a possible or probable relationship to drug in 1% or more of Sanamisol-treated patients and occurred at a greater rate in Sanamisol-treated patients than placebo-treated patients in Table 1.
| Body System/Adverse Event | Sanamisol (N= 2768) % | Placebo (N= 1023) % |
|---|---|---|
| Body as a Whole Abdominal Pain | 2.1 | 1.2 |
| Digestive System Constipation Diarrhea Nausea | 1.0 3.8 1.3 | 0.4 2.3 1.2 |
Headache was also seen at greater than 1% incidence but was more common on placebo. The incidence of diarrhea was similar between patients who received placebo and patients who received 15 mg and 30 mg of Sanamisol, but higher in the patients who received 60 mg of Sanamisol (2.9%, 1.4%, 4.2%, and 7.4%, respectively).
The most commonly reported possibly or probably treatment-related adverse event during maintenance therapy was diarrhea.
In the risk reduction study of Sanamisol for NSAID-associated gastric ulcers, the incidence of diarrhea for patients treated with Sanamisol, misoprostol, and placebo was 5%, 22%, and 3%, respectively.
Another study for the same indication, where patients took either a COX-2 inhibitor or Sanamisol and naproxen, demonstrated that the safety profile was similar to the prior study. Additional reactions from this study not previously observed in other clinical trials with Sanamisol included contusion, duodenitis, epigastric discomfort, esophageal disorder, fatigue, hunger, hiatal hernia, hoarseness, impaired gastric emptying, metaplasia, and renal impairment.
Additional adverse experiences occurring in less than 1% of patients or subjects who received Sanamisol in domestic trials are shown below:
Body as a Whole – abdomen enlarged, allergic reaction, asthenia, back pain, candidiasis, carcinoma, chest pain (not otherwise specified), chills, edema, fever, flu syndrome, halitosis, infection (not otherwise specified), malaise, neck pain, neck rigidity, pain, pelvic pain
Cardiovascular System – angina, arrhythmia, bradycardia, cerebrovascular accident/cerebral infarction, hypertension/hypotension, migraine, myocardial infarction, palpitations, shock (circulatory failure), syncope, tachycardia, vasodilation
Digestive System – abnormal stools, anorexia, bezoar, cardiospasm, cholelithiasis, colitis, dry mouth, dyspepsia, dysphagia, enteritis, eructation, esophageal stenosis, esophageal ulcer, esophagitis, fecal discoloration, flatulence, gastric nodules/fundic gland polyps, gastritis, gastroenteritis, gastrointestinal anomaly, gastrointestinal disorder, gastrointestinal hemorrhage, glossitis, gum hemorrhage, hematemesis, increased appetite, increased salivation, melena, mouth ulceration, nausea and vomiting, nausea and vomiting and diarrhea, gastrointestinal moniliasis, rectal disorder, rectal hemorrhage, stomatitis, tenesmus, thirst, tongue disorder, ulcerative colitis, ulcerative stomatitis
Endocrine System – diabetes mellitus, goiter, hypothyroidism
Hemic and Lymphatic System – anemia, hemolysis, lymphadenopathy
Metabolic and Nutritional Disorders – avitaminosis, gout, dehydration, hyperglycemia/hypoglycemia, peripheral edema, weight gain/loss
Musculoskeletal System – arthralgia, arthritis, bone disorder, joint disorder, leg cramps, musculoskeletal pain, myalgia, myasthenia, ptosis, synovitis
Nervous System – abnormal dreams, agitation, amnesia, anxiety, apathy, confusion, convulsion, dementia, depersonalization, depression, diplopia, dizziness, emotional lability, hallucinations, hemiplegia, hostility aggravated, hyperkinesia, hypertonia, hypesthesia, insomnia, libido decreased/increased, nervousness, neurosis, paresthesia, sleep disorder, somnolence, thinking abnormality, tremor, vertigo
