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Betapred adverse events reported to FDA.

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Summary

FDA Adverse Reports: 2. View All

Betapred FDA safety alerts: No

Reported deaths: 2

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

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5227218-2 | Adrenal Cortical Insufficiency, Adrenocortical Insufficiency Acute, Blood Potassium Increased, Cardiac Arrest, Diarrhoea, Gastroenteritis, Vomiting
on Jan 26, 2007 Female patient from SWEDEN , 33 years of age, was diagnosed with iritis, gastritis, obesity (What is obesity?) and was treated with Betapred (View Usage). Patient experienced the following unwanted or unexpected effects: adrenal cortical insufficiency, adrenocortical insufficiency acute, blood potassium increased, cardiac arrest (What is cardiac arrest?), diarrhoea, gastroenteritis (What is gastroenteritis?), vomiting. Betapred dosage: . During the same period patient was treated with ZANTAC (600mg Per Day) (View Zantac Review and Zantac Label ), REDUCTIL (10mg Per Day) (View Reductil Review and Reductil Label ).

5222853-X | Adrenal Cortical Insufficiency
Patient was taking Betapred (View Usage). Patient had the following side effects: adrenal cortical insufficiency on Jan 18, 2007 from SWEDEN Additional patient health information: Female patient , 33 years of age, was diagnosed with iritis, gastritis, obesity (What is obesity?) and. Betapred dosage: 2.5mg Per Day. During the same period patient was treated with ZANTAC (600mg Per Day) (View Zantac Review and Zantac Label ), REDUCTIL (10mg Per Day) (View Reductil Review and Reductil 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 Betapred 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 Betapred quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Betapred 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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BETAPRED (.5 Mg, Unk) (View Betapred Review and Betapred Label ), ETALPHA (.25 Mcg, Unk) (View Etalpha Review and Etalpha Label ), ASPIRIN (75 Mg ...<<<<

During the same period patient was treated with DESOLETT (View Desolett Review and Desolett Label ), BETAPRED (View Betapred Review and Betapred Label ).<<<<

Report a Drug Side Effect. ... This anonymous Drug Side Effect Survey has 13 questions and takes less than 2 minutes to complete.<<<<

(View Isosorbidmononitrat Mylan Review and Isosorbidmononitrat Mylan Label ), BETAPRED (View Betapred Review and ... During the same period patient was treated with SELOKEN ...<<<<

During the same period patient was treated with PROPYLENE GLYCOL CREAM, BETAPRED. Aerius Side Effects Report: 4973530-1,Diabetes Mellitus Insulin-dependent on Mar 29 ...<<<<

... Amlodipine Label ), ACETAMINOPHEN (Film Coated Tablet) (View Acetaminophen Review and Acetaminophen Label ), BETAPRED (Tab) (View Betapred Review and Betapred Label ), ...<<<<

During the same period patient was treated with BETAPRED, MOLLIPECT (MOLLIPECT), FUROSEMIDE. Patient was hospitalized. Tarceva Side Effects Report: 5102779-2,Disseminated ...<<<<

... 20 Mg, As Needed) (View Omeprazole Review and Omeprazole Label ), NEULASTA (View Neulasta Review and Neulasta Label ), BETAPRED (View Betapred Review and Betapred Label ), ...<<<<

During the same period patient was treated with ACETAMINOPHEN, PROMITEN, PLASMODEX, CATAPRESSAN, CYKLOKAPRON, CLINDAMYCIN, THEOPHYLLAMIN, BETAPRED.<<<<

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Betapred Reactions
Adrenal Cortical Insufficiency
Adrenocortical Insufficiency Acute
Blood Potassium Increased
Cardiac ArrestWhat is Cardiac arrest?
Diarrhoea
GastroenteritisWhat is Gastroenteritis?
Sudden Death
Vomiting
Betapred 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 Betapred 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!