THERAPEUTIC RESPONSE DECREASED side effect
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Drugs associated with THERAPEUTIC RESPONSE DECREASED
ABATACEPT ACTONEL ADDERALL ADVAIR ALTACE ARANESP AROMASIN ATROVENT AVANDIA AVODART BARACLUDE BETAMETHASONE BEXXAR BOTOX BUPIVACAINE BUPROPION BYETTA CARDURA CEFUROXIME CELLCEPT CIALIS CISPLATIN CLOLAR COMBIVENT CONCERTA CYANOCOBALAMIN DEXEDRINE DEXTROAMPHETAMIN DURAGESIC ENABLEX ENBREL EPOGEN FENTANYL FLOMAX FLOVENT FORTOVASE FOSAMAX GLEEVEC HEPARIN HUMIRA HUMULIN IMITREX INFLIXIMAB INSULIN INVEGA JANUVIA LAMICTAL LAMIVUDINE LEVEMIR LEVOTHYROXINE LORAZEPAM LOTRONEX LOVAZA METHYLPHENIDATE METHYLPREDNISOLO MICARDIS MIRAPEX NABUMETONE NEORAL NEULASTA NEUPOGEN NEXIUM NICOTINE NIFEDIPINE NOVOSEVEN OLMESARTAN OMACOR OPANA ORENCIA PACLITAXELECTION PACLITAZELECTION PAROXETINE PAXIL PEGASYS PEGETRON PRAVASTATIN PREDNISOLONE PROCRIT PROGRAF PROTONIX QUETIAPINE RANITIDINE REBIF REMICADE REQUIP RISPERDAL RITUXAN ROACUTAN ROZEREM RYTHMOL SENSORCAINE SIMVASTATIN SINEMET SPIRIVA TEGRETOL TERBINAFINE TESTOSTERONE TOPAMAX TYLENOL VALTREX VERAMYST VIREAD WELLBUTRIN ZANTAC ZOMIG ZOVIRAXRanitidine Side Effects Report #5648386-4
Health Professional from UNITED STATES reported RANITIDINE problem on Mar 03, 2008. Male patient, 50 years of age, weighting 200.0 lb, was diagnosed with gastrooesophageal reflux disease, schizophrenia and was treated with RANITIDINE. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . RANITIDINE dosage: 150MG 1 PO BID ORAL. Patient recovered.
Requip Side Effects Report #5654822-X
REQUIP problem was reported by a Consumer or non-health professional from UNITED STATES on July 31, 2007. Female patient, 51 years of age, was diagnosed with restless legs syndrome and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . REQUIP dosage: 1MG SEE TEXT. During the same period patient was treated with PREVACID, TRICOR, SIMVASTATIN, FISH OIL, ASPIRIN, CALCIUM. Patient recovered.
Requip Side Effects Report #5654873-5
Consumer or non-health professional from UNITED STATES reported REQUIP problem on Aug 14, 2007. Female patient was diagnosed with restless legs syndrome and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . REQUIP dosage: 1MG AT NIGHT. During the same period patient was treated with METFORMIN. Patient recovered.
Altace Side Effects Report #5672691-9
ALTACE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 26, 2007. Female patient was diagnosed with hypertension and was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ALTACE dosage: 10 MG, QD. Patient recovered.
Mirapex Side Effects Report #5677713-7
Consumer or non-health professional from UNITED STATES reported MIRAPEX problem on Feb 29, 2008. Male patient, 72 years of age, weighting 260.1 lb, was diagnosed with restless legs syndrome and was treated with MIRAPEX. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . MIRAPEX dosage: unknown. During the same period patient was treated with REQUIP, AVAPEX. Patient recovered.
Mirapex Side Effects Report #5680722-5
MIRAPEX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 03, 2008. Female patient, 51 years of age, was diagnosed with restless legs syndrome and was treated with MIRAPEX. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . MIRAPEX dosage: unknown. During the same period patient was treated with LIPITOR. Patient recovered.
Heparin Side Effects Report #5682212-2
Consumer or non-health professional from UNITED STATES reported HEPARIN problem on Mar 27, 2008. Male patient, weighting 205.0 lb, was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . HEPARIN dosage: unknown. Patient recovered.
Heparin Side Effects Report #5682213-4
HEPARIN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 27, 2008. Female patient was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . HEPARIN dosage: unknown. Patient recovered.