Respiratory System – asthma, bronchitis, cough increased, dyspnea, epistaxis, hemoptysis, hiccup, laryngeal neoplasia, lung fibrosis, pharyngitis, pleural disorder, pneumonia, respiratory disorder, upper respiratory inflammation/infection, rhinitis, sinusitis, stridor
Skin and Appendages – acne, alopecia, contact dermatitis, dry skin, fixed eruption, hair disorder, maculopapular rash, nail disorder, pruritus, rash, skin carcinoma, skin disorder, sweating, urticaria
Special Senses – abnormal vision, amblyopia, blepharitis, blurred vision, cataract, conjunctivitis, deafness, dry eyes, ear/eye disorder, eye pain, glaucoma, otitis media, parosmia, photophobia, retinal degeneration/disorder, taste loss, taste perversion, tinnitus, visual field defect
Urogenital System – abnormal menses, breast enlargement, breast pain, breast tenderness, dysmenorrhea, dysuria, gynecomastia, impotence, kidney calculus, kidney pain, leukorrhea, menorrhagia, menstrual disorder, penis disorder, polyuria, testis disorder, urethral pain, urinary frequency, urinary retention, urinary tract infection, urinary urgency, urination impaired, vaginitis.
Postmarketing Experience
Additional adverse experiences have been reported since Sanamisol delayed-release capsules and Sanamisol delayed-release orally disintegrating tablets have been marketed. The majority of these cases are foreign-sourced and a relationship to Sanamisol delayed-release capsules and Sanamisol delayed-release orally disintegrating tablets have not been established. Because these reactions were reported voluntarily from a population of unknown size, estimates of frequency cannot be made. These events are listed below by COSTART body system.
Body as a Whole – anaphylactic/anaphylactoid reactions; Digestive System - hepatotoxicity, pancreatitis, vomiting; Hemic and Lymphatic System - agranulocytosis, aplastic anemia, hemolytic anemia, leukopenia, neutropenia, pancytopenia, thrombocytopenia, and thrombotic thrombocytopenic purpura; Musculoskeletal System – bone fracture, myositis; Skin and Appendages – severe dermatologic reactions including erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis (some fatal); Special Senses - speech disorder; Urogenital System – interstitial nephritis, urinary retention.
Combination Therapy with Amoxicillin and Clarithromycin
In clinical trials using combination therapy with Sanamisol plus amoxicillin and clarithromycin, and Sanamisol plus amoxicillin, no adverse reactions peculiar to these drug combinations were observed. Adverse reactions that have occurred have been limited to those that had been previously reported with Sanamisol, amoxicillin, or clarithromycin.
Triple Therapy: Sanamisol/amoxicillin/clarithromycin
The most frequently reported adverse reactions for patients who received triple therapy for 14 days were diarrhea (7%), headache (6%), and taste perversion (5%). There were no statistically significant differences in the frequency of reported adverse reactions between the 10- and 14-day triple therapy regimens. No treatment-emergent adverse reactions were observed at significantly higher rates with triple therapy than with any dual therapy regimen.
Dual Therapy: Sanamisol/amoxicillin
The most frequently reported adverse reactions for patients who received Sanamisol three times daily plus amoxicillin three times daily dual therapy were diarrhea (8%) and headache (7%). No treatment-emergent adverse reactions were observed at significantly higher rates with Sanamisol three times daily plus amoxicillin three times daily dual therapy than with Sanamisol alone.
For information on adverse reactions with amoxicillin or clarithromycin, refer to their full prescribing information, ADVERSE REACTIONS sections.
