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FDA Adverse Reports: 1. View All

Reserpine FDA safety alerts: No

Reported hospitalizations: 1

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

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5345133-0 | Blood Pressure Increased
on May 24, 2006 Male patient from UNITED STATES , 63 years of age, weighting 239.9 lb, was diagnosed with hypertension and was treated with Reserpine (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased. Reserpine dosage: 0.125 Mg, Qd, Oral. During the same period patient was treated with CHLORTHALIDONE (View Chlorthalidone Review and Chlorthalidone Label ), VERAPAMIL (View Verapamil Review and Verapamil Label ), LIPITOR /NET/ (ATORVASTATIN CALCIUM) (View Lipitor /net/ (atorvastatin Calcium) Review and Lipitor /net/ (atorvastatin Calcium) 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 Reserpine 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 Reserpine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Reserpine 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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Report a Drug Side Effect. ... This anonymous Drug Side Effect Survey has 13 questions and takes less than 2 minutes to complete.

Diazepam, unlike chlorpromazine and reserpine, has no demonstrable peripheral autonomic blocking action, nor does it produce extrapyramidal side effects.

Alteration of synaptic concentrations of catecholamines with either reserpine or tricyclic antidepressants does not alter the actions of dobutamine in animals, which ...

Atarax is unrelated chemically to the phenothiazines, reserpine, meprobamate, or the benzodiazepines. Atarax is not a cortical depressant, but its action may be due to a ...

The signs of hypoglycemia may be reduced or absent in patients taking sympatholytic products such as beta-blockers, clonidine, guanethidine, and reserpine.

Patients receiving catecholamine-depleting drugs, such as reserpine or guanethidine, should be closely monitored, because the added β-blocking action of BYSTOLIC may ...

During the same period patient was treated with RESERPINE (0.25 Mg Bid Po) (View Reserpine Review and Reserpine Label ). Patient was hospitalized.

The signs of hypoglycemia may be reduced or absent in patients taking anti-adrenergic drugs such as beta-blockers, clonidine, guanethidine, and reserpine.

Do not use parenteral reserpine. PRECAUTIONS. Hypotension. Hypotension has been observed during therapy with PARNATE. Symptoms of postural hypotension are seen most commonly ...

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Reserpine 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 Reserpine 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!