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Predopa adverse events reported to FDA.

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Summary

FDA Adverse Reports: 3. View All

Predopa FDA safety alerts: No

Reported deaths: 3

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

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5363818-7 | Abnormal Behaviour, Delirium, Fall, Muscle Twitching
on Jun 08, 2007 Male patient from JAPAN , 62 years of age, weighting 108.0 lb, was diagnosed with hypotension, abdominal pain (What is abdominal pain?), ileus and was treated with Predopa (View Usage). Patient experienced the following unwanted or unexpected effects: abnormal behaviour, delirium, fall (What is fall?), muscle twitching. Predopa dosage: . During the same period patient was treated with SUBVITAN (1 Df) (View Subvitan Review and Subvitan Label ), ATARAX (View Atarax Review and Atarax Label ), BUSCOPAN (View Buscopan Review and Buscopan Label ), ISOTONIC SODIUM CHLORIDE (120 Ml) (View Isotonic Sodium Chloride Review and Isotonic Sodium Chloride Label ).

5344155-3 | Abnormal Behaviour, Delirium, Fall, Muscle Twitching
Patient was taking Predopa (View Usage). Patient had the following side effects: abnormal behaviour, delirium, fall (What is fall?), muscle twitching on May 23, 2007 from JAPAN Additional patient health information: Male patient , 62 years of age, weighting 108.0 lb, was diagnosed with hypotension, enteritis, abdominal pain (What is abdominal pain?), ileus and. Predopa dosage: 1 Df. During the same period patient was treated with PANSPORIN (2 G) (View Pansporin Review and Pansporin Label ), SUBVITAN (1 Df) (View Subvitan Review and Subvitan Label ), ATARAX (View Atarax Review and Atarax Label ), BUSCOPAN (100 Mg) (View Buscopan Review and Buscopan Label ), ISOTONIC SODIUM CHLORIDE (120 Ml) (View Isotonic Sodium Chloride Review and Isotonic Sodium Chloride Label ).

5333924-1 | Abnormal Behaviour, Delirium, Fall
Adverse event was reported on May 16, 2007 by a Male patient taking Predopa (View Usage) (Dosage: 1 Df) was diagnosed with hypotension, abdominal pain (What is abdominal pain?), ileus and. Location: JAPAN , 62 years of age, weighting 108.0 lb, After Predopa was administered, patient had the following side effects: abnormal behaviour, delirium, fall (What is fall?). During the same period patient was treated with PANSPORIN (2 G) (View Pansporin Review and Pansporin Label ), SUBVITAN (1 Df) (View Subvitan Review and Subvitan Label ), PENTAGIN (View Pentagin Review and Pentagin Label ), ATARAX (View Atarax Review and Atarax Label ), BUSCOPAN (100 Mg) (View Buscopan Review and Buscopan 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 Predopa 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 Predopa quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Predopa 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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Abnormal Behaviour
Delirium
FallWhat is Fall?
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