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INCREASED TENDENCY TO BRUISE side effect

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Aleve Side Effects Report #5658878-X
Consumer or non-health professional from UNITED STATES reported ALEVE problem on Apr 30, 2007. Female patient, weighting 187.4 lb, was diagnosed with pain and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, rash, . ALEVE dosage: UNIT DOSE: 220 MG. During the same period patient was treated with ATENOLOL, ACCUPRIL, SYNTHROID, MACRODANTIN, ELAVIL, NEXIUM, AMBIEN, OROVITE. Patient recovered.

Plavix Side Effects Report #5671087-3
PLAVIX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 17, 2008. Female patient, 71 years of age, weighting 140.0 lb, was diagnosed with cerebrovascular accident and was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, . PLAVIX dosage: unknown. Patient recovered.

Arixtra Side Effects Report #5615139-2
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on July 18, 2007. Female patient was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, . ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.

Paroxetine Side Effects Report #5617266-2
PAROXETINE problem was reported by a Consumer or non-health professional from UNITED STATES on June 19, 2007. Female patient was diagnosed with depression and was treated with PAROXETINE. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, . PAROXETINE dosage: 20MG PER DAY. During the same period patient was treated with ASPIRIN. Patient recovered.


Januvia Side Effects Report #5656809-X
Physician from UNITED STATES reported JANUVIA problem on Dec 10, 2007. Female patient was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, . JANUVIA dosage: unknown. Patient recovered.

Plavix Side Effects Report #5622441-7
PLAVIX problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 03, 2007. Female patient was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, scar, thrombotic thrombocytopenic purpura, . PLAVIX dosage: unknown. Patient recovered.

Fosamax Side Effects Report #5535017-7
Health Professional from UNITED KINGDOM reported FOSAMAX problem on Nov 30, 2007. Male patient, 87 years of age, was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, . FOSAMAX dosage: unknown. During the same period patient was treated with CALCIUM CARBONATE AND CHOLECALCIFEROL, ASPIRIN, PREDNISOLONE, SIMVASTATIN. Patient recovered.

Humira Side Effects Report #5559021-8
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 13, 2007. Female patient, weighting 150.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, skin atrophy, skin lesion, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISONE, OXYCODONE HYDROCHLORIDE, VICODIN. Patient recovered.

Concerta Side Effects Report #5464414-3
Consumer or non-health professional from UNITED STATES reported CONCERTA problem on Sept 14, 2007. Female patient, weighting 205.0 lb, was diagnosed with depression, attention deficit/hyperactivity disorder and was treated with CONCERTA. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, menorrhagia, . CONCERTA dosage: unknown. Patient recovered.


Fosamax Side Effects Report #5466186-5
FOSAMAX problem was reported by a Health Professional from UNITED KINGDOM on Sept 19, 2007. Male patient, 87 years of age, was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, . FOSAMAX dosage: unknown. During the same period patient was treated with CALCIUM CARBONATE AND CHOLECALCIFEROL, ASPIRIN, PREDNISOLONE. Patient recovered.

Paxil Side Effects Report #5410502-7
Physician from UNITED STATES reported PAXIL problem on Feb 12, 2007. Female patient, 42 years of age, was diagnosed with depression and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, . PAXIL dosage: 40MG PER DAY. During the same period patient was treated with CELEXA. Patient recovered.

Wellbutrin Side Effects Report #5431459-9
WELLBUTRIN problem was reported by a Consumer or non-health professional from UNITED STATES on July 06, 2007. Female patient, 43 years of age, was treated with WELLBUTRIN. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, . WELLBUTRIN dosage: 300MG PER DAY. During the same period patient was treated with ZOLOFT, AMBIEN, BUSPAR. Patient recovered.

Xenical Side Effects Report #5383948-3
Consumer or non-health professional from UNITED KINGDOM reported XENICAL problem on June 29, 2007. Male patient, 46 years of age, weighting 308.0 lb, was diagnosed with obesity and was treated with XENICAL. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, thrombosis, . XENICAL dosage: unknown. Patient recovered.

