DEVICE MALFUNCTION side effect
What is DEVICE MALFUNCTION ?Drugs associated with DEVICE MALFUNCTION
ADVAIR ALBUTEROL ASMANEX AVONEX BAMIFIX BYETTA CARDIAC CAVERJECT CLIMARA CLOBETASOL CORTIFOAM DAYTRANA DIASTAT DOPAMINE ENBREL EPINEPHERINE EPINEPHRINE EPIPEN EPOGEN ESTRADERM EXUBERA FENTANYL FORADIL FORASEQ FORTEO HEPARIN HUMALOG HUMIRA IMITREX INOMAX LANTUS LEVEMIR LIORESAL LOVENOX MAXAIR MEDROXYPROGESTER NITRIC NITROGLYCERIN NOVOLOG OPTICLIK PEGASYS PHYTONADIONE PRIMATENE PROAIR PROVENTIL SERETIDE SEVORANE SPIRIVA SYMBICORT TEMODAR TOP TRANSDERM TWINJECT TYSABRI VIAGRA VITAMIN XALATANDEVICE MALFUNCTION : Lioresal Side Effects Report #5654407-5
Consumer or non-health professional from UNITED STATES reported LIORESAL problem on Feb 27, 2008. Male patient was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: device malfunction, ileus, muscle spasms, . LIORESAL dosage: unknown. Patient was hospitalized. Patient recovered.
DEVICE MALFUNCTION : Albuterol Side Effects Report #5671856-X
ALBUTEROL problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 17, 2008. Male patient, 80 years of age, weighting 140.0 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with ALBUTEROL. After drug was administered, patient experienced the following problems/side effects: device malfunction, . ALBUTEROL dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Foradil Side Effects Report #5672541-0
Consumer or non-health professional from UNITED STATES reported FORADIL problem on Mar 10, 2008. Male patient, 62 years of age, was diagnosed with asthma and was treated with FORADIL. After drug was administered, patient experienced the following problems/side effects: device malfunction, dyspnoea, feeling abnormal, lung disorder, pharyngolaryngeal pain, tooth infection, tooth loss, tooth repair, . FORADIL dosage: unknown. During the same period patient was treated with ALBUTEROL. Patient recovered.
DEVICE MALFUNCTION : Foradil Side Effects Report #5612127-7
FORADIL problem was reported by a Physician from UNITED STATES on Jan 29, 2008. Female patient, 66 years of age, weighting 127.0 lb, was diagnosed with bronchial hyperreactivity and was treated with FORADIL. After drug was administered, patient experienced the following problems/side effects: device malfunction, dyspnoea, pneumonia, . FORADIL dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Proventil Side Effects Report #5615518-3
Consumer or non-health professional from UNITED STATES reported PROVENTIL problem on Feb 04, 2008. Female patient, 40 years of age, weighting 150.0 lb, was diagnosed with asthma and was treated with PROVENTIL. After drug was administered, patient experienced the following problems/side effects: device malfunction, . PROVENTIL dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Opticlik Side Effects Report #5620119-7
OPTICLIK problem was reported by a Physician from JAPAN on Feb 01, 2008. Female patient was treated with OPTICLIK. After drug was administered, patient experienced the following problems/side effects: device malfunction, no adverse event, . OPTICLIK dosage: unknown. During the same period patient was treated with LANTUS. Patient recovered.
DEVICE MALFUNCTION : Inomax Side Effects Report #5622585-X
Health Professional from UNITED STATES reported INOMAX problem on Feb 08, 2008. Male patient, 51 years of age, weighting 388.0 lb, was diagnosed with vasodilation procedure and was treated with INOMAX. After drug was administered, patient experienced the following problems/side effects: device malfunction, oxygen saturation decreased, . INOMAX dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Epinephrine Side Effects Report #5626417-5
EPINEPHRINE problem was reported by a Pharmacist from CANADA on Jan 25, 2008. Male patient, weighting 155.0 lb, was diagnosed with hypersensitivity and was treated with EPINEPHRINE. After drug was administered, patient experienced the following problems/side effects: device malfunction, incorrect dose administered, injection site haemorrhage, . EPINEPHRINE dosage: 0.3 MG INTRAMUSCULAR/SUBCUTANEOUS. Patient was hospitalized. Patient recovered.