Novoseven Side Effects Report #5612198-8
Physician from JAPAN reported NOVOSEVEN problem on Jan 25, 2008. Female patient was diagnosed with acquired haemophilia and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . NOVOSEVEN dosage: 4.8 MG, AT 12:00. During the same period patient was treated with THROMBIN LOCAL SOLUTION, DOPAMINE HYDROCHLORIDE, DOBUTAMINE HYDROCHLORIDE, METOCLOPRAMIDE. Patient was hospitalized. Patient died on 04/13/2004.
Simvastatin Side Effects Report #5615477-3
SIMVASTATIN problem was reported by a Pharmacist from UNITED STATES on Feb 04, 2008. Male patient, 65 years of age, was diagnosed with blood cholesterol increased and was treated with SIMVASTATIN. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . SIMVASTATIN dosage: unknown. During the same period patient was treated with AMLODIPINE, METOPRO SUC. Patient recovered.
Paxil Side Effects Report #5616586-5
Consumer or non-health professional from UNITED STATES reported PAXIL CR problem on Aug 15, 2007. Male patient was diagnosed with panic attack and was treated with PAXIL CR. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . PAXIL CR dosage: 25MG PER DAY. Patient recovered.
Valtrex Side Effects Report #5644897-6
VALTREX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 09, 2007. Male patient was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . VALTREX dosage: 500MG PER DAY. Patient recovered.
Enbrel Side Effects Report #5555221-1
Physician from UNITED STATES reported ENBREL problem on Aug 14, 2007. Male patient, weighting 280.2 lb, was diagnosed with psoriasis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ENBREL dosage: unknown. Patient recovered.
Betamethasone Side Effects Report #5556925-7
BETAMETHASONE problem was reported by a Physician from UNITED STATES on Dec 11, 2007. Female patient was treated with BETAMETHASONE. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . BETAMETHASONE dosage: unknown. Patient recovered.
Humira Side Effects Report #5559532-5
Physician from UNITED STATES reported HUMIRA problem on Oct 03, 2007. Female patient, weighting 400.8 lb, was diagnosed with psoriatic arthropathy and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . HUMIRA dosage: unknown. Patient recovered.
Enbrel Side Effects Report #5562104-X
ENBREL problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 28, 2007. Male patient, weighting 190.3 lb, was diagnosed with psoriasis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ENBREL dosage: unknown. Patient recovered.
Aranesp Side Effects Report #5562451-1
Physician from UNITED STATES reported ARANESP problem on July 20, 2007. Male patient, weighting 210.1 lb, was diagnosed with renal failure chronic and was treated with ARANESP. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ARANESP dosage: unknown. During the same period patient was treated with NORVASC, PHOSLO, CELEXA, VITAMIN CAP, PROTONIX, PREDNISONE, CYTOXAN, FERROUS SULPHATE. Patient recovered.
Avodart Side Effects Report #5568902-0
AVODART problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 30, 2007. Male patient, 74 years of age, was diagnosed with benign prostatic hyperplasia and was treated with AVODART. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . AVODART dosage: .5MG PER DAY. During the same period patient was treated with DIOVAN. Patient recovered.
Avodart Side Effects Report #5569015-4
Consumer or non-health professional from UNITED STATES reported AVODART problem on June 18, 2007. Male patient, 69 years of age, was diagnosed with benign prostatic hyperplasia and was treated with AVODART. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . AVODART dosage: .5MG PER DAY. During the same period patient was treated with TRIAMTERENE AND HYDROCHLOROTHIAZIDE, NORVASC. Patient recovered.
Lovaza Side Effects Report #5588591-9
LOVAZA problem was reported by a Health Professional from UNITED STATES on Nov 01, 2007. Male patient, 40 years of age, was diagnosed with blood triglycerides increased and was treated with LOVAZA. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . LOVAZA dosage: unknown. Patient recovered.
Januvia Side Effects Report #5535349-2
Consumer or non-health professional from UNITED STATES reported JANUVIA problem on Aug 14, 2007. Female patient, 68 years of age, was diagnosed with diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . JANUVIA dosage: 100 MG DAILY PO. During the same period patient was treated with OMEPRAZOLE, PRAVASTATIN. Patient recovered.
Byetta Side Effects Report #5575687-0
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 25, 2007. Female patient, 57 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . BYETTA dosage: unknown. During the same period patient was treated with FORTAMET, COUMADIN. Patient recovered.
Aranesp Side Effects Report #5472506-8
Physician from UNITED KINGDOM reported ARANESP problem on Sept 18, 2007. Female patient, 31 years of age, was diagnosed with renal failure chronic and was treated with ARANESP. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ARANESP dosage: unknown. Patient recovered.