Laboratory Values
The following changes in laboratory parameters in patients who received Sanamisol were reported as adverse reactions:
Abnormal liver function tests, increased SGOT (AST), increased SGPT (ALT), increased creatinine, increased alkaline phosphatase, increased globulins, increased GGTP, increased/decreased/abnormal WBC, abnormal AG ratio, abnormal RBC, bilirubinemia, blood potassium increased, blood urea increased, crystal urine present, eosinophilia, hemoglobin decreased, hyperlipemia, increased/decreased electrolytes, increased/decreased cholesterol, increased glucocorticoids, increased LDH, increased/decreased/abnormal platelets, increased gastrin levels and positive fecal occult blood. Urine abnormalities such as albuminuria, glycosuria, and hematuria were also reported. Additional isolated laboratory abnormalities were reported.
In the placebo controlled studies, when SGOT (AST) and SGPT (ALT) were evaluated, 0.4% (4/978) and 0.4% (11/2677) patients, who received placebo and Sanamisol, respectively, had enzyme elevations greater than three times the upper limit of normal range at the final treatment visit. None of these patients who received Sanamisol reported jaundice at any time during the study.
In clinical trials using combination therapy with Sanamisol plus amoxicillin and clarithromycin, and Sanamisol plus amoxicillin, no increased laboratory abnormalities particular to these drug combinations were observed.
For information on laboratory value changes with amoxicillin or clarithromycin, refer to their full prescribing information, ADVERSE REACTIONS sections.
Sanamisol contraindications
See also:
What is the most important information I should know about Sanamisol?
Heartburn is often confused with the first symptoms of a heart attack. Seek emergency medical attention if you have chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, and a general ill feeling.
Ask a doctor or pharmacist if it is safe for you to take Sanamisol if you have liver disease, or low levels of magnesium in your blood.
Sanamisol is not for immediate relief of heartburn symptoms.
Some conditions are treated with a combination of Sanamisol and antibiotics. Use all medications as directed by your doctor. Read the medication guide or patient instructions provided with each medication. Do not change your doses or medication schedule without your doctor's advice.
If you also take sucralfate (Carafate), avoid taking it at the same time you take Sanamisol. Sucralfate can make it harder for your body to absorb Sanamisol. Wait at least 30 minutes after taking Sanamisol before you take sucralfate.
Take this medication for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared.
Sanamisol 24HR should be taken only once every 24 hours for 14 days. It may take up to 4 days for full effect. Do not take more than one tablet every 24 hours.
Allow at least 4 months to pass before you start another 14-day treatment with Sanamisol 24HR. Call your doctor if you have additional symptoms and need treatment before the 4 months has passed.
Active ingredient matches for Sanamisol:
Lansoprazole in Vietnam.
| Unit description / dosage (Manufacturer) | Price, USD |
| Sanamisol 30 mg x 3 Blister x 10 Tablet | |
List of Sanamisol substitutes (brand and generic names): | |
| Salproz (Vietnam) | |
| Salproz 30 mg x 3 Blister x 10 Tablet | |
| Sandoz Lansoprazole (Canada) | |
| Sandoz Lansoprazole tablet 30 mg (Sandoz Canada Incorporated (Canada)) | |
| Sandoz Lansoprazole capsule / delayed release 15 mg (Sandoz Canada Incorporated (Canada)) | |