DEVICE MALFUNCTION : Primatene Side Effects Report #5631348-0
Consumer or non-health professional from UNITED STATES reported PRIMATENE MIST problem on Jan 28, 2008. Male patient, 45 years of age, was diagnosed with asthma and was treated with PRIMATENE MIST. After drug was administered, patient experienced the following problems/side effects: device malfunction, . PRIMATENE MIST dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Foraseq Side Effects Report #5635979-3
FORASEQ problem was reported by a Consumer or non-health professional from BRAZIL on Feb 13, 2008. Female patient, 30 years of age, weighting 242.5 lb, was diagnosed with asthma and was treated with FORASEQ. After drug was administered, patient experienced the following problems/side effects: device malfunction, dyspnoea, endodontic procedure, erythema, hypersensitivity, weight increased, . FORASEQ dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Imitrex Side Effects Report #5638490-9
Consumer or non-health professional from UNITED STATES reported IMITREX problem on Mar 27, 2007. Female patient, 38 years of age, was diagnosed with migraine and was treated with IMITREX. After drug was administered, patient experienced the following problems/side effects: device malfunction, injection site bruising, injection site irritation, . IMITREX dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Xalatan Side Effects Report #5639465-6
XALATAN problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 19, 2008. Female patient was diagnosed with glaucoma and was treated with XALATAN. After drug was administered, patient experienced the following problems/side effects: device malfunction, eye operation, ocular vascular disorder, vascular injury, visual acuity reduced, weight decreased, . XALATAN dosage: unknown. During the same period patient was treated with DILANTIN, PHENOBARBITAL. Patient recovered.
DEVICE MALFUNCTION : Epinephrine Side Effects Report #5639709-0
Consumer or non-health professional from UNITED STATES reported EPINEPHRINE problem on Feb 06, 2008. Female patient was diagnosed with anaphylactic reaction and was treated with EPINEPHRINE. After drug was administered, patient experienced the following problems/side effects: device malfunction, . EPINEPHRINE dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Imitrex Side Effects Report #5640814-3
IMITREX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 12, 2008. Male patient was diagnosed with migraine and was treated with IMITREX. After drug was administered, patient experienced the following problems/side effects: device malfunction, injection site vesicles, . IMITREX dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Opticlik Side Effects Report #5645076-9
Physician from JAPAN reported OPTICLIK problem on Feb 20, 2008. Female patient was treated with OPTICLIK. After drug was administered, patient experienced the following problems/side effects: device malfunction, no adverse event, . OPTICLIK dosage: unknown. During the same period patient was treated with LANTUS. Patient recovered.
DEVICE MALFUNCTION : Lioresal Side Effects Report #5649077-6
LIORESAL problem was reported by a Health Professional from UNITED STATES on Feb 19, 2008. Female patient, 46 years of age, was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: device malfunction, muscle rigidity, muscle spasticity, pyrexia, . LIORESAL dosage: unknown. During the same period patient was treated with ORAL BACLOFEN. Patient recovered.
DEVICE MALFUNCTION : Tysabri Side Effects Report #5590771-3
Consumer or non-health professional from UNITED STATES reported TYSABRI problem on Dec 26, 2007. Female patient, 61 years of age, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: device malfunction, eye swelling, ocular hyperaemia, . TYSABRI dosage: unknown. During the same period patient was treated with REBIF, SYNTHROID, FOSAMAX, LIPITOR, BACTRIM. Patient was hospitalized. Patient recovered.