Xenical Side Effects Report #5383948-3
XENICAL problem was reported by a Consumer or non-health professional from UNITED KINGDOM on June 29, 2007. Male patient, 46 years of age, weighting 308.0 lb, was diagnosed with obesity and was treated with XENICAL. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, thrombosis, . XENICAL dosage: unknown. Patient recovered.


Humira Side Effects Report #5769764-9
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Apr 08, 2008. Female patient, weighting 110.1 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, . HUMIRA dosage: unknown. Patient recovered.

Citalopram Side Effects Report #5753743-1
CITALOPRAM HYDROBROMIDE problem was reported by a Health Professional from UNITED KINGDOM on May 07, 2008. Female patient, 28 years of age, was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, rash pruritic, . CITALOPRAM HYDROBROMIDE dosage: 20 MG; ORAL. Patient recovered.

Citalopram Side Effects Report #5755947-0
Health Professional from UNITED KINGDOM reported CITALOPRAM HYDROBROMIDE problem on May 12, 2008. Female patient, 28 years of age, was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, rash pruritic, . CITALOPRAM HYDROBROMIDE dosage: 20 MG QD PO. Patient recovered.

Cephalexin Side Effects Report #5325357-9
CEPHALEXIN problem was reported by a Health Professional from UNITED KINGDOM on Apr 23, 2007. Female patient, 45 years of age, weighting 165.3 lb, was diagnosed with urinary tract infection and was treated with CEPHALEXIN. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, jaundice, liver disorder, . CEPHALEXIN dosage: 500 MG, BID, ORAL. Patient recovered.

Dacogen Side Effects Report #5336035-4
Pharmacist from UNITED STATES reported DACOGEN problem on Dec 14, 2006. Female patient was treated with DACOGEN. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, off label use, platelet count decreased, white blood cell count decreased, . DACOGEN dosage: 20 MG/M**2; QD; IV. Patient recovered.


Trileptal Side Effects Report #5337690-5
TRILEPTAL problem was reported by a Health Professional from UNITED STATES on Apr 10, 2006. Female patient, 23 years of age, was diagnosed with grand mal convulsion, depression and was treated with TRILEPTAL. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, platelet count decreased, . TRILEPTAL dosage: 300 MG, BID. During the same period patient was treated with LEXAPRO. Patient recovered.

Crestor Side Effects Report #5237224-X
Consumer or non-health professional from UNITED STATES reported CRESTOR problem on May 24, 2005. Female patient, 73 years of age, weighting 135.0 lb, was diagnosed with blood cholesterol increased and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, muscle atrophy, skin atrophy, weight decreased, . CRESTOR dosage: 5 MG PO. During the same period patient was treated with ELAVIL. Patient recovered.

Crestor Side Effects Report #5241602-2
CRESTOR problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 12, 2005. Female patient, 77 years of age, weighting 169.0 lb, was diagnosed with blood cholesterol increased and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, . CRESTOR dosage: 5 MG QOD PO. During the same period patient was treated with PLAVIX, NORVASC, COZAAR, ISOSORBIDE, TENORMIN, WATER S. Patient recovered.

Byetta Side Effects Report #5244576-3
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Aug 17, 2006. Female patient, 62 years of age, was diagnosed with diabetes mellitus non-insulin-dependent, convulsion and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, injection site rash, rash pruritic, . BYETTA dosage: unknown. During the same period patient was treated with LYRICA, ACTOS. Patient recovered.

Byetta Side Effects Report #5244882-2
BYETTA problem was reported by a Health Professional from UNITED STATES on Aug 10, 2006. Female patient was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: increased tendency to bruise, injection site bruising, . BYETTA dosage: unknown. During the same period patient was treated with ASPIRIN. Patient recovered.

