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Twinject adverse events reported to FDA.

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Summary

FDA Adverse Reports: 11. View All

Twinject FDA safety alerts: No

Reported hospitalizations: 4

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

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5527454-1 | Device Malfunction
on Nov 07, 2007 Female patient from UNITED STATES , weighting 32.00 lb, was diagnosed with anaphylactic reaction and was treated with Twinject (View Usage). Patient experienced the following unwanted or unexpected effects: device malfunction. Twinject dosage: 0.15 Mg Intramuscular.

5518640-5 | Chest Discomfort, Device Failure
Patient was taking Twinject (View Usage). Patient had the following side effects: chest discomfort, device failure on Oct 25, 2007 from CANADA Additional patient health information: Male patient , 40 years of age, was diagnosed with anaphylactic reaction and. Twinject dosage: (0.3 Mg Intramuscular). Patient was hospitalized.

5391011-0 | Anaphylactic Reaction, Cardio-respiratory Arrest
Adverse event was reported on Jun 28, 2007 by a Female patient taking Twinject (View Usage) (Dosage: (0.3 Mg Prn Intramuscular)) was diagnosed with food allergy (What is food allergy?), hypersensitivity and. Location: UNITED STATES , weighting 167.0 lb, After Twinject was administered, patient had the following side effects: anaphylactic reaction, cardio-respiratory arrest. During the same period patient was treated with PROTONIX /01236201/ (View Protonix /01236201/ Review and Protonix /01236201/ Label ).

5214737-8 | Feeling Jittery
on Jun 02, 2006 Female patient from UNITED STATES , 40 years of age, weighting 107.0 lb, was diagnosed with anaphylactic reaction and was treated with Twinject (View Usage). Patient experienced the following unwanted or unexpected effects: feeling jittery. Twinject dosage: 1 Df Once Sc.


5148233-3 | Device Failure
on Oct 19, 2006 Male patient from CANADA , child 4 years of age, was diagnosed with anaphylactic reaction and was treated with Twinject (View Usage). Patient had the following side effects: device failure. Twinject dosage: 1 Df Twice; Sc.

5122411-1 | Device Malfunction
Patient was taking Twinject (View Usage). After Twinject was administered, patient had the following side effects: device malfunction on Sep 18, 2006 from UNITED STATES Additional patient health information: Female patient , 34 years of age, was diagnosed with hypersensitivity and. Twinject dosage: 1 U Once Sc.

5093137-8 | Device Malfunction
Adverse event was reported on Aug 11, 2006 by a Male patient taking Twinject (View Usage) (Dosage: 1 Df Once Sc) was diagnosed with anaphylactic reaction and. Location: CANADA , 44 years of age, Patient experienced the following unwanted or unexpected effects: device malfunction. Patient was hospitalized.

5086095-3 | Device Failure
on Aug 02, 2006 Male patient from CANADA , 32 years of age, was diagnosed with anaphylactic reaction and was treated with Twinject (View Usage). Patient had the following side effects: device failure. Twinject dosage: 2 Df Once Sc.

5066305-9 | Device Failure
on Jul 11, 2006 Female patient from UNITED STATES , 34 years of age, was diagnosed with hypersensitivity and was treated with Twinject (View Usage). After Twinject was administered, patient had the following side effects: device failure. Twinject dosage: 1 U Once Sc.

5058988-4 | Anaphylactoid Reaction, Contusion
Patient was taking Twinject (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactoid reaction, contusion on Jul 03, 2006 from UNITED STATES Additional patient health information: Female patient , 37 years of age, weighting 125.0 lb, was diagnosed with anaphylactic reaction and. Twinject dosage: 1 Df Once Sc.

5042401-7 | Device Failure
Adverse event was reported on Jun 07, 2006 by a Female patient taking Twinject (View Usage) (Dosage: 1 Df Once Sc) was diagnosed with food allergy (What is food allergy?) and. Location: CANADA , 25 years of age, Patient had the following side effects: device failure. 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 Twinject 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 Twinject quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Twinject 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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Twinject Reactions
Anaphylactic Reaction
Anaphylactoid Reaction
Cardio-respiratory Arrest
Chest Discomfort
Contusion
Device Failure
Device Malfunction
Feeling Jittery
Twinject 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 Twinject 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!