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Mylanta adverse events reported to FDA.

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

Summary

FDA Adverse Reports: 4. View All

Mylanta FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 3

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Often additional risks of using a medication, such as Mylanta, 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 Mylanta users, Learn more about unwanted side effects & find ways to reduce them. Browse Mylanta Adverse Reports reported to FDA and participate in Mylanta discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Mylanta. 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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Mylanta Adverse Effect Reports (FDA)

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6929342-2 | Therapeutic Agent Toxicity
on Aug 05, 2010 Female patient from UNITED STATES , 29 years of age, weighting 82.01 lb, was treated with Mylanta (View Usage). Patient experienced the following unwanted or unexpected effects: therapeutic agent toxicity. Mylanta dosage: . During the same period patient was treated with ROLAIDS (View Rolaids Review and Rolaids Label ), ASPIRIN (8-12 Tablets Per Day) (View Aspirin Review and Aspirin Label ), ALKA SELTZER (No More Than 4 Tablets Per Day) (View Alka Seltzer Review and Alka Seltzer Label ). Patient was hospitalized.

6518487-7 | Hypocalciuria, Hypophosphataemic Rickets
Patient was taking Mylanta (View Usage). Patient had the following side effects: hypocalciuria, hypophosphataemic rickets on Dec 15, 2009 from UNITED STATES Additional patient health information: Male patient , 18 years of age, weighting 48.50 lb, was diagnosed with convulsion and. Mylanta dosage: 4-8 Teaspoons Daily. During the same period patient was treated with OSMOLITE (16-32 Ounces Daily) (View Osmolite Review and Osmolite Label ), PHENOBARBITAL (60-90 Mg Daily) (View Phenobarbital Review and Phenobarbital Label ). Patient was hospitalized.

6516909-9 | Hypophosphataemia, Nephrocalcinosis, Rickets
Adverse event was reported on Dec 11, 2009 by a Female patient taking Mylanta (View Usage) (Dosage: 5 Ml To Each Bottle) was diagnosed with vomiting, medical diet and. Location: UNITED STATES , weighting 10.19 lb, After Mylanta was administered, patient had the following side effects: hypophosphataemia, nephrocalcinosis, rickets (What is rickets?). During the same period patient was treated with INFANTS FORMULA (View Infants Formula Review and Infants Formula Label ). Patient was hospitalized.

4883694-6 | Anencephaly, Caesarean Section, Metal Poisoning
on Jan 05, 2006 Female patient from BRAZIL , 38 years of age, was diagnosed with dyspepsia and was treated with Mylanta (View Usage). Patient experienced the following unwanted or unexpected effects: anencephaly, caesarean section, metal poisoning. Mylanta dosage: 2 Soup Spoons Daily, Oral.


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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 Mylanta 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 Mylanta quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Mylanta 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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Mylanta Reactions
Anencephaly
Caesarean Section
Death Neonatal
Hypocalciuria
Hypophosphataemia
Hypophosphataemic Rickets
Metal Poisoning
Nephrocalcinosis
RicketsWhat is Rickets?
Therapeutic Agent Toxicity
Mylanta Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Mylanta adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!