Enbrel Side Effects Report #5548157-3
Physician from UNITED STATES reported ENBREL problem on Mar 14, 2007. Female patient, weighting 148.2 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: depression, increased tendency to bruise, rheumatoid arthritis, . ENBREL dosage: unknown. During the same period patient was treated with TOPROL, DIOVAN, FOLIC ACID, EFFEXOR, SULFASALAZINE, RESTORIL, TYLOX, CALCIUM. Patient recovered.

Humira Side Effects Report #5560295-8
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 31, 2007. Female patient, weighting 145.1 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: haemorrhage, increased tendency to bruise, injection site pain, injection site reaction, . HUMIRA dosage: unknown. Patient recovered.

Humira Side Effects Report #5560361-7
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Nov 01, 2007. Male patient, weighting 178.2 lb, was diagnosed with psoriatic arthropathy, hypertension, blood cholesterol and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: dyspnoea, increased tendency to bruise, . HUMIRA dosage: unknown. During the same period patient was treated with IRBESARTAN, SIMVASTATIN. Patient recovered.

Flovent Side Effects Report #5576569-0
FLOVENT problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 25, 2007. Female patient, 70 years of age, was diagnosed with asthma and was treated with FLOVENT. After drug was administered, patient experienced the following problems/side effects: diarrhoea, increased tendency to bruise, palpitations, skin discolouration, . FLOVENT dosage: unknown. During the same period patient was treated with SYMBICORT. Patient recovered.

Raptiva Side Effects Report #5513560-4
Consumer or non-health professional from SWITZERLAND reported RAPTIVA problem on Nov 12, 2007. Female patient was diagnosed with psoriasis, pain, mineral supplementation, thyroid disorder, anxiety disorder and was treated with RAPTIVA. After drug was administered, patient experienced the following problems/side effects: haematoma, increased tendency to bruise, purpura, . RAPTIVA dosage: unknown. During the same period patient was treated with DAIVOBET, IBUPROFEN, ASCORBIC ACID, CALCIUM, LEVOTHYROXINE, PRAZEPAM, RALOXIFENE, SULPIRIDE. Patient recovered.

Raptiva Side Effects Report #5494673-2
RAPTIVA problem was reported by a Consumer or non-health professional from SWITZERLAND on Oct 12, 2007. Female patient was diagnosed with psoriasis, pain, mineral supplementation, thyroid disorder, anxiety disorder and was treated with RAPTIVA. After drug was administered, patient experienced the following problems/side effects: haematoma, increased tendency to bruise, purpura, . RAPTIVA dosage: unknown. During the same period patient was treated with DAIVOBET, IBUPROFEN, ASCORBIC ACID, CALCIUM, LEVOTHYROXINE, PRAZEPAM, RALOXIFENE, SULPIRIDE. Patient recovered.

Advair Side Effects Report #5496808-4
Consumer or non-health professional from UNITED STATES reported ADVAIR DISKUS problem on Aug 20, 2007. Male patient, 70 years of age, was diagnosed with asthma and was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: contusion, increased tendency to bruise, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with BETOPTIC, TRUSOPT, NASAREL, SINGULAIR, ALLOPURINOL, FUROSEMIDE, POTASSIUM SUPPLEMENT, LISINOPRIL. Patient recovered.

Raptiva Side Effects Report #5472160-5
RAPTIVA problem was reported by a Consumer or non-health professional from SWITZERLAND on Sept 20, 2007. Female patient was diagnosed with psoriasis, pain, mineral supplementation, thyroid disorder, anxiety disorder and was treated with RAPTIVA. After drug was administered, patient experienced the following problems/side effects: haematoma, increased tendency to bruise, purpura, . RAPTIVA dosage: unknown. During the same period patient was treated with DAIVOBET, IBUPROFEN, ASCORBIC ACID, CALCIUM, LEVOTHYROXINE, PRAZEPAM, RALOXIFENE, SULPIRIDE. Patient recovered.

Citalopram Side Effects Report #5743584-3
Physician from UNITED KINGDOM reported CITALOPRAM HYDROBROMIDE problem on May 07, 2008. Female patient, 28 years of age, was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: coagulation test abnormal, increased tendency to bruise, rash pruritic, . CITALOPRAM HYDROBROMIDE dosage: 20 MG, PO. Patient recovered.