| SANLAP (India) | |
| 30 mg x 100's (Arvincare) | $ 6.02 |
| Sanlap 30mg SG-CAP / 100 (Arvincare) | $ 6.02 |
| SANLAP soft-gelatin cap 30 mg x 10's (Arvincare) | $ 0.60 |
| Sanlap 30mg SG-CAP / 100 (Arvincare) | $ 6.02 |
| Selanz (Myanmar) | |
| Selanz SR (Philippines) | |
| Sofran (South Korea) | |
| Solans (Indonesia) | |
| Solans 30 mg x 20's (Soho) | $ 27.28 |
| Solanza | |
| Solanza 30 mg Capsule (Emcee Pharmaceuticals Pvt.Ltd.) | $ 0.05 |
| Sopralan (Indonesia) | |
| Sopralan 30 mg x 4 x 6's (Mersifarma TM) | $ 23.81 |
| Sorifran | |
| Capsule; Oral; Lansoprazole 30 mg | |
| Spentase | |
| Spentase 30 mg Capsule (Therapeutic Pharmaceuticals) | $ 0.06 |
| Splanz (India) | |
| SPLANZ Capsule/ Tablet / 30mg / 10 units (Natco Pharma Ltd) | $ 0.80 |
| SPLANZ Capsule/ Tablet / 15mg / 10 units (Natco Pharma Ltd) | $ 0.35 |
| Splanz 15mg3 CAP / 10 (Natco Pharma Ltd) | $ 0.35 |
| Splanz 30mg CAP / 10 (Natco Pharma Ltd) | $ 0.54 |
| 15 mg x 10's (Natco Pharma Ltd) | $ 0.35 |
| 30 mg x 10's (Natco Pharma Ltd) | $ 0.54 |
| Splanz 15 mg Natco Pharma Capsule (Natco Pharma Ltd) | $ 0.04 |
| Splanz 30 mg Natco Pharma Capsule (Natco Pharma Ltd) | $ 0.06 |
| Splanz 30 mg Solarase Capsule (Natco Pharma Ltd) | $ 0.06 |
| Splanz 15 mg Solarase Capsule (Natco Pharma Ltd) | $ 0.03 |
| SPLANZ 15 MG CAPSULE 1 strip / 10 capsules each (Natco Pharma Ltd) | $ 0.39 |
| SPLANZ 30 MG CAPSULE 1 strip / 10 capsules each (Natco Pharma Ltd) | $ 1.44 |
| SPLANZ cap 15 mg x 10's (Natco Pharma Ltd) | $ 0.35 |
| SPLANZ cap 30 mg x 10's (Natco Pharma Ltd) | $ 0.54 |
| Splanz 15mg Capsule (Natco Pharma Ltd) | $ 0.04 |
| Splanz 30mg Capsule (Natco Pharma Ltd) | $ 0.14 |
| Stanzome (Japan) | |
| Stoklan | |
| Stoklan 15mg CAP / 10 (Chemo Biological) | $ 0.42 |
| Stoklan 30mg CAP / 10 (Chemo Biological) | $ 0.55 |
| Stoklan 30 mg Capsule (Chemo Biological) | $ 0.05 |
| Stoklan 15 mg Capsule (Chemo Biological) | $ 0.04 |
| Suncid | |
| Suncid 30 mg Tablet (Sunmax Pharma Limited) | $ 0.05 |
| Suncid 40 mg Tablet (Sunmax Pharma Limited) | $ 0.05 |
| Suncid 20 mg Capsule (Sunmax Pharma Limited) | $ 0.04 |
| Suprecid | |
| Synpraz (Vietnam) | |
| Synpraz 30 mg x 30 Tablet | |
| Taiproton (Japan) | |
See 1496 substitutes for Sanamisol | |
References
- DailyMed. "LANSOPRAZOLE: DailyMed provides trustworthy information about marketed drugs in the United States. DailyMed is the official provider of FDA label information (package inserts).". https://dailymed.nlm.nih.gov/dailyme... (accessed September 17, 2018).
- PubChem. "lansoprazole". https://pubchem.ncbi.nlm.nih.gov/com... (accessed September 17, 2018).
- DrugBank. "lansoprazole". http://www.drugbank.ca/drugs/DB00448 (accessed September 17, 2018).
Reviews
The results of a survey conducted on ndrugs.com for Sanamisol are given in detail below. The results of the survey conducted are based on the impressions and views of the website users and consumers taking Sanamisol. We implore you to kindly base your medical condition or therapeutic choices on the result or test conducted by a physician or licensed medical practitioners.User reports
Consumer reported useful
No survey data has been collected yetConsumer reported price estimates
No survey data has been collected yetConsumer reported time for results
No survey data has been collected yetConsumer reported age
No survey data has been collected yetConsumer reviews
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Information checked by Dr. Sachin Kumar, MD Pharmacology
