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Have You Experienced unusual Rize symptoms? PatientsVille.com collects and analyzes Rize side effect and adverse reports submitted by Rize users, such as Fatigue and blood pressure is 75/43 pulse|severe facial swelling, burning, irritation, reddening of|Elevated blood pressure (personally unprecedented) 160/110 sitting,|.

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

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6216845-1 | Bradycardia
on May 22, 2009 Female patient from JAPAN , 67 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and was treated with Rize (View Usage). Patient experienced the following unwanted or unexpected effects: bradycardia. Rize dosage: Unk. During the same period patient was treated with BEPRICOR (Unk) (View Bepricor Review and Bepricor Label ), SEDIEL (Unk) (View Sediel Review and Sediel Label ), DOGMATYL (Unk) (View Dogmatyl Review and Dogmatyl Label ), SILECE (Unk) (View Silece Review and Silece Label ), MYSLEE (Unk) (View Myslee Review and Myslee Label ), WARFARIN SODIUM (Unk) (View Warfarin Sodium Review and Warfarin Sodium Label ).

6204634-3 | Bradycardia
Patient was taking Rize (View Usage). Patient had the following side effects: bradycardia on May 15, 2009 from JAPAN Additional patient health information: Female patient , 67 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and. Rize dosage: Unk. During the same period patient was treated with BEPRICOR (Unk) (View Bepricor Review and Bepricor Label ), SEDIEL (Unk) (View Sediel Review and Sediel Label ), DOGMATYL (Unk) (View Dogmatyl Review and Dogmatyl Label ), SILECE (Unk) (View Silece Review and Silece Label ), MYSLEE (Unk) (View Myslee Review and Myslee Label ), WARFARIN SODIUM (Unk) (View Warfarin Sodium Review and Warfarin Sodium Label ).

4801391-X | Neuroleptic Malignant Syndrome
Adverse event was reported on Jun 27, 2005 by a Male patient taking Rize (View Usage) (Dosage: Daily Dose: 1 Dosage Form) was diagnosed with insomnia, depression (What is depression?), mania, nasopharyngitis and. Location: JAPAN , weighting 154.3 lb, After Rize was administered, patient had the following side effects: neuroleptic malignant syndrome. During the same period patient was treated with DEPROMEL 25 (Daily Dose: 200 Milligram(s)) (View Depromel 25 Review and Depromel 25 Label ), LIMAS (Daily Dose: 200 Milligram(s)) (View Limas Review and Limas Label ), AMOBAN (Daily Dose: 10 Milligram(s)) (View Amoban Review and Amoban Label ), BETAMAC (Daily Dose: 75 Milligram(s)) (View Betamac Review and Betamac Label ), PL (View Pl Review and Pl Label ), PABRON (View Pabron Review and Pabron Label ). Patient was hospitalized.

4749428-0 | Neuroleptic Malignant Syndrome
on Jun 27, 2005 Male patient from JAPAN , weighting 154.3 lb, was diagnosed with insomnia, depression (What is depression?), mania, nasopharyngitis and was treated with Rize (View Usage). Patient experienced the following unwanted or unexpected effects: neuroleptic malignant syndrome. Rize dosage: Daily Dose: 1 Dosage Form. During the same period patient was treated with DEPROMEL 25 (Daily Dose: 200 Milligram(s)) (View Depromel 25 Review and Depromel 25 Label ), AMOBAN (Daily Dose: 10 Milligram(s)) (View Amoban Review and Amoban Label ), LIMAS (Daily Dose: 200 Milligram(s)) (View Limas Review and Limas Label ), BETAMAC (Daily Dose: 75 Milligram(s)) (View Betamac Review and Betamac Label ), PL (View Pl Review and Pl Label ), PABRON (View Pabron Review and Pabron Label ). Patient was hospitalized.


4592749-5 | Abdominal Pain, Blood Calcium Decreased, Blood Potassium Decreased, Blood Pressure Diastolic Increased, Differential White Blood Cell Count Abnormal, Dysuria, Glucose Urine, Hepatic Enzyme Increased, Inappropriate Antidiuretic Hormone Secretion
on Jun 11, 2004 Female patient from , 31 years of age, weighting 112.4 lb, was diagnosed with depression (What is depression?), anxiety (What is anxiety?), gastritis erosive, pain (What is pain?) and was treated with Rize (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), blood calcium decreased, blood potassium decreased, blood pressure diastolic increased, differential white blood cell count abnormal, dysuria, glucose urine, hepatic enzyme increased, inappropriate antidiuretic hormone secretion. Rize dosage: Daily Dose: 15 Milligram(s). During the same period patient was treated with DEPROMEL 25 (Daily Dose: 25 Milligram(s)) (View Depromel 25 Review and Depromel 25 Label ), DEPAS (Daily Dose: 1 Milligram(s)) (View Depas Review and Depas Label ), SOLANAX (Daily Dose: .4 Milligram(s)) (View Solanax Review and Solanax Label ), ZANTAC (View Zantac Review and Zantac Label ), GASMOTIN (View Gasmotin Review and Gasmotin Label ), VOLTAREN (Daily Dose: 50 Milligram(s)) (View Voltaren Review and Voltaren 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 Rize 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 Rize quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Rize 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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During the same period patient was treated with RIZE (View Rize Review and Rize Label ), NIVADIL (View Nivadil Review and Nivadil Label ), ALMARL (View Almarl Review and Almarl ...<<<<

During the same period patient was treated with EURODIN (2 Mg) (View Eurodin Review and Eurodin Label ), RIZE (15 Mg) (View Rize Review and Rize Label ), FLOMOX (Unk) (View ...<<<<

... Depas Review and Depas Label ), ERSIBON (View Ersibon Review and Ersibon Label ), MUCOSTA (View Mucosta Review and Mucosta Label ), RIZE (View Rize Review and Rize Label ).<<<<

During the same period patient was treated with RIZE /00624801/ (View Rize /00624801/ Review and Rize ...<<<<

... Diovan Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), NEUQUINON (View Neuquinon Review and Neuquinon Label ), ADALAT (View Adalat Review and Adalat Label ), RIZE ...<<<<

During the same period patient was treated with ALINAMIN (View Alinamin Review and Alinamin Label ), SYMMETREL (View Symmetrel Review and Symmetrel Label ), RIZE (View ...<<<<

During the same period patient was treated with ZOLPIDEM TARTRATE (View Zolpidem Tartrate Review and Zolpidem Tartrate Label ), RIZE (CLOTIAZEPAM) (View Rize (clotiazepam ...<<<<

During the same period patient was treated with ALINAMIN (View Alinamin Review and Alinamin Label ), SYMMETREL (View Symmetrel Review and Symmetrel Label ), RIZE (View Rize ...<<<<

Rize Review and Rize Label ), FLOMOX (Unk) (View Flomox Review and Flomox Label ), BRUFEN (Unk) (View Brufen Review and Brufen Label ), RULID (Unk) (View Rulid Review and ...<<<<

During the same period patient was treated with RIZE/00624801/(CLOTIAZEPAM) (Oral) (View Rize/00624801/(clotiazepam) Review and Rize/00624801/(clotiazepam) Label ).<<<<

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Rize Reactions
Abdominal PainWhat is Abdominal pain?
Blood Calcium Decreased
Blood Potassium Decreased
Blood Pressure Diastolic Increased
Bradycardia
Differential White Blood Cell Count Abnormal
Dysuria
Glucose Urine
Hepatic Enzyme Increased
Inappropriate Antidiuretic Hormone Secretion
Neuroleptic Malignant Syndrome
Rize 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 Rize 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!