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Prodif adverse events reported to FDA.

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Summary

FDA Adverse Reports: 5. View All

Prodif FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 3

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

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6905531-8 | International Normalised Ratio Increased
on Jul 23, 2010 Female patient from JAPAN , 42 years of age, was diagnosed with systemic candida, atrial fibrillation (What is atrial fibrillation?), basedow's disease, cardiac failure, agranulocytosis and was treated with Prodif (View Usage). Patient experienced the following unwanted or unexpected effects: international normalised ratio increased. Prodif dosage: 200 Mg, 1x/day. During the same period patient was treated with VFEND (200 Mg, 2x/day) (View Vfend Review and Vfend Label ), THYRADIN S (25 Ug, 1x/day) (View Thyradin S Review and Thyradin S Label ), WARFARIN (0.5 Mg, 1x/day) (View Warfarin Review and Warfarin Label ), LUGOL CAP (70 Mg, 1x/day) (View Lugol Cap Review and Lugol Cap Label ), ARTIST (2.5 Mg, 1x/day) (View Artist Review and Artist Label ), ALDACTONE (2.5 Mg, 1x/day) (View Aldactone Review and Aldactone Label ), COTRIM (Unk) (View Cotrim Review and Cotrim Label ).

6819402-9 | International Normalised Ratio Increased
Patient was taking Prodif (View Usage). Patient had the following side effects: international normalised ratio increased on Jun 25, 2010 from JAPAN Additional patient health information: Female patient , 40 years of age, . Prodif dosage: . During the same period patient was treated with VFEND (600 Mg, 1x/day) (View Vfend Review and Vfend Label ), WARFARIN (View Warfarin Review and Warfarin Label ).

6490862-9 | Adrenocortical Insufficiency Acute, Agranulocytosis, Anaemia, Hepatic Failure, Liver Disorder, Thrombocytopenia
Adverse event was reported on Dec 01, 2009 by a Male patient taking Prodif (View Usage) (Dosage: 1009 Mg, 1x/day) was diagnosed with systemic mycosis, rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: JAPAN , 59 years of age, weighting 132.3 lb, After Prodif was administered, patient had the following side effects: adrenocortical insufficiency acute, agranulocytosis, anaemia, hepatic failure, liver disorder, thrombocytopenia. During the same period patient was treated with AZULFIDINE (View Azulfidine Review and Azulfidine Label ), RHEUMATREX (2 Mg, 2x/day) (View Rheumatrex Review and Rheumatrex Label ), ASPIRIN (Unk) (View Aspirin Review and Aspirin Label ), ADALAT CC (Unk) (View Adalat Cc Review and Adalat Cc Label ), CARDENALIN (Unk) (View Cardenalin Review and Cardenalin Label ), LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (Unk) (View Losartan Potassium And Hydrochlorothiazide Review and Losartan Potassium And Hydrochlorothiazide Label ), EPLERENONE (Unk) (View Eplerenone Review and Eplerenone Label ). Patient was hospitalized.

4684444-9 | Acute Respiratory Distress Syndrome, Blood Beta-d-glucan Increased, Blood Culture Positive, Blood Pressure Decreased, C-reactive Protein Increased, Chest X-ray Abnormal, Coronary Arterial Stent Insertion, Diarrhoea
on Apr 08, 2005 Male patient from , 66 years of age, weighting 132.3 lb, was diagnosed with systemic mycosis, shock and was treated with Prodif (View Usage). Patient experienced the following unwanted or unexpected effects: acute respiratory distress syndrome, blood beta-d-glucan increased, blood culture positive, blood pressure decreased, c-reactive protein increased, chest x-ray abnormal, coronary arterial stent insertion, diarrhoea. Prodif dosage: 400 Mg/d. During the same period patient was treated with PREDNISOLONE ACETATE (30 Mg/d) (View Prednisolone Acetate Review and Prednisolone Acetate Label ), SOLU MEDROL (1 G/d) (View Solu-medrol Review and Solu-medrol Label ), CATABON (10 Ml/d) (View Catabon Review and Catabon Label ), FLUMARIN (1 G/d) (View Flumarin Review and Flumarin Label ), MODACIN (1 G/d) (View Modacin Review and Modacin Label ), PERSANTIN (View Persantin Review and Persantin Label ). Patient was hospitalized.


