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Dopacol adverse events reported to FDA.

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Summary

FDA Adverse Reports: 3. View All

Dopacol FDA safety alerts: No

Reported deaths: 3

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

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5519401-3 | Cerebral Haemorrhage, Hypertension
on Nov 12, 2007 Female patient from JAPAN , 62 years of age, weighting 94.80 lb, was diagnosed with parkinson's disease (What is parkinson's disease?), iron deficiency anaemia and was treated with Dopacol (View Usage). Patient experienced the following unwanted or unexpected effects: cerebral haemorrhage, hypertension. Dopacol dosage: 4.5 Df/d. During the same period patient was treated with FERROMIA (50 Mg/d) (View Ferromia Review and Ferromia Label ), COMTAN (300 Mg/day) (View Comtan Review and Comtan Label ).

5487122-1 | Cerebral Haemorrhage, Hypertension
Patient was taking Dopacol (View Usage). Patient had the following side effects: cerebral haemorrhage, hypertension on Oct 09, 2007 from JAPAN Additional patient health information: Female patient , 62 years of age, weighting 94.80 lb, was diagnosed with parkinson's disease (What is parkinson's disease?), iron deficiency anaemia and. Dopacol dosage: 4.5 Df/d. During the same period patient was treated with FERROMIA (50 Mg/d) (View Ferromia Review and Ferromia Label ), COMTAN (300 Mg/day) (View Comtan Review and Comtan Label ).

5405620-3 | Cerebral Haemorrhage
Adverse event was reported on Aug 02, 2007 by a Female patient taking Dopacol (View Usage) (Dosage: 600 Mg, Unk) . Location: JAPAN , 63 years of age, After Dopacol was administered, patient had the following side effects: cerebral haemorrhage. During the same period patient was treated with FERROMIA (50 Mg, Unk) (View Ferromia Review and Ferromia Label ), COMTADE (300 Mg/day) (View Comtade Review and Comtade 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 Dopacol 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 Dopacol quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Dopacol 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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