DEVICE MALFUNCTION : Spiriva Side Effects Report #5595474-7
SPIRIVA problem was reported by a Pharmacist from UNITED STATES on Jan 16, 2008. Female patient was diagnosed with asthma and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: device malfunction, . SPIRIVA dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Epinephrine Side Effects Report #5613317-X
Consumer or non-health professional from CANADA reported EPINEPHRINE problem on Jan 10, 2008. Female patient was diagnosed with anaphylactic reaction and was treated with EPINEPHRINE. After drug was administered, patient experienced the following problems/side effects: device malfunction, dyspnoea, obstructive airways disorder, . EPINEPHRINE dosage: 0.3 MG INTRAMUSCULAR. Patient was hospitalized. Patient recovered.
DEVICE MALFUNCTION : Lioresal Side Effects Report #5614699-5
LIORESAL problem was reported by a Physician from UNITED STATES on Dec 21, 2007. Female patient was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: device malfunction, inappropriate device programming, pneumonia, respiratory failure, . LIORESAL dosage: unknown. Patient was hospitalized. Patient recovered.
DEVICE MALFUNCTION : Enbrel Side Effects Report #5553287-6
Consumer or non-health professional from UNITED STATES reported ENBREL problem on July 13, 2007. Female patient was diagnosed with psoriatic arthropathy, psoriasis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: device malfunction, productive cough, psoriasis, respiratory tract congestion, . ENBREL dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Enbrel Side Effects Report #5555375-7
ENBREL problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 17, 2007. Female patient was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: device malfunction, injection site pain, malaise, rheumatoid arthritis, . ENBREL dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Epinephrine Side Effects Report #5568024-9
Physician from UNITED STATES reported EPINEPHRINE problem on Dec 05, 2007. Male patient was treated with EPINEPHRINE. After drug was administered, patient experienced the following problems/side effects: device malfunction, . EPINEPHRINE dosage: 0.3 MG INTRAMUSCULAR. Patient recovered.
DEVICE MALFUNCTION : Foradil Side Effects Report #5518982-3
FORADIL problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 12, 2007. Female patient was treated with FORADIL. After drug was administered, patient experienced the following problems/side effects: device malfunction, pneumonia, . FORADIL dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Humalog Side Effects Report #5520311-6
Consumer or non-health professional from UNITED STATES reported HUMALOG problem on Nov 15, 2007. Male patient, weighting 290.0 lb, was diagnosed with diabetes mellitus and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: device malfunction, . HUMALOG dosage: unknown. During the same period patient was treated with HUMULIN U. Patient recovered.
DEVICE MALFUNCTION : Maxair Side Effects Report #5520325-6
MAXAIR problem was reported by a Pharmacist from UNITED STATES on Nov 15, 2007. Female patient was treated with MAXAIR. After drug was administered, patient experienced the following problems/side effects: device malfunction, incorrect dose administered, . MAXAIR dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Seretide Side Effects Report #5520879-X
Consumer or non-health professional from BELGIUM reported SERETIDE problem on Nov 09, 2007. Female patient was treated with SERETIDE. After drug was administered, patient experienced the following problems/side effects: device malfunction, . SERETIDE dosage: unknown. During the same period patient was treated with ANTIBIOTICS. Patient recovered.
DEVICE MALFUNCTION : Twinject Side Effects Report #5527454-1
TWINJECT problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 07, 2007. Female patient, weighting 32.00 lb, was diagnosed with anaphylactic reaction and was treated with TWINJECT. After drug was administered, patient experienced the following problems/side effects: device malfunction, . TWINJECT dosage: 0.15 MG INTRAMUSCULAR. Patient recovered.
DEVICE MALFUNCTION : Advair Side Effects Report #5527626-6
Pharmacist from UNITED STATES reported ADVAIR DISKUS problem on Nov 26, 2007. Female patient, 60 years of age, was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: device malfunction, incorrect dose administered, . ADVAIR DISKUS dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Byetta Side Effects Report #5527728-4
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 19, 2007. Female patient was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: device malfunction, . BYETTA dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Proair Side Effects Report #5528050-2
Pharmacist from UNITED STATES reported PROAIR HFA problem on Nov 26, 2007. Male patient, 68 years of age, weighting 220.0 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: device malfunction, . PROAIR HFA dosage: unknown. During the same period patient was treated with PROAIR HFA, FLOVENT HFA. Patient recovered.
