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Nivadil adverse events reported to FDA.

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Summary

FDA Adverse Reports: 13. View All

Nivadil FDA safety alerts: No

Reported deaths: 3

Reported hospitalizations: 8

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

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5293087-8 | Dizziness, Hypoacusis, Pyrexia, Sudden Hearing Loss, Vomiting
on Mar 30, 2007 Male patient from JAPAN , 67 years of age, was diagnosed with hypertension, hypersensitivity, insomnia, gastric ulcer and was treated with Nivadil (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), hypoacusis, pyrexia, sudden hearing loss, vomiting. Nivadil dosage: . During the same period patient was treated with AZELASTINE HCL (View Azelastine Hcl Review and Azelastine Hcl Label ), CYANOCOBALAMIN (View Cyanocobalamin Review and Cyanocobalamin Label ), MEVALOTIN (View Mevalotin Review and Mevalotin Label ), AMOBAN (View Amoban Review and Amoban Label ), GASTER D (View Gaster D Review and Gaster D Label ), LENDORMIN (View Lendormin Review and Lendormin Label ), TERNELIN (View Ternelin Review and Ternelin Label ), CALBLOCK (View Calblock Review and Calblock Label ). Patient was hospitalized.

5292929-X | Dizziness, Hypoacusis, Pyrexia, Sudden Hearing Loss, Vomiting
Patient was taking Nivadil (View Usage). Patient had the following side effects: dizziness (What is dizziness?), hypoacusis, pyrexia, sudden hearing loss, vomiting on Mar 30, 2007 from JAPAN Additional patient health information: Male patient , 67 years of age, was diagnosed with hypertension, hypersensitivity, insomnia, gastric ulcer and. Nivadil dosage: . During the same period patient was treated with AZELASTINE HCL (View Azelastine Hcl Review and Azelastine Hcl Label ), CYANOCOBALAMIN (View Cyanocobalamin Review and Cyanocobalamin Label ), MEVALOTIN (View Mevalotin Review and Mevalotin Label ), AMOBAN (View Amoban Review and Amoban Label ), GASTER D (View Gaster D Review and Gaster D Label ), LENDORMIN (View Lendormin Review and Lendormin Label ), TERNELIN (View Ternelin Review and Ternelin Label ), CALBLOCK (View Calblock Review and Calblock Label ). Patient was hospitalized.

5098377-X | Anaemia, Anorexia, Blood Lactate Dehydrogenase Increased, Haematocrit Decreased, Haemoglobin Decreased, Malaise, Mean Cell Volume Abnormal, Pancytopenia, Platelet Count Decreased
Adverse event was reported on Jul 11, 2006 by a Male patient taking Nivadil (View Usage) (Dosage: 8 Mg/day) was diagnosed with hypertension, cerebral infarction, benign prostatic hyperplasia, nail tinea and. Location: JAPAN , 70 years of age, weighting 127.9 lb, After Nivadil was administered, patient had the following side effects: anaemia, anorexia, blood lactate dehydrogenase increased, haematocrit decreased, haemoglobin decreased, malaise, mean cell volume abnormal, pancytopenia, platelet count decreased. During the same period patient was treated with PANALDINE (200 Mg/day) (View Panaldine Review and Panaldine Label ), HARNAL (0.2 Mg/day) (View Harnal Review and Harnal Label ), LAMISIL (125 Mg/d) (View Lamisil Review and Lamisil Label ). Patient was hospitalized.

5098233-7 | Anaemia, Anorexia, Blood Lactate Dehydrogenase Increased, Haematocrit Decreased, Haemoglobin Decreased, Malaise, Mean Cell Volume Abnormal, Pancytopenia, Platelet Count Decreased
on Jul 11, 2006 Male patient from JAPAN , 70 years of age, weighting 127.9 lb, was diagnosed with hypertension, cerebral infarction, benign prostatic hyperplasia, nail tinea and was treated with Nivadil (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, anorexia, blood lactate dehydrogenase increased, haematocrit decreased, haemoglobin decreased, malaise, mean cell volume abnormal, pancytopenia, platelet count decreased. Nivadil dosage: 8 Mg/day. During the same period patient was treated with PANALDINE (200 Mg/day) (View Panaldine Review and Panaldine Label ), HARNAL (0.2 Mg/day) (View Harnal Review and Harnal Label ), LAMISIL (125 Mg/d) (View Lamisil Review and Lamisil Label ). Patient was hospitalized.