4664541-4 | Blood Beta-d-glucan Increased, Blood Culture Positive, Blood Pressure Decreased, C-reactive Protein Increased, Chest X-ray Abnormal, Escherichia Infection, Granulocytopenia, Hypoxia
on Apr 08, 2005 Male patient from , 66 years of age, weighting 132.3 lb, was diagnosed with systemic mycosis, shock and was treated with Prodif (View Usage). Patient had the following side effects: blood beta-d-glucan increased, blood culture positive, blood pressure decreased, c-reactive protein increased, chest x-ray abnormal, escherichia infection, granulocytopenia, hypoxia. Prodif dosage: 400 Mg/d. During the same period patient was treated with PREDNISOLONE ACETATE (30 Mg/d) (View Prednisolone Acetate Review and Prednisolone Acetate Label ), SOLU MEDROL (1 G/d) (View Solu-medrol Review and Solu-medrol Label ), CATABON (10 Ml/d) (View Catabon Review and Catabon Label ), FLUMARIN (1 G/d) (View Flumarin Review and Flumarin Label ), MODACIN (1 G/d) (View Modacin Review and Modacin Label ), PERSANTIN (View Persantin Review and Persantin 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 Prodif 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 Prodif quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Prodif 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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Pradif Side Effects - Complete Patient's Guide | User Reviews: Male patient, 69 years of age, weighting 163.1 |Headache|Pradif 400<<<<

During the same period patient was treated with PRODIF (252.3 Mg, 1x/day) (View Prodif Review and Prodif Label ), VANCOMYCIN (0.5 G, 1x/day) (View Vancomycin Review and ...<<<<

During the same period patient was treated with PRODIF (23-mar-2005 To 24-mar-2005 200 Mg/day, Then 25-mar-2005 To 11-apr-2005 100 Mg/day) (View Prodif Review and Prodif ...<<<<

During the same period patient was treated with PRODIF (252.3 Mg Iv) (View Prodif Review and Prodif Label ), KIPRES (10 Mg Qd 050) (View Kipres Review and Kipres Label ), ...<<<<

prodif Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: profenid Episodes: 1: Diagnosed with major depression.Side ...<<<<

During the same period patient was treated with PREDNISOLONE, PRODIF. Solu-medrol Side Effects Report: 5367843-1,Hepatic Failure, Liver Disorder, Transaminases Increased ...<<<<

prodif Episodes: 2: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: prograf Episodes: 2: Diagnosed with major depression.Side ...<<<<

During the same period patient was treated with PRODIF (View Prodif Review and Prodif Label ), CEFMETAZOLE (View Cefmetazole Review and Cefmetazole Label ), GASTER (View ...<<<<

During the same period patient was treated with PRODIF (FOSFLUCONAZOLE) (View Prodif (fosfluconazole) Review and Prodif (fosfluconazole) Label ), VFEND (View Vfend Review and ...<<<<

prodif Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: prograf Episodes: 1: Diagnosed with major depression.Side ...<<<<

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Prodif Reactions
Acute Respiratory Distress Syndrome
Adrenocortical Insufficiency Acute
Agranulocytosis
Anaemia
Blood Beta-d-glucan Increased
Blood Culture Positive
Blood Pressure Decreased
C-reactive Protein Increased
Chest X-ray Abnormal
Coronary Arterial Stent Insertion
Diarrhoea
Escherichia Infection
Granulocytopenia
Hepatic Failure
Hypoxia
International Normalised Ratio Increased
Liver Disorder
Thrombocytopenia
Prodif 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 Prodif 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!