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estou tomando esse medicamento esperamos que passe essa azia orrivel :(...Keep Reading

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Anagastra adverse events reported to FDA.

Have You Experienced unusual Anagastra symptoms? PatientsVille.com collects and analyzes Anagastra side effect and adverse reports submitted by Anagastra users, such as .

Summary

FDA Adverse Reports: 3. View All

Anagastra FDA safety alerts: No

Reported hospitalizations: 1

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Often additional risks of using a medication, such as Anagastra, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Anagastra users, Learn more about unwanted side effects & find ways to reduce them. Browse Anagastra Adverse Reports reported to FDA and participate in Anagastra discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Anagastra. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Anagastra Adverse Effect Reports (FDA)

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5664648-9 | Paranoia
on Sep 27, 2007 Female patient from SPAIN , 86 years of age, was diagnosed with anxiety (What is anxiety?) and was treated with Anagastra (View Usage). Patient experienced the following unwanted or unexpected effects: paranoia. Anagastra dosage: . During the same period patient was treated with FUROSEMIDE (View Furosemide Review and Furosemide Label ), ALPRAZOLAM (View Alprazolam Review and Alprazolam Label ).

5328626-1 | Blood Osmolarity Increased, Diabetes Mellitus
Patient was taking Anagastra (View Usage). Patient had the following side effects: blood osmolarity increased, diabetes mellitus on May 07, 2007 from SPAIN Additional patient health information: Female patient , 82 years of age, . Anagastra dosage: . During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), TROMALYT (View Tromalyt Review and Tromalyt Label ), RISPERDAL (1 Mg, Frequency Not Specified) (View Risperdal Review and Risperdal Label ). Patient was hospitalized.

5277364-2 | Anaemia
Adverse event was reported on Mar 15, 2007 by a Female patient taking Anagastra (View Usage) (Dosage: ) was diagnosed with peptic ulcer (What is peptic ulcer?), grand mal convulsion and. Location: SPAIN , 48 years of age, After Anagastra was administered, patient had the following side effects: anaemia. During the same period patient was treated with VALPROIC ACID (^df^) (View Valproic Acid Review and Valproic Acid Label ), PHENYTOIN (Daily Dose 450 Mg) (View Phenytoin Review and Phenytoin Label ), NEOSIDANTOINA (View Neosidantoina Review and Neosidantoina Label ).


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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Anagastra risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Anagastra quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Anagastra use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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