Citalopram Side Effects Report #5757413-5
CITALOPRAM HYDROBROMIDE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on May 12, 2008. Female patient, 28 years of age, was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: coagulopathy, increased tendency to bruise, rash pruritic, . CITALOPRAM HYDROBROMIDE dosage: 20 MG QD PO. Patient recovered.

Cephalexin Side Effects Report #5318402-8
Consumer or non-health professional from UNITED KINGDOM reported CEPHALEXIN problem on Apr 18, 2007. Female patient, 45 years of age, was diagnosed with urinary tract infection and was treated with CEPHALEXIN. After drug was administered, patient experienced the following problems/side effects: gamma-glutamyltransferase increased, increased tendency to bruise, jaundice, liver disorder, . CEPHALEXIN dosage: 500 MG (2/ 1DAYS), ORAL. Patient recovered.

Cephalexin Side Effects Report #5324392-4
CEPHALEXIN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Apr 23, 2007. Female patient, 45 years of age, weighting 165.3 lb, was diagnosed with urinary tract infection and was treated with CEPHALEXIN. After drug was administered, patient experienced the following problems/side effects: gamma-glutamyltransferase increased, increased tendency to bruise, jaundice, liver disorder, . CEPHALEXIN dosage: 500 MG; BID; PO. Patient recovered.

Hydrea Side Effects Report #5306058-X
Consumer or non-health professional from UNITED STATES reported HYDREA problem on May 09, 2006. Male patient, 74 years of age, weighting 196.2 lb, was diagnosed with polycythaemia and was treated with HYDREA. After drug was administered, patient experienced the following problems/side effects: fatigue, increased tendency to bruise, rash, . HYDREA dosage: unknown. During the same period patient was treated with PROSCAR. Patient recovered.

Coreg Side Effects Report #5310029-7
COREG problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 25, 2007. Male patient, 72 years of age, was diagnosed with cardiac failure congestive and was treated with COREG. After drug was administered, patient experienced the following problems/side effects: haemorrhage, increased tendency to bruise, . COREG dosage: 3.125MG PER DAY. During the same period patient was treated with LISINOPRIL, LASIX. Patient recovered.

Quetiapine Side Effects Report #5256583-5
Health Professional from UNITED KINGDOM reported QUETIAPINE FUMARATE problem on Feb 21, 2007. Female patient, weighting 173.1 lb, was diagnosed with mania, atrial fibrillation, haemoglobin decreased, gastritis and was treated with QUETIAPINE FUMARATE. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, increased tendency to bruise, international normalised ratio increased, neutropenia, thrombocytopenia, . QUETIAPINE FUMARATE dosage: unknown. During the same period patient was treated with QUETIAPINE FUMARATE, DEPAKOTE, DIGOXIN, ASPIRIN, FERROUS SULPHATE, OMEPRAZOLE. Patient was hospitalized. Patient recovered.

Acitretin Side Effects Report #5283779-9
ACITRETIN problem was reported by a Physician from UNITED KINGDOM on Mar 20, 2006. Male patient, 45 years of age, was diagnosed with pityriasis rubra pilaris, psoriasis and was treated with ACITRETIN. After drug was administered, patient experienced the following problems/side effects: exostosis, increased tendency to bruise, . ACITRETIN dosage: unknown. Patient recovered.

Humira Side Effects Report #5666629-8
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Dec 20, 2007. Female patient, weighting 115.1 lb, was diagnosed with psoriasis, palpitations and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: fatigue, headache, increased tendency to bruise, rash macular, skin lesion, . HUMIRA dosage: unknown. During the same period patient was treated with ATENOLOL, PROGESTERONE, HORMONES. Patient recovered.

