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Tubertest adverse events reported to FDA.

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Summary

FDA Adverse Reports: 17. View All

Tubertest FDA safety alerts: No

Reported hospitalizations: 10

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

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5744934-4 | Deafness, Local Reaction, Mobility Decreased, Monoparesis, Multiple Sclerosis Relapse, Overdose, Paraplegia, Tuberculin Test Positive
on May 14, 2008 Male patient from FRANCE , 38 years of age, weighting 114.6 lb, was diagnosed with tuberculin test and was treated with Tubertest (View Usage). Patient experienced the following unwanted or unexpected effects: deafness, local reaction, mobility decreased, monoparesis, multiple sclerosis relapse, overdose, paraplegia, tuberculin test positive. Tubertest dosage: 0.1 Ml.

5695492-4 | Injection Site Erythema, Overdose
Patient was taking Tubertest (View Usage). Patient had the following side effects: injection site erythema, overdose on Mar 27, 2008 from FRANCE Additional patient health information: Female patient , 20 years of age, weighting 132.3 lb, was diagnosed with tuberculin test and. Tubertest dosage: .

5691158-5 | Injection Site Erythema, Overdose
Adverse event was reported on Mar 27, 2008 by a Female patient taking Tubertest (View Usage) (Dosage: ) was diagnosed with tuberculin test and. Location: FRANCE , 20 years of age, weighting 132.3 lb, After Tubertest was administered, patient had the following side effects: injection site erythema, overdose.

5621296-4 | Angioedema, Hypersensitivity, Injection Site Reaction, Respiratory Disorder, Urticaria
on Jan 31, 2008 Female patient from FRANCE , 23 years of age, weighting 138.9 lb, was diagnosed with tuberculin test and was treated with Tubertest (View Usage). Patient experienced the following unwanted or unexpected effects: angioedema, hypersensitivity, injection site reaction, respiratory disorder, urticaria. Tubertest dosage: . During the same period patient was treated with AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ).


5607441-5 | Angioedema, Hypersensitivity, Injection Site Reaction, Respiratory Disorder, Urticaria
on Jan 21, 2008 Female patient from FRANCE , 23 years of age, weighting 138.9 lb, was diagnosed with tuberculin test and was treated with Tubertest (View Usage). Patient had the following side effects: angioedema, hypersensitivity, injection site reaction, respiratory disorder, urticaria. Tubertest dosage: . During the same period patient was treated with AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ).

5464075-3 | Abscess, Chills, Depressive Symptom, Feeling Hot, Hemiplegia, Infection, Inflammation, Influenza Like Illness, Injected Limb Mobility Decreased
Patient was taking Tubertest (View Usage). After Tubertest was administered, patient had the following side effects: abscess (What is abscess?), chills, depressive symptom, feeling hot, hemiplegia, infection (What is infection?), inflammation, influenza like illness, injected limb mobility decreased on Sep 10, 2007 from FRANCE Additional patient health information: Male patient , 21 years of age, was diagnosed with tuberculin test, immunisation and. Tubertest dosage: . During the same period patient was treated with TICE BCG (Not Rep) (View Tice Bcg Review and Tice Bcg Label ), PRIORIX (View Priorix Review and Priorix Label ), LEGALON (SILYMARIN) (View Legalon (silymarin) Review and Legalon (silymarin) Label ), ORBENINE (CLOXACILLIN) (View Orbenine (cloxacillin) Review and Orbenine (cloxacillin) Label ), VOLTAREN (View Voltaren Review and Voltaren Label ), DEXTROPROPOXYPHENE PARACETAMOL ISOMED (View Dextropropoxyphene Paracetamol Isomed Review and Dextropropoxyphene Paracetamol Isomed Label ), CEFPODOXIME PROXETIL (View Cefpodoxime Proxetil Review and Cefpodoxime Proxetil Label ), HELICIDINE 10% (View Helicidine 10% Review and Helicidine 10% Label ). Patient was hospitalized and became disabled.

5420836-8 | Abscess, Chills, Feeling Hot, Hemiplegia, Inflammation, Injected Limb Mobility Decreased, Pain, Pyrexia
Adverse event was reported on Aug 07, 2007 by a Male patient taking Tubertest (View Usage) (Dosage: ) was diagnosed with tuberculin test and. Location: FRANCE , 21 years of age, Patient experienced the following unwanted or unexpected effects: abscess (What is abscess?), chills, feeling hot, hemiplegia, inflammation, injected limb mobility decreased, pain (What is pain?), pyrexia. Patient was hospitalized and became disabled.

5364644-5 | Chills, Malaise
on Jun 15, 2007 Female patient from FRANCE , 24 years of age, weighting 116.8 lb, was diagnosed with tuberculin test and was treated with Tubertest (View Usage). Patient had the following side effects: chills, malaise. Tubertest dosage: . Patient was hospitalized.