5078780-4 | Anaemia, Anorexia, Blood Lactate Dehydrogenase Increased, Haematocrit Decreased, Haemoglobin Decreased, Malaise, Mean Cell Volume Abnormal, Pancytopenia, Platelet Count Decreased
on Jul 11, 2006 Male patient from JAPAN , 70 years of age, weighting 127.9 lb, was diagnosed with hypertension, cerebral infarction, benign prostatic hyperplasia, nail tinea and was treated with Nivadil (View Usage). Patient had the following side effects: anaemia, anorexia, blood lactate dehydrogenase increased, haematocrit decreased, haemoglobin decreased, malaise, mean cell volume abnormal, pancytopenia, platelet count decreased. Nivadil dosage: 8 Mg/day. During the same period patient was treated with PANALDINE (200 Mg/day) (View Panaldine Review and Panaldine Label ), HARNAL (0.2 Mg/day) (View Harnal Review and Harnal Label ), LAMISIL (125 Mg/d) (View Lamisil Review and Lamisil Label ). Patient was hospitalized.

5054636-8 | Anorexia, Blood Lactate Dehydrogenase Increased, Haematocrit Decreased, Haemoglobin Decreased, Malaise, Mean Cell Volume Abnormal, Pancytopenia, Platelet Count Decreased, Red Blood Cell Count Decreased
Patient was taking Nivadil (View Usage). After Nivadil was administered, patient had the following side effects: anorexia, blood lactate dehydrogenase increased, haematocrit decreased, haemoglobin decreased, malaise, mean cell volume abnormal, pancytopenia, platelet count decreased, red blood cell count decreased on Jul 11, 2006 from JAPAN Additional patient health information: Male patient , 70 years of age, was diagnosed with nail tinea and. Nivadil dosage: . During the same period patient was treated with PANALDINE (View Panaldine Review and Panaldine Label ), HARNAL (View Harnal Review and Harnal Label ), LAMISIL (125 Mg/d) (View Lamisil Review and Lamisil Label ). Patient was hospitalized.

4899933-1 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Bile Duct Cancer, Biliary Neoplasm, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Lactate Dehydrogenase Increased, Gamma-glutamyltransferase Increased, Hepatic Function Abnormal
Adverse event was reported on Aug 22, 2005 by a Female patient taking Nivadil (View Usage) (Dosage: 8 Mg/d) was diagnosed with essential hypertension, nail tinea and. Location: JAPAN , 76 years of age, weighting 103.6 lb, Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, bile duct cancer, biliary neoplasm, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, hepatic function abnormal. During the same period patient was treated with TENORMIN (5 Mg/d) (View Tenormin Review and Tenormin Label ), APLACE (300 Mg/d) (View Aplace Review and Aplace Label ), KARIKUROMONE (150 Mg/d) (View Karikuromone Review and Karikuromone Label ), LAMISIL (125 Mg, Qd) (View Lamisil Review and Lamisil Label ), SALUMOSIN (15 Mg/d) (View Salumosin Review and Salumosin Label ).

4832813-6 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Lactate Dehydrogenase Increased, Gamma-glutamyltransferase Increased, Hepatic Function Abnormal, Hepatic Neoplasm Malignant, Jaundice
on Aug 22, 2005 Female patient from JAPAN , 76 years of age, weighting 103.6 lb, was diagnosed with essential hypertension, nail tinea and was treated with Nivadil (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, hepatic function abnormal, hepatic neoplasm malignant, jaundice (What is jaundice?). Nivadil dosage: 8 Mg/d. During the same period patient was treated with TENORMIN (5 Mg/d) (View Tenormin Review and Tenormin Label ), APLACE (300 Mg/d) (View Aplace Review and Aplace Label ), KARIKUROMONE (150 Mg/d) (View Karikuromone Review and Karikuromone Label ), LAMISIL (125 Mg, Qd) (View Lamisil Review and Lamisil Label ), SALUMOSIN (15 Mg/d) (View Salumosin Review and Salumosin Label ).

4821525-0 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Bile Duct Cancer, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Lactate Dehydrogenase Increased, Gamma-glutamyltransferase Increased, Hepatic Function Abnormal, Hepatic Neoplasm Malignant
on Aug 22, 2005 Female patient from JAPAN , 76 years of age, weighting 103.6 lb, was diagnosed with essential hypertension, nail tinea and was treated with Nivadil (View Usage). After Nivadil was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, bile duct cancer, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, hepatic function abnormal, hepatic neoplasm malignant. Nivadil dosage: 4 Mg/d. During the same period patient was treated with TENORMIN (5 Mg/d) (View Tenormin Review and Tenormin Label ), APLACE (View Aplace Review and Aplace Label ), KARIKUROMONE (View Karikuromone Review and Karikuromone Label ), LAMISIL (125 Mg, Qd) (View Lamisil Review and Lamisil Label ).