Altace Side Effects Report #5672778-0
ALTACE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 09, 2007. Female patient was diagnosed with stent placement and was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: fatigue, hypotension, increased tendency to bruise, muscle spasms, . ALTACE dosage: 1.25 MG, QD. During the same period patient was treated with LIPITOR, PLAVIX, ATENOLOL. Patient recovered.

Plavix Side Effects Report #5622309-6
Consumer or non-health professional from UNITED STATES reported PLAVIX problem on Oct 22, 2007. Female patient, 83 years of age, weighting 135.0 lb, was diagnosed with transient ischaemic attack and was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: decreased appetite, fatigue, increased tendency to bruise, muscular weakness, skin laceration, somnolence, transient ischaemic attack, weight decreased, . PLAVIX dosage: 75 MG QD - ORAL. During the same period patient was treated with ACETYLSALICYLIC ACID SRT, ROPINIROLE, TOLTERODINE TARTRATE, RISEDRONATE, ESOMEPRAZOLE. Patient was hospitalized. Patient recovered.

Plavix Side Effects Report #5622311-4
PLAVIX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 22, 2007. Male patient, 71 years of age, weighting 190.0 lb, was diagnosed with cardiac operation and was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: cystitis, haemorrhage, increased tendency to bruise, . PLAVIX dosage: 75 MG QD - ORAL. During the same period patient was treated with SIMVASTATIN, FUROSEMIDE. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5642410-0
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Dec 03, 2007. Male patient, 63 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: accommodation disorder, cataract, increased tendency to bruise, injection site bruising, skin atrophy, waist circumference increased, . BYETTA dosage: unknown. Patient recovered.

Humira Side Effects Report #5558852-8
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 10, 2007. Male patient, weighting 160.1 lb, was diagnosed with psoriatic arthropathy, glaucoma and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: dizziness, haemorrhagic diathesis, increased tendency to bruise, skin disorder, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, FOSOMAX, GLAUCOMA EYE DROPS. Patient recovered.

Humira Side Effects Report #5558992-3
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Sept 13, 2007. Male patient, weighting 235.5 lb, was diagnosed with psoriasis, psoriatic arthropathy, diabetes mellitus, pain and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: blister, haemorrhagic diathesis, increased tendency to bruise, skin atrophy, skin disorder, . HUMIRA dosage: unknown. During the same period patient was treated with METFORMIN, NAPROXEN. Patient recovered.

Humira Side Effects Report #5560031-5
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 26, 2007. Male patient, weighting 165.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: accidental exposure, impaired healing, increased tendency to bruise, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient recovered.

Humira Side Effects Report #5560402-7
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Nov 01, 2007. Male patient, weighting 116.1 lb, was diagnosed with crohn's disease, depression and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: burning sensation, haemorrhagic diathesis, increased tendency to bruise, libido decreased, rash, throat irritation, vomiting, . HUMIRA dosage: 160MG EVERY TWO WEEKS, THEN 80MG X1, AND THEN 40MG EVERY TWO WEEKS. During the same period patient was treated with AZATHIOPRINE, VENLAFAXIINE, BUPROPION. Patient recovered.

Orencia Side Effects Report #5570458-3
ORENCIA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 18, 2007. Female patient, 35 years of age, weighting 191.8 lb, was treated with ORENCIA. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, fatigue, increased tendency to bruise, joint swelling, . ORENCIA dosage: unknown. During the same period patient was treated with PREDNISONE, SINGULAIR, CYMBALTA, TYLENOL, SONATA, SKELAXIN, MOBIC. Patient recovered.

Betaseron Side Effects Report #5484094-0
Consumer or non-health professional from UNITED STATES reported BETASERON problem on Oct 05, 2007. Female patient, 52 years of age, weighting 138.9 lb, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: idiopathic thrombocytopenic purpura, increased tendency to bruise, multiple sclerosis, . BETASERON dosage: unknown. During the same period patient was treated with IMMUNOGLOBULINS, SOLGAR VM, MAGNESIUM SULPHATE, EPA XTRA FISH OIL, TIZANIDINE. Patient recovered.