5363143-4 | Haemoptysis, Pruritus, Rash Maculo-papular
on Jun 18, 2007 Female patient from FRANCE , 16 years of age, was diagnosed with tuberculin test and was treated with Tubertest (View Usage). After Tubertest was administered, patient had the following side effects: haemoptysis, pruritus, rash maculo-papular. Tubertest dosage: . Patient was hospitalized.

5359994-2 | Pruritus, Rash Maculo-papular
Patient was taking Tubertest (View Usage). Patient experienced the following unwanted or unexpected effects: pruritus, rash maculo-papular on Jun 12, 2007 from FRANCE Additional patient health information: Female patient , 16 years of age, was diagnosed with tuberculin test and. Tubertest dosage: . Patient was hospitalized.

5359993-0 | Pruritus, Rash, Rash Pruritic
Adverse event was reported on Jun 12, 2007 by a Female patient taking Tubertest (View Usage) (Dosage: ) was diagnosed with tuberculin test and. Location: FRANCE , child 10 years of age, weighting 103.6 lb, Patient had the following side effects: pruritus, rash (What is rash?), rash pruritic. Patient was hospitalized.

5153761-0 | Back Pain, Fatigue, Injection Site Induration, Musculoskeletal Pain, Viral Infection
on Aug 09, 2006 Female patient from FRANCE , 23 years of age, was diagnosed with tuberculin test and was treated with Tubertest (View Usage). After Tubertest was administered, patient had the following side effects: back pain (What is back pain?), fatigue, injection site induration, musculoskeletal pain, viral infection (What is viral infection?). Tubertest dosage: . Patient was hospitalized.

4914884-1 | Hypersensitivity, Leukocyturia, Urticaria
on Feb 09, 2006 Female patient from FRANCE , 77 years of age, weighting 125.7 lb, was diagnosed with tuberculin test and was treated with Tubertest (View Usage). Patient experienced the following unwanted or unexpected effects: hypersensitivity, leukocyturia, urticaria. Tubertest dosage: . During the same period patient was treated with OFLOCET (OFLOXACINE) (View Oflocet (ofloxacine) Review and Oflocet (ofloxacine) Label ), HYPERIUM (RILMENIDINE) (View Hyperium (rilmenidine) Review and Hyperium (rilmenidine) Label ), TANAKAN (GINKGO BILOBA) (View Tanakan (ginkgo Biloba) Review and Tanakan (ginkgo Biloba) Label ), NISISCO (VALSARTAN) (View Nisisco (valsartan) Review and Nisisco (valsartan) Label ). Patient was hospitalized.

4902640-X | Injection Site Erythema, Injection Site Necrosis, Injection Site Oedema, Injection Site Ulcer
Patient was taking Tubertest (View Usage). Patient had the following side effects: injection site erythema, injection site necrosis, injection site oedema, injection site ulcer on Jun 28, 2004 from FRANCE Additional patient health information: Female patient , child 12 years of age, was diagnosed with tuberculin test and. Tubertest dosage: .

4894693-2 | Injection Site Erythema, Injection Site Necrosis, Injection Site Oedema, Injection Site Ulcer
Adverse event was reported on Jun 11, 2004 by a Male patient taking Tubertest (View Usage) (Dosage: ) was diagnosed with tuberculin test and. Location: FRANCE , 39 years of age, After Tubertest was administered, patient had the following side effects: injection site erythema, injection site necrosis, injection site oedema, injection site ulcer.

4758669-8 | Abdominal Pain, Albuminuria, Asthenia, Henoch-schonlein Purpura, Oedema, Pain In Extremity, Petechiae, Pyrexia, Vomiting
on Apr 25, 2005 Male patient from FRANCE , child 3 years of age, was diagnosed with tuberculin test and was treated with Tubertest (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), albuminuria, asthenia, henoch-schonlein purpura, oedema, pain in extremity, petechiae, pyrexia, vomiting. Tubertest dosage: . Patient was hospitalized.

4650588-0 | Henoch-schonlein Purpura, Vomiting
on Apr 25, 2005 Male patient from , child 3 years of age, was diagnosed with tuberculin test and was treated with Tubertest (View Usage). Patient had the following side effects: henoch-schonlein purpura, vomiting. Tubertest dosage: . 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 Tubertest 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 Tubertest quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Tubertest 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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Tubertest Reactions
Abdominal PainWhat is Abdominal pain?
AbscessWhat is Abscess?
Albuminuria
Angioedema
Asthenia
Back PainWhat is Back pain?
Chills
Deafness
Depressive Symptom
Fatigue
Feeling Hot
Haemoptysis
Hemiplegia
Henoch-schonlein Purpura
Hypersensitivity
InfectionWhat is Infection?
Inflammation
Injected Limb Mobility Decreased
Injection Site Erythema
Injection Site Necrosis
Injection Site Oedema
Injection Site Reaction
Injection Site Ulcer
Overdose
Pruritus
Pyrexia
Rash Maculo-papular
Respiratory Disorder
Urticaria
Vomiting
Tubertest 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 Tubertest 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!