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FDA Adverse Reports: 4. View All

Adona FDA safety alerts: No

Reported hospitalizations: 3

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

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4981738-4 | Dyspnoea, Pleural Effusion
on Jan 10, 2006 Female patient from JAPAN , 59 years of age, weighting 108.0 lb, was diagnosed with aplastic anaemia and was treated with Adona (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, pleural effusion. Adona dosage: 90 Mg/d. During the same period patient was treated with MARZULENE S (2 G/d) (View Marzulene S Review and Marzulene S Label ), ZYLORIC (200 Mg/d) (View Zyloric Review and Zyloric Label ), ALFAROL (1 Ug/d) (View Alfarol Review and Alfarol Label ), NEORAL (150 Mg/d) (View Neoral Review and Neoral Label ), NORVASC (5 Mg/d) (View Norvasc Review and Norvasc Label ). Patient was hospitalized.

4762824-0 | Blood Creatinine Increased, Blood Urea Increased, Henoch-schonlein Purpura, Infection, Petechiae, Pyrexia, Renal Impairment
Patient was taking Adona (View Usage). Patient had the following side effects: blood creatinine increased, blood urea increased, henoch-schonlein purpura, infection (What is infection?), petechiae, pyrexia, renal impairment on Oct 27, 2004 from JAPAN Additional patient health information: Male patient , 70 years of age, weighting 156.5 lb, was diagnosed with haemorrhagic diathesis, myelodysplastic syndrome and. Adona dosage: 30 Mg/d. During the same period patient was treated with TRANSAMIN (750 Mg/d) (View Transamin Review and Transamin Label ), PRIMOBOLAN DEPOT INJ (10 Mg/d) (View Primobolan-depot Inj Review and Primobolan-depot Inj Label ), BIOFERMIN R (View Biofermin R Review and Biofermin R Label ), DIFLUCAN (100 Mg/d) (View Diflucan Review and Diflucan Label ), NEORAL (300 Mg/d) (View Neoral Review and Neoral Label ). Patient was hospitalized.

4745300-0 | Blood Creatinine Increased, Blood Urea Increased, Henoch-schonlein Purpura, Infection, Petechiae, Pyrexia, Renal Impairment
Adverse event was reported on Oct 27, 2004 by a Male patient taking Adona (View Usage) (Dosage: 30 Mg/d) was diagnosed with haemorrhagic diathesis, myelodysplastic syndrome and. Location: JAPAN , 70 years of age, weighting 156.5 lb, After Adona was administered, patient had the following side effects: blood creatinine increased, blood urea increased, henoch-schonlein purpura, infection (What is infection?), petechiae, pyrexia, renal impairment. During the same period patient was treated with TRANSAMIN (750 Mg/d) (View Transamin Review and Transamin Label ), PRIMOBOLAN DEPOT INJ (10 Mg/d) (View Primobolan-depot Inj Review and Primobolan-depot Inj Label ), BIOFERMIN R (View Biofermin R Review and Biofermin R Label ), DIFLUCAN (100 Mg/d) (View Diflucan Review and Diflucan Label ), NEORAL (300 Mg/d) (View Neoral Review and Neoral Label ).

4578837-8 | Blood Creatinine Increased, Blood Urea Increased, Henoch-schonlein Purpura, Infection, Petechiae, Pyrexia, Renal Impairment
on Oct 27, 2004 Male patient from , 70 years of age, weighting 156.5 lb, was diagnosed with haemorrhagic diathesis, myelodysplastic syndrome and was treated with Adona (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatinine increased, blood urea increased, henoch-schonlein purpura, infection (What is infection?), petechiae, pyrexia, renal impairment. Adona dosage: 30 Mg/d. During the same period patient was treated with TRANSAMIN (750 Mg/d) (View Transamin Review and Transamin Label ), PRIMOBOLAN DEPOT INJ (10 Mg/d) (View Primobolan-depot Inj Review and Primobolan-depot Inj Label ), BIOFERMIN R (View Biofermin R Review and Biofermin R Label ), DIFLUCAN (100 Mg/d) (View Diflucan Review and Diflucan Label ), NEORAL (Unk, Unk) (View Neoral Review and Neoral 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 Adona 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 Adona quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Adona 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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... same period patient was treated with ASPIRIN, VALSARTAN, LASIX (Dose: Twice A Day; 40 Mg In The Morning And 20 Mg At Noon), NOVORAPID (Dose:5 Unit(s)), ALFACALCIDOL, ADONA.<<<<

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Adona Reactions
Blood Creatinine Increased
Blood Urea Increased
Dyspnoea
Henoch-schonlein Purpura
InfectionWhat is Infection?
Petechiae
Pleural Effusion
Pyrexia
Renal Impairment
Adona 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 Adona 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!