Atrovent Side Effects Report #5495170-0
ATROVENT HFA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 03, 2007. Female patient, 86 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with ATROVENT HFA. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ATROVENT HFA dosage: unknown. During the same period patient was treated with SEREVENT, ALBUTEROL, SINGULAIR, ZYRTEC, ACTONEL, ASPIRIN, VITAMIN CAP. Patient recovered.
Advair Side Effects Report #5495794-0
Consumer or non-health professional from UNITED STATES reported ADVAIR DISKUS problem on Oct 23, 2006. Male patient, 20 years of age, was diagnosed with asthma and was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with SINGULAIR, ALBUTEROL, ALLEGRA. Patient recovered.
Advair Side Effects Report #5496070-2
ADVAIR DISKUS problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 18, 2007. Female patient, 61 years of age, was diagnosed with asthma and was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with ASCORBIC ACID, DIETARY SUPPLEMENT, ASPIRIN. Patient recovered.
Advair Side Effects Report #5496119-7
Consumer or non-health professional from UNITED STATES reported ADVAIR DISKUS problem on Jan 25, 2007. Female patient, 81 years of age, was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ADVAIR DISKUS dosage: unknown. Patient recovered.
Advair Side Effects Report #5496746-7
ADVAIR DISKUS problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 03, 2007. Male patient, 49 years of age, was diagnosed with lung disorder and was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with BENADRYL. Patient recovered.
Advair Side Effects Report #5497243-5
Consumer or non-health professional from UNITED STATES reported ADVAIR DISKUS problem on Sept 18, 2006. Female patient, 61 years of age, was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with CALAN, CLARITIN, VIVELLE. Patient recovered.
Advair Side Effects Report #5498844-0
ADVAIR DISKUS problem was reported by a Consumer or non-health professional from UNITED STATES on July 23, 2007. Female patient, 95 years of age, was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ADVAIR DISKUS dosage: unknown. Patient recovered.
Advair Side Effects Report #5499088-9
Consumer or non-health professional from UNITED STATES reported ADVAIR DISKUS problem on May 29, 2007. Male patient, child 10 years of age, was diagnosed with asthma and was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with ZYRTEC, RHINOCORT, ALBUTEROL, ALLERGY SHOTS. Patient recovered.
Flomax Side Effects Report #5499729-6
FLOMAX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 09, 2007. Male patient, 71 years of age, was diagnosed with benign prostatic hyperplasia, hypertension, diabetes mellitus, gastrooesophageal reflux disease and was treated with FLOMAX. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . FLOMAX dosage: unknown. During the same period patient was treated with ULTRAFLEX, ALTACE, PROSTATA, ASPIRIN, METFORMIN, METOPROLOL, OMEPRAZOLE. Patient recovered.
Spiriva Side Effects Report #5503370-6
Consumer or non-health professional from reported SPIRIVA problem on Oct 30, 2007. Male patient, 66 years of age, was diagnosed with asthma and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . SPIRIVA dosage: unknown. Patient recovered.
Neoral Side Effects Report #5444173-0
NEORAL problem was reported by a Physician from UNITED STATES on Sept 04, 2007. Female patient, child 6 years of age, weighting 98.55 lb, was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . NEORAL dosage: unknown. Patient recovered.
Procrit Side Effects Report #5450262-7
Physician from UNITED STATES reported PROCRIT problem on Sept 04, 2007. Male patient, weighting 173.9 lb, was diagnosed with hiv infection and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . PROCRIT dosage: unknown. During the same period patient was treated with TRUVADA, SUSTIVA, BACTRIM, NEXIUM, ANDROGEL, AMITRIPTYLINE, SEROQUEL. Patient recovered.
Combivent Side Effects Report #5450482-1
COMBIVENT problem was reported by a Pharmacist from UNITED STATES on Sept 04, 2007. Female patient, 62 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with COMBIVENT. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . COMBIVENT dosage: unknown. During the same period patient was treated with BONIVA. Patient recovered.
Procrit Side Effects Report #5455968-1
Physician from UNITED STATES reported PROCRIT problem on Sept 13, 2007. Male patient, weighting 173.9 lb, was diagnosed with hiv infection and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . PROCRIT dosage: unknown. During the same period patient was treated with TRUVADA, SUSTIVA, BACTRIM, NEXIUM, ANDROGEL, AMITRIPTYLINE, SEROQUEL. Patient recovered.
Neoral Side Effects Report #5456599-X
NEORAL problem was reported by a Physician from UNITED STATES on Sept 14, 2007. Female patient, child 10 years of age, weighting 98.33 lb, was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . NEORAL dosage: 100 BID WITH 25MG TABS TOTAL 125MG BD. Patient recovered.
Orencia Side Effects Report #5468477-0
Consumer or non-health professional from UNITED STATES reported ORENCIA problem on June 20, 2007. Female patient, 60 years of age, weighting 220.5 lb, was diagnosed with rheumatoid arthritis and was treated with ORENCIA. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, weight increased, . ORENCIA dosage: unknown. During the same period patient was treated with METHOTREXATE, WARFARIN, CYMBALTA, AMBIEN CR, ETODOLAC, LORTAB. Patient recovered.
Atrovent Side Effects Report #5468829-9
ATROVENT HFA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 17, 2007. Female patient, 86 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with ATROVENT HFA. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ATROVENT HFA dosage: unknown. During the same period patient was treated with SEREVENT, ALBUTEROL, SINGULAIR, ZYRTEC, ACTONEL, ASPIRIN, VITAMIN CAP. Patient recovered.
Neupogen Side Effects Report #5469781-2
Health Professional from UNITED STATES reported NEUPOGEN problem on May 18, 2007. Male patient, 71 years of age, was diagnosed with peripheral blood stem cell apheresis and was treated with NEUPOGEN. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . NEUPOGEN dosage: unknown. Patient recovered.
Procrit Side Effects Report #5469801-5
PROCRIT problem was reported by a Physician from UNITED STATES on Sept 18, 2007. Male patient, weighting 173.9 lb, was diagnosed with hiv infection and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . PROCRIT dosage: unknown. During the same period patient was treated with TRUVADA, SUSTIVA, BACTRIM, NEXIUM, ANDROGEL, AMITRIPTYLINE, SEROQUEL. Patient recovered.
Enablex Side Effects Report #5476479-3
Consumer or non-health professional from UNITED STATES reported ENABLEX problem on May 02, 2007. Female patient, 70 years of age, was diagnosed with hypertonic bladder and was treated with ENABLEX. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . ENABLEX dosage: 7.5 MG, QD, ORAL. Patient recovered.
Imitrex Side Effects Report #5402465-5
IMITREX problem was reported by a Consumer or non-health professional from UNITED STATES on June 19, 2006. Female patient, 54 years of age, was diagnosed with migraine and was treated with IMITREX. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . IMITREX dosage: 100MG TWICE PER DAY. During the same period patient was treated with ZELNORM. Patient recovered.
Concerta Side Effects Report #5407075-1
Pharmacist from CANADA reported CONCERTA problem on July 27, 2007. Male patient, child 12 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with CONCERTA. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . CONCERTA dosage: unknown. Patient recovered.
Fentanyl Side Effects Report #5409331-X
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 01, 2007. Female patient, weighting 170.0 lb, was diagnosed with headache, hypothyroidism, anxiety, depression, blood cholesterol, cardiac disorder, breakthrough pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, type 2 diabetes mellitus, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with SYNTHROID, CYMBALTA, GEMFIBROZIL, ATENOLOL, OXYCODONE. Patient recovered.
Paroxetine Side Effects Report #5410644-6
Consumer or non-health professional from UNITED STATES reported PAROXETINE problem on May 04, 2007. Female patient, 42 years of age, was diagnosed with depression and was treated with PAROXETINE. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . PAROXETINE dosage: 20MG PER DAY. During the same period patient was treated with BUPROPION, XANAX. Patient recovered.
Combivent Side Effects Report #5415891-5
COMBIVENT problem was reported by a Pharmacist from UNITED STATES on July 27, 2007. Female patient, 62 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with COMBIVENT. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . COMBIVENT dosage: unknown. During the same period patient was treated with BONIVA. Patient recovered.
Concerta Side Effects Report #5416929-1
Pharmacist from CANADA reported CONCERTA problem on Aug 13, 2007. Male patient, child 12 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with CONCERTA. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . CONCERTA dosage: unknown. Patient recovered.
Bexxar Side Effects Report #5418020-7
BEXXAR problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 26, 2006. Male patient, 53 years of age, was diagnosed with non-hodgkin's lymphoma and was treated with BEXXAR. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . BEXXAR dosage: unknown. Patient recovered.
Neoral Side Effects Report #5420465-6
Physician from UNITED STATES reported NEORAL problem on Aug 17, 2007. Female patient, child 10 years of age, weighting 98.55 lb, was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: therapeutic response decreased, . NEORAL dosage: unknown. Patient recovered.