4820489-3 | Alanine Aminotransferase Increased, Anal Cancer, Aspartate Aminotransferase Increased, Bile Duct Cancer, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Lactate Dehydrogenase Increased, Gamma-glutamyltransferase Increased, Hepatic Function Abnormal
Patient was taking Nivadil (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, anal cancer (What is anal cancer?), aspartate aminotransferase increased, bile duct cancer, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, hepatic function abnormal on Aug 22, 2005 from JAPAN Additional patient health information: Female patient , 76 years of age, weighting 103.6 lb, was diagnosed with essential hypertension, nail tinea and. Nivadil dosage: 4 Mg/d. During the same period patient was treated with TENORMIN (5 Mg/d) (View Tenormin Review and Tenormin Label ), APLACE (View Aplace Review and Aplace Label ), KARIKUROMONE (View Karikuromone Review and Karikuromone Label ), LAMISIL (125 Mg, Qd) (View Lamisil Review and Lamisil Label ).

4780073-7 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Bile Duct Cancer, Gamma-glutamyltransferase Increased, Hepatic Function Abnormal
Adverse event was reported on Aug 22, 2005 by a Female patient taking Nivadil (View Usage) (Dosage: 4 Mg/d) was diagnosed with nail tinea and. Location: JAPAN , 77 years of age, Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, bile duct cancer, gamma-glutamyltransferase increased, hepatic function abnormal. During the same period patient was treated with TENORMIN (5 Mg/d) (View Tenormin Review and Tenormin Label ), APLACE (View Aplace Review and Aplace Label ), KARIKUROMONE (View Karikuromone Review and Karikuromone Label ), LAMISIL (View Lamisil Review and Lamisil Label ).

4598692-X | Cerebral Infarction, Cerebral Thrombosis, Depressed Level Of Consciousness, Dysarthria, Facial Palsy
on Jan 15, 2004 Female patient from , 83 years of age, weighting 132.3 lb, was diagnosed with hypertension, angina pectoris, hypercholesterolaemia and was treated with Nivadil (View Usage). After Nivadil was administered, patient had the following side effects: cerebral infarction, cerebral thrombosis, depressed level of consciousness, dysarthria, facial palsy. Nivadil dosage: Unk, Unk. During the same period patient was treated with BUFFERIN (81mg Daily Dose) (View Bufferin Review and Bufferin Label ), EPADEL (1.2g Daily Dose) (View Epadel Review and Epadel Label ), DIOVAN (Unk, Unk) (View Diovan Review and Diovan Label ). Patient was hospitalized.

4588150-0 | Cerebral Infarction, Cerebral Thrombosis, Depressed Level Of Consciousness, Dysarthria, Facial Palsy
on Jan 15, 2004 Female patient from , 83 years of age, weighting 132.3 lb, was diagnosed with hypertension, angina pectoris, hypercholesterolaemia and was treated with Nivadil (View Usage). Patient experienced the following unwanted or unexpected effects: cerebral infarction, cerebral thrombosis, depressed level of consciousness, dysarthria, facial palsy. Nivadil dosage: Unk, Unk. During the same period patient was treated with BUFFERIN (81mg Daily Dose) (View Bufferin Review and Bufferin Label ), EPADEL (1.2g Daily Dose) (View Epadel Review and Epadel Label ), DIOVAN (Unk, Unk) (View Diovan Review and Diovan 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 Nivadil 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 Nivadil quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Nivadil 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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Nivadil Reactions
Alanine Aminotransferase Increased
Anaemia
Anal CancerWhat is Anal cancer?
Anorexia
Aspartate Aminotransferase Increased
Bile Duct Cancer
Biliary Neoplasm
Blood Alkaline Phosphatase Increased
Blood Bilirubin Increased
Blood Lactate Dehydrogenase Increased
Cerebral Infarction
Cerebral Thrombosis
Depressed Level Of Consciousness
DizzinessWhat is Dizziness?
Dysarthria
Facial Palsy
Gamma-glutamyltransferase Increased
Haematocrit Decreased
Haemoglobin Decreased
Hepatic Function Abnormal
Hepatic Neoplasm Malignant
Hypoacusis
JaundiceWhat is Jaundice?
Malaise
Mean Cell Volume Abnormal
Pancytopenia
Platelet Count Decreased
Pyrexia
Sudden Hearing Loss
Vomiting
Nivadil 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 Nivadil 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!