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Pemetrexed Disodium reports

Browse community reports connected to Pemetrexed Disodium. These reports can show that other people are describing similar experiences, but they do not prove that Pemetrexed Disodium caused a symptom or reaction.

⚕️ Medicine safety note

Community reports do not prove causation, cannot be used to estimate how common a reaction is, and are not medical advice.

25 problems

Abdominal Pain while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and abdominal pain appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Back Pain while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and back pain appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Constipation while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and constipation appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Cough while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and cough appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Decreased Appetite while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and decreased appetite appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Dehydration while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and dehydration appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Diarrhea while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and diarrhea appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Dizziness while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and dizziness appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Fatigue while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and fatigue appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Headache while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and headache appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Hypotension while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and hypotension appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Itching while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and itching appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Malaise while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and malaise appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Nausea while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and nausea appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Pain while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and pain appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Peripheral swelling while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and peripheral swelling appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Rash Maculo-papular while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and rash maculo-papular appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Rash while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and rash appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Shortness of breath while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and shortness of breath appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Skin redness while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and skin redness appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Swelling while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and swelling appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Tachycardia while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and tachycardia appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Vomiting while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and vomiting appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Weakness while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and weakness appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Decreased while using Pemetrexed Disodium

FDA FAERS contains adverse-event reports in which Pemetrexed Disodium and weight decreased appear together. This does not establish that Pemetrexed Disodium caused the reported reaction and cannot be used to estimate how often it occurs.

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