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Alteis adverse events reported to FDA.

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Summary

FDA Adverse Reports: 8. View All

Alteis FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 6

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

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5228631-X | Dry Mouth, Malaise, Tachyarrhythmia
on Jan 17, 2007 Female patient from FRANCE , 61 years of age, was diagnosed with hypertension and was treated with Alteis (View Usage). Patient experienced the following unwanted or unexpected effects: dry mouth, malaise, tachyarrhythmia. Alteis dosage: 20 Mg Qd Po. During the same period patient was treated with FLUDEX (1.5 Mg Qd Po) (View Fludex Review and Fludex Label ), PRAVASTATIN (View Pravastatin Review and Pravastatin Label ).

5086047-3 | Gastric Ulcer Perforation, Hyperkalaemia, Myoglobinaemia, Neutrophil Percentage Increased, Peritonitis, Platelet Count Increased, Renal Failure Acute, Septic Shock, White Blood Cell Count Increased
Patient was taking Alteis (View Usage). Patient had the following side effects: gastric ulcer perforation, hyperkalaemia, myoglobinaemia, neutrophil percentage increased, peritonitis, platelet count increased, renal failure acute, septic shock, white blood cell count increased on Aug 03, 2006 from FRANCE Additional patient health information: Female patient , 55 years of age, weighting 273.4 lb, was diagnosed with essential hypertension, musculoskeletal pain and. Alteis dosage: 10 Mg Qd Po. During the same period patient was treated with SEROPRAM (View Seropram Review and Seropram Label ), DAFALGAN CODEINE (View Dafalgan Codeine Review and Dafalgan Codeine Label ), PLAVIX (75 Mg Daily Po) (View Plavix Review and Plavix Label ), PARIET (View Pariet Review and Pariet Label ), BUFLOMEDIL (View Buflomedil Review and Buflomedil Label ). Patient was hospitalized.

5062292-8 | Anaphylactic Reaction, Angioneurotic Oedema, Respiratory Disorder
Adverse event was reported on Jul 10, 2006 by a Female patient taking Alteis (View Usage) (Dosage: 10 Mg Qd Po) was diagnosed with essential hypertension and. Location: FRANCE , 78 years of age, After Alteis was administered, patient had the following side effects: anaphylactic reaction, angioneurotic oedema, respiratory disorder. Patient was hospitalized.

4831022-4 | Acute Febrile Neutrophilic Dermatosis, Myalgia
on Nov 02, 2005 Male patient from FRANCE , 62 years of age, was diagnosed with hypertension and was treated with Alteis (View Usage). Patient experienced the following unwanted or unexpected effects: acute febrile neutrophilic dermatosis, myalgia. Alteis dosage: . During the same period patient was treated with STILNOX (View Stilnox Review and Stilnox Label ), DAFALGAN (View Dafalgan Review and Dafalgan Label ). Patient was hospitalized.


4693762-X | Abdominal Pain, Blood Sodium Decreased, Constipation, Syncope Vasovagal
on Jun 06, 2005 Female patient from , 74 years of age, was diagnosed with essential hypertension, depression (What is depression?) and was treated with Alteis (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), blood sodium decreased, constipation (What is constipation?), syncope vasovagal. Alteis dosage: 20 Mg Qd Po. During the same period patient was treated with FLUDEX (1.5 Mg Po) (View Fludex Review and Fludex Label ), TEMESTA (View Temesta Review and Temesta Label ), ZOCOR (View Zocor Review and Zocor Label ), NORSET (60 Mg Po) (View Norset Review and Norset Label ). Patient was hospitalized.

4674004-8 | Abdominal Pain, Constipation, Depression, Hypercholesterolaemia, Hyponatraemia, Syncope Vasovagal
Patient was taking Alteis (View Usage). After Alteis was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), constipation (What is constipation?), depression (What is depression?), hypercholesterolaemia, hyponatraemia, syncope vasovagal on May 12, 2005 from Additional patient health information: Female patient , 74 years of age, was diagnosed with essential hypertension, depression (What is depression?) and. Alteis dosage: 20 Mg Qd Po. During the same period patient was treated with FLUDEX (1.5 Mg Po) (View Fludex Review and Fludex Label ), NORSET (60 Mg Po) (View Norset Review and Norset Label ), TEMESTA (View Temesta Review and Temesta Label ), ZOCOR (View Zocor Review and Zocor Label ). Patient was hospitalized.

4640603-2 | Chest Discomfort, Dyspnoea Paroxysmal Nocturnal
Adverse event was reported on Apr 06, 2005 by a Female patient taking Alteis (View Usage) (Dosage: 20 Mg Qd Po) was diagnosed with essential hypertension and. Location: , 54 years of age, Patient experienced the following unwanted or unexpected effects: chest discomfort, dyspnoea paroxysmal nocturnal.

4607427-3 | Amnesia, Insomnia, Malaise, Road Traffic Accident
on Feb 25, 2005 Male patient from , 54 years of age, was diagnosed with essential hypertension and was treated with Alteis (View Usage). Patient had the following side effects: amnesia, insomnia, malaise, road traffic accident. Alteis dosage: 10 Mg Qd Po. 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 Alteis 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 Alteis quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Alteis 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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Complete Guide to Alteis Duo (hydrochlorothiazide Olmesartan Medoxomil) (tablet) (hydroc Side Effects | Female patient, 70 years of age, weighting 169.8 |Page 1

alteis Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: cefamezin Episodes: 2: Diagnosed with major depression.Side ...

During the same period patient was treated with ALTEIS (View Alteis Review and Alteis Label ), PARIET (View Pariet Review and Pariet Label ), BUFLOMEDIL (Unk) (View Buflomedil ...

During the same period patient was treated with ASPEGIC 325 (Unk) (View Aspegic 325 Review and Aspegic 325 Label ), ALTEIS (Unk) (View Alteis Review and Alteis Label ), ...

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

... Qd) (View Kardegic /00002703/ Review and Kardegic /00002703/ Label ), ALTEIS (40 Mg, Unk) (View Alteis Review and Alteis ...

During the same period patient was treated with ASPEGIC 325 (Unk) (View Aspegic 325 Review and Aspegic 325 Label ), ALTEIS (Unk) ... (View Lercan Review and Lercan Label ...

(View Bristopen /00040801/ Review and Bristopen /00040801/ Label ), ALTEIS (3 Df, Qd) (View Alteis Review and Alteis Label ), ..... Amarel Label ), AUGMENTIN '125' (1 G ...

... Bid) (View Bristopen /00040801/ Review and Bristopen /00040801/ Label ), ALTEIS (3 Df, Qd) (View Alteis Review and Alteis ...

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Alteis Reactions
Abdominal PainWhat is Abdominal pain?
Acute Febrile Neutrophilic Dermatosis
Amnesia
Anaphylactic Reaction
Angioneurotic Oedema
Blood Sodium Decreased
Chest Discomfort
ConstipationWhat is Constipation?
DepressionWhat is Depression?
Dry Mouth
Dyspnoea Paroxysmal Nocturnal
Gastric Ulcer Perforation
Hypercholesterolaemia
Hyperkalaemia
Hyponatraemia
Insomnia
Malaise
Myalgia
Myoglobinaemia
Neutrophil Percentage Increased
Peritonitis
Platelet Count Increased
Renal Failure Acute
Respiratory Disorder
Road Traffic Accident
Septic Shock
Syncope Vasovagal
Tachyarrhythmia
White Blood Cell Count Increased
Alteis 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 Alteis 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!