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1.5 million people annually are harmed from drug errors.
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From simple mix-ups to fatal overdoses, medication mistakes happen, on average, once a day to every hospital patient, a new report says. Nationwide, at least 1.5 million people annually are harmed from drug errors, more than half of them in nursing homes.
Many Unfavorable Drug Studies Aren’t Published. Nearly a third of antidepressant drug studies are never published in the medical literature, and nearly all of those happen to show that the drug being tests failed to work.
Only Drugs That are Safe Should be put on the Market. Drug developers are just beginning to come to grips with recent FDA oversight reforms and how they will affect drug safety. But, it appears that industry and consumer advocates are not together on how well the overhaul will be able to prevent future drug safety scandals.

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Community-reported Factive side effects:

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Review Factive Safety Reports submitted to FDA

Total Factive reports: 23.
Factive FDA safety alerts: No.
Reported deaths: 2    Reported hospitalizations: 16.
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FDA Reported Factive Side Effects: rash pruritic, rash macular, rash maculo-papular, rash papular, urticaria, dyspnoea, swelling face, rash erythematous, nausea, vision blurred, oedema peripheral.
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Factive Side Effects Report #5676770-1
Consumer or non-health professional from UNITED STATES reported FACTIVE problem on Mar 05, 2008. Female patient, 29 years of age, was diagnosed with bronchopneumonia and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: rash macular, skin exfoliation. FACTIVE dosage: 320 MG, QD, ORAL. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5615248-8
FACTIVE problem was reported by a Consumer or non-health professional from MEXICO on Jan 25, 2008. Female patient, 48 years of age, weighting 143.3 lb, was diagnosed with bronchitis and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, anaphylactic shock, face oedema, heart rate increased, neutrophilia, rash. FACTIVE dosage: 320 MG, QD, ORAL. During the same period patient was treated with DESLORATADINE. Patient recovered.

Factive Side Effects Report #5623833-2
Physician from UNITED STATES reported FACTIVE problem on Jan 24, 2008. Male patient, 38 years of age, weighting 229.9 lb, was diagnosed with lobar pneumonia, influenza immunisation and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, anorexia, asthenia, blood chloride decreased, blood glucose increased, dysstasia, faecal incontinence, fatigue. FACTIVE dosage: 320 MG,QD; ORAL. During the same period patient was treated with FLUVAX, CRESTOR, IMITREX, LEVAQUIN, ZITHROMAX, ALBUTEROL, SYMBICORT, ROCEPHIN. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5627161-0
FACTIVE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 13, 2008. Female patient, 49 years of age, weighting 260.0 lb, was diagnosed with sinusitis and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: anaphylactic reaction. FACTIVE dosage: unknown. Patient recovered.

Factive Side Effects Report #5630025-X
Physician from MEXICO reported FACTIVE problem on Feb 06, 2008. Male patient, 83 years of age, weighting 154.3 lb, was diagnosed with bronchitis and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: hallucination, hypoxia, incoherent, loss of consciousness, pneumonia. FACTIVE dosage: 320 MG, QD, ORAL. During the same period patient was treated with ACETAMINOPHEN, AMBROXOL. Patient died on 01/13/2008.

Factive Side Effects Report #5641085-4
FACTIVE problem was reported by a Physician from MEXICO on Feb 11, 2008. Male patient, 83 years of age, weighting 154.3 lb, was diagnosed with bronchitis, pneumonia and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: hallucination, hypoxia, incoherent, loss of consciousness. FACTIVE dosage: 320 MG, QD, ORAL. During the same period patient was treated with ACETAMINOPHEN, AMBROXOL, SYMBICORT. Patient died on 01/13/2008.

Factive Side Effects Report #5642247-2
Physician from UNITED STATES reported FACTIVE problem on Feb 12, 2008. Male patient, 38 years of age, weighting 229.9 lb, was diagnosed with pneumonia, influenza immunisation and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, anorexia, asthenia, blood chloride decreased, blood glucose increased, dysstasia, faecal incontinence, fatigue. FACTIVE dosage: 320 MG, QD, ORAL. During the same period patient was treated with FLUVAX, CRESTOR, IMITREX, LEVAQUIN, ZITHROMAX, ALBUTEROL, SYMBICORT, ROCEPHIN. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5589457-0
FACTIVE problem was reported by a Pharmacist from UNITED STATES on Jan 10, 2008. Female patient, 55 years of age, weighting 160.0 lb, was diagnosed with bronchitis, sinusitis and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: rash. FACTIVE dosage: unknown. Patient recovered.

Factive Side Effects Report #5599584-X
Physician from UNITED STATES reported FACTIVE problem on Jan 03, 2008. Female patient, 40 years of age, weighting 170.0 lb, was diagnosed with pneumonia and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, atelectasis, blood alkaline phosphatase increased, chills, erythema multiforme, nausea, pain, pulmonary congestion, pyrexia. FACTIVE dosage: 320 MG, QD, ORAL. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5604409-X
FACTIVE problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 23, 2008. Female patient, 71 years of age, weighting 130.0 lb, was diagnosed with bronchitis and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: anaphylactic shock, loss of consciousness, respiratory arrest. FACTIVE dosage: unknown. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5535780-5
Physician from UNITED STATES reported FACTIVE problem on Nov 19, 2007. Male patient, 79 years of age, was diagnosed with pneumonia and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased. FACTIVE dosage: 320 MG, ORAL. During the same period patient was treated with CEFTRIAXONE, GLYBURIDE, LISINOPRIL, SIMVASTATIN, TAMSULOSIN, BISOPROLOL FUMARATE, CLOPIDOGREL. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5543115-7
FACTIVE problem was reported by a Physician from UNITED STATES on Nov 21, 2007. Male patient, 45 years of age, was diagnosed with pneumonia and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: guillain-barre syndrome, nervous system disorder. FACTIVE dosage: 320 MG QD. During the same period patient was treated with CRESTOR, IMITREX, LEVAQUIN, AZITHROMYCIN, ALBUTEROL, SYMBICORT. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5546363-5
Consumer or non-health professional from UNITED STATES reported FACTIVE problem on Dec 06, 2007. Female patient, weighting 151.0 lb, was diagnosed with pneumonia and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: dyspnoea, rash macular, skin burning sensation. FACTIVE dosage: unknown. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5578911-3
FACTIVE problem was reported by a Health Professional from UNITED STATES on Dec 12, 2007. Female patient, 49 years of age, was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: constipation, dyspepsia, dysphonia, stevens-johnson syndrome, tongue blistering, upper respiratory tract infection. FACTIVE dosage: unknown. During the same period patient was treated with SYNTHROID, NADOLOL, ATIVAN, ALBUTEROL. Patient recovered.

Factive Side Effects Report #5523105-0
Health Professional from UNITED STATES reported FACTIVE problem on Nov 01, 2007. Female patient, 31 years of age, was diagnosed with bronchitis and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: stevens-johnson syndrome. FACTIVE dosage: 320 MG, QD. During the same period patient was treated with ACETAMINOPHEN, IBUPROFEN. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5525057-6
FACTIVE problem was reported by a Physician from UNITED STATES on Nov 06, 2007. Male patient, 45 years of age, was diagnosed with pneumonia and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: guillain-barre syndrome. FACTIVE dosage: 320 MG, QD. During the same period patient was treated with CRESTOR, IMITREX, LEVAQUIN, AZITHROMYCIN, ALBUTEROL, SYMBICORT. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5532361-4
Physician from UNITED STATES reported FACTIVE problem on Nov 19, 2007. Female patient, 31 years of age, was diagnosed with bronchitis and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: beta haemolytic streptococcal infection, blood sodium decreased, culture urine positive, ectropion, neutrophil percentage increased, psychotic disorder, toxic shock syndrome streptococcal. FACTIVE dosage: 320 MG, QD. During the same period patient was treated with ACETAMINOPHEN, IBUPROFEN, VITAMIN. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5487929-0
FACTIVE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 12, 2007. Male patient, weighting 248.0 lb, was diagnosed with infection, pulmonary congestion and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: pyrexia, rash papular. FACTIVE dosage: unknown. Patient recovered.

Factive Side Effects Report #5503479-7
Physician from MEXICO reported FACTIVE problem on Oct 11, 2007. Female patient was diagnosed with bronchitis and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: anaphylactic shock, rash vesicular. FACTIVE dosage: 320 MG, QD, ORAL. During the same period patient was treated with DEXAMETHASONE. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5472374-4
FACTIVE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 13, 2007. Female patient, 48 years of age, was diagnosed with urinary tract infection and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: catheter related infection, convulsion, depressed level of consciousness, hallucination, incoherent, movement disorder, renal failure acute, sinusitis, thirst. FACTIVE dosage: unknown. During the same period patient was treated with HYDROCORTISONE, VALSARTAN, BYETTA, MORPHINE. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5452084-X
Physician from UNITED STATES reported FACTIVE problem on May 09, 2007. Female patient, 35 years of age, weighting 153.9 lb, was diagnosed with respiratory disorder and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: rash pruritic. FACTIVE dosage: 320 MG. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5403393-1
FACTIVE problem was reported by a Physician from JORDAN on July 13, 2007. Female patient, 25 years of age, was diagnosed with bronchitis and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: acarodermatitis. FACTIVE dosage: 320 MG, QD. Patient was hospitalized. Patient recovered.

Factive Side Effects Report #5403393-1
Physician from JORDAN reported FACTIVE problem on July 13, 2007. Female patient, 25 years of age, was diagnosed with bronchitis and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: acarodermatitis. FACTIVE dosage: 320 MG, QD. Patient was hospitalized. Patient recovered.


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rash macular, skin exfoliation, alanine aminotransferase increased, anaphylactic shock, face oedema, heart rate increased, neutrophilia, rash, , was diagnosed with bronchopneumonia and was diagnosed with bronchitis and was diagnosed with lobar pneumonia, influenza immunisation and