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Rancepine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 4. View All

Rancepine FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 1

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

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6614711-0 | Cardiac Arrest, Cardio-respiratory Arrest
on Feb 19, 2010 Female patient from UNITED STATES , 31 years of age, was treated with Rancepine (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac arrest (What is cardiac arrest?), cardio-respiratory arrest. Rancepine dosage: . During the same period patient was treated with TOPIRAMATE (View Topiramate Review and Topiramate Label ), ALPRAZOLAM (View Alprazolam Review and Alprazolam Label ), ZIPRASIDONE HCL (View Ziprasidone Hcl Review and Ziprasidone Hcl Label ).

6612934-8 |
Patient was taking Rancepine (View Usage). on Feb 19, 2010 from UNITED STATES Additional patient health information: Female patient , 50 years of age, . Rancepine dosage: . During the same period patient was treated with HYDROCODONE BITARTRATE AND ACETAMINOPHEN (View Hydrocodone Bitartrate And Acetaminophen Review and Hydrocodone Bitartrate And Acetaminophen Label ), OXYCODONE AND ACETAMINOPHEN (View Oxycodone And Acetaminophen Review and Oxycodone And Acetaminophen Label ), PERPHENAZINE (View Perphenazine Review and Perphenazine Label ).

6426014-8 | Inappropriate Antidiuretic Hormone Secretion
Adverse event was reported on Oct 26, 2009 by a Female patient taking Rancepine (View Usage) (Dosage: 200 Mg, Unk) was diagnosed with hypertension, prophylaxis against gastrointestinal ulcer and. Location: GERMANY , 80 years of age, weighting 220.5 lb, After Rancepine was administered, patient had the following side effects: inappropriate antidiuretic hormone secretion. During the same period patient was treated with ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE (1 Df, Qd) (View Enalapril Maleate And Hydrochlorothiazide Review and Enalapril Maleate And Hydrochlorothiazide Label ), TORASEMIDE (2.5 Mg, Qd) (View Torasemide Review and Torasemide Label ), METOPROLOL (50 Mg, Bid) (View Metoprolol Review and Metoprolol Label ), NIFEDIPINE (10 Mg, Bid) (View Nifedipine Review and Nifedipine Label ), OMEPRAZOLE (20 Mg, Qd) (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

6090962-1 | Coma, Suicide Attempt
on Feb 17, 2009 Female patient from NETHERLANDS , 14 years of age, was treated with Rancepine (View Usage). Patient experienced the following unwanted or unexpected effects: coma, suicide attempt. Rancepine dosage: . During the same period patient was treated with PARACETAMOL (View Paracetamol Review and Paracetamol Label ), PHENYTOIN (View Phenytoin Review and Phenytoin 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 Rancepine 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 Rancepine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Rancepine 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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Rancepine Reactions
Cardiac ArrestWhat is Cardiac arrest?
Cardio-respiratory Arrest
Coma
Death
Inappropriate Antidiuretic Hormone Secretion
Respiratory Arrest
Suicide Attempt
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