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PULMONARY FUNCTION TEST DECREASED side effect

What is PULMONARY FUNCTION TEST DECREASED ?
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Drugs associated with PULMONARY FUNCTION TEST DECREASED

ADVAIR  AERX  ATIVAN  CIPROFLOXACIN  COREG  ENDOTOXIN  EXUBERA  FLOVENT  INSULIN  MYFORTIC  PROAIR  PULMICORT  QVAR  RAPAMUNE  RHINOCORT  SEROQUEL  SPIRIVA  SYMBICORT  TACROLIMUS  VELCADE  


Aerx Side Effects Report #5654615-3
Physician from UNITED KINGDOM reported AERX SOLUTION problem on Feb 27, 2008. Female patient, weighting 124.8 lb, was diagnosed with insulin-requiring type 2 diabetes mellitus and was treated with AERX SOLUTION. After drug was administered, patient experienced the following problems/side effects: pulmonary function test decreased, . AERX SOLUTION dosage: unknown. During the same period patient was treated with INSULIN DETEMIR FLEXPEN, ASPIRIN, FLUVASTATIN, SERTRALINE, ESTRACOMBI. Patient recovered.

Endotoxin Side Effects Report #5688318-6
ENDOTOXIN problem was reported by a Physician from UNITED STATES on Mar 28, 2008. Male patient, weighting 194.4 lb, was treated with ENDOTOXIN. After drug was administered, patient experienced the following problems/side effects: pulmonary function test decreased, . ENDOTOXIN dosage: unknown. During the same period patient was treated with AMOXICILLIN, LACTOSE. Patient was hospitalized. Patient recovered.

Aerx Side Effects Report #5514226-7
Physician from UNITED KINGDOM reported AERX SOLUTION problem on Nov 02, 2007. Female patient, weighting 124.8 lb, was diagnosed with insulin-requiring type ii diabetes mellitus and was treated with AERX SOLUTION. After drug was administered, patient experienced the following problems/side effects: pulmonary function test decreased, . AERX SOLUTION dosage: unknown. During the same period patient was treated with INSULIN DETEMIR FLEXPEN, ASPIRINE, FLUVASTATIN, SERTRALINE, ESTRACOMBI. Patient recovered.

Insulin Side Effects Report #5518029-9
INSULIN DETEMIR FLEXPEN problem was reported by a Physician from UNITED KINGDOM on Nov 02, 2007. Female patient, weighting 124.8 lb, was diagnosed with insulin-requiring type ii diabetes mellitus and was treated with INSULIN DETEMIR FLEXPEN. After drug was administered, patient experienced the following problems/side effects: pulmonary function test decreased, . INSULIN DETEMIR FLEXPEN dosage: unknown. During the same period patient was treated with AERX SOLUTION, ASPIRINE, FLUVASTATIN, SERTRALINE, ESTRACOMBI. Patient recovered.


Ciprofloxacin Side Effects Report #5389364-2
Pharmacist from JAPAN reported CIPROFLOXACIN problem on July 12, 2007. Female patient was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: pulmonary function test decreased, . CIPROFLOXACIN dosage: UNIT DOSE: 200 MG. Patient recovered.

Velcade Side Effects Report #5392963-5
VELCADE problem was reported by a Physician from UNITED STATES on July 06, 2007. Male patient, 73 years of age, was diagnosed with mantle cell lymphoma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: pulmonary function test decreased, pulmonary toxicity, . VELCADE dosage: 2.75 MG, INTRAVENOUS. During the same period patient was treated with RITUXIMAB, CYCLOPHOSPHAMIDE, VINCRISTINE, ADRIAMYCIN PFS, DEXAMETHASONE, CLONIDINE, CRESTOR, ASPIRIN. Patient recovered.

Ciprofloxacin Side Effects Report #5389364-2
Pharmacist from JAPAN reported CIPROFLOXACIN problem on July 12, 2007. Female patient was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: pulmonary function test decreased, . CIPROFLOXACIN dosage: UNIT DOSE: 200 MG. Patient recovered.

Velcade Side Effects Report #5392963-5
VELCADE problem was reported by a Physician from UNITED STATES on July 06, 2007. Male patient, 73 years of age, was diagnosed with mantle cell lymphoma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: pulmonary function test decreased, pulmonary toxicity, . VELCADE dosage: 2.75 MG, INTRAVENOUS. During the same period patient was treated with RITUXIMAB, CYCLOPHOSPHAMIDE, VINCRISTINE, ADRIAMYCIN PFS, DEXAMETHASONE, CLONIDINE, CRESTOR, ASPIRIN. Patient recovered.

