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Nimodipine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 6. View All

Nimodipine FDA safety alerts: 2006

Reported deaths: 2

Reported hospitalizations: 3

Nimodipine Dosage, Warnings, Usage.

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

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5935184-7 | Familial Hemiplegic Migraine, Grand Mal Convulsion
on Oct 21, 2008 Male patient from NORWAY , 16 years of age, was diagnosed with cerebral vasoconstriction, nausea (What is nausea?), migraine (What is migraine?), familial hemiplegic migraine and was treated with Nimodipine (View Usage). Patient experienced the following unwanted or unexpected effects: familial hemiplegic migraine, grand mal convulsion. Nimodipine dosage: . During the same period patient was treated with VERAPAMIL (View Verapamil Review and Verapamil Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), KETOBEMIDONE (View Ketobemidone Review and Ketobemidone Label ), SODIUM CHLORIDE (View Sodium Chloride Review and Sodium Chloride Label ), ACETYLSALICYLIC ACID SRT (View Acetylsalicylic Acid Srt Review and Acetylsalicylic Acid Srt Label ), PROPRANOLOL (View Propranolol Review and Propranolol Label ). Patient was hospitalized.

5614954-9 | Renal Failure Acute
Patient was taking Nimodipine (View Usage). Patient had the following side effects: renal failure acute on Jan 29, 2008 from SPAIN Additional patient health information: Male patient , 80 years of age, weighting 187.4 lb, was diagnosed with metastatic renal cell carcinoma and. Nimodipine dosage: . During the same period patient was treated with SUNITINIB MALATE (View Sunitinib Malate Review and Sunitinib Malate Label ), COZAAR (View Cozaar Review and Cozaar Label ). Patient was hospitalized.

5610608-3 | Blood Pressure Decreased, Breath Sounds Abnormal, Cerebrovascular Accident, Liver Scan Abnormal, Oxygen Saturation Decreased
Adverse event was reported on Jan 23, 2008 by a Female patient taking Nimodipine (View Usage) (Dosage: 2 Poked Caps, Under The Tongue 2 Caps, Single, Intravenous) . Location: UNITED STATES , 63 years of age, weighting 140.0 lb, After Nimodipine was administered, patient had the following side effects: blood pressure decreased, breath sounds abnormal, cerebrovascular accident, liver scan abnormal, oxygen saturation decreased. Patient was hospitalized.

5025044-0 | Gingival Bleeding, Haemorrhage, Increased Tendency To Bruise
on Jun 08, 2006 Female patient from UNITED STATES , 48 years of age, weighting 140.0 lb, was diagnosed with bipolar disorder (What is bipolar disorder?) and was treated with Nimodipine (View Usage). Patient experienced the following unwanted or unexpected effects: gingival bleeding, haemorrhage, increased tendency to bruise. Nimodipine dosage: 1 Q Am Po. During the same period patient was treated with LAMICTAL (View Lamictal Review and Lamictal Label ), ATIVAN (View Ativan Review and Ativan Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), CYTOMEL (View Cytomel Review and Cytomel Label ), DEXEDRINE (View Dexedrine Review and Dexedrine Label ).


4886868-3 | Asphyxia, Disease Recurrence, Dyspnoea, Heart Rate Increased, Pyrexia, Subarachnoid Haemorrhage
on Jan 10, 2006 Male patient from CHINA , 67 years of age, was diagnosed with prophylaxis, vasospasm and was treated with Nimodipine (View Usage). Patient had the following side effects: asphyxia, disease recurrence, dyspnoea, heart rate increased, pyrexia, subarachnoid haemorrhage. Nimodipine dosage: 10 Mg, Total Daily, Intravenous. During the same period patient was treated with CEREBROLYSIN (View Cerebrolysin Review and Cerebrolysin Label ), SODIUM CYTIDINE TRIPHOSPHATE (View Sodium Cytidine Triphosphate Review and Sodium Cytidine Triphosphate Label ), CEFTAZIDIME (View Ceftazidime Review and Ceftazidime Label ), ISOSORBIDE DINITRATE (View Isosorbide Dinitrate Review and Isosorbide Dinitrate Label ), AZOSEMIDE (View Azosemide Review and Azosemide Label ), METOPROLOL (View Metoprolol Review and Metoprolol Label ).

4869718-0 | Asphyxia, Disease Recurrence, Dyspnoea, Infection, Pyrexia, Subarachnoid Haemorrhage, Tachycardia
Patient was taking Nimodipine (View Usage). After Nimodipine was administered, patient had the following side effects: asphyxia, disease recurrence, dyspnoea, infection (What is infection?), pyrexia, subarachnoid haemorrhage, tachycardia on Dec 15, 2005 from CHINA Additional patient health information: Male patient , 67 years of age, was diagnosed with prophylaxis, vasospasm and. Nimodipine dosage: 10 Mg, Total Daily, Intravenous. During the same period patient was treated with CEREBROLYSIN (View Cerebrolysin Review and Cerebrolysin Label ), SODIUM CYTIDINE TRIPHOSPHATE (View Sodium Cytidine Triphosphate Review and Sodium Cytidine Triphosphate Label ), CEFTAZIDIME (View Ceftazidime Review and Ceftazidime Label ), ISOSORBIDE DINITRATE (View Isosorbide Dinitrate Review and Isosorbide Dinitrate Label ), AZOSEMIDE (View Azosemide Review and Azosemide Label ), METOPROLOL (View Metoprolol Review and Metoprolol Label ).


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Nimodipine Questions, Answers, Feedback and Comments

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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 Nimodipine 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 Nimodipine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Nimodipine 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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How Did You Deal with Side Effects?

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During the same period patient was treated with ARADOIS (View Aradois Review and Aradois Label ), NIMODIPINE (View Nimodipine Review and Nimodipine Label ), TARGIFOR (1/3 ...

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During the same period patient was treated with NIMODIPINE, OMEPRAZOLE. Galvus Side Effects Report: 6274092-1,Infarction on Jul 07, 2009 Male patient from BRAZIL, was ...

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Nimodipine Reactions
Asphyxia
Blood Pressure Decreased
Breath Sounds Abnormal
Cerebrovascular Accident
Disease Recurrence
Dyspnoea
Familial Hemiplegic Migraine
Gingival Bleeding
Grand Mal Convulsion
Haemorrhage
Heart Rate Increased
Increased Tendency To Bruise
InfectionWhat is Infection?
Liver Scan Abnormal
Oxygen Saturation Decreased
Pyrexia
Renal Failure Acute
Subarachnoid Haemorrhage
Tachycardia
Nimodipine 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 Nimodipine 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!