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Kaleorid adverse events reported to FDA.

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Summary

FDA Adverse Reports: 4. View All

Kaleorid FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 1

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

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5110382-3 | Dysphagia, Oesophagitis
on Sep 14, 2006 Male patient from FRANCE , 56 years of age, weighting 167.6 lb, was treated with Kaleorid (View Usage). Patient experienced the following unwanted or unexpected effects: dysphagia, oesophagitis. Kaleorid dosage: 1200 Mg. During the same period patient was treated with CAPTOPRIL (50 Mg) (View Captopril Review and Captopril Label ), CAPTEA (View Captea Review and Captea Label ), PLAVIX (View Plavix Review and Plavix Label ).

5085000-3 | Abdominal Pain Upper
Patient was taking Kaleorid (View Usage). Patient had the following side effects: abdominal pain upper on Aug 07, 2006 from DENMARK Additional patient health information: Female patient , 61 years of age, weighting 105.8 lb, was diagnosed with ill-defined disorder, cardiomyopathy (What is cardiomyopathy?) and. Kaleorid dosage: . During the same period patient was treated with COVERSYL (Daily Dose: 8 Milligram(s)) (View Coversyl Review and Coversyl Label ), FURIX (Daily Dose: 20 Milligram(s)) (View Furix Review and Furix Label ), PAMOL (View Pamol Review and Pamol Label ), MAGNESIA (View Magnesia Review and Magnesia Label ).

5084999-9 | Abdominal Pain Upper
Adverse event was reported on Aug 07, 2006 by a Female patient taking Kaleorid (View Usage) (Dosage: ) was diagnosed with ill-defined disorder, cardiomyopathy (What is cardiomyopathy?) and. Location: DENMARK , 61 years of age, weighting 105.8 lb, After Kaleorid was administered, patient had the following side effects: abdominal pain upper. During the same period patient was treated with COVERSYL (Daily Dose: 8 Milligram(s)) (View Coversyl Review and Coversyl Label ), FURIX (Daily Dose: 20 Milligram(s)) (View Furix Review and Furix Label ), PAMOL (View Pamol Review and Pamol Label ), MAGNESIA (View Magnesia Review and Magnesia Label ).

4558345-0 | Blood Creatine Phosphokinase Increased, Muscular Weakness, Myositis
on Nov 29, 2004 Male patient from , 59 years of age, was diagnosed with diabetes mellitus, polymyalgia rheumatica (What is polymyalgia rheumatica?) and was treated with Kaleorid (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, muscular weakness, myositis (What is myositis?). Kaleorid dosage: 1 Df, Tid. During the same period patient was treated with DIURAL (40 Mg, Bid) (View Diural Review and Diural Label ), NEXIUM (40 Mg, Qd) (View Nexium Review and Nexium Label ), LESCOL (80 Mg, Qd) (View Lescol Review and Lescol Label ), AVANDIA (4 Mg, Qd) (View Avandia Review and Avandia Label ), PREDNISOLONE (5 Mg, Qd) (View Prednisolone Review and Prednisolone Label ), AMARYL (3 Mg, Qd) (View Amaryl Review and Amaryl Label ). Patient was hospitalized.


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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 Kaleorid 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 Kaleorid quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Kaleorid 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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... Kenzen Label ), MEDIATENSYL (View Mediatensyl Review and Mediatensyl Label ), ZANIDIP (View Zanidip Review and Zanidip Label ), KALEORID (View Kaleorid Review and Kaleorid Label ).

(View Mediatensyl Review and Mediatensyl Label ), ZANIDIP (View Zanidip Review and Zanidip Label ), KALEORID (View ..... Enalapril Label ), INDAPEN SR (1.5 Mg, 1 Tablet ...

)During the same period patient was treated with METRONIDAZOLE (View Metronidazole Review and Metronidazole Label ), KALEORID (View Kaleorid Review and Kaleorid Label ).

During the same period patient was treated with SINEMET (10/100 Mg X 1/day) (View Sinemet Review and Sinemet Label ), KALEORID (2 G/week) (View Kaleorid Review and Kaleorid ...

During the same period patient was treated with KALEORID (750 Mg/d) (View Kaleorid Review and Kaleorid Label ), MAGNESIA (2 Df, Qd) (View Magnesia Review and Magnesia Label ...

... Inegy Label ), KENZEN (Unk) (View Kenzen Review and Kenzen Label ), CARDENSIEL (Unk) (View Cardensiel Review and Cardensiel Label ), KALEORID (View Kaleorid Review and Kaleorid ...

During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), AMLOR (View Amlor Review and Amlor Label ), KALEORID (View Kaleorid Review and ...

... Imovane Review and Imovane Label ), TENORMIN (Daily Dose: 100 Milligram(s)) (View Tenormin Review and Tenormin Label ), KALEORID (View Kaleorid Review and Kaleorid Label ).

... acetylsalicylate Lysine) Review and Kardegic Sachets (acetylsalicylate Lysine) Label ), MOLSIDOMINE (View Molsidomine Review and Molsidomine Label ), KALEORID (View Kaleorid ...

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Kaleorid Reactions
Abdominal Pain Upper
Blood Creatine Phosphokinase Increased
Dysphagia
Muscular Weakness
MyositisWhat is Myositis?
Oesophagitis
Kaleorid 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 Kaleorid 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!