Please choose an event type to view the corresponding MedsFacts report:

FALL ( 26 FDA reports)
DIARRHOEA ( 23 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 20 FDA reports)
RESPIRATORY FAILURE ( 17 FDA reports)
CELLULITIS ( 16 FDA reports)
FEMORAL ARTERY EMBOLISM ( 15 FDA reports)
PERIPHERAL ISCHAEMIA ( 15 FDA reports)
PNEUMONIA ( 15 FDA reports)
UROSEPSIS ( 15 FDA reports)
DYSPNOEA ( 14 FDA reports)
ASTHENIA ( 12 FDA reports)
FATIGUE ( 12 FDA reports)
HAEMOGLOBIN DECREASED ( 12 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 12 FDA reports)
RENAL IMPAIRMENT ( 12 FDA reports)
ANAEMIA ( 11 FDA reports)
ARTHRALGIA ( 11 FDA reports)
HYPERTENSION ( 11 FDA reports)
PULMONARY EMBOLISM ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
VOMITING ( 11 FDA reports)
ATRIAL FIBRILLATION ( 10 FDA reports)
ABDOMINAL DISTENSION ( 9 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 9 FDA reports)
DEATH ( 9 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
CHEST PAIN ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
NEOPLASM MALIGNANT ( 7 FDA reports)
RHEUMATOID ARTHRITIS ( 7 FDA reports)
BRONCHOPNEUMONIA ( 6 FDA reports)
CHOREA ( 6 FDA reports)
CLOSTRIDIUM COLITIS ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
FEMUR FRACTURE ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
MOUTH ULCERATION ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
NEUTROPENIC SEPSIS ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
RASH ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
METASTATIC NEOPLASM ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
COUGH ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
H1N1 INFLUENZA ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
MANIA ( 4 FDA reports)
MENINGITIS ASEPTIC ( 4 FDA reports)
METASTASES TO BONE ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
TEARFULNESS ( 4 FDA reports)
THIRST ( 4 FDA reports)
TUBERCULOSIS ( 4 FDA reports)
ULCER ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BLISTER ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEART TRANSPLANT REJECTION ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HISTIOCYTIC NECROTISING LYMPHADENITIS ( 3 FDA reports)
HUMERUS FRACTURE ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
MULTIPLE FRACTURES ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
PAIN ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
PSORIATIC ARTHROPATHY ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PYELONEPHRITIS ACUTE ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VASCULAR DEMENTIA ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ADENOMA BENIGN ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BOWEN'S DISEASE ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EXPOSED BONE IN JAW ( 2 FDA reports)
EYELID INFECTION ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 2 FDA reports)
PROCTITIS ULCERATIVE ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 2 FDA reports)
SEDATION ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TENDON INJURY ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FISTULA REPAIR ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE UNSPECIFIED ( 1 FDA reports)
HODGKIN'S DISEASE STAGE II ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NIPPLE EXUDATE BLOODY ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAGET'S DISEASE OF THE VULVA ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SCAR EXCISION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STILL'S DISEASE ADULT ONSET ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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