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Hyperium adverse events reported to FDA.

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Summary

FDA Adverse Reports: 7. View All

Hyperium FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 7

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

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5315990-2 | Acute Prerenal Failure, Fall, Rhabdomyolysis
on Apr 24, 2007 Female patient from FRANCE , 92 years of age, weighting 156.5 lb, was diagnosed with essential hypertension and was treated with Hyperium (View Usage). Patient experienced the following unwanted or unexpected effects: acute prerenal failure, fall (What is fall?), rhabdomyolysis. Hyperium dosage: . During the same period patient was treated with PLAVIX (Unk) (View Plavix Review and Plavix Label ), VASTEN (View Vasten Review and Vasten Label ), STILNOX (View Stilnox Review and Stilnox Label ), CHRONOADALATE (View Chronoadalate Review and Chronoadalate Label ). Patient was hospitalized.

5296496-6 | Acute Prerenal Failure, Atrial Fibrillation, Escherichia Urinary Tract Infection, Fall, Rhabdomyolysis, Tachyarrhythmia
Patient was taking Hyperium (View Usage). Patient had the following side effects: acute prerenal failure, atrial fibrillation (What is atrial fibrillation?), escherichia urinary tract infection, fall (What is fall?), rhabdomyolysis, tachyarrhythmia on Apr 04, 2007 from FRANCE Additional patient health information: Female patient , 92 years of age, weighting 156.5 lb, was diagnosed with essential hypertension and. Hyperium dosage: . During the same period patient was treated with PLAVIX (Unk) (View Plavix Review and Plavix Label ), CHRONOADALATE (Unk) (View Chronoadalate Review and Chronoadalate Label ), VASTEN (View Vasten Review and Vasten Label ), STILNOX (View Stilnox Review and Stilnox Label ). Patient was hospitalized.

5039897-3 | Abdominal Pain, Abnormal Faeces, Alpha Globulin Increased, Anaemia, Appendicectomy, Asthenia, Blood Alkaline Phosphatase Increased, Blood Lactate Dehydrogenase Increased, Blood Uric Acid Increased
Adverse event was reported on May 29, 2006 by a Female patient taking Hyperium (View Usage) (Dosage: Unk, Unk) was diagnosed with hypertension, venous insufficiency, anxiety (What is anxiety?), anaemia, peritonitis, chronic myeloid leukaemia and. Location: FRANCE , 75 years of age, weighting 141.1 lb, After Hyperium was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), abnormal faeces, alpha globulin increased, anaemia, appendicectomy, asthenia, blood alkaline phosphatase increased, blood lactate dehydrogenase increased, blood uric acid increased. During the same period patient was treated with PRACTAZIN (Unk, Unk) (View Practazin Review and Practazin Label ), VEINAMITOL (Unk, Unk) (View Veinamitol Review and Veinamitol Label ), TEMESTA (View Temesta Review and Temesta Label ), TARDYFERON (View Tardyferon Review and Tardyferon Label ), AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), GLEEVEC (400 Mg Daily) (View Gleevec Review and Gleevec Label ). Patient was hospitalized.

5011873-6 | Diarrhoea, Pancreatitis, Vomiting
on May 03, 2006 Female patient from FRANCE , 64 years of age, was diagnosed with epilepsy (What is epilepsy?) and was treated with Hyperium (View Usage). Patient experienced the following unwanted or unexpected effects: diarrhoea, pancreatitis, vomiting. Hyperium dosage: . During the same period patient was treated with EUCALCIC (View Eucalcic Review and Eucalcic Label ), VASTEN (View Vasten Review and Vasten Label ), STILNOX (View Stilnox Review and Stilnox Label ), DEPAKENE (1000 Mg) (View Depakene Review and Depakene Label ), KAYEXALATE (View Kayexalate Review and Kayexalate Label ). Patient was hospitalized.


4617927-8 | Abdominal Distension, Abdominal Pain, Alanine Aminotransferase Increased, Bilirubin Conjugated Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Bilirubin Unconjugated Increased, Cholelithiasis, Flatulence
on Feb 18, 2005 Male patient from , 61 years of age, weighting 273.4 lb, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and was treated with Hyperium (View Usage). Patient had the following side effects: abdominal distension, abdominal pain (What is abdominal pain?), alanine aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, blood bilirubin unconjugated increased, cholelithiasis, flatulence. Hyperium dosage: 1 Mg, Qd. During the same period patient was treated with CORDARONE (450 Mg Per Day) (View Cordarone Review and Cordarone Label ), SECTRAL (400 Mg Per Day) (View Sectral Review and Sectral Label ), AMLOR (10 Mg Per Day) (View Amlor Review and Amlor Label ), STABLON (View Stablon Review and Stablon Label ), ATARAX (View Atarax Review and Atarax Label ). Patient was hospitalized.

4616039-7 | Blood Pressure Inadequately Controlled, Pancreatitis
Patient was taking Hyperium (View Usage). After Hyperium was administered, patient had the following side effects: blood pressure inadequately controlled, pancreatitis on Mar 18, 2005 from Additional patient health information: Male patient , 70 years of age, was diagnosed with hypertension and. Hyperium dosage: . During the same period patient was treated with LOPRESSOR (View Lopressor Review and Lopressor Label ). Patient was hospitalized.

4588127-5 | Abdominal Distension, Abdominal Pain, Alanine Aminotransferase Increased, Bilirubin Conjugated Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Bilirubin Unconjugated Increased, Cholelithiasis, Flatulence
Adverse event was reported on Feb 18, 2005 by a Male patient taking Hyperium (View Usage) (Dosage: 1 Mg, Qd) was diagnosed with atrial fibrillation (What is atrial fibrillation?), epilepsy (What is epilepsy?) and. Location: , 61 years of age, weighting 273.4 lb, Patient experienced the following unwanted or unexpected effects: abdominal distension, abdominal pain (What is abdominal pain?), alanine aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, blood bilirubin unconjugated increased, cholelithiasis, flatulence. During the same period patient was treated with CORDARONE (450 Mg Per Day) (View Cordarone Review and Cordarone Label ), SECTRAL (400 Mg Per Day) (View Sectral Review and Sectral Label ), AMLOR (10 Mg Per Day) (View Amlor Review and Amlor Label ), STABLON (View Stablon Review and Stablon Label ), ATARAX (View Atarax Review and Atarax Label ), TRILEPTAL (150 Mg Per Day) (View Trileptal Review and Trileptal 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 Hyperium 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 Hyperium quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Hyperium 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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An arrhythmia is a problem with the speed or rhythm of the heartbeat.

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Hyperium Reactions
Abdominal Distension
Abdominal PainWhat is Abdominal pain?
Abnormal Faeces
Acute Prerenal Failure
Alanine Aminotransferase Increased
Alpha Globulin Increased
Anaemia
Appendicectomy
Asthenia
Atrial FibrillationWhat is Atrial fibrillation?
Bilirubin Conjugated Increased
Blood Alkaline Phosphatase Increased
Blood Bilirubin Increased
Blood Bilirubin Unconjugated Increased
Blood Lactate Dehydrogenase Increased
Blood Pressure Inadequately Controlled
Blood Uric Acid Increased
Cholelithiasis
Diarrhoea
Escherichia Urinary Tract Infection
FallWhat is Fall?
Flatulence
Pancreatitis
Rhabdomyolysis
Tachyarrhythmia
Vomiting
Hyperium 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 Hyperium 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!