DEVICE MALFUNCTION : Byetta Side Effects Report #5528135-0
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 26, 2007. Female patient, 72 years of age, was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: device malfunction, incorrect dose administered, . BYETTA dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Dopamine Side Effects Report #5466625-X
Pharmacist from UNITED STATES reported DOPAMINE HYDROCHLORIDE problem on Sept 21, 2007. Male patient, 80 years of age, was treated with DOPAMINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: device malfunction, incorrect dose administered, loss of consciousness, therapeutic response decreased, . DOPAMINE HYDROCHLORIDE dosage: unknown. During the same period patient was treated with BAXTER COLLEAGUE INFUSION PUMP. Patient recovered.
DEVICE MALFUNCTION : Epinephrine Side Effects Report #5478773-9
EPINEPHRINE problem was reported by a Pharmacist from UNITED STATES on Sept 17, 2007. Male patient was diagnosed with hypersensitivity and was treated with EPINEPHRINE. After drug was administered, patient experienced the following problems/side effects: device malfunction, musculoskeletal chest pain, . EPINEPHRINE dosage: 0.3 MG INTRAMUSCULAR/SUBCUTANEOUS. During the same period patient was treated with ETHANOL. Patient recovered.
DEVICE MALFUNCTION : Advair Side Effects Report #5480469-4
Consumer or non-health professional from UNITED STATES reported ADVAIR HFA problem on Oct 04, 2007. Female patient was treated with ADVAIR HFA. After drug was administered, patient experienced the following problems/side effects: device malfunction, . ADVAIR HFA dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Climara Side Effects Report #5481347-7
CLIMARA PRO problem was reported by a Pharmacist from UNITED STATES on Oct 05, 2007. Female patient, 63 years of age, was diagnosed with hot flush and was treated with CLIMARA PRO. After drug was administered, patient experienced the following problems/side effects: device malfunction, . CLIMARA PRO dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Daytrana Side Effects Report #5481352-0
Pharmacist from UNITED STATES reported DAYTRANA problem on Oct 05, 2007. Female patient, child 9 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with DAYTRANA. After drug was administered, patient experienced the following problems/side effects: device malfunction, . DAYTRANA dosage: 10MG -1.1 MG/HR- QD TRANSDERMAL. Patient recovered.
DEVICE MALFUNCTION : Humalog Side Effects Report #5481378-7
HUMALOG problem was reported by a Pharmacist from UNITED STATES on Oct 05, 2007. Male patient, 64 years of age, was diagnosed with diabetes mellitus and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: device malfunction, . HUMALOG dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Proair Side Effects Report #5485539-2
Consumer or non-health professional from UNITED STATES reported PROAIR HFA problem on Oct 11, 2007. Female patient, 72 years of age, weighting 155.0 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: device malfunction, . PROAIR HFA dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Medroxyprogester Side Effects Report #5487041-0
MEDROXYPROGESTERONE problem was reported by a Health Professional from UNITED STATES on Oct 12, 2007. Female patient was diagnosed with contraception and was treated with MEDROXYPROGESTERONE. After drug was administered, patient experienced the following problems/side effects: device malfunction, . MEDROXYPROGESTERONE dosage: 150MG IM. Patient recovered.
