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

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5297424-X | Cerebrovascular Accident, Hypercoagulation, Hypomagnesaemia, Vascular Injury
on Apr 13, 2007 Female patient from JAPAN , 29 years of age, was diagnosed with gastric cancer and was treated with Randa (View Usage). Patient experienced the following unwanted or unexpected effects: cerebrovascular accident, hypercoagulation, hypomagnesaemia, vascular injury. Randa dosage: . During the same period patient was treated with S 1 (View S-1 Review and S-1 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 Randa 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 Randa quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Randa 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 RANDA (Cycle 1 On 17nov08: 25mg/day X5;route Dr Cyc2 Unk-12dec08:17mg/day X5;total Dose 210mg) (View Randa Review and Randa ...

During the same period patient was treated with RANDA (View Randa Review and Randa Label ), TS 1 (View Ts-1 Review and Ts-1 Label ). 6921776-5 | Abdominal Abscess ...

Report a Drug Side Effect. ... This anonymous Drug Side Effect Survey has 13 questions and takes less than 2 minutes to complete.

During the same period patient was treated with PARAPLATIN (View Paraplatin Review and Paraplatin Label ), VEPESID (View Vepesid Review and Vepesid Label ), RANDA (View Randa ...

)During the same period patient was treated with RANDA (16 Mg; 7x/months) (View Randa Review and Randa Label ), IFOMIDE (1 G; 4x/months) (View Ifomide Review and Ifomide Label ).

During the same period patient was treated with FLUOROURACIL (View Fluorouracil Review and Fluorouracil Label ), RANDA (View Randa Review and Randa Label ), DECADRON (View ...

During the same period patient was treated with RANDA (30-90 Mg* Intravenous) (View Randa Review and Randa Label ). 4885893-6 | Corneal Epithelium Disorder, Enophthalmos ...

During the same period patient was treated with RANDA (100 Mg, Other), FOLIAMIN (0.5 Mg, Daily (1/d)), PANVITAN (1 G, Daily (1/d)), CYANOCOBALAMIN (1 Mg, Other), DECADRON ...

During the same period patient was treated with RANDA (View Randa Review and Randa Label ). Patient was hospitalized. 6749712-5 | Dizziness on May 12, 2010 Male patient from ...

During the same period patient was treated with METHOTREXATE SODIUM (View Methotrexate Sodium Review and Methotrexate Sodium Label ), RANDA (View Randa Review and Randa Label ).

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Randa Reactions
Cerebrovascular Accident
Hypercoagulation
Hypomagnesaemia
Vascular Injury
Randa 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 Randa 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!