Spiriva Side Effects Report #5756083-X
Physician from JAPAN reported SPIRIVA problem on May 27, 2008. Male patient, 82 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: pulmonary function test decreased, . SPIRIVA dosage: unknown. During the same period patient was treated with BLOPRESS, SEREVENT. Patient recovered.


Spiriva Side Effects Report #5726324-3
SPIRIVA problem was reported by a Physician from JAPAN on Apr 28, 2008. Male patient, 82 years of age, was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: pulmonary function test decreased, . SPIRIVA dosage: unknown. During the same period patient was treated with SEREVENT, BLOPRESS. Patient recovered.

Spiriva Side Effects Report #5744570-X
Physician from JAPAN reported SPIRIVA problem on May 14, 2008. Male patient, 82 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: pulmonary function test decreased, . SPIRIVA dosage: unknown. During the same period patient was treated with SEREVENT, BLOPRESS. Patient recovered.

Qvar Side Effects Report #5693567-7
QVAR problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 02, 2008. Female patient, weighting 150.0 lb, was diagnosed with asthma and was treated with QVAR. After drug was administered, patient experienced the following problems/side effects: pulmonary function test decreased, . QVAR dosage: unknown. During the same period patient was treated with PROVENTIL. Patient recovered.

Myfortic Side Effects Report #5672380-0
Physician from SWITZERLAND reported MYFORTIC VS EVEROLIMUS problem on Mar 11, 2008. Female patient, 35 years of age, weighting 112.4 lb, was diagnosed with lung transplant and was treated with MYFORTIC VS EVEROLIMUS. After drug was administered, patient experienced the following problems/side effects: c-reactive protein increased, pulmonary function test decreased, respiratory tract infection, . MYFORTIC VS EVEROLIMUS dosage: 360 MG 2 X 4. During the same period patient was treated with MYFORTIC VS EVEROLIMUS. Patient was hospitalized. Patient recovered.

Proair Side Effects Report #5586308-5
PROAIR HFA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 07, 2008. Male patient, weighting 235.0 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with PROAIR HFA. After drug was administered, patient experienced the following problems/side effects: pulmonary function test decreased, respiratory disorder, . PROAIR HFA dosage: unknown. Patient recovered.


Tacrolimus Side Effects Report #5578689-3
Physician from GERMANY reported TACROLIMUS problem on Dec 11, 2007. Female patient, 60 years of age, was diagnosed with lung transplant and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: lung transplant rejection, pulmonary function test decreased, . TACROLIMUS dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL, CORTICOSTEROIDS. Patient was hospitalized. Patient recovered.

Advair Side Effects Report #5498304-7
ADVAIR DISKUS problem was reported by a Consumer or non-health professional from UNITED STATES on June 04, 2007. Male patient, 66 years of age, was diagnosed with asthma and was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: pulmonary function test decreased, respiratory disorder, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with COMBIVENT, LIPITOR, METOPROLOL TARTRATE, WARFARIN, ASPIRIN. Patient recovered.

Symbicort Side Effects Report #5763620-8
Physician from UNITED STATES reported SYMBICORT problem on June 05, 2008. Male patient, 15 years of age, was treated with SYMBICORT. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, pulmonary function test decreased, . SYMBICORT dosage: unknown. During the same period patient was treated with ALBUTEROL. Patient recovered.

Pulmicort Side Effects Report #5786406-7
PULMICORT problem was reported by a Physician from UNITED STATES on June 26, 2007. Female patient, 17 years of age, was treated with PULMICORT. After drug was administered, patient experienced the following problems/side effects: asthma, pulmonary function test decreased, wheezing, . PULMICORT dosage: unknown. Patient recovered.

Myfortic Side Effects Report #5703687-6
Physician from SWITZERLAND reported MYFORTIC VS EVEROLIMUS problem on Apr 04, 2008. Female patient, 35 years of age, weighting 112.4 lb, was diagnosed with lung transplant and was treated with MYFORTIC VS EVEROLIMUS. After drug was administered, patient experienced the following problems/side effects: c-reactive protein increased, pulmonary function test decreased, respiratory tract infection, . MYFORTIC VS EVEROLIMUS dosage: 360 MG 2 X 4. During the same period patient was treated with MYFORTIC VS EVEROLIMUS. Patient was hospitalized. Patient recovered.


Seroquel Side Effects Report #5259740-7
SEROQUEL problem was reported by a Physician from UNITED STATES on Mar 06, 2007. Female patient, 53 years of age, was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: oxygen saturation decreased, pulmonary function test decreased, . SEROQUEL dosage: unknown. Patient was hospitalized. Patient recovered.

Ativan Side Effects Report #5657988-0
Consumer or non-health professional from UNITED STATES reported ATIVAN problem on Feb 29, 2008. Female patient, weighting 77.00 lb, was diagnosed with anxiety and was treated with ATIVAN. After drug was administered, patient experienced the following problems/side effects: coma, pneumonia, pulmonary function test decreased, respiratory disorder, total lung capacity decreased, . ATIVAN dosage: (0.25 MG BID ORAL). During the same period patient was treated with DORIBAX. Patient died on 02/09/2008.

Coreg Side Effects Report #5515495-X
COREG problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 06, 2007. Male patient, 88 years of age, was diagnosed with atrial fibrillation and was treated with COREG. After drug was administered, patient experienced the following problems/side effects: dyspnoea exertional, pruritus, pulmonary function test decreased, . COREG dosage: 6.25MG TWICE PER DAY. During the same period patient was treated with COUMADIN, PREVACID. Patient recovered.

Exubera Side Effects Report #5549626-2
Physician from UNITED STATES reported EXUBERA problem on Aug 23, 2007. Female patient, 60 years of age, was treated with EXUBERA. After drug was administered, patient experienced the following problems/side effects: chest pain, cough, pulmonary function test decreased, . EXUBERA dosage: unknown. Patient recovered.

Advair Side Effects Report #5497304-0
ADVAIR DISKUS problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 06, 2006. Female patient, 57 years of age, was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, pulmonary function test decreased, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with ALBUTEROL, SINGULAIR. Patient recovered.

Advair Side Effects Report #5497592-0
Consumer or non-health professional from UNITED STATES reported ADVAIR DISKUS problem on Jan 02, 2007. Female patient, 58 years of age, was diagnosed with asthma and was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: pharyngolaryngeal pain, pulmonary function test decreased, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with SYNTHROID, KLONOPIN, LEXAPRO, XOPENEX. Patient recovered.

Rapamune Side Effects Report #5443658-0
RAPAMUNE problem was reported by a Health Professional from AUSTRALIA on Sept 03, 2007. Male patient, weighting 158.7 lb, was treated with RAPAMUNE. After drug was administered, patient experienced the following problems/side effects: dyspnoea, lung infiltration, pulmonary function test decreased, pyrexia, . RAPAMUNE dosage: 1 MG DAILY. During the same period patient was treated with CALTRATE, HYOSCINE, DILTIAZEM, DOXYCYCLINE HYDROCHLORIDE. Patient recovered.

Rhinocort Side Effects Report #5781535-6
Consumer or non-health professional from UNITED STATES reported RHINOCORT problem on Apr 30, 2007. Female patient was diagnosed with seasonal allergy and was treated with RHINOCORT. After drug was administered, patient experienced the following problems/side effects: cough, pseudomembranous colitis, pulmonary function test decreased, sinusitis, . RHINOCORT dosage: unknown. During the same period patient was treated with ADVAIR DISKUS, PULMICORT. Patient recovered.

Pulmicort Side Effects Report #5784266-1
PULMICORT problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 30, 2007. Female patient was diagnosed with seasonal allergy and was treated with PULMICORT. After drug was administered, patient experienced the following problems/side effects: cough, pseudomembranous colitis, pulmonary function test decreased, sinusitis, . PULMICORT dosage: unknown. During the same period patient was treated with ADVAIR DISKUS, RHINOCORT. Patient recovered.

Flovent Side Effects Report #5793123-6
Consumer or non-health professional from UNITED STATES reported FLOVENT problem on June 12, 2008. Male patient, 48 years of age, was treated with FLOVENT. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, pulmonary function test decreased, . FLOVENT dosage: unknown. Patient recovered.

Spiriva Side Effects Report #5333598-X
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 17, 2007. Female patient, 63 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: dyspnoea, pulmonary function test decreased, . SPIRIVA dosage: unknown. During the same period patient was treated with ADVAIR, ALBUTEROL, CLONAPIN, LEXAPRO. Patient recovered.

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