DEVICE MALFUNCTION : Albuterol Side Effects Report #5487714-X
Consumer or non-health professional from UNITED STATES reported ALBUTEROL SULPHATE problem on Oct 15, 2007. Female patient was treated with ALBUTEROL SULPHATE. After drug was administered, patient experienced the following problems/side effects: device malfunction, . ALBUTEROL SULPHATE dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Epipen Side Effects Report #5489712-9
EPIPEN problem was reported by a Health Professional from UNITED STATES on Oct 17, 2007. Female patient was treated with EPIPEN. After drug was administered, patient experienced the following problems/side effects: device malfunction, . EPIPEN dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Proair Side Effects Report #5498520-4
Health Professional from UNITED STATES reported PROAIR HFA problem on Oct 24, 2007. Female patient, 33 years of age, weighting 125.0 lb, was diagnosed with asthma and was treated with PROAIR HFA. After drug was administered, patient experienced the following problems/side effects: device malfunction, respiratory disorder, . PROAIR HFA dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Novolog Side Effects Report #5498542-3
NOVOLOG problem was reported by a Pharmacist from UNITED STATES on Oct 24, 2007. Female patient, 64 years of age, was diagnosed with diabetes mellitus and was treated with NOVOLOG. After drug was administered, patient experienced the following problems/side effects: device malfunction, . NOVOLOG dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Proair Side Effects Report #5500359-8
Consumer or non-health professional from UNITED STATES reported PROAIR HFA problem on Oct 25, 2007. Female patient, 36 years of age, weighting 135.0 lb, was diagnosed with asthma and was treated with PROAIR HFA. After drug was administered, patient experienced the following problems/side effects: device malfunction, . PROAIR HFA dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Viagra Side Effects Report #5502355-3
VIAGRA problem was reported by a Physician from UNITED STATES on Oct 19, 2007. Male patient, weighting 155.4 lb, was diagnosed with erectile dysfunction, diabetes mellitus, anxiety and was treated with VIAGRA. After drug was administered, patient experienced the following problems/side effects: device malfunction, paraesthesia, prostate cancer, . VIAGRA dosage: unknown. During the same period patient was treated with CAVERJECT, GLUCOPHAGE, XANAX. Patient recovered.
DEVICE MALFUNCTION : Proair Side Effects Report #5504804-3
Pharmacist from UNITED STATES reported PROAIR HFA problem on Oct 31, 2007. Male patient, 77 years of age, was diagnosed with asthma and was treated with PROAIR HFA. After drug was administered, patient experienced the following problems/side effects: device malfunction, . PROAIR HFA dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Proair Side Effects Report #5504805-5
PROAIR HFA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 31, 2007. Female patient, weighting 155.0 lb, was diagnosed with asthma and was treated with PROAIR HFA. After drug was administered, patient experienced the following problems/side effects: device malfunction, fear, . PROAIR HFA dosage: unknown. During the same period patient was treated with PROAIR HFA. Patient recovered.
DEVICE MALFUNCTION : Levemir Side Effects Report #5508112-6
Consumer or non-health professional from UNITED STATES reported LEVEMIR problem on July 05, 2007. Male patient, 61 years of age, was diagnosed with insulin-requiring type ii diabetes mellitus and was treated with LEVEMIR. After drug was administered, patient experienced the following problems/side effects: device malfunction, . LEVEMIR dosage: unknown. Patient recovered.
DEVICE MALFUNCTION : Estraderm Side Effects Report #5444255-3
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 04, 2007. Female patient, 32 years of age, weighting 150.0 lb, was diagnosed with assisted fertilisation and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: device malfunction, . ESTRADERM dosage: 0.1MG/DAY 2 PATCHES/ 48 HOURS TRANSDERMAL. Patient recovered.
DEVICE MALFUNCTION : Epinephrine Side Effects Report #5450654-6
Consumer or non-health professional from UNITED STATES reported EPINEPHRINE problem on Aug 27, 2007. Male patient, weighting 118.0 lb, was diagnosed with anaphylactic reaction and was treated with EPINEPHRINE. After drug was administered, patient experienced the following problems/side effects: device malfunction, . EPINEPHRINE dosage: (0.3 MG INTRAMUSCULAR/SUBCUTANEOUS). During the same period patient was treated with ANTIHISTAMINES. Patient recovered.