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Orapred adverse events reported to FDA.

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Summary

FDA Adverse Reports: 7. View All

Orapred FDA safety alerts: No

Reported hospitalizations: 2

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

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5401914-6 | Blood Creatine Phosphokinase Increased, Dysstasia, Electrocardiogram Normal, Extrasystoles, Fatigue, Gait Disturbance, Hypokalaemia, Myalgia, Paralysis
on Jul 11, 2007 Male patient from FRANCE , 19 years of age, was treated with Orapred (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, dysstasia, electrocardiogram normal, extrasystoles, fatigue, gait disturbance, hypokalaemia, myalgia, paralysis (What is paralysis?). Orapred dosage: . Patient was hospitalized.

5295952-4 | Abnormal Behaviour, Blood Glucose Increased, Breath Sounds Abnormal, Phaehyphomycosis
Patient was taking Orapred (View Usage). Patient had the following side effects: abnormal behaviour, blood glucose increased, breath sounds abnormal, phaehyphomycosis on Mar 17, 2007 from INDIA Additional patient health information: Male patient , 40 years of age, was diagnosed with asthma (What is asthma?) and. Orapred dosage: Qd; Po. Patient was hospitalized.

4954438-4 | B-cell Lymphoma, Bedridden, Blood Pressure Decreased, Dehydration, Dilatation Ventricular, Dyspnoea Exertional, Embolism Venous, Mobility Decreased
Adverse event was reported on Mar 07, 2006 by a Female patient taking Orapred (View Usage) (Dosage: 60 Mg, Qd, Oral) was diagnosed with paraneoplastic syndrome and. Location: JAPAN , 67 years of age, After Orapred was administered, patient had the following side effects: b-cell lymphoma, bedridden, blood pressure decreased, dehydration, dilatation ventricular, dyspnoea exertional, embolism venous, mobility decreased.

4666452-7 | Agitation, Atelectasis, Dyspnoea Exacerbated, Flushing, Pneumonia, Pruritus, Respiratory Rate Increased, Swelling Face, Urticaria
on May 04, 2005 Female patient from , weighting 22.05 lb, was diagnosed with bronchospasm and was treated with Orapred (View Usage). Patient experienced the following unwanted or unexpected effects: agitation, atelectasis, dyspnoea exacerbated, flushing, pneumonia (What is pneumonia?), pruritus, respiratory rate increased, swelling face, urticaria. Orapred dosage: 2 Mg/kg, Once, Po. During the same period patient was treated with MONTELUKAST SODIUM (View Montelukast Sodium Review and Montelukast Sodium Label ), ALBUTEROL SULFATE HFA (View Albuterol Sulfate Hfa Review and Albuterol Sulfate Hfa Label ).


4661057-6 | Agitation, Anaphylactic Reaction, Flushing, Respiratory Rate Increased
on Apr 26, 2005 Male patient from , weighting 22.05 lb, was diagnosed with bronchospasm and was treated with Orapred (View Usage). Patient had the following side effects: agitation, anaphylactic reaction, flushing, respiratory rate increased. Orapred dosage: 2 Mg/kg, Once, Po. During the same period patient was treated with MONTELUKAST SODIUM (View Montelukast Sodium Review and Montelukast Sodium Label ), SALBUTAMOL SULFATE (View Salbutamol Sulfate Review and Salbutamol Sulfate Label ).

4604039-2 | Abnormal Behaviour, Affect Lability, Crying, Screaming, Sleep Disorder
Patient was taking Orapred (View Usage). After Orapred was administered, patient had the following side effects: abnormal behaviour, affect lability, crying, screaming, sleep disorder (What is sleep disorder?) on Mar 08, 2005 from Additional patient health information: Male patient , weighting 25.00 lb, was diagnosed with asthma (What is asthma?), bronchiectasis and. Orapred dosage: 4 Ml Daily X 5 Days Oral.

4599393-4 | Abnormal Behaviour, Aggression, Personality Change, Psychomotor Hyperactivity
Adverse event was reported on Mar 03, 2005 by a Female patient taking Orapred (View Usage) (Dosage: 1/2 Tsp A Da For 2 Days Oral) . Location: , weighting 23.00 lb, Patient experienced the following unwanted or unexpected effects: abnormal behaviour, aggression, personality change, psychomotor hyperactivity.


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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 Orapred 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 Orapred quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Orapred 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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During the same period patient was treated with HEPARIN, ORAPRED. Patient died. Prednisone Side Effects Report: 5613405-8,Bronchitis, Memory Impairment, Pulmonary ...

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Orapred Reactions
Abnormal Behaviour
Affect Lability
Aggression
Agitation
Anaphylactic Reaction
Atelectasis
B-cell Lymphoma
Bedridden
Blood Creatine Phosphokinase Increased
Blood Glucose Increased
Blood Pressure Decreased
Breath Sounds Abnormal
Crying
Dehydration
Dilatation Ventricular
Dyspnoea Exacerbated
Dyspnoea Exertional
Dysstasia
Electrocardiogram Normal
Embolism Venous
Extrasystoles
Fatigue
Flushing
Gait Disturbance
Hypokalaemia
Mobility Decreased
Myalgia
ParalysisWhat is Paralysis?
Personality Change
Respiratory Rate Increased
Orapred 